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血清或血浆中雷尼替丁的机器人固相萃取和高效液相色谱分析

Robotic solid phase extraction and high performance liquid chromatographic analysis of ranitidine in serum or plasma.

作者信息

Lloyd T L, Perschy T B, Gooding A E, Tomlinson J J

机构信息

Glaxo Inc. Research Institute, Research Triangle Park, NC 27709.

出版信息

Biomed Chromatogr. 1992 Nov-Dec;6(6):311-6. doi: 10.1002/bmc.1130060613.

Abstract

A fully automated assay for the analysis of ranitidine in serum and plasma, with and without an internal standard, was validated. It utilizes robotic solid phase extraction with on-line high performance liquid chromatographic (HPLC) analysis. The ruggedness of the assay was demonstrated over a three-year period. A Zymark Py Technology II robotic system was used for serial processing from initial aspiration of samples from original collection containers, to final direct injection onto the on-line HPLC system. Automated serial processing with on-line analysis provided uniform sample history and increased productivity by freeing the chemist to analyse data and perform other tasks. The solid phase extraction efficiency was 94% throughout the assay range of 10-250 ng/mL. The coefficients of variation for within- and between-day quality control samples ranged from 1 to 6% and 1 to 5%, respectively. Mean accuracy for between-day standards and quality control results ranged from 97 to 102% of the respective theoretical concentrations.

摘要

一种用于分析血清和血浆中雷尼替丁的全自动检测方法得到了验证,该方法有内标和无内标两种情况。它采用机器人固相萃取结合在线高效液相色谱(HPLC)分析。该检测方法在三年期间展现出了耐用性。使用Zymark Py Technology II机器人系统进行系列处理,从最初从原始采集容器中吸取样品,到最终直接注入在线HPLC系统。在线分析的自动系列处理提供了统一的样品历史记录,并通过让化学家腾出时间分析数据和执行其他任务提高了工作效率。在10 - 250 ng/mL的整个检测范围内,固相萃取效率为94%。日内和日间质量控制样品的变异系数分别为1%至6%和1%至5%。日间标准品和质量控制结果的平均准确度分别为各自理论浓度的97%至102%。

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