HPLC methods of fexofenadine quantitative analysis in rabbits’ liver

P. Mylnikov, I. V. Chernykh, A. Shchulkin, N. M. Popova, E. Yakusheva
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引用次数: 1

Abstract

The investigation of pharmacokinetics of marker substrates of carrier protein P-glycoprotein (Pgp, ABCB1-protein) including fexofenadine, is one of the methods of its functional activity evaluation.The aim of the study was to work out the HPLC methods of the quantitative determination of fexofenadine in rabbits’ liver.Materials and methods. The quantitative determination of fexofenadine was performed using Stayer chromatographic system (Akvilon, Russia) with UVV 104 ultraviolet detector. Reverse-phased chromatographic column Luna C18 100Å (250*4.6) was used with 5 µm granulation at 45°С. The сoncentration of fexofenadine was determined by methods of absolute peak area calibration.Results. The work was conducted in the isocratic mode. The composition of the mobile phase consisted of deionized water, acetonitrile and glacial acetic acid at the ratio of 267.4:120:4.33 brought to pH=6.7 with triethylamine. The sample processing was in the form of homogenization of 500 mg of ground liver in 500 µl of purified water with the subsequent centrifugation (1750 g) and selection of the supernatant. The proteins were precipitated by acetonitrile (2.5 ml) acidified with 375 µl of hydrochloric acid by shaking at 500 rev/min. The supernatant was transported into a separate test tube, where methylene chloride, diethyl ether and ethyl acetate were added (2 ml each). Then the solution was again shaken for 10 minutes (500 rev/min). After that, the solution was centrifuged (1750 g) and the supernatant was evaporated on a rotor-vacuum evaporator at 50°С. 300 µl of the mobile phase was added to the dry residue, and 100 µl was injected into the chromatograph. The method was validated in the linear range from 3 to 60 µg/g of fexofenadine with the acceptable intra- and intercycle accuracy, precision and stability. The method was tested on rabbits after the intravenous administration of fexofenadine at the dose of 11 mg/kg.Conclusion. The HPLC methods of fexofenadine quantitative determination in the hepatic tissue of rabbits has been worked out. It can be used for the evaluation of the functional activity of Pgp in preclinical studies.Abbreviations: Pgp – P-glycoprotein, HPLC – high performance liquid chromatography, rev/min – revolutions per minute
非索非那定在家兔肝脏中定量分析的高效液相色谱方法
非索非那定等载体蛋白p -糖蛋白(Pgp、abcb1蛋白)标记底物的药代动力学研究是评价其功能活性的方法之一。建立了兔肝脏中非索非那定的高效液相色谱定量测定方法。材料和方法。采用Stayer色谱系统(Akvilon, Russia), uvv104紫外检测器对非索非那定进行定量测定。反相色谱柱Luna C18 100Å(250*4.6), 45°С, 5µm造粒。采用绝对峰面积校准法测定非索非那定的浓度。这项工作是在等距模式下进行的。流动相由去离子水、乙腈和冰醋酸组成,以267.4:120:4.33的比例加入三乙胺,溶液pH=6.7。样品处理为500mg磨碎的肝脏在500µl纯净水中均质,随后离心(1750 g)并选择上清。用用375µl盐酸酸化的乙腈(2.5 ml)以500转/分钟振荡沉淀蛋白质。将上清输送到单独的试管中,在试管中加入二氯甲烷、乙醚和乙酸乙酯(各2ml)。然后再次搅拌10分钟(500转/分钟)。之后,将溶液离心(1750 g),上清液在50°С的转子真空蒸发器上蒸发。在干燥残渣中加入300µl流动相,并将100µl注入色谱仪。在非索非那定浓度为3 ~ 60µg/g的线性范围内验证了该方法的准确度、精密度和稳定性。以非索非那定11 mg/kg剂量静脉给药后,在家兔身上进行了实验。建立了兔肝组织中非索非那定的高效液相色谱定量测定方法。可用于临床前研究中Pgp功能活性的评价。缩写:Pgp - p -糖蛋白,HPLC -高效液相色谱,rev/min -每分钟转数
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