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智能抗菌肽:修饰的纳米结构脂质载体可提高抗菌肽在慢性感染烧伤创面的疗效

Smart-AMPs: Decorated Nanostructured Lipid Carriers for Improved Efficacy of Antimicrobial Peptides in Chronically Infected Burn Wounds.

作者信息

Müller Daniela, Nallbati Laura, Keck Cornelia M

机构信息

Institute for Pharmaceutics and Biopharmaceutics, Philipps-Universität Marburg, Robert-Koch-Str. 4, 35037 Marburg, Germany.

出版信息

Pharmaceutics. 2025 Aug 10;17(8):1039. doi: 10.3390/pharmaceutics17081039.

DOI:10.3390/pharmaceutics17081039
PMID:40871060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12389237/
Abstract

: Burn wound infections present significant clinical challenges due to multidrug-resistant pathogens and the limitations of traditional antimicrobials. While antimicrobial peptides (AMPs) have broad-spectrum effectiveness, their instability in wound environments limits their use. This study compares properties of AMP-decorated nanostructured lipid carriers (NLCs) to free AMPs, focusing on their dermal penetration, retention, and antimicrobial efficacy in simulated ex vivo burn wound models. : AMP-decorated NLCs (smart-AMPs) were produced by electrostatic and hydrophobic surface adsorption and characterized regarding their size, zeta potential, and physical short-term stability. The distribution of AMPs within the wounds was evaluated using an ex vivo porcine ear model with various wound types. The antimicrobial efficacy was assessed by monitoring the bioluminescence of as a live bacterial marker for 24 h. : The size and zeta potential measurements confirmed the successful formation of smart-AMPs. The dermal penetration of AMPs was influenced by the type of wound and the type of AMP formulation (free AMPs vs. smart-AMPs). In the chronically infected burn wounds, which were characterized by the formation of a biofilm in a protein-rich wound fluid, the smart-AMPs resulted in a 1.5-fold higher and deeper penetration of the AMPs, and the antimicrobial activity was 6-fold higher compared to the free AMPs. : smart-AMPs present an innovative approach for treating chronic, biofilm-associated wounds more efficiently than the current treatment options.

摘要

由于多重耐药病原体和传统抗菌药物的局限性,烧伤创面感染带来了重大的临床挑战。虽然抗菌肽(AMPs)具有广谱有效性,但其在创面环境中的不稳定性限制了其应用。本研究比较了载有AMPs的纳米结构脂质载体(NLCs)与游离AMPs的特性,重点关注它们在模拟离体烧伤创面模型中的皮肤渗透、滞留和抗菌效果。通过静电和疏水表面吸附制备了载有AMPs的NLCs(智能AMPs),并对其大小、zeta电位和物理短期稳定性进行了表征。使用具有不同创面类型的离体猪耳模型评估AMPs在创面内的分布。通过监测作为活细菌标志物的生物发光24小时来评估抗菌效果。大小和zeta电位测量证实了智能AMPs的成功形成。AMPs的皮肤渗透受创面类型和AMPs制剂类型(游离AMPs与智能AMPs)的影响。在以富含蛋白质的创面液中形成生物膜为特征的慢性感染烧伤创面中,智能AMPs使AMPs的渗透提高了1.5倍且更深,抗菌活性比游离AMPs高6倍。智能AMPs提供了一种创新方法,比目前的治疗方案更有效地治疗慢性、生物膜相关创面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/2b2c53d13c5e/pharmaceutics-17-01039-g012.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/8c35fa917f92/pharmaceutics-17-01039-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/17a6090e0923/pharmaceutics-17-01039-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/f9c2166ee290/pharmaceutics-17-01039-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/1e74d4ebdcc3/pharmaceutics-17-01039-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/2b2c53d13c5e/pharmaceutics-17-01039-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/19bed3da1bed/pharmaceutics-17-01039-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/8e5d7c761944/pharmaceutics-17-01039-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/4b88f7d0fff1/pharmaceutics-17-01039-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/030b307845f8/pharmaceutics-17-01039-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/23fcb87fa80c/pharmaceutics-17-01039-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/8c35fa917f92/pharmaceutics-17-01039-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/17a6090e0923/pharmaceutics-17-01039-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/f9c2166ee290/pharmaceutics-17-01039-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/4566e990d009/pharmaceutics-17-01039-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/7f62c9936763/pharmaceutics-17-01039-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/1e74d4ebdcc3/pharmaceutics-17-01039-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2d9/12389237/2b2c53d13c5e/pharmaceutics-17-01039-g012.jpg

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