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生物基质中药物和/或药物代谢物的定量选择离子监测(QSIM)。

Quantitative selected ion monitoring (QSIM) of drugs and/or drug metabolites in biological matrices.

作者信息

Garland W A, Powell M L

出版信息

J Chromatogr Sci. 1981 Aug;19(8):392-434. doi: 10.1093/chromsci/19.8.392.

Abstract

From a modest beginning, QSIM has established itself with over three hundred applications in the 1970s as not only a reference technique for other methods but also as a useful method in its own right for the quantitation of drugs in biological matrices. Relative to its potential sensitivity, the actual sensitivity of QSIM drug assays is disappointing, although a number of QSIM drug assays report LOQs of 250 pg ml-1 or less. The mean reported precision of QSIM drug assays (approximately 6%) is similar to that of traditional GC and LC assays, but is an order of magnitude less than either what is theoretically possible or what has been demonstrated in a few selected QSIM assays.

摘要

从一个适度的开端起步,QSIM在20世纪70年代凭借三百多项应用确立了自身地位,它不仅是其他方法的参考技术,而且本身就是一种用于生物基质中药物定量的有用方法。相对于其潜在灵敏度而言,QSIM药物分析的实际灵敏度令人失望,尽管一些QSIM药物分析报告的检测限为250 pg ml-1或更低。QSIM药物分析报告的平均精密度(约6%)与传统气相色谱和液相色谱分析的精密度相似,但比理论上可能达到的精密度或少数选定的QSIM分析中所证明的精密度低一个数量级。

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