Functional peptide-based nanoparticles for photodynamic therapy

被引:58
作者
Han, Kai [1 ]
Ma, Zhaoyu [1 ]
Han, Heyou [1 ]
机构
[1] Huazhong Agr Univ, Coll Sci, Biomed Ctr, State Key Lab Agr Microbiol, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
AGGREGATION-INDUCED EMISSION; MESOPOROUS SILICA NANOPARTICLES; FIBROBLAST-ACTIVATION PROTEIN; TARGETED CHIMERIC PEPTIDE; IRON-OXIDE NANOPARTICLES; DRUG-DELIVERY; TUMOR MICROENVIRONMENT; IN-VITRO; ENHANCED PERMEABILITY; CHARGE-REVERSAL;
D O I
10.1039/c7tb02804k
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Photodynamic therapy as a non-invasive approach has obtained great research attention during the last decade. However, photodynamic therapy still suffers from low tumor selectivity and therapeutic inefficacy due to the unspecific distribution of photosensitizers in normal tissues/cells. To overcome these hurdles, functional peptides have been introduced in photodynamic therapy systems due to their advantages of functional diversity, bioactivity, high biocompatibility and biodegradability. Herein, we review various peptide-based self-assemblies or hybrid nanoparticles that have already been reported to achieve tumor tissue, cell or subcellular organelle targeted photodynamic therapy. The role of tumor microenvironments, cellular/subcellular location, and physical/chemical properties of peptide-based nanoparticles in facilitating the photodynamic therapy efficiency are discussed in-depth. The novel development of peptide-based nanoparticles described here should offer great potential to achieve better photodynamic therapy in tumors.
引用
收藏
页码:25 / 38
页数:14
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