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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/49959


    Title: Multifunctional hollow nanoparticles based on graft-diblock copolymers for doxorubicin delivery
    Authors: Lu,PL;Chen,YC;Ou,TW;Chen,HH;Tsai,HC;Wen,CJ;Lo,CL;Wey,SP;Lin,KJ;Yen,TC;Hsiue,GH
    Contributors: 化學工程與材料工程學系
    Keywords: DRUG-DELIVERY;QUANTUM DOTS;MICELLES;CANCER;ADRIAMYCIN;SIZE;BIODISTRIBUTION;TOXICITY;THERAPY;CARRIER
    Date: 2011
    Issue Date: 2012-03-27 16:27:25 (UTC+8)
    Publisher: 國立中央大學
    Abstract: This article reports a flexible hollow nanoparticles, self-assembling from poly(N-vinylimidazole-co-N-vinylpyrrolidone)-g-poly(D,L-lactide) graft copolymers and methoxyl/functionalized-PEG-PLA diblock copolymers, as an anticancer drug doxorubicin (Dox) carrier for cancer targeting, imaging, and cancer therapy. This multifunctional hollow nanoparticle exhibited a specific on-off switch drug release behavior, owning to the pH-sensitive structure of imidazole, to release Dox in acidic surroundings (intracellular endosomes) and to capsulate Dox in neutral surroundings (blood circulation or extracellular matrix). Imaging by SPECT/CT shows that nanoparticle conjugated with folic acids ensures a high intratumoral accumulation due to the folate-binding protein (FBP)-binding effect. In vivo tumor growth inhibition shows that nanoparticles exhibited excellent antitumor activity and a high rate of apoptosis in cancer cells. After 80-day treatment course of nanoparticles, it did not appreciably cause heart, liver and kidney damage by inactive Dox or polymeric materials. The results indicate that the flexible carriers with an on-off switched drug release may be allowed to accurately deliver to targeted tumors for cancer therapy. (C) 2010 Elsevier Ltd. All rights reserved.
    Relation: BIOMATERIALS
    Appears in Collections:[化學工程與材料工程學系 ] 期刊論文

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