Thermosensitive hydrogel drug delivery system containing doxorubicin loaded CS - GO nanocarriers for controlled release drug in situ

被引:20
|
作者
Guo, Q. F. [1 ]
Cao, H. [1 ]
Li, X. H. [1 ]
Liu, S. W. [1 ]
机构
[1] Weifang Univ, Key Lab Biochem & Mol Biol Univ Shandong, Weifang 261061, Shandong, Peoples R China
关键词
PLA-PEG-PLA; CS-GO; DOX; Nanocarriers; Thermosensitive hydrogel; Sol-gel; GRAPHENE OXIDE; INTRAPERITONEAL CHEMOTHERAPY; PERITONEAL CARCINOMATOSIS; PROPERTY RELATIONSHIP; COLORECTAL-CANCER; CARBON NANOTUBES; GENE DELIVERY; COPOLYMERS; OSTEOBLASTS; SCAFFOLDS;
D O I
10.1179/1753555715Y.0000000006
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Local delivery of antitumour drugs provided a high local concentration, the intention of increased antitumour and decreased systemic therapy. An injectable thermosensitive hydrogel is commonly used as a local drug delivery system (DDS). In this paper, a novel local hydrophilic doxorubicin (DOX) DDS, chitosan functionalised graphene oxide (CS-GO) nanocarriers in polylactide (PLA)-poly( ethylene glycol) (PEG)-PLA thermosensitive hydrogel, was demonstrated. The DOX loaded CS-GO nanocarriers (DOX/CS-GO) were prepared via pi-pi stacking and hydrophobic interactions, which presented a superior loading capacity for DOX, and then DOX/CS-GO were incorporated into the thermosensitive hydrous matrix. The obtained injectable hydrophilic DOX delivery system was flowing sol at ambient temperature but became non-flowing gel at body temperature and can act as a depot for sustained release of DOX in situ. The in vitro cytotoxicity test showed that the PLA-PEG-PLA hydrogel and CS-GO nanocarriers were non-cytotoxic. The obtained CS-GO/DOX nanocarriers not only showed increased cellular uptake but also enhanced cytotoxicity. The in vitro release of PLA-PEG-PLA/(CS-GO/DOX) complexes was sustained for >200 h. These results suggested that this injectable composite hydrogel is a potential candidate as drug carrier and in clinical applications in situ.
引用
收藏
页码:294 / 300
页数:7
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