Sulfonated Polyethylenimine for Photosensitizer Conjugation and Targeting

被引:6
作者
Chitgupi, Upendra [1 ]
Zhang, Yumiao [1 ,2 ]
Lo, Chi Y. [2 ]
Shao, Shuai [1 ]
Song, Wentao [1 ]
Geng, Jumin [1 ]
Neelamegham, Sriram [1 ,2 ]
Lovell, Jonathan F. [1 ,2 ]
机构
[1] SUNY Buffalo, Dept Biomed Engn, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Dept Chem & Biol Engn, Buffalo, NY 14260 USA
基金
美国国家卫生研究院;
关键词
DENDRITIC POLYGLYCEROL SULFATES; PHOTODYNAMIC THERAPY; E-SELECTIN; P-SELECTIN; IN-VIVO; BIOLOGICAL EVALUATION; GENE DELIVERY; INFLAMMATION; CANCER; LIGANDS;
D O I
10.1021/acs.bioconjchem.5b00241
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Polysulfonated macromolecules are known to bind selectins, adhesion membrane proteins which are broadly implicated in inflammation. Commercially available branched polyethylenimine (PEI) was reacted with chlorosulfonic acid to generate sulfonated PEI with varying degrees of sulfonation. Remaining unreacted amine groups were then used for straightforward conjugation with pyropheophoribide-a, a near-infrared photosensitizer. Photosensitizer-labeled sulfonated PEI conjugates inhibited blood coagulation and were demonstrated to specifically bind to cells genetically programmed to overexpress L-selectin (CD62L) or P-selectin (CD62P). In vitro, following targeting, selectin-expressing cells could be destroyed via photodynamic therapy.
引用
收藏
页码:1633 / 1639
页数:7
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