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Cited by 220

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

Peptides for nucleic acid delivery

Open access
Lehto, Taavi, Ezzat, Kariem, Wood, Matthew J.A., EL Andaloussi, Samir·2016·Advanced Drug Delivery Reviews

Abstract

Nucleic acids and their synthetic oligonucleotide (ON) analogs are a group of gene therapeutic compounds which hold enormous clinical potential. Despite their undoubted potential, clinical translation of these molecules, however, has been largely held back by their limited bioavailability in the target tissues/cells. To overcome this, many different drug delivery systems have been devised. Among others, short delivery peptides, called cell-penetrating peptides (CPPs), have been demonstrated to allow for efficient delivery of nucleic acids and their ON analogs, in both cell culture and animal models. In this review, we provide brief overview of the latest advances in nucleic acid delivery with CPPs, covering the two main vectorization strategies, covalent conjugation and nanoparticle formation-based approach. In conclusion, CPP-based drug delivery systems have the capacity to overcome the hurdle of delivery and thus have the potential to facilitate the clinical translation of nucleic acid-based therapeutics.

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Metadata

Authors
Lehto, T., Ezzat, K., Wood, M. J. A., & EL Andaloussi, S.
Venue
Advanced Drug Delivery Reviews
Publisher
Elsevier BV
Published
2016-11
Volume
106
Issue
Pt A
Pages
172-182
ISSN
0169-409X (ISSN-L)
OpenAlex
W2467743933
Cited by
220
References
6
FWCI
2.03
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Peptides for nucleic acid delivery. https://app.cochat.ai/papers/10.1016/j.addr.2016.06.008
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Lehto, T., Ezzat, K., Wood, M. J. A., & EL Andaloussi, S. (2016). Peptides for nucleic acid delivery. Advanced Drug Delivery Reviews. https://doi.org/10.1016/j.addr.2016.06.008

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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