Towards Robust Delivery of Antimicrobial Peptides to Combat Bacterial Resistance
- PMID: 32635310
- PMCID: PMC7412191
- DOI: 10.3390/molecules25133048
Towards Robust Delivery of Antimicrobial Peptides to Combat Bacterial Resistance
Abstract
Antimicrobial peptides (AMPs), otherwise known as host defence peptides (HDPs), are naturally occurring biomolecules expressed by a large array of species across the phylogenetic kingdoms. They have great potential to combat microbial infections by directly killing or inhibiting bacterial activity and/or by modulating the immune response of the host. Due to their multimodal properties, broad spectrum activity, and minimal resistance generation, these peptides have emerged as a promising response to the rapidly concerning problem of multidrug resistance (MDR). However, their therapeutic efficacy is limited by a number of factors, including rapid degradation, systemic toxicity, and low bioavailability. As such, many strategies have been developed to mitigate these limitations, such as peptide modification and delivery vehicle conjugation/encapsulation. Oftentimes, however, particularly in the case of the latter, this can hinder the activity of the parent AMP. Here, we review current delivery strategies used for AMP formulation, focusing on methodologies utilized for _targeted infection site release of AMPs. This specificity unites the improved biocompatibility of the delivery vehicle with the unhindered activity of the free AMP, providing a promising means to effectively translate AMP therapy into clinical practice.
Keywords: antimicrobial peptide (AMP); bioconjugation; delivery vehicles; encapsulation; multidrug resistance (MDR).
Conflict of interest statement
The authors declare no conflict of interest.
Figures
Similar articles
-
Anti-bacterial activity of inorganic nanomaterials and their antimicrobial peptide conjugates against resistant and non-resistant pathogens.Int J Pharm. 2020 Aug 30;586:119531. doi: 10.1016/j.ijpharm.2020.119531. Epub 2020 Jun 12. Int J Pharm. 2020. PMID: 32540348 Review.
-
Rediscovery of antimicrobial peptides as therapeutic agents.J Microbiol. 2021 Feb;59(2):113-123. doi: 10.1007/s12275-021-0649-z. Epub 2021 Feb 1. J Microbiol. 2021. PMID: 33527313 Review.
-
Lipidation of Antimicrobial Peptides as a Design Strategy for Future Alternatives to Antibiotics.Int J Mol Sci. 2020 Dec 18;21(24):9692. doi: 10.3390/ijms21249692. Int J Mol Sci. 2020. PMID: 33353161 Free PMC article. Review.
-
Host Defense Peptides: Dual Antimicrobial and Immunomodulatory Action.Int J Mol Sci. 2021 Oct 16;22(20):11172. doi: 10.3390/ijms222011172. Int J Mol Sci. 2021. PMID: 34681833 Free PMC article. Review.
-
Topical antimicrobial peptide formulations for wound healing: Current developments and future prospects.Acta Biomater. 2020 Feb;103:52-67. doi: 10.1016/j.actbio.2019.12.025. Epub 2019 Dec 23. Acta Biomater. 2020. PMID: 31874224 Review.
Cited by
-
Advancements in antimicrobial nanoscale materials and self-assembling systems.Chem Soc Rev. 2022 Oct 17;51(20):8696-8755. doi: 10.1039/d1cs00915j. Chem Soc Rev. 2022. PMID: 36190355 Free PMC article. Review.
-
A Novel Dimeric Short Peptide Derived from α-Defensin-Related Rattusin with Improved Antimicrobial and DNA-Binding Activities.Biomolecules. 2024 Jun 5;14(6):659. doi: 10.3390/biom14060659. Biomolecules. 2024. PMID: 38927062 Free PMC article.
-
_targeting Multidrug Resistance With Antimicrobial Peptide-Decorated Nanoparticles and Polymers.Front Microbiol. 2022 Mar 31;13:831655. doi: 10.3389/fmicb.2022.831655. eCollection 2022. Front Microbiol. 2022. PMID: 35432230 Free PMC article. Review.
-
Polymeric Nanomaterials for Efficient Delivery of Antimicrobial Agents.Pharmaceutics. 2021 Dec 7;13(12):2108. doi: 10.3390/pharmaceutics13122108. Pharmaceutics. 2021. PMID: 34959388 Free PMC article. Review.
-
Improving the biocompatibility and antibacterial efficacy of silver nanoparticles functionalized with (LLRR)3 antimicrobial peptide.World J Microbiol Biotechnol. 2023 Nov 4;40(1):1. doi: 10.1007/s11274-023-03792-0. World J Microbiol Biotechnol. 2023. PMID: 37923918
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials