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使用在线净化柱同时测定牛乳中磺胺甲恶唑和甲氧苄啶的高效液相色谱法

High-performance liquid chromatography method for the simultaneous determination of sulfamethoxazole and trimethoprim in bovine milk using an on-line clean-up column.

作者信息

Pereira A V, Cass Q B

机构信息

Departamento de Ciências Farmacêuticas, Universidade Estadual de Ponta Grossa, 84030-900, Ponta Grossa, PR, Brazil.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Nov 5;826(1-2):139-46. doi: 10.1016/j.jchromb.2005.08.006. Epub 2005 Oct 5.

Abstract

A bidimensional HPLC method for the simultaneous determination of sulfamethoxazole (SMX) and trimethoprim (TMP) in bovine milk has been developed and validated. After centrifugation, aliquots (150 microl) of milk samples were directly injected to a column-switching HPLC system. At the first step a RAM octyl-BSA column was employed to automatically remove proteins that otherwise would interfere with milk analysis. The mobile phase 0.01 M phosphate buffer pH 6.0:acetonitrile (95:5, v/v) was used in the first 5 min for the elution of milk proteins and then 0.01 M phosphate buffer pH 6.0:acetonitrile (83:17, v/v) for transfer SMX and TMP to the analytical column. The separation of SMX and TMP from one another and from other remaining milk components was performed on an octyl column using the mobile phase 0.01 M phosphate buffer pH 5.0:acetonitrile (82:18, v/v), which were detected by UV at 265 nm. The calibration graphs were linear in the concentration ranges of 25-800 ng/ml and 50-400 ng/ml for SMX and TMP, respectively. The intra- and inter-assay coefficients of variation were less than 15% for both drugs. The validated method was applied to the analysis of milk samples of twelve (two groups of six) cows after administration (intramuscular or subcutaneous) of a single recommended therapeutic dose of the SMX-TMP combination.

摘要

已开发并验证了一种用于同时测定牛奶中磺胺甲恶唑(SMX)和甲氧苄啶(TMP)的二维高效液相色谱法。离心后,将牛奶样品的等分试样(150微升)直接注入柱切换高效液相色谱系统。第一步,使用RAM辛基-BSA柱自动去除否则会干扰牛奶分析的蛋白质。在最初5分钟内,使用流动相0.01 M pH 6.0的磷酸盐缓冲液:乙腈(95:5,v/v)洗脱牛奶蛋白,然后使用0.01 M pH 6.0的磷酸盐缓冲液:乙腈(83:17,v/v)将SMX和TMP转移至分析柱。在辛基柱上,使用流动相0.01 M pH 5.0的磷酸盐缓冲液:乙腈(82:18,v/v)将SMX和TMP彼此分离并与其他剩余的牛奶成分分离,在265 nm处通过紫外检测。SMX和TMP的校准曲线在浓度范围分别为25 - 800 ng/ml和50 - 400 ng/ml时呈线性。两种药物的批内和批间变异系数均小于15%。经验证的方法应用于对12头(两组,每组6头)奶牛单次肌肉注射或皮下注射推荐治疗剂量的SMX - TMP组合后的牛奶样品进行分析。

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