Mass spectrometry imaging is a promising technique for measuring drugs and drug metabolites in cells and tissues. In this manuscript we describe a method for the imaging of HIV protease inhibitors. As a model system we used Mono Mac 6 cells cultured with the HIV protease inhibitors saquinavir and nelfinavir deposited on glass slides using a cytocentrifuge. A sublimation/deposition device for homogeneous matrix deposition was constructed which allows imaging of these HIV protease inhibitors at clinically relevant concentrations. Using this matrix sublimation/deposition method, glass slides containing the cytocentrifuged cells can be measured and analyzed by two types of mass spectrometry techniques, viz. matrix-assisted laser desorption/ionization time-of-flght (MALDI-TOF) and MALDI Fourier transform ion cyclotron resonance (FTICR), and this makes it possible to perform imaging rapidly (MALDI-TOF) and with a very high selectivity (MALDI-FTICR). Copyright

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Persistent URL dx.doi.org/10.1002/rcm.3981, hdl.handle.net/1765/24123
Citation
Dekker, L.J.M., Kampert, J.J.A.V., Reedijk, M.L., Burgers, P.C., Gruters, R.A., Osterhaus, A.D.M.E., & Lyider, T.M.. (2009). A Mass spectrometry based imaging method developed for the intracellular detection of HIV protease inhibitors. Rapid Communications in Mass Spectrometry, 23(8), 1183–1188. doi:10.1002/rcm.3981