| Literature DB >> 35150468 |
Takeshi Fukuda1,2, Shinya Yokomizo1,3, Stefanie Casa4, Hailey Monaco1, Sophia Manganiello1, Haoran Wang1, Xiangmin Lv5, Amy Daniel Ulumben1, Chengeng Yang1, Min-Woong Kang1,6, Kazumasa Inoue3, Masahiro Fukushi3, Toshiyuki Sumi2, Cheng Wang5, Homan Kang1, Kai Bao1, Maged Henary4,7, Satoshi Kashiwagi1, Hak Soo Choi1.
Abstract
The residual tumor after surgery is the most significant prognostic factor of patients with epithelial ovarian cancer. Near-infrared (NIR) fluorescence-guided surgery is actively utilized for tumor localization and complete resection during surgery. However, currently available contrast-enhancing agents display low on-target binding, unfavorable pharmacokinetics, and toxicity, thus not ideal for clinical use. Here we report ultrabright and stable squaraine fluorophores with optimal pharmacokinetics by introducing an asymmetric molecular conformation and surface charges for rapid transporter-mediated cellular uptake. Among the tested, OCTL14 shows low serum binding and rapid distribution into cancer tissue via organic cation transporters (OCTs). Additionally, the charged squaraine fluorophores are retained in lysosomes, providing durable intraoperative imaging in a preclinical murine model of ovarian cancer up to 24 h post-injection. OCTL14 represents a significant departure from the current bioconjugation approach of using a non-targeted fluorophore and would provide surgeons with an indispensable tool to achieve optimal resection.Entities:
Keywords: Intraoperative Near-Infrared Fluorescence Imaging; Lysosome; Organic Cation Transporter; Ovarian Cancer; Squaraine
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Year: 2022 PMID: 35150468 PMCID: PMC9007913 DOI: 10.1002/anie.202117330
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336