Liposomal Nanotechnology for Cancer Theranostics

被引:47
作者
Yue, Xiuli [1 ]
Dai, Zhifei [2 ]
机构
[1] Harbin Inst Technol, Sch Municipal & Environm Engn, Harbin 150001, Heilongjiang, Peoples R China
[2] Peking Univ, Coll Engn, Dept Biomed Engn, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
Liposomes; cerasomes; cancer theranostics; drug delivery; contrast enhanced imaging; drug nanocarrier; TEMPERATURE-SENSITIVE LIPOSOMES; IN-VIVO PHARMACOKINETICS; CONTROLLED DRUG-RELEASE; PHOTODYNAMIC-THERAPY; NANOHYBRID CERASOMES; ENCAPSULATING DOXORUBICIN; PHOTOTHERMAL THERAPY; QUANTUM DOTS; NANOPARTICLES; PORPHYRIN;
D O I
10.2174/0929867324666170306105350
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
Liposomes are a type of biomimetic nanoparticles generated from self-assembling concentric lipid bilayer enclosing an aqueous core domain. They have been attractive nano-carriers for the delivery of many drugs (e.g. radiopharmaceuticals, chemotherapeutic agents, porphyrin) and diagnostic agents (e.g. fluorescent dyes, quantum dots, Gadolinium complex and Fe3O4) by encapsulating (or adsorbing) hydrophilic one inside the liposomal aqueous core domain (or on the bilayer membrane surface), and by entrapping hydrophobic one within the liposomal bilayer. Additionally, the liposome surface can be easily conjugated with targeting molecules. Liposomes may accumulate in cancerous tissues not only passively via enhanced permeability and retention (EPR) effect, but also actively by targeting cancer cell or angiogenic marker specifically. The multimodality imaging functionalization of liposomal therapeutic agents makes them highly attractive for individualized monitoring of the in vivo cancer targeting and pharmacokinetics of liposomes loading therapeutic drugs, and predicting therapeutic efficacy in combination with the helpful information from each imaging technique. The present review article will highlight some main advances of cancer theranostic liposomes with a view to activate further research in the nanomedicine community.
引用
收藏
页码:1397 / 1408
页数:12
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