GSH-mediated photoactivity of pheophorbide a-conjugated heparin/gold nanoparticle for photodynamic therapy

被引:78
作者
Li, Li [1 ]
Nurunnabi, Md. [2 ]
Nafiujjaman, Md. [3 ]
Lee, Yong-kyu [3 ]
Huh, Kang Moo [1 ]
机构
[1] Chungnam Natl Univ, Dept Polymer Sci & Engn, Taejon 305764, South Korea
[2] Korean Natl Univ Transportat, Dept Polymer Sci & Engn, Chungju 380702, Chungbuk, South Korea
[3] Korean Natl Univ Transportat, Dept Green Bio Engn, Chungju 380702, Chungbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Switchable photoactivity; Photodynamic therapy; Pheophorbide a (PubChem CID: 5323510); Heparin (PubChem CID: 772); Gold nanoparticle (PubChem CID: 23985); Glutathione (PubChem CID: 124886); GOLD NANOPARTICLES; GLUTATHIONE LEVELS; DELIVERY; MECHANISMS; DRUG;
D O I
10.1016/j.jconrel.2013.07.002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this study, we developed a new photosensitizer (PS)-conjugated hybrid nanoparticle comprised of gold nanoparticle (AuNP) as an efficient energy quencher, polysaccharide heparin and a second generation PS, pheophorbide a (PhA) for PDT. The hybrid nanoparticles (PhA-H/AuNPs) with an average size of 40 nm were prepared by surface coating of AuNPs with PhA conjugated heparins via gold-thiol interaction. The glutathione (GSH)-mediated switchable photoactivity of the PhA-H/AuNPs was observed by fluorescence quenching and dequenching behaviors in the absence and presence of GSH. The photoactivity was significantly suppressed in aqueous media, but instantaneously restored at the GSH-rich intracellular environment to generate a strong fluorescence signal together with active production of singlet oxygen species with light treatment. In vitro cell tests revealed marked phototoxicity and high intracellular uptake of PhA-H/AuNPs in contrast with free PhA. The PhA-H/AuNPs also exhibited a prolonged circulation characteristic, enhanced tumor specificity, and improved photodynamic therapeutic efficacy compared with free PhA in tumor-bearing mice. As a result, the PhA-H/AuNPs may serve as an effective smart nanomedicine platform for PDT and have great potential for the clinical treatment of various tumors. (C) 2013 Elsevier B. V. All rights reserved.
引用
收藏
页码:241 / 250
页数:10
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