Supramolecular Nanodrugs Constructed by Self-Assembly of Peptide Nucleic Acid-Photosensitizer Conjugates for Photodynamic Therapy

被引:39
作者
Chang, Rui [1 ,5 ]
Nikoloudakis, Emmanouil [2 ]
Zou, Qianli [1 ]
Mitraki, Anna [3 ,4 ]
Coutsolelos, Athanassios G. [2 ]
Yan, Xuehai [1 ,5 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, Beijing 100190, Peoples R China
[2] Univ Crete, Dept Chem, Lab Bioinorgan Chem, Voutes Campus, Iraklion 70013, Greece
[3] Univ Crete, Fdn Res & Technol Hellas FORTH, Dept Mat Sci & Technol, Iraklion 70013, Crete, Greece
[4] Univ Crete, Fdn Res & Technol Hellas FORTH, Inst Elect Struct & Laser IESL, Iraklion 70013, Crete, Greece
[5] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
peptide nucleic acid; porphyrin; self-assembly; nanodrug; photodynamic therapy; AGGREGATION-INDUCED EMISSION; DRUG-DELIVERY; NANOPARTICLES; PORPHYRINS; TRANSFORMATION; VEHICLES; PROTEIN; PNA;
D O I
10.1021/acsabm.9b00558
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Two hybrid materials were designed by conjugating peptide nucleic acids (PNAs) to porphyrin or boron-dipyrromethene, generating PNA-porphyrin (PNA-TPP) and PNA-BODIPY (PNA-BDP) conjugates, respectively. Because of the combination of the supramolecular characteristics of PNAs and photosensitizers, the two hybrid conjugates readily self-assemble in aqueous solutions and produce well-defined nanoparticles with uniform particle sizes. The resulting two kinds of nanoparticles show good stability in biological solutions and upon dilution. Importantly, the nanoparticles can efficiently interact with cancer cells and the internalized nanoparticles are mainly distributed in the cytoplasm without discernible cytotoxicity in the dark, enabling them to be applied as photodynamic nanoagents for selective killing cells. Hence, self-assembly of PNA-photosensitizer conjugates may hold promise for advancing the rational design and construction of photodynamic nanoagents for cancer therapy.
引用
收藏
页码:2 / 9
页数:8
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