首页> 外文期刊>Analytical and Bioanalytical Chemistry >Analytical development for analysis of pharmaceuticals in water samples by SPE and GC–MS
【24h】

Analytical development for analysis of pharmaceuticals in water samples by SPE and GC–MS

机译:通过SPE和GC-MS分析水样品中的药物的分析开发

获取原文
获取原文并翻译 | 示例
           

摘要

An analytical procedure involving solid-phase extraction (SPE) and gas chromatography–mass spectrometry (GC–MS) has been developed for determination of pharmaceutical compounds (aspirin, caffeine, carbamazepine, diclofenac, ketoprofen, naproxen, ibuprofen, clofibrate, clofibric acid, and gemfibrozil) in a variety of aqueous samples (wastewater and surface water). After filtration, samples were extracted and concentrated using C18 or HLB cartridges, depending on the type of compound. Sample storage conditions were checked and optimized to ensure preservation of the pharmaceutical substance, taking into consideration environmental sampling conditions. For most of the pharmaceuticals monitored, recovery was in the range 53 to 99% and the variability was below 15% for the complete procedure, with limits of detection ranging from 0.4 to 2.5 ng L?1, depending on the compound. The methods were successfully applied to monitoring of pharmaceutical contamination of the Seine estuary. Concentrations varied from several dozens of nanograms per liter for surface waters to several hundreds of nanograms per liter for wastewaters.
机译:已开发出一种涉及固相萃取(SPE)和气相色谱-质谱(GC-MS)的分析程序,用于测定药物化合物(阿司匹林,咖啡因,卡马西平,双氯芬酸,酮洛芬,萘普生,布洛芬,氯贝贝特,氯贝酸,和吉非贝齐(gemfibrozil))中的各种水样(废水和地表水)中。过滤后,根据化合物的类型,使用C18 或HLB柱提取样品并进行浓缩。考虑到环境采样条件,检查并优化了样品存储条件以确保药物的保存。对于大多数被监测的药物,整个过程的回收率在53%到99%之间,变异性在15%以下,检测限在0.4到2.5 ng L?1 之间,具体取决于化合物。该方法已成功应用于监测塞纳河河口的药物污染。浓度从地表水的每升几十纳克到废水的每升数百纳克不等。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号