Journal
ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY
Volume 46, Issue -, Pages 874-882Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/21691401.2018.1470529
Keywords
Glycol chitosan; visible light irradiation; doxorubicinhydrochloride; cross-linking density; local drug delivery system
Categories
Funding
- Technology Innovation Program - Ministry of Trade, Industry and Energy (MOTIE, Republic of Korea) [10053595]
- National Research Foundation of Korea (NRF) [NRF-2015R1C1A1A01053168, 2014R1A1A1002697, 2017R1D1A1B03033195]
Ask authors/readers for more resources
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 doxorubicinhydrochloride (DOXHCl) 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 10s (GC(10)/DOX) was greater than in 60s (GC(60)/DOX). In vitro release test showed that DOX was rapidly released in GC(10)/DOX compared with GC(60)/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 GC(10)/DOX yielded substantially greater antitumor effect compared with that of GC(60)/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.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available