Antimicrobial Peptides and Antimicrobial Nanomaterials in Biomedicine

A special issue of Pharmaceutics (ISSN 1999-4923). This special issue belongs to the section "Nanomedicine and Nanotechnology".

Deadline for manuscript submissions: closed (20 September 2023) | Viewed by 2988

Special Issue Editor


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Guest Editor
i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal
Interests: bioengineering; nanotechnology; medical biotechnology; biomaterials; biological sciences; microbiology; antimicrobial drugs; non-antibiotic therapeutics; treatment of bacterial infections; gastric infection; gut microbiome

Special Issue Information

Dear Colleagues,

The development of antibiotics is one of the greatest medical achievements of the 20th Century, saving countless lives. However, as the use of these drugs increased, so did bacterial resistance. Antibiotic resistance is growing faster than it was expected to, being considered a main public health challenge and one of the biggest threats to global health and development.

Using antimicrobial peptides (AMPs) and antimicrobial nanomaterials is an excellent strategy to overcome this problem.

AMPs have a large spectrum of activity and low propensity to induce bacteria resistance. Nonetheless, their in vivo performance may be affected as they tend to self-aggregate and undergo enzymatic degradation, which often leads to toxicity issues, and high concentrations are then required to solve these. The key this dilemma may dwell in their immobilization on biomaterials.

Over the last few decades, biomedical research has largely benefited from advances in nanotechnology. A broad range of nanomaterials, besides those functionalized with AMPs (e.g., micelles, liposomes nanocomposites, and nanoemulsions), have excellent antimicrobial properties, providing more benefits than traditional antibiotics do in terms of countering the microbial resistance mechanisms. Additionally, nanomaterials have remarkable features for targeted drug-delivery.

Altogether, this bioengineered approach may allow researchers to simultaneously tackle antimicrobial resistance and enhance the performance of conventional drugs.

Authors are kindly invited to submit original papers, communications, and reviews regarding the potential of Antimicrobial Peptides and Antimicrobial Nanomaterials to be published in this Special Issue of Pharmaceutics.

Dr. Paula Parreira
Guest Editor

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Published Papers (2 papers)

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Research

19 pages, 6521 KiB  
Article
Matrix-Mediated Delivery of Silver Nanoparticles for Prevention of Staphylococcus aureus and Pseudomonas aeruginosa Biofilm Formation in Chronic Rhinosinusitis
by Bhuvanesh Yathavan, Tanya Chhibber, Douglas Steinhauff, Abigail Pulsipher, Jeremiah A. Alt, Hamidreza Ghandehari and Paris Jafari
Pharmaceutics 2023, 15(10), 2426; https://doi.org/10.3390/pharmaceutics15102426 - 05 Oct 2023
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Abstract
Chronic rhinosinusitis (CRS) is a chronic health condition affecting the sinonasal cavity. CRS-associated mucosal inflammation leads to sinonasal epithelial cell death and epithelial cell barrier disruption, which may result in recurrent bacterial infections and biofilm formation. For patients who fail medical management and [...] Read more.
Chronic rhinosinusitis (CRS) is a chronic health condition affecting the sinonasal cavity. CRS-associated mucosal inflammation leads to sinonasal epithelial cell death and epithelial cell barrier disruption, which may result in recurrent bacterial infections and biofilm formation. For patients who fail medical management and elect endoscopic sinus surgery for disease control, bacterial biofilm formation is particularly detrimental, as it reduces the efficacy of surgical intervention. Effective treatments that prevent biofilm formation in post-operative patients in CRS are currently limited. To address this unmet need, we report the controlled release of silver nanoparticles (AgNps) with silk-elastinlike protein-based polymers (SELPs) to prevent bacterial biofilm formation in CRS. This polymeric network is liquid at room temperature and forms a hydrogel at body temperature, and is hence, capable of conforming to the sinonasal cavity upon administration. SELP hydrogels demonstrated sustained AgNp and silver ion release for the studied period of three days, potent in vitro antibacterial activity against Pseudomonas aeruginosa (**** p < 0.0001) and Staphylococcus aureus (**** p < 0.0001), two of the most commonly virulent bacterial strains observed in patients with post-operative CRS, and high cytocompatibility with human nasal epithelial cells. Antibacterial controlled release platform shows promise for treating patients suffering from prolonged sinonasal cavity infections due to biofilms. Full article
(This article belongs to the Special Issue Antimicrobial Peptides and Antimicrobial Nanomaterials in Biomedicine)
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19 pages, 3908 KiB  
Article
Influence of Immobilization Strategies on the Antibacterial Properties of Antimicrobial Peptide-Chitosan Coatings
by Mariana Barbosa, Pedro M. Alves, Fabíola Costa, Cláudia Monteiro, Paula Parreira, Cátia Teixeira, Paula Gomes and Maria Cristina L. Martins
Pharmaceutics 2023, 15(5), 1510; https://doi.org/10.3390/pharmaceutics15051510 - 16 May 2023
Cited by 1 | Viewed by 1562
Abstract
It is key to fight bacterial adhesion to prevent biofilm establishment on biomaterials. Surface immobilization of antimicrobial peptides (AMP) is a promising strategy to avoid bacterial colonization. This work aimed to investigate whether the direct surface immobilization of Dhvar5, an AMP with head-to-tail [...] Read more.
It is key to fight bacterial adhesion to prevent biofilm establishment on biomaterials. Surface immobilization of antimicrobial peptides (AMP) is a promising strategy to avoid bacterial colonization. This work aimed to investigate whether the direct surface immobilization of Dhvar5, an AMP with head-to-tail amphipathicity, would improve the antimicrobial activity of chitosan ultrathin coatings. The peptide was grafted by copper-catalyzed azide-alkyne cycloaddition (CuAAC) chemistry by either its C- or N- terminus to assess the influence of peptide orientation on surface properties and antimicrobial activity. These features were compared with those of coatings fabricated using previously described Dhvar5-chitosan conjugates (immobilized in bulk). The peptide was chemoselectively immobilized onto the coating by both termini. Moreover, the covalent immobilization of Dhvar5 by either terminus enhanced the antimicrobial effect of the chitosan coating by decreasing colonization by both Gram-positive (Staphylococcus aureus, Staphylococcus epidermidis) and Gram-negative (Escherichia coli, Pseudomonas aeruginosa) bacteria. Relevantly, the antimicrobial performance of the surface on Gram-positive bacteria depended on how Dhvar5-chitosan coatings were produced. An antiadhesive effect was observed when the peptide was grafted onto prefabricated chitosan coatings (film), and a bactericidal effect was exhibited when coatings were prepared from Dhvar5-chitosan conjugates (bulk). This antiadhesive effect was not due to changes in surface wettability or protein adsorption but rather depended on variations in peptide concentration, exposure, and surface roughness. Results reported in this study show that the antibacterial potency and effect of immobilized AMP vary greatly with the immobilization procedure. Overall, independently of the fabrication protocol and mechanism of action, Dhvar5-chitosan coatings are a promising strategy for the development of antimicrobial medical devices, either as an antiadhesive or contact-killing surface. Full article
(This article belongs to the Special Issue Antimicrobial Peptides and Antimicrobial Nanomaterials in Biomedicine)
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