A rapid high performance liquid chromatographic determination of methyldopa in human serum with fluorescence detection and alumina extraction: Application to a bioequivalence study


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نویسندگان: غلامرضا بهرامی , امیر کیانی , شهلا میرزایی

کلمات کلیدی: Reverse phase chromatography; HPLC; Methyldopa; Bioequivalence study

نشریه: Journal of Chromatography B , 2 , 832 ,

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کد مقاله 10514
عنوان فارسی مقاله
عنوان لاتین مقاله A rapid high performance liquid chromatographic determination of methyldopa in human serum with fluorescence detection and alumina extraction: Application to a bioequivalence study
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 2
دوره 832
تاریخ انتشار شمسی 1384/12/15
تاریخ انتشار میلادی
آدرس لینک مقاله/ همایش در شبکه اینترنت http://www.sciencedirect.com/science/article/pii/S1570023206000213
DOI
آدرس علمی (Affiliation) نویسنده متقاضی School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran

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A simple and ultra rapid high performance liquid chromatographic (HPLC) method coupled with alumina extraction and fluorescence detection was described for determination of methyldopa in human serum. The drug and an internal standard were adsorbed onto alumina and eluted using acidic methanol. The eluate was directly injected onto ODS reverse phase column using a mixture of phosphate buffer (0.05 M) containing triethylamine (100l/l, v/v; pH 2.3) and methanol (92:8, v/v) at a flow rate of 2.1 ml/min as the mobile phase. The fluorescence detector excitation and emission wavelengths were set at 270 and 320 nm, respectively. No interference in the assay from any endogenous substances or other concurrently used drugs was observed and the retention times of I.S. and the drug were 1.7 and 2.4 min, respectively with total run time (injection to injection) of less than 3.5 min. The limit of quantification was evaluated to be 20 ng/ml. Validity of the method was studied and the method was precise and accurate with a linearity range from 20 ng/ml to 5000 ng/ml. This method has been used in a randomized crossover bioequivalence study of two different methyldopa preparations in 24 healthy volunteers.

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نویسنده نفر چندم مقاله نویسنده مسئول
غلامرضا بهرامیاولبلي
امیر کیانیدومخير
شهلا میرزاییسومخير

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