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首页> 外文期刊>Journal of liquid chromatography and related technologies >Development and Validation of a Method forDetermination of Tilmicosin Residues in EquinePlasma and Tissues Using HPLC
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Development and Validation of a Method forDetermination of Tilmicosin Residues in EquinePlasma and Tissues Using HPLC

机译:高效液相色谱法测定马血浆和组织中Tilmicosin残留的方法的开发和验证

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摘要

A sensitive liquid chromatographic method with UV detection has been developed for the analysis of tilmicosin concentrations in equine tissues and plasma. Tilmicosin is extracted from plasma or tissues using acetonitrile and a phosphate buffer. The extract is centrifuged, filtered, and cleaned up on a conditioned C_(18) solid phase extraction cartridge. Tilmicosin is eluted with ammonium acetate in methanol and diluted with ammonium acetate. It is analyzed by reversed phase liquid chromatography with UV detection at 287 nm. The method was shown to be suitable for detecting tilmicosin in equine plasma, muscle, liver, kidney, and lung tissues. The limit of detection of the method was 13ng/mL in plasma and 181 ng/g in lung tissue.
机译:已经开发了一种具有紫外线检测功能的灵敏液相色谱方法,用于分析马组织和血浆中的替米考星浓度。使用乙腈和磷酸盐缓冲液从血浆或组织中提取提尔米可辛。将提取物离心,过滤并在条件良好的C_(18)固相萃取柱上纯化。将Tilmicosin用甲醇中的乙酸铵洗脱,并用乙酸铵稀释。通过反相液相色谱法在287 nm处进行UV分析。结果表明该方法适用于检测马血浆,肌肉,肝,肾和肺组织中的替米考星。该方法的检测极限是血浆中13ng / mL,肺组织中181ng / g。

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