Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2024MeXpose─A Modular Imaging Pipeline for the Quantitative Assessment of Cellular Metal Bioaccumulationcitations
  • 2022Elemental Mapping of Human Malignant Mesothelioma Tissue Samples Using High-Speed LA-ICP-TOFMS Imaging.8citations
  • 2019Laser Ablation-Inductively Coupled Plasma Time-of-Flight Mass Spectrometry Imaging of Trace Elements at the Single-Cell Level for Clinical Practice.46citations

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Fyhrquist, Nanna
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Wisgrill, Lukas
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Werner, Paulina
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Koellensperger, Gunda
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Braun, Gabriel
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Schaier, Martin
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Zanghellini, Jürgen
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Haywood-Small, Sarah
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Clench, Malcolm
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Cole, Laura
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Voloaca, Oana M.
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Sjm, Van Malderen
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Schoeberl, A.
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Neumayer, S.
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Jilma, P.
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Koellensperger, G.
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Peyrl, Andreas
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Schweikert, A.
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Co-Authors (by relevance)

  • Fyhrquist, Nanna
  • Wisgrill, Lukas
  • Werner, Paulina
  • Koellensperger, Gunda
  • Braun, Gabriel
  • Schaier, Martin
  • Zanghellini, Jürgen
  • Haywood-Small, Sarah
  • Clench, Malcolm
  • Cole, Laura
  • Voloaca, Oana M.
  • Sjm, Van Malderen
  • Schoeberl, A.
  • Neumayer, S.
  • Jilma, P.
  • Koellensperger, G.
  • Peyrl, Andreas
  • Schweikert, A.
OrganizationsLocationPeople

article

Laser Ablation-Inductively Coupled Plasma Time-of-Flight Mass Spectrometry Imaging of Trace Elements at the Single-Cell Level for Clinical Practice.

  • Sjm, Van Malderen
  • Schoeberl, A.
  • Neumayer, S.
  • Jilma, P.
  • Koellensperger, G.
  • Theiner, Sarah
  • Peyrl, Andreas
  • Schweikert, A.
Abstract

In this work, a combination of routine clinical practice and state-of-the-art laser ablation-inductively coupled plasma time-of-flight mass spectrometry (LA-ICP-TOFMS) imaging is presented for multielement analysis of single cells on clinical samples. More specifically, routinely drawn blood thin films of a patient undergoing treatment with the anticancer drug cisplatin were studied. The presented label-free approach enabled rapid analysis of hundreds of cells at the single-cell level within a few minutes without additional tailored sample preparation. The employed low-dispersion LA setup is based on the tube-type COBALT ablation cell in combination with the aerosol rapid introduction system (ARIS) providing pixel-resolved imaging at 250-500 Hz for biological sample material. In order to cope with the short transient signals of only a few milliseconds delivered by the laser ablation setup, an icpTOF 2R TOF-based ICP-MS instrument was used for analysis, which has a mass coverage of m/ z = 14-256. Leukocytes and erythrocytes, imaged with a laser beam of 4 μm and pixel interspacing of 2 μm, were differentiated on the basis of their intrinsic trace-elemental pattern. Overall, red blood cells displayed high iron intensities, whereas individual white blood cells were characterized by their high phosphorus content and increased sulfur signal. Unsupervised multivariate statistical analysis was applied to the data set. Principal component plots showed a clear clustering of leukocytes versus erythrocytes. The approach allowed studying not only the drug distribution between plasma and cells but also, for the first time, the preferential accumulation of platinum in different blood cell types without the need of cell fixation and labeling. Extracellular hotspots of platinum were observed, whereas only a small fraction of platinum was associated with erythrocytes. The investigation demonstrates the potential of low-dispersion LA-ICP-TOFMS as a rapid and powerful tool for label-free single-cell imaging in the clinical context.

Topics
  • impedance spectroscopy
  • dispersion
  • thin film
  • Platinum
  • cobalt
  • iron
  • spectrometry
  • clustering
  • Phosphorus
  • trace element
  • laser ablation
  • time-of-flight mass spectrometry
  • inductively coupled plasma mass spectrometry