TY - JOUR
T1 - Dendritic Nanogels Directed Dual-Encapsulation Topical Delivery System of Antimicrobial Peptides Targeting Skin Infections
AU - Zhang, Yuning
AU - Håkansson, Joakim
AU - Fan, Yanmiao
AU - Andrén, Oliver C.J.
AU - San Jacinto García, Jorge
AU - Qin, Liguo
AU - Umerska, Anita
AU - Hutchinson, Daniel J.
AU - Lüchow, Mads
AU - Mahlapuu, Margit
AU - Malkoch, Michael
N1 - Publisher Copyright:
© 2023 The Authors. Macromolecular Bioscience published by Wiley-VCH GmbH.
PY - 2023/4
Y1 - 2023/4
N2 - Antimicrobial 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.
AB - Antimicrobial 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.
KW - DPK-060
KW - antimicrobial peptide delivery
KW - dendritic nanogels
KW - poloxamer gels
UR - https://www.scopus.com/pages/publications/85146683018
U2 - 10.1002/mabi.202200433
DO - 10.1002/mabi.202200433
M3 - 文章
C2 - 36639138
AN - SCOPUS:85146683018
SN - 1616-5187
VL - 23
JO - Macromolecular Bioscience
JF - Macromolecular Bioscience
IS - 4
M1 - 2200433
ER -