Dendritic Nanogels Directed Dual‐Encapsulation Topical Delivery System of Antimicrobial Peptides Targeting Skin Infections

Author:

Zhang Yuning12,Håkansson Joakim34,Fan Yanmiao1,Andrén Oliver C. J.1,San Jacinto García Jorge1,Qin Liguo15,Umerska Anita3,Hutchinson Daniel J.1,Lüchow Mads1,Mahlapuu Margit6,Malkoch Michael1ORCID

Affiliation:

1. Department of Fibre and Polymer Technology KTH Royal Institute of Technology Stockholm SE‐100 44 Sweden

2. Key Laboratory of Organ Regeneration and Transplantation of Ministry of Education, Institute of Immunology, The First Hospital Jilin University Changchun 130061 P. R. China

3. Biological Function Unit RISE Research Institutes of Sweden, Methodology, Textile and Medical Devices Borås SE‐501 15 Sweden

4. Department of Laboratory Medicine, Institute of Biomedicine University of Gothenburg P.O. Box 440 Gothenburg SE‐40530 Sweden

5. Institute of Design Science and Basic Components, School of Mechanical Engineering Xi'an Jiaotong University Xi'an 710049 P. R. China

6. Promore Pharma AB Solna SE‐171 65 Sweden

Abstract

AbstractAntimicrobial peptides (AMPs) are promising antibacterial agents in the fight against multidrug resistant pathogens. However, their application to skin infections is limited by the absence of a realizable topical delivery strategy. Herein, a hybrid hierarchical delivery system for topical delivery of AMPs is accomplished through the incorporation of AMPs into dendritic nanogels (DNGs) and their subsequent embedding into poloxamer gel. The high level of control over the crosslink density and the number of chosen functionalities makes DNGs ideal capsules with tunable loading capacity for DPK‐060, a human kininogen‐derived AMP. Once embedded into the poloxamer gel, DPK‐060 encapsulated in DNGs displays a slower release rate compared to those entrapped directly in the gels. In vitro EpiDerm Skin Irritation Tests show good biocompatibility, while MIC and time‐kill curves reveal the potency of the peptide toward Staphylococcus aureus. Anti‐infection tests on ex vivo pig skin and in vivo mouse infection models demonstrate that formulations with 0.5% and 1% AMPs significantly inhibit the growth of S. aureus. Similar outcomes are observed for an in vivo mouse surgical site infection model. Importantly, when normalizing the bacteria inhibition to released/free DPK‐060 at the wound site, all formulations display superior efficacy compared to DPK‐060 in solution.

Funder

Seventh Framework Programme

Barncancerfonden

Publisher

Wiley

Subject

Materials Chemistry,Polymers and Plastics,Biomaterials,Bioengineering,Biotechnology

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