首页> 外文会议>CARBON'09;Annual world conference on carbon;World conference on carbon >Cork-based activated carbons as enrichment materials for analysis of ibuprofen and clofibric acid at trace levels in environmental matrices
【24h】

Cork-based activated carbons as enrichment materials for analysis of ibuprofen and clofibric acid at trace levels in environmental matrices

机译:基于软木的活性炭作为富集材料,用于在环境基质中痕量分析布洛芬和氯纤维酸

获取原文

摘要

In this contribution, a novel sample preparation technique for trace enrichment prior to chromatographic analysis, using cork-based activated carbons in powder form, was applied to monitor two pharmaceutical compounds. Extractions with two cork-based activated carbons followed by liquid desorption and high performance liquid chromatography with diode array detection (LD/HPLC-DAD) analysis were developed for assessment of ibuprofen and clofibric acid in real water samples and also a biologic fluid (urine). Activated carbons used present apparent surface areas around 1000 m~2 g~(-1). Sample C1 is a microporous carbon and C2 is a microporous carbon with an important development of the mesoporous structure. Both samples have basic nature: C1 has a pH_(PZC) near the neutral pH and C2 has a pH_(PZC) of 9.9. Assays performed on 30 mL water samples spiked at the 25.0 μg L~(-1) levels under optimized experimental conditions yielded recoveries between 80 and 96 %. The analytical performance showed good precision (relative standard deviation < 15 %), detection limits between 0.21 and 0.28 μg L~(-1) and linear ranges (1.0-600.0 μg L~(-1)) with r~2 > 0.99. By using the standard addition method, the application of the present method to water matrices such as surface water, wastewater, tap water, estuary water and underground water, allowed very good performances at the trace level. The present method was also applied with success to a biologic matrix, i.e. urine. The proposed methodology proved to be a suitable alternative for the analysis of polar compounds, showing to be easy to implement, reliable, sensitive and requiring a low sample volume to monitor these pharmaceutical compounds in environmental and biological matrices.
机译:在这一贡献中,采用了粉末形式的基于软木塞的活性炭,在色谱分析之前用于痕量富集的新型样品制备技术被用于监测两种药物化合物。开发了两种基于软木塞的活性炭萃取,然后进行液相脱附和具有二极管阵列检测(LD / HPLC-DAD)分析的高效液相色谱仪,用于评估实际水样样品中的布洛芬和氯纤维酸以及一种生物液体(尿液) 。所用活性炭的表观表面积约为1000 m〜2 g〜(-1)。样品C1是微孔碳,C2是中孔结构有重要发展的微孔碳。两种样品都具有基本性质:C1的pH_(PZC)接近中性pH,C2的pH_(PZC)为9.9。在优化的实验条件下,对加标浓度为25.0μgL〜(-1)的30 mL水样品进行的测定,回收率在80%至96%之间。分析性能显示出良好的精密度(相对标准偏差<15%),检测限在0.21至0.28μgL〜(-1)和线性范围(1.0-600.0μgL〜(-1)),r〜2> 0.99。通过使用标准添加方法,本方法在水基质如地表水,废水,自来水,河口水和地下水中的应用在痕量水平上具有非常好的性能。本方法也成功地应用于生物基质,即尿液。所提出的方法被证明是分析极性化合物的合适替代方法,显示出易于实施,可靠,灵敏并且需要少量样品量来监测环境和生物基质中的这些药物化合物。

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