| Literature DB >> 31368257 |
Seunghun Lee1, Won Yeong Park1, Hoonchul Chang2, Bumju Kim2, Won Hyuk Jang2, Seonghan Kim1, Younghoon Shin3, Myoung Joon Kim4, Kyung Hwa Lee5, Eui Hyun Kim6, Euiheon Chung3, Ki Hean Kim1,2.
Abstract
Delineation of brain tumor margins during surgery is critical to maximize tumor removal while preserving normal brain tissue to obtain optimal clinical outcomes. Although various imaging methods have been developed, they have limitations to be used in clinical practice. We developed a high-speed cellular imaging method by using clinically compatible moxifloxacin and confocal microscopy for sensitive brain tumor detection and delineation. Moxifloxacin is a Food and Drug Administration (FDA) approved antibiotic and was used as a cell labeling agent through topical administration. Its strong fluorescence at short visible excitation wavelengths allowed video-rate cellular imaging. Moxifloxacin-based confocal microscopy (MBCM) was characterized in normal mouse brain specimens and visualized their cytoarchitecture clearly. Then, MBCM was applied to both brain tumor murine models and two malignant human brain tumors of glioblastoma and metastatic cancer. MBCM detected tumors in all the specimens by visualizing dense and irregular cell distributions, and tumor margins were easily delineated based on the cytoarchitecture. An image analysis method was developed for automated detection and delineation. MBCM demonstrated sensitive delineation of brain tumors through cytoarchitecture visualization and would have potentials for human applications, such as a surgery-guiding method for tumor removal.Entities:
Keywords: anti-bacterial agents; brain neoplasms; confocal microscopy; fluorescence; topical administration
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Year: 2019 PMID: 31368257 DOI: 10.1002/jbio.201900197
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.207