Polymeric iron chelators for enhancing 5-aminolevulinic acid-induced photodynamic therapy

被引:8
|
作者
Nomoto, Takahiro [1 ,2 ]
Komoto, Kana [1 ,2 ]
Nagano, Tomoya [3 ]
Ishii, Takuya [3 ]
Guo, Haochen [1 ,2 ]
Honda, Yuto [1 ,2 ]
Ogura, Shun-ichiro [2 ]
Ishizuka, Masahiro [3 ]
Nishiyama, Nobuhiro [1 ,2 ,4 ]
机构
[1] Tokyo Inst Technol, Inst Innovat Res, Lab Chem & Life Sci, Yokohama, Kanagawa, Japan
[2] Tokyo Inst Technol, Sch Life Sci & Technol, Dept Life Sci & Technol, Yokohama, Kanagawa, Japan
[3] SBI Pharmaceut Co Ltd, Kawasaki, Kanagawa, Japan
[4] Kawasaki Inst Ind Promot, Innovat Ctr Nanomed iCONM, Kawasaki, Kanagawa, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
aminolevulinic acid; deferoxamine; drug delivery systems; iron; photodynamic therapy; PROTOPORPHYRIN-IX; CANCER; DEFEROXAMINE; DESFERRIOXAMINE; ACCUMULATION;
D O I
10.1111/cas.15637
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
5-Aminolevulinic acid (5-ALA) is an amino acid that can be metabolized into a photosensitizer, protoporphyrin IX (PpIX) selectively in a tumor cell, permitting minimally invasive photodynamic diagnosis/therapy. However, some malignant tumor cells have excess intracellular labile iron and facilitate the conversion of PpIX into heme, which compromises the therapeutic potency of 5-ALA. Here, we examined the potential of chelation of such unfavorable intratumoral labile iron in photodynamic therapy (PDT) with 5-ALA hydrochloride, using polymeric iron chelators that we recently developed. The polymeric iron chelator efficiently inactivated the intracellular labile iron in cultured cancer cells and importantly enhanced the accumulation of PpIX, thereby improving the cytotoxicity upon photoirradiation. Even in in vivo study with subcutaneous tumor models, the polymeric iron chelator augmented the intratumoral accumulation of PpIX and the PDT effect. This study suggests that our polymeric iron chelator could be a tool for boosting the effect of 5-ALA-induced PDT by modulating tumor microenvironment.
引用
收藏
页码:1086 / 1094
页数:9
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