54 results about "Lactobionic acid" patented technology

The invention discloses a composition for improving the stability of oleuropein in a solution as well as a preparation method and application of the composition. The composition comprises oleuropein and at least one stabilizer, and the stabilizer is selected from the group consisting of anisic acid, lactobionic acid, glycyrrhizic acid, 3, 3-thiodipropionic acid, N-acetyl-L-glutamine, propyl-cysteine and lauramidopropyl betaine; and the pH value of the aqueous solution of the composition is 4.0-8.0. The preparation method comprises the following steps: dissolving oleuropein in water, adding the stabilizer, and uniformly mixing. Through simple physical mixing, by utilizing the synergistic effect of the specific stabilizer and the oleuropein, the degradation and discoloration of the oleuropein in the storage process are remarkably inhibited. Experiments show that after the preferable composition is preserved for 30 days in an open manner, the retention rate of the oleuropein still reaches up to 80% or above, and is far superior to that of blank control and a traditional liposome wrapping method. The composition is simple and convenient in preparation process and low in cost, and provides reliable technical support for wide application of oleuropein in liquid products such as food, medicine and cosmetics.

The invention discloses an oil-controlling and acne-removing synergistic composition which comprises the following components in percentage by weight: 0.8 to 2.0 percent of succinic acid, 0.3 to 1.0 percent of salicylic acid derivative and 0.5 to 1.5 percent of PCA (Principal Component Analysis) zinc. The invention also provides a sustained-release body. The sustained-release body is prepared from the following components in percentage by weight: 0.8 to 2.0 percent of succinic acid, 0.3 to 1.0 percent of salicylic acid derivative, 0.5 to 1.5 percent of PCA zinc, 1.0 to 2.5 percent of lactobionic acid, 1.0 to 3.0 percent of lactobacillus fermentation product, 2.0 to 4.0 percent of aminated modified diatomite and 0.1 to 0.3 percent of citric acid. The invention also provides a preparation method and application of the sustained release body. The acne-removing shampoo has low irritation, and can be used for controlling oil and removing acnes for a long time and efficiently dredging hair follicles.

The invention discloses a pore cleaning mud mask and a preparation method thereof, belongs to the technical field of cosmetics, and particularly relates to a pore cleaning mud mask. Comprising 14 to 18 parts of kaolin, 7 to 9 parts of Manny root ice river mud, 4.5 to 5.5 parts of Amazon white mud, 10 to 12 parts of wheat germ oil, 43 to 47 parts of tea water, 0.1 to 0.14 part of a phellinus linteus extract, 1 to 2 parts of swertia mileensis powder, 2 to 4 parts of lactobionic acid, 0.08 to 0.12 part of salicylic acid and 0.4 to 0.6 part of gluconolactone. The pore cleaning mud mask provided by the invention is uniform in particle size distribution, uniform in mixing and capable of keeping the state of the mud mask moist and not dry in the use process, the cleaning strength of controlling oil, dredging pores and resisting inflammation is improved, meanwhile, skin sensitivity caused by excessive cleaning is avoided, and the cleaning effect is good. The invention provides a novel cleaning mud mask formula for realizing the goal of cleaning pores and an efficient and stable preparation method of the novel cleaning mud mask formula.

The invention relates to an allergy-relieving acne-removing composition and a preparation method and application thereof, and the allergy-relieving acne-removing composition comprises the following raw materials in parts by mass: 1-10 parts of VB-IP, 5-20 parts of hydroxyethyl urea, 1-5 parts of coated salicylic acid, 2-10 parts of wild soybean, 1-5 parts of clerodendranthus spicatus, 1-5 parts of rosewood seeds, 1-10 parts of lactobionic acid, 1-10 parts of gluconolactone, 1-10 parts of mandelic acid, 1-10 parts of glycollic acid, 1-5 parts of octyl dodecyl glucoside and 1-5 parts of cetearyl glucoside. 0.5 to 2 parts of phenoxyethanol and 5 to 30 parts of deionized water; the composition comprises the following components: a wild soybean fermentation extract, a clerodendranthus spicatus fermentation extract and a rosewood seed fermentation extract. Compared with the prior art, the formula is stable, penetration can be promoted, cutin renewal can be accelerated, a sebum film can be repaired, sebum can be adjusted, and the acne removing and skin care effects are good.

The invention relates to a halogen-free heavy oil removal surfactant and a preparation method thereof, and belongs to the technical field of surfactants. The heavy oil removal surfactant is prepared from fatty alcohol-polyoxyethylene ether, hydrophilic alkyl quaternary ammonium salt, a glycosyl nonionic surfactant and an alcohol compound, the glycosyl nonionic surfactant is prepared by sequentially carrying out hydrophobic amidation and hydrophobic epoxy addition on lactobionic acid lactone; the heavy oil removal surfactant is good in oil removal effect, safe, free of halogen and small in corrosivity, and the use performance is improved through compound use of the fatty alcohol-polyoxyethylene ether, the hydrophilic alkyl quaternary ammonium salt and the glycosyl nonionic surfactant.

The invention relates to a composition with exfoliating and whitening effects and application of the composition in cosmetics, and belongs to the technical field of cosmetics. The composition consists of the following components in parts by weight: 1-4 parts of lactobionic acid, 3-5 parts of a tea polysaccharide solution and 1-3 parts of kale leaf extract, the tea polysaccharide solution is prepared by fermenting bacillus subtilis, trametes hirsutum and tea, extracting and purifying. The content of tea polysaccharide in the tea polysaccharide solution is increased, the content of small molecular substances is increased, and permeation and absorption are facilitated. Meanwhile, the tea polysaccharide solution, lactobionic acid and kale leaf extract are combined for use, so that compared with other substances with similar effects, the combination effect is better, internal and external dual whitening and brightening can be realized, the effects are stably and lastingly played, the skin is not irritated, and the mask is fine and glossy.

The invention discloses a preparation method of zero-lactose yoghurt fermented milk for infants, which specifically comprises the following steps: firstly, performing high-temperature sterilization on raw milk, then cooling, and adding lactase Nola Fit 5500 before fermentation to perform pre-hydrolysis of lactose so as to ensure zero lactose of the product from the source. Then, compound probiotics composed of bifidobacterium animalis subsp. Lactis HN019, lactobacillus mucus fermentation CECT5716, lactobacillus rhamnosus HN001 and bifidobacterium breve M-16V are added, low-temperature slow fermentation is carried out for 15 hours at the temperature of 41 + / -1 DEG C, and no exogenous sugar is added in the whole process. According to the process, nutritional ingredients are reserved to the maximum extent through mild fermentation, formation of natural flavor is promoted, and the obtained product is safe, nutritional and easy to digest and can effectively improve intestinal health of infants and reduce the risk of digestion discomfort.

The present invention relates to the field of cosmetic technology, and particularly, to a whitening and anti-aging composition, a method for preparing same, and use thereof. The whitening and anti-aging composition is prepared from the following ingredients in parts by weight: 0.1-2 parts of hydroxypropyl cyclodextrin; 0.1-2 parts of tocopherol; 1-5 parts of an emulsifier; 0.5-1 part of a preservative; 1-5 parts of a functional solvent; 0.1-0.9 part of retinol; 0.1-3 parts of an adjusting mixed acid agent; and 90-100 parts of deionized water. The adjusting mixed acid agent consists of lactobionic acid, inositol hexaphosphate, and ferulic acid, and the ratio of lactobionic acid to inositol hexaphosphate to ferulic acid is (5-7):(0.5-1):1. The method for preparing the whitening and anti-aging composition comprises: dissolving the adjusting mixed acid agent in a portion of deionized water; adding hydroxypropyl cyclodextrin, the emulsifier, and retinol into the remaining deionized water and heating for dissolution; and finally, mixing and stirring the two resulting solutions along with the addition of tocopherol and the preservative during the process to give the composition. The composition exhibits excellent whitening and anti-aging effects with low irritation, and is also suitable for populations having sensitive skin with damaged skin barriers.

The application belongs to the technical field of cosmetics, and discloses a Rosa chinensis / Rhizopus stolonifer fermenting composition and a moisturizing and oil-controlling composition. The preparation method of the Rosa chinensis / Rhizopus stolonifer fermenting composition is as follows: dried Rosa chinensis petals are ground and sieved, inoculated into a fermentation medium, and then inoculated with Lactobacillus pentosus for fermentation culture; the obtained fermentation liquor is inactivated, filtered, concentrated and purified to obtain a Rosa chinensis fermentation product filtrate; then the Rosa chinensis fermentation product filtrate is mixed with a Rhizopus stolonifer fermentation product filtrate to obtain the Rosa chinensis / Rhizopus stolonifer fermenting composition. The moisturizing and oil-controlling composition comprises Hamamelis virginiana extract, Buxus seed extract, lactobionic acid, tea tree essential oil, the Rosa chinensis / Rhizopus stolonifer fermenting composition, supermolecular inclusion suberic acid, a surfactant and water. The composition has the synergistic effects of moisturizing, oil-controlling and skin tightening.

This invention relates to the field of cosmetic technology, specifically disclosing a synergistic exfoliating composition and a method for preparing a controlled-release carrier containing the composition. The synergistic exfoliating composition is a compound of adenosine, N-acetylneuraminic acid, and lactobionic acid. This invention has the advantage of maintaining good exfoliating efficacy while reducing skin irritation.

The invention discloses micro-molecular metastructured 4-butylresorcinol and a preparation method and application thereof, a skin external preparation and cosmetics, and belongs to the technical field of cosmetics. According to the technical scheme, the micro-molecular metastructured 4-butylresorcinol is obtained through hydrogen bond interaction of lactobionic acid and 4-butylresorcinol in water; according to the supramolecular complex provided by the invention, the lactobionic acid and the 4-butylresorcinol form the supramolecular complex, on one hand, both the lactobionic acid and the 4-butylresorcinol have certain whitening and antioxidant capacities, and on the other hand, due to a supramolecular complex structure formed by the lactobionic acid and the 4-butylresorcinol, the water solubility of the 4-butylresorcinol can be improved; hydroxyl on 4-butylresorcinol can be prevented from being oxidized, so that the 4-butylresorcinol can keep good oxidation resistance.

A biphasic product comprising lactobionic acid, lactic acid or corresponding salts thereof and / or gluconolactone.

The invention relates to the technical field of cosmetics, in particular to a blue copper peptide-containing composition and application thereof in cosmetics. The composition comprises the following components in parts by mass: 1 part of blue copper peptide; 0.5 to 5 parts of tetrahydromethylpyrimidine carboxylic acid; 0.05 to 0.5 part of sodium hyaluronate; and 0.05 to 0.5 part of beta-glucan. Preferably, the composition further comprises allantoin and lactobionic acid, based on 1 part by mass of the blue copper peptide, the content of the allantoin is 0.1-0.5 part, the content of the lactobionic acid is 0.2-1.0 part, and the mass ratio of the allantoin to the lactobionic acid is 1: (2-4). In-vitro efficacy experiments prove that the specific combination and proportion can generate a remarkable synergistic effect, and meanwhile, the capabilities of inhibiting the activity of elastinase and promoting epidermal cell repair are improved, so that the excellent dual effects of wrinkle resistance and skin barrier repair are realized. The composition can be used for preparing cosmetics such as essence, emulsion and face cream.

The present application discloses a method for detecting the purity of lactobionic acid in the preparation process of erythromycin lactobionate, comprising the following steps: establishing a linear regression equation between conductivity and the concentration of sodium lactobionate solution, and deriving the relationship between the theoretical concentration of lactobionic acid and conductivity; detecting the actual concentration of lactobionic acid using titration; measuring the conductivity of the solution after titration, and calculating the theoretical concentration of lactobionic acid according to the relationship; the ratio of the actual concentration to the theoretical concentration is the purity. This detection method can detect the purity of lactobionic acid after cation exchange in real time, ensuring that its value is above the standard, which is conducive to the preparation of erythromycin lactobionate with stable quality and ensuring the safety of patients' medication. The above detection method is simple and easy to control, low cost and strong stability.

The invention discloses a pH self-adaptive private care lotion based on a composite biological antibacterial system. The pH self-adaptive private care lotion is prepared from 8 to 12 parts of cocamidopropyl betaine, 0.5 to 1.5 parts of polylysine hydrochloride, 0.3 to 0.8 part of tea tree essential oil, 1.2 to 2.0 parts of lactic acid-sodium lactate buffer agent, 0.1 to 0.3 part of dipotassium glycyrrhizinate, 0.5 to 1.2 parts of chamomile extract, 0.3 to 0.7 part of lactobionic acid, 1.0 to 2.0 parts of aloe polysaccharide and the balance of deionized water. During preparation, the tea tree essential oil and beta-cyclodextrin are subjected to clathration for 30 minutes at 35 DEG C to form a clathrate compound, so that the volatile loss is reduced by 80%; dissolving polylysine hydrochloride in deionized water at 4 DEG C, and adding a lactic acid-sodium lactate buffer solution; lactobionic acid and a chamomile extract are added; homogenizing for 3 minutes by using a homogenizer at the speed of 2000rpm; and carrying out vacuum defoaming under 0.08 MPa. Dynamic pH buffering is achieved, and a lactic acid-lactobionic acid double-buffering layer resists secreta impact; a preservative-free process is adopted, and vacuum defoaming and PES membrane filtration are used for replacing chemical preservatives; and gender differentiation adaptation: cranberry polyphenol, female adhesion prevention and succinic acid buffer male pH adaptation.

This application provides a skin-renewing composition containing an acid-enzyme peptide, comprising lactobionic acid, hexanoyl dipeptide-3-leucine, and papain; the mass ratio of lactobionic acid, hexanoyl dipeptide-3-leucine, and papain is 0.1~15:0.5~15:0.05~5. This application also provides a product comprising the above composition and its application. This application combines lactobionic acid, papain, and hexanoyl dipeptide-3-leucine for biological skin renewal, i.e., exfoliation. The three components interact synergistically, significantly increasing the content of exfoliated keratin proteins and providing excellent exfoliation effects. Furthermore, the composition provided in this application has low irritation.

A perfusion stock composition, for preserving a donor organ for transplantation, comprising: a source of 60 to 100 mM Na+; a source of 10 to 20 mM K+; a source of 5 to 10 mM Mg2+; a source of 0.25 to 0.75 mM Ca2+; 10 to 40 mM Tris(hydroxymethyl)aminomethane hydrochloride (Tris or THAM), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), 3-(N-morpholino)propanesulfonic acid (MOPS), 2-(N-morpholino)ethanesulfonic acid (IviES), N,N-bis-(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), or N / -tris(hydroxymethyl)methyl-2-aminoethanesulfonic acid (TES); a source of 10 to 30 mM HCO3; 1 to 30 mM glucose; 1 to 20 U / L insulin; 1 to 10 mM fructose diphosphate or a salt thereof, 1 to 40 mM aspartate or glutamate; 1 to 10 mM adenosine, cAMP or cGMP; 1 to 10 mM reduced glutathione; and 30 to 100 mM lactobionate or mannitol; and, optionally, a diluent. The present disclosure also provides a perfusion composition, a kit, a method, and a perfusion apparatus, each related to the perfusion stock composition.

The invention relates to the technical field of nano-drug delivery systems, in particular to a liver-targeting, long-circulating and acid-responsive nano-drug delivery system for loading oleuropein as well as a preparation method and application of the liver-targeting, long-circulating and acid-responsive nano-drug delivery system. The nano-drug delivery system comprises a drug-loading inner core and a functionalized surface modification layer, the medicine carrying inner core is a zeolite imidazate framework loaded with oleuropein; the functional surface modification layer is a lactobionic acid-polyethylene glycol conjugate. According to the invention, by constructing a three-stage modular nano-drug delivery system of liver targeting-long circulation-acid response, precise delivery and efficient release of oleuropein at a sepsis liver injury part are realized. According to the technical scheme, the technical problems that the bioavailability of the oleuropein is low, the targeted delivery efficiency of the oleuropein at the sepsis liver injury part is not ideal and the like can be solved. According to the technical scheme, the pharmacokinetic characteristics and targeted treatment efficiency of OLE are comprehensively improved, and an efficient and safe nano-drug delivery system is provided for precise treatment of sepsis liver injury.

The invention discloses galactosyl fluorinated chitosan-EGCG (epigallocatechin gallate) nanoparticles and application thereof, and belongs to the field of steady-state delivery of functional foods. The preparation method comprises the following steps: firstly, synthesizing galactosyl modified fluorinated chitosan by utilizing an amidation reaction between lactobionic acid carboxyl and fluorinated chitosan amino, and successfully preparing the tea polyphenol EGCG-loaded nano steady-state delivery carrier through an ionic gel method. The carrier can utilize the fluorine effect of the fluorinated group on the surface of the carrier and the interaction of the galactose-SGLT1 receptor to enhance the intestinal targeted delivery of EGCG (epigallocatechin gallate). The preparation method is simple to operate, the prepared galactosyl-modified fluorinated chitosan nanoparticle delivery carrier has high loading rate on EGCG (epigallocatechin gallate), the bioavailability of EGCG can be improved, and the galactosyl-modified fluorinated chitosan nanoparticle delivery carrier is of great significance in promoting development and application of functional food.

The present invention belongs to the field of biomedicine technology and specifically relates to a small molecule ligand-rucaparib conjugate and a preparation method thereof. The small molecule ligand-rucaparib conjugate is a combination of one or both of a biotin-rucaparib conjugate and a lactobionic acid-rucaparib conjugate. Rucaparib is coupled to the small molecule ligand through an amidation reaction, thereby improving rucaparib's tumor targeting ability and thereby enhancing its inhibitory effect on tumor cells. In particular, the dual-targeting effect of biotin / lactobionic acid-rucaparib composite nanoparticles, which are self-assembled from the small molecule ligand complex, is more significantly inhibited against double-positive tumor cells such as biotin receptors and asialoglycoprotein receptors. Furthermore, the biotin / lactobionic acid-rucaparib composite nanoparticles have a significant application prospect due to their safety advantage over normal cells.

The invention relates to the technical field of cosmetics, in particular to a cosmetic for removing acnes and a preparation method of the cosmetic. The composition comprises the following components in percentage by weight: a humectant (propylene glycol, betaine and the like), a skin conditioner (2-6% of nicotinamide and various plant extracts of schisandra chinensis, scutellaria baicalensis, coptis chinensis and the like), an exfoliating agent (lactobionic acid, betaine salicylate), an antioxidant and the like. The preparation method comprises the following steps: heating a water phase to dissolve the humectant and the like, cooling to 40-50 DEG C, adding the skin conditioner and the functional components, adjusting the pH value to 5.0-6.0 with arginine, homogenizing, cooling and filling. The cosmetic for removing acnes and the preparation method thereof have the effects of relieving, repairing, controlling oil and removing acnes, are mild and low in irritation, are adaptive to easily acnes and sensitive skin, are good in stability, are simple in preparation process, and are suitable for large-scale production. The industrial production is easy.

The invention discloses a hepatocyte cryopreservation solution which comprises a first cryopreservation mixed solution, a second cryopreservation mixed solution and fetal calf serum, the first cryopreservation mixed solution is prepared from a Leibovitz's L-15 culture medium, lactobionic acid, raffinose, reduced glutathione, ademetionine, curcumin, bicyclol, ursodesoxycholic acid, silymarin and glycyrrhizic acid; the second cryopreservation mixed solution comprises cane sugar, trehalose, hydroxyethyl starch and polyene phosphatidylcholine. On the other hand, the invention discloses a cryopreservation method and a recovery method of primary mouse hepatocytes based on the hepatocyte cryopreservation liquid. The cryopreservation method comprises the following steps: pre-culturing, re-suspending, slowly dropwise adding DMSO (dimethylsulfoxide) and cooling and cryopreserving step by step. The resuscitation method comprises the steps of rapid unfreezing, centrifugal purification and resuscitation culture. The liver cell cryopreservation liquid and the cryopreservation and resuscitation method can play roles in regulating osmotic pressure, inhibiting ice crystal formation, stabilizing cell membrane structure, resisting oxidation, promoting protein synthesis and the like, and the resuscitated cells are high in survival rate and strong in adherence capability and functional activity.

The present application relates to the technical field of nanomedicine delivery system, and particularly relates to a liver-targeting, long-circulating and acid-responsive nanomedicine delivery system loaded with oleuropein and a preparation method and application thereof. The nanomedicine delivery system comprises a drug-loaded core and a functional surface modification layer; the drug-loaded core is a zeolitic imidazolate framework loaded with oleuropein; and the functional surface modification layer is a lactobionic acid-polyethylene glycol conjugate. The present application realizes the precise delivery and efficient release of oleuropein at the site of sepsis liver injury by constructing a liver-targeting, long-circulating and acid-responsive three-level modular nanomedicine delivery system. The technical scheme can solve the technical problems of low bioavailability of oleuropein and unsatisfactory targeting delivery efficiency at the site of sepsis liver injury. The technical scheme comprehensively improves the pharmacokinetic characteristics and targeted treatment efficiency of OLE, and provides an efficient and safe nanomedicine delivery system for the precise treatment of sepsis liver injury.

The invention provides a skin care composition containing acid enzyme peptide. The skin care composition comprises lactobionic acid, hexanoyl dipeptide-3-n-leucine and papain, the mass ratio of the lactobionic acid to the hexanoyl dipeptide-3-n-leucine to the papain is (0.1 to 15) to (0.5 to 15) to (0.05 to 5). The invention further provides a product containing the composition and application of the product. According to the invention, lactobionic acid, papain and hexanoyl dipeptide-3-n-leucine are compounded for use, when the composition is used for biological skin renewal, namely exfoliating, the three components interact with each other and have a synergistic effect, the content of eluted keratin can be remarkably increased, and the composition has a good exfoliating effect. In addition, the composition provided by the invention is relatively low in irritation.

The invention discloses a preparation method of crocodile skin collagen peptide and application of a composition of the crocodile skin collagen peptide in antisepsis, anti-inflammation and skin repair. The crocodile skin collagen peptide provided by the invention is composed of 17 peptide fragments with the molecular weight of 700-1800 Da. The composition obtained by compounding crocodile skin collagen peptide, mandelic acid, lactobionic acid, asiaticoside and nicotinamide has multiple functions of antisepsis, anti-inflammation, skin repair and the like through multi-target point synergism, and the crocodile skin collagen peptide dominates oxidation resistance and skin repair and delays skin aging; mandelic acid is used for mildly conditioning cutin, effectively dredging pores and inhibiting growth and reproduction of acne-related flora; lactobionic acid promotes epidermis renewal, makes the skin moist and delicate, and reduces fine wrinkles; the asiaticoside is used for relieving, diminishing inflammation and relieving irritation reactions such as skin redness and swelling; nicotinamide can regulate sebum secretion, block melanin migration and brighten the skin color. The composition can effectively deal with acnes and complications, and solves the problems that an existing product is high in irritation, easy to leave marks and the like.

The invention belongs to the technical field of food chemistry and biological catalysis, and particularly relates to an enzymolysis reaction additive in low-sugar food and a preparation method of the enzymolysis reaction additive. According to the additive, tea polyphenol subjected to glycosylation-amidation synergistic modification and gluconic acid-acetamide are used as main components, sodium lactobionate, levulinic acid, 1-ethyl-3-methylimidazolium acetate, sodium citrate, polyethylene glycol-400 and ascorbic acid are used as auxiliary components, and through a synergistic modification and small molecule stabilization strategy, the tea polyphenol-gluconic acid-ascorbic acid composite additive is prepared. The hydrophilicity, the stability and the interaction capability with enzyme molecules of the tea polyphenol are improved. The prepared additive can significantly improve the reaction rate and thermal stability of amylase and protease in a low-sugar system, and improve the dispersity and uniformity of the system. The method has the advantages of scientific and reasonable formula, mild reaction conditions, high stability, excellent food compatibility and the like, and can be widely applied to the field of enzymatic processing of low-sugar foods, sugar substitutes and functional foods.

The invention relates to a hair care and / or scalp care composition comprising rhamnose, trehalose and lactobionic acid. Said composition moisturizes the scalp, protects the scalp from dehydration, promotes the growth of Staphylococcus epidermis and / or Cutibacterium acnes on the scalp and can be used for treating or preventing dandruff.

A perfusion stock composition, for preserving a donor organ for transplantation, comprising: a source of 60 to 100 mM Na+; a source of 10 to 20 mM K+; a source of 5 to 10 mM Mg2+; a source of 0.25 to 0.75 mM Ca2+; 10 to 40 mM Tris(hydroxymethyl)aminomethane hydrochloride (Tris or THAM), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), 3-(N-morpholino)propanesulfonic acid (MOPS), 2-(N-morpholino)ethanesulfonic acid (IviES), N,N-bis-(2-hydroxyethyl)-2-aminoethanesulfonic acid (BES), or N / -tris(hydroxymethyl)methyl-2-aminoethanesulfonic acid (TES); a source of 10 to 30 mM HCO3; 1 to 30 mM glucose; 1 to 20 U / L insulin; 1 to 10 mM fructose diphosphate or a salt thereof; 1 to 40 mM aspartate or glutamate; 1 to 10 mM adenosine, cAMP or cGMP; 1 to 10 mM reduced glutathione; and 30 to 100 mM lactobionate or mannitol; and, optionally, a diluent. The present disclosure also provides a perfusion composition, a kit, a method, and a perfusion apparatus, each related to the perfusion stock composition.

The invention belongs to the field of drug delivery and oral preparations, and provides an 8-O-acetyl harpagide nano-composition and a preparation method thereof.The 8-O-acetyl harpagide-soybean lecithin compound is used as a nuclear phase, lactobionic acid and thioglycolic acid dual-modified chitosan and sodium tripolyphosphate are subjected to ionic crosslinking to form a shell layer, and the 8-O-acetyl harpagide nano-composition is prepared. Compared with the prior art, the freeze-dried powder has the advantages of high loading capacity, high solid content, low viscosity and wide processing window, small particle size, low polydispersity index and stable nano dispersion are obtained, ethanol residue and water content of the freeze-dried powder are reduced, freeze-dried storage stability, redissolution redispersibility and oral release and absorption performance are improved, and the freeze-dried powder is suitable for large-scale production. The method is suitable for the development of oral preparations for preventing the acetaminophen-induced liver injury.

The invention relates to the technical field of tissue preservation solutions, and provides a solid tissue flow detection sample preservation solution and a preparation method thereof, and the preservation solution comprises N-acetylcysteine, melatonin, lactobionic acid and an HBSS buffer solution. NAC, melatonin and lactobionic acid jointly act on an antioxidant pathway, ROS is removed, accumulation of lipid peroxidation products (MDA) is reduced, the mitochondrial function is protected, and the cell survival rate is increased. The melatonin and lactobionic acid act together to inhibit ferroptosis paths, maintain the health state of cells and improve the cell survival rate and the stability of antigen epitopes. All the components and a stable environment provided by HBSS act together to maintain the high activity of cells and the stability of antigen epitopes.