生物分析
分析物
口译(哲学)
计算生物学
化学
生化工程
色谱法
配体结合分析
药物开发
组合化学
计算机科学
纳米技术
药品
生物系统
药理学
生物化学
医学
生物
材料科学
工程类
受体
程序设计语言
出处
期刊:Bioanalysis
[Future Science Ltd]
日期:2011-06-01
卷期号:3 (11): 1287-1295
被引量:26
摘要
Ligand-binding assays are used to determine concentration levels of biopharmaceuticals in biological matrices. The whole molecule does not serve as a basis for quantification, but subregions are captured and detected by specific binding critical reagents that have been produced for the sole purpose of bioanalysis. An assay can be designed to measure the free or the total analyte. Depending on the format of the assay, different observations and interpretations could be deemed. In the case studies presented in this article, the same serum samples were subjected to analysis in parallel by two different assay formats. In three out of the four cases presented, the results and the data interpretation were remarkably different. Therefore, it is essential for the bioanalyst to communicate to other stake-holders, such as toxicologists and pharmacokineticists, what the assay detects and measures for plausible data interpretation and implication.
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