中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Determination of atenolol in human plasma by pseudo reversed phase liquid chromatography-tandem mass spectrometry

文献类型:期刊论文

作者Dong, Lili; Huang, Junxiong
刊名CHROMATOGRAPHIA
出版日期2006
卷号64期号:2015-09-10页码:583-586
关键词column liquid chromatography pseudo-RPLC MS-MS bare silica as stationary phase atenolol
英文摘要Previous HPLC determination of atenolol on reversed-phase packings has often required a mobile phase containing three components: organic modifier, buffer and ion-pairing reagent or organic amine. In addition to the complexity of the eluents employed, alkyl sulphonates and organic amines in the mobile phase can reduce the life of silica-based bonded columns. A new simple, rapid and sensitive method-pseudo reversed-phase liquid chromatography/tandem mass spectrometry has been developed for the analysis of atenolol in human plasma using bare silica as the stationary phase coupled with a simple mobile phase consisted of 5% acetonitrile and 95% formate buffer. The optimization of separation is fast and easy. The assay was validated for the concentration range 1-100 ng mL(-1) with a detection limit of 1 ng mL(-1). Moreover, the silica column was durable with the mainly aqueous eluents. No obvious loss in performance was observed for 30,000 column volumes of eluent.
WOS记录号WOS:000242425600015
源URL[http://ir.rcees.ac.cn/handle/311016/22854]  
专题生态环境研究中心_环境化学与生态毒理学国家重点实验室
推荐引用方式
GB/T 7714
Dong, Lili,Huang, Junxiong. Determination of atenolol in human plasma by pseudo reversed phase liquid chromatography-tandem mass spectrometry[J]. CHROMATOGRAPHIA,2006,64(2015-09-10):583-586.
APA Dong, Lili,&Huang, Junxiong.(2006).Determination of atenolol in human plasma by pseudo reversed phase liquid chromatography-tandem mass spectrometry.CHROMATOGRAPHIA,64(2015-09-10),583-586.
MLA Dong, Lili,et al."Determination of atenolol in human plasma by pseudo reversed phase liquid chromatography-tandem mass spectrometry".CHROMATOGRAPHIA 64.2015-09-10(2006):583-586.

入库方式: OAI收割

来源:生态环境研究中心

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