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Development of HPTLC method for determination of cefpodoxime proxetil and ambroxol hydrochloride in human plasma by liquid–liquid extraction

机译:液液萃取法测定人血浆中头孢泊肟酯和盐酸氨溴索的高效液相色谱法的建立

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Aim: To develop a simple, sensitive, rapid, and economic high performance thinlayer chromatographic method for determination of cefpodoxime proxetil (CEFPO)and ambroxol hydrochloride (AMBRO) in human plasma by liquid–liquid extractionusing paracetamol as an internal standard. Materials and Methods: The plasmasample was extracted by a mixture of methanol and acetonitrile. A concentrationrange from 500 to 3500 ng/spot for CEFPO and 1000 to 7000 ng/spot for AMBROwere used for the calibration curve, respectively. This recovery was found to be 74.40and 94.50 for CEFPO and AMBRO, respectively. The mobile phase used consistsof chloroform: methanol (9:1v/v). Densitometric analysis was carried out at awavelength of 240 nm. Results: The Rf values for CEFPO, AMBRO, and paracetamolwere found to be 0.69 ± 0.005, 0.49 ± 0.0057, and 0.31 ± 0.0054, respectively. Thestability of CEFPO and AMBRO in plasma was confirmed during three freeze–thawcycles (-20°C), on bench during 24 h and post preparative during 48 h. Conclusion:The proposed method was validated statistically and by performing a recoverystudy for determination of CEFPO and AMBRO in human plasma.
机译:目的:建立一种简单,灵敏,快速,经济的高性能薄层色谱方法,以对乙酰氨基酚为内标,通过液-液萃取法测定人血浆中的头孢泊肟肟(CEFPO)和盐酸氨溴索(AMBRO)。材料和方法:用甲醇和乙腈的混合物萃取血浆样品。 CEFPO的浓度范围为500至3500 ng /点,AMBRO的浓度范围为1000至7000 ng /点。 CEFPO和AMBRO的回收率分别为74.40和94.50。所用的流动相由氯仿:甲醇(9:1v / v)组成。在240nm的波长下进行光密度分析。结果:CEFPO,AMBRO和扑热息痛的Rf值分别为0.69±0.005、0.49±0.0057和0.31±0.0054。在三个冻融循环(-20°C)期间,在长凳上24小时内以及制备后48小时内,证实了CEFPO和AMBRO在血浆中的稳定性。结论:该方法经统计学验证,并通过回收法测定人血浆中的CEFPO和AMBRO。

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