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使用超高效液相色谱-混合三重四极杆线性离子阱质谱法定量测定小檗属植物中的异喹啉生物碱和绿原酸。

Quantitative determination of isoquinoline alkaloids and chlorogenic acid in Berberis species using ultra high performance liquid chromatography with hybrid triple quadrupole linear ion trap mass spectrometry.

作者信息

Singh Awantika, Bajpai Vikas, Kumar Sunil, Arya Kamal Ram, Sharma Kulwant Rai, Kumar Brijesh

机构信息

Sophisticated Analytical Instrument Facility Division, CSIR-Central Drug Research Institute, Lucknow, India.

Academy of Scientific and Innovative Research, New Delhi, India.

出版信息

J Sep Sci. 2015 Jun;38(12):2007-13. doi: 10.1002/jssc.201500063. Epub 2015 May 8.

DOI:10.1002/jssc.201500063
PMID:25847792
Abstract

Berberis species are well known and used extensively as medicinal plants in traditional medicine. They have many medicinal values attributable to the presence of alkaloids having different pharmacological activities. In this study, a method was developed and validated as per international conference on harmonization guidelines using ultra high performance liquid chromatography with hybrid triple quadrupole-linear ion trap mass spectrometry operated in the multiple reaction monitoring mode for nine bioactive compounds, including protoberberine alkaloids, aporphine alkaloids and chlorogenic acid. This method was applied in different plant parts of eight Berberis species to determine variations in content of nine bioactive compounds. The separation was achieved on an ACQUITY UPLC CSH™ C18 column using a gradient mobile phase at flow rate 0.3 mL/min. Calibration curves for all the nine analytes provided optimum linear detector response (with R(2) ≥0.9989) over the concentration range of 0.5-1000 ng/mL. The precision and accuracy were within RSDs ≤2.4 and ≤2.3%, respectively. The results indicated significant variation in the total contents of the nine compounds in Berberis species.

摘要

小檗属植物广为人知,在传统医学中被广泛用作药用植物。由于存在具有不同药理活性的生物碱,它们具有许多药用价值。在本研究中,根据国际协调会议指南,开发并验证了一种方法,该方法使用超高效液相色谱仪与混合三重四极杆-线性离子阱质谱联用,在多反应监测模式下测定包括原小檗碱生物碱、阿朴啡生物碱和绿原酸在内的九种生物活性化合物。该方法应用于八种小檗属植物的不同植物部位,以确定九种生物活性化合物含量的变化。使用梯度流动相,流速为0.3 mL/min,在ACQUITY UPLC CSH™ C18柱上实现分离。所有九种分析物的校准曲线在0.5-1000 ng/mL的浓度范围内提供了最佳线性检测器响应(R(2)≥0.9989)。精密度和准确度的相对标准偏差分别≤2.4%和≤2.3%。结果表明,小檗属植物中九种化合物的总含量存在显著差异。

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