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Cited by 1,227

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Antimicrobial Peptides: Diversity, Mechanism of Action and Strategies to Improve the Activity and Biocompatibility In Vivo

Open access
Kumar, Prashant, Kizhakkedathu, Jayachandran, Straus, Suzana·2018·Biomolecules

Abstract

Antibiotic resistance is projected as one of the greatest threats to human health in the future and hence alternatives are being explored to combat resistance. Antimicrobial peptides (AMPs) have shown great promise, because use of AMPs leads bacteria to develop no or low resistance. In this review, we discuss the diversity, history and the various mechanisms of action of AMPs. Although many AMPs have reached clinical trials, to date not many have been approved by the US Food and Drug Administration (FDA) due to issues with toxicity, protease cleavage and short half-life. Some of the recent strategies developed to improve the activity and biocompatibility of AMPs, such as chemical modifications and the use of delivery systems, are also reviewed in this article.

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Crossref · 10.3390/biom8010004

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Metadata

Authors
Kumar, P., Kizhakkedathu, J., & Straus, S.
Venue
Biomolecules
Publisher
MDPI AG
Published
2018-01-19
Volume
8
Issue
1
Pages
4
ISSN
2218-273X (ISSN-L)
OpenAlex
W2788314593
Cited by
1,227
References
6
FWCI
76.37
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Antimicrobial Peptides: Diversity, Mechanism of Action and Strategies to Improve the Activity and Biocompatibility In Vivo. https://app.cochat.ai/papers/10.3390/biom8010004
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Kumar, P., Kizhakkedathu, J., & Straus, S. (2018). Antimicrobial Peptides: Diversity, Mechanism of Action and Strategies to Improve the Activity and Biocompatibility In Vivo. Biomolecules. https://doi.org/10.3390/biom8010004

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

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

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.