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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:用指纹和化学计量分析的指纹和多组分定量组合龙丹谢Gan丸的质量分析

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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. 0is 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 0.046-1.16mg·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. 0e study provided sound basis for improving quality control standards. 0is study also provided practical strategy for overall quality control of traditional Chinese medicines.
机译:龙丹谢甘丸是一种传统的复杂复合品制备,历史悠久,用于治疗疾病,包括肝脏湿润,头晕,耳鸣和耳聋。不同厂商的产品质量可能会改变。这项研究旨在以全面而有效的方式控制产品质量,旨在为整体质量控制建立一种实用而方便的方法。 0IS研究包括定性和定量作品,分别用于获取整体组成和主要成分的信息。结果,所有50个样品的HPLC指纹(UV 240nm)相似性在0.65〜0.99的范围内。结果表明,来自不同制造商的产品存在差异。另外,通过LC-MS暂时识别指纹的10个特征峰。进一步的化学计量学分析用于评估不同制造商的产品。同时,HPLC(UV 285nm)多组分定量结果表明,醋栗霉素,黄芩苷,黄芩素和Wogonin的含量为0.61-5.40,1.96-5.33,0.10-3.40和0.046-1.16mg· G-1分别。数据分析从指纹统计分析中验证了Baicalein的主要不同分量。值得一提的是,通过具有双通道的HPLC-DAD同时完成定性指纹和定量多组分测定。 0E研究为提高质量控制标准提供了合理的基础。 0IS研究还为中药总体质量控制提供了实际策略。

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