ArticleBiomedical optics express2021
High-fidelity and rapid cellular-level Mueller matrix imaging for tissue identification with unstained sections.
Article in Biomedical optics express, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed, 21 citations in OpenAlex.
- Evaluating backscattering polarized light imaging microstructural mapping capabilities through neural tissue and analogous phantom imaging.Journal of biomedical optics · 2024Article
- Mechanical stability of polarization signatures in biological tissue characterization.Biomedical optics express · 2024Article
- The LMIT: Light-mediated minimally-invasive theranostics in oncology.Theranostics · 2024Review
- Stokes Dynamic Polarimeter for Non-Organic and Organic Samples Characterization.Sensors (Basel, Switzerland) · 2022Article
- Erratum: High-fidelity and rapid cellular-level Mueller matrix imaging for tissue identification with unstained sections: erratum.Biomedical optics express · 2022Article
Corrections and comments
- Erratum issued
Authors and funding
5 authors at 2 institutions in 2 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mueller matrix polarimetry is regarded as a promising technique in the field of biomedicine, especially for pathological diagnosis. However, the current studies on Mueller imaging of pathological sections are all at the tissue-level, and the cellular-level polarization information is difficult to obtain. To overcome this challenge, we first propose a cellular-level Mueller matrix imaging method for accurate quantitative identification of tissues in this study. Benefiting from the significant birefringent behavior of paraffin in unstained sections, the proposed method can locate the paraffin distribution areas of retardance images by involving Otsu's algorithm. Then, the real cellular-level polarization information (e.g., depolarization) is acquired. The efficiency of the proposed method was demonstrated on unstained rat tissue samples. The results showed that the obtained depolarization images are highly consistent with the stained microscopic images in terms of the morphology and arrangement of the tissues at cellular level. Finally, this method was preliminarily applied to the detection of human lung cancer tissue section, effectively realizing the quantitative differentiation of normal, inflamed, and malignant areas in unstained section. This study provides a possible approach for the rapid and accurate diagnosis of cancer.
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Registered trials
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