首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Bone distribution study of anti leprotic drug clofazimine in rat bone marrow cells by a sensitive reverse phase liquid chromatography method
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Bone distribution study of anti leprotic drug clofazimine in rat bone marrow cells by a sensitive reverse phase liquid chromatography method

机译:灵敏反相液相色谱法研究抗麻风病药物氯氟齐明在大鼠骨髓细胞中的骨分布

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The aim of the present study was to investigate the distribution of clofazimine (CLF) in rat bone marrow cells by a validated reverse phase high performance liquid chromatography. CLF and chlorzoxazone (I.S) were extracted by liquid-liquid extraction from plasma and rat bone marrow cells. The chromatographic separation was performed in isocratic mode by the mobile phase consisting of 10 mM ammonium formate (pH 3.0 with formic acid) and acetonitrile in a ratio of 50:50 (v/v). The method was accurate and precise in the linear range of 15.6-2000.0ng/mL with a correlation coefficient (r~2) of 0.996 and 0.995 in rat plasma and bone marrow cells, respectively. After single oral dose of 20 mg/kg, the maximum concentration of CLF in plasma and bone marrow cells were obtained at 12 h with the concentrations of 593.2 and 915.4 ng/mL, respectively. The AUC_(0-t) and mean elimination half life (t_(1/2)) of CLF in bone marrow cells were 54339.02 ng*h/mL and 52.46 h, respectively, which signified the low body clearance and high distribution of CLF in bone marrow cells. The single oral dose pharmacokinetic investigation was confirmed the CLF endure for a long period in rat due to high distribution in various tissues. The developed method was successfully applied to the estimation of the pharmacokinetic parameters of CLF in plasma and bone marrow cells after administration of single oral dose of 20 mg/kg to rats.
机译:本研究的目的是通过经过验证的反相高效液相色谱法研究氯法齐明(CLF)在大鼠骨髓细胞中的分布。通过液-液萃取从血浆和大鼠骨髓细胞中萃取CLF和氯唑沙宗(I.S)。色谱分离是通过等流动相模式进行的,该流动相由10 mM甲酸铵(pH 3.0,甲酸)和乙腈按50:50(v / v)的比例组成。该方法在15.6-2000.0ng / mL的线性范围内是准确的,在大鼠血浆和骨髓细胞中的相关系数(r〜2)分别为0.996和0.995。单次口服剂量为20 mg / kg后,在12 h血浆和骨髓细胞中的CLF最高浓度分别为593.2 ng / mL和915.4 ng / mL。骨髓细胞中CLF的AUC_(0-t)和平均消除半衰期(t_(1/2))分别为54339.02 ng * h / mL和52.46 h,这表明CLF的低清除率和高分布在骨髓细胞中。由于在各种组织中的高度分布,单次口服剂量药代动力学研究证实了CLF在大鼠中可以长期忍受。该方法成功应用于大鼠单次口服20 mg / kg血浆和骨髓细胞中CLF的药代动力学参数估计。

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