Improved Stability and Photodynamic Activity of Water-Soluble 5,15-Diazaporphyrins Incorporated in β-(1,3-1,6)-d-Glucan with On-Off Switch

被引:20
作者
Hino, Shodai [1 ]
Satake, Shuhei [1 ]
Shinmori, Hideyuki [2 ]
Kawabata, Shigeki [3 ]
Koumoto, Kazuya [4 ]
Suzuki, Toshio [5 ]
Nagasaki, Takeshi [5 ]
Sugikawa, Kouta [1 ]
Kawasaki, Riku [1 ]
Ikeda, Atsushi [1 ]
机构
[1] Hiroshima Univ, Grad Sch Engn, Dept Appl Chem, 1-4-1 Kagamiyama, Higashihiroshima, Hiroshima 7398527, Japan
[2] Univ Yamanashi, Grad Fac Interdisciplinary Res, Fac Life & Environm Sci, Dept Biotechnol, 4-4-37 Takeda, Kofu, Yamanashi 4008510, Japan
[3] Toyama Prefectural Univ, Fac Engn, Dept Liberal Arts & Sci, 5180 Kurokawa, Imizu, Toyama 9390398, Japan
[4] Konan Univ, FIRST, Dept Nanobiochem, 7-1-20 Minatojima Minamimachi, Kobe, Hyogo 6500047, Japan
[5] Osaka City Univ, Grad Sch Engn, Dept Appl Chem & Bioengn, Sumiyoshi Ku, 3-3-138 Sugimoto, Osaka 5588585, Japan
关键词
aggregation; fluorescent probes; host-guest systems; polysaccharide; porphyrinoids; WALLED CARBON NANOTUBES; ONE-DIMENSIONAL HOST; LIPOSOMAL MEMBRANES; GAMMA-CYCLODEXTRIN; SCHIZOPHYLLAN; BETA-1,3-GLUCAN; COMPLEXATION; DERIVATIVES; ACETATE; CURDLAN;
D O I
10.1002/asia.201901582
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
5,15-Diazaporphyrins, which have a large absorption at wavelengths over 600 nm, were dissolved in water by complex formation with beta-(1,3-1,6)-d-glucans. Aqueous solutions of these complexes were relatively stable compared with their trimethyl-beta-cyclodextrin-complexed analogues. beta-Glucan-complexed diazaporphyrins showed quenched fluorescence and had low singlet-oxygen-generation abilities owing to random self-aggregation. However, external stimuli, such as the presence of liposomes or intracellular uptake, restored the fluorescence and singlet-oxygen-generation abilities of beta-glucan-complexed diazaporphyrins. Consequently, beta-glucan-complexed diazaporphyrins showed very high photodynamic activities toward HeLa cells.
引用
收藏
页码:365 / 370
页数:6
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