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    Cell-acquiring fallopian endoscope for detection of ovarian cancer via reflectance imaging, fluorescence imaging and cell collection

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    1235603.pdf
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    Author
    Galvez, D.
    Cordova, R.
    Kiekens, K.
    Rocha, A.
    Drake, W.
    Rice, P.
    Heusinkveld, J.M.
    Barton, J.
    Affiliation
    Wyant College of Optical Sciences, University of Arizona
    Deptartment of Biomedical Engineering, University of Arizona
    Department of Obstetrics and Gynecology, University of Arizona
    Issue Date
    2023-03-14
    Keywords
    cancer screening
    endoscopic biopsy
    Fallopian tubes
    fluorescence imaging
    microendoscope
    ovarian cancer
    
    Metadata
    Show full item record
    Publisher
    SPIE
    Citation
    Dominique Galvez, Ricky Cordova, Kelli Kiekens, Andrew Rocha, William Drake, Photini Rice, John M. Heusinkveld, and Jennifer Barton "Cell-acquiring fallopian endoscope for detection of ovarian cancer via reflectance imaging, fluorescence imaging, and cell collection", Proc. SPIE 12356, Endoscopic Microscopy XVIII, 1235603 (14 March 2023); https://doi.org/10.1117/12.2650875
    Journal
    Progress in Biomedical Optics and Imaging - Proceedings of SPIE
    Rights
    © 2023 SPIE.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Ovarian cancer is the deadliest gynecological cancer, with most cases of high-grade serous ovarian carcinoma originating as serous tubal intraepithelial carcinoma (STIC) lesions in the fallopian tube epithelium. The Cell-Acquiring Fallopian Endoscope (CAFE) was designed to optically detect these STIC lesions and collect cells from the suspicious site for further analysis. While approximately 0.93 mm in diameter, the CAFE is able to perform multispectral fluorescence imaging (MFI), white light imaging for navigation, and cell collection. Each of these modalities is useful to locating potentially pathological areas. To find these regions, the CAFE looks for alterations of the autofluorescence of the tissue. Upon identification of a potential STIC lesion, a scrape biopsy collects cells from the region of interest. The prototype CAFE achieved an imaging resolution of 88 μm at a 5 mm distance, and 45° full field of view in air. When tested on ex vivo porcine tissue, hemocytometry counts determined that on the order of 105 cells per scrape biopsy could be collected. Current progress on the CAFE includes cell collection testing on ex vivo porcine and human tissue, and improvements in the imaging resolution. © 2023 SPIE.
    Note
    Immediate access
    ISSN
    1605-7422
    DOI
    10.1117/12.2650875
    Version
    Final Published Version
    ae974a485f413a2113503eed53cd6c53
    10.1117/12.2650875
    Scopus Count
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    UA Faculty Publications

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