Injected nanocrystals for targeted drug delivery

被引:142
作者
Lu, Yi [1 ]
Li, Ye [2 ]
Wu, Wei [1 ]
机构
[1] Fudan Univ, Sch Pharm, Dept Pharmaceut, Shanghai 201203, Peoples R China
[2] Shaanxi Acad Tradit Chinese Med, Xian 710003, Peoples R China
关键词
Nanocrystals; Targeted drug delivery; Biodistribution; Ligand; Stimuli response; Encapsulation; POORLY SOLUBLE DRUGS; PARTICLE ENGINEERING TECHNOLOGY; HYBRID PACLITAXEL NANOCRYSTALS; IN-VIVO EVALUATION; NEVIRAPINE NANOSUSPENSIONS; ANTISOLVENT PRECIPITATION; NUCLEATION KINETICS; ENHANCE DISSOLUTION; TISSUE DISTRIBUTION; INSOLUBLE DRUG;
D O I
10.1016/j.apsb.2015.11.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nanocrystals are pure drug crystals with sizes in the nanometer range. Due to the advantages of high drug loading, platform stability, and ease of scaling-up, nanocrystals have been widely used to deliver poorly water-soluble drugs. Nanocrystals in the blood stream can be recognized and sequestered as exogenous materials by mononuclear phagocytic system (MPS) cells, leading to passive accumulation in MPS-rich organs, such as liver, spleen and lung. Particle size, morphology and surface modification affect the biodistribution of nanocrystals. Ligand conjugation and stimuli-responsive polymers can also be used to target nanocrystals to specific pathogenic sites. In this review, the progress on injected nanocrystals for targeted drug delivery is discussed following a brief introduction to nanocrystal preparation methods, i.e., top-down and bottom-up technologies. (C) 2016 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:106 / 113
页数:8
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