Multifunctionality of lipid-core micelles for drug delivery and tumour targeting

被引:74
|
作者
Sawant, Rupa R.
Torchilin, Vladimir P. [1 ]
机构
[1] Northeastern Univ, Dept Pharmaceut Sci, Boston, MA 02115 USA
关键词
Phospholipid micelles; cancer targeting; stimuli-sensitive nanocarriers; BLOCK-COPOLYMER MICELLES; CELL-PENETRATING PEPTIDES; BIODEGRADABLE POLYMERIC MICELLES; LEWIS LUNG-CARCINOMA; IN-VIVO EVALUATION; PEG-PE MICELLES; TAT-PEPTIDE; ANTICANCER ACTIVITY; DIBLOCK COPOLYMER; MIXED MICELLES;
D O I
10.3109/09687688.2010.516276
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
Phospholipid micelles have proven to be the versatile pharmaceutical nanocarrier of choice for the delivery of poorly soluble chemotherapeutics for cancer therapy using various treatment modalities. Phospholipid micelles are typically expected to increase the accumulation of the loaded drugs in tumour tissues by taking advantage of the enhanced permeability and retention effect and by ligand-mediated active targeting. Furthermore, by tailoring the composition of the micelles, it is possible to enhance the intracellular delivery of the cargo. This review highlights the important advancements in our laboratory with polyethyleneglycol phosphatidylethanolamine (PEG-PE)-based micellar drug delivery systems for improvement of the therapeutic efficacy of poorly soluble anticancer drugs.
引用
收藏
页码:232 / 246
页数:15
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