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Development of dual acid-visible light-degradable core-crosslinked nanogels with extended conjugate aromatic imines for enhanced drug delivery

Authors: Bairagi KShamekhi MTountas ILetourneau NPeslherbe GHPiekny AOh JK


Affiliations

1 Department of Chemistry and Biochemistry, Concordia University, Montreal, Quebec, H4B 1R6, Canada. john.oh@concordia.ca.
2 Department of Physics, Concordia University, Montreal, Quebec, H4B 1R6, Canada.
3 Center for Research in Molecular Modeling, Concordia University, Montreal, Quebec, H4B 1R6, Canada.
4 Department of Biology, Concordia University, Montreal, Quebec, H4B 1R6, Canada.

Description

The development of stimuli-responsive amphiphilic block copolymers and their nanoassemblies/nanogels integrated with degradable covalent chemistry undergoing chemical transitions has been extensively explored as a promising platform for tumor-targeting controlled/enhanced drug delivery. The conjugate aromatic imine bond is unique in responding to acidic pH through acid-catalyzed hydrolysis and visible light through photo-induced E/Z isomerization, thus allowing for a dual acid-light response via a single conjugate aromatic imine bond. Herein, we report a robust strategy for fabricating well-defined core-crosslinked nanogels bearing extended conjugate aromatic imine linkages that exhibit controlled degradation in response to acidic pH and visible light. This approach utilizes the pre-crosslinking of a poly(ethylene glycol)-based block copolymer bearing reactive imidazole pendants with a diol crosslinker bearing an extended conjugate aromatic imine, followed by the mechanical dispersion of the formed crosslinked polymers in an aqueous solution. The fabricated core-crosslinked nanogels with a hydrodynamic diameter of 119 nm are non-cytotoxic, colloidally stable, and capable of encapsulating cancer drug curcumin. They exhibit controlled/enhanced release of encapsulated curcumin at pH = 5 (acidic) or upon irradiation with visible light (? = 420 nm) as well as exhibit promisingly accelerated and synergistic release under the combination of the above conditions. Furthermore, curcumin-loaded nanogels reduce cell viability in a controlled manner, unlike free drugs. This simplified yet efficient synthetic approach paves the way for the development of smart nanocarriers with potential applications in controlled drug release and cancer therapy.


Links

PubMed: https://pubmed.ncbi.nlm.nih.gov/40637173/

DOI: 10.1039/d5tb00734h