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Quality Analysis of Long dan Xie gan Pill by a Combination of Fingerprint and Multicomponent Quantification with Chemometrics Analysis

机译:指纹图谱与多组分定量结合化学计量学分析龙胆泻肝丸的质量

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摘要

Long dan Xie gan pill is a traditional complex compound preparation with a long history for treatment of diseases, including hepatocolic hygropyrexia, dizziness, tinnitus, and deafness. Quality of products from different manufacturers may be varied. Since the current standard could not control the quality of products in a comprehensive and effective way, this study aimed at establishing a practical and convenient approach for holistic quality control of the preparation. This study included both qualitative and quantitative works to get information on the overall composition and main components, respectively. As a result, HPLC fingerprint (UV 240 nm) similarities of all fifty samples were in the range of 0.65∼0.99. Results indicated that there was a difference among products from different manufacturers. Additionally, ten characteristic peaks of the fingerprint were tentatively identified by LC-MS. Further chemometrics analysis was utilized to evaluate the products from different manufacturers. At the same time, the HPLC (UV 285 nm) multicomponent quantification result showed that contents of gentiopicrin, baicalin, baicalein, and wogonin were in the range of 0.61–5.40, 1.96–5.33, 0.10–3.40, and 0.046–1.16 mg·g−1, respectively. Data analysis verified the main different component of baicalein from the fingerprint statistical analysis. It is worth mentioning that the qualitative fingerprint and quantitative multicomponent determination were simultaneously accomplished by HPLC-DAD with dual channels. The study provided sound basis for improving quality control standards. This study also provided practical strategy for overall quality control of traditional Chinese medicines.
机译:龙胆泻肝丸是一种传统的复方制剂,具有悠久的历史,用于治疗包括肝炎性潮热,头晕,耳鸣和耳聋的疾病。来自不同制造商的产品质量可能会有所不同。由于当前标准无法全面有效地控制产品质量,因此本研究旨在建立一种实用且方便的方法来对制剂进行整体质量控制。这项研究包括定性和定量工作,以分别获取有关总体成分和主要成分的信息。结果,所有五十个样品的HPLC指纹图谱相似度(UV 240 nm)在0.65至0.99之间。结果表明,不同制造商的产品之间存在差异。另外,通过LC-MS初步鉴定出指纹的十个特征峰。利用进一步的化学计量学分析来评估来自不同制造商的产品。同时,高效液相色谱(UV 285 nm)的定量分析结果表明,龙胆苦素,黄in苷,黄e素和沃戈宁的含量在0.61–5.40、1.96–5.33、0.10–3.40和0.046–1.16 mg·之间。 g -1 。数据分析从指纹统计分析中证实了黄ical素的主要不同成分。值得一提的是,HPLC-DAD双通道同时完成了定性指纹图谱和定量多组分测定。该研究为提高质量控制标准提供了良好的基础。该研究还为中药的全面质量控制提供了可行的策略。

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