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电膜萃取结合毛细管电泳法测定生物样品中的氨氯地平对映体。

Electro membrane extraction combined with capillary electrophoresis for the determination of amlodipine enantiomers in biological samples.

机构信息

Department of Chemistry, Faculty of Sciences, Shahid Beheshti University, Evin, Tehran, Iran.

出版信息

J Sep Sci. 2010 Oct;33(20):3231-8. doi: 10.1002/jssc.201000242.

Abstract

Electro membrane extraction as a new microextraction method was applied for the extraction of amlodipine (AM) enantiomers from biological samples. During the extraction time of 15  min, AM enantiomers migrated from a 3  mL sample solution, through a supported liquid membrane into a 20  μL acceptor solution presented inside the lumen of the hollow fiber. The driving force of the extraction was 200  V potential, with the negative electrode in the acceptor solution and the positive electrode in the sample solution. 2-Nitro phenyl octylether was used as the supported liquid membrane. Using 10  mM HCl as background electrolyte in the sample and acceptor solution, enrichment up to 124 times was achieved. Then, the extract was analyzed using CD modified CE method for separation of AM enantiomers. Best results were achieved using a phosphate running buffer (100  mM, pH 2.0) containing 5  mM hydroxypropyl-α-CD. The range of quantitation for both enantiomers was 10-500  ng/mL. Intra- and interday RSD (n=6) were less than 14%. The limits of quantitation and detection for both enantiomers were 10 and 3  ng/mL respectively. Finally, this procedure was applied to determine the concentration of AM enantiomers in plasma and urine samples.

摘要

电膜萃取作为一种新的微萃取方法,被应用于从生物样品中萃取氨氯地平(AM)对映异构体。在 15 分钟的萃取时间内,AM 对映异构体从 3 mL 样品溶液中通过支撑液膜迁移到空心纤维内腔内的 20 μL 接受溶液中。萃取的驱动力是 200 V 的电势,负电极在接受溶液中,正电极在样品溶液中。2-硝基苯辛醚被用作支撑液膜。在样品和接受溶液中使用 10 mM HCl 作为背景电解质,可以实现高达 124 倍的富集。然后,使用 CD 修饰的 CE 方法分析提取物,以分离 AM 对映异构体。使用含有 5 mM 羟丙基-α-CD 的磷酸盐运行缓冲液(100 mM,pH 2.0)可以获得最佳结果。两种对映异构体的定量范围均为 10-500 ng/mL。日内和日间 RSD(n=6)均小于 14%。两种对映异构体的定量下限和检测下限分别为 10 和 3 ng/mL。最后,该方法应用于测定血浆和尿液样品中 AM 对映异构体的浓度。

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