| Literature DB >> 26701101 |
Richard J A Goodwin1, Anna Nilsson2, C Logan Mackay3, John G Swales4, Maria K Johansson5, Martin Billger5, Per E Andrén2, Suzanne L Iverson5.
Abstract
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.Entities:
Keywords: label-free; mass spectrometry imaging; screening
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Year: 2015 PMID: 26701101 DOI: 10.1177/1087057115623740
Source DB: PubMed Journal: J Biomol Screen ISSN: 1087-0571