Cheng Wenhao, Li Yinghui, Yang Wei, Wu Siyang, Wei Mengmeng, Gao Yang, Kang Chen, Zhang Shuofeng, Li Yingfei
School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 100102, China.
Center for DMPK Research of Herbal Medicines, Institute of Chinese Materia Medica, China Academy of Chinese, Beijing 100700, China.
Int J Anal Chem. 2020 Mar 3;2020:4508374. doi: 10.1155/2020/4508374. eCollection 2020.
Radix Polygoni Multiflori (RPM) has been widely used to treat various diseases in Asian countries for many centuries. Although, stilbenes and anthraquinones, two major components of RPM, show various bioactive effects, it has been speculated that the idiosyncratic hepatotoxicity induced by RPM may be related to these constituents. However, information on the pharmacokinetics of stilbenes and anthraquinones at a subtoxic dose of RPM is limited. A simple and sensitive UPLC-MS/MS bioanalytical method for the simultaneous determination of 13 ingredients of RPM, including chrysophanol, emodin, aloe-emodin, rhein, physcion, questin, citreorosein, questinol, 2,3,5,4'-tetrahydroxystilbene-2-O--D-glucoside, torachrysone-8-O-glucoside, chrysophanol-8-O--D-glucoside, emodin-8-O--D-glucoside, and physcion-8-O--D-glucoside, in rat plasma was established. Acetonitrile was employed to precipitate the plasma with appropriate sensitivity and acceptable matrix effects. Chromatographic separation was performed using a waters HSS C18 column with a gradient elution using water and acetonitrile both containing 0.025% formic acid within a run time of 9 min. The constituents were detected in negative ionization mode using multiple reaction monitoring. The method was fully validated in terms of selectivity, linearity, accuracy, precision, recovery, matrix effects, and stability. The lower limit of quantitation of the analytes was 0.1-1 ng/mL. The intrabatch and interbatch accuracies were 87.1-109%, and the precision was within the acceptable limits. The method was applied to a pharmacokinetic study after oral administration of RPM extract to rats at a subtoxic dose of 36 g/kg.
何首乌在亚洲国家已被广泛用于治疗各种疾病达数百年之久。尽管何首乌的两种主要成分芪类和蒽醌类具有多种生物活性作用,但据推测,何首乌引起的特异质性肝毒性可能与这些成分有关。然而,关于芪类和蒽醌类在亚毒性剂量何首乌下的药代动力学信息有限。建立了一种简单灵敏的超高效液相色谱-串联质谱(UPLC-MS/MS)生物分析方法,用于同时测定大鼠血浆中何首乌的13种成分,包括大黄酚、大黄素、芦荟大黄素、大黄酸、大黄素甲醚、虎杖苷、橙黄决明素、决明蒽醌、2,3,5,4'-四羟基二苯乙烯-2-O-β-D-葡萄糖苷、大黄素-8-O-β-D-葡萄糖苷、大黄酚-8-O-β-D-葡萄糖苷、大黄素甲醚-8-O-β-D-葡萄糖苷。采用乙腈沉淀血浆,具有适当的灵敏度和可接受的基质效应。使用waters HSS C18柱进行色谱分离,采用梯度洗脱,流动相为含0.025%甲酸的水和乙腈,运行时间为9分钟。采用多反应监测在负离子模式下检测各成分。该方法在选择性、线性、准确性、精密度、回收率、基质效应和稳定性方面均得到充分验证。分析物的定量下限为0.1-1 ng/mL。批内和批间准确度为87.1-109%,精密度在可接受范围内。该方法应用于以36 g/kg亚毒性剂量给大鼠口服何首乌提取物后的药代动力学研究。