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Sample preparation of bone tissue for MALDI-MSI for forensic and (pre)clinical applications

In the past decades, matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) has been applied to a broad range of biological samples, e.g., forensics and preclinical samples. The use of MALDI-MSI for the analysis of bone tissue has been limited due to the insulating propert...

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Autores principales: Vandenbosch, Michiel, Nauta, Sylvia P., Svirkova, Anastasiya, Poeze, Martijn, Heeren, Ron M.A., Siegel, Tiffany Porta, Cuypers, Eva, Marchetti-Deschmann, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007508/
https://www.ncbi.nlm.nih.gov/pubmed/32930817
http://dx.doi.org/10.1007/s00216-020-02920-1
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author Vandenbosch, Michiel
Nauta, Sylvia P.
Svirkova, Anastasiya
Poeze, Martijn
Heeren, Ron M.A.
Siegel, Tiffany Porta
Cuypers, Eva
Marchetti-Deschmann, Martina
author_facet Vandenbosch, Michiel
Nauta, Sylvia P.
Svirkova, Anastasiya
Poeze, Martijn
Heeren, Ron M.A.
Siegel, Tiffany Porta
Cuypers, Eva
Marchetti-Deschmann, Martina
author_sort Vandenbosch, Michiel
collection PubMed
description In the past decades, matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) has been applied to a broad range of biological samples, e.g., forensics and preclinical samples. The use of MALDI-MSI for the analysis of bone tissue has been limited due to the insulating properties of the material but more importantly the absence of a proper sample preparation protocol for undecalcified bone tissue. Undecalcified sections are preferred to retain sample integrity as much as possible or to study the tissue-bone bio interface in particular. Here, we optimized the sample preparation protocol of undecalcified bone samples, aimed at both targeted and untargeted applications for forensic and preclinical applications, respectively. Different concentrations of gelatin and carboxymethyl cellulose (CMC) were tested as embedding materials. The composition of 20% gelatin and 7.5% CMC showed to support the tissue best while sectioning. Bone tissue has to be sectioned with a tungsten carbide knife in a longitudinal fashion, while the sections need to be supported with double-sided tapes to maintain the morphology of the tissue. The developed sectioning method was shown to be applicable on rat and mouse as well as human bone samples. Targeted (methadone and EDDP) as well as untargeted (unknown lipids) detection was demonstrated. DHB proved to be the most suitable matrix for the detection of methadone and EDDP in positive ion mode. The limit of detection (LOD) is estimated to approximately 50 pg/spot on bone tissue. The protocol was successfully applied to detect the presence of methadone and EDDP in a dosed rat femur and a dosed human clavicle. The best matrices for the untargeted detection of unknown lipids in mouse hind legs in positive ion mode were CHCA and DHB based on the number of tissue-specific peaks and signal-to-noise ratios. The developed and optimized sample preparation method, applicable on animal and human bones, opens the door for future forensic and (pre)clinical investigations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-020-02920-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-80075082021-04-16 Sample preparation of bone tissue for MALDI-MSI for forensic and (pre)clinical applications Vandenbosch, Michiel Nauta, Sylvia P. Svirkova, Anastasiya Poeze, Martijn Heeren, Ron M.A. Siegel, Tiffany Porta Cuypers, Eva Marchetti-Deschmann, Martina Anal Bioanal Chem Research Paper In the past decades, matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) has been applied to a broad range of biological samples, e.g., forensics and preclinical samples. The use of MALDI-MSI for the analysis of bone tissue has been limited due to the insulating properties of the material but more importantly the absence of a proper sample preparation protocol for undecalcified bone tissue. Undecalcified sections are preferred to retain sample integrity as much as possible or to study the tissue-bone bio interface in particular. Here, we optimized the sample preparation protocol of undecalcified bone samples, aimed at both targeted and untargeted applications for forensic and preclinical applications, respectively. Different concentrations of gelatin and carboxymethyl cellulose (CMC) were tested as embedding materials. The composition of 20% gelatin and 7.5% CMC showed to support the tissue best while sectioning. Bone tissue has to be sectioned with a tungsten carbide knife in a longitudinal fashion, while the sections need to be supported with double-sided tapes to maintain the morphology of the tissue. The developed sectioning method was shown to be applicable on rat and mouse as well as human bone samples. Targeted (methadone and EDDP) as well as untargeted (unknown lipids) detection was demonstrated. DHB proved to be the most suitable matrix for the detection of methadone and EDDP in positive ion mode. The limit of detection (LOD) is estimated to approximately 50 pg/spot on bone tissue. The protocol was successfully applied to detect the presence of methadone and EDDP in a dosed rat femur and a dosed human clavicle. The best matrices for the untargeted detection of unknown lipids in mouse hind legs in positive ion mode were CHCA and DHB based on the number of tissue-specific peaks and signal-to-noise ratios. The developed and optimized sample preparation method, applicable on animal and human bones, opens the door for future forensic and (pre)clinical investigations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-020-02920-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-09-15 2021 /pmc/articles/PMC8007508/ /pubmed/32930817 http://dx.doi.org/10.1007/s00216-020-02920-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Paper
Vandenbosch, Michiel
Nauta, Sylvia P.
Svirkova, Anastasiya
Poeze, Martijn
Heeren, Ron M.A.
Siegel, Tiffany Porta
Cuypers, Eva
Marchetti-Deschmann, Martina
Sample preparation of bone tissue for MALDI-MSI for forensic and (pre)clinical applications
title Sample preparation of bone tissue for MALDI-MSI for forensic and (pre)clinical applications
title_full Sample preparation of bone tissue for MALDI-MSI for forensic and (pre)clinical applications
title_fullStr Sample preparation of bone tissue for MALDI-MSI for forensic and (pre)clinical applications
title_full_unstemmed Sample preparation of bone tissue for MALDI-MSI for forensic and (pre)clinical applications
title_short Sample preparation of bone tissue for MALDI-MSI for forensic and (pre)clinical applications
title_sort sample preparation of bone tissue for maldi-msi for forensic and (pre)clinical applications
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007508/
https://www.ncbi.nlm.nih.gov/pubmed/32930817
http://dx.doi.org/10.1007/s00216-020-02920-1
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