傅里叶变换离子回旋共振
代谢物
质谱成像
化学
药品
质谱法
药物发现
计算生物学
色谱法
药理学
生物化学
生物
作者
Richard J. A. Goodwin,Anna Nilsson,C. Logan Mackay,John G. Swales,Maria K. Johansson,Martin Billger,Per E. Andrén,Suzanne L. Iverson
出处
期刊:
[Elsevier BV]
日期:2015-12-23
卷期号:21 (2): 187-193
被引量:37
标识
DOI:10.1177/1087057115623740
摘要
Mass spectrometry imaging (MSI) provides pharmaceutical researchers with a suite of technologies to screen and assess compound distributions and relative abundances directly from tissue sections and offer insight into drug discovery-applicable queries such as blood-brain barrier access, tumor penetration/retention, and compound toxicity related to drug retention in specific organs/cell types. Label-free MSI offers advantages over label-based assays, such as quantitative whole-body autoradiography (QWBA), in the ability to simultaneously differentiate and monitor both drug and drug metabolites. Such discrimination is not possible by label-based assays if a drug metabolite still contains the radiolabel. Here, we present data exemplifying the advantages of MSI analysis. Data of the distribution of AZD2820, a therapeutic cyclic peptide, are related to corresponding QWBA data. Distribution of AZD2820 and two metabolites is achieved by MSI, which [(14)C]AZD2820 QWBA fails to differentiate. Furthermore, the high mass-resolving power of Fourier transform ion cyclotron resonance MS is used to separate closely associated ions.
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