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UHPLC-MS/MS method for pharmacokinetic and bioavailability determination of five bioactive components in raw and various processed products of Polygala tenuifolia in rat plasma

机译:UHPLC-MS / MS / MS方法用于药代动力学和生物利用度,在大鼠等离子体中的GOVALA Tenuifolia中生物和各种加工产品中的五种生物活性成分

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Context Sibiricose A5 (A5), sibiricose A6 (A6), 3,6′-disinapoyl sucrose (DSS), tenuifoliside A (TFSA) and 3,4,5-trimethoxycinnamic acid (TMCA) are the main active components of Polygala tenuifolia Willd. (Polygalaceae) (PT) that are active against Alzheimer's disease. Objective To compare the pharmacokinetics and bioavailability of five active components in the roots of raw PT (RPT), liquorice-boiled PT (LPT) and honey-stir-baked PT (HPT). Materials and methods The median lethal dose (LD50) was evaluated through acute toxicity test. The pharmacokinetics of five components after oral administration of extracts of RPT, LPT, HPT (all equivalent to 1.9?g/kg of RPT extract for one dose) and 0.5% CMC-Na solution (control group) were investigated, respectively, in Sprague-Dawley rats (four groups, n?=?6) using UHPLC-MS/MS. In addition, the absolute bioavailability of A5, A6, DSS, TFSA and TMCA after oral administration (7.40, 11.60, 16.00, 50.00 and 3.11?mg/kg, respectively) and intravenous injection (1/10 of the corresponding oral dose) in rats (n?=?6) was studied. Results The LD50 of RPT, LPT and HPT was 7.79, 14.55 and 15.99?g/kg, respectively. AUC 0- t of RPT, LPT and HPT were as follows: A5 (433.18?±?65.48, 680.40?±?89.21, 552.02?±?31.10?ng h/mL), A6 (314.55?±?62.73, 545.76?±?123.16, 570.06?±?178.93?ng h/mL) and DSS (100.30?±?62.44, 232.00?±?66.08, 197.58?±?57.37?ng h/mL). The absolute bioavailability of A5, A6, DSS, TFSA and TMCA was 3.25, 2.95, 2.36, 1.17 and 42.91%, respectively. Discussion and conclusions The pharmacokinetic and bioavailability parameters of each compound can facilitate future clinical studies.
机译:上下文Sibiricose A5(A5),Sibiricose A6(A6),3,6'-脱脂蔗糖蔗糖(DSS),Tenuifoliside A(TFSA)和3,4,5-三甲氧基氨基酸(TMCA)是Polygala Tenuifolia Willd的主要活性组分。 (polygalaceae)(pt)对阿尔茨海默病有效。目的将五种活性成分的药代动力学和生物有效性与原料PT(RPT),甘草沸腾的Pt(LPT)和蜂蜜搅拌烘焙PT(HPT)进行比较。材料和方法通过急性毒性试验评价中值致命剂量(LD50)。在Sprague中分别研究了RPT,LPT,HPT提取物(一种量相当于1.9×g / kg的RPT提取物)和0.5%CMC-Na溶液(对照组)后的五种组分后的药代动力学分别在SPRAGUE中进行了调查 - 使用UHPLC-MS / MS(四组,N?= 3)此外,A5,A6,DSS,TFSA和TMCA的绝对生物利用度口服给药后(7.40,11.60,16.00,50.00和3.11?Mg / kg)和静脉注射(相应口服剂量的1/10)研究了大鼠(N?=?6)。结果RPT,LPT和HPT的LD50分别为7.79,14.55和15.99?g / kg。 AUC 0-T的RPT,LPT和HPT如下:A5(433.18?±65.48,680.40?±89.21,552.02?±31.10?ng h / ml),a6(314.55?±62.73,545.76? ±123.16,570.06?±178.93?ng h / ml)和dss(100.30?±62.44,232.00?±66.08,197.58?±57.37?ng h / ml)。 A5,A6,DSS,TFSA和TMCA的绝对生物利用度分别为3.25,2.95,2.36,1.17和42.91%。讨论和结论每个化合物的药代动力学和生物利用度参数可以促进未来的临床研究。

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