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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous determination of amantadine and rimantadine by HPLC in rat plasma with pre-column derivatization and fluorescence detection for pharmacokinetic studies.
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Simultaneous determination of amantadine and rimantadine by HPLC in rat plasma with pre-column derivatization and fluorescence detection for pharmacokinetic studies.

机译:高效液相色谱法同时测定大鼠血浆中金刚烷胺和金刚烷胺的含量,并进行柱前衍生化和荧光检测,用于药代动力学研究。

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摘要

We investigated simultaneous high-performance liquid chromatographic (HPLC) determination of amantadine hydrochloride (AMA) and rimantadine hydrochloride (RIM) levels in rat plasma after fluorescent derivatization with o-phthalaldehyde and 2-mercaptoethanol. Afterwards, the method was applied to determine their pharmacokinetics. The retention times of AMA and RIM derivatives were 12.6 and 22.2 min and the lower limits of detection were 0.025 and 0.016 microg/mL, respectively. The coefficients of variation for intra- and inter-day assay of AMA and RIM were less than 5.1 and 7.6%, respectively. After i.v. administration of AMA or RIM to rats, the total body clearance and distribution volume at the steady-state of RIM were higher than those of AMA. Bioavailability of AMA and RIM was 34.9 and 37.2%, respectively. When AMA and RIM were p.o. co-administered, the area under the plasma concentration--time curve of RIM was significantly lower than that after RIM alone. On the other hand, pharmacokinetic parameters of AMA did not significantly change. These results indicate that our HPLC assay is simple, rapid, sensitive and reproducible for simultaneously determining AMA and RIM concentrations in rat plasma and is applicable to their pharmacokinetic studies. Also, co-administration of AMA and RIM may result in the lack of pharmacological effects of RIM.
机译:我们研究了高效液相色谱(HPLC)同时测定邻苯二甲醛和2-巯基乙醇进行荧光衍生后大鼠血浆中金刚烷胺盐酸盐(AMA)和金刚烷胺盐酸盐(RIM)的含量。之后,将该方法应用于确定其药代动力学。 AMA和RIM衍生物的保留时间分别为12.6和22.2 min,检测下限分别为0.025和0.016 microg / mL。日间和日间AMA和RIM测定的变异系数分别小于5.1和7.6%。在i.v.之后在大鼠身上施用AMA或RIM后,RIM稳态时的总体清除率和分布体积均高于AMA。 AMA和RIM的生物利用度分别为34.9%和37.2%。当AMA和RIM成为p.o.与RIM并用时,血浆浓度-时间曲线下的面积显着低于RIM之后。另一方面,AMA的药代动力学参数没有显着变化。这些结果表明,我们的HPLC测定方法简单,快速,灵敏且可重现,可同时测定大鼠血浆中的AMA和RIM浓度,适用于它们的药代动力学研究。同样,AMA和RIM的共同给药可能会导致RIM缺乏药理作用。

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