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Sub-millimeter endoscope demonstrates feasibility of in vivo reflectance imaging, fluorescence imaging, and cell collection in the fallopian tubes

Significance: Most cases of high-grade serous ovarian carcinoma originate as serous tubal intraepithelial carcinoma (STIC) lesions in the fallopian tube epithelium (FTE), enabling early endoscopic detection. Aim: The cell-acquiring fallopian endoscope (CAFE) was built to meet requirements for locati...

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Detalles Bibliográficos
Autores principales: Cordova, Ricky, Kiekens, Kelli, Burrell, Susan, Drake, William, Kmeid, Zaynah, Rice, Photini, Rocha, Andrew, Diaz, Sebastian, Yamada, Shigehiro, Yozwiak, Michael, Nelson, Omar L., Rodriguez, Gustavo C., Heusinkveld, John, Shih, Ie-Ming, Alberts, David S., Barton, Jennifer K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Photo-Optical Instrumentation Engineers 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253554/
https://www.ncbi.nlm.nih.gov/pubmed/34216135
http://dx.doi.org/10.1117/1.JBO.26.7.076001
Descripción
Sumario:Significance: Most cases of high-grade serous ovarian carcinoma originate as serous tubal intraepithelial carcinoma (STIC) lesions in the fallopian tube epithelium (FTE), enabling early endoscopic detection. Aim: The cell-acquiring fallopian endoscope (CAFE) was built to meet requirements for locating potentially pathological tissue indicated by an alteration in autofluorescence or presence of a targeted fluorophore. A channel was included for directed scrape biopsy of cells from regions of interest. Approach: Imaging resolution and fluorescence sensitivity were measured using a standard resolution target and fluorescence standards, respectively. A prototype was tested in ex vivo tissue, and collected cells were counted and processed. Results: Measured imaging resolution was [Formula: see text] at a 5-mm distance, and full field of view was [Formula: see text] in air. Reflectance and fluorescence images in ex vivo porcine reproductive tracts were captured, and fit through human tracts was verified. Hemocytometry counts showed that on the order of [Formula: see text] per scrape biopsy could be collected from ex vivo porcine tissue. Conclusions: All requirements for viewing STIC in the FTE were met, and collected cell counts exceeded input requirements for relevant analyses. Our benchtop findings suggest the potential utility of the CAFE device for in vivo imaging and cell collection in future clinical trials.