Peritoneal Deterioration Inhibitory Composition, Peritoneal Deterioration Inhibitory Composition Kit, Peritoneal Dialysis Solution, and Peritoneal Dialysis Solution Kit

Abstract

Provided is a composition capable of inhibiting peritoneal deterioration.　A peritoneal deterioration inhibiting composition according to the present invention comprises carbon monoxide.

Description

[Technical Field]

[0001] The present invention relates to a peritoneal deterioration-inhibiting composition, a peritoneal deterioration-inhibiting composition kit, a peritoneal dialysis solution, and a peritoneal dialysis solution kit. [Background technology]

[0002] Artificial dialysis is performed as a treatment method to compensate for renal function in patients with impaired renal function. Artificial dialysis includes hemodialysis and peritoneal dialysis. Hemodialysis is performed about three times a week, and each session takes 4 to 5 hours. On the other hand, peritoneal dialysis can be performed once a day with the dialysis fluid changed while the patient is asleep, and has the advantage of improving the patient's quality of life (Non-Patent Document 1). [Prior art documents] [Non-patent literature]

[0003] [Non-Patent Document 1] Qin Zhou et al., “Preventing peritoneal membrane fibrosis in peritoneal dialysis patients”, Kidney International, Volume 90, Issue 3, 2016, Pages 515-524 Summary of the Invention [Problem to be solved by the invention]

[0004] However, in patients undergoing peritoneal dialysis, the peritoneal membrane's function, such as its ability to remove water, deteriorates over time, and peritoneal dialysis becomes impossible 6 to 7 years after the start of peritoneal dialysis. In this case, the patient discontinues peritoneal dialysis and switches to hemodialysis. Therefore, there is a need for a composition that can suppress peritoneal membrane deterioration in order to maintain the duration of peritoneal dialysis for a longer period of time.

[0005] Therefore, an object of the present invention is to provide a composition capable of suppressing deterioration of the peritoneum. [Means for solving the problem]

[0006] To achieve the above object, the composition for inhibiting peritoneal deterioration of the present invention (hereinafter also referred to as "composition") contains carbon monoxide.

[0007] The peritoneal deterioration-suppressing composition kit of the present invention (hereinafter also referred to as "composition kit") contains a peritoneal deterioration-suppressing composition and other components, The peritoneal deterioration inhibiting composition and the other components are arranged separately, The composition for inhibiting peritoneal deterioration is the composition of the present invention.

[0008] The peritoneal dialysis solution of the present invention comprises the composition of the present invention.

[0009] The peritoneal dialysis solution kit of the present invention includes a composition and a peritoneal dialysis solution, The composition and the peritoneal dialysis solution are placed separately, The composition is the composition of the present invention.

[0010] The composition of the present invention is a pharmaceutical composition (hereinafter also referred to as "pharmaceutical composition") for use in preventing or suppressing diseases caused by peritoneal dialysis, and contains carbon monoxide.

[0011] The composition kit of the present invention is a pharmaceutical composition kit (hereinafter also referred to as a "pharmaceutical kit" or "pharmaceutical composition kit") for use in preventing or suppressing diseases caused by peritoneal dialysis, comprising: composition and other ingredients, The composition and the other components are arranged separately, The composition is the composition of the present invention. [Effects of the Invention]

[0012] The composition of the present invention can inhibit deterioration of the peritoneum. [Brief explanation of the drawings]

[0013] [Figure 1] FIG. 1 is a cross-sectional view showing an example of a multi-chamber container containing the composition of the present invention and other components. [Figure 2] FIG. 2 is a schematic diagram showing a microbubble production device in Example 1. [Figure 3] FIG. 3 is a graph showing the amount of drainage in Example 1. [Figure 4] FIG. 4 is a photograph showing peritoneal thickening by tissue staining in Example 1. [Figure 5] FIG. 5 is a photograph showing inflammatory cells by tissue staining in Example 1. [Figure 6] FIG. 6 is a photograph showing the results of CD68 (macrophage marker) staining by immunohistochemical staining in Example 1. [Figure 7] FIG. 7 is a graph showing the macrophage-positive area (%) in Example 1. [Figure 8] FIG. 8 is a photograph showing the results of CD31 (vascular endothelial cell marker) staining by immunohistochemical staining in Example 1. [Figure 9] FIG. 9 is a graph showing the vascular endothelial cell-positive area (%) in Example 1. [Figure 10] FIG. 10 is a photograph showing the results of Lyve-1 (lymphatic vessel marker) staining by immunohistochemical staining in Example 1. [Figure 11] FIG. 11 is a graph showing the results of lymphatic vessel-positive area (%) in Example 1. [Figure 12] FIG. 12 is a graph showing the expression level of each gene in Example 1. [Figure 13] FIG. 13 is a graph showing the amount of peritoneal fluid in Example 2. [Figure 14] FIG. 14 is a graph showing the thickness of the peritoneal surface (peritoneal thickness) in Example 2. [Figure 15] FIG. 15 is a graph showing the expression level of the IL-6 gene in Example 3. [Figure 16]Figure 16 is a graph showing the peritoneal fluid volume in Example 4. Figure 16(A) shows the results for CO-UFB. Figure 16(B) shows the results for CO-UFB 1 / 4. Figure 16(C) shows the results for CO-UFB 1 / 10. Figure 16(D) shows the results for CO-UFB 1 / 50. Figure 16(E) shows the results for CO-dis. Figure 16(F) shows the results for CO-dis 1 / 4. Figure 16(G) shows the results for CO-dis 1 / 10. Figure 16(H) shows the results for CO-dis 1 / 50. DETAILED DESCRIPTION OF THE INVENTION

[0014] <Definition> As used herein, "peritoneum" refers to a membrane that covers part or all of the abdominal organs. The peritoneum is composed of the parietal peritoneum and the visceral peritoneum (including the diaphragm). Under normal conditions, the peritoneum covers the outer surface and is composed of a mesothelial cell layer composed of mesothelial cells and a submesothelial layer composed of connective tissue.

[0015] As used herein, "peritoneal deterioration" refers to a decline in peritoneal function and / or a change in peritoneal morphology. The peritoneal deterioration is preferably peritoneal deterioration occurring during peritoneal dialysis. The "decrease in peritoneal function" refers to a decline or failure in the ultrafiltration function of the peritoneal membrane and / or an increase in peritoneal permeability. The "change in peritoneal morphology" refers to fibrous thickening of the peritoneal membrane and / or sclerotic thickening of the peritoneal membrane. The "peritoneal deterioration" can be evaluated by examining the peritoneal function and / or peritoneal morphology of a subject. The peritoneal function can be evaluated, for example, by a peritoneal equilibration test (PET). The peritoneal function may also be evaluated based on the water removal function in accordance with Example 1 described below. The peritoneal morphology can be evaluated, for example, by biopsy of the subject's peritoneum.

[0016] As used herein, "peritoneal fibrosis" refers to a state in which extracellular matrix such as collagen is deposited in the peritoneum.

[0017] As used herein, "inhibition of peritoneal deterioration" may mean preventing, inhibiting, or stopping a decline in peritoneal function, inhibiting or stopping the progression of a decline in peritoneal function, and / or improving or alleviating (relieving) peritoneal function, or may mean preventing, inhibiting, inhibiting, or stopping changes in peritoneal morphology, inhibiting or stopping the progression of changes in peritoneal morphology, and / or improving or normalizing altered peritoneal morphology.

[0018] As used herein, "inhibition of peritoneal fibrosis" means significant inhibition of peritoneal fibrosis in a subject. The "inhibition of peritoneal fibrosis" can also be expressed, for example, as prevention, suppression, or arrest of peritoneal fibrosis in a subject, inhibition or arrest of the progression of peritoneal fibrosis, and / or improvement or normalization of fibrotic peritoneal tissue. The "inhibition of peritoneal fibrosis" can be evaluated, for example, by determining whether fibrosis is significantly inhibited under conditions in which peritoneal fibrosis is induced. Specifically, the "inhibition of peritoneal fibrosis" can be evaluated as having peritoneal fibrosis-inhibiting activity when, under conditions in which peritoneal fibrosis is induced, fibrosis is significantly inhibited in a group treated with a test substance compared to a control group not treated with the test substance or a control group treated with a substance (control substance) that does not have peritoneal fibrosis-inhibiting activity. The inhibition of peritoneal fibrosis may be evaluated based on peritoneal thickening in a peritoneal deterioration model induced by chlorhexidine gluconate solution, according to Example 1(4) described below.

[0019] As used herein, "suppression of peritoneal inflammation" means that peritoneal inflammation in a subject is significantly suppressed. The "suppression of peritoneal inflammation" can also be expressed, for example, as the prevention, suppression, or arrest of peritoneal inflammation in a subject, and / or the suppression or arrest of the progression (exacerbation) of peritoneal inflammation. The "suppression of peritoneal inflammation" can be evaluated, for example, by determining whether inflammation is significantly suppressed under conditions in which peritoneal inflammation is induced. Specifically, the "suppression of peritoneal inflammation" can be evaluated as having peritoneal inflammation suppressing activity when, under conditions in which peritoneal inflammation is induced, inflammation is significantly suppressed in a group treated with a test substance compared to a control group not treated with the test substance or a control group treated with a substance (control substance) that does not have the activity of suppressing peritoneal inflammation. The suppression of peritoneal inflammation may be evaluated based on the infiltration of macrophages into the peritoneum in a chlorhexidine gluconate solution-induced peritoneal deterioration model in accordance with Example 1(5) described below, and / or the expression level of peritoneal inflammatory cytokines in Example 1(6).

[0020] As used herein, "inhibition of angiogenesis" means significant inhibition of angiogenesis in the peritoneum. Specifically, the "inhibition of angiogenesis" can be evaluated as having angiogenesis inhibitory activity when, under conditions for inducing peritoneal angiogenesis, angiogenesis is significantly inhibited in a group treated with a test substance, compared to a control group not treated with the test substance or a control group treated with a substance (control substance) that does not have inhibitory activity against peritoneal angiogenesis. Inhibition of peritoneal angiogenesis may also be evaluated based on the positive area of ​​a vascular endothelial cell marker in the peritoneum of a chlorhexidine gluconate solution-induced peritoneal deterioration model, as described in Example 1(5) below.

[0021] As used herein, "inhibition of lymphangiogenesis" means significant inhibition of lymphangiogenesis in the peritoneum. Specifically, the "inhibition of lymphangiogenesis" can be evaluated as having lymphangiogenesis inhibitory activity when, under conditions for inducing peritoneal lymphangiogenesis, lymphangiogenesis is significantly inhibited in a test substance-treated group compared to a control group not treated with the test substance or a control group treated with a substance (control substance) that does not have the activity of inhibiting peritoneal lymphangiogenesis. The inhibition of peritoneal lymphangiogenesis may also be evaluated based on the positive area of ​​lymphatic endothelial cell markers in the peritoneum of a chlorhexidine gluconate solution-induced peritoneal deterioration model, as described in Example 1(5) below. In the evaluation of lymphangiogenesis, the peritoneum is preferably the diaphragm.

[0022] As used herein, "positive (+)" means that a higher signal is detected by an analytical method such as immunohistochemical staining, which utilizes an antigen-antibody reaction, compared to a negative control reaction using negative control cells that do not express the antigen or an antibody that does not react with the antigen.

[0023] As used herein, "negative (-)" means that a signal equivalent to or less than that detected in a negative control reaction using negative control cells that do not express the antigen or an antibody that does not react with the antigen is detected.

[0024] In this specification, "microbubbles" refers to a closed, minute space made of gas and surrounded by something other than gas. The "microbubbles" can also be referred to as, for example, fine bubbles. Examples of the microbubbles include fine bubbles. The fine bubbles generally refer to microbubbles having a diameter of less than 100 μm. The bubble diameter refers to the equivalent sphere diameter of the bubbles. The bubble diameter may be the average diameter (arithmetic mean diameter) of microbubbles obtained by the measurement method described below. The fine bubbles (FB) may be microbubbles or ultrafine bubbles (UFB). The microbubbles generally refer to microbubbles having a diameter of 1 μm or more and less than 100 μm. The ultrafine bubbles generally refer to microbubbles having a diameter of less than 1 μm. The ultrafine bubbles have a diameter of, for example, 1 nm or more and less than 1,000 nm, 1 to 750 nm, or 1 to 500 nm.

[0025] As used herein, the term "subject" refers to an animal or a cell, tissue, or organ derived from an animal, and particularly includes humans. The term "animal" refers to both humans and non-human animals. Examples of non-human animals include mammals such as mice, rats, rabbits, dogs, cats, cows, horses, pigs, monkeys, dolphins, and sea lions.

[0026] As used herein, "treatment" means therapeutic treatment and / or prophylactic treatment. As used herein, "treatment" means treating, curing, preventing, suppressing, ameliorating, or improving a disease, pathology, or disorder, or halting, inhibiting, reducing, or delaying the progression of a disease, pathology, or disorder. As used herein, "prevention" means reducing the likelihood of developing a disease or pathology, or delaying the onset of a disease or pathology. The "treatment" may be, for example, treatment of a patient who develops a target disease, or treatment of an animal model of the target disease.

[0027] The present invention will be described below using examples, but the present invention is not limited to the following examples and can be practiced with any modifications. Furthermore, each description in the present invention can be mutually incorporated unless otherwise specified. In this specification, when the expression "to" is used, it is used to mean including the numerical or physical values ​​before and after it. In addition, in this specification, the expression "A and / or B" includes "A only," "B only," and "both A and B."

[0028] <Peritoneal deterioration inhibiting composition> The present invention provides a composition that inhibits peritoneal deterioration. The composition that inhibits peritoneal deterioration of the present invention contains carbon monoxide. The composition of the present invention is characterized by containing carbon monoxide (CO), and other configurations and conditions are not particularly limited. The composition of the present invention can inhibit peritoneal deterioration. Because the composition of the present invention contains CO, it can be administered directly into the body of a recipient, for example, into the peritoneum or abdominal cavity.

[0029] The carbon monoxide is present, for example, in a medium. The carbon monoxide may exist in the medium in a state separate from the medium or in a state integrated with the medium. When the carbon monoxide exists in a state separate from the medium, the carbon monoxide exists, for example, in a state that can be separated or distinguished from the medium. In this case, the carbon monoxide exists, for example, in a space surrounded by the medium, and specifically exists as bubbles. Examples of the bubbles include microbubbles. When the carbon monoxide exists in a state integrated with the medium, the carbon monoxide exists, for example, in a state that cannot be separated or distinguished from the medium. In this case, the carbon monoxide exists in a dissolved or dissolved state in the medium. When the medium is a liquid solvent, the medium in which the carbon monoxide is dissolved or dissolved can also be referred to, for example, as a carbon monoxide-dissolved liquid or a carbon monoxide-dissolved liquid.

[0030] The medium may be, for example, a liquid or a solid. Examples of the liquid include a water-containing aqueous solvent, an oil-based solvent, or a mixture thereof. The liquid may also include a sol. Examples of the solid include a solidified liquid. Examples of the solid include a gel. Examples of the liquid include physiological saline; buffer solutions such as phosphate buffer; infusion solutions such as extracellular fluid and intracellular fluid; water such as distilled water and pure water; cell culture solutions such as DMEM and RPMI1640; organ preservation solutions; and the like. Examples of the solid include a solidified product of the liquid.

[0031] The microbubbles exist in a dispersed state in the medium. Therefore, it can be said that the gas components of the microbubbles are surrounded by the medium. It is preferable that the gas components in the microbubbles are in direct contact with the medium. The microbubbles exist in a dispersed state throughout or in part of the medium. In the latter case, it can be said that the microbubbles are localized in part of the medium.

[0032] The composition of the present invention contains carbon monoxide as a gas component. The composition of the present invention may contain only carbon monoxide (CO) as a gas (gaseous component), or may contain other gases. The CO can be, for example, an active ingredient in the composition of the present invention. Examples of the other gases include biological gases such as nitric oxide (NO), hydrogen sulfide (HS), and hydrogen (H); rare gases such as helium (He), argon (Ar), krypton (Kr), and xenon (Xe); carbon dioxide (CO), nitrous oxide (NO), carbon dioxide (CO), nitrogen (N), methane (CH), ethane (CHCH), propane (CHCHCH), fluoromethane (CHF), difluoromethane (CHF), carbon tetrafluoride (CF), ethylene oxide (CHO), and air. In the present invention, "biogas" refers to a gas containing carbon monoxide (CO), nitric oxide (NO), hydrogen sulfide (HS), or hydrogen (H), or a mixed gas containing two or more of these. When the composition of the present invention contains two or more gas components, the gas components other than CO are preferably gas components that do not react with CO, such as the noble gases or nitrogen. The carbon monoxide does not refer to, for example, cases in which the gas is air alone. In the present invention, the "air" refers to, for example, the air (atmospheric air) used in producing the composition of the present invention. In the composition of the present invention, when the carbon monoxide and the other gases are gases of medical gas grade, they are preferably gases derived from medical gas. The other gas components may exist in the medium in the same state as CO, or in a different state. As a specific example, when the carbon monoxide forms bubbles in the medium, the other gas components may form bubbles in the medium together with or separately from the carbon monoxide, or may exist in a dissolved or dissolved state in the medium. When the carbon monoxide is present in the medium in a dissolved or dissolved state, the other gaseous components may form bubbles in the medium, or may be present in the medium in a dissolved or dissolved state together with the carbon monoxide.

[0033] In the composition of the present invention, the carbon monoxide content can be set, for example, depending on the dosage to be administered to a subject, as described below. The lower limit of the carbon monoxide content (concentration) may be, for example, 0.01 μmol / L or more, 0.1 μmol / L or more, 1 μmol / L or more, 10 μmol / L or more, 15 μmol / L, 50 μmol / L or more, 75 μmol / L or more, or 100 μmol / L or more. The upper limit of the carbon monoxide content (concentration) may be, for example, 5 mmol / L or less, 1 mmol / L or less, 0.75 mmol / L or less, 0.5 mmol / L or less, or 0.25 mmol / L or less. The range of the carbon monoxide content (concentration) in the composition of the present invention is, for example, 0.01 μmol / l to 5 mmol / l, 0.1 μmol / l to 1 mmol / l, 1 μmol / l to 1 mmol / l, 10 μmol / l to 1 mmol / l, or 100 μmol / l to 1 mmol / l.

[0034] When the composition of the present invention contains carbon monoxide as bubbles and / or microbubbles, the density of the bubbles and / or microbubbles refers to the number of bubbles and / or microbubbles relative to the volume of the medium. The "density" can also be referred to as the number concentration. The lower limit of the density of the bubbles and / or microbubbles is, for example, 5 x 10 5 pieces / ml, 1×10 6 pieces / ml, 5×10 6 pieces / ml, 1×10 7 pieces / ml, 5×10 7 pieces / ml, 1×10 8 pieces / ml, 5×10 8 pieces / ml, 1×10 9 cells / ml, preferably 1 x 10 6 pieces / ml, 5×10 6 pieces / ml, 1×10 7 pieces / ml, 5×10 7 pieces / ml, 1×10 8 pieces / ml, 5×10 8 The upper limit of the density of the bubbles and / or microbubbles is, for example, 1.5 × 10 9 pieces / ml, 2×10 9 pieces / ml, 3×10 9 pieces / ml, 5×109 pieces / ml, 7×10 9 pieces / ml, 9×10 9 pieces / ml, 1×10 10 pieces / ml, 5×10 10 pieces / ml, 1×10 11 pieces / ml, 5×10 11 pieces / ml, 1×10 12 pieces / ml, 5×10 12 The density range of the bubbles and / or microbubbles is, for example, 5×10 5 pieces / ml~5×10 12 pieces / ml, 5×10 5 pieces / ml~1×10 12 pieces / ml, 5×10 5 pieces / ml~5×10 11 pieces / ml, 5×10 5 pieces / ml~1×10 11 pieces / ml, 5×10 5 pieces / ml~5×10 10 pieces / ml, 5×10 5 pieces / ml~1×10 10 pieces / ml, 1×10 6 pieces / ml~9×10 9 pieces / ml, 5×10 6 pieces / ml~9×10 9 pieces / ml, 1×10 7 pieces / ml~7×10 9 pieces / ml, 5×10 7 pieces / ml~7×10 9 pieces / ml, 1×10 8 pieces / ml~5×10 9 pieces / ml, 5×10 8 pieces / ml~5×10 9 pieces / ml, 1×10 9 pieces / ml~3×10 9 pieces / ml, 5×10 8 pieces / ml~2×10 9 pieces / ml, 5×10 8 pieces / ml~1.5×10 9 pieces / ml.

[0035] The density, bubble diameter, and average diameter (hereinafter also referred to as "characteristics") of the bubbles and / or microbubbles can be measured appropriately depending on the medium in which the bubbles and / or microbubbles are dispersed. When the bubbles and / or microbubbles are dispersed in a liquid medium, the characteristics of the bubbles and / or microbubbles can be calculated by analyzing the bubbles in the composition of the present invention using particle trajectory analysis. The particle trajectory analysis can be performed, for example, using a NanoSight (registered trademark) NS300 (manufactured by Malvern Instrument) in accordance with Example 1 described below. The characteristics of the bubbles and / or microbubbles may be calculated using an analysis method other than particle trajectory analysis. In this case, the characteristics of the bubbles and / or microbubbles obtained by other analysis methods satisfy the above-mentioned examples when converted to calculated values ​​obtained by particle trajectory analysis. When the gas bubbles and / or microbubbles are dispersed in a solid medium, the properties of the gas bubbles and / or microbubbles can be calculated based on the properties of the gas bubbles and / or microbubbles in the liquid before the medium solidifies and the properties of the gas bubbles and / or microbubbles in the liquid obtained by dissolving the solid medium.

[0036] The proportion of CO in the gas is, for example, more than 0% and 100% or less, 10 to 100%, 20 to 100%, 30 to 100%, 40 to 100%, 50 to 100%, 60 to 100%, 70 to 100%, 80 to 100%, 90 to 100%, 95 to 100%, 96 to 100%, 97 to 100%, 98 to 100%, or 99 to 100%, and preferably 90 to 100%.

[0037] The composition of the present invention preferably exhibits any one, two, three or four of the following activities (1) to (4): The following activities (1) to (4) can be evaluated by the above-mentioned methods. (1) Inhibitory activity against peritoneal fibrosis (2) Anti-inflammatory activity of the peritoneum (3) Inhibitory activity against angiogenesis in the peritoneum (4) Inhibitory activity of lymphangiogenesis in the peritoneum

[0038] In (1) above, the composition of the present invention has the activity of inhibiting the peritoneal thickness by 5% or more, 10% or more, 15% or more, 20% or more, 25% or more, 30% or more, 35% or more, 40% or more, 45% or more, 50% or more, 55% or more, 60% or more, 65% or more, 70% or more, 75% or more, 80% or more, 85% or more, 90% or more, or 95% or more, based on the peritoneal thickness of the control group, for example, in an assay using the peritoneal deterioration model, 9 or 16 days after the induction of peritoneal deterioration.

[0039] In (2) above, the composition of the present invention has the activity of suppressing the expression level of inflammatory cytokines in the peritoneum of the control group by 5% or more, 10% or more, 15% or more, 20% or more, 25% or more, 30% or more, 35% or more, 40% or more, 45% or more, 50% or more, 55% or more, 60% or more, 65% or more, 70% or more, 75% or more, 80% or more, 85% or more, 90% or more, or 95% or more, for example, in an assay using the peritoneal deterioration model, 9 or 16 days after the induction of peritoneal deterioration, based on the expression level of inflammatory cytokines in the peritoneum of the control group in the group to which the composition of the present invention is administered.

[0040] In (3) above, the composition of the present invention has the activity of suppressing the area of ​​the vascular endothelial cell marker-positive area by 5% or more, 10% or more, 15% or more, 20% or more, 25% or more, 30% or more, 35% or more, 40% or more, 45% or more, 50% or more, 55% or more, 60% or more, 65% or more, 70% or more, 75% or more, 80% or more, 85% or more, 90% or more, or 95% or more, based on the area of ​​the vascular endothelial cell marker-positive area in the peritoneum of the control group, for example, 9 or 16 days after the induction of peritoneal deterioration, in an assay using the peritoneal deterioration model.

[0041] In (4) above, the composition of the present invention has the activity of suppressing the area of ​​the lymphatic endothelial cell marker-positive area by 5% or more, 10% or more, 15% or more, 20% or more, 25% or more, 30% or more, 35% or more, 40% or more, 45% or more, 50% or more, 55% or more, 60% or more, 65% or more, 70% or more, 75% or more, 80% or more, 85% or more, 90% or more, or 95% or more, based on the area of ​​the lymphatic endothelial cell marker-positive area in the peritoneum of the control group, for example, 9 or 16 days after the induction of peritoneal deterioration, in an assay using the peritoneal deterioration model.

[0042] The composition of the present invention can be produced using a method for producing a medium containing dissolved gas or a method for producing a medium containing bubbles, depending on the state of CO in the composition. When the CO is dissolved in the medium, the composition of the present invention can be produced by, for example, placing the medium, such as physiological saline, and the gas in a sealable container and then mixing them. The volume ratio of the medium to the gas can be set, for example, depending on the gas content in the medium. For example, the volume ratio (S:G) of the medium (S) to the gas (G) is, for example, 1:0.01-100, 1:0.1-10, or 1:0.5-5. The mixing time is, for example, 1 minute to 24 hours, 10 minutes to 12 hours, or 20 minutes to 1 hour. Furthermore, when the CO forms bubbles in the composition of the present invention, the composition of the present invention can be produced, for example, by a method for producing microbubbles such as fine bubbles using any gas. Therefore, the method for producing the composition of the present invention includes, for example, a bubble production step in which microbubbles are produced using a CO2-containing gas and a medium. Specifically, when the composition of the present invention is a liquid, the liquid composition can be produced using, for example, a CO2-containing gas, the medium, and a microbubble-producing device using a swirl flow system, an ejector system, a Venturi system, a static mixer system, a micropore system, a pressure dissolution system, or an ultrasonic cavitation system. When the composition of the present invention is a solid, the solid composition can be produced by solidifying the liquid composition using a known method. When the solid is a gel, the gel composition can be produced, for example, by mixing the liquid composition with a gelling agent. At the start of the bubble-producing process, the CO2-containing gas is in a gaseous, liquid, or solid state. The gas containing the CO2 may contain multiple types of gases. In this case, each gas may be subjected to the bubble-producing process separately, or all or a portion of the CO2-containing gas may be subjected to the bubble-producing process simultaneously. Specifically, when the gas is CO2 and a gas other than CO2, the CO2 and the gas other than CO2 may be introduced simultaneously or separately.

[0043] The composition of the present invention may be, for example, in vivo You can also use in In vitro The composition of the present invention can be used, for example, as a research reagent or as a pharmaceutical. In the latter case, the composition of the present invention can also be called a medicine or a pharmaceutical composition.

[0044] There are no particular limitations on the subject (subject) to which the composition of the present invention is administered. in vivo When the composition of the present invention is used in the above, the subject of administration can be, for example, the subject described above. in In vitro When used in the above, the subject to be administered can be, for example, a cell, a tissue, an organ, etc., and examples of the cells can be, for example, cells collected from a living body, cultured cells, etc., and examples of the tissue or organ can be, for example, tissue (living tissue) or organ collected from a living body, etc. Examples of the cells can be, for example, peritoneal endothelial cells, peritoneal mesothelial cells, etc.

[0045] The subjects to which the composition of the present invention is administered are preferably subjects who are scheduled to undergo peritoneal dialysis, subjects who are undergoing peritoneal dialysis, subjects who have been undergoing peritoneal dialysis, and / or subjects who are suspected of having deteriorated peritoneal function due to peritoneal dialysis.

[0046] The conditions for use (administration conditions) of the composition of the present invention are not particularly limited, and the administration form, administration time, dosage, etc. can be appropriately determined depending on the type of subject to be administered, etc.

[0047] The dosage of the composition of the present invention is not particularly limited, and is, for example, a therapeutically effective amount. in vivo When used in the above range, the density of the microbubbles can be appropriately determined depending on, for example, the type, symptoms, age, and administration method of the subject. 8 pieces / ml (carbon monoxide content: approx. 0.0002mm 3 / ml) ~ 5 × 10 12 pieces / ml (carbon monoxide content: approx. 10mm 3When a composition having a carbon monoxide content (concentration) of 0.01 μmol / L to 5 mmol / L is intraperitoneally or intravenously administered to a mouse or human, the total daily dose of the composition is, for example, 1 to 80 ml / kg body weight or 20 to 80 ml / kg body weight. In this case, the composition of the present invention is administered, for example, 1 to 5 times, 1 to 3 times, or preferably once a day. When the density of the microbubbles is 1×10 8 pieces / ml~5×10 12 When a composition containing 0.01 μmol / L to 5 mmol / L of carbon monoxide is administered into the peritoneal cavity of a human as a peritoneal dialysis solution, the daily dose of the composition is, for example, 2 to 5 L per administration. The total daily dose is, for example, 2 to 30 L, 5 to 20 L, or 8 to 18 L. In this case, the number of times the composition of the present invention is administered per day is, for example, 1 to 15 times, 1 to 13 times, or 3 to 10 times. Furthermore, when the density of the microbubbles is 1×10 8 pieces / ml~5×10 12 When a composition containing 0.01 μmol / L to 5 mmol / L of carbon monoxide is administered to a mouse or human for prophylactic purposes, the daily dose of the composition is, for example, 0.00001 to 500 ml. In this case, the number of times the composition of the present invention is administered per day is, for example, 1 to 5 times, 1 to 3 times, or preferably 1 time. The content of the gas component in the composition is not particularly limited and can be appropriately determined, for example, depending on the daily dose. The composition of the present invention may be administered, for example, continuously or discontinuously. The discontinuous administration can also be referred to as intermittent administration. The composition of the present invention may be administered, for example, at predetermined intervals. The predetermined intervals may be approximately equal or regular intervals, or may be unequal intervals. The predetermined intervals may be, for example, every 8 to 12 hours or every day.

[0048] The administration form of the composition of the present invention is not particularly limited. in vivoWhen the composition of the present invention is administered intraperitoneally, it may be administered orally or parenterally. Examples of parenteral administration include intravenous injection (intravenous administration), intramuscular injection (intramuscular administration), transdermal administration, subcutaneous administration, intradermal administration, enteral administration, rectal administration, vaginal administration, nasal administration, pulmonary administration, intraperitoneal administration, and topical administration. When the composition of the present invention is administered intraperitoneally, the composition administered intraperitoneally may be recovered from the abdominal cavity.

[0049] The dosage form of the composition of the present invention is not particularly limited and can be appropriately determined depending on, for example, the administration form. Examples of the dosage form include liquid and solid forms. Specific examples of the dosage form include oral preparations such as modified-release preparations (enteric preparations, sustained-release preparations, etc.), capsules, oral liquids (elixirs, suspensions, emulsions, perfumes, lemonades, etc.), syrups (syrup preparations, etc.), granules (effervescent granules, fine granules, etc.), powders, tablets (orally disintegrating tablets, chewable tablets, effervescent tablets, dispersible tablets, dissolving agents, coated tablets, etc.), pills, and oral jellies; oral preparations such as oral tablets (gums, sublingual tablets, troches, drops, buccal tablets, adhesive tablets, etc.), oral sprays, oral semisolid preparations, and mouthwashes; injections (implanted injections, sustained-release injections, infusions (infusion preparations, etc.), freeze-dried injections, powder injections, pre-filled syringes, nasal preparations such as nasal drops (nasal liquid preparations, nasal powder preparations, etc.); rectal preparations such as suppositories, rectal semisolid preparations, and enemas; vaginal preparations such as vaginal suppositories and vaginal tablets; skin preparations such as topical liquid preparations (spirits, liniments, lotions, etc.), creams, gels, topical solid preparations (topical powder preparations, etc.), sprays (topical aerosols, pump sprays, etc.), patches (tapes, poultices, etc.), and ointments. When the composition of the present invention is administered orally, the dosage form may be, for example, a tablet, a coated tablet, a pill, fine granules, granules, powder, capsule, liquid, syrup, emulsion, suspension, etc. When the composition of the present invention is administered parenterally, the dosage form may be, for example, an injection preparation, an intravenous drip preparation, etc. When the composition of the present invention is administered transdermally, the dosage form may be, for example, a patch, an ointment, an ointment, a cream, a lotion, or other topical agent.

[0050] The composition of the present invention may contain, for example, additives as needed. When the composition of the present invention is used as a medicine or pharmaceutical composition, the additive preferably comprises a pharmaceutically acceptable additive or a pharmaceutically acceptable carrier. The additive is not particularly limited, and examples thereof include osmotic pressure regulators such as salts, base raw materials, excipients, colorants, lubricants, binders, disintegrants, stabilizers, coating agents, preservatives, pH adjusters, and flavoring agents such as fragrances. In the present invention, the amount of the additive is not particularly limited as long as it does not interfere with the function of CO.

[0051] Examples of the excipient include sugar derivatives such as lactose, lactose hydrate, sucrose, glucose, mannitol, and sorbitol; starch derivatives such as corn starch, potato starch, alpha starch, and dextrin; cellulose derivatives such as crystalline cellulose; organic excipients such as gum arabic, dextran, and pullulan; silicate derivatives such as light anhydrous silicic acid, synthetic aluminum silicate, calcium silicate, and magnesium aluminometasilicate; phosphates such as calcium hydrogen phosphate; carbonates such as calcium carbonate; and sulfates such as calcium sulfate. Examples of the colorant include yellow ferric oxide. Examples of the lubricant include metal stearates such as stearic acid, calcium stearate, and magnesium stearate; talc; polyethylene glycol; silica; and hydrogenated vegetable oil. Examples of the flavoring agent include flavorings such as cocoa powder, peppermint, aromatic powder, peppermint oil, borneol, and cinnamon powder, as well as sweeteners and acidulants. Examples of the binder include hydroxypropyl cellulose, hydroxypropylmethyl cellulose, polyvinylpyrrolidone, macrogol, etc. Examples of the disintegrant include cellulose derivatives such as carboxymethyl cellulose and carboxymethyl cellulose calcium; chemically modified starches and chemically modified celluloses such as carboxymethyl starch, carboxymethyl starch sodium, cross-linked polyvinylpyrrolidone, and sodium starch glycolate; examples of the stabilizer include parahydroxybenzoic acid esters such as methylparaben and propylparaben; alcohols such as chlorobutanol, benzyl alcohol, and phenylethyl alcohol; benzalkonium chloride; phenols such as phenol and cresol; thimerosal; dehydroacetic acid; sorbic acid; and examples of the coating agent include hypromellose, macrogols such as Macrogol 6000, talc, titanium oxide, etc.

[0052] The composition of the present invention can, for example, suppress peritoneal deterioration in a subject to administration, and can therefore be suitably used, for example, as a composition for suppressing peritoneal deterioration caused by peritoneal dialysis, preventing or suppressing peritoneal inflammation and / or peritoneal fibrosis caused during the peritoneal deterioration process, and preventing or suppressing encapsulating peritoneal sclerosis caused by the peritoneal deterioration.

[0053] <Peritoneal Deterioration Inhibition Composition Kit> In one aspect, the present invention provides a composition kit for inhibiting peritoneal deterioration. As described above, the peritoneal deterioration-inhibiting composition kit of the present invention comprises the peritoneal deterioration-inhibiting composition of the present invention and other components, wherein the peritoneal deterioration-inhibiting composition and the other components are arranged separately, and the peritoneal deterioration-inhibiting composition is the peritoneal deterioration-inhibiting composition of the present invention. The composition kit of the present invention is characterized by comprising the composition of the present invention, and other configurations and conditions are not particularly limited. According to the composition kit of the present invention, the dosage of CO can be adjusted by adjusting the dosage of the composition. The description of the composition of the present invention above can be used for the composition kit of the present invention.

[0054] The other components are not particularly limited and can be appropriately determined depending on the contents of the composition and the purpose of administration to the recipient. Examples of the other components include additives, drugs, nutrients, etc. Examples of the drug include antibiotics, etc. When the osmotic pressure of the composition is not adjusted, the other components preferably include an osmotic pressure adjuster (substance). Examples of the osmotic pressure adjuster include sugars such as glucose and icodextrin; salts (electrolytes) such as sodium chloride, sodium lactate, calcium chloride, calcium chloride, sodium bicarbonate, and magnesium chloride; amino acids; proteins, etc. Examples of the nutrient include sugars such as glucose, vitamins, etc. The other components may be solid or liquid. In the former case, the other components are preferably disposed in an undissolved state in a solvent or the like and are preferably configured to dissolve, for example, when mixed with the composition. In the latter case, the other components are preferably dissolved, for example, in a solvent.

[0055] In the composition kit of the present invention, the composition and the other components are arranged separately, i.e., the composition and the other components are arranged in an unmixed state or in a state where they are not in contact with each other. Specifically, the composition and the other components are arranged in different locations in a container that contains them.

[0056] In the composition kit of the present invention, the composition and the other components are preferably contained in a container. In this case, the container has multiple chambers, and the composition and the other components are contained in different chambers. That is, the container is preferably a multi-chamber container. The number of chambers in one container is not particularly limited and can be determined, for example, depending on the number of components to be arranged separately, specifically 2 to 10 chambers or 2 to 5 chambers. Specific examples of the container include a first chamber for containing the composition and a second chamber for containing the other components. In the container, the first chamber and the second chamber may each be configured independently, i.e., as separate containers, or may be integrated, i.e., as a single container. When the first chamber and the second chamber are configured as a single container, the container preferably has a partition that can separate the first chamber and the second chamber. When the container has a partition, the first chamber and the second chamber are, for example, arranged via the partition. When the composition is mixed with the other component and administered to a subject, the isolation part is preferably configured to allow communication between the first chamber and the second chamber.

[0057] The container having the first and second chambers can be, for example, a medical multi-chamber container. Examples of the multi-chamber container include a plastic double bag in which multiple chambers are formed by providing the separating section inside a plastic bag (e.g., JP 2016-190646 A, JP 2016-131577 A, etc.), a dissolution kit in which a container containing other components and a container containing a dissolution solution (corresponding to the composition) are integrated so as to be able to communicate with each other (e.g., WO 96 / 25136 A, etc.), and a double-chamber pre-filled syringe (e.g., JP 2012-245086 A, etc.).

[0058] An example of the multi-chamber container containing the composition and the other components in the composition kit of the present invention will be described with reference to FIG. 1. FIG. 1 is a cross-sectional view showing an example of the composition kit of the present invention. As shown in FIG. 1, the composition kit includes a container 10, a composition 11, and other components 21. The container 10 includes a first chamber 1 containing the composition 11, a second chamber 2 containing the other components 21, and a separating section 3 that separates the first chamber 1 from the second chamber 2 and allows communication between the first chamber 1 and the second chamber 2. The container 10 further includes a hanging section 5 from which the container 10 can be hung.

[0059] As shown in FIG. 1, container 10 is formed from sheets 13 and 14 and a discharge section (discharge port) 22. As shown in FIG. 1, sheets 13 and 14 are welded to sheet 13 at the upper end thereof to form upper end 12 of first chamber 1, and are connected to discharge section 22 at the lower end sides of sheets 13 and 14. Sheets 13 and 14 are also welded to each other at their centers to form isolation section 3. The weld of isolation section 3 is peelable, and by applying pressure to first chamber 1, the weld of sheets 13 and 14 in isolation section 3 is released, allowing first chamber 1 and second chamber 2 to communicate with each other. In container 10, first chamber 1 is the space from upper end 12 of sheets 13 and 14 to isolation section 3. In container 10, second chamber 2 is the space from isolation section 3 to discharge section 22 of sheets 13 and 14.

[0060] Plastic sheets can be used for sheets 13 and 14. The plastic sheet is preferably composed of multiple layers, for example, including an inner layer, an outer layer, and an intermediate layer. Thermoplastic resins such as thermoplastic olefin resins, thermoplastic propylene resins, and thermoplastic polyethylene resins can be used for the inner layer and the outer layer. By using such thermoplastic resins, the outer peripheries of first chamber 1 and second chamber 2, upper end 12, and separator 3 can be easily formed by stacking sheets 13 and 14 facing each other and heat sealing them, thereby producing container 10. The intermediate layer is preferably made of, for example, a highly flexible resin, and a thermoplastic olefin resin composition can be used as a specific example.

[0061] The volumes and shapes of the first chamber 1 and the second chamber 2 are not particularly limited and can be set appropriately depending on, for example, the amounts of the composition and other ingredients to be administered.

[0062] The kit of the present invention can suppress peritoneal deterioration in a subject to administration, for example, and can therefore be suitably used as a kit for suppressing peritoneal deterioration caused by peritoneal dialysis, preventing or suppressing peritoneal inflammation and / or peritoneal fibrosis that occur during the peritoneal deterioration process, and preventing or suppressing encapsulating peritoneal sclerosis that occurs as a result of the peritoneal deterioration.

[0063] <Peritoneal dialysis solution> In another aspect, the present invention provides a peritoneal dialysis solution that inhibits peritoneal deterioration. The peritoneal dialysis solution of the present invention is characterized by containing the peritoneal deterioration-inhibiting composition of the present invention. The peritoneal dialysis solution of the present invention can inhibit peritoneal deterioration during peritoneal dialysis. The peritoneal dialysis solution of the present invention is characterized by containing CO as the composition of the present invention, i.e., as a gas component, and other configurations and conditions are not particularly limited. The peritoneal dialysis solution of the present invention can inhibit peritoneal deterioration during peritoneal dialysis. Because the composition of the present invention contains CO, it can be administered directly into the body of a recipient, for example, into the peritoneum or abdominal cavity.

[0064] The peritoneal dialysis solution of the present invention contains, in addition to the composition of the present invention, other components that are contained in peritoneal dialysis solutions. That is, the peritoneal dialysis solution of the present invention contains, in addition to the components contained in ordinary peritoneal dialysis solutions, the composition of the present invention, i.e., CO as a gas component. Examples of the other components include osmotic pressure adjusting substances; ions of metals such as calcium, sodium, magnesium, and chromium; alkalinizing agents; organic acids; etc.

[0065] Examples of the osmotic pressure adjusting substance include sugars such as glucose and icodextrin; amino acids; proteins; and the like.

[0066] Examples of the alkaline agent include lactate ions and bicarbonate ions.

[0067] Examples of the organic acid include propionic acid, malic acid, fumaric acid, succinic acid, oxalacetic acid, N-acetylglycine, N-acetyl-L-cysteine, glutaric acid, glucuronic acid, ascorbic acid, citric acid, isocitric acid, gluconic acid, N-acetyl-L-aspartic acid, N-acetyl-L-glutamic acid, N-acetyl-L-methionine, N-acetyl-L-proline, N-acetyl-L-valine, N-acetyl-L-glutamine, N-acetyl-L-arginine, N-acetyl-L-histidine, N-acetyl-L-leucine, N-acetyl-L-tryptophan, and salts thereof.

[0068] The concentration of the other components can be appropriately set depending on the type of the other components.

[0069] The pH of the peritoneal dialysis solution of the present invention is, for example, about pH 5.0 to 7.5, and preferably about pH 6.5 to 7.5.

[0070] The osmotic pressure of the peritoneal dialysis solution of the present invention is, for example, about 300 to 500 mOsm / kg, and preferably about 330 to 450 mOsm / kg.

[0071] The amount of the peritoneal dialysis solution of the present invention injected per administration is, for example, 1.5 to 2 L in the case of a human being. The retention time of the peritoneal dialysis solution of the present invention per administration is, for example, 4 to 8 hours. After the retention time, the peritoneal dialysis solution of the present invention is drained. The peritoneal dialysis solution of the present invention is continuously administered 3 to 5 times per day, with each of these procedures counting as one administration.

[0072] The peritoneal dialysis solution of the present invention can be prepared, for example, by mixing the composition of the present invention with other components such as the osmotic pressure adjuster. Therefore, it is preferable that the other components are prepared as concentrated solutions, and that the concentrations of the other components are adjusted so as to achieve a desired concentration after mixing with the composition of the present invention. It is preferable that the composition of the present invention and the other components are sterilized in advance.

[0073] The peritoneal dialysis solution of the present invention is preferably enclosed in a soft plastic bag, a glass container, or the like.

[0074] <Peritoneal dialysis solution kit> In another aspect, the present invention provides a peritoneal dialysis solution kit that suppresses peritoneal deterioration. The peritoneal dialysis solution kit of the present invention is characterized by comprising the composition of the present invention and a peritoneal dialysis solution. The peritoneal dialysis solution of the present invention can suppress peritoneal deterioration during peritoneal dialysis. The peritoneal dialysis solution of the present invention is characterized by containing CO as the composition of the present invention, i.e., as a gas component, and other configurations and conditions are not particularly limited. The peritoneal dialysis solution of the present invention can suppress peritoneal deterioration. Because the composition of the present invention contains CO, it can be administered directly into the body of a recipient, for example, to the peritoneum or intraperitoneal cavity.

[0075] In the peritoneal dialysis kit of the present invention, the peritoneal dialysis solution is mixed with the composition of the present invention at the time of use to prepare a mixed solution, and the mixed solution is used. Therefore, the peritoneal dialysis solution is preferably, for example, a concentrated solution of a conventional peritoneal dialysis solution. The concentrations of each component (other components) in the concentrated peritoneal dialysis solution can be set so as to achieve a desired concentration after mixing with the composition of the present invention.

[0076] In the peritoneal dialysis kit of the present invention, the composition and the other components are preferably contained in a container. For the container, for example, the description of the container in the composition kit can be applied.

[0077] <Pharmaceutical Composition> In another aspect, the present invention provides a composition capable of treating diseases caused by peritoneal dialysis or peritoneal deterioration. The pharmaceutical composition for treating diseases caused by peritoneal dialysis or peritoneal deterioration (hereinafter also referred to as "pharmaceutical composition") of the present invention comprises the composition for inhibiting peritoneal deterioration of the present invention. The pharmaceutical composition of the present invention is characterized by comprising the composition of the present invention, and other configurations and conditions are not particularly limited. The pharmaceutical composition of the present invention can inhibit peritoneal deterioration in a subject to administration. Therefore, the pharmaceutical composition of the present invention can be suitably used, for example, as a pharmaceutical composition for inhibiting peritoneal deterioration caused by peritoneal dialysis, preventing or inhibiting peritoneal inflammation and / or peritoneal fibrosis that occur during the peritoneal deterioration process, and preventing encapsulating peritoneal sclerosis that occurs as a result of the peritoneal deterioration. According to the pharmaceutical composition of the present invention, the amount of CO administered can be adjusted by adjusting the amount of the composition administered.

[0078] The pharmaceutical composition of the present invention may contain, for example, the above-mentioned pharmaceutically acceptable additives or pharmaceutically acceptable carriers.

[0079] <Medicine kit> In another aspect, the present invention provides a kit of compositions capable of treating diseases caused by peritoneal dialysis or peritoneal deterioration. The pharmaceutical kit for treating diseases caused by peritoneal dialysis or peritoneal deterioration (hereinafter also referred to as the "pharmaceutical kit") of the present invention includes the peritoneal deterioration-inhibiting composition kit of the present invention, i.e., includes the peritoneal deterioration-inhibiting composition of the present invention and other ingredients. The pharmaceutical kit of the present invention is characterized by including the composition kit of the present invention, and other configurations and conditions are not particularly limited. The pharmaceutical kit of the present invention can inhibit peritoneal deterioration in a subject to administration. Therefore, the pharmaceutical kit of the present invention can be suitably used, for example, as a pharmaceutical composition for inhibiting peritoneal deterioration caused by peritoneal dialysis, preventing peritoneal inflammation and / or peritoneal fibrosis that occur during the peritoneal deterioration process, and preventing encapsulating peritoneal sclerosis that occurs as a result of the peritoneal deterioration. According to the pharmaceutical kit of the present invention, the amount of CO administered can be adjusted by adjusting the amount of the composition administered.

[0080] <Suppression method> In another aspect, the present invention provides a method for inhibiting peritoneal deterioration. The inhibition method of the present invention is a method for inhibiting peritoneal deterioration, which uses the peritoneal deterioration-inhibiting composition of the present invention or the peritoneal deterioration-inhibiting composition kit of the present invention. The inhibition method of the present invention is characterized by using the peritoneal deterioration-inhibiting composition of the present invention or the peritoneal deterioration-inhibiting composition kit of the present invention, and other steps and conditions are not particularly limited. According to the inhibition method of the present invention, peritoneal deterioration can be inhibited.

[0081] The suppression method of the present invention includes, for example, an administration step of administering the composition or the composition kit to a subject. The administration is preferably intraperitoneal administration.

[0082] In the suppression method of the present invention, the subject can be the same as the subject described above, and specific examples include a subject who is scheduled to undergo peritoneal dialysis, a subject who is undergoing peritoneal dialysis, or a subject who has undergone peritoneal dialysis.

[0083] In the suppression method of the present invention, the composition or composition kit is in In vitroYou can also use in vivo It may also be used in

[0084] In the suppression method of the present invention, the target of the peritoneal deterioration is, for example, peritoneal fibrosis, decreased peritoneal function, and the like.

[0085] <Dialysis method> In another aspect, the present invention provides a dialysis method in which peritoneal deterioration is suppressed. The dialysis method of the present invention is a peritoneal dialysis method in which the peritoneal dialysis solution of the present invention or the peritoneal dialysis solution kit of the present invention is used. The dialysis method of the present invention is characterized by using the peritoneal dialysis solution of the present invention or the peritoneal dialysis solution kit of the present invention, and other steps and conditions are not particularly limited. According to the dialysis method of the present invention, peritoneal deterioration during peritoneal dialysis can be suppressed.

[0086] The dialysis method of the present invention includes, for example, the steps of injecting the peritoneal dialysis solution or the mixed solution of the peritoneal dialysis solution kit into the peritoneal cavity of a subject, storing the peritoneal dialysis solution or the mixed solution, and draining the peritoneal dialysis solution or the mixed solution. The dialysis conditions, such as the injection amount and storage time, in each step can be determined from the above explanation.

[0087] <Treatment method> In another aspect, the present invention provides a method for treating a disease caused by peritoneal dialysis or peritoneal deterioration. The treatment method of the present invention (hereinafter also referred to as the "treatment method") is a method for treating a disease caused by peritoneal dialysis or peritoneal deterioration, and uses the pharmaceutical composition of the present invention or the pharmaceutical composition kit of the present invention. The treatment method of the present invention is characterized by using the pharmaceutical composition of the present invention or the pharmaceutical composition kit of the present invention, and other steps and conditions are not particularly limited. The treatment method of the present invention can suppress peritoneal deterioration in peritoneal dialysis of a subject to be administered. Therefore, the treatment method of the present invention can prevent or suppress, for example, the suppression of peritoneal deterioration caused by peritoneal dialysis, peritoneal inflammation and / or peritoneal fibrosis that occur during the peritoneal deterioration process, and diseases such as encapsulating peritoneal sclerosis that occur as a result of the peritoneal deterioration.

[0088] The treatment method of the present invention includes, for example, an administration step of administering the composition for inhibiting peritoneal deterioration of the present invention to a patient.

[0089] The treatment method of the present invention may use the pharmaceutical composition as the composition. Also, the treatment method of the present invention may use a composition kit or a pharmaceutical kit (hereinafter, collectively referred to as a "kit") as the composition.

[0090] When the treatment method of the present invention uses the kit, the composition and the other components may be administered simultaneously or separately in the administration step. When the composition and the other components are administered simultaneously, the treatment method of the present invention preferably includes a mixing step of mixing the composition and the other components in the kit prior to the administration step. In this case, the resulting mixture is administered to a patient in the administration step.

[0091] The administration conditions in the administration step can be as described above.

[0092] In the treatment method of the present invention, the patient is preferably a patient diagnosed with or suspected of having a disease caused by peritoneal deterioration. The patient may also be a patient with or suspected of having peritoneal fibrosis, or a patient with or suspected of having peritoneal inflammation. Peritoneal deterioration can be evaluated, for example, by biopsy of the patient's peritoneum.

[0093] <Use> In another aspect, the present invention is a composition for use in inhibiting peritoneal deterioration, peritoneal dialysis, or treating peritoneal dialysis or a disease caused by peritoneal deterioration, wherein the composition comprises carbon monoxide. Also, the present invention is a composition kit for use in inhibiting peritoneal deterioration, peritoneal dialysis, or treating peritoneal dialysis or a disease caused by peritoneal deterioration, wherein the composition kit comprises a composition and other components, the composition and the other components being disposed separately, and the composition comprises carbon monoxide. [Example]

[0094] [Example 1] The composition of the present invention was prepared and confirmed to be capable of reducing peritoneal deterioration.

[0095] (1) Preparation of the composition The composition of the present invention was produced using a microbubble-producing apparatus 100 shown in FIG. 2. As shown in FIG. 2, the production apparatus 100 has syringes 32 and 33 arranged on two sides of a three-way stopcock 31. In the production apparatus 100, the syringes 32 and 33 are connected via the three-way stopcock 31. First, the syringe 32 was removed from the three-way stopcock 31, and 20 ml of physiological saline was introduced into the syringe. Next, the syringe 32 was reconnected to the three-way stopcock 31, and the gas inside the three-way stopcock 31 was removed. After the gas removal, the syringe 33 was removed from the three-way stopcock 31, and 20 ml of medical carbon monoxide (manufactured by Taiyo Nippon Sanso Corporation or Japan Fine Products Co., Ltd., CO concentration: 99.95% or higher (G1)) was introduced into the syringe. Then, the syringe 33 was reconnected to the three-way stopcock 31. After the connection, the plungers of the syringes 32 and 33 were continuously moved piston-like within the outer cylinders for 10 minutes to produce microbubbles containing CO as a gas component, thereby producing the composition of the present invention (the composition of Example 1).

[0096] The resulting composition was allowed to stand for about 1 hour, and then the physical properties of the composition were measured using a NanoSight (registered trademark) NS300 (manufactured by Malvern Instrument) with default parameters. The measurements were carried out at 25°C. As a result, the average diameter and density of the microbubbles in the composition were as follows: (Composition of Example 1 (CO-UFB)) Average diameter: 136.3 ± 1.4 nm, density: 1.54×10 9 ±1.87×10 7 pieces / ml

[0097] (2) Creation of a mouse model of peritoneal membrane deterioration A mouse model of peritoneal deterioration was generated by intraperitoneally administering chlorhexidine gluconate solution (CG solution) to mice (strain: C57BL / 6JJmsSlc, purchased from Japan SLC). The CG solution was prepared as follows: First, 1.5 ml of 99.5% ethanol (Wako, Cat. No. 057-00456) and 50 μl of 20% CG (Wako, Cat. No. 034-10871) were added to 8.5 ml of physiological saline and thoroughly mixed. The resulting mixture was sterilized through a 0.2 μm filter to prepare 0.1% CG solution. Next, 300 μl of 0.1% CG solution was intraperitoneally administered to the mice. Two hours after administration of the CG solution, 1.0 ml of CO-UFB was intraperitoneally administered. The administration was performed every other day for a total of seven times (CG + CO-UFB, Example group). The control group (Control) was treated in the same manner except that an equal volume of saline was used instead of the 0.1% CG solution and saline was used instead of the CO-UFB. The reference group (CG) was treated in the same manner except that saline was used instead of the CO-UFB.

[0098] (3) Measurement of peritoneal function On the 16th day after the start of administration, peritoneal function was measured to confirm the occurrence of peritoneal deterioration. Specifically, a Peritoneal Equilibration Test (PET) was performed on the mice of each group on the 16th day after the start of administration. Each group of mice was intraperitoneally administered 2 ml of 4.25% Dianeal (registered trademark). Two hours after administration, drainage fluid intake and blood sampling were performed to evaluate the amount of fluid removed and drainage. These results are shown in Table 1 and Figure 3.

[0099] [Table 1]

[0100] Table 1 shows the mortality rate, drainage volume, and amount of water removed. FIG. 3 is a graph showing the drainage volume. In FIG. 3, the horizontal axis shows the type of sample, and the vertical axis shows the drainage volume. As shown in Table 1, in the reference example group (CG), the mortality rate increased to 30.4% due to the induction of peritoneal deterioration. In contrast, in the example group (CG+CO-UFB), the mortality rate was 12.5%, indicating a decrease in mortality. As shown in Table 1 and FIG. 3, the reference example group showed a tendency for the amount of fluid to decrease compared to the control group. In contrast, there was no significant difference in the amount of drainage between the example group (CG+CO-UFB) and the control group.

[0101] From the above, it was found that administration of CO-UFB, the composition of the present invention, alleviates the decline in water removal function caused by peritoneal deterioration.

[0102] (4) Measurement of peritoneal thickness On day 16 after the start of CG solution administration in Example 1(1), peritoneal thickening and inflammatory cell infiltration into the peritoneum were examined as indicators of peritoneal deterioration. Specifically, on day 16 after the administration of CG solution, the parietal peritoneum and diaphragm of each mouse group were collected and fixed in 10% neutral buffered formalin. After fixation, the parietal peritoneum and diaphragm were embedded in paraffin, and 3 μm-thick paraffin-embedded sections were prepared. The obtained paraffin-embedded sections were subjected to HE staining using standard methods. After staining, the thickness of each section from the basement membrane to the peritoneal surface (peritoneal surface layer) was measured using an optical microscope (OLYMPUS BX50, Olympus) and a camera (OLYMPUS DP22, Olympus). Additionally, the presence or absence of inflammatory cell infiltration was examined for each section. These results are shown in Figures 4 and 5.

[0103] Figure 4 is a photograph showing peritoneal thickening by histological staining. In Figure 4, the arrow indicates the region from the basement membrane to the peritoneal surface. As shown in Figure 2, in the reference group (CG), the peritoneal thickness was an average of 166.6 μm, while in the control group (control), the peritoneal thickness was an average of 54.4 μm, confirming that administration of CG solution causes peritoneal thickening. In contrast, in the example group (CG + CO-UFB), the peritoneal thickness was an average of 109.9 μm. These results demonstrate that administration of CO-UFB, the composition of the present invention, can reduce peritoneal thickening that occurs during peritoneal deterioration.

[0104] Next, Figure 5 is a photograph showing inflammatory cells by histological staining. As shown in Figure 5, infiltration of inflammatory cells into the peritoneal surface was not observed in the control group (control). On the other hand, infiltration of inflammatory cells into the peritoneal surface was confirmed in the reference group (CG) in the area indicated by the arrow, compared to the control group. In contrast, in the example group (CG+CO-UFB), a decrease in the number of inflammatory cells infiltrating into the peritoneal surface was observed in the area indicated by the arrow, compared to the reference group.

[0105] From the above, it was found that administration of CO-UFB, the composition of the present invention, reduced peritoneal thickening caused by peritoneal deterioration and inhibited the infiltration of inflammatory cells.

[0106] (5) Measurement of inflammatory response to peritoneal deterioration On the 16th day after the start of administration of the CG solution in Example 1(1), the infiltration of inflammatory cells, macrophages, and the formation of blood vessels and lymphatic vessels related to the ability to remove water were examined as indicators of peritoneal deterioration. First, paraffin-embedded sections were prepared in the same manner as in Example 1(4).

[0107] The paraffin-embedded sections were then reacted with a primary antibody, followed by a secondary antibody and HRP (HRP Rb, Cell Signaling Technology, reagent code: 8114S, lot number: 21). The primary antibodies used were CD68 antibody (Rt×Mo CD68, Bio-Rad, reagent code: MCA1957, lot number: 1807-14) for macrophage staining, CD31 antibody (Rt×Mo CD31, Merck, reagent code: CBL1337, lot number: 3123230) for vascular endothelial cell staining, and Lyve-1 antibody (Rb×Mo / Rt Lyve-1, Acris, reagent code: DP3513P, lot number: 1410R24) for lymphatic vessel staining. After the reaction, the sections were stained with 3,3'-diaminobenzidine (DAB) as a chromogenic substrate. After the staining, counterstaining was performed with hematoxylin. The areas of CD68-positive macrophages, CD31-positive vascular endothelial cells, and Lyve-1-positive lymphatic endothelial cells were counted under the optical microscope, and the percentage of each area per field was calculated. The results are shown in Figures 6 to 11.

[0108] Figure 6 is a photograph showing the results of CD68 (macrophage marker) staining by immunohistochemical staining, and Figure 7 is a graph showing the macrophage-positive area (%). As shown in Figures 6 and 7, no macrophage infiltration was observed in the control group. On the other hand, the macrophage marker-positive area increased in the reference group (CG) compared to the control group. In contrast, the macrophage marker-positive area decreased in the example group (CG+CO-UFB) compared to the reference group, as indicated by the arrow.

[0109] Next, Figure 8 is a photograph showing the results of CD31 (vascular endothelial cell marker) staining by immunohistochemical staining, and Figure 9 is a graph showing the vascular endothelial cell-positive area (%). As shown in Figures 8 and 9, the vascular endothelial cell marker-positive area increased in the reference example group (CG) compared to the control group (control), as indicated by the arrows. In contrast, the example group (CG+CO-UFB) showed a tendency for the vascular endothelial cell marker-positive area to decrease, as indicated by the arrows, compared to the reference example group.

[0110] Next, Figure 10 is a photograph showing the results of Lyve-1 (lymphatic vessel marker) staining by immunohistochemical staining, and Figure 11 is a graph showing the results of lymphatic vessel positive area (%). In Figure 10, the void areas are areas where lymphangiogenesis occurred. As shown in Figures 10 and 11, the reference example group (CG) showed a tendency for the lymphatic vessel marker positive area to increase compared to the control group (Control), as indicated by the arrows. In contrast, the example group (CG+CO-UFB) showed a tendency for the lymphatic vessel marker positive area to decrease compared to the reference example group, as indicated by the arrows.

[0111] These results demonstrate that administration of the composition of the present invention, CO-UFB, inhibits the infiltration of inflammatory cells, such as macrophages, and inhibits the formation of new blood vessels and lymphatic vessels in a peritoneal deterioration model. As mentioned above, peritoneal functions, such as water removal ability, are impaired in the peritoneal deterioration model, and administration of CO-UFB inhibits the decline in peritoneal function. This is presumably due to the fact that CO-UFB inhibits inflammatory responses, such as macrophage infiltration, and the decline in water removal function due to the formation of new blood vessels and lymphatic vessels, which occur during peritoneal deterioration.

[0112] (6) Measurement of gene expression in peritoneal deterioration On day 16 after the start of administration of the CG solution described in Example 1(1), the expression of genes related to angiogenesis, lymphangiogenesis, and inflammation was examined. Specifically, the parietal peritoneum and diaphragm of each mouse group were collected, and total RNA was extracted from each membrane by standard methods. cDNA was synthesized using the obtained RNA, reverse transcriptase (High Capacity cDNA Reverse Transcription Kit, Appliedbiosystems), and a PCR device (Thermal Cycler Dice, Takara). The cDNA and the primer set below were then used with an RT-PCR reagent (RTB Green™ Premix™ Taq™ II, manufactured by Takara) and a real-time PCR analyzer (Quant Studio 3, manufactured by Appliedbiosystems) to measure the gene expression levels of VEGF-A (vascular endothelial growth factor), VEGF-C (lymphangiogenic factor), PECAM-1 (vascular endothelial cell adhesion molecule), LYVE-1 (lymphatic endothelial cell marker), and IL-6 (inflammatory cytokine). GAPDH was used as an internal standard gene, and the expression level of each gene was calculated as a relative expression level to that of the internal standard gene. These results are shown in Figure 12.

[0113] Primer set for VEGF-A Forward primer (SEQ ID NO: 1) 5'-caggctgctgtaacgatgaa-3' Reverse primer (SEQ ID NO: 2) 5'-gctttggtgaggtttgatcc-3' Primer set for VEGF-C Forward primer (SEQ ID NO: 3) 5'-cagacaagttcattcaattattagacg-3' Reverse primer (SEQ ID NO: 4) 5'-catgtcttgttagctgcctga-3' Primer set for PECAM-1 Forward primer (SEQ ID NO: 5) 5'-cggtgttcagcgagatcc-3' Reverse primer (SEQ ID NO: 6) 5'-actcgacaggatggaaatcac-3' Primer set for LYVE-1 Forward primer (SEQ ID NO: 7) 5'-gaagcagctgggtttggag-3' Reverse primer (SEQ ID NO: 8) 5'-cgtagcaaacagccagcac-3' IL-6 primer set Forward primer (SEQ ID NO: 9) 5'-gctaccaaactggatataatcagga-3' Reverse primer (SEQ ID NO: 10) 5'-ccaggtagctatggtactccagaa-3' Primer set for internal control gene (GAPDH) Forward primer (SEQ ID NO: 11) 5'-tgtgtccgtcgtggatctga-3' Reverse primer (SEQ ID NO: 12) 5'-ttgctgttgaagtcgcaggag-3'

[0114] Figure 12 is a graph showing the expression level of each gene. In Figure 12, the horizontal axis represents the type of sample, and the vertical axis represents the expression level of each gene. As shown in Figure 12, the reference group (CG) showed increased gene expression levels for vascular endothelial growth factor, lymphangiogenesis factor, vascular endothelial cell adhesion molecule, lymphatic endothelial cell marker, and inflammatory cytokine compared to the control group (control). In contrast, the example group (CG+CO-UFB) showed decreased gene expression levels for vascular endothelial growth factor, lymphangiogenesis factor, vascular endothelial cell adhesion molecule, lymphatic endothelial cell marker, and inflammatory cytokine compared to the reference group.

[0115] These results demonstrate that administration of CO-UFB, a composition of the present invention, suppresses the expression of vascular endothelial growth factor, lymphangiogenesis factor, vascular endothelial cell adhesion molecule, lymphatic endothelial cell marker, and inflammatory cytokines, which are upregulated in the peritoneal deterioration model. As mentioned above, peritoneal function, such as water removal ability, is reduced in the peritoneal deterioration model, and administration of CO-UFB suppresses the decline in peritoneal function. This is presumably due to CO-UFB suppressing the upregulation of genes related to inflammatory responses, such as macrophage infiltration, and the decline in water removal function due to angiogenesis and lymphangiogenesis, which occur in peritoneal deterioration.

[0116] [Example 2] The composition of the present invention was prepared and confirmed to be capable of reducing peritoneal deterioration.

[0117] (1) Preparation of the composition A composition containing CO as microbubbles was produced in the same manner as in Example 1(1) above (composition of Example 2(1)). The average diameter and density of the microbubbles in the composition of Example 2(1) were measured in the same manner as in Example 1(1) above, and the results were as follows. (Composition (CO-UFB) of Example 2(1)) Average diameter: 155.2 nm, density: 1.03×10 8 pieces / ml

[0118] Furthermore, a composition in which CO was dissolved in physiological saline (the composition of Example 2(2)) was produced by the following procedure. Specifically, physiological saline and the medical carbon monoxide were charged into a syringe at a volume ratio of 1:1, and then the mixture was shaken and mixed for 30 minutes to dissolve the CO in the physiological saline, thereby producing the composition of Example 2(2). The carbon monoxide concentration in the composition of Example 2(2) was measured, and the results were as follows: (Composition of Example 2(2) (CO-Dissolve)) Concentration: 839 μM

[0119] (2) Creation of a mouse model of peritoneal membrane deterioration A peritoneal deterioration model mouse was prepared in the same manner as in Example 1(2), except that the composition of Example 2(1) and the composition of Example 2(2) were administered instead of CO-UFB.

[0120] (3) Measurement of peritoneal function Next, peritoneal function was measured two days after the seventh administration (9 days after the start of CG solution administration). The peritoneal function measurement was performed in the same manner as in Example 1(3), and the amount of fluid in the peritoneal cavity of each mouse (peritoneal fluid volume) was calculated. The negative control was performed in the same manner except that it was untreated, and the control was performed in the same manner except that physiological saline was used instead of the composition of Example 2(1) and the composition of Example 2(2). These results are shown in Figure 13. In the figure, * indicates p<0.05, ** indicates p<0.01, *** indicates p<0.001, and **** indicates p<0.0001.

[0121] Figure 13 is a graph showing the amount of peritoneal fluid. In Figure 13, the horizontal axis indicates the type of sample, and the vertical axis indicates the amount of peritoneal fluid (mL). As shown in Figure 13, the control showed a significantly reduced amount of water removal compared to the negative control. In contrast, the groups administered with the composition of Example 2(1) (CO-UFB+CG) and the composition of Example 2(2) (CO-Dissolve+CG) showed a significantly reduced decrease in the amount of water removed compared to the control, demonstrating that the decline in water removal function caused by peritoneal deterioration was alleviated.

[0122] (4) Measurement of peritoneal thickness Next, two days after the seventh administration (the ninth day after the start of CG administration), the thickness of the peritoneal surface was measured as an index of peritoneal deterioration. The measurement of the thickness of the peritoneal surface was carried out in the same manner as in Example 1(4). The results are shown in Figure 14.

[0123] FIG. 14 is a graph showing the thickness of the peritoneal surface (peritoneal thickness). In FIG. 14, the horizontal axis indicates the type of sample, and the vertical axis indicates the thickness of the peritoneal surface. As shown in FIG. 14, the control showed a significant increase in peritoneal thickness compared to the negative control. In contrast, the groups administered with the composition of Example 2(1) (CO-UFB+CG) and the composition of Example 2(2) (CO-Dissolve+CG) showed a significantly reduced increase in peritoneal thickness compared to the control, demonstrating that the thickening of the peritoneal membrane that occurs during peritoneal deterioration can be alleviated. Furthermore, the group administered with the composition of Example 2(1) tended to show a smaller increase in peritoneal thickness compared to the group administered with the composition of Example 2(2).

[0124] [Example 3] The composition of the present invention was prepared and confirmed to be capable of preventing peritoneal deterioration.

[0125] (1) Preparation of the composition A composition containing CO as microbubbles and a composition in which CO is dissolved in physiological saline were prepared in the same manner as the compositions of Example 1(1) and Example 2(1), respectively (the compositions of Example 3(1) and Example 3(2)). The average diameter and density of the microbubbles in the composition of Example 3(1) were measured in the same manner as Example 1(1), and the results were as follows: The carbon monoxide concentration in the composition of Example 3(2) was measured and the results were as follows: (Composition (CO-UFB) of Example 3(1)) Average diameter: 155.2 nm, density: 1.03×10 8 pieces / ml (Composition of Example 3(2) (CO-Dissolve)) CO concentration: 755 μM

[0126] (2) Prevention of peritoneal deterioration The ability of the compositions of the present invention to prevent peritoneal deterioration was examined by administering the compositions of each Example before administration of CG. Specifically, 1.0 mL of the composition of Example 3(1) or the composition of Example 3(2) was intraperitoneally administered to the mice. One hour after administration, 300 μL of 0.1% CG solution was intraperitoneally administered to the mice. Next, 6 hours after administration of the CG solution, the parietal peritoneum and diaphragm of each mouse were collected. The relative expression level of the IL-6 gene was calculated in the same manner as in Example 1(6), except that the parietal peritoneum and diaphragm were used. A negative control was prepared in the same manner except that it was untreated. A control was prepared in the same manner except that physiological saline was used instead of the composition of Example 3(1) or the composition of Example 3(2). The results are shown in Figure 15.

[0127] Figure 15 is a graph showing the expression level of the IL-6 gene. In Figure 15, the horizontal axis indicates the type of sample, and the vertical axis indicates the expression level of the IL-6 gene. As shown in Figure 15, the control showed a significant increase in the expression level of the IL-6 gene compared to the negative control. In contrast, the groups administered with the composition of Example 3(1) (CO-UFB+CG) and the composition of Example 3(2) (CO-Dissolve+CG) showed a significant decrease in the expression level of the IL-6 gene compared to the control, demonstrating that inflammation occurring before peritoneal deterioration can be alleviated. Furthermore, the group administered with the composition of Example 3(1) showed a tendency for the increase in the expression level of the IL-6 gene to be more reduced compared to the group administered with the composition of Example 3(2).

[0128] [Example 4] A dilution series of the composition of the present invention was prepared to confirm the effect of CO concentration on the reduction of peritoneal deterioration.

[0129] (1) Preparation of the composition A composition containing CO as microbubbles was prepared in the same manner as in Example 1(1), and then a stock solution, a 4-fold diluted solution, a 10-fold diluted solution, and a 50-fold diluted solution were produced as the composition of Example 4(1) (CO-UFB, CO-UFB 1 / 4, CO-UFB 1 / 10, and CO-UFB 1 / 50, respectively). A composition in which CO was dissolved in physiological saline was prepared in the same manner as in Example 2(2), and then a stock solution, a 4-fold diluted solution, a 10-fold diluted solution, and a 50-fold diluted solution were produced as the composition of Example 4(2) (CO-dis, CO-dis 1 / 4, CO-dis 1 / 10, and CO-dis 1 / 50, respectively).

[0130] (2) Creation of a mouse model of peritoneal membrane deterioration A peritoneal deterioration model mouse was prepared in the same manner as in Example 1(2), except that the composition of Example 4(1) or the composition of Example 4(2) was administered instead of CO-UFB.

[0131] (3) Measurement of peritoneal function A Peritoneal Equilibration Test (PET) was performed in the same manner as in Example 1(3), except that peritoneal function was measured on day 14 from the start of administration, and the amount of fluid in the peritoneal cavity (peritoneal fluid volume) of each mouse was calculated. A control (saline) was performed in the same manner, except that physiological saline was used instead of the composition of Example 4(1) or the composition of Example 4(2). These results are shown in Figures 16(A) to (H). * in the figures indicates p<0.05.

[0132] Figure 16 is a graph showing peritoneal fluid volume. In Figures 16(A) to (H), the horizontal axis indicates the type of sample, and the vertical axis indicates the peritoneal fluid volume (mL). The peritoneal fluid volume, which indicates the permeability of the peritoneum, was higher in the groups administered with the compositions of the Examples than in the control (saline). In particular, the groups administered with the compositions of the Examples (CO-UFB, CO-UFB 1 / 4, CO-UFB 1 / 10, and CO-UFB 1 / 50) had significantly higher peritoneal fluid volumes than the control (saline). Furthermore, in the group administered with the composition of Example 4(2), the peritoneal fluid volumes were significantly higher in Figures 16(E) and (G) (CO-dis and CO-dis 1 / 10) than in the control (saline). In Figures 16(F) and (H) (CO-dis 1 / 4 and CO-dis 1 / 50), the mean peritoneal fluid volumes were higher than in the control (saline). These results demonstrate that the composition of the present invention can alleviate the decline in water removal function caused by peritoneal deterioration even at low CO concentrations.

[0133] Although the present invention has been described above with reference to the embodiments and examples, the present invention is not limited to the above-described embodiments and examples. Various modifications that can be understood by those skilled in the art can be made to the configuration and details of the present invention within the scope of the present invention.

[0134] <Additional Notes> Some or all of the above-described embodiments and examples can be described as, but are not limited to, the following supplementary notes. <Composition for inhibiting peritoneal deterioration> (Appendix 1) A composition for use in inhibiting peritoneal deterioration, comprising: A composition comprising carbon monoxide. (Appendix 2) Contains microbubbles, 2. The composition of claim 1, wherein the microbubbles contain carbon monoxide as a gaseous component. (Appendix 3) The density of the microbubbles is 5×10 5 ~5×10 12 The composition of claim 2, wherein the composition is 0.01g / ml. (Appendix 4) 4. The composition according to claim 2, wherein the proportion of carbon monoxide in the gaseous components is 80% or more. (Appendix 5) 5. The composition of any one of claims 2 to 4, wherein in the microbubbles, the gas component is surrounded by an aqueous solvent. (Appendix 6) Further, the medium includes 6. The composition of any one of claims 2 to 5, wherein the medium is at least one of a liquid and a solid. (Appendix 7) Includes media, 2. The composition of claim 1, wherein the carbon monoxide is dissolved in the medium. (Appendix 8) 8. The composition according to claim 7, wherein the content of the carbon monoxide dissolved in the medium is 0.01 μmol / L to 5 mmol / L. (Appendix 9) The composition of any one of claims 1 to 8, wherein the peritoneal deterioration is peritoneal fibrosis. (Appendix 10) The composition of any one of claims 1 to 9, wherein the peritoneal deterioration is a decrease in peritoneal function. (Appendix 11) 11. A composition according to any one of claims 1 to 10 for use in intraperitoneal administration. <Peritoneal Deterioration Inhibition Composition Kit> (Appendix 12) A composition kit for use in inhibiting peritoneal deterioration, comprising: composition and other ingredients, The composition and the other components are arranged separately, 12. A composition kit, wherein the composition is a composition described in any one of Appendices 1 to 11. (Appendix 13) Further comprising a container, The container has a plurality of chambers and isolation portions that isolate the chambers, the plurality of chambers includes at least a first chamber and a second chamber; The composition is contained in the first chamber; The other ingredients are contained in the second chamber, 13. The composition kit according to claim 12, wherein the isolation section isolates the first chamber from the second chamber and allows communication between the first chamber and the second chamber. (Appendix 14) 14. The composition kit of claim 12 or 13, wherein the other components include an osmolyte. <Peritoneal dialysis solution> (Appendix 15) 12. A peritoneal dialysis solution comprising the composition of any of claims 1 to 11. <Peritoneal dialysis solution kit> (Appendix 16) a composition and a peritoneal dialysis solution, The composition and the peritoneal dialysis solution are placed separately, 12. A peritoneal dialysis solution kit, wherein the composition is a composition described in any one of appendices 1 to 11. (Appendix 17) Further comprising a container, The container has a plurality of chambers and isolation portions that isolate the chambers, the plurality of chambers includes at least a first chamber and a second chamber; The composition is contained in the first chamber; The peritoneal dialysis solution is contained in the second chamber; 17. The peritoneal dialysis solution kit according to claim 16, wherein the isolation section isolates the first chamber from the second chamber and allows communication between the first chamber and the second chamber. <Composition for treating diseases caused by peritoneal dialysis or peritoneal deterioration> (Appendix 18) A pharmaceutical composition for use in treating peritoneal dialysis or diseases caused by peritoneal deterioration, comprising: A pharmaceutical composition comprising carbon monoxide. (Appendix 19) Contains microbubbles, 19. The pharmaceutical composition of claim 18, wherein the microbubbles contain carbon monoxide as a gaseous component. (Appendix 20) The density of the microbubbles is 5×10 5 ~5×10 12 19. The pharmaceutical composition of claim 18, wherein the total number of cells per ml is 100. (Appendix 21) 21. The pharmaceutical composition according to claim 19 or 20, wherein the proportion of carbon monoxide in the gaseous components is 80% or more. (Appendix 22) 22. The pharmaceutical composition of any one of claims 19 to 21, wherein in the microbubbles, the gas component is surrounded by an aqueous solvent. (Appendix 23) Further, the medium includes 23. The pharmaceutical composition of any of claims 19 to 22, wherein the vehicle is at least one of a liquid and a solid. (Appendix 24) Includes media, 19. The pharmaceutical composition of claim 18, wherein the carbon monoxide is dissolved in the medium. (Appendix 25) 25. The pharmaceutical composition according to any one of claims 19 to 24, wherein the disease caused by peritoneal dialysis is peritoneal fibrosis, peritonitis, and / or encapsulating peritoneal sclerosis. (Appendix 26) 26. A pharmaceutical composition according to any one of claims 19 to 25, for use in intraperitoneal administration. <Composition kit for treating diseases caused by peritoneal dialysis or peritoneal deterioration> (Appendix 27) A pharmaceutical composition kit for use in treating diseases caused by peritoneal dialysis or peritoneal deterioration, comprising: composition and other ingredients, The composition and the other components are arranged separately, 12. A pharmaceutical composition kit, wherein the composition is a composition according to any one of appendices 1 to 11. (Appendix 28) Further comprising a container, The container has a plurality of chambers and isolation portions that isolate the chambers, the plurality of chambers includes at least a first chamber and a second chamber; The composition is contained in the first chamber; The other ingredients are contained in the second chamber, 28. The pharmaceutical composition kit according to claim 27, wherein the isolation section isolates the first chamber from the second chamber and allows communication between the first chamber and the second chamber. (Appendix 29) 29. The pharmaceutical composition kit of claim 27 or 28, wherein the other components include an osmolyte. <Method to prevent peritoneal deterioration> (Appendix 30) A method for inhibiting peritoneal deterioration, comprising: A method of suppression using a composition according to any one of Appendices 1 to 11 or a kit of compositions according to any one of Appendices 12 to 14. (Appendix 31) The suppression method described in Appendix 30, comprising an administration step of administering the composition or the composition kit to a subject. (Appendix 32) The suppression method of claim 31, wherein the compound is administered intraperitoneally. (Appendix 33) The suppression method according to claim 31 or 32, wherein the subject is a subject who is scheduled to undergo peritoneal dialysis, a subject who is undergoing peritoneal dialysis, or a subject who has undergone peritoneal dialysis. (Appendix 34) The composition or composition kit, in In vitro or in vivo 34. The method of any one of appendices 30 to 33, wherein the method is used in (Appendix 35) The method for suppressing peritoneal deterioration described in any one of Appendices 30 to 34, wherein the peritoneal deterioration is peritoneal fibrosis. (Appendix 36) The method for suppressing peritoneal deterioration according to any one of claims 30 to 35, wherein the peritoneal deterioration is a decrease in peritoneal function. <Peritoneal dialysis method> (Appendix 37) 1. A method of peritoneal dialysis comprising: A dialysis method using the peritoneal dialysis solution described in Appendix 15 or the peritoneal dialysis solution kit described in Appendix 16 or 17. (Appendix 38) injecting the peritoneal dialysis solution or the mixture of the peritoneal dialysis solution kit into the peritoneal cavity of the subject; storing the peritoneal dialysis solution or the mixture; and draining the peritoneal dialysis solution or the mixture. <Method for treating diseases caused by peritoneal dialysis or peritoneal deterioration> (Appendix 39) A method for treating diseases caused by peritoneal dialysis or peritoneal deterioration, comprising: A method of treatment using a pharmaceutical composition according to any one of appendices 18 to 26 or a pharmaceutical composition kit according to any one of appendices 27 to 29. (Appendix 40) The method of treatment described in Appendix 39, comprising an administration step of administering the pharmaceutical composition or the pharmaceutical composition kit to a subject. (Appendix 41) 41. The method of treatment of claim 40, wherein the treatment is administered intraperitoneally. (Appendix 42) 42. The method of claim 40 or 41, wherein the subject is scheduled to undergo peritoneal dialysis, is undergoing peritoneal dialysis, or has been undergoing peritoneal dialysis. (Appendix 43) The composition or composition kit, in In vitro or in vivo 43. The method of any one of appendices 39 to 42, wherein (Appendix 44) 44. The method of any one of claims 39 to 43, wherein the peritoneal deterioration is peritoneal fibrosis. (Appendix 45) 45. The method of any one of claims 39 to 44, wherein the peritoneal deterioration is a decrease in peritoneal function. (Appendix 46) 46. ​​The method of any one of claims 39 to 45, wherein the disease caused by peritoneal dialysis is peritoneal fibrosis, peritonitis, and / or encapsulating peritoneal sclerosis. (Appendix 47) 47. The method of any of claims 39 to 46, wherein the treatment is prevention or suppression. <Use> (Appendix 48) A composition for use in inhibiting deterioration of the peritoneum, The composition comprises a composition according to any one of claims 1 to 11. (Appendix 49) A composition kit for use in inhibiting peritoneal deterioration, The composition kit includes a composition and other components, The composition and the other components are arranged separately, A composition kit, wherein the composition comprises a composition described in any one of Appendices 1 to 11. (Appendix 50) A composition for use in peritoneal dialysis, The composition comprises a composition according to any one of claims 1 to 11. (Appendix 51) A composition kit for use in peritoneal dialysis, The composition kit includes a composition and other components, The composition and the other components are arranged separately, A composition kit, wherein the composition comprises a composition described in any one of Appendices 1 to 11. (Appendix 52) A composition for use in peritoneal dialysis or the treatment of diseases caused by peritoneal deterioration, The composition comprises a composition according to any one of claims 1 to 11. (Appendix 53) A composition kit for use in treating peritoneal dialysis or diseases caused by peritoneal deterioration, The composition kit includes a composition and other components, The composition and the other components are arranged separately, A composition kit, wherein the composition comprises a composition described in any one of Appendices 1 to 11. [Industrial Applicability]

[0135] As described above, the present invention can suppress peritoneal deterioration. Therefore, the present invention can suppress peritoneal deterioration caused by peritoneal dialysis, and prevent or suppress encapsulating peritoneal sclerosis caused by peritoneal deterioration. Therefore, the present invention can be suitably used, for example, in the treatment of diseases caused by peritoneal deterioration, and is extremely useful in the medical and pharmaceutical fields, etc.

[0136] This application claims priority based on Japanese Patent Application No. 2022-100790, filed on June 23, 2022, the disclosure of which is incorporated herein in its entirety. [Explanation of symbols]

[0137] 1 Room 1 10 containers 11 Composition 12 Upper end 13, 14 sheets 2 Room 2 21 Other ingredients 22 Discharge section 3 Isolation section 5 Hanging section

Claims

1. A composition for use in inhibiting peritoneal deterioration, comprising: A composition comprising carbon monoxide.

2. Contains microbubbles, The composition of claim 1 , wherein the microbubbles contain carbon monoxide as a gaseous component.

3. The density of the microbubbles is 5×10 ５ ~5 x 10 １２ The composition of claim 2, wherein the concentration is 0.015 mg / ml.

4. 4. The composition according to claim 2, wherein the proportion of carbon monoxide in the gaseous components is 80% or more.

5. The composition according to claim 2 or 3, wherein in the microbubbles, the gas component is surrounded by an aqueous solvent.

6. Further, the medium includes The composition according to claim 2 or 3, wherein the medium is at least one of a liquid and a solid.

7. Includes media, 10. The composition of claim 1, wherein the carbon monoxide is dissolved in the medium.

8. 8. The composition according to claim 7, wherein the content of carbon monoxide dissolved in the medium is 0.01 μmol / L to 5 mmol / L.

9. The composition of claim 1 , 2 , 7 or 8 , wherein the peritoneal deterioration is peritoneal fibrosis.

10. The composition according to claim 1 , wherein the peritoneal deterioration is a decrease in peritoneal function.

11. 10. The composition of any one of claims 1, 2, 7 or 8 for use in intraperitoneal administration.

12. A composition kit for use in inhibiting peritoneal deterioration, comprising: composition and other ingredients, The composition and the other components are arranged separately, 10. A composition kit, wherein the composition is a composition according to any one of claims 1, 2, 7 or 8.

13. Further comprising a container, The container has a plurality of chambers and isolation portions that isolate the chambers, the plurality of chambers includes at least a first chamber and a second chamber; The composition is contained in the first chamber; The other ingredients are contained in the second chamber, The composition kit according to claim 12 , wherein the isolation portion isolates the first chamber from the second chamber and allows the first chamber to communicate with the second chamber.

14. The composition kit of claim 12 , wherein the other components include an osmolyte.

15. A peritoneal dialysis solution comprising the composition of any one of claims 1, 2, 7 or 8.

16. a composition and a peritoneal dialysis solution, The composition and the peritoneal dialysis solution are placed separately, 10. A peritoneal dialysis solution kit, wherein the composition is the composition of any one of claims 1, 2, 7 or 8.

17. Further comprising a container, The container has a plurality of chambers and isolation portions that isolate the chambers, the plurality of chambers includes at least a first chamber and a second chamber; The composition is contained in the first chamber; The peritoneal dialysis solution is contained in the second chamber; The peritoneal dialysis solution kit according to claim 16, wherein the isolation section isolates the first chamber from the second chamber and allows the first chamber to communicate with the second chamber.

18. A pharmaceutical composition for use in preventing or suppressing diseases caused by peritoneal dialysis, comprising: A pharmaceutical composition comprising carbon monoxide.

19. A pharmaceutical composition kit for use in preventing or suppressing diseases caused by peritoneal dialysis, comprising: composition and other ingredients, The composition and the other components are arranged separately, 10. A composition kit, wherein the composition is a composition according to any one of claims 1, 2, 7 or 8.

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