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Recovery of the analytes and the IS from human plasma.

NIAID Data Ecosystem2026-03-10 收录

生物医药分析方法验证

血浆样品前处理

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https://figshare.com/articles/dataset/Recovery_of_the_analytes_and_the_IS_from_human_plasma_/5922808 数据链接链接失效反馈

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Recovery of the analytes and the IS from human plasma.

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创建时间：

2018-02-24

生物医药分析方法验证

生物检测精密度评估

Abstract–In the pharmaceutical industry, all analytical methods must be shown to deliver unbiased and precise results. In an assay qualification or validation study, the trueness, accuracy, and interm

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Method validation data for a UPLC-MS/MS method for simultaneous quantification of aspirin, its metabolite salicylic acid, and salvianolic acid B in human plasma.

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Recovery and matrix effect of the antidiabetic agents and internal standards.

生物医药分析方法验证

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Recovery and matrix effect of the antidiabetic agents and internal standards.

Figshare2016-12-09 更新50

Validation parameters of the analytical method by UPLC-MS/MS, to quantify ifosfamide in DBS at 30% HTC.

治疗反应监测

生物医药分析方法验证

SD: Standard Deviation. CV: Coefficient of Variation. N/R: Not required according to the guidelines. Theoretical amounts for QC1, QC2 and QC3 were 300, 4000 and 8000 ng/mL, respectively. Validation pa

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LRV status of the analyzed strains according to detection method.

利什曼原虫病毒检测

生物医药分析方法验证

aAs shown in Ives et al., 2011; by qRT-PCR analysis, Lg 1881, Lg 03 and Lg 17 were classified as LRVlow harboring at least 10,000 fold less viral transcripts than the highly infected strains.bAs shown

Figshare2015-12-02 更新70

Recovery of the analytes and the IS from human plasma.

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