A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples

    Research output: Contribution to journalArticleScientificpeer-review

    7 Citations (Scopus)
    27 Downloads (Pure)

    Abstract

    Development and study of cell-cultured constructs, such as tissue-engineering scaffolds or organ-on-a-chip platforms require a comprehensive, representative view on the cells inside the used materials. However, common characteristics of biomedical materials, for example, in porous, fibrous, rough-surfaced, and composite materials, can severely disturb low-energy imaging. In order to image and quantify cell structures in optically challenging samples, we combined labeling, 3D X-ray imaging, and in silico processing into a methodological pipeline. Cell-structure images were acquired by a tube-source X-ray microtomography device and compared to optical references for assessing the visual and quantitative accuracy. The spatial coverage of the X-ray imaging was demonstrated by investigating stem-cell nuclei inside clinically relevant-sized tissue-engineering scaffolds (5x13 mm) that were difficult to examine with the optical methods. Our results highlight the potential of the readily available X-ray microtomography devices that can be used to thoroughly study relative large cell-cultured samples with microscopic 3D accuracy.

    Original languageEnglish
    Article number548
    JournalCommunications biology
    Volume3
    Issue number1
    DOIs
    Publication statusPublished - 2020
    Publication typeA1 Journal article-refereed

    Publication forum classification

    • Publication forum level 1

    ASJC Scopus subject areas

    • General Biochemistry,Genetics and Molecular Biology
    • General Agricultural and Biological Sciences
    • Medicine (miscellaneous)

    Fingerprint

    Dive into the research topics of 'A tube-source X-ray microtomography approach for quantitative 3D microscopy of optically challenging cell-cultured samples'. Together they form a unique fingerprint.

    Cite this