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基于液相色谱-飞行时间质谱联用(LC-TOF/MS)和高效液相色谱-紫外检测法(HPLC-UV)的独一味成分分析与质量控制

Constituent analysis and quality control of Lamiophlomis rotata by LC-TOF/MS and HPLC-UV.

作者信息

La Mingping, Zhang Feng, Gao Shouhong, Liu Xiaowei, Wu Zhijun, Sun Lianna, Tao Xia, Chen Wansheng

机构信息

Department of Pharmacy, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai 200003, PR China.

Department of Pharmacy, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai 200003, PR China.

出版信息

J Pharm Biomed Anal. 2015 Jan;102:366-76. doi: 10.1016/j.jpba.2014.09.038. Epub 2014 Oct 8.

Abstract

In the present study, chemical profile analysis for Lamiophlomis rotata, a classic Tibetan folk medicine, was illustrated by an ultra-high performance liquid chromatography quadrupole time-of-flight mass spectrometry (LC-TOF/MS) method, which provided evidence for the certain identification of the main constituents, including iridoids, flavonoids and phenylethanoid glycosides. Among these compounds, nine of them were regarded as marker compounds for the quantitative evaluation of L. rotata, using a simple and reliable method by HPLC with ultraviolet, in combination of chromatographic fingerprint analysis. Separation was achieved on a Waters SunFire C18 analytical column with linear gradient elution of acetonitrile and 0.1% formic acid aqueous solution. The validated method was successfully applied to evaluate twelve batches of L. rotata. Assay results showed that nine compounds did not vary significantly from the aerial parts and the whole plant for each batch, and was consistent with the fingerprint analysis, which confirmed the medicine parts alteration in Chinese Pharmacopoeia from the perspective of chemical components.

摘要

在本研究中,采用超高效液相色谱四极杆飞行时间质谱(LC-TOF/MS)法对经典藏药独一味进行了化学特征分析,为确定包括环烯醚萜、黄酮类和苯乙醇苷类在内的主要成分提供了依据。在这些化合物中,其中9种被视为独一味定量评价的标记化合物,采用高效液相色谱-紫外检测的简单可靠方法,并结合色谱指纹图谱分析。在Waters SunFire C18分析柱上进行分离,以乙腈和0.1%甲酸水溶液进行线性梯度洗脱。该验证方法成功应用于评价12批独一味。测定结果表明,每批独一味地上部分和全草中的9种化合物含量无显著差异,且与指纹图谱分析结果一致,从化学成分角度证实了《中国药典》中该药部位的变更。

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