Near-infrared light activated photodynamic therapy of THP-1 macrophages based on core-shell structured upconversion nanoparticles

被引:19
作者
Wang, Hao [1 ]
Zhu, Xing [2 ]
Han, Renlu [1 ]
Wang, Xin [1 ]
Yang, Liming [2 ]
Wang, You [1 ]
机构
[1] Harbin Inst Technol, Sch Mat Sci & Engn, Harbin 150001, Peoples R China
[2] Harbin Med Univ, Dept Pathophysiol, Harbin 150081, Peoples R China
基金
中国国家自然科学基金;
关键词
Photodynamic therapy; Cell imaging; Upconversion nanoparticles; Near infrared light; DRUG-DELIVERY; PHOTOANGIOPLASTY; LUMINESCENT; DIAGNOSIS; RELEASE; PLAQUES; DESIGN;
D O I
10.1016/j.micromeso.2016.09.048
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Upconversion nanoparticles (UCNPs) with fascinating properties hold great potential as nanotransducers for solving the light penetration problem that traditional photodynamic therapy (PDT) is facing. In this report, the synthesis and utility of UCNPs/silica core-shell structured nanoparticles for upconversion (UC) PDT and imaging of THP-1 macrophages were described. The UCNPs (NaYF4:Yb, Er) with a uniform diameter of 28 +/- 1 nm were synthesized as core and 10 nm thick biocompatible mesoporous silica was coated as shell. Photosensitizer (PS) was covalently grafted inside mesoporous silica shell. Upon excitation, NIR light is converted into visible one by UCNPs for the absorption of PS to generate singlet oxygen for killing THP-1 macrophages and inhibiting the development of atherosclerosis. The fluorescence images showed the resulting nanoparticles are readily taken up by macrophages and TEM results indicated that they are highly phototoxic. The statistical in vitro results revealed PDT could cause the apoptosis of THP-1 macrophages with a remarkable therapeutic efficacy of cell inhibition ratio of 40%. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:78 / 85
页数:8
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