High‐contrast visualization of human skin cancers with combined reflectance confocal and moxifloxacin‐based two‐photon microscopy: An ex vivo study

• Published in: Lasers in surgery and medicine Vol. 54; no. 9; pp. 1226 - 1237
• Main Authors: Park, Won Yeong, Kim, Bumju, Chun, Ji Hyun, Hong, Seung‐Mo, Oh, Byung Ho, Kim, Ki Hean
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc 01.11.2022
• Subjects: Antibiotics; Basal cell carcinoma; Cancer; Cancer surgery; Cellular structure; Confocal microscopy; Dermis; Extracellular matrix; Fluorescence; Follicles; Histology; Labeling; Microscopy; Moxifloxacin; multiphoton microscopy; Photons; Second harmonic generation; Skin cancer; Squamous cell carcinoma; Surgery; surgery guiding; two‐photon microscopy
• ISSN: 0196-8092; 1096-9101
• DOI: 10.1002/lsm.23600

Background and Objectives Precise determination of cancer margin during skin cancer surgery is crucial for complete resection and further clinical prognosis. Although reflection confocal microscopy (RCM) has been used for perioperative guiding, its reflection contrast has limitations in detecting cancer cells in the dermis. We previously developed combined reflection confocal (RC) and moxifloxacin‐based two‐photon (MB‐TP) microscopy for sensitive cancer detection by using multiple contrast mechanisms. In this study, the performance of combined microscopy was characterized in various skin cancer specimens and compared with standard methods. Materials and Methods Seven human skin specimens in total including two normal ones, three basal cell carcinomas (BCCs), and two squamous cell carcinomas (SCCs) were collected and imaged in fresh condition. Moxifloxacin ophthalmic solution was topically instilled for cell labeling for 3–5 minutes, then mosaic imaging with the combined microscopy was conducted. The imaged specimens were imaged again after exogenous nuclear labeling for comparison and then processed for standard hematoxylin and eosin histology. Results Combined RC and MB‐TP microscopy visualized both cell and extracellular matrix structures of the skin specimens with multiple contrasts of reflection, moxifloxacin fluorescence, autofluorescence, and second harmonic generation. It distinguished normal cell structures in the skin dermis such as hair follicles, sebaceous and eccrine glands from BCC nests, and SCCs based on cell organization. Normal cell structures had organized cell arrangements for their functions, while cancer cell structures had dense and disorganized cell arrangements. Cellular features found by combined microscopy images were confirmed by both TP microscopy with nuclear labeling and histological examination. Conclusions The imaging results showed the potential of combined microscopy for sensitive cancer detection and in vivo guiding of skin cancer surgery.