Simultaneous multielement imaging of liver tissue using laser ablation inductively coupled plasma mass spectrometry.

Biological tissues Chemical imaging Elemental analysis LA-ICP-MS Laser ablation inductively coupled plasma mass spectrometry Principal component analysis

Journal

Talanta
ISSN: 1873-3573
Titre abrégé: Talanta
Pays: Netherlands
ID NLM: 2984816R

Informations de publication

Date de publication:
01 Dec 2021
Historique:
received: 05 06 2021
revised: 16 07 2021
accepted: 17 07 2021
entrez: 14 9 2021
pubmed: 15 9 2021
medline: 16 9 2021
Statut: ppublish

Résumé

Analysis of the spatial distribution of metals, metalloids, and non-metals in biological tissues is of significant interest in the life sciences, helping to illuminate the function and roles these elements play within various biological pathways. Chemical imaging methods are commonly employed to address biological questions and reveal individual spatial distributions of analytes of interest. Elucidation of these spatial distributions can help determine key elemental and molecular information within the respective biological specimens. However, traditionally utilized imaging methods prove challenging for certain biological tissue analysis, especially with respect to applications that require high spatial resolution or depth profiling. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been shown to be effective for direct elemental analysis of solid materials with high levels of precision. In this work, chemical imaging using LA-ICP-MS has been applied as a powerful analytical methodology for the analysis of liver tissue samples. The proposed analytical methodology successfully produced both qualitative and quantitative information regarding specific elemental distributions within images of thin tissue sections with high levels of sensitivity and spatial resolution. The spatial resolution of the analytical methodology was innovatively enhanced, helping to broaden applicability of this technique to applications requiring significantly high spatial resolutions. This information can be used to further understand the role these elements play within biological systems and impacts dysregulation may have.

Identifiants

pubmed: 34517593
pii: S0039-9140(21)00646-9
doi: 10.1016/j.talanta.2021.122725
pii:
doi:

Substances chimiques

Metals 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122725

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Nicole M Ralbovsky (NM)

Analytical Research & Development, MRL, Merck & Co., Inc., West Point, PA, 19486, USA.

Lanfang Zou (L)

Analytical Research & Development, MRL, Merck & Co., Inc., West Point, PA, 19486, USA.

Bingming Chen (B)

Pharmacokinetics, Pharmacodynamics and Drug Metabolism, MRL, Merck & Co., Inc., West Point, PA, 19486, USA.

Nanyan Rena Zhang (NR)

Pharmacokinetics, Pharmacodynamics and Drug Metabolism, MRL, Merck & Co., Inc., West Point, PA, 19486, USA.

Catherine D G Hines (CDG)

Translational Imaging Biomarkers, MRL, Merck & Co., Inc., West Point, PA, 19486, USA.

Marissa Vavrek (M)

Pharmacokinetics, Pharmacodynamics and Drug Metabolism, MRL, Merck & Co., Inc., West Point, PA, 19486, USA.

Wendy Zhong (W)

Analytical Research & Development, MRL, Merck & Co., Inc., West Point, PA, 19486, USA.

Joseph P Smith (JP)

Analytical Research & Development, MRL, Merck & Co., Inc., West Point, PA, 19486, USA. Electronic address: joseph.smith@merck.com.

Xiaodong Bu (X)

Analytical Research & Development, MRL, Merck & Co., Inc., West Point, PA, 19486, USA. Electronic address: xiaodong_bu@merck.com.

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Classifications MeSH