| Literature DB >> 33790990 |
Hung V-T Nguyen1,2,3,4,5, Alexandre Detappe2,3,4,6,5, Peter Harvey7, Nolan Gallagher1, Clelia Mathieu3,4, Michael P Agius3,4, Oksana Zavidij3,4, Wencong Wang1, Yivan Jiang1, Andrzej Rajca8, Alan Jasanoff7,9,10, Irene M Ghobrial3,4, P Peter Ghoroghchian2,3,4, Jeremiah A Johnson1,2.
Abstract
Nitroxide-based organic-radical contrast agents (ORCAs) are promising as safe, next-generation magnetic resonance imaging (MRI) tools. Nevertheless, stimuli-responsive ORCAs that enable MRI monitoring of prodrug activation have not been reported; such systems could open new avenues for prodrug validation and image-guided drug delivery. Here, we introduce a novel "pro-ORCA" concept that addresses this challenge. By covalent conjugation of nitroxides and drug molecules (doxorubicin, DOX) to the same brush-arm star polymer (BASP) through chemically identical cleavable linkers, we demonstrate that pro-ORCA and prodrug activation, i.e., ORCA and DOX release, leads to significant changes in MRI contrast that correlate with cytotoxicity. This approach is shown to be general for a range of commonly used linker cleavage mechanisms (e.g., photolysis and hydrolysis) and release rates. Pro-ORCAs could find applications as research tools or clinically viable "reporter theranostics" for in vitro and in vivo MRI-correlated prodrug activation.Entities:
Year: 2020 PMID: 33790990 PMCID: PMC8009311 DOI: 10.1039/d0py00558d
Source DB: PubMed Journal: Polym Chem ISSN: 1759-9954 Impact factor: 5.582