Redox-Responsive Porphyrin-Based Polysilsesquioxane Nanoparticles for Photodynamic Therapy of Cancer Cells

被引:19
|
作者
Vega, Daniel L. [1 ,2 ]
Lodge, Patrick [1 ]
Vivero-Escoto, Juan L. [1 ,2 ]
机构
[1] Univ N Carolina, Dept Chem, Charlotte, NC 28223 USA
[2] Univ N Carolina, Ctr Biomed Engn & Sci, Charlotte, NC 28223 USA
基金
美国国家科学基金会;
关键词
photodynamic therapy; photosensitizer delivery; porphyrin; stimulus-responsive materials; polysilsesquioxane nanoparticles; cancer therapy; IN-VITRO; BASIC PRINCIPLES; DELIVERY; PHOTOSENSITIZERS; NANOTECHNOLOGY; NANOMATERIALS; FLUORESCENCE; ONCOLOGY; LIGHT;
D O I
10.3390/ijms17010056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of stimulus-responsive photosensitizer delivery systems that carry a high payload of photosensitizers is of great importance in photodynamic therapy. In this study, redox-responsive polysilsesquioxane nanoparticles (PSilQNPs) built by a reverse microemulsion approach using 5,10,15,20-tetrakis(carboxyphenyl) porphyrin (TCPP) silane derivatives as building blocks, were successfully fabricated. The structural properties of TCPP-PSilQNPs were characterized by dynamic light scattering (DLS)/zeta- potential, scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). The photophysical properties were determined by UV-vis and fluorescence spectroscopy. The quantity of singlet oxygen generated in solution was measured using 1,3-diphenylisobenzofuran. The redox-responsive release of TCPP molecules was successfully demonstrated in solution in the presence of a reducing agent. The internalization of TCPP-PSilQNPs in cancer cells was investigated using laser scanning confocal microscopy. Phototoxicity experiments in vitro showed that the redox-responsive TCPP-PSilQNPs exhibited an improved phototherapeutic effect on cervical cancer cells compared to a non-responsive TCPP-PSilQNP control material.
引用
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页数:16
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