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In situ Gelation of Supramolecular Hydrogel for Anti-Tumor Drug Delivery
來源:何斌教授個(gè)人網(wǎng)站 發(fā)布日期:2012-04-14
作者:10. Bin He*, Jing Zeng, Yu Nie, Li Ji, Rui Wang, Yao Wu, Li Li, Gang Wang, Zhongwei Gu*
關(guān)鍵字:biodegradable, supramolecular hydrogel, gelation
論文來源:期刊
具體來源:Macromol. Biosci. 2009, 9, 1169–1175
發(fā)表時(shí)間:2009年

A supramolecular injectable hydrogel was fabricated. The hydrogel was in situ gelated by the host-guest interaction between a-cyclodextrins (a-CDs) and methylated poly(ethylene glycol) grafted poly(a,b-malic acid) (mPEG-g-PMA). The hydrogel was characterized by 1NMR, XRD, DSC, TGA and SEM. The results showed that the polyrotaxanes of alpha-CDs/mPEG-g-PMA acted as physical crosslink sites in the hydrogel. Anti-tumor drug doxorubicin hydrochloride (DOX) was loaded in the hydrogel. The release and anti-tumor
effect were studied in vitro. The burst release of DOX was restrained obviously. The sustaining release time lasted more than 3 d and the cell viability decreased greatly. This hydrogel is a promising injectable hydrogel for minimally invasive therapeutic drug delivery.

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