Zhou Wei, Tam Kin Y, Meng Minxin, Shan Jinjun, Wang Shouchuan, Ju Wenzheng, Cai Baochang, Di Liuqing
College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210046, PR China; Jiangsu Engineering Research Center for Efficient Delivery System of TCM, PR China; Nanjing Engineering Research Center for Industrialization of Chinese Medicine Pellets, PR China; Jiangsu Key Laboratory of Pediatric Respiratory Disease, Institute of Pediatrics, Nanjing University of Chinese Medicine, Nanjing 210046, PR China.
Faculty of Health Sciences, University of Macau, Macau SAR, PR China.
J Chromatogr A. 2015 Jan 9;1376:84-97. doi: 10.1016/j.chroma.2014.12.018. Epub 2014 Dec 15.
The current study aims to investigate the pharmacokinetics of multi-components (caffeic acid, quinic acid, genistein, luteolin, quercetin, neochlorogenic acid, chlorogenic acid, cryptochlorogenic acid, arctigenin, genistin, luteoloside, astragalin, hyperoside, isoquercitrin, 3,5-dicaffeoylquinic acid, 3,4-dicaffeoylquinic acid, rutin, loganin, pinoresinol-β-d-glucoside, phillyrin, isoforsythoside, forsythoside A and forsythoside B) following oral administration of Flos Lonicerae Japonicae-Fructus Forsythiae herb couple in rats. A rapid and sensitive UPLC-ESI-MS/MS with sequential positive and negative ionization modes was developed to determine the 23 absorbed ingredients using one sample preparation combined with three chromatographic conditions in rat plasma. After mixing with internal standard (IS) (tinidazole and chloramphenicol), samples were pretreated by liquid-liquid extraction (LLE) with n-butyl alcohol/ethyl acetate (1:1, v/v). The separations for pinoresinol-β-d-glucoside, phillyrin, isoforsythoside, forsythoside A and forsythoside B were performed on an ACQUITY UPLC BEH C18 column (100mm×2.1mm, 1.7μm) with acetonitrile/methanol (4:1, v/v)-water as mobile phase. For analyzing quinic acid, an ACQUITY UPLC HSS T3 column (100mm×2.1mm, 1.8μm) was applied with acetonitrile/methanol (4:1, v/v)-0.01% formic acid as mobile phase after dilution up to 25-fold. The same column was applied to the other components with acetonitrile/methanol (4:1, v/v)-0.4% formic acid as mobile phase. The method validation results demonstrated that the proposed method was sensitive, specific and reliable, which was successfully applied to the pharmacokinetic study of the multi-components after oral administration of Flos Lonicerae Japonicae-Fructus Forsythiae herb couple.
本研究旨在考察大鼠口服金银花 - 连翘药对后多成分(咖啡酸、奎宁酸、染料木黄酮、木犀草素、槲皮素、新绿原酸、绿原酸、隐绿原酸、牛蒡子苷元、染料木苷、木犀草苷、黄芪苷、金丝桃苷、异槲皮苷、3,5 - 二咖啡酰奎宁酸、3,4 - 二咖啡酰奎宁酸、芦丁、马钱苷、松脂醇 - β - D - 葡萄糖苷、连翘苷、异连翘酯苷、连翘酯苷A和连翘酯苷B)的药代动力学。建立了一种快速灵敏的超高效液相色谱 - 电喷雾串联质谱法(UPLC - ESI - MS/MS),采用一种样品制备方法结合三种色谱条件,在大鼠血浆中测定23种吸收成分。样品与内标(IS)(替硝唑和氯霉素)混合后,用正丁醇/乙酸乙酯(1:1,v/v)液 - 液萃取(LLE)进行预处理。松脂醇 - β - D - 葡萄糖苷、连翘苷、异连翘酯苷、连翘酯苷A和连翘酯苷B在ACQUITY UPLC BEH C18柱(100mm×2.1mm,1.7μm)上分离,以乙腈/甲醇(4:1,v/v) - 水为流动相。分析奎宁酸时,则应用ACQUITY UPLC HSS T3柱(100mm×2.1mm,1.8μm),稀释25倍后,以乙腈/甲醇(4:1,v/v) - 0.01%甲酸为流动相。同一根柱子用于分析其他成分,流动相为乙腈/甲醇(4:1,v/v) - 0.4%甲酸。方法验证结果表明,所建立的方法灵敏、特异、可靠,成功应用于金银花 - 连翘药对口服给药后多成分的药代动力学研究。