Cell penetrating peptides: Efficient vectors for delivery of nanoparticles, nanocarriers, therapeutic and diagnostic molecules

被引:214
|
作者
Farkhani, Samad Mussa [1 ,5 ]
Valizadeh, Alireza [1 ]
Karami, Hadi [2 ]
Mohammadi, Samane [1 ]
Sohrabi, Nasrin [3 ]
Badrzadeh, Fariba [4 ]
机构
[1] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Med Nanotechnol, Tabriz 51664, Iran
[2] Arak Univ Med Sci, Dept Med Biotechnol, Fac Med, Sardasht 38481, Arak, Iran
[3] Tabriz Univ Med Sci, Dept Med Genet, Fac Med, Tabriz 51664, Iran
[4] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Med Biotechnol, Tabriz 51664, Iran
[5] Tabriz Univ Med Sci, Res Ctr Pharmaceut Nanotechnol, Tabriz 51664, Iran
关键词
Cell penetrating peptides; Drug delivery; Endosomal escape; Nanocarrier; Nanoparticle; Gene delivery; BLOOD-BRAIN-BARRIER; ARGININE-RICH PEPTIDES; PEG-PLA NANOPARTICLES; MESOPOROUS SILICA NANOPARTICLES; OVERCOMING MULTIDRUG-RESISTANCE; ANTICANCER DRUG-DELIVERY; IRON-OXIDE NANOPARTICLES; CONJUGATED QUANTUM DOTS; MESENCHYMAL STEM-CELLS; TAT-PEPTIDE;
D O I
10.1016/j.peptides.2014.04.015
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
Efficient delivery of therapeutic and diagnostic molecules to the cells and tissues is a difficult challenge. The cellular membrane is very effective in its role as a selectively permeable barrier. While it is essential for cell survival and function, also presents a major barrier for intracellular delivery of cargo such as therapeutic and diagnostic agents. In recent years, cell-penetrating peptides (CPPs), that are relatively short cationic and/or amphipathic peptides, received great attention as efficient cellular delivery vectors due to their intrinsic ability to enter cells and mediate uptake of a wide range of macromolecular cargo such as plasmid DNA (pDNA), small interfering RNA (siRNAs), drugs, and nanoparticulate pharmaceutical carriers. This review discusses the various uptake mechanisms of these peptides. Furthermore, we discuss recent advances in the use of CPP for the efficient delivery of nanoparticles, nanocarriers, DNA, siRNA, and anticancer drugs to the cells. In addition, we have been highlighting new results for improving endosomal escape of CPP-cargo molecules. Finally, pH-responsive and activable CPPs for tumor-targeting therapy have been described. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:78 / 94
页数:17
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