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采用高效液相色谱-二极管阵列检测法同时测定人血浆中雷尼替丁和甲硝唑的含量。

Simultaneous determination of ranitidine and metronidazole in human plasma using high performance liquid chromatography with diode array detection.

作者信息

do Nascimento Ticiano Gomes, Oliveira Eduardo de Jesus, Macêdo Rui Oliveira

机构信息

Unidade de Desenvolvimento e Ensaios de Medicamentos (UDEM/ LTF), Universidade Federal da Paraíba-UFPB, Campus I, Cidade Universitária, 58051-970 João Pessoa, Paraíba, Brazil.

出版信息

J Pharm Biomed Anal. 2005 Apr 1;37(4):777-83. doi: 10.1016/j.jpba.2004.11.042. Epub 2004 Dec 28.

Abstract

The development and validation of a simple method for the simultaneous determination of ranitidine and metronidazole in human plasma is described. Plasma samples (250 microL) were deproteinized by precipitation with 60% perchloric acid, centrifuged and the supernatant directly injected into the HPLC. Separation was achieved in isocratic mode with a Shimpak C(18) column and a mobile phase consisting of 10mM potassium dihydrogen phosphate pH 3.5:acetonitrile (90:10, v/v) with UV detection at 315 nm. The method showed good selectivity and sensitivity. Good and consistent recovery for metronidazole and ranitidine was obtained: 96.22+/-3.52 and 95.00+/-4.50% for ranitidine (25-1000 ng/mL) and metronidazole (60-10,000 ng/mL), respectively (n=3). With this one-step sample preparation method, both ranitidine and metronidazole could be quantified simultaneously in human plasma with good precision (R.S.D.<15%) and accuracy (bias values below 15%). The limit of quantification for ranitidine and metronidazole were 20 and 40 ng/mL plasma, respectively.

摘要

本文描述了一种同时测定人血浆中雷尼替丁和甲硝唑的简单方法的开发与验证。取250微升血浆样品,用60%高氯酸沉淀法进行脱蛋白处理,离心后将上清液直接注入高效液相色谱仪。采用岛津C(18)柱,以等度洗脱模式进行分离,流动相为10mM磷酸二氢钾(pH 3.5):乙腈(90:10,v/v),于315nm处进行紫外检测。该方法具有良好的选择性和灵敏度。雷尼替丁和甲硝唑的回收率良好且一致:雷尼替丁(25 - 1000 ng/mL)回收率为96.22±3.52%,甲硝唑(60 - 10,000 ng/mL)回收率为95.00±4.50%(n = 3)。采用这种一步样品制备方法,雷尼替丁和甲硝唑均可在人血浆中同时进行定量分析,精密度良好(相对标准偏差<15%),准确度高(偏差值低于15%)。雷尼替丁和甲硝唑的定量限分别为血浆中20和40 ng/mL。

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