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Wiley, Journal of Mass Spectrometry, 8(40), p. 985-999, 2005

DOI: 10.1002/jms.902

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Biological tissue imaging with time‐of‐flight secondary ion mass spectrometry and cluster ion sources

Journal article published in 2005 by Alain Brunelle, David Touboul ORCID, Olivier Laprévote
This paper is available in a repository.
This paper is available in a repository.

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Abstract

Time-of-flight secondary ion mass spectrometry (TOF-SIMS) using liquid metal ion guns (LMIGs) is now sensitive enough to produce molecular-ion images directly from biological tissue samples. Primary cluster ions strike a spot on the sample to produce a mass spectrum. An image of this sample is achieved by rastering the irradiated point over the sample surface. The use of secondary ion mass spectrometry for mapping biological tissue surfaces provides unique analytical capabilities; in particular, it enables in a single acquisition a large variety of biological compounds to be localised on a micrometer scale and scrutinised for colocalisations. Without any treatment of the sample, this method is fully compatible with subsequent and complementary analyses like fluorescence microscopy, histochemical staining, or even matrix-assisted laser desorption/ionisation imaging. Basic physical concepts, required instrumentation (ion source and mass analyzer), sample preparation methods, image acquisition, image processing, and emerging biological applications will be described and discussed.