Literature DB >> 24377103

A review of complementary separation methods and matrix assisted laser desorption ionization-mass spectrometry imaging: lowering sample complexity.

Karolina Škrášková, Ron M A Heeren.   

Abstract

Matrix-assisted laser desorption ionization (MALDI) mass spectrometry imaging (MSI) brings unique combined information on molecular identity and molecular distribution of a sample surface. During the past decade, it has matured and is now routinely employed for biomedical tissue sections analysis. However, owing to the high molecular complexity of tissue, MALDI-MSI suffers from ionization suppression effects. This directly results in a reduced ability to detect low-abundant molecular species. At the same time, the spatial resolution of separation techniques can be insufficient for an unambiguous determination of the local composition of a mixture. As analytical separation techniques can significantly reduce ion suppression, and MALDI-MSI has an ability to improve their spatial resolution, the two analytical approaches can successfully be combined in a pursuit of comprehensive local sample composition information. In the following review we summarize strategies of mutually beneficial combinations of MALDI-MSI and different separation techniques and discuss limitations and future developments.

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Year:  2013        PMID: 24377103     DOI: 10.1016/j.chroma.2013.10.027

Source DB:  PubMed          Journal:  J Chromatogr A        ISSN: 0021-9673            Impact factor:   4.759


  3 in total

1.  Laser Ablation with Vacuum Capture for MALDI Mass Spectrometry of Tissue.

Authors:  Fabrizio Donnarumma; Fan Cao; Kermit K Murray
Journal:  J Am Soc Mass Spectrom       Date:  2015-09-15       Impact factor: 3.109

2.  Solvent separating secondary metabolites directly from biosynthetic tissue for surface-assisted laser desorption ionisation mass spectrometry.

Authors:  David Rudd; Kirsten Benkendorff; Nicolas H Voelcker
Journal:  Mar Drugs       Date:  2015-03-16       Impact factor: 5.118

3.  Decrease in Sphingomyelin (d18:1/16:0) in Stem Villi and Phosphatidylcholine (16:0/20:4) in Terminal Villi of Human Term Placentas with Pathohistological Maternal Malperfusion.

Authors:  Kaori Yamazaki; Noritaka Masaki; Yukiko Kohmura-Kobayashi; Chizuko Yaguchi; Takahiro Hayasaka; Hiroaki Itoh; Mitsutoshi Setou; Naohiro Kanayama
Journal:  PLoS One       Date:  2015-11-16       Impact factor: 3.240

  3 in total

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