一种宣肺败毒中药组合物多指标成分的检测方法

By combining high performance liquid chromatography (HPLC) and ultra-high performance liquid chromatography (UHPLC) with a gradient elution procedure and optimizing extraction conditions, a fingerprint spectrum and content determination method for Xuanfei Baidu Granules were established. This solved the instability problem in the detection of components of Xuanfei Baidu Granules, achieved accurate control of multiple indicator components, and ensured the consistency of product quality.

CN118443846BActive Publication Date: 2026-07-17SHANDONG BUCHANG PHARMA +1

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
SHANDONG BUCHANG PHARMA
Filing Date
2024-05-21
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Existing technologies are insufficient to comprehensively and accurately control the content and quality of various active ingredients in Xuanfei Baidu Granules, and lack a systematic method for establishing fingerprint spectra, resulting in unstable product quality.

Method used

High performance liquid chromatography (HPLC) and ultra-high performance liquid chromatography (UHPLC), combined with gradient elution procedures and characteristic index components, were used to establish a fingerprint spectrum and content determination method for Xuanfei Baidu Granules. By optimizing the extraction solvent, material-liquid ratio, and extraction time, the contents of verbenacin, verbenin, glutinin, verbascoside, isoverascoside, naringin, and glycyrrhizic acid were identified to ensure product quality consistency.

Benefits of technology

The stability and accuracy of the multi-index component detection method for Xuanfei Baidu Granules have been achieved, ensuring the intrinsic quality of the product, providing a systematic quality control means, and improving the similarity and consistency of the product components.

✦ Generated by Eureka AI based on patent content.

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Abstract

本发明提供一种宣肺败毒中药组合物多指标成分的检测方法,该检测方法包括指纹图谱和有效物质成分含量方法,并确定认8个色谱峰,包括峰戟叶马鞭草苷、马鞭草苷、虎杖苷、毛蕊花糖苷、异毛蕊花糖苷、柚皮苷紫铆因及甘草酸。本发明所建立的含量检测方法稳定、准确可靠,用于本发明宣肺败毒中药组合物的质量检测标准中,以保障其内在质量。经方法学考察,该方法具有检测效率高、控制指标成分多、精密度、稳定性、加样回收率良好特点,从而有效保证本发明宣肺败毒中药组合物的内在质量。
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