首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Stereoselective HPLC assay of donepezil enantiomers with UV detection and its application to pharmacokinetics in rats
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Stereoselective HPLC assay of donepezil enantiomers with UV detection and its application to pharmacokinetics in rats

机译:紫外检测多奈哌齐对映体的立体选择性HPLC分析及其在大鼠药代动力学中的应用

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This investigation describes a new precise, sensitive and accurate stereoselective HPLC method for the simultaneous determination of donepezil enantiomers in tablets and plasma with enough sensitivity to follow its pharmacokinetics in rats up to 12 h after single oral dosing. Enantiomeric resolution was achieved on a cellulose tris (3,5-dimethylphenyl carbamate) column known as Chiralcel OD, with UV detection at 268 nm, and the mobile phase consisted of n-hexane, isopropanol and triethylamine (87:12.9:0.1). Using the chromatographic conditions described, donepezil enantiomers were well resolved with mean retention times of 12.8 and 16.3 min, respectively. Linear response (r > 0.994) was observed over the range of 0.05-2 mu g/ml of donepezil enantiomers, with detection limit of 20 ng/ml. The mean relative standard deviation (R.S.D.%) of the results of within-day precision and accuracy of the drug were <= 10%. There was no significant difference (p > 0.05) between inter- and intra-day studies for each enantiomers which confirmed the reproducibility of the assay method. The mean extraction efficiency was 92.6-93.2% of the enantiomers. The proposed method was found to be suitable and accurate for the quantitative determination of donepezil enantiomers in tablets. The assay method also shows good specificity to donepezil enantiomers, and it could be successfully applied to its pharmacokinetic studies and to therapeutic drug monitoring. (c) 2005 Elsevier B.V. All rights reserved.
机译:这项研究描述了一种新的精确,灵敏和准确的立体选择性HPLC方法,该方法可同时测定片剂和血浆中的多奈哌齐对映异构体,其灵敏度足以跟踪其在大鼠一次口服给药后长达12 h在大鼠体内的药代动力学。在称为Chiralcel OD的纤维素三(3,5-二甲基苯基氨基甲酸酯)色谱柱上实现对映体拆分,并在268 nm处进行紫外检测,流动相由正己烷,异丙醇和三乙胺(87:12.9:0.1)组成。使用所描述的色谱条件,多奈哌齐对映体的分离度很好,平均保留时间分别为12.8和16.3分钟。在多奈哌齐对映体的0.05-2μg / ml范围内观察到线性响应(r> 0.994),检出限为20 ng / ml。药物日内准确度和准确度结果的平均相对标准偏差(R.S.D.%)≤10%。在日间研究和日内研究之间,每种对映异构体之间均无显着差异(p> 0.05),这证实了该测定方法的可重复性。平均萃取效率为对映异构体的92.6-93.2%。发现该方法适用于定量测定片剂中多奈哌齐对映异构体的准确度。该测定方法对多奈哌齐对映体也显示出良好的特异性,可以成功地用于其药代动力学研究和治疗药物监测。 (c)2005 Elsevier B.V.保留所有权利。

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