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超高效液相色谱指纹图谱结合一测多评法对丹参注射液进行质量评价

[UPLC fingerprint combined with quantitative analysis of multi-components by single marker for quality assessment of Danshen Injection].

作者信息

Zhang Han, Li Zhen-Hao, Fan Xiao-Hui

机构信息

Graduate College,Tianjin University of Traditional Chinese Medicine Tianjin 301617,China.

Department of Chinese Medical Science and Engineering,College of Pharmaceutical Science,Zhejiang University Hangzhou 310058,China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2019 Sep;44(17):3724-3731. doi: 10.19540/j.cnki.cjcmm.20190410.310.

Abstract

Testing and analysis of chemical markers is currently the prevailing approach for quality assessment of traditional Chinese medicines. However,several important issues remain to be addressed,including the trade-off between accuracy and coverage. In this study,in order to give full play to the advantages of their respective methods and provide technical support for more comprehensively and rapidly evaluate the quality of Danshen Injection products,a fingerprint method was coupled with quantitative analysis of multicomponents by single marker( QAMS),with Danshen Injection as the carrier. Ultra performance liquid chromatography( UPLC) was used to establish the quantitative fingerprint. The UPLC fingerprints contained 13 common peaks,11 of which were identified by using ultra performance liquid chromatography-quadrupole time-of-flight mass spectrometry( UPLC-QTOF-MS). Furthermore,with sodium danshensu as the internal reference substance,relative correction factors( RCFs) of protocatechuic aldehyde,caffeic acid,rosmarinic acid,lithospermic acid,and salvianolic acid B were calculated through slope analysis method,and the QAMS method was adopted to determine the contents of these 6 components. The UPLC fingerprint was employed to assess the consistency of 12 batches of Danshen Injection,which showed good batch-to-batch consistency with similarity higher than 0. 99. In the comparison of contents of the six constituents obtained by QAMS and external standard method( ESM),RSD was all less than 4. 3%,indicating the good accuracy of the QAMS method. The QAMS method developed in this study combined with UPLC fingerprint can comprehensively reflect the internal quality of Danshen Injection when only the reference substance sodium danshensu is consumed,with greatly reduced detection cost and time. It provides a technical basis for further improving the quality standard of Danshen Injection.

摘要

化学标志物的检测与分析是目前中药质量评价的主流方法。然而,仍有几个重要问题有待解决,包括准确性和覆盖范围之间的权衡。在本研究中,为充分发挥各自方法的优势,为更全面、快速地评价丹参注射液产品质量提供技术支持,以丹参注射液为载体,将指纹图谱法与一测多评法(QAMS)相结合。采用超高效液相色谱(UPLC)建立定量指纹图谱。该UPLC指纹图谱包含13个共有峰,其中11个通过超高效液相色谱-四极杆飞行时间质谱(UPLC-QTOF-MS)进行了鉴定。此外,以丹参素钠为内参物,通过斜率分析法计算了原儿茶醛、咖啡酸、迷迭香酸、紫草酸和丹酚酸B的相对校正因子(RCFs),并采用QAMS法测定了这6种成分的含量。采用UPLC指纹图谱对12批丹参注射液的一致性进行评价,结果显示批次间一致性良好,相似度均高于0.99。在QAMS法与外标法(ESM)测定6种成分含量的比较中,相对标准偏差(RSD)均小于4.3%,表明QAMS法准确性良好。本研究建立的QAMS法结合UPLC指纹图谱,仅消耗丹参素钠对照品即可全面反映丹参注射液的内在质量,大大降低了检测成本和时间。为进一步提高丹参注射液的质量标准提供了技术依据。

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