Treatment of inflammatory conditions in mucous membranes or on the skin

Abstract

The present invention relates to a pharmaceutical composition comprising 0.001-2% (w / v) propane-1,2-diol as the sole anti-inflammatory agent and at least one bioadhesive polymer. The pharmaceutical composition can be used to ameliorate, prevent, or treat inflammatory conditions of the mucosa or skin of a subject, and / or to treat pain associated with such inflammatory conditions.

Description

[Technical field]

[0001] The present invention relates to pharmaceutical compositions used to ameliorate, prevent or treat inflammatory conditions of the mucous membranes or skin of a subject, and to the treatment of pain associated with such inflammatory conditions. [Background technology]

[0002] Wound healing is a complex process involving the overlapping of a series of processes: inflammatory responses, proliferative processes leading to tissue repair, and finally tissue remodeling. The wound healing process is greatly influenced and regulated by various cellular elements, which can be bioactive compounds such as growth factors and cytokines at the wound site.

[0003] The initial inflammatory phase of the wound healing process involves a vascular response characterized by cellular events including the infiltration of leukocytes and inflammatory cells with various functions including blood clotting and hemostasis, as well as the release of antimicrobial factors and cytokines, which initiate a proliferative response for wound repair. Some authors add further stages, emphasizing the importance of the vascular response while leaving the first stage as hemostasis. During the proliferative phase, there is the formation of an epithelium to cover the wound surface, accompanied by the growth of granulation tissue to fill the wound space. Granulation tissue involves the proliferation of fibroblasts, the deposition of collagen and other extracellular matrix, and the initiation of new blood vessel development. Once new tissue elements are generated within the wound, the remodeling phase begins to restore the structural integrity and functional capacity of the tissue. The stages of typical wound repair are usually not simple linear events, but rather complex and overlapping in time.

[0004] When the cellular elements appear at the wound site, they become activated and the macrophages start to release several growth factors and cytokines that influence the formation of granulation and tissue.

[0005] The development of novel and effective interventions in wound care remains an area of ​​active research. The role of various inflammatory cells, vasoactive amines, serotonin, coagulation factors, arachidonic acid metabolites, free radicals, platelet factors, cytokines, chemokines and gene regulation are being actively investigated with respect to the impact related to the inflammatory process. Despite many scientific discoveries and advances, the understanding of the mechanisms and pathways involved in normal and abnormal wound healing is still poor. Thus, there is a great deal of room for improvement in the management of certain inflammatory conditions.

[0006] No. 8,513,225 discloses a hydrogel containing 80% propylene glycol that is applied to prodermal lesions in patients suffering from recurrent ulcerative stomatitis. The pain subsided, but the lesions did not disappear. Summary of the Invention [Problem to be solved by the invention]

[0007] It is the overall objective to provide treatment for inflammatory conditions of the mucous membranes or skin. [Means for solving the problem]

[0008] This and other objectives are met by the embodiments disclosed herein.

[0009] The invention is defined in the independent claims. Further embodiments of the invention are defined in the dependent claims.

[0010] Briefly, the present invention relates to a pharmaceutical composition for use in the amelioration, prevention or treatment of an inflammatory condition in the mucosa or skin of a subject, and / or for use in treating pain associated with such an inflammatory condition in the mucosa or skin of a subject. The pharmaceutical composition comprises 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer. The pharmaceutical composition does not comprise any anti-inflammatory agent other than propane-1,2-diol.

[0011] The pharmaceutical compositions of the present invention are capable of significantly reducing the amount of tumor necrosis factor alpha (TNF-α) and interleukin 2 (IL-2), two cytokines involved in the inflammatory process. The present invention has been shown to treat inflammatory conditions and to reduce the pain and discomfort associated with such inflammatory conditions and pathologies. [Brief description of the drawings]

[0012] [Figure 1A] Concentration-dependent effect of propane-1,2-diol, i.e. propylene glycol (PG), on TNF-α production by peripheral blood mononuclear cells (PBMC) from four patients stimulated with lipopolysaccharide (LPS). A strong inhibition of TNF-α concentration was obtained at 100 mM propane-1,2-diol. [Figure 1B] Concentration-dependent effect of propane-1,2-diol, i.e. propylene glycol (PG), on TNF-α production by peripheral blood mononuclear cells (PBMC) from four patients stimulated with lipopolysaccharide (LPS). A strong inhibition of TNF-α concentration was obtained at 100 mM propane-1,2-diol. [Figure 1C] Concentration-dependent effect of propane-1,2-diol, i.e. propylene glycol (PG), on TNF-α production by peripheral blood mononuclear cells (PBMC) from four patients stimulated with lipopolysaccharide (LPS). A strong inhibition of TNF-α concentration was obtained at 100 mM propane-1,2-diol. [Figure 1D] Concentration-dependent effect of propane-1,2-diol, i.e. propylene glycol (PG), on TNF-α production by peripheral blood mononuclear cells (PBMC) from four patients stimulated with lipopolysaccharide (LPS). A strong inhibition of TNF-α concentration was obtained at 100 mM propane-1,2-diol. [Diagram 2] Figure 2 shows the effect of 100 mM propane-1,2-diol on TNF-α inhibition when PBMCs (buffy coats from 12 patients) were stimulated with LPS. [Diagram 3] IL-2 production following increasing concentrations of phytohemagglutinin (PHA) is shown. [Figure 4] FIG. 1 shows the effect of different concentrations of propane-1,2-diol on IL-2 production by 1 μg / ml PHA stimulated PBMC from two different patients. [Figure 5A] The difference between the mucosal tissue weight and its water content after contact with water or propylene glycol solution is shown. [Figure 5B] The difference between the mucosal tissue weight and its water content after contact with water or propylene glycol solution is shown. [Figure 6] TNFR1 signaling pathway. [Figure 7] PBMC cell death rates at different concentrations of propane-1,2-diol are shown. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] The present invention relates to pharmaceutical compositions used to ameliorate, prevent or treat inflammatory conditions of the mucous membranes or skin of a subject, and to the treatment of pain associated with such inflammatory conditions.

[0014] It has surprisingly been found that propane-1,2-diol is useful for ameliorating, preventing and / or treating inflammatory conditions of mucous membranes and skin in a subject.

[0015] Propane-1,2-diol, commonly called propylene glycol (PG), is a synthetic diol alcohol with the chemical formula C3H8O2. The compound is sometimes called α-propylene glycol to distinguish it from the isomer propane-1,3-diol, known as β-propylene glycol. Other alternative names include 1,2-propanediol, 1,2-dihydroxypropane, methyl ethyl glycol (MEG), and methyl ethylene glycol.

[0016] Propane-1,2-diol is a tasteless, odorless, colorless, transparent liquid that is miscible with water, acetone and chloroform and is hygroscopic. Propane-1,2-diol has many uses, including, for example, the manufacture of polymers. It can also be used in food processing and as a process fluid in low-temperature heat exchange applications. Propane-1,2-diol is known to be used in cosmetic and pharmaceutical compositions as a solvent, co-solvent, humectant, plasticizer in polymer films, and as a permeation enhancer.

[0017] For a long time, propane-1,2-diol has been considered an inert organic solvent (Seidenfeld and Hanzlik (1932) J. Pharmac. Exp. Ther. 44, 109-121; Braun and Cartland (1936) J. Am. Pharm. Ass. 25, 746-749; Weatherby and Haag (1938) J. Am. Pharm. Assoc. 27, 466-471). However, adverse effects have occurred after topical, oral, and intravenous administration of propane-1,2-diol (Glascow, et al. (1983) Pediatrics 72(3), 353-355). Adverse effects associated with propane-1,2-diol include central nervous system (CNS) toxicity, hyperosmolarity, hemolysis, cardiac arrhythmias, and lactic acidosis. Despite these adverse effects, it has been proposed for topical use in high concentrations (15-100%) on various skin lesions to kill bacteria, fungi, and / or viruses (U.S. Patent No. 8,513,225). However, low concentrations of propane-1,2-diol have not been shown to have any adverse effects on organisms.

[0018] The experimental data presented herein show that even low concentrations of propane-1,2-diol have a therapeutic effect on inflammatory conditions of the mucosa or skin, particularly by causing a significant reduction in tumor necrosis factor alpha (TNF-α) and interleukin-2 (IL-2).

[0019] TNF-α, also called cachexin or cachectin, is a cytokine involved in systemic inflammation in mammalian tissues. TNF-α plays a major role in regulating the cellular components of the immune system. TNF-α is known as a major pro-inflammatory mediator, and overexpression of TNF-α, along with the resulting overactivation of nuclear factor kappa light-chain-enhancer of activated B cells (NF-κB), is thought to be a key element in the progression and maintenance of various inflammatory conditions. TNF-α can induce fever, apoptotic cell death, cachexia, inflammation, and act to respond to sepsis via cells that produce IL-1 and IL-6.

[0020] TNF-α is known to be produced primarily by various cell types, such as macrophages (Olszewski et al. (2007) Journal of Immunology 178, 5701-5709), lymphoid cells, endothelial cells, cardiac myocytes, adipose tissue cells, and fibroblasts. Large amounts of TNF-α are released in response to lipopolysaccharide (LPS), other bacterial products, and IL-1. In the skin, mast cells are the major source of TNF-α, which can be released in response to inflammatory stimuli, such as LPS (Walsh et al. (1991) Proc. Natl. Acad. Sci. USA 88(10), 4220-4224).

[0021] TNF-α is primarily produced as a 233 amino acid long type II transmembrane protein that forms a stable homotrimer and is released via proteolytic cleavage by the metalloprotease TNF-α converting enzyme (TACE), also called ADAM17. Both secreted and membrane-bound forms are biologically active (Palladino et al. (2003) Nature Reviews Drug Discovery 2(9), 736-746). TNF-α can bind to two receptors: TNF receptor type 1 (TNFR1), also called CD120a or p55 / 60, and TNFR2, also called CD120b or p75 / 80. TNFR1 is expressed in most tissues and can be fully activated by both membrane-bound and soluble trimeric TNF-α, whereas TNFR2 is typically found in cells of the immune system and responds to membrane-bound TNF-α homotrimers. Upon contact with ligand, TNF receptor binding can result in (1) activation of NF-κB, (2) activation of the mitogen-activated protein kinase (MAPK) pathway, or (3) induction of death signaling. Thus, TNF-α activation can result in complex and often opposing effects mediated by these pathways in various tissues.

[0022] Figure 6 shows the TNFR1 signaling pathway. Upon binding of TNF-α to TNFR1, TNF receptor-associated factor 2 (TRAF2), receptor interacting protein (RIP), and Fas-associated protein with death domain (FADD) are recruited to TNFR1 via the adaptor protein TRADD. TRAF2 and RIP lead to activation of the transcription factor activator protein 1 (AP-1) via activation of mitogen-activated protein (MAP) kinase kinase kinase (MAP3K) as well as c-Jun N-terminal kinase (JNK) and p38 MAPK. TRAF2 and RIP also activate the transcription factor NF-kB via activation of the kinase IκB kinase (IKK). Phosphorylation of IkB leads to proteasomal degradation of the latter and nuclear translocation of activated NF-kB. Many of the genes transcribed by NF-kB and AP-1 are anti-apoptotic or oncogenic. FADD recruits and activates the proapoptotic caspase 8. TNF-α signaling and expression can be inhibited by targeting the proteolysis of TNF-α precursor to TNF-α or by interfering with the downstream MAP3K and NF-kB cascades. TNF-α expression can also be inhibited by compounds that target molecules along the IRAK4 signaling pathway, activate adenylate cyclase, or prevent the translation of TNF-α precursor messenger ribonucleic acid (mRNA) into TNF-α precursor. TNF-α expression can also be inhibited by compounds that interfere with phosphodiesterase 4 (PDE4), which converts cyclic adenosine monophosphate (cAMP) to adenosine monophosphate (AMP), since PDE4 is required for the transcription of TNF-α by NF-kB. The diagram in Figure 6 is taken from Folmer et al. (2012) Current Topics in Medicinal Chemistry 12, 1392-1407.

[0023] It is clear that whenever this cytokine is released, due to the complex signaling that follows its release, a wide variety of cells with highly diverse functions and conditions will generate inflammatory responses that may be present or progress in various anatomical locations in the mucosa or skin. TNF-α-related conditions include, for example, several diseases involving the skin, such as psoriasis and atopic dermatitis, as well as diseases of the mucosa, such as recurrent aphthous stomatitis (RAS), inflammatory bowel disease (IBD), and oral lichen planus (Mozaffari et al. (2017) Oral Surg Oral Med Oral Pathol Oral Radiol. 124(3), e183-e189). TNF-α has been suggested as a key cytokine in such conditions.

[0024] In particular, TNF-α is believed to play a key role in the progression of new RAS lesions, also called aphthous stomatitis or stomatitis, and has been found to be increased 2-5 fold in the saliva of affected patients (Chaudhuri et al. (2018) J Dent Res Dent Clin Dent Prospect 12(1), 45-48). The involvement of TNF-α in the progression of RAS gains credibility due to the fact that immunomodulatory drugs such as thalidomide and pentoxifylline have been found to be effective in the treatment of RAS (Natah et al. (2000) Int J Oral Maxillofac Surg 29, 375-80; Sampaio et al. (1991) J Exp Med; 173, 699-703).

[0025] IL-2 is a cytokine and one of the most important signaling molecules in the immune system. It is secreted by clonally expanding naive T cells that have just been activated by antigen. IL-2 is an autocrine messenger secreted by the same cells that IL-2 acts on. IL-2 stimulates T cells to undergo mitosis, leading to an increase in the amount of specific T cells to eliminate pathogens. IL-2 is also a potent activation signal for natural killer (NK) cells and B cells. In addition, IL-2 stimulates regulatory T cells to turn off the immune response when a stimulus such as an infection is eliminated.

[0026] IL-2 is a member of the cytokine family, each member of which contains four α-helical bundles. This family also includes IL-4, IL-7, IL-9, IL-15, and IL-21. IL-2 signals through the IL-2 receptor, a complex of three chains called α (CD25), β (CD122), and γ (CD132). All cytokine family members share the γ chain.

[0027] The pleiotropic effects of IL-2 are made possible by the fact that IL-2 signals can be transduced through three different signaling pathways, namely the Janus kinase-signal transduction and activator of transcription (JAK-STAT), phosphoinositide 3-kinase / protein kinase B / mammalian target of rapamycin (PI3K / Akt / mTOR) and MAPK / extracellular signal-regulated kinase (MAPK / ERK) pathways. After IL-2 binds to its receptor, the cytoplasmic domains of CD122 and CD132 heterodimerize, leading to the activation of the Janus kinases JAK1 and JAK3, which subsequently phosphorylate Tyr-338 on CD122. This phosphorylation recruits STAT transcription factors, mainly STAT5, which dimerize and translocate to the cell nucleus, where they bind to deoxyribonucleic acid (DNA).

[0028] IL-2 has an essential role in the important functions of the immune system, tolerance and immunity, mainly through its direct effect on T cells. In the thymus, where T cells mature, it prevents autoimmune diseases by promoting the differentiation of certain immature T cells into regulatory T cells, which suppress other T cells that would otherwise be primed to attack normal healthy cells in the body. IL-2 enhances activation-induced cell death (AICD). IL-2 also promotes the differentiation of T cells into effector and memory T cells, if the initial T cells are also stimulated by antigen, thus helping the body fight infection. Together with other polarizing cytokines, IL-2 stimulates the differentiation of naive CD4+ T cells into Th1 and Th2 lymphocytes, while preventing the differentiation into Th17 and follicular Th lymphocytes.

[0029] IL-2 expression and secretion are tightly regulated and function as part of both transient positive and negative feedback loops in the initiation and suppression of immune responses. Through its role in the development of T cell immunological memory, which depends on the expansion in number and function of antigen-selective T cell clones, IL-2 plays a key role in the maintenance of cell-mediated immunity.

[0030] Apparently, the complex signaling that follows IL-2 release will ensure that whenever this cytokine is released, a large number of different cells with highly diverse functions and states will be present or develop an inflammatory response that may occur in various anatomical locations of the mucosa or skin.

[0031] IL-2-related conditions include several skin-related diseases, such as psoriasis and atopic dermatitis, as well as diseases of the mucous membranes, such as RAS, IBD, and oral lichen planus. For a review, see Vasovic, et al. (2016) Cent Eur J Immunol. 41(3), 302-310. IL-2 has been suggested as a key cytokine in such conditions. IL-2 is also thought to play an important role in the progression of new RAS lesions (Kalpana et al. (2014) J Oral Maxillofac Pathol. 18(3), 361-364; Bhosale et al. (2018) J Contemp Dent Pract. 19(10), 1242-1245). IL-2 has also been implicated in the progression of IBD (Ebrahimpour, (2017) J Biol Regul Homeost Agents. 31(2), 279-287) as well as oral lichen planus (Qian et al. (2018) Med Sci Monit. 24: 8716-8721).

[0032] The propane-1,2-diol of the present invention can significantly reduce the amount of TNF-α and IL-2 even when administered in small amounts. Therefore, propane-1,2-diol can be used to improve, prevent or treat inflammatory conditions of the mucosa or skin, for example by inducing a decrease in TNF-α and / or IL-2.

[0033] One aspect of the present invention relates to a pharmaceutical composition for use in the amelioration, prevention or treatment of an inflammatory condition in the mucosa or skin of a subject. The pharmaceutical composition comprises 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer. The pharmaceutical composition does not contain any anti-inflammatory agent other than propane-1,2-diol.

[0034] Thereby, the pharmaceutical composition of the present invention comprises a relatively small amount of propane-1,2-diol, i.e., up to 2% (w / v), and at least one bioadhesive polymer. It was very surprising that this small amount of propane-1,2-diol could have a therapeutic effect, when the prior art, such as that presented by U.S. Pat. No. 8,513,225, requires at least 15% propane-1,2-diol and disclosed a hydrogel containing 80% propane-1,2-diol. However, such high concentrations of propane-1,2-diol are associated with adverse effects after topical, oral, and intravenous administration, including CNS toxicity, hyperosmolarity, hemolysis, cardiac arrhythmia, and lactic acidosis (Glascow et al. (1983) Pediatrics 72(3), 353-355). Moreover, topical administration of high concentrations of propane-1,2-diol further has adverse dehydrating effects, as shown in Table 1 below.

[0035] Hereinafter, the amount of propane-1,2-diol in the pharmaceutical composition is defined as mass volume % (w / v). In many practical applications of pharmaceutical compositions, %w / v is substantially the same as weight % (w / w). Thus, in some embodiments, the concentration of propane-1,2-diol in the pharmaceutical composition expressed as %w / v also encompasses the corresponding concentration of propane-1,2-diol in the pharmaceutical composition expressed as %w / w.

[0036] The at least one bioadhesive polymer allows the pharmaceutical composition to adhere to the mucosa or skin, thereby achieving local administration and release of the propane-1,2-diol to the mucosa or skin.The at least one bioadhesive polymer thus allows the pharmaceutical composition to cover the lesion or inflamed area of ​​the mucosa or skin over the treatment period.

[0037] The inflammatory condition ameliorated, prevented or treated by the pharmaceutical composition of the present invention is an inflammatory condition in the mucosa or skin of a subject. In one embodiment, the inflammatory condition is an inflammatory lesion of the mucosa or skin.

[0038] The mucosa may be any mucosa within the subject's body, including, for example, the bronchial mucosa, the mucosa of the uterus (endometrium), the esophageal mucosa, the gastric mucosa, the intestinal mucosa, the nasal mucosa, the olfactory mucosa, the oral mucosa, the lingual frenulum, the mucosa of the tongue, the penile mucosa, the vaginal mucosa, the mucosa of the anal canal, and the palpebral conjunctiva. In certain embodiments, the mucosa is the oral mucosa.

[0039] In one embodiment, the inflammatory condition is an inflammatory condition or disorder of the mucosa, such as stomatitis, mucositis, recurrent aphthous stomatitis (RAS, also called aphthous stomatitis or stomatitis), minor aphthae, major aphthae, recurrent aphthous ulcers (RAU), herpetiform aphthae, bullous erosions or ulcerative lesions, pemphigus family of disorders, pemphigoid family of disorders, linear immunoglobulin A (IgA) disorder, dermatitis herpetiformis, discoid lupus erythematosus, radiotherapeutic mucositis, chemotherapy-induced mucositis, or oral lichen planus. In one embodiment, the inflammatory condition in the mucosa is an inflammatory condition in the oral mucosa, preferably RAS.

[0040] In one embodiment, the inflammatory condition is an inflammatory condition of the skin, for example, eczema, seborrheic eczema, contact dermatitis, atopic dermatitis, ichthyosis, dry skin, UV dermatitis, blisters, acne, psoriasis, herpes, pressure sores, diabetic ulcers, urticaria, hyperhidrosis, rosacea, keratosis pilaris, actinic keratosis, warts, fungal infections (e.g., ringworm, athlete's foot), viral disease rashes, for example from herpes simplex, shingles, chickenpox or measles, and bacterial infections such as impetigo or carbuncles.

[0041] In one embodiment, the pharmaceutical composition comprises 0.001% up to 2% (w / v) propane-1,2-diol. In another embodiment, the pharmaceutical composition comprises 0.001% up to less than 2% (w / v) propane-1,2-diol.

[0042] In one embodiment, the pharmaceutical composition comprises 0.01% to 2% (w / v) propane-1,2-diol. In another embodiment, the pharmaceutical composition comprises 0.01% to less than a maximum of 2% (w / v) propane-1,2-diol.

[0043] In one embodiment, the pharmaceutical composition comprises 0.5% to 2% (w / v) propane-1,2-diol. In another embodiment, the pharmaceutical composition comprises 0.5% to less than a maximum of 2% (w / v) propane-1,2-diol.

[0044] In another embodiment, the pharmaceutical composition comprises 0.5-1.5% (w / v) propane-1,2-diol, preferably 0.5-1.25% (w / v) propane-1,2-diol, more preferably 0.5-1.0% (w / v) propane-1,2-diol, such as 0.6-1.0% (w / v) propane-1,2-diol, or 0.7-0.9% (w / v) propane-1,2-diol, such as about 0.8% (w / v) propane-1,2-diol.

[0045] A preferred concentration of propane-1,2-diol in the pharmaceutical composition is 0.001-2% (w / v), however, embodiments of the pharmaceutical composition may also include up to 2.75% (w / v) propane-1,2-diol, such as up to 2.5% (w / v) or up to 2.25% (w / v) propane-1,2-diol.

[0046] The amount of propane-1,2-diol contained in the pharmaceutical composition of the present invention has a medical effect as disclosed herein, but without the adverse effects seen with pharmaceutical compositions containing significantly higher concentrations of propane-1,2-diol, as disclosed in U.S. Pat. No. 8,513,225. The pharmaceutical composition of the present invention does not have adverse hydrating effects, whereas compositions containing higher concentrations of propane-1,2-diol are dehydrating. Thus, application of compositions containing high amounts of propane-1,2-diol, for example, more than 15%, more than 50% or more, for example 80%, can dehydrate the tissue to which the composition is applied.

[0047] Furthermore, the experimental data presented herein show that propane-1,2-diol in the amounts according to the invention has no significant toxic effect and does not induce significant cell death, however, already at a concentration of 5% (w / v), propane-1,2-diol induced significant cell death and was therefore toxic to peripheral blood mononuclear cells.

[0048] Thus, the pharmaceutical compositions of the present invention have medical effects, particularly as seen in significant inhibition of TNF-α and / or IL-2, but without the deleterious effects, particularly in terms of dehydration and toxicity, seen with higher concentrations of propane-1,2-diol.

[0049] In one embodiment, the pharmaceutical composition comprises 50-99% (w / v) of at least one bioadhesive polymer, preferably 60-99% (w / v), for example 70-99% (w / v) or 80-99% (w / v), more preferably 90-99% (w / v) of at least one bioadhesive polymer.

[0050] The at least one bioadhesive polymer is capable of adhering to the biological tissue to which the pharmaceutical composition is applied. Thus, the at least one bioadhesive polymer is preferably capable of adhering to the mucosa and / or skin of a subject.

[0051] In one embodiment, the at least one bioadhesive polymer is at least one mucoadhesive polymer, ie at least one polymer capable of adhering to a mucosa.

[0052] In one embodiment, the at least one mucoadhesive polymer is poly(acrylic acid) (PAA).

[0053] PAA, also known by its trade name Carbomer, is a synthetic high molecular weight polymer of acrylic acid. PAA may be a homopolymer of acrylic acid or may be crosslinked with allyl ethers of pentaerythritol, allyl ethers of sucrose, or allyl ethers of propylene. In aqueous solutions at neutral pH, PAA is an anionic polymer, i.e., many of the side chains of PAA lose protons and acquire a negative charge. This makes PAA a polyelectrolyte with the ability to absorb and retain water and swell to many times its original volume. The pharmaceutical uses of PAA are described in the Pharmacopoeia (BP 93) and USP 23. In general, carbomer resins intended for oral and mucosal application are designated by a "P" (934P, 974P, 971P).

[0054] PAA is swellable in water due to the high proportion of carboxylic acid groups in the polymer. When dispersed in water, the PAA molecules partially swell, increasing the viscosity. When neutralized with a water-soluble base, the PAA molecules swell completely, dramatically increasing the viscosity. In an alkaline environment, the carboxyl groups of PAA dissociate. Electrostatic repulsion between the negatively charged carboxyl groups causes the PAA molecules to unravel and expand. This causes the polymer to swell, forming a gel. The gel is composed of closely packed swollen particles that swell more and more with increasing pH.

[0055] PAA is advantageous as a bioadhesive polymer because it is physiologically inert and is not absorbed from the gastrointestinal tract into the systemic circulation. PAA has good mucoadhesive properties. When used as a carrier for propane-1,2-diol, the PAA polymer could increase the propane-1,2-diol concentration at the administration site by localizing the propane-1,2-diol at its absorption site. Thus, absorption would be enhanced and bioavailability would increase. Furthermore, PAA formulations could provide sustained release properties to pharmaceutical compositions. Under both simulated gastric and intestinal fluids, PAA provides CR at lower concentrations than other controlled release (CR) systems. Furthermore, PAA protects the underlying cell layer, forming a thick barrier that separates the cells from the environment due to its continuous crosslinking and the fact that it is water insoluble. For tablet dosage forms, PAA is a good disintegrant and a directly compressible vehicle. PAA produces tablets with excellent hardness and friability over a range of compression forces.

[0056] In certain embodiments, the PAA is selected from the group consisting of PAAs having an average viscosity of 29,400 to 39,400 cP at 25° C. in a 0.5 wt % aqueous solution at pH 7.3 to maximum 7.8, as measured by a Brookfield Viscometer (Brookfield RVT, 20 rpm, spindle #6), PAAs having an average viscosity of 4,000 to 11,000 cP at 25° C. in a 0.5 wt % aqueous solution, as measured by a Brookfield Viscometer (Brookfield RVT, 20 rpm, spindle #5), as measured by a Brookfield Viscometer (Brookfield RVT, 20 rpm, spindle #5), and combinations thereof. Such PAAs are commercially available as Carbopol 974P NF, Carbopol 971P NF, and Carbopol 71G NF, respectively.

[0057] Carbopol 71G NF polymer is a free-flowing granular form of Carbopol 971P NF polymer for use in direct compression formulations. It is produced by roller compacting Carbopol 971P NF polymer and is a chemically identical product without additives. The resulting granules are free-flowing, have increased bulk density, and contain minimal amounts of very small particles that may cause dusting and / or static adherence compared to powdered polymers.

[0058] Other examples of bioadhesive polymers that can be used according to the invention include alginate polymers. Alginates, salts of alginic acid, are linear polysaccharides that are naturally produced by brown seaweeds (Phaeonphyceae, including Laminaria). Alginates are composed of a large number of monomeric residues, typically between 100 and 3,000 monomers, linked together in flexible chains. These residues are primarily β-(1→4) linked D-mannuronic acid (M) residues and β-(1→4) linked L-guluronic acid (G) residues. These two residues are epimers, differing only at C5. In the polymer chain, they give rise to very different conformations, and as shown in formula I, any two D-mannuronic acid residues are 4 The bond linking either to the L-guluronic acid residue is 1 C4-diaxially bonded. [ka] The residues are generally organized into blocks of identical or strictly alternating residues, for example MMMMMM..., GGGGGG..., or GMGMGM....

[0059] Alginate polymers form soluble solid particles in the presence of monovalent cations. This is because alginate polymers are instead Ca 2+This is in clear contrast to when the alginate polymer is exposed to divalent cations such as 1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,50,51,60,71,82, which form links between different alginate polymers, thereby cross-linking the alginate polymers. This cross-linking then results in the formation of an alginate film that is generally insoluble, or at least difficult to dissolve in a moist environment.

[0060] Suitable monovalent cations that can be used include sodium ions (Na + ), potassium ion (K + ) and ammonium ion (NH4 + ), preferably Na + Includes:

[0061] In one embodiment, the pharmaceutical composition comprises at least one excipient in addition to propane-1,2-diol and at least one bioadhesive polymer. Non-limiting but illustrative examples of such excipients include anti-adhesive agents, binders, coatings, colorants, disintegrants, flavorings, glidants, lubricants, preservatives, adsorbents, solvents, buffers, stabilizers, adjuvants, diluents, wetting agents, surfactants, osmotic agents, sweeteners and vehicles. In certain embodiments, the at least one excipient is selected from the group consisting of microcrystalline cellulose, povidone (also called polyvinylpyrrolidone (PVP)), magnesium stearate and combinations thereof.

[0062] In one embodiment, the pharmaceutical composition comprises microcrystalline cellulose in an amount of 2.5-15% (w / w), preferably 5-10% (w / w), more preferably 7-9% (w / w) or 7-8% (w / w), for example about 7.9% (w / w).

[0063] In one embodiment, the pharmaceutical composition comprises povidone in an amount of 0.01-5% (w / w), preferably 0.01-1% (w / w), more preferably 0.05-0.5% (w / w), for example about 0.1% (w / w). Povidone as used herein does not include povidone iodine. In one embodiment, povidone as used herein is 1-ethenylpyrrolidin-2-one.

[0064] In one embodiment, the pharmaceutical composition comprises magnesium stearate in an amount of 0.01-5% (w / w), preferably 0.01-2.5% (w / w), more preferably 0.1-1% (w / w), for example about 0.5% (w / w).

[0065] In one embodiment, the pharmaceutical composition is formulated, i.e., converted into a suitable form, for local application to the inflamed area or lesion. In a preferred embodiment, the pharmaceutical composition is formulated for topical application or administration. Such topical application may include skin, mucous membrane, sublingual, buccal, intranasal, ocular, rectal, or intravaginal application, depending on the location of the inflamed area or lesion.

[0066] The pharmaceutical composition, in one embodiment, is in a dosage form selected from the group consisting of a patch, a film, a tablet, a cream, an ointment, a foam, a gel, and a spray.

[0067] For example, the patch may be in the form of a mucoadhesive patch, such as a skin patch or a mucoadhesive oral patch, such as a skin patch or a mucoadhesive oral patch, which may be shaped to cover the inflamed area or lesion and adhere to the inflamed area or lesion throughout the treatment period due to the presence of at least one bioadhesive polymer, such as at least one mucoadhesive polymer.

[0068] The mucoadhesive patch can be manufactured according to a variety of embodiments, including in the form of a mucoadhesive tablet, a mucoadhesive film, or a mucoadhesive gel, depending on the particular components and concentrations of the pharmaceutical composition.

[0069] In the case of a film, cream, ointment, foam or gel, the film, cream, ointment, foam or gel can preferably be attached to mucosa and / or skin, i.e. preferably a mucoadhesive film, such as a skin film, a mucoadhesive buccal film, etc. If at least one bioadhesive polymer is present in the pharmaceutical composition, the film, cream, ointment, foam or gel can be attached to an inflamed area or lesion of mucosa and / or skin. Thus, such a film, cream, ointment, foam or gel can be used as a "medical dressing" or patch to cover an inflamed area or lesion, and at the same time release propane-1,2-diol to promote the healing process.

[0070] The pharmaceutical composition formulated as a tablet is preferably in the form of a skin or mucoadhesive tablet, i.e., such a tablet can be attached to the skin or mucosa of a subject.Such a tablet can contain, in addition to propane-1,2-diol and at least one bioadhesive polymer, a filler such as microcrystalline cellulose (MCC), a binder such as povidone, and a lubricant such as magnesium stearate.The presence of at least one bioadhesive polymer provides the formed tablet with adhesive properties, such as mucoadhesive properties, which means that when the tablet comes into contact with an inflamed or lesioned area of ​​mucosa or skin, the tablet adheres thereto and the propane-1,2-diol is continuously released to the inflamed or lesioned area.

[0071] The pharmaceutical composition in the form of a spray also has adhesive properties due to the presence of at least one bioadhesive polymer. The spray is preferably sprayed onto the mucous membrane or skin inflamed areas or lesions. The hygroscopicity and / or viscosity properties of the spray formulation can be adjusted by including various excipients that adjust the viscosity and / or hygroscopicity of the pharmaceutical composition.

[0072] In general, the galenic properties of the pharmaceutical composition can be adjusted by ingredients such as dextran, starch-acrylonitrile copolymers, soy protein / poly(acrylic acid) superabsorbent polymers, polyacrylate / polyacrylamide copolymers, polyacrylamide copolymers, ethylene maleic anhydride copolymers, crosslinked carboxymethylcellulose, polyvinyl alcohol copolymers, crosslinked polyethylene oxide, and / or starch graft copolymers of polyacrylonitrile.

[0073] The pharmaceutical composition may be applied to the inflamed area or lesion by an applicator. In such an embodiment, a handheld applicator can be used to allow convenient and hygienic dispensing and uniform spreading of topical formulations such as creams, ointments, foams and gels, and to easily apply oral patch formulations. The applicator can be used to orally deliver the pharmaceutical composition to a desired mucosal site in the oral cavity. When an applicator is used, the applicator can include three main components: an applicator barrel, a tip for holding the pharmaceutical composition to be delivered, and a plunger. In practical use, the medical formulation can be placed in the tip. The tip, which conforms to the shape of the medical intervention, firmly grips or encases the pharmaceutical composition depending on the size or volume. The applicator is then inserted into or applied onto the desired application site. Once placed, the plunger is depressed to apply the pharmaceutical composition to the desired anatomical site.

[0074] Mucoadhesion is a complex phenomenon involving wetting, adsorption and interpenetration of polymer chains. Relating this mechanism to pharmacology, mucoadhesion describes the attractive forces between a pharmaceutical composition and mucus or mucous membranes.

[0075] The mucoadhesion process involves two general steps: a contact phase and a solidification phase. The contact phase is the initial wetting that occurs between the pharmaceutical composition and the mucosa. This can occur mechanically, by bringing two surfaces together, as when particles are deposited in the nasal cavity by inhalation, or through the body system. The solidification phase of mucoadhesion involves the establishment of adhesive interactions to reinforce a strong or long-term attachment. In the presence of moisture, the mucoadhesive material is activated and the system is plasticized. This stimulus allows the mucoadhesive molecules to separate and break free while proceeding to be bound by weak van der Waals and hydrogen bonds. There are multiple mucoadhesion theories that explain the solidification phase, the two main theories of which focus on macromolecular interpenetration and dehydration.

[0076] The subject treated with the pharmaceutical composition of the present invention is preferably a human subject. However, the pharmaceutical composition may also be applied for veterinary use, where the subject is an animal, preferably a non-human mammal, such as a cat, dog, horse, sheep, pig, cow, goat, rabbit, guinea pig, rat, mouse, etc.

[0077] In accordance with the present invention, the pharmaceutical composition is devoid of anti-inflammatory agents other than propane-1,2-diol, and thus, propane-1,2-diol is the only active anti-inflammatory agent in the pharmaceutical composition.

[0078] In one embodiment, the pharmaceutical composition does not contain any active agent or ingredient in addition to propane-1,2-diol, in particular does not contain any active agent or ingredient with anti-inflammatory effect.Therefore, optional additional components of the pharmaceutical composition are one or more bioadhesive polymers and one or more excipients.These one or more excipients and one or more bioadhesive polymers are not considered as active agents or ingredients in the pharmaceutical composition.

[0079] The pharmaceutical composition of the present invention can be used not only to ameliorate, prevent or treat the inflammatory conditions disclosed herein. The pharmaceutical composition can also or alternatively be used to treat pain associated with or caused by an inflammatory condition of the mucosa or skin of a subject. In such cases, the pharmaceutical composition comprises 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer. The pharmaceutical composition is devoid of anti-inflammatory agents other than propane-1,2-diol.

[0080] The pharmaceutical composition therefore relieves discomfort and pain caused by inflammatory conditions of the skin or mucous membranes, particularly inflammatory conditions of the oral cavity such as RAS.

[0081] Related aspects of the invention include methods of ameliorating, preventing or treating an inflammatory condition of a mucosa or skin in a subject, or treating pain associated with an inflammatory condition of a mucosa or skin in a subject, comprising administering a pharmaceutical composition of the invention, i.e., a pharmaceutical composition comprising 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer, and lacking an anti-inflammatory agent other than propane-1,2-diol.

[0082] The pharmaceutical compositions are preferably administered locally to the inflamed area or lesion, such as by topical application to the inflamed area or lesion of the mucosa or skin disclosed herein.

[0083] As used herein, treating an inflammatory condition or treating pain associated with an inflammatory condition also encompasses inhibiting an inflammatory condition or inhibiting pain associated with an inflammatory condition. As used herein, inhibiting an inflammatory condition or pain associated with an inflammatory condition means that the symptoms and effects of the condition are reduced by the pharmaceutical compositions of the invention, even if a 100% treatment or cure does not necessarily occur.

[0084] A further related aspect of the invention includes the use of a pharmaceutical composition of the invention, i.e. a pharmaceutical composition comprising 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer, and devoid of anti-inflammatory agents other than propane-1,2-diol, for the manufacture of a medicament for ameliorating, preventing or treating an inflammatory condition of the mucosa or skin of a subject, or for treating pain associated with an inflammatory condition of the mucosa or skin of a subject.

[0085] Another aspect of the present invention relates to an anti-inflammatory pharmaceutical composition comprising 0.001-2% (w / v) propane-1,2-diol and 50-99% (w / v) poly(acrylic acid) (PAA).

[0086] In one embodiment, the anti-inflammatory pharmaceutical composition comprises 0.01-2% (w / v) propane-1,2-diol, preferably 0.5-2% (w / v) propane-1,2-diol, more preferably 0.8-2% (w / v) propane-1,2-diol.

[0087] In one embodiment, the anti-inflammatory pharmaceutical composition contains 60 to 99% (w / v), for example 70 to 99% (w / v) or 80 to 99% (w / v), preferably 90 to 99% (w / v) PAA.

[0088] In one embodiment, the PAA is selected from the group consisting of PAA having an average viscosity of 29,400 to 39,400 cP in a 0.5 wt % aqueous solution at 25° C., measured by a Brookfield viscometer, at a pH of 7.3 to a maximum of 7.8, PAA having an average viscosity of 4,000 to 11,000 cP in a 0.5 wt % aqueous solution at 25° C., measured by a Brookfield viscometer, at a pH of 7.3 to a maximum of 7.8, and combinations thereof.

[0089] In one embodiment, the anti-inflammatory pharmaceutical composition comprises at least one excipient selected from the group consisting of microcrystalline cellulose, povidone, magnesium stearate, and combinations thereof.

[0090] In a particular embodiment, the anti-inflammatory pharmaceutical composition comprises microcrystalline cellulose in an amount of 2.5-15% (w / w), preferably 5-10% (w / w), more preferably 7-9% (w / w) or 7-8% (w / w), for example about 7.9% (w / w). In another particular embodiment, the anti-inflammatory pharmaceutical composition comprises instead or in addition povidone in an amount of 0.01-5% (w / w), preferably 0.01-1% (w / w), more preferably 0.05-0.5% (w / w), for example about 0.1% (w / w). In a further particular embodiment, the anti-inflammatory pharmaceutical composition comprises instead or in addition magnesium stearate in an amount of 0.01-5% (w / w), preferably 0.01-2.5% (w / w), more preferably 0.1-1% (w / w), for example about 0.5% (w / w).

[0091] In one embodiment, the anti-inflammatory pharmaceutical composition is devoid of anti-inflammatory agents other than propane-1,2-diol.

[0092] In one embodiment, the anti-inflammatory pharmaceutical composition comprises 0.001-2% (w / v) propane-1,2-diol and 50-99% (w / v) PAA. In another particular embodiment, the anti-inflammatory pharmaceutical composition comprises 0.001-2% (w / v) propane-1,2-diol, 50-99% (w / v) PAA, and at least one excipient selected from the group consisting of microcrystalline cellulose in an amount of 2.5-15% (w / w), povidone in an amount of 0.01-5% (w / w), and magnesium stearate in an amount of 0.01-5% (w / w). In these embodiments, the amounts of all components in the anti-inflammatory pharmaceutical composition total 100%.

[0093] Further aspects of the invention include anti-inflammatory compositions for use as a medicine, for use in the amelioration, prevention or treatment of an inflammatory condition of the mucosa or skin of a subject, and / or for use in the treatment of pain associated with an inflammatory condition of the mucosa or skin of a subject.

[0094] Related aspects of the invention include methods of ameliorating, preventing or treating an inflammatory condition of a mucosa or skin in a subject, or treating pain associated with an inflammatory condition of a mucosa or skin in a subject, comprising administering an anti-inflammatory pharmaceutical composition comprising 0.001-2% (w / v) propane-1,2-diol and 50-99% (w / v) PAA.

[0095] The anti-inflammatory pharmaceutical compositions are preferably administered locally to the inflamed area or lesion, such as by topical application to the inflamed area or lesion of the mucosa or skin disclosed herein.

[0096] The present invention also relates to use of an anti-inflammatory pharmaceutical composition comprising 0.001-2% (w / v) propane-1,2-diol and 50-99% (w / v) PAA for the manufacture of a medicament for use in the amelioration, prevention or treatment of an inflammatory condition of the mucosa or skin of a subject, and / or for use in the treatment of pain associated with an inflammatory condition of the mucosa or skin of a subject.

[0097] A further aspect of the present invention relates to a mucoadhesive tablet, such as a mucoadhesive buccal tablet, which comprises the pharmaceutical composition according to the present invention or the anti-inflammatory pharmaceutical composition according to the present invention.

[0098] example Example 1: In vitro culture of human PBMCs Human venous blood was sampled and collected in heparinized vials and mixed well by gently inverting the tube several times. Human peripheral blood mononuclear cells (PBMCs) were isolated by gradient centrifugation using Ficoll-Histopaque®.

[0099] The cells were washed with sterile phosphate-buffered saline (PBS) (centrifugation at 400 × g for 10 min). The PBS was discarded and the cell pellet was resuspended in sterile Dulbecco's Modified Eagle Medium (DMEM). The cells were then counted by hemocytometer using a white blood cell (WBC) diluent: 15 μl of cell suspension was added to 15 μl of trypan blue and mixed thoroughly. The cell suspension was loaded onto a hemocytometer and the cells were counted. The cell concentration was adjusted to 2 × 10 using DMEM supplemented with 1% penicillin-streptomycin solution and 5% human serum. 6 The approximate cell yield was adjusted to 10 cells / ml. 7 ~10 8 The cells / ml varied.

[0100] 1 ml of cell suspension was seeded in 24-well culture plates. 1 ml of propane-1,2-diol diluted in DMEM was added at various concentrations (0-100 mM). 15 μl of phytohemagglutinin (PHA) was added to a final concentration of 1 μg / ml. When investigating the effect of different concentrations of PHA (Figure 1), the range used was 0-25 μg / ml. Plates were incubated for 24 h at +37 °C and 5% CO2. Plates were then frozen at -20 °C until further analysis. After thawing the samples, enzyme-linked immunosorbent assays (ELISAs) were performed according to the manufacturer's specifications.

[0101] Example 2: Inhibition of TNF-α production in human PBMCs in vitro The immunopathogenesis of aphthous stomatitis is thought to be T cell mediated. The aim of this example was to characterize the cytokine profile of PBMCs with a special emphasis on the effect of using propane-1,2-diol. The production of the cytokine tumor necrosis factor-α (TNF-α) in lipopolysaccharide (LPS)-stimulated PBMCs was analyzed.

[0102] In vitro culture of human PBMC was performed as in Example 1 above. Briefly, 1 ml of propane-1,2-diol was added to 1 ml of PBMC to give a final concentration range of 30 (0-100 mM). 15 μl of LPS was added to a final concentration of 100 nM and the cell suspension was incubated at 37°C, 5% CO2 for 24 hours. Plates were then frozen at -20°C until ELISA analysis.

[0103] TNF-α production was determined by ELISA using a procedure according to the manufacturer's specifications (BioSite, Sweden; Art No.: EA102165).

[0104] The results (Figure 1A-D) show a concentration-dependent inhibition of TNF-α when PBMCs were stimulated with LPS. As expected, the curves were somewhat different because PBMCs were obtained from four different individuals. Maximal inhibition of TNF-α was obtained with 100 mM propane-1,2-diol.

[0105] Figure 2 shows the inhibition of TNF-α by 100 mM propane-1,2-diol using LPS-stimulated PBMC from 12 different individuals. Inhibition was observed in all 12 individuals.

[0106] Example 3: Inhibition of IL-2 production in human PBMCs in vitro The immunopathogenesis of aphthous stomatitis is thought to be T cell mediated. The aim of this example was to characterize the cytokine profile of PBMCs with a special emphasis on the effect of using propane-1,2-diol. The production of the cytokine interleukin-2 (IL-2) in PHA-stimulated PBMCs was analyzed.

[0107] In vitro culture of human PBMC was performed as in Example 1 above. Briefly, 1 ml of propane-1,2-diol was added to 1 ml of PBMC to give a range of final concentrations (0-100 mM). 15 μl of PHA was added to a final concentration of 1 μg / ml and the cell suspension was incubated at +37°C, 5% CO2 for 24 hours. Plates were then frozen at -20°C until ELISA analysis.

[0108] IL-2 production was determined by ELISA using a procedure according to the manufacturer's specifications (BioSite, Sweden; Art. No.: EA102165).

[0109] Figure 3 shows IL-2 production after increasing PHA concentrations. Experiments were performed to establish a suboptimal concentration to be used to study the effect of increasing propane-1,2-diol concentrations on IL-2 PBMC production.

[0110] Figure 4 shows the effect of different concentrations of propane-1,2-diol on IL-2 production by 1 μg / ml PHA-stimulated PBMC from two different patients. IL-2 production was reduced by 53% in patient A and 64% in patient B at 100 mM propane-1,2-diol.

[0111] Example 4: Osmotic effect of the preparation A study was performed to demonstrate the relationship between the concentration of propane-1,2-diol and its dehydrating effect on the oral mucosa. Fresh porcine oral mucosa (300-700 mg) was equilibrated at room temperature and 40% relative humidity (RH), weighed and immersed in 5 ml of the investigated solution for 20 h at room temperature (RT, approximately 20-25 °C). The tissue was removed from the solution, dried by blotting and weighed. Finally, it was dried for 24 h at +40 °C.

[0112] Table 1 shows the calculated osmolality of the solutions investigated and the dehydrating effect observed after immersion of mucosal tissue in the solutions for 24 hours. [Table 1]

[0113] From the results shown in Table 1 and Figure 5, the following conclusions can be drawn: - No dehydrating effect was observed for 1% and 5% propane-1,2-diol solutions. - The dehydrating effect was evident for propane-1,2-diol solutions at concentrations of 50%, 80% and 100%, with no differences between mixtures with water or glycerol (85%). The concentration of propane-1,2-diol required to obtain the dehydrating effect exceeds the concentration (100 mM; equivalent to 0.8% w / v) sufficient to obtain the TNF-α production inhibitory effect (Example 2) and the IL-2 production inhibitory effect (Example 3). Therefore, the inhibitory effects shown in Examples 2 and 3 were not due to the dehydrating effect.

[0114] Example 5: Preparation of the composition The compositions may be prepared according to standard methods, as illustrated by the following examples.

[0115] Batch 1 Preparation and testing of solutions and gels containing propane-1,2-diol (propylene glycol). Mucosal sprays or liquids (1a) and gels (1b) for topical use were then prepared according to the compositions provided below. These propane-1,2-diol formulations had a completely acceptable fragrance and slight sweetness.

[0116] For liquids, sprays and gels, the pH is advantageously adjusted to 6.0 to 6.5 and a preservative may be added.

[0117] (1a) Mucosal sprays or liquids for topical use -Propane-1,2-diol 0.8g - 0.5g carbomer or hydroxyethyl cellulose 5.0 g glycerol, and -Add water to make 100.0g.

[0118] (1b) Mucoadhesive gels for topical use -Propane-1,2-diol 0.8g -Carbomer or carmellose sodium 1.0g 5.0 g glycerol, and -Add water to make 100.0g.

[0119] Batch 2 Preparation and testing of a mucoadhesive patch. The patch was circular and approximately 1 cm in diameter. The patch contained 0.8% propane-1,2-diol, allowing sufficient volume to reach the ulcer tissue at the site of patch application. It was manufactured by mixing the components propane-1,2-diol, Carbopol 974P NF, and additional components according to the formulation described below, followed by drying, i.e., compressing without water.

[0120] (2a) Mucoadhesive patch formulations for use on mucous membranes Carbomer: Carbopol 974P NF (Lubrizol, Brussels, Belgium) 99.0% Propane-1,2-diol (propylene glycol) (POCH, Gliwice, Poland) 0.8% Menthol 0.2% Colourants E131 and E132

[0121] Appearance and manufacturing details: Diameter: 11mm Thickness: 1.40mm Weight: 0.85~0.90mg Compression: 300kg

[0122] Batch 3 Preparation of mucoadhesive patches for testing. The patches contained carbomer, Carbopol 71G NF polymer (Lubrizol). The patches were circular and approximately 1 cm in diameter. The components propane-1,2-diol, Carbopol, 71G NF, microcrystalline cellulose, povidone, and magnesium stearate were mixed and then prepared by compression, as described below.

[0123] (3a) A mucoadhesive patch in the form of a mucoadhesive buccal tablet containing propylene glycol (propane-1,2-diol). [Table 2]

[0124] Manufacturing process: 1.Wet granulation: Dry excipients: Microcrystalline cellulose (Vivapur 101) - 10.0 g Binding solution: 2.5 g of 5% Kollidon 30 solution and 2.5 g of propylene glycol Procedure: Wet mixing in a mortar, wet sieving (0.6 mm), drying (30 min / 50°C), dry sieving (0.5 mm) 2. Dry mix with Carbopol G71 3. Magnesium stearate (0.5%) mixed with lubricant 4.Compression using a Gamlen D series laboratory press, 7mm flat punch with 300kg compression load, compression speed 120mm / min. Tablet weight: 50mg Tablet thickness: 1.2mm

[0125] (3b) A mucoadhesive patch in the form of a mucoadhesive buccal tablet containing propylene glycol (propane-1,2-diol). [Table 3]

[0126] Preparation was carried out as described above for (3a) mucoadhesive patches. Tablet weight: 50mg Tablet thickness: 1.2mm

[0127] Example 6: Treatment or prevention of RAS Patient cases are described to illustrate the properties of the gel or patch formulations for managing aphthous ulcers of various severity and distribution. Furthermore, application of the patch or gel formulations to the buccal mucosa of healthy volunteers is described to demonstrate the mucoadhesive properties of the various formulations, as well as the duration of patch or gel attachment and tolerability aspects.

[0128] Subject 1 was a 25-year-old female who experienced 5-6 painful episodes per year of recurrent aphthous stomatitis (RAS) that routinely required up to 2 weeks to heal, with or without various standard treatments. The day after the appearance of the stomatitis, a mucoadhesive buccal gel (batch 1b in case 5) containing propane-1,2-diol was applied and left on for 1 hour. This provided immediate relief of pain from the RAS lesions. The patient's experience with the patch containing propane-1,2-diol was similar to treatment with topical corticosteroids.

[0129] Subject 2 was a 34 year old male experiencing severe pain and inflammation from aphthous ulcers on his lower lip and tongue. The patient also experienced prodromal symptoms on the right side of his lower lip. A patch containing propane-1,2-diol (Batch 2a of Example 5) was applied to both sides of the lower lip. At the follow-up visit 3 days later, the patient reported no symptoms from the left side of his lower lip, but had a small aphthous ulcer at this location with minimal visible inflammation. There was no progression of the aphthous ulcer on the right side of the lower lip. The untreated ulcer on the tongue remained and no healing was observed.

[0130] Subject 3 was a 66-year-old male with no signs of developing RAS ulcers. A mucoadhesive patch (Batch 2a of Example 5) containing propane-1,2-diol was prepared according to the present invention and applied to normal buccal mucosa. The subject experienced that the patch immediately and strongly adhered to the mucosal tissue and remained in place for at least 60 minutes. There were no adverse reactions and the subject experienced no adverse effects while the patch was in place on the buccal mucosa. After 60 minutes, the buccal patch had completely dissolved.

[0131] Subject 4 was a 65 year old male with a history of recurrent aphthous ulcers, but no ulcers at the time of testing the mucoadhesive gel containing propane-1,2-diol prepared according to the present invention (Batch 1b of Example 5). The gel was applied to the right buccal mucosa in the oral cavity. An applicator device was used to apply 2 ml of the mucoadhesive gel. The subject experienced that the gel formed a mucoadhesive layer on the mucosa and that the gel remained in place on the mucosal surface for 40-60 minutes, after which the gel completely dissolved. No adverse events were reported by the subject.

[0132] Subject 5 was a 74-year-old male with no pathology or signs of oral aphthous lesions at the time of testing. A patch containing propane-1,2-diol (Batch 2a of Example 5) was prepared according to the present invention and applied to the right buccal mucosa of the oral cavity. The subject reported that the patch adhered firmly to the mucosa and was completely dissolved approximately 1 hour after application. The subject reported no adverse events.

[0133] Example 7 In this example, it was investigated whether inhibition of TNF-α in Example 2 and / or IL-2 in Example 3 resulted in cell death of PBMCs.

[0134] PBMCs were isolated from one donor as described in Example 1 and plated at 2 × 10 6 1 ml of PBMC cells was added. 1 ml of 2,000 mM propane-1,2-diol was added to two wells to a final concentration of 1,000 mM (8% propane-1,2-diol). The same procedure was used to add lower concentrations of propane-1,2-diol: 500 mM (4% propane-1,2-diol), 250 mM (2% propane-1,2-diol), 125 mM (1% propane-1,2-diol), 62.5 mM (0.5% propane-1,2-diol). After 24 hours of incubation at 37°C and 5% CO2, 15 μl of each cell culture was mixed with 15 μl of tryptan blue and dead cells out of 100 cells were counted under a light microscope.

[0135] As can be seen from the results shown in Figure 7, propane-1,2-diol concentrations up to 1% had no significant toxic effects compared to the control and did not cause significant cell death in PBMCs. A concentration of 2% propane-1,2-diol had minor or mild toxic effects, but higher concentrations of propane-1,2-diol caused significant cell death in PBMCs and were therefore toxic.

[0136] The above embodiments should be understood as some illustrative examples of the present invention. Those skilled in the art will understand that various modifications, combinations and changes can be made to the embodiments without departing from the scope of the present invention. In particular, different part solutions in different embodiments can be combined in other configurations, if technically possible. However, the scope of the present invention is defined by the appended claims.

Claims

1. 1. A pharmaceutical composition for use in the amelioration, prevention or treatment of recurrent aphthous stomatitis or aphthous ulcers in a subject, comprising: 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer; and A pharmaceutical composition that is devoid of any active agent or ingredient having anti-inflammatory effects other than propane-1,2-diol.

2. 1. A pharmaceutical composition for use in treating pain associated with recurrent aphthous stomatitis or aphthous ulcers in a subject, comprising: 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer; and A pharmaceutical composition that is devoid of any active agent or ingredient having anti-inflammatory effects other than propane-1,2-diol.

3. The pharmaceutical composition for use according to claim 1 or 2, wherein said pharmaceutical composition comprises 0.01 to 2% (w / v) propane-1,2-diol.

4. 4. The pharmaceutical composition for use according to claim 3, wherein said pharmaceutical composition comprises 0.5 to 2% (w / v) propane-1,2-diol.

5. 5. The pharmaceutical composition for use according to claim 4, wherein the pharmaceutical composition comprises 0.5-1.5% (w / v) propane-1,2-diol, 0.5-1.25% (w / v) propane-1,2-diol, 0.5-1.0% (w / v) propane-1,2-diol, 0.6-1.0% (w / v) propane-1,2-diol, 0.7-0.9% (w / v) propane-1,2-diol, or about 0.8% (w / v) propane-1,2-diol.

6. A pharmaceutical composition for use according to any one of claims 1 to 5, wherein said pharmaceutical composition comprises 50-99% (w / v) of said at least one bioadhesive polymer.

7. 7. The pharmaceutical composition for use according to claim 6, wherein said pharmaceutical composition comprises 60-99% (w / v), 70-99% (w / v), 80-99% (w / v), or 90-99% (w / v) of said at least one bioadhesive polymer.

8. 8. The pharmaceutical composition for use according to any one of claims 1 to 7, wherein said at least one bioadhesive polymer is at least one mucoadhesive polymer.

9. 9. The pharmaceutical composition for use according to claim 8, wherein said at least one mucoadhesive polymer is poly(acrylic acid) (PAA).

10. 10. The pharmaceutical composition for use according to claim 9, wherein the PAA is selected from the group consisting of PAA having an average viscosity of 29,400 to 39,400 cP at 25°C in a 0.5 wt% aqueous solution, measured by a Brookfield viscometer, at pH 7.3 to maximum 7.8, PAA having an average viscosity of 4,000 to 11,000 cP at 25°C in a 0.5 wt% aqueous solution, measured by a Brookfield viscometer, at pH 7.3 to maximum 7.8, and combinations thereof.

11. 10. The pharmaceutical composition for use according to any one of claims 1 to 9, wherein said pharmaceutical composition comprises at least one excipient selected from the group consisting of microcrystalline cellulose, povidone, magnesium stearate and combinations thereof.

12. 12. The pharmaceutical composition for use according to claim 11, wherein the pharmaceutical composition comprises microcrystalline cellulose in an amount of 2.5-15% (w / w), 5-10% (w / w), 7-9% (w / w), 7-8% (w / w), or about 7.9% (w / w).

13. 13. The pharmaceutical composition for use according to claim 11 or 12, wherein the pharmaceutical composition comprises povidone in an amount of 0.01-5% (w / w), 0.01-1% (w / w), 0.05-0.5% (w / w), or about 0.1% (w / w).

14. 14. A pharmaceutical composition for use according to any one of claims 11 to 13, wherein the pharmaceutical composition comprises magnesium stearate in an amount of 0.01 to 5% (w / w), 0.01 to 2.5% (w / w), 0.1 to 1% (w / w), or about 0.5% (w / w).

15. 15. The pharmaceutical composition for use according to any one of claims 1 to 14, wherein said pharmaceutical composition is formulated for topical application.

16. 16. The pharmaceutical composition for use according to any one of claims 1 to 15, wherein the pharmaceutical composition is in a dosage form selected from the group consisting of a patch, a film, a tablet, a cream, an ointment, a gel, a foam and a spray.

17. 17. The pharmaceutical composition for use according to claim 16, wherein the dosage form is a mucoadhesive patch.

18. 18. The pharmaceutical composition for use according to claim 17, wherein said mucoadhesive patch is selected from the group consisting of a mucoadhesive tablet, a mucoadhesive film and a mucoadhesive gel.

19. 1. Use of a pharmaceutical composition in the manufacture of a medicament for ameliorating, preventing or treating recurrent aphthous stomatitis or aphthous ulcers in a subject, comprising: The pharmaceutical composition comprises 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer; and The pharmaceutical composition is devoid of any active agent or ingredient having an anti-inflammatory effect other than propane-1,2-diol.

20. 1. Use of a pharmaceutical composition in the manufacture of a medicament for treating pain associated with recurrent aphthous stomatitis or aphthous ulcers in a subject, comprising: The pharmaceutical composition comprises 0.001-2% (w / v) propane-1,2-diol and at least one bioadhesive polymer; and The pharmaceutical composition is devoid of any active agent or ingredient having an anti-inflammatory effect other than propane-1,2-diol.

21. An anti-inflammatory agent for use in ameliorating, preventing or treating recurrent aphthous stomatitis or aphthous ulcers in a subject, or in treating pain associated with recurrent aphthous stomatitis or aphthous ulcers in a subject, said anti-inflammatory agent comprising 0.001 to 2% (w / v) propane-1,2-diol and 50 to 99% (w / v) poly(acrylic acid) (PAA).

22. 22. The anti-inflammatory agent of claim 21, wherein the anti-inflammatory agent comprises 0.01-2% (w / v) propane-1,2-diol, 0.5-2% (w / v) propane-1,2-diol, or 0.8-2% (w / v) propane-1,2-diol.

23. The anti-inflammatory agent of claim 21 or 22, wherein the anti-inflammatory agent comprises 60-99% (w / v), 70-99% (w / v), 80-99% (w / v), or 90-99% (w / v) PAA.

24. The anti-inflammatory agent according to any one of claims 21 to 23, wherein the PAA is selected from the group consisting of PAA having an average viscosity of 29,400 to 39,400 cP at 25°C in a 0.5 wt% aqueous solution, measured with a Brookfield viscometer, at pH 7.3 to a maximum of 7.8, PAA having an average viscosity of 4,000 to 11,000 cP at 25°C in a 0.5 wt% aqueous solution, measured with a Brookfield viscometer, and a combination thereof.

25. 25. The anti-inflammatory agent of any one of claims 21 to 24, further comprising at least one excipient selected from the group consisting of microcrystalline cellulose, povidone, magnesium stearate, and combinations thereof.

26. 26. The anti-inflammatory agent of claim 25, further comprising microcrystalline cellulose in an amount of 2.5-15% (w / w), 5-10% (w / w), 7-9% (w / w), 7-8% (w / w), or about 7.9% (w / w).

27. 27. The anti-inflammatory agent of claim 25 or 26, further comprising povidone in an amount of 0.01-5% (w / w), 0.01-1% (w / w), 0.05-0.5% (w / w), or about 0.1% (w / w).

28. 28. The anti-inflammatory agent of any one of claims 25 to 27, further comprising magnesium stearate in an amount of 0.01-5% (w / w), 0.01-2.5% (w / w), 0.1-1% (w / w), or about 0.5% (w / w).

29. 29. The anti-inflammatory agent of any one of claims 21 to 28, wherein the anti-inflammatory agent is devoid of any active agent or ingredient having an anti-inflammatory effect other than propane-1,2-diol.

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