Peptide Targeted Lipid Nanoparticles for Anticancer Drug Delivery

被引:164
作者
Pearce, Timothy R. [2 ]
Shroff, Kamlesh [1 ]
Kokkoli, Efrosini [1 ]
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Biomed Engn, Minneapolis, MN 55455 USA
关键词
peptides; lipid nanoparticles; liposomes; cancer; drug delivery; FIBRONECTIN-MIMETIC PEPTIDE; CELL-ADHESION MOLECULE; CANCER-CELLS; IN-VITRO; BREAST-CANCER; INTRACELLULAR DELIVERY; LIPOSOMAL DOXORUBICIN; THERAPEUTIC-EFFICACY; PEGYLATED LIPOSOMES; LOADED LIPOSOMES;
D O I
10.1002/adma.201200832
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Encapsulating anticancer drugs in nanoparticles has proven to be an effective mechanism to alter the pharmacokinetic and pharmacodynamic profiles of the drugs, leading to clinically useful cancer therapeutics like Doxil and DaunoXome. Underdeveloped tumor vasculature and lymphatics allow these first-generation nanoparticles to passively accumulate within the tumor, but work to create the next-generation nanoparticles that actively participate in the tumor targeting process is underway. Lipid nanoparticles functionalized with targeting peptides are among the most often studied. The goal of this article is to review the recently published literature of targeted nanoparticles to highlight successful designs that improved in vivo tumor therapy, and to discuss the current challenges of designing these nanoparticles for effective in vivo performance.
引用
收藏
页码:3803 / 3822
页数:20
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