王红艳, 孔爱英, 杨波, 闫亮平, 邸欣. 手性HPLC方法测定布洛芬对映体及其在比格犬体内的药代动力学J. 药学学报, 2015,50(12): 1607-1612.
引用本文: 王红艳, 孔爱英, 杨波, 闫亮平, 邸欣. 手性HPLC方法测定布洛芬对映体及其在比格犬体内的药代动力学J. 药学学报, 2015,50(12): 1607-1612.
WANG Hong-yan, KONG Ai-ying, YANG Bo, YAN Liang-ping, DI Xin. Plasma ibuprofen enantiomers and their pharmacokinetics in Beagle dogs determined by HPLCJ. Acta Pharmaceutica Sinica, 2015,50(12): 1607-1612.
Citation: WANG Hong-yan, KONG Ai-ying, YANG Bo, YAN Liang-ping, DI Xin. Plasma ibuprofen enantiomers and their pharmacokinetics in Beagle dogs determined by HPLCJ. Acta Pharmaceutica Sinica, 2015,50(12): 1607-1612.

手性HPLC方法测定布洛芬对映体及其在比格犬体内的药代动力学

Plasma ibuprofen enantiomers and their pharmacokinetics in Beagle dogs determined by HPLC

  • 摘要: 建立高效液相色谱法测定比格犬血浆中布洛芬对映体浓度,采用该方法比较比格犬分别静脉输注消旋布洛芬、S-布洛芬和R-布洛芬后的药代动力学参数。以酮洛芬为内标,血浆样品前处理以甲醇沉淀蛋白,流动相为乙腈-20 mmol·L-1磷酸盐缓冲液(pH 3.0,含5%甲醇)(60:40),采用手性色谱柱Kromasil 100-5CHI-TBB(250 mm×4.6 mm, 5μm)分离,检测波长220 nm。S-布洛芬和R-布洛芬的标准曲线线性范围均为0.5~50μg·mL-1,定量下限均为0.5μg·mL-1,日内和日间精密度(RSD)均小于7%,方法回收率为93.1%~100.4%。本方法简便、快速、灵敏,可同时定量测定血浆中S-布洛芬和R-布洛芬的浓度。应用此法测定了比格犬分别静脉输注消旋布洛芬、S-布洛芬和R-布洛芬注射液后血浆中布洛芬对映体的浓度,给药剂量均为9 mg·kg-1,依据药-时曲线计算药代动力学参数,且3组实验测得的S-布洛芬Cmax分别为(30.8±4.7)、(46.1±5.9)和(20.0±2.6) µg·mL-1S-布洛芬注射液组的Cmax和AUC值显著大于其他两组。本文探讨了R-布洛芬在比格犬体内的转化行为,通过比较比格犬分别给予消旋布洛芬、S-和R-布洛芬后的药代参数,计算得静脉输注消旋布洛芬和R-布洛芬的手性转化率分别为(70.1±36.6)%和(76.4±36.2)%,此研究为开发S-布洛芬注射液安全用药方案提供理论依据。

     

    Abstract: A chiral high-performance liquid chromatography method was developed for the simultaneous determination of ibuprofen enantiomers in dog plasma. It was used to study the pharmacokinetics in the Beagle dog after intravenous administration of racemic-ibuprofen, S-ibuprofen and R-ibuprofen. Ketoprofen was chosen as the internal standard. After a simple precipitation using methanol as the precipitating solvent, both analytes and IS were separated on a Kromasil 100-5CHI-TBB chiral column(250 mm × 4.6 mm, 5μm) with isocratic elution using acetonitrile-20 mmol·L-1 phosphate buffer(pH 3.0, containing 5% methanol)(6:4) as the mobile phase. The detection wavelength was 220 nm. Liner calibration curves for both of the ibuprofen enantiomers were over the concentration range from 0.5 to 50μg·mL-1 with a lower limit of quantification of 0.5μg·mL-1, the accuracies were all in standard ranges. The intra-and inter-assay precisions were all below 7%. The recovery rate was 93.1% to 100.4%. The experiments proved that the method was simple, rapid and sensitive. It can be used in the quantitative determination of ibuprofen enantiomers in dog plasma. The method was used to determine the concentration of ibuprofen enantiomers in Beagle dog plasma after a single intravenous administration of racemic-ibuprofen, S-ibuprofen and R-ibuprofen(9 mg·kg-1) and the pharmacokinetics parameters were calculated based on the concentration-time curves. The Cmax of S-ibuprofen in Beagle dog plasma after a single intravenous administration of racemic-ibuprofen, S-ibuprofen and R-ibuprofen were 30.8±4.7, 46.1±5.9 and 20.0±2.6µg·mL-1, respectively. In terms of the exposure of active ingredient, it revealed a significant difference between the administration of S-ibuprofen and the other two groups. The systematical R-to S-chiral inversion was discussed. Comparing the pharmacokinetic parameters at different doses, chiral inversion were 70.1% ±36.6% and 76.4% ±36.2%, respectively, after intravenous administration of racemic-and R-ibuprofen. This study provides a theoretical basis for the safety of ibuprofen formula of injection drug.

     

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