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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Pharmacokinetics screening for multi-components absorbed in the rat plasma after oral administration of traditional Chinese medicine Flos Lonicerae Japonicae Fructus Forsythiae herb couple by sequential negative and positive ionization ultra-high-performance liquid chromatography/tandem triple quadrupole mass spectrometric detection
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Pharmacokinetics screening for multi-components absorbed in the rat plasma after oral administration of traditional Chinese medicine Flos Lonicerae Japonicae Fructus Forsythiae herb couple by sequential negative and positive ionization ultra-high-performance liquid chromatography/tandem triple quadrupole mass spectrometric detection

机译:连续负电离和正电离超高效液相色谱/串联三重四极杆质谱检测药理动力学筛选口服中药金银花药材后大鼠血浆中吸收的多种成分

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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, pinoresino1-beta-D-glucoside, phillyrin, isoforsythoside, forsythoside A and forsythoside B) following oral administration of Flos Lonicerae Japotticae-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-beta-D-glucoside, phillyrin, isoforsythoside, forsythoside A and forsythoside B were performed on an ACQUITY UPLC BEH C-18 column (100 mm x 2.1 mm, 1.7 mu m) with acetonitrile/methanol (4:1, v/v)-water as mobile phase. For analyzing quinic acid, an ACQUITY UPLC HSS T3 column (100 mm x 2.1 mm, 1.8 mu m) 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. (C) 2014 Elsevier B.V. All rights reserved.
机译:当前的研究旨在研究多组分(咖啡酸,奎尼酸,金雀异黄素,木犀草素,槲皮素,新绿原酸,绿原酸,隐绿原酸,阿替加汀,黄连木苷,黄体苷,黄芪素,高糖苷,异槲皮苷,3,5-羟色胺的药代动力学。在大鼠口服Flos Lonicerae Japotticae-Fructus Forsythiae药草夫妇后,加入了二咖啡酰奎尼酸,3,4-二咖啡酰奎尼酸,芦丁,loganin,pinoresino1-beta-D-葡萄糖苷,phillyrin,异佛菊酯,连翘苷A和连翘苷B)。开发了一种快速灵敏的UPLC-ESI-MS / MS,具有顺序的正电离和负电离模式,使用一种样品制备方法和三种血浆条件在大鼠血浆中测定23种吸收成分。与内标(IS)(替硝唑和氯霉素)混合后,通过正丁醇/乙酸乙酯(1:1,v / v)的液-液萃取(LLE)对样品进行预处理。在ACQUITY UPLC BEH C-18色谱柱(100 mm x 2.1 mm,1.7μm)上用乙腈/甲醇(4:1)分离松油醇-β-D-葡萄糖苷,phillyrin,异连翘苷,连翘苷A和连翘苷B ,v / v)-水作为流动相。为了分析奎尼酸,将ACQUITY UPLC HSS T3色谱柱(100 mm x 2.1 mm,1.8μm)应用于乙腈/甲醇(4:1,v / v)-0.01%甲酸,稀释至25倍后作为流动相。 -折。使用乙腈/甲醇(4:1,v / v)-0.4%甲酸作为流动相,将相同的色谱柱应用于其他组分。方法验证结果表明,该方法灵敏,特异,可靠,已成功应用于金银花连翘药材口服后对多组分的药代动力学研究。 (C)2014 Elsevier B.V.保留所有权利。

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