Abstract |
Currently available chemotherapy is associated with serious side effects, and therefore novel drug delivery systems (DDSs) are required to specifically deliver anticancer drugs to targeted sites. In this study, we evaluated the feasibility of visible light-cured glycol chitosan (GC) hydrogels with controlled release of doxorubicin⋅hydrochloride (DOX⋅HCl) as local DDSs for effective cancer therapy in vivo. The storage modulus of the hydrogel precursor solutions was increased as a function of visible light irradiation time. In addition, the swelling ratio of the hydrogel irradiated for 10 s (GC10/DOX) was greater than in 60 s (GC60/DOX). In vitro release test showed that DOX was rapidly released in GC10/DOX compared with GC60/DOX due to the density of cross-linking. In vitro and in vivo tests including cell viability and measurement of tumor volume showed that the local treatment of GC10/DOX yielded substantially greater antitumor effect compared with that of GC60/DOX. Therefore, the visible light-cured GC hydrogel system may exhibit clinical potential as a local DDS of anticancer drugs with controlled release, by modulating cross-linking density.
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Authors | Hoon Hyun, Min Ho Park, Wonbong Lim, So Yeon Kim, Danbi Jo, Jin Seok Jung, Gayoung Jo, Sewook Um, Deok-Won Lee, Dae Hyeok Yang |
Journal | Artificial cells, nanomedicine, and biotechnology
(Artif Cells Nanomed Biotechnol)
Vol. 46
Issue sup2
Pg. 874-882
( 2018)
ISSN: 2169-141X [Electronic] England |
PMID | 29749265
(Publication Type: Journal Article)
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Chemical References |
- Antineoplastic Agents
- Delayed-Action Preparations
- Hydrogels
- glycol-chitosan
- Doxorubicin
- Chitosan
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Topics |
- Animals
- Antineoplastic Agents
(chemistry, pharmacology)
- Cell Survival
(drug effects)
- Chitosan
(chemistry)
- Delayed-Action Preparations
- Doxorubicin
(chemistry, pharmacology)
- Feasibility Studies
- Humans
- Hydrogels
(chemistry)
- Injections
- Light
- MCF-7 Cells
- Mice
- Xenograft Model Antitumor Assays
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