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 >Integrated on-line sample clean-up using cation exchange restricted access sorbent for the LC determination of atropine in human plasma coupled to UV detection.
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Integrated on-line sample clean-up using cation exchange restricted access sorbent for the LC determination of atropine in human plasma coupled to UV detection.

机译:使用阳离子交换限制访问吸附剂进行的在线样品综合净化,用于LC测定人血浆中的阿托品和紫外检测。

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摘要

A new, simple and fully automated liquid chromatographic (LC) method with UV detection has been developed for the direct determination of atropine in plasma. Sample clean-up was based on the use of cation exchange restricted access material (RAM) in a pre-column, coupled to LC by means of a column switching system. After direct injection of a 200mul-volume of plasma sample, the biological matrix was washed out for 10min using a washing liquid composed of 2mM lithium perchlorate adjusted to pH 3.0 and methanol (97:3; v/v). By rotation of the switching valve, atropine was then eluted in the back-flush mode for 2min and transferred to the analytical column packed with octadecyl silica by the LC mobile phase constituted of a mixture of acetonitrile and potassium phosphate buffer (pH 3.0; 50mM) containing 2mM sodium heptanesulfonate (16:84; v/v). The UV detection was performed at 220nm. The method was validated according to a new approach based on accuracy profile over a concentration range from 25ng/ml, corresponding to the limit of quantitation, to 1000ng/ml. The method was then applied for the determination of atropine in plasma after intravenous administration to hospitalised patients.
机译:已开发出一种具有紫外线检测功能的新型,简单且全自动的液相色谱(LC)方法,用于直接测定血浆中的阿托品。样品净化是基于在预柱中使用阳离子交换限制进样材料(RAM),并通过色谱柱切换系统将其与LC偶联。直接注入200 mul-vol的血浆样品后,使用由2mM的高氯酸锂和pH值为3.0的甲醇(97:3; v / v)组成的洗涤液将生物基质洗涤10分钟。然后,通过切换阀的旋转,将阿托品在反吹模式下洗脱2分钟,然后通过由乙腈和磷酸钾缓冲液(pH 3.0; 50mM)组成的LC流动相转移到装有十八烷基二氧化硅的分析柱中。含有2mM庚烷磺酸钠(16:84; v / v)。 UV检测在220nm进行。根据一种新方法对方法进行了验证,该方法基于精度范围为25ng / ml(对应于定量极限)至1000ng / ml的浓度范围。然后将该方法用于住院患者的静脉内给药后测定血浆中的阿托品。

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