School of Pharmacy, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang, PR China.
J Pharm Biomed Anal. 2011 Mar 25;54(4):717-21. doi: 10.1016/j.jpba.2010.11.002. Epub 2010 Nov 12.
The present paper describes a novel, sensitive and selective liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the simultaneous analysis of ganoderic acids C(2), B, A, H, D in Ganoderma lucidum and its related species. Ganoderma samples were prepared using simple ultrasonic extraction. Chromatographic separation was carried out on an Agilent Zorbax XDB C(18) column (250 mm × 4.6 mm i.d., 5μm) with an isocratic mobile phase consisting of acetonitrile, water and formic acid (42:58:0.5, v/v/v). Mass spectrometric detection was achieved by a triple-quadrupole mass spectrometer equipped with an atmospheric pressure chemical ionization (APCI) interface operating in negative and positive ionization mode via a single within-run polarity switching. Quantitation of five ganoderic acids was performed using selective reaction monitoring (SRM) mode. The intra- and inter-day precision was less than 6.2% and the accuracy ranged from 90.0% to 105.7%. The limit of quantification (LOQ) was 20.0-40.0 ng/mL and the limit of detection (LOD) was 3.0-25.0 ng/mL. With this method, low levels of ganoderic acids in the fruiting bodies of Ganoderma sinense and Ganoderma applanatum were accurately quantified for the first time. Importantly, the method allows unequivocal quantification of the five ganoderic acids in the spores and fruiting bodies of Ganoderma lucidum, whereas the previously published methods have lacked the capability. The method presented will be a powerful tool for quality control of Ganoderma lucidum and its related species.
本文描述了一种新颖、灵敏和选择性的液相色谱-串联质谱(LC-MS/MS)方法,用于同时分析灵芝及其相关种属中的灵芝酸 C(2)、B、A、H、D。灵芝样品采用简单的超声提取法制备。色谱分离在 Agilent Zorbax XDB C(18)柱(250mm×4.6mm id,5μm)上进行,采用乙腈、水和甲酸(42:58:0.5,v/v/v)的等度流动相。质谱检测采用配有大气压化学电离(APCI)接口的三重四极杆质谱仪,通过单次运行内极性切换,以正、负离子模式进行。五种灵芝酸的定量采用选择反应监测(SRM)模式。日内和日间精密度小于 6.2%,准确度在 90.0%至 105.7%之间。定量限(LOQ)为 20.0-40.0ng/mL,检测限(LOD)为 3.0-25.0ng/mL。使用该方法,首次准确地定量了灵芝和无柄灵芝子实体中的低水平灵芝酸。重要的是,该方法允许在灵芝的孢子和子实体中明确地定量五种灵芝酸,而以前发表的方法缺乏这种能力。所提出的方法将成为灵芝及其相关种属质量控制的有力工具。