| Literature DB >> 28830061 |
Wei Li1, Hongjie Zhou2, Yang Chu3, Xiangyang Wang3, Ruizhi Luo3, Liu Yang3, Navaneethakrishnan Polachi3, Xiao Li3, Min Chen4, Luqi Huang5, Xueying Yan6, Zhixin Guo3, He Sun7.
Abstract
Compound Danshen Dripping Pills (CDDP), a herbal patent medicine, is widely used in China for the prevention and treatment of cardiovascular diseases. A simple, sensitive and reliable method for simultaneous determination of danshensu (DSS), protocatechuic aldehyde (PCA), and their related metabolites, 4-hydroxy-3-methyloxyphenyl lactic acid (HMLA) and protocatechuic acid (PAA) in human plasma was developed and validated based on liquid chromatography tandem mass spectrometry (LC-MS/MS). The analytes and internal standard (IS), vanillic acid (VAA), were extracted from plasma with ethyl acetate and separated on a C18 column by using the mobile phase consisted of methanol-0.1% formic acid via gradient elution. The electrospray ionization (ESI) source was applied and operated under the multiple reaction monitoring (MRM) mode. The linear calibration curves were obtained at the concentration ranges of 0.46-1000ng/mL for DSS and PAA, and 1.38-1000ng/mL for PCA and HMLA, respectively. The inter- and intra-day precisions (RSD%) were less than 13.5%, and the accuracy (±RE%) was within 13.4%. The described method was successfully applied for the clinical pharmacokinetics of CDDP in Chinese healthy volunteers.Entities:
Keywords: Clinical pharmacokinetics; Compound Danshen Dripping Pills; LC–MS/MS; Salvia miltiorrhizae
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Year: 2017 PMID: 28830061 DOI: 10.1016/j.jpba.2017.06.014
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935