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 >The use of human plasma as matrix for calibration standards in pre-clinical LC-MS/MS methods--a way to reduce animal use.
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The use of human plasma as matrix for calibration standards in pre-clinical LC-MS/MS methods--a way to reduce animal use.

机译:在临床前LC-MS / MS方法中将人血浆用作校准标准品的基质-一种减少动物使用的方法。

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摘要

The option, for practical and ethical reasons, to replace animal plasma with human plasma for calibration standards was successfully applied to 73 analytical methods developed in our laboratory during the last years. The animals used for obtaining blank plasma could then be reduced with a number corresponding to about 25% of mice or 5% of rats in ordinary one-month toxicology studies. This is of important public concern and also in accordance with the 3R-strategy. The methods were successfully validated for determination of drug concentrations in plasma from rat, dog, mouse, rabbit and cynomolgus monkey. Reproducibility of study samples from dosed animals was established, showing a mean accuracy of 100.8% with a CV of 7.2% (n=1339). The purpose of this paper is to present a scientific basis for the alternative approach to adopt human plasma matrix for calibration standards, which will reduce animal use, without compromising the quality of appropriately validated assays. Additional advantages are cheaper and simplified plasma maintenance and the possibility to validate methods for several species in the same analytical batch.
机译:出于实际和道德原因,用人血浆替代动物血浆作为校准标准的选择已成功应用于我们实验室近几年开发的73种分析方法。在普通的一个月的毒理学研究中,用于获得空白血浆的动物数量可以减少,大约相当于小鼠的25%或大鼠的5%。这是重要的公众关注点,也符合3R策略。该方法已成功验证了测定大鼠,狗,小鼠,兔和食蟹猴血浆中药物浓度的方法。建立了来自剂量动物的研究样品的可重复性,显示平均准确度为100.8%,CV为7.2%(n = 1339)。本文的目的是为采用人血浆基质作为校准标准品的替代方法提供科学依据,这将减少动物的使用,而不会损害经过适当验证的测定的质量。额外的优势是更便宜且简化的血浆维护,并且可以验证同一分析批次中几种物质的方法。

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