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      Absolute Quantitative MALDI Imaging Mass Spectrometry: A Case of Rifampicin in Liver Tissues

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          Abstract

          Matrix-assisted laser desorption/ionization (MALDI) imaging mass spectrometry (IMS) elucidates molecular distributions in thin tissue sections. Absolute pixel-to-pixel quantitation has remained a challenge, primarily lacking validation of the appropriate analytical methods. In the present work, isotopically labeled internal standards are applied to tissue sections to maximize quantitative reproducibility and yield accurate quantitative results. We have developed a tissue model for rifampicin (RIF), an antibiotic used to treat tuberculosis, and have tested different methods of applying an isotopically labeled internal standard for MALDI IMS analysis. The application of the standard and subsequently the matrix onto tissue sections resulted in quantitation that was not statistically significantly different from results obtained using HPLC-MS/MS of tissue extracts. Quantitative IMS experiments were performed on liver tissue from an animal dosed in vivo. Each microspot in the quantitative images measures the local concentration of RIF in the thin tissue section. Lower concentrations were detected from the blood vessels and around the portal tracts. The quantitative values obtained from these measurements were comparable (>90% similarity) to HPLC-MS/MS results obtained from extracts of the same tissue.

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          Journal
          0370536
          519
          Anal Chem
          Anal. Chem.
          Analytical chemistry
          0003-2700
          1520-6882
          21 October 2016
          05 February 2016
          16 February 2016
          26 October 2016
          : 88
          : 4
          : 2392-2398
          Affiliations
          []Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235, United States
          []Mass Spectrometry Research Center, Vanderbilt University, Nashville, Tennessee 37240, United States
          [§ ]Tuberculosis Research Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, United States
          []Institute of Infectious Disease and Molecular Medicine, Department of Clinical Laboratory Sciences, University of Cape Town, Cape Town, South Africa
          [|| ]Departments of Pharmacology, Biochemistry, and Medicine, Vanderbilt University, 465 21st Avenue South, Medical Research Building III, Nashville, Tennessee 37240, United States
          Author notes
          [* ]Corresponding Author: Phone: 615-322-4336. r.caprioli@ 123456vanderbilt.edu
          Article
          PMC5080977 PMC5080977 5080977 nihpa824303
          10.1021/acs.analchem.5b04409
          5080977
          26814665
          a6d6c72e-c545-483f-9bb8-69df9e35c6bb
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