期刊
BIOCONJUGATE CHEMISTRY
卷 24, 期 11, 页码 1784-1789出版社
AMER CHEMICAL SOC
DOI: 10.1021/bc400322h
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资金
- Small Animal Imaging Core
- Radiochemistry and Molecular Imaging Probes Core
- NIH [R01 CA138468, R25 CA096945, K25 EB016673]
- Brain Tumor Center of Memorial Sloan-Kettering Cancer
- Nanotechnology Center of Memorial Sloan-Kettering Cancer Center
Liposomes are attractive vehicles for the controlled release of drugs and cytotoxins and have a long-standing history in medical research and clinical practice. In addition to established therapeutic indications, liposomes have several favorable properties for molecular imaging, including high stability and the ability to be labeled with radioisotopes, as well as paramagnetic and fluorescent contrast agents. However, long circulation times and difficulties in creating targeted liposomes have proven challenges for imaging. In this study, we have addressed these limitations using a recently developed strategy for bioorthogonal conjugation, the reaction between tetrazines and trans-cyclooctenes. By coating radiolabeled liposomes with trans-cyclooctene and pretargeting with a tetrazine coupled to a targeted peptide, we were able to selectively enhance the retention of liposomes and bind them to tumor tissue in live animals. The rapid reaction between tetrazines and trans-cyclooctenes allowed imaging to be performed with the short-lived PET tracer F-18, yielding signal-to-background activity ratios of 7:1. The covalent, bioorthogonally driven tumor-targeting of liposomes by in vivo click chemistry is promising and should be explored for more selective and rapid delivery of radiodiagnostics and radiotherapeutics, two classes of drugs which particularly benefit from fast clearance, low nonspecific binding, and the associated reduced toxicity to kidneys and bone marrow.
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