High performance liquid chromatographic determination of azithromycin in serum using fluorescence detection and its application in human pharmacokinetic studies


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نویسندگان: غلامرضا بهرامی , امیر کیانی , بهاره محمدی , شهلا میرزایی

کلمات کلیدی: Reverse phase chromatography; HPLC; Azithromycin; Serum; Bioequivalence study; Macrolide antibiotics

نشریه: JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES , 2 , 823 ,

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کد مقاله 10519
عنوان فارسی مقاله
عنوان لاتین مقاله High performance liquid chromatographic determination of azithromycin in serum using fluorescence detection and its application in human pharmacokinetic studies
نوع مقاله گزارش کوتاه (Policy Brife,Short Communication, Short Report, Brief report)
بالاترین نمایه نامه بین‌المللی ISI
سطح مقاله هیچکدام
IF 2.603
عنوان نشریه JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
نوع نشریه خارجی ایندکس شده
شماره نشریه 2
دوره 823
تاریخ انتشار شمسی 1384/06/15
تاریخ انتشار میلادی
آدرس لینک مقاله/ همایش در شبکه اینترنت http://www.sciencedirect.com/science/article/pii/S1570023205002047
DOI
آدرس علمی (Affiliation) نویسنده متقاضی School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran

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Afast and sensitive high-performance liquid chromatographic method for determination of azithromycin in human serum using fluorescence detection was developed. The drug and an internal standard (clarithromycin) were extracted from serum using n-hexan and subjected to precolumn derivatization with 9-fluorenylmethyl chloroformate as labeling agent. Analysis was performed on a phenyl packing material column with sodium phosphate buffer containing 2 ml/l triethylamine (pH 5.9) and methanol (29:71, v/v) as the mobile phase. The standard curve was linear over the range of 10–500 ng/ml of azithromycin in human serum. The means between-days precision were from 13.3% (for 10 ng/ml) to 2% (500 ng/ml) and the within-day precision from 11.9 to 1.7% determined on spiked samples. The accuracy of the method was 100.7–107.2% (between days) and 100.3–107.8% (within day). The limit of quantification was 10 ng/ml. This method was applied in a bioequivalence study of four different azithromycin preparations in 12 healthy volunteers.

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

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