Injectable Coacervate Hydrogel for Delivery of Anticancer Drug-Loaded Nanoparticles in vivo
journal contributionposted on 29.03.2018, 00:00 authored by Ashlynn L. Z. Lee, Zhi Xiang Voo, Willy Chin, Robert J. Ono, Chuan Yang, Shujun Gao, James L. Hedrick, Yi Yan Yang
In this study, bortezomib (BTZ, a cytotoxic water-insoluble anticancer drug) was encapsulated in micellar nanoparticles having a catechol-functionalized polycarbonate core through a pH-sensitive covalent bond between phenylboronic acid (PBA) in BTZ and catechol, and these drug-loaded micelles were incorporated into hydrogels to form micelle/hydrogel composites. A series of injectable, biodegradable hydrogels with readily tunable mechanical properties were formed and optimized for sustained delivery of the BTZ-loaded micelles through ionic coacervation between PBA-functionalized polycarbonate/poly(ethylene glycol) (PEG) “ABA” triblock copolymer and a cationic one having guanidinium- or thiouronium-functionalized polycarbonate as “A” block. An in vitro release study showed the pH dependence in BTZ release. At pH 7.4, the BTZ release from the micelle/hydrogel composite remained low at 7%, whereas in an acidic environment, ∼85% of BTZ was released gradually over 9 days. In vivo studies performed in a multiple myeloma MM.1S xenograft mouse model showed that the tumor progression of mice treated with BTZ-loaded micelle solution was similar to that of the control group, whereas those treated with the BTZ-loaded micelle/hydrogel composite resulted in significant delay in the tumor progression. The results demonstrate that this hydrogel has great potential for use in subcutaneous and sustained delivery of drug-loaded micelles with superior therapeutic efficacy.
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tumor progressiondrug-loaded micellespH-sensitive covalent bondPBAPEGcatechol-functionalized polycarbonate coreInjectable Coacervate Hydrogelcytotoxic water-insoluble anticancer drugAnticancer Drug-Loaded NanoparticleshydrogelBTZ releasemyeloma MM .1S xenograft mouse modelABABTZ-loaded micelle solution