Polyacrylamide Nanoparticles with Visible and Near-Infrared Autofluorescence

被引:5
|
作者
Xie, Hongmei [1 ]
Zhang, Ling [1 ]
Wu, Lin [1 ]
Wang, Jinke [1 ]
机构
[1] Southeast Univ, Sch Biol Sci & Med Engn, State Key Lab Bioelect, Nanjing 210096, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
autofluorescence; biocompatibility; imaging; NIR; polyacrylamide nanoparticle; IRON-OXIDE NANOPARTICLES; CROSS-LINKED CHITOSAN; POLY-L-LYSINE; QUANTUM DOTS; EPSILON-POLYLYSINE; CANCER-CELLS; PHOTODYNAMIC THERAPY; SURFACE-CHARGE; LIVING CELLS; IN-VIVO;
D O I
10.1002/ppsc.201700222
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nowadays, self-fluorescent materials such as quantum dots are widely studied and applied in biomedical field. However, the biggest obstacle is biocompatibility. Here, a novel autofluorescent nanoparticle is constructed by crosslinking polyacrylamide nanoparticles (PAANPs) that contain epsilon-poly-L-lysine with glutaraldehyde (named fPAANPs). The nanoparticle has a mean size of about 16 nm, a zeta potential of about + 16 mV, and strong visible and near-infrared autofluorescence. The nanoparticle can be efficiently internalized into cells with high biocompatibility, the LC50 of which in RAW264.7, HepG2, and Hepa1-6 cells is 6, 9, and 7.5 mg mL(-1), respectively. The nanoparticle shows no visible impact on the mice vitality even at a high intravenously administered dose (126 mg kg(-1)). The autofluorescence of fPAANPs shows high stability, persistence, allowing long-term dynamic imaging for 25 d in subcutaneous injections and 18 d in xenograft tumors in mice. The nanoparticle thus provides a self-traceable nanomaterial that can be exploited as drug carrier and potential photodynamic therapy photosensitizer.
引用
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页数:10
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