A quantitation method for mass spectrometry imaging

被引:79
|
作者
Koeniger, Stormy L. [1 ]
Talaty, Nari [1 ]
Luo, Yanping [1 ]
Ready, Damien [1 ]
Voorbach, Martin [1 ]
Seifert, Terese [1 ]
Cepa, Steve [1 ]
Fagerland, Jane A. [2 ]
Bouska, Jennifer [3 ]
Buck, Wayne [1 ]
Johnson, Robert W. [1 ]
Spanton, Stephen [1 ]
机构
[1] Abbott Labs, GPRD, Adv Technol, Abbott Pk, IL 60064 USA
[2] Abbott Labs, GPRD, Global Preclin Safety, Abbott Pk, IL 60064 USA
[3] Abbott Labs, GPRD, Exploratory Kinet, Abbott Pk, IL 60064 USA
关键词
LASER-DESORPTION-IONIZATION; RAT-BRAIN; CHEMICAL INFORMATION; TISSUE-SECTIONS; MALDI; LOCALIZATION; CELLS; DRUG; MS; METABOLITES;
D O I
10.1002/rcm.4891
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new quantitation method for mass spectrometry imaging (MSI) with matrix-assisted laser desorption/ionization (MALDI) has been developed. In this method, drug concentrations were determined by tissue homogenization of five 10 mu m tissue sections adjacent to those analyzed by MSI. Drug levels in tissue extracts were measured by liquid chromatography coupled to tandem mass spectrometry (LC/MS/MS). The integrated MSI response was correlated to the LC/MS/MS drug concentrations to determine the amount of drug detected per MSI ion count. The study reported here evaluates olanzapine in liver tissue. Tissue samples containing a range of concentrations were created from liver harvested from rats administered a single dose of olanzapine at 0, 1, 4, 8, 16, 30, or 100 mg/kg. The liver samples were then analyzed by MALDI-MSI and LC/MS/MS. The MALDI-MSI and LC/MS/MS correlation was determined for tissue concentrations of similar to 300 to 60 000 ng/g and yielded a linear relationship over two orders of magnitude (R-2 = 0.9792). From this correlation, a conversion factor of 6.3 +/- 0.23 fg/ion count was used to quantitate MSI responses at the pixel level (100 mu m). The details of the method, its importance in pharmaceutical analysis, and the considerations necessary when implementing it are presented. Copyright (C) 2011 John Wiley & Sons, Ltd.
引用
收藏
页码:503 / 510
页数:8
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