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采用液相色谱-质谱联用技术测定绞股蓝中叶绿素及其衍生物的含量。

Determination of chlorophylls and their derivatives in Gynostemma pentaphyllum Makino by liquid chromatography-mass spectrometry.

作者信息

Huang S C, Hung C F, Wu W B, Chen B H

机构信息

Department of Food Science, School of Medicine, Fu Jen University, Taipei 242, Taiwan.

出版信息

J Pharm Biomed Anal. 2008 Sep 10;48(1):105-12. doi: 10.1016/j.jpba.2008.05.009. Epub 2008 May 17.

Abstract

The objectives of this study were to develop a high performance liquid chromatography-mass spectrometry (HPLC-MS) method for determination of chlorophylls and their derivatives in Gynostemma pentaphyllum Makino, a traditional Chinese herb possessing vital biological activities. Chlorophylls were extracted with a quaternary solvent system of hexane-acetone-ethanol-toluene (10:7:6:7, v/v/v/v), followed by separation of a total of 15 chlorophylls and their derivatives within 32 min using a gradient mobile phase of acetone, acetonitrile and methanol and a HyPURITY C18 column, with detection at 660 nm and flow rate at 1 mL/min. Identification was carried out on the basis of retention behavior, absorption spectra and mass spectra using atmospheric pressure chemical ionization (APCI) in positive ion mode for detection. Of the 15 analytes, chlorophyll a, chlorophyll b, pheophytin a and pheophytin b were quantified by using standard calibration curves, with the other 11 being quantified with an internal standard Fast Green FCF. Chlorophyll extracts in G. pentaphyllum were found to contain pheophytin a (2508.3 microg/g), pheophytin a' (111.2 microg/g), chlorophyll a (113.8 microg/g), chlorophyll a' (11.0 microg/g), hydroxypheophytin a (88.6 microg/g), hydroxypheophytin a' (66.5 microg/g), pyropheophytin a (76.0 microg/g), hydroxychlorophyll a (23.8 microg/g), pheophytin b (319.6 microg/g), pheophytin b' (13.2 microg/g), chlorophyll b (287.9 microg/g), chlorophyll b' (11.1 microg/g), hydroxychlorophyll b (15.0 microg/g), hydroxypheophytin b (11.2 microg/g) and hydroxypheophytin b' (8.5 microg/g).

摘要

本研究的目的是开发一种高效液相色谱 - 质谱联用(HPLC-MS)方法,用于测定绞股蓝(一种具有重要生物活性的传统中草药)中的叶绿素及其衍生物。叶绿素用己烷 - 丙酮 - 乙醇 - 甲苯(10:7:6:7,v/v/v/v)的四元溶剂体系提取,然后使用丙酮、乙腈和甲醇的梯度流动相以及HyPURITY C18柱,在32分钟内分离总共15种叶绿素及其衍生物,检测波长为660 nm,流速为1 mL/min。采用大气压化学电离(APCI)正离子模式,根据保留行为、吸收光谱和质谱进行鉴定。在这15种分析物中,叶绿素a、叶绿素b、脱镁叶绿素a和脱镁叶绿素b通过标准校准曲线进行定量,另外11种则用内标亮绿FCF进行定量。发现绞股蓝中的叶绿素提取物含有脱镁叶绿素a(2508.3 μg/g)、脱镁叶绿素a'(111.2 μg/g)、叶绿素a(113.8 μg/g)、叶绿素a'(11.0 μg/g)、羟基脱镁叶绿素a(88.6 μg/g)、羟基脱镁叶绿素a'(66.5 μg/g)、焦脱镁叶绿素a(76.0 μg/g)、羟基叶绿素a(23.8 μg/g)、脱镁叶绿素b(319.6 μg/g)、脱镁叶绿素b'(13.2 μg/g)、叶绿素b(287.9 μg/g)、叶绿素b'(11.1 μg/g)、羟基叶绿素b(15.0 μg/g)、羟基脱镁叶绿素b(11.2 μg/g)和羟基脱镁叶绿素b'(8.5 μg/g)。

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