Separation method of compound with pancreatic lipase inhibitory activity in Tibetan medicine Sibiraea angustata and application of compound in preparation of weight-losing and lipid-lowering medicine

CN119302974APending Publication Date: 2025-01-14HEXI UNIV
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Patent Information

Application Number
CN202411484231.4
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2024-10-23
Publication Date
2025-01-14

AI Technical Summary

Technical Problem

Existing weight loss drugs such as orlistat have liver damage and adverse gastrointestinal side effects. The method of screening pancreatic lipase inhibitors from natural products is complex and time-consuming, making it difficult to effectively screen out significant weight loss and lipid-lowering effects. Element.

Method used

Affinity ultrafiltration-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry technology was used to screen a variety of pancreatic lipase inhibitors from Liucha, combined with molecular docking technology and macroporous resin preparation chromatography method, and directional separation was strong Flavonoids with binding ability such as quercetin 3,4'-diglucoside and schizonepetin were verified for their pancreatic lipase inhibitory activity.

Benefits of technology

A variety of novel pancreatic lipase inhibitors were screened, especially quercetin 3,4'-diglucoside and schizonepetin, which had strong pancreatic lipase inhibitory activity, providing a new direction for the development of weight loss and lipid-lowering drugs, and through High performance liquid chromatography detection achieved high purity preparation of the target compound.

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Abstract

The invention provides a separation method of a compound with pancreatic lipase inhibitory activity in Tibetan medicine Sibiraea angustata and application of the compound in preparation of weight-losing and lipid-lowering medicines. According to the invention, 14 new pancreatic lipase inhibitory activity compounds are screened from a Sibiraea angustata extract by adopting an affinity ultrafiltration-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry method; the binding capacity of the target compound and the pancreatic lipase is compared by adopting a molecular docking technology; macroporous resin and a preparative chromatography method are adopted for directional separation of two flavonoid components with high binding capacity; further inspecting the in-vitro pancreatic lipase inhibition activity by adopting an in-vitro pancreatic lipase inhibition experiment; the method provides technical support for rapid screening of the pancreatic lipase inhibitor, lays a good foundation for discovery of weight-losing and lipid-lowering drugs, and has a wide application prospect.
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