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低温液相-液相萃取结合超高效液相色谱-串联质谱法同时测定中药葛根芩连汤中的12种生物活性成分

Subzero-Temperature Liquid-Liquid Extraction Coupled with UPLC-MS-MS for the Simultaneous Determination of 12 Bioactive Components in Traditional Chinese Medicine Gegen-Qinlian Decoction.

作者信息

Shi Zhihong, Li Zhimin, Zhang Shulan, Fu Hongna, Zhang Hongyi

机构信息

College of Chemistry and Environmental Science, Key Laboratory of Analytical Science and Technology of Hebei Province, Hebei University, Baoding 071002, China.

College of Chemistry and Environmental Science, Key Laboratory of Analytical Science and Technology of Hebei Province, Hebei University, Baoding 071002, China

出版信息

J Chromatogr Sci. 2015 Sep;53(8):1407-13. doi: 10.1093/chromsci/bmu226. Epub 2015 Feb 5.

Abstract

Based on the phase separation phenomenon of acetonitrile-water system at subzero temperature, a subzero-temperature liquid-liquid extraction coupled with ultra-performance liquid chromatography tandem quadrupole mass spectrometry : UPLC-MS-MS) method was developed for the simultaneous determination of 12 bioactive components in Gegen-Qinlian decoction. After optimization, the extraction conditions were set as follows: 3.0 mL of aqueous sample solution (pH 5.86) was extracted with 2 mL of acetonitrile at -35°C for 35 min. The separated acetonitrile phase was diluted 10-fold with water before UPLC-MS-MS analysis. Separation was performed on a Waters ACQUITY UPLC(®)BEH C18 column (2.1 × 100 mm i.d., 1.7 µm) with ammonium formate buffer solution (20 mmol L(-1), pH 3.2, adjusted by formic acid) and acetonitrile as mobile phase with gradient elution. Twelve target components could be separated within 10 min and quantified in multiple reaction monitoring mode, both positive and negative ionization modes were employed. Limits of detection were in the range of 0.0003-0.0451 μg mL(-1). Relative standard deviation values for intra- and interday precision were <2.71 and 8.94%, respectively. The established method provides a simple and effective framework for the quality control of Gegen-Qinlian decoction and related traditional Chinese medicinal preparations.

摘要

基于乙腈 - 水体系在零下温度下的相分离现象,建立了一种零下温度液 - 液萃取结合超高效液相色谱串联四极杆质谱(UPLC - MS - MS)法,用于同时测定葛根芩连汤中的12种生物活性成分。经过优化,萃取条件设定如下:取3.0 mL水样溶液(pH 5.86),加入2 mL乙腈,在 - 35°C下萃取35 min。分离得到的乙腈相在进行UPLC - MS - MS分析前用水稀释10倍。采用Waters ACQUITY UPLC(®)BEH C18柱(内径2.1×100 mm,粒径1.7 µm)进行分离,以甲酸铵缓冲溶液(20 mmol L(-1),pH 3.2,用甲酸调节)和乙腈为流动相进行梯度洗脱。12种目标成分可在10 min内分离,并在多反应监测模式下进行定量,同时采用正离子和负离子电离模式。检测限在0.0003 - 0.0451 μg mL(-1)范围内。日内和日间精密度的相对标准偏差值分别<2.71%和8.94%。所建立的方法为葛根芩连汤及相关中药制剂的质量控制提供了一种简单有效的框架。

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