Pheophorbide a-Conjugated pH-Sensitive Nanoparticle Vectors for Highly Efficient Photodynamic Therapy of Cancer

被引:9
|
作者
Zhao, Linlin [1 ]
Kim, Tae-Hyun [2 ,3 ,4 ]
Kim, Hae-Won [2 ,3 ,4 ]
Kim, So Yeon [1 ,5 ]
机构
[1] Chungnam Natl Univ, Grad Sch Energy Sci & Technol, Taejon 305764, South Korea
[2] Dankook Univ, Dept Nanobiomed Sci, Cheonan, South Korea
[3] Dankook Univ, WCU Res Ctr, Cheonan, South Korea
[4] Dankook Univ, Inst Tissue Regenerat Engn ITREN, Cheonan, South Korea
[5] Chungnam Natl Univ, Dept Chem Engn Educ, Coll Educ, Taejon 305764, South Korea
基金
新加坡国家研究基金会;
关键词
Drug delivery system; nanoparticle; PBLA; PEG; photodynamic therapy; SCUTELLARIA-BARBATA; COPOLYMER MICELLES; POLYMERIC MICELLE; SINGLET OXYGEN; PHOTOSENSITIZERS; CYTOTOXICITY; PERMEABILITY; SYSTEM;
D O I
10.1080/00914037.2014.1002131
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
To achieve a tumor-targeted drug delivery system for photodynamic therapy, we designed ligand-mediated nanoparticles with stable formulations of a hydrophobic photosensitizer. Folic acid (FA)-conjugated amphiphilic block copolymers of PEG and poly--benzyl-L-aspartate with the potential to act as pH-sensitive drug release reservoirs were synthesized. The photosensitizer was conjugated to the copolymers through pH-sensitive hydrazone (Hyd) linkages. The FA-PEG-P(Asp-Hyd)-Pheo nanoparticles had average diameters of 76-217nm. The pH-dependent photosensitizer release property may ensure intracellular drug release inside tumor cells due to the lower pH inside the endosomes and lysosomes of tumor cells. The FA-PEG-P(Asp-Hyd)-Pheo nanoparticles demonstrated marked phototoxicity and minimal dark toxicity. [GRAPHICS] .
引用
收藏
页码:733 / 744
页数:12
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