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87 results about "Primary biliary cirrhosis" patented technology

An auto-immune disease that causes progressive destruction of the bile ducts.

Sulfonylurea derivative and pharmaceutical composition and application thereof

The invention relates to a preparation method and application of a sulfonylurea compound and a composition containing the same component as FXR and / or TGR5 agonist, the FXR and / or TGR5 agonist is a compound shown as a formula (I), or a pharmaceutically acceptable salt, a solvate, a prodrug, an isomer and a stable isotope derivative thereof. The compounds can be used for treatment of FXR and / or TGR5 mediated diseases including primary biliary cirrhosis, nonalcoholic fatty liver, portal hypertension, bile acid diarrhea and cholestasis, type II diabetes and obesity and other field.
Owner:SHANGHAI DE NOVO PHARMA

Application of norisoboldine in preparing medicament for treating autoimmune disease

The invention relates to the medicine filed, in particular to a medicinal purpose of norisoboldine. The medicinal purpose is characterized in that the norisoboldine can be used in the application of preparing drugs for the treatment of autoimmune diseases. The autoimmune diseases are: rheumatoid arthritis, multiple sclerosis, systemic lupus erythematosus, multiple sclerosis, type-I diabetes, psoriasis, ulcerative colitis, Sjogren syndrome, scleroderma, polymyositis, chronic active hepatitis, mixed connective tissue disease, primary biliary cirrhosis, autoimmune hemolytic anemia and other diseases.
Owner:CHINA PHARM UNIV

SNP in KRT8 gene exon area and determination method thereof

InactiveCN103602671ALiver cirrhosis controlLiver transplantation success rate controlMicrobiological testing/measurementDNA/RNA fragmentationPrimary biliary cirrhosisNucleotide
The invention discloses a SNP in KRT8 gene exon area and determination method thereof, and the SNP locus with G / T polymorphisms (GG) is at 12563 site of the eighth exon area of the KRT8 gene and has nucleotide sequences SEQ ID NO:1 and SEQ ID NO:2. The invention also provides a determination method of the SNP locus, and research and development of the polymorphisms can be applied to researches in the aspect of primary biliary cirrhosis, for example, control of primary biliary cirrhosis attack and hepatic cirrhosis degree or improvement of liver transplantation success rate.
Owner:FOURTH MILITARY MEDICAL UNIVERSITY

Method for breeding IL-12p40 (-/-) IL-2R alpha (-/-) mice used as hepatic fibrosis and primary biliary cirrhosis animal models

InactiveCN103749388ALow specificityStrong destructionAnimal husbandryPrimary biliary cirrhosisIl 12p40
The invention discloses a method for breeding IL-12p40 (- / -) IL-2R alpha (- / -) mice used as novel hepatic fibrosis and primary biliary cirrhosis animal models. The method includes steps of (1), performing cross breeding on IL-2R alpha (+ / -) mice and IL-12p40(- / -) mice to obtain IL-12p40(+ / -) IL-2R alpha (+ / -) mice by means of breeding; (2), performing cross breeding on IL-12p40(- / -) mice and the IL-12p40(+ / -) IL-2R alpha (+ / -) mice obtained in the step (1) to obtain IL-12p40(- / -) IL-2R alpha (+ / -) mice by means of breeding; (3), performing inbreeding on the IL-12p40(- / -) IL-2R alpha (+ / -) mice obtained in the step (2) and obtaining the identified IL-12p40(- / -) IL-2R alpha (- / -) mice. The method has the advantages that IL-12p40 is an important cell factor in the immune system of a patient, and functions and differentiation of CD4+T and CD8+T cells can be affected by the IL-12p40; IL-2R alpha is an alpha chain of an IL-2 receptor and plays a key role in keeping the balance of the immune system of the patient.
Owner:UNIV OF SCI & TECH OF CHINA

Pharmaceutical compositions for combination therapy

ActiveUS20180008616A1Metabolism disorderDigestive systemLiver enzyme levelsPPAR-delta Agonists
The present invention relates to a pharmaceutical composition comprising a combination of an FXR agonist and at least one lipid lowering agent (e.g., PPAR-alpha agonist, PPAR-delta agonist, PPAR-alpha and delta dual agonist, and / or statin). Also disclosed is use of the combination for the treatment or prevention of a FXR mediated disease or condition, such as primary biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC), portal hypertension, bile acid diarrhea, NAFLD (nonalcoholic fatty liver disease), NASH (non-alcohol-induced steatohepatitis), and other chronic liver diseases. The combination of the present invention is useful for the treatment or prevention of conditions related to elevated lipid and liver enzyme levels. The present invention also relates to packs or kits including the pharmaceutical combination.
Owner:INTERCEPT PHARMA INC

Use of Adefovir or Tenofovir for Inhibiting Mmtv-Like Viruses Involved in Breast Cancer and Primary Biliary Cirrhosis

The active metabolites of adefovir and tenofovir (PMEApp and PMPApp) are active against the MMTV RT. They are 25-fold more potent than 3TCppp, suggesting that tenofovir and adefovir may be effective at inhibiting the MMTV-like retroviruses, which may be the etiological agents involved in PBC and breast cancer.
Owner:GILEAD SCI INC

Chinese medicine composition for treating autoimmune liver disease, and preparation method thereof

The invention discloses a Chinese medicine composition for treating an autoimmune liver disease. The Chinese medicine composition is prepared from the Chinese medicinal materials, namely rheum officinale, radix rubiae, fructus forsythia, herba siegesbeckiae, large-leaved gentian and liquorice. The invention also discloses a preparation method of the Chinese medicine composition and application of the Chinese medicine composition. The composition has the effects of clearing away heat and toxic materials, smoothing liver-gallbladder, and promoting blood circulation to remove blood stasis, and is mainly used for treating autoimmune hepatitis, primary biliary cirrhosis and primary sclerosing cholangitis.
Owner:THE FIFTH MEDICAL CENT OF CHINESE PLA GENERAL HOSPITAL

Identification of a novel retrovirus associated with primary biliary cirrhosis and autoimmune disorders

InactiveUS6468737B1Reduced responseReactivity is smallOrganic active ingredientsAntipyreticAutoimmune thyroiditisS syndrome
The present invention relates, first, to the discovery, identification, and characterization of novel nucleic acid molecules, that are associated with PBC, Sjögren's syndrome, scleroderma, SLE, autoimmune thyroiditis and various other connective tissue disorders. The novel nucleotide sequences of the present invention are retroviral in origin and are indicative of a PBC retrovirus which bears a strong correlation with PBC. The present invention is based, in part, on the Applicant's data which is the first evidence to suggest that PBC patient's tissue may harbor a transmissible agent. The association of a retroviral infectious agent with PBC was first demonstrated by Applicants in vitro by co-culture of periportal lymph nodes derived from patients at time of transplantation and healthy biliary epithelium cells. The Applicant's discoveries as described herein, report the characterization of PBC-associated infectious agent as retroviral as demonstrated by electron microscopy and immunoblot reactivity. In addition, Applicants have characterized novel nucleotide sequences which are associated with the PBC-associated retrovirus.
Owner:ALTON OCHSNER MEDICAL FOUND

Colloidal gold chromatography anti-SSB antibody detection test paper and preparation method thereof

The invention discloses a colloidal gold chromatography anti-SSB antibody detection test paper and a preparation method thereof. The colloidal gold chromatography anti-SSB antibody detection test paper comprises a sample pad, a combination pad, a cellulose nitrate coated film and a water absorption pad, and the sample pad, the combination pad, the cellulose nitrate coated film and the water absorption pad are pasted on a base plate sequentially from one side of the base plate to the other side of the base plate, wherein the combination pad is coated with a gold-labeled antibody a and a gold-labeled antibody b; and the cellulose nitrate coated film is provided with a detection line and a quality control line, the detection line is coated with an SSB antigen protein, and the quality control line is coated with a gold-labeled antibody c. By adopting indirect immunoassay to introduce the SSB antigen protein in the invention to carry out process optimization on the combination pad and the sample pad, so high sensitivity, high specificity and high accuracy detection performances of the anti-SSB antibody are realized, and a reference basis is provided for the auxiliary diagnosis of primary biliary cirrhosis.
Owner:SHANGHAI KEXIN BIOTECH

Therapeutic agent for primary biliary cirrhosis

Disclosed is a therapeutic agent for primary biliary cirrhosis, which contains L-alanine or a pharmaceutically acceptable salt thereof as the active ingredient. The effect of this therapeutic agent is to reduce serum total bilirubin and transaminase value, thereby effectively curing primary biliary cirrhosis. This therapeutic agent can be chronically administrated for a long period of time and exhibits an effect superior to that obtained in ordinary medical therapy.
Owner:THE CITY OF OSAKA +1

Alpha crystal form of obeticholic acid as well as preparation method, medicine composition and application thereof

The invention relates to an alpha crystal form of obeticholic acid and a preparation method thereof. The preparation method comprises the following steps: (a) fully dissolving obeticholic acid under a backflow state in a mixed solvent of toluene or toluene and another kind of solvent forming a homogeneous system; (b) cooling the obtained obeticholic acid solution, so the alpha crystal form of the obeticholic acid precipitates out from the solution; (c) separating the alpha crystal form of the obeticholic acid out from the solution; and (d) placing the alpha crystal form of the obeticholic acid under 30-70 DEG C and drying for 3-30 hours at reduced pressure or ordinary pressure. The prepared alpha crystal form of obeticholic acid has the characteristics of better stability, higher purity, stable moisture content and the like. Furthermore, the invention also relates to a medicine composition of the alpha crystal form and the application of the alpha crystal form in preparing medicines for treating hepatic diseases such as biliary atresia, cholestatic liver disease, chronic liver disease, primary biliary cirrhosis, alcoholic fatty liver, non-alcoholic fatty liver disease and the like.
Owner:SICHUAN RUIXIKANG BIOLOGICAL MEDICINE CO LTD

Specific autoantibody of PBC (primary biliary cirrhosis) and application

InactiveCN103044548ADiagnosis helpsAids in differential diagnosisImmunoglobulins against animals/humansBiological testingAnti-mitochondrial antibodyAntigen
The invention provides a specific autoantibody of the PBC and a corresponding antigen. RBE (relative biological effectiveness) TP (total protein) of cholangiocarcinoma cells is taken as the antigen of the specific autoantibody; an IB (immunoblotting) method is adopted to detect the serum of a PBC patient; an autoantibody aiming at protein with the molecular weight about 20kD is detected and named Sp20 antibody; and then the Sp20 antibody is separated and obtained from the serum of the PBC patient through two-dimensional electrophoresis. The invention further provides an application of the Sp20 antibody in preparation of a kit for PBC diagnosis. By means of research on the mechanism of the Sp20 antibody in PBC incidence, theoretical basis is provided for early diagnosis, early treatment and prognostic judgment of PBC patients, diagnosis for AMA (anti mitochondrial antibody)-negative PBC patients is facilitated, and differential diagnosis with other autoimmune diseases is facilitated.
Owner:PEOPLES HOSPITAL PEKING UNIV

Efficient amplifying and culturing method for biliary epithelial cells

The invention discloses an efficient amplifying and culturing method for biliary epithelial cells in rabbit livers and belongs to the technical field of biological medicines. The efficient amplifying and culturing method comprises the following steps of: (1) separating, purifying and culturing the epithelial cells; (2) detecting cell growth lines; and (3) identifying the epithelial cells. The efficient amplifying and culturing method for the biliary epithelial cells, disclosed by the invention, has the advantages as follows: through a multi-step separating method, biliary epithelial cells with higher purities are obtained and a long-time multiplication culturing system for the biliary epithelial cells is established; a fact that the multiplication of the biliary epithelial cells in the livers can be obviously promoted through an Rho kinase inhibitor Y-27632 is first found; and the efficient amplifying and culturing method for the biliary epithelial cells, disclosed by the invention, has the advantages of simpler operation and the like, is suitable for promotion and application and can provide a platform for researches on a plurality of disease mechanisms including biliary atresia, primary biliary cirrhosis and the like.
Owner:SHAOXING UNIVERSITY

Specific autoantigen of primary biliary cirrhosis (PBC) and application thereof

The invention discloses a specific autoantigen EIF2C1 of primary biliary cirrhosis (PBC). According to the specific autoantigen of PBC and the application thereof, six novel autoantigens of PBC are obtained through screening; during the detection on the blood serum of a PBC patient, the positive rate of each autoantigen reaches over 15%, so that the new-found autoantigens are potential biomarkers which are used for accurately diagnosing PBC through distinguishing other autoimmune diseases.
Owner:PEKING UNION MEDICAL COLLEGE HOSPITAL CHINESE ACAD OF MEDICAL SCI +1

Methods and Compositions for Diagnosis of Inflammatory Liver Disease

The present disclosure provides methods and compositions that find use in facilitating a diagnosis of inflammatory liver disease in a subject. The methods and compositions generally involve detection of eotaxin-3 (E3) levels, either alone or with levels of eotaxin-1 (E1), and optionally, with levels of CCL22 and, further optionally, with levels of IL15. These levels can be used to facilitate a diagnosis of a liver disease of at least one of autoimmune hepatitis (AIH), primary biliary cirrhosis (PBC), and primary sclerosing cholangitis (PSC), and / or to facilitate a differential diagnosis between AIH, PBC, and PSC. The methods and compositions of the present disclosure also find use in facilitating treatment decisions for a subject.
Owner:MEDIZINISCHE HOCHSCHULE HANNOVER +1

Traditional Chinese medicine for treating primary biliary cirrhosis and preparation method and application of traditional Chinese medicine

The invention discloses a traditional Chinese medicine for treating primary biliary cirrhosis and a preparation method and application of the traditional Chinese medicine. The traditional Chinese medicine comprises the following raw materials in parts by weight: 500-1500 parts of oriental wormwood, 1000-2500 parts of roots of common peony, 500-1000 parts of scorpio, 1000-2000 parts of cortex dictamni, 1000-2500 parts of malt and 500-2000 parts of licorice roots. The traditional Chinese medicine disclosed by the invention has the main effects of clearing heat and removing toxin, soothing livers and dispersing gallbladder as well as activating blood and removing stasis, is capable of treating overlap syndromes of primary biliary cirrhosis caused by endoretention of damp heat, liver and gall stasis and Qi-stagnancy and blood stasis, and is simple in composition formula, outstanding in medicinal effect, free of toxic or side effect and convenient to prepare.
Owner:YUNNAN UNIV OF TRADITIONAL CHINESE MEDICINE

FXR (farnesol X receptor) agonist

ActiveCN109575008AExcellent FXR receptor agonistic activityPrevent non-alcoholic fatty liver diseaseOrganic active ingredientsSenses disorderDiseaseDiabetic complication
The invention belongs to the technical field of medicine and particularly relates to a compound shown as formula (I) that is shown in the description, and its pharmaceutically acceptable salts, estersor stereoisomers, with R1, R2, R3, M1, M2, Q, L, ring A, ring B and m defined as in the description and the claims. The invention also relates to a preparation method these compounds, pharmaceuticalpreparations and their application in the preparation of drugs for the treatment and / or prevention of FXR-mediated non-alcoholic fatty liver disease, primary biliary cirrhosis, lipid metabolism disorder, diabetic complications, malignant tumors and related diseases.
Owner:XUANZHU BIOPHARMACEUTICAL CO LTD

FXR receptor agonist

ActiveCN109265471AExcellent FXR receptor agonistic activityPrevent non-alcoholic fatty liver diseaseOrganic active ingredientsSenses disorderDiseaseDiabetic complication
The present invention discloses an FXR receptor agonist, belongs to the technical field of medicine, and particularly relates to a compound represented by a formula (I), a pharmaceutically acceptablesalt, an ester or a stereoisomer thereof, wherein R<1>, R<2>, R<3>, M, L, L1, W, A , B, Q, m and n are defined in the specification. The present invention further relates to a preparation method of the compound, a pharmaceutical preparation, and applications in preparation of drugs for treatment and / or prevention of nonalcoholic fatty liver disease, primary biliary cirrhosis, lipid metabolism disorder, diabetic complication, malignant tumors and other related diseases mediated by FXR receptors. The formula I is defined in the specification.
Owner:XUANZHU BIOPHARMACEUTICAL CO LTD

Traditional Chinese medicine for treating primary biliary cirrhosis

InactiveCN103356886ASafe and effective in primary biliary cirrhosisNo significant differenceDigestive systemPlant ingredientsPrimary biliary cirrhosisClinical tests
The invention relates to a traditional Chinese medicine for treating primary biliary cirrhosis, which is prepared from the following medicinal materials in parts by weight: 12 parts of fructus rosae laevigatae, 14 parts of radix scrophulariae, 6 parts of euphorbia jolkinii, 10 parts of beggarweed, 12 parts of climbing entada, 14 parts of elsholtzia rugulosa hemsl, 10 parts of michelia champaca, 14 parts of radix bupleuri, 10 parts of semen cassiae, 8 parts of rhizoma cyperi, 14 parts of semiliquidambar cathayensis, 10 parts of abutilon peniculatum flower, 14 parts of dysosma difformis, 12 parts of osbeckia chinensis, 14 parts of penthorum chinense pursh, 10 parts of twisted-stalk, 8 parts of all-grass of winkled marshweed, 10 parts of bryoniifolia root and 10 parts of gynura divaricata. Clinical tests prove that the traditional Chinese medicine disclosed by the invention can safely and effectively treat primary biliary cirrhosis.
Owner:丁漫漫

Method for analyzing primary biliary cirrhosis metabolite based on H1NMR technology

The invention provides a method for analyzing primary biliary cirrhosis metabolites based on H1NMR technology, belongs to the field of biotechnology, and relates to primary biliary cirrhosis. The invention mainly comprises the following flow: step 1, sample collection and preparation, liver function testing; step 2, extraction, alignment, and normalization of original data; step 3, primary component analysis (PCA); step 4, orthogonal partial least squares-discriminant analysis (OPLS-DA); step 5, searching of metabolites causing intergroup differences; steo 6, statistical test. The advantages of the invention are that: the analysis method provided by the invention provides a new approach and method for the analysis research of primary biliary cirrhosis metabolites; the method has reasonable and feasible design, provides new landmarks for the research of the diagnosis and treatment of PCB, and also provides new thoughts for the research of the pathogenesis.
Owner:SHANGHAI CLUSTER BIOTECH

Preparation method of high-purity natural ursodesoxycholic acid and application thereof in medicament

The invention belongs to the technical field of medical biology, in particular to a preparation method of high-purity natural ursodesoxycholic acid. The high-purity natural ursodesoxycholic acid is obtained by separating and purifying bear gall powder prepared from a manual drained bear gall, and the high performance liquid chromatography purity is not lower than 98 percent. The preparation method comprises the following steps of: firstly, separating and purifying by applying a cation exchange medium to prepare tauroursodeoxycholic acid with purity not lower than 90 percent; and then thoroughly hydrolyzing the tauroursodeoxycholic acid into ursodesoxycholic acid and taurine in the presence of alkali and separating and purifying by applying a silica gel adsorption chromatography technology to prepare the ursodesoxycholic acid with purity not lower than 98 percent. The natural ursodesoxycholic acid prepared by the invention has the effects on treating primary biliary cirrhosis and primary sclerosing cholangitis.
Owner:重庆寰瑞生物技术有限公司

Deuterated chenodeoxycholic acid derivative and pharmaceutical composition comprising compound thereof

Disclosed are deuterated chenodeoxycholic acid derivatives and pharmaceutical compositions containing the deuterated chenodeoxycholic acid derivatives. In particular, disclosed is a deuterated chenodeoxycholic acid derivative of formula (I), or a crystal form, pharmaceutically acceptable salt, hydrate or solvate thereof, and a pharmaceutical composition containing the same. The deuterated chenodeoxycholic acid derivatives of formula (I) can be used to treat and / or prevent diseases related to the farnesoid X receptor (FXR) and / or G-protein coupled bile acid receptor, such as nonalcoholic steatohepatitis, nonalcoholic fatty liver diseases, gallstones, primary biliary cirrhosis, and cirrhosis.
Owner:SUZHOU ZELGEN BIOPHARML

Methods and compositions for diagnosis of inflammatory liver disease

The present disclosure provides methods and compositions that find use in facilitating a diagnosis of inflammatory liver disease in a subject. The methods and compositions generally involve detection of eotaxin-3 (E3) levels, either alone or with levels of eotaxin-1 (E1), and optionally, with levels of CCL22 and, further optionally, with levels of IL15. These levels can be used to facilitate a diagnosis of a liver disease of at least one of autoimmune hepatitis (AIH), primary biliary cirrhosis (PBC), and primary sclerosing cholangitis (PSC), and / or to facilitate a differential diagnosis between AIH, PBC, and PSC. The methods and compositions of the present disclosure also find use in facilitating treatment decisions for a subject.
Owner:MEDIZINISCHE HOCHSCHULE HANNOVER +1
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