个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:吉林大学
学位:博士
所在单位:化工学院
学科:高分子材料. 高分子化学与物理
办公地点:西部校区化工实验楼A207
联系方式:13052731242
电子邮箱:zyb1104@dlut.edu.cn
Poly(photosensitizer) Nanoparticles for Enhanced in Vivo Photodynamic Therapy by Interrupting the pi-pi Stacking and Extending Circulation Time
点击次数:
论文类型:期刊论文
发表时间:2019-05-22
发表刊物:ACS APPLIED MATERIALS & INTERFACES
收录刊物:PubMed、SCIE、EI
卷号:11
期号:20
页面范围:18224-18232
ISSN号:1944-8244
关键字:photodynamic therapy; pi-pi interactions; ROS degradable poly(TPP); quantitative TPP loading; improved singlet oxygen quantum yield
摘要:The natural planar and rigid structures of most of the hydrophobic photosensitizers (PSs) [such as tetraphenyl porphyrin (TPP)] significantly reduce their loading efficiencies in polymeric nanoparticles (NPs) because of the strong pi-pi interaction-induced aggregation. This aggregation-caused quenching will further reduce the quantum yield of singlet oxygen (O-1(2)) generation and weaken the efficiency of photodynamic therapy (PDT). In addition, the small molecular PSs exhibit short tumor retention time and tend to be easily cleared once released. Herein, poly(TPP) NPs, prepared by cross-linking of reactive oxygen species degradable, thioketal linkers and TPP derivatives, followed by coprecipitation, were first developed with quantitative loading efficiency (>99%), uniform NP sizes (without aggregation), increased singlet oxygen quantum yield (Phi(Delta) = 0.79 in dimethyl sulfoxide compared with 0.52 for original TPP), increased in vitro phototoxicity, extended tumor retention time, light-triggered on-demand release, and enhanced in vivo antitumor efficacy, which comprehensively address the multiple issues for most of the PSs in the PDT area.