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dc.contributor.authorFarkhani, SM
dc.contributor.authorValizadeh, A
dc.contributor.authorKarami, H
dc.contributor.authorMohammadi, S
dc.contributor.authorSohrabi, N
dc.contributor.authorBadrzadeh, F
dc.date.accessioned2018-08-26T06:05:06Z
dc.date.available2018-08-26T06:05:06Z
dc.date.issued2014
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41674
dc.description.abstractEfficient 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.
dc.language.isoEnglish
dc.relation.ispartofPeptides
dc.subjectBiological Transport
dc.subjectCell-Penetrating Peptides
dc.subjectDrug Delivery Systems
dc.subjectEndosomes
dc.subjectGenetic Vectors
dc.subjectHumans
dc.subjectNanoparticles
dc.subjectNeoplasms
dc.subjectRNA, Small Interfering
dc.titleCell penetrating peptides: efficient vectors for delivery of nanoparticles, nanocarriers, therapeutic and diagnostic molecules.
dc.typearticle
dc.citation.volume57
dc.citation.spage78
dc.citation.epage94
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1016/j.peptides.2014.04.015


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