Liver organ chip-based anti-fibrosis active component high-throughput screening method and application thereof

CN119506389APending Publication Date: 2025-02-25TIANJIN INST OF IND BIOTECH CHINESE ACADEMY OF SCI +1
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Patent Information

Application Number
CN202411515857.7
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2024-10-29
Publication Date
2025-02-25

AI Technical Summary

Technical Problem

The prior art is difficult to truly simulate human liver responses in vitro, resulting in complex and time-consuming drug development processes, especially when screening anti-hepatic fibrosis drugs, which lacks a high-throughput, rapid testing platform.

Method used

通过结合商业化孔板与器官芯片,构建3D肝纤维化类器官模型,并利用人诱导多能干细胞技术进行原位分化和干预,实现司美格鲁肽等药物的高通量筛选。

Benefits of technology

It has achieved efficient construction of a 3D liver organoid model with liver-specific functions in vitro, which can truly simulate the human liver's response to drugs, quickly screen out drugs with anti-fibrotic activity, and promoted the research and development of anti-liver fibrotic drugs.

✦ Generated by Eureka AI based on patent content.

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Abstract

The invention discloses an anti-fibrosis active ingredient high-throughput screening method based on a liver organ chip and application of the anti-fibrosis active ingredient high-throughput screening method. The invention provides a liver organ chip combined with a pore plate. The liver organ chip is used for high-throughput screening of anti-fibrosis active ingredients. The method specifically comprises the steps of building a high-throughput organ-like chip, forming a 3D fibrosis liver organ and screening the biological activity of an anti-fibrosis drug. According to the invention, the physiological state of the human liver is reproduced in an in-vitro culture environment by utilizing the principles of stem cell development and engineering, and the pharmacological action of the liver tissue on the medicines obeticholic acid and semeglutide under the pathological state of the human liver is remodeled; the method has great application value in the aspects of in-vitro organ simulation, high-throughput screening of drug efficacy and exploration of a response mechanism of an organism to a drug, and the construction mode of combining with a commercial pore plate is extremely simple, convenient, expansible and practical.
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