Determination of acyclovir in human serum by high-performance liquid chromatography using liquid-liquid extraction and its application in pharmacokinetic studies.


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نویسندگان: غلامرضا بهرامی , امیر کیانی , شهلا میرزایی

کلمات کلیدی: Reverse phase chromatography; HPLC; Acyclovir; Serum; Bioequivalence study

نشریه: Journal of Chromatography B , 1 , 816 ,

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کد مقاله 10554
عنوان فارسی مقاله
عنوان لاتین مقاله Determination of acyclovir in human serum by high-performance liquid chromatography using liquid-liquid extraction and its application in pharmacokinetic studies.
نوع مقاله مقاله اصیل (پژوهشی، Original)
بالاترین نمایه نامه بین‌المللی ISI
سطح مقاله هیچکدام
IF 2.603
عنوان نشریه Journal of Chromatography B
نوع نشریه خارجی ایندکس شده
شماره نشریه 1
دوره 816
تاریخ انتشار شمسی 1385/11/18
تاریخ انتشار میلادی
آدرس لینک مقاله/ همایش در شبکه اینترنت http://www.sciencedirect.com/science/article/pii/S1570023204009572
DOI
آدرس علمی (Affiliation) نویسنده متقاضی Medical Biology Research Center, Medical School, Kermanshah University of Medical Sciences, Kermanshah, Iran

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A fast, simple and sensitive high performance liquid chromatographic (HPLC) method has been described for determination of acyclovir in human serum. Since acyclovir is a polar compound and soluble in aqueous medium and practically insoluble in most of organic solvents, its analysis in biological fluids in currently published HPLC methods, involve pre-treatment of acyclovir plasma sample including deproteinization or solid phase extraction. In present method liquid–liquid extraction of acyclovir and internal standard (vanillin) is achieved using dichloromethane-isopropyl alcohol (1:1, v/v) as an extracting solvent. Analysis was carried out on ODS column using methanol-phosphate buffer (0.05 M) containing sodium dodecyl sulfate (200 mg/L) and triethylamine (2 mL/L, v/v) as mobile phase (pH = 2.3; 5:95, v/v) at flow rate of 2 ml/min. The method was shown to be selective and linear into the concentration range of 10–2560 ng/mL. Accuracy and precision of the method were also studied. The limit of quantitation was evaluated to be 10 ng/mL. This method was applied in bioequivalence study of two different acyclovir preparations after administration of 400 mg in 12 healthy volunteers. © 2004 Elsevier B.V. All rights reserved.

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نویسنده نفر چندم مقاله نویسنده مسئول
غلامرضا بهرامیاولبلي
امیر کیانیسومخير
شهلا میرزاییدومخير

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Determination of acyclovir in human serum by high-performance.pdf1396/04/24102297دانلود