30 results about "Choleretic" patented technology

The invention provides a strain of high-temperature-resistant and inflammation-relieving Witzia ciliaris and an application thereof, the high-temperature-resistant and inflammation-relieving Witzia ciliaris is Witzia ciliaris CN985 and is preserved in the China Center for Type Culture Collection (CCTCC), the preservation date is April 7, 2024, and the preservation number is CCTCC NO: M 2024641. The invention further provides a preparation method of the high-temperature-resistant and inflammation-relieving Witzia ciliaris strain for preventing and treating inflammation of the high-temperature-resistant and inflammation-relieving Witzia ciliaris strain for preventing and treating inflammation of the high-temperature-resistant and inflammation-relieving Witzia ciliaris strain. The invention provides a brand new strain of Witzia ciliaris CN985, which is resistant to high temperature, has better acid resistance and bile resistance, and has no hemolysis risk when being applied to a human body. The Witzia coagulans CN985 has excellent antibacterial performance, and especially can significantly inhibit streptococcus pyogenes, salmonella enteritidis and / or group B streptococcus; besides, experimental results show that the Witzia ciliaris CN985 can relieve enteritis, improve the immunity of the organism and relieve pharyngitis, and especially when the Witzia ciliaris CN985 and the phytobacterium plantarum CE18 are combined for use, the Witzia ciliaris CN985 and the phytobacterium plantarum CE18 have a synergistic interaction effect, so that the relieving effect on enteritis can be remarkably improved.

This invention relates to the use of a recombinant protein ANG in the preparation of medicaments for treating cholestatic liver disease. Specifically, this invention provides the use of the angiopoietin ANG gene, or its protein, or its promoter, for the preparation of medicaments, compositions, or formulations for the prevention, improvement, and / or treatment of cholestatic liver disease. It is particularly effective in treating primary biliary cholangitis and primary sclerosing cholangitis.

The invention provides a biomarker for diagnosing primary biliary cholangitis and application of the biomarker, and belongs to the technical field of biomarkers. The biomarker disclosed by the invention comprises serum protein and / or N-glycopeptide. According to the method, the improvement of PBC diagnosis is taken as a starting point, the serum protein and the N-glycopeptide are taken as screening templates, a more accurate non-invasive prediction means for differential diagnosis of PBC is provided, and a theoretical basis is provided for rapid and accurate diagnosis of PBC.

The present disclosure provides methods and compositions for treating a disease or condition involving inflammation and / or fibrosis in the liver, e.g., metabolic dysfunction-associated steatohepatitis (MASH), metabolic dysfunction-associated steatotic liver disease (MASLD), primary biliary cholangitis, primary sclerosing cholangitis, alcoholic cirrhosis, hepatitis cirrhosis, cholestasis, autoimmune hepatitis, viral hepatitis B, viral hepatitis C, hemochromatosis, Wilson's disease, or alcoholic steatohepatitis, with a therapeutic dose of an anti-TNF-like ligand 1A (TL1A) antibody.

The present invention relates to a pharmaceutical composition comprising elafibranor or a pharmaceutically acceptable salt thereof for use in treating primary biliary cholangitis (PBC) in subjects intolerant to ursodeoxycholic acid (UDCA).

The present application provides a kind of PRMT5 inhibitor, PRMT5 inhibitor includes: recombinant adeno-associated virus vector AAV-shPrmt5 and GSK3326595;Recombinant adeno-associated virus vector AAV-shPrmt5 includes the shRNA of targeting PRMT5, the nucleotide sequence of shRNA is as shown in SEQ ID No:1.The present application also provides the application of the above-mentioned PRMT5 inhibitor in the preparation of drug for improving primary biliary cholangitis, PRMT5 inhibitor is all PRMT5 gene / protein as target point, by inhibiting the expression of PRMT5 gene / protein, reduce liver tissue and spleen tissue Tfh cell and GC B cell, serum autoantibody and transaminase level, can effectively delay the disease progression of primary biliary cholangitis.

This invention relates to the field of biomedical technology, specifically to the application of TXNIP gene expression inhibitors in the preparation of drugs for treating primary biliary cholangitis. This invention discovers the complete mechanism by which hepatocytes regulate glucose uptake through TXNIP, thereby influencing T cell metabolism and driving Th1 differentiation, thus exacerbating intrahepatic inflammation in primary biliary cholangitis (PBC). This clarifies TXNIP as a potential new target for intervening in the progression of PBC, and therefore proposes the application of TXNIP gene expression inhibitors in the preparation of drugs for treating PBC.

The disclosure herein relates to the development and production of novel antibodies and antigen-binding fragments thereof that bind to TL1A and are useful in the treatment, prevention, and diagnosis of diseases, disorders, or inflammation, including, for example, autoimmune diseases, including rheumatoid arthritis, inflammatory bowel disease, atopic dermatitis, systemic lupus erythematosus, asthma, ulcerative colitis, Crohn's disease, psoriasis, primary biliary cirrhosis, primary biliary cholangitis, ankylosing spondylitis, and fibrosis, including intestinal fibrosis, pulmonary fibrosis, and liver fibrosis. Some of the elements of the final antibody structure are designed de novo by a computer system and its data training set, without reference to a particular reference molecule.

The invention provides a biomarker for predicting the prognosis effect of ursodesoxycholic acid for primary biliary cholangitis and application of the biomarker, and belongs to the technical field of biomarkers. The biomarker disclosed by the invention comprises an activating agent AHSA1 of a 90 kDa heat shock protein ATPase homolog 1 and a glycosylated form C4BN226HexNAc (2) Hex( 7) of a complement C4-B. The invention further discloses a preparation method of the biomarker. According to the method, the improvement of the PBC medication efficiency is taken as a starting point, the serum protein and the N-glycopeptide are taken as screening templates, a more accurate non-invasive prediction means for the curative effect of the PBC medication UDCA is provided, and a theoretical basis is provided for personalized treatment of PBC.

The present disclosure finds that TGFBI in a plasma sample can serve as a diagnostic molecular marker for primary biliary cholangitis, provides a molecular marker and diagnostic model with high specificity and high sensitivity for individualized diagnosis and treatment of primary biliary cholangitis, and provides a new, efficient and non-invasive auxiliary tool for the clinician to formulate a diagnostic scheme for primary biliary cholangitis.

The invention relates to the field of medicine, in particular to solid dosage forms for the treatment of primary biliary cholangitis (PBC). The invention provides a modified release solid dosage form comprising two active pharmaceutical ingredients, obeticholic acid and ursodeoxycholic acid, arranged to release sequentially over time. The solid dosage form is designed to achieve a controlled, separate release of each API to provide a desired therapeutic profile.

The invention relates to a pharmaceutical composition comprising elafibranor or a pharmaceutically acceptable salt thereof, for use to treat primary biliary cholangitis (PBC) in a subject intolerant to ursodeoxycholic acid (UDCA).

The present invention relates to a pharmaceutical composition comprising a compound selected from the group consisting of elafibranor, 2-[2,6-dimethyl-4-[3-[4-(methylthio)phenyl]-3-oxo- propyl]phenoxy]-2-methylpropanoic acid (GFT1007), and a pharmaceutically acceptable salt of elafibranor or GFT1007, for use in a method for treating primary biliary cholangitis (PBC) in a subject having advanced stage primary biliary cholangitis (PBC).

The invention provides a biomarker for pathological staging judgment of primary biliary cholangitis and application of the biomarker, and belongs to the technical field of biomarkers. The biomarker disclosed by the invention comprises a peroxisome bifunctional enzyme, phosphoenolpyruvate carboxykinase, a receptor expression enhancing protein 6, an HLA (human leukocyte antigen) II histocompatibility antigen gamma chain and a C-X-C motif chemotactic factor 10. According to the method, the improvement of the PBC diagnosis efficiency is taken as a starting point, the serum protein and the N-glycopeptide are taken as screening templates, a more accurate non-invasive PBC pathological staging judgment method is provided, and a theoretical basis is provided for early diagnosis of PBC.

The present invention concerns elafibranor for use for the treatment of Primary Biliary Cholangitis (PBC) in a subject with PBC and with liver cirrhosis, and preferably a subject having Child-Pugh score A or having Child-Pugh score B.

The application relates to the medical technical field, in particular to application of sulfasalazine in preparation of a medicine for treating primary biliary cholangitis (PBC) which is poorly responsive to ursodeoxycholic acid (UDCA), aiming at the clinical problem that about 40% of PBC patients are poorly responsive to the first-line drug UDCA, have high disease progression risk and limited second-line treatment options, and providing a new treatment use of the mature drug sulfasalazine. Through prospective clinical research, it is confirmed that, on the basis of UDCA standard treatment, combined use of sulfasalazine (1.5g / day, a treatment course of 48 weeks) can significantly improve liver biochemical indexes of UDCA non-responders, including alkaline phosphatase and gamma-glutamyltransferase, and 62.5% of the patients reach composite biochemical response. The application provides a new, effective, safe and highly accessible second-line treatment strategy for PBC patients who are poorly responsive to UDCA, and has a good clinical application prospect.

This invention relates to a novel use of synephrine in the preparation of drugs for treating cholestatic liver disease, belonging to the field of pharmaceutical technology. Cholestatic liver disease is characterized by jaundice and conjugated bilirubin and / or total bilirubin hyperconjugation caused by impaired bilirubin excretion due to various reasons. Its causes include common bile duct stones, pancreatic duct cancer, common bile duct malignant tumors, pancreatic cancer, biliary parasitic diseases, viral hepatitis cirrhosis, alcoholic liver disease, fatty liver disease, drug-induced liver injury, primary biliary cirrhosis, intrahepatic sclerosing cholangitis, and certain congenital diseases such as Dubin-Johnson syndrome and Rotor syndrome. This invention establishes a mouse cholestasis model using bile duct ligation and administers synephrine by gavage to evaluate its protective effect against liver injury. The results showed that synephrine significantly improved jaundice caused by cholestasis, reduced hepatocellular necrosis and inflammatory infiltration caused by cholestasis, alleviated bile duct dilation, decreased serum total bilirubin (TBIL) and direct bilirubin (DBIL), and reduced the levels of total bile acids (BA) in liver tissue and plasma. Furthermore, the above-mentioned effects of synephrine in improving cholestasis showed a clear dose-dependent effect. This invention reveals for the first time the application of synephrine in cholestatic liver disease, demonstrating good safety and promising clinical development prospects.

The present invention relates to a pharmaceutical composition comprising a compound selected from the group consisting of Eraffibularor, 2-[2, 6-dimethyl-4-[3-[4-(methylthio) phenyl]-3-oxo-propyl] phenoxy]-2-methyl propionic acid (GFT1007), and a pharmaceutically acceptable salt of Eraffibularor or GFT1007, and a pharmaceutical composition comprising a compound selected from the group consisting of a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor Methods for reducing fatigue in a subject suffering from primary biliary cholangitis (PBC). The pharmaceutical composition of the present invention significantly reduces the PROMIS Fatigue T score (PROMIS profile-Fatigue 7a questionnaire (V1.0)) relative to the baseline in a subject suffering from PBC.

The present disclosure relates to a method of a method of treating a cholangiopathy (e.g., Primary Sclerosing Cholangitis or Primary Biliary Cholangitis) in a human subject in need thereof, comprising administering a therapeutically effective amount of an anti-Claudin-1 antibody to the human subject.

The present invention relates to the use of Eraffibularox for the treatment of primary biliary cholangitis (PBC) and cirrhosis in a subject suffering from PBC, preferably in a subject having a Child-Pugh score A or a Child-Pugh score B. The present invention also relates to the use of Eraffibularox for the treatment of PBC in a subject having a Child-Pugh score A or a Child-Pugh score B.

The present invention relates to a pharmaceutical composition comprising a compound selected from the group consisting of Eraffibularor, 2-[2, 6-dimethyl-4-[3-[4-(methylthio) phenyl]-3-oxo-propyl] phenoxy]-2-methyl propionic acid (GFT1007), and a pharmaceutically acceptable salt of Eraffibularor or GFT1007, and a pharmaceutical composition comprising a compound selected from the group consisting of a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor, a compound of Eraffibularor The pharmaceutical composition is used in a method of treating primary biliary cholangitis (PBC) in a subject with primary biliary cholangitis (PBC) at baseline plasma alkaline phosphatase (ALP) levels of more than 1.67 * ULN and up to 3 * ULN.

The present application relates to the technical field of polysaccharide extraction, and particularly relates to a Chinese hairy cap polysaccharide, a preparation method and application thereof. Polysaccharides in the Chinese hairy cap are extracted, separated and purified, and four polysaccharide components are obtained. The four polysaccharides can inhibit HIBEC-EMT, avoid liver damage, and can be used for treating and / or preventing primary biliary cholangitis.

The present disclosure relates to a coated probiotic having enhanced acid tolerance, bile tolerance, gastrointestinal survivability, cold storage stability and room temperature storage stability by including milk-derived phospholipid and Aloe vera gel as a coating agent, a food composition containing the same, and a method for producing the same. As the coated probiotic includes the Aloe vera gel and the milk-derived phospholipid as the coating agent, it may have increased stabilities against external environmental stress, such as lyophilization stability and storage stability of the probiotic itself, and may have significantly enhanced acid tolerance and bile tolerance which are the indices of the gastrointestinal stability of the probiotic after taking.

The application relates to preparation of a cholestatic liver fibrosis mouse model and application thereof, and belongs to the technical field of biological medicines. The preparation of the cholestatic liver fibrosis mouse model comprises preparing Zfyve19 gene knockout mice, and performing an isothiocyanate-A-naphthyl ester drug induction on the Zfyve19 gene knockout mice to obtain the cholestatic liver fibrosis mouse model. The model preparation method has the advantages of good simulation of human diseases, high success rate of modeling, short modeling time and high modeling stability.

The present invention relates to a substituted benzimidazole derivative as represented by formula (I) and a pharmaceutically acceptable salt, a polymorph, a tautomer, a stereoisomer, a hydrate, a solvate or an isotopic variant of the derivative. The compound is a PPAR α and / or PPAR δ agonist, therefore the compound can be used for treating and / or preventing diseases associated with by PPAR α and / or PPAR δ, such as non-alcoholic steatohepatitis, Duchenne muscular dystrophy syndrome, Alzheimer's disease, tumors and PBC (primary biliary cholangitis)

The present invention relates to a novel Bifidobacterium breve IDCC 4401 strain (accession number: KCTC13169BP) and dead cell thereof ID-BBR4401, which are superb in acid tolerance and bile tolerance and have a preventive or therapeutic effect on dyslipidemia. Having not only an excellent effect of reducing a cholesterol level in the body but alto a very high level of acid tolerance and bile tolerance in contrast to previously known B. breve, the novel Bifidobacterium breve IDCC 4401 strain (accession number: KCTC13169BP) of the present invention well exhibits the functionality that the strain has in the digestive duct of animals (especially humans), has an excellent growth potential, and provides sustainable and effective functionality of reducing a level of cholesterol in vivo.

The invention belongs to the field of biological medicines, and provides application of miR-1291 in mesenchymal stem cell exosomes in treatment of hepatic fibrosis and other hepatic diseases caused by primary cholangitis. Primary biliary cholangitis is a chronic autoimmune liver disease, and is mainly characterized by bile duct destruction accompanied by hepatic fibrosis. Currently, liver transplantation and drug therapy have many restrictions. These limiting factors highlight the urgent need to develop a safer and more effective therapeutic alternative. When the miR-1291 in the mesenchymal stem cell exosome is used in a hepatic fibrosis animal model caused by DDC diet, the degree of hepatic fibrosis can be reduced, and proliferation and differentiation of hepatic cells can be promoted. The traditional Chinese medicine composition can inhibit polarization of M1 type macrophages in the liver, promote polarization of M2 type macrophages, inhibit chronic inflammation of the liver and slow down liver injury.