Exemplifying the Screening Power of Mass Spectrometry Imaging over Label-Based Technologies for Simultaneous Monitoring of Drug and Metabolite Distributions in Tissue Sections

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 [14C]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.

[1]  C. Mackay,et al.  Future technology insight: mass spectrometry imaging as a tool in drug research and development , 2015, British journal of pharmacology.

[2]  L. Cohen,et al.  Small molecule analysis by MALDI mass spectrometry , 2002, Analytical and bioanalytical chemistry.

[3]  P. Edlund,et al.  Determination of corticosteroids in tissue samples by liquid chromatography-tandem mass spectrometry. , 2005, Journal of pharmaceutical and biomedical analysis.

[4]  A. Walch,et al.  High‐resolution metabolite imaging of light and dark treated retina using MALDI‐FTICR mass spectrometry , 2014, Proteomics.

[5]  P. Svenningsson,et al.  Controlled-pH tissue cleanup protocol for signal enhancement of small molecule drugs analyzed by MALDI-MS imaging. , 2012, Analytical chemistry.

[6]  Lars Farde,et al.  Qualitative and quantitative MALDI imaging of the positron emission tomography ligands raclopride (a D2 dopamine antagonist) and SCH 23390 (a D1 dopamine antagonist) in rat brain tissue sections using a solvent-free dry matrix application method. , 2011, Analytical chemistry.

[7]  D. Drexler,et al.  Utility of quantitative whole-body autoradiography (QWBA) and imaging mass spectrometry (IMS) by matrix-assisted laser desorption/ionization (MALDI) in the assessment of ocular distribution of drugs. , 2011, Journal of pharmacological and toxicological methods.

[8]  R. Caprioli,et al.  Molecular imaging of biological samples: localization of peptides and proteins using MALDI-TOF MS. , 1997, Analytical chemistry.

[9]  Walter A. Korfmacher,et al.  Direct analysis of drug candidates in tissue by matrix-assisted laser desorption/ionization mass spectrometry. , 2003, Journal of mass spectrometry : JMS.

[10]  Kristine Glunde,et al.  An Alternative Paper Based Tissue Washing Method for Mass Spectrometry Imaging: Localized Washing and Fragile Tissue Analysis , 2011, Journal of the American Society for Mass Spectrometry.

[11]  Nicholas E. Manicke,et al.  Desorption electrospray ionization mass spectrometry: Imaging drugs and metabolites in tissues , 2008, Proceedings of the National Academy of Sciences.

[12]  R. D'argy,et al.  Quantitative whole-body radioluminography-future strategy for balance and tissue distribution studies. , 2000, Regulatory toxicology and pharmacology : RTP.

[13]  Peter J H Webborn,et al.  Mass spectrometry imaging in drug development. , 2015, Analytical chemistry.

[14]  C. Dollery,et al.  Single-Cell Analysis: Visualizing Pharmaceutical and Metabolite Uptake in Cells with Label-Free 3D Mass Spectrometry Imaging. , 2015, Analytical chemistry.

[15]  R. Cooks,et al.  Mass Spectrometry Sampling Under Ambient Conditions with Desorption Electrospray Ionization , 2004, Science.

[16]  D. Muddiman,et al.  Assessing drug and metabolite detection in liver tissue by UV-MALDI and IR-MALDESI mass spectrometry imaging coupled to FT-ICR MS. , 2015, International journal of mass spectrometry.

[17]  Alain Schweitzer,et al.  Autoradiography, MALDI-MS, and SIMS-MS Imaging in Pharmaceutical Discovery and Development , 2010, The AAPS Journal.

[18]  C. Morris,et al.  The imaging and quantification of aluminium in the human brain using dynamic secondary ion mass spectrometry (SIMS) , 1992, Biology of the cell.

[19]  Richard J A Goodwin,et al.  Sample preparation for mass spectrometry imaging: small mistakes can lead to big consequences. , 2012, Journal of proteomics.

[20]  E. Solon Autoradiography: high-resolution molecular imaging in pharmaceutical discovery and development , 2007, Expert opinion on drug discovery.

[21]  P. Chaurand,et al.  Enhancement of protein sensitivity for MALDI imaging mass spectrometry after chemical treatment of tissue sections , 2008, Journal of the American Society for Mass Spectrometry.

[22]  Amanda B Hummon,et al.  Imaging mass spectrometry: from tissue sections to cell cultures. , 2013, Advanced drug delivery reviews.

[23]  R. Heeren,et al.  A concise review of mass spectrometry imaging. , 2010, Journal of chromatography. A.