盐炙对杜仲中京尼平苷酸体内药代动力学的影响

Evaluation of Salt Processing on Pharmacokinetics of Geniposidic Acid in Eucommia ulmoides Oliver

  • 摘要: 目的 建立测定大鼠血浆中京尼平苷酸的UHPLC-MS/MS方法,研究盐炙对杜仲中京尼平苷酸药代动力学的影响。方法 色谱柱:BEH-C18(100 mm×2.1 mm,1.7 μm);流动相:0.1%甲酸水-乙腈梯度洗脱;流速:0.3 mL/min。结果 所建立的UHPLC-MS/MS测定大鼠血浆中京尼平苷酸的方法灵敏度、选择性、稳定性较好,回收率和基质效应皆满足体内样品的测试要求。京尼平苷酸在生品和盐炙品组大鼠体内的药动学参数分别为:AUC(0-t)(1 547.18±272.28)、(2 120.694±664.532)ng·h/mL;AUC(0-∞)(1 564.42±273.97)、(2 145.61±659.983)ng·h/mL;Cmax(517.59±51.24)、(733.292±261.34)ng/mL;MRT(2.68±0.11)、(2.551±0.08)h;T1/2(1.37±0.08)、(1.43±0.17)h;Tmax(1.52±0.1)、(1.51±0.1)h。结论 杜仲盐炙后有助于促进京尼平苷酸的吸收,一定程度上增加了其生物利用度。

     

    Abstract: OBJECTIVE To establish UHPLC-MS/MS method to determine geniposidic acid in rat plasma and to investigate the effect of salt processing on pharmacokinetics of geniposidic acid in Eucommia ulmoides Oliver. METHODS Chromatographic column: BEH-C18(100 mm×2.1 mm, 1.7 μm); the mobile phase: acetonitrile-0.1% formic acid aqueous solution. The gradient elution program was performed at a flow rate of 0.3 mL/min. RESULTS The main pharmacokinetic parameters of geniposidic acid in raw and salt products were that:AUC(0-t) were (1 47.18±272.28), (2 120.694±664.532)ng·h/mL;AUC(0-∞) were (1 564.42±273.97), (2 145.61±659.983)ng·h/mL;Cmax were (517.59±51.24), (733.292±261.34)ng/mL;MRT were (2.68±0.11), (2.551±0.08)h;T1/2 were (1.37±0.08), (1.43±0.17) h;T max were (1.52±0.1), (1.51±0.1)h. CONCLUSION Salt processing can obviously enhance the absorption of geniposidic acid in Eucommia ulmoides Oliver, and increase the bioavailability.

     

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