首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of troglitazone stereoisomers in rat plasma using semi-micro HPLC with electrochemical detection.
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Determination of troglitazone stereoisomers in rat plasma using semi-micro HPLC with electrochemical detection.

机译:使用电化学检测的半微量HPLC测定大鼠血浆中曲格列酮立体异构体。

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摘要

A highly sensitive determination method for troglitazone stereoisomers was developed by high-performance liquid chromatography with electrochemical detection (HPLC-ECD). The oxidation behavior of troglitazone was investigated for the application of ECD by measuring the cyclic voltammogram. The separation was performed on a semi-micro chiral column (Chiralcel OJ-RH) using a mobile phase consisting of methanol-acetic acid (1000:1, v/v) containing 50mM LiClO(4) at a flow rate of 20mul/min. The peak areas of the stereoisomers separated from 0.1 to 50ng/ml of troglitazone had good linearity with correlation coefficients of >0.999, and had similar response. The limit of detection was 1.3fmol (signal-to-noise ratio of 3). This method was applied to the determination of troglitazone stereoisomers in rat plasma. The levels of troglitazone stereoisomers in rat plasma could be monitored until 24h after the oral administration.
机译:通过高效液相色谱-电化学检测(HPLC-ECD)建立了曲格列酮立体异构体的高灵敏度测定方法。通过测量循环伏安图,研究了曲格列酮在ECD应用中的氧化行为。使用包含50mM LiClO(4)的甲醇-乙酸(1000:1,v / v)组成的流动相,在半微手性柱(Chiralcel OJ-RH)上进行分离,流速为20mul / min 。曲格列酮从0.1至50ng / ml的立体异构体的峰面积具有良好的线性,相关系数> 0.999,并且具有相似的响应。检测限为1.3fmol(信噪比为3)。该方法用于大鼠血浆曲格列酮立体异构体的测定。可以监测大鼠血浆中曲格列酮立体异构体的水平,直到口服后24小时。

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