Human Glioblastoma Visualization: Triple Receptor-Targeting Fluorescent Complex of Dye, SIWV Tetra-Peptide, and Serum Albumin Protein

• DOI: 10.1021/acssensors.1c00320
• Publication Date: 2021-06-08T15:15:25Z
• Authors: Jong Min An; Heejo Moon; Peter Verwilst; Jinwoo Shin; B. Moon Kim; Chul-Kee Park; Jong Seung Kim; Seung Geun Yeo; Hyo Young Kim; Dokyoung Kim
• Keywords: glioblastoma targeting; Optical Imaging; Serum Albumin, Bovine; albumin complex; 01 natural sciences; 0104 chemical sciences; 3. Good health; fluorescent probe; Animals; Humans; Cattle; Osteonectin; two-photon microscopy; Glioblastoma; Peptides; fluorescence-guided surgery

Fluorescence guided surgery (FGS) has been highlighted in the clinical site for guiding surgical procedures and providing the surgeon with a real-time visualization of the operating field. FGS is a powerful technique for precise surgery, particularly tumor resection; however, clinically approved fluorescent dyes have often shown several limitations during FGS, such as non-tumor-targeting, low in vivo stability, insufficient emission intensity, and low blood-brain barrier penetration. In this study, we disclose a fluorescent dye complex, peptide, and protein for the targeted visualization of human glioblastoma (GBM) cells and tissues. Our noble triple receptor-targeting fluorescent complex (named BSA-OXN-SIWV) consists of (i) dipolar oxazepine dye (OXN), which has high stability, low cytotoxicity, bright fluorescence, and two-photon excitable, (ii) tetra-peptide (SIWV) for the targeting of the caveolin-1 receptor, and (iii) bovine serum-albumin (BSA) protein for the targeting of albondin (gp60) and secreted protein acidic and rich in cysteine receptor. The photophysical properties and binding mode of BSA-OXN-SIWV were analyzed, and the imaging of GBM cell lines and human clinical GBM tissues were successfully demonstrated in this study. Our findings hold great promise for the application of BSA-OXN-SIWV to GBM identification and the surgery at clinical sites, as a new FGS agent.