Activated carbon-chitosan hydrogel dressing loaded with LL37 microspheres for the treatment of infected wounds: In vivo antimicrobial and antitoxin assessment.

IF 5.5 3区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Drug Delivery and Translational Research Pub Date : 2025-11-01 Epub Date: 2025-03-22 DOI:10.1007/s13346-025-01835-7
Bee-Yee Lim, Fazren Azmi, Shiow-Fern Ng
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Abstract

Wound healing is a complex process which is crucial for recovery. Delayed wound healing which is caused by the presence of pathogens has posed significant clinical implications affecting millions of patients globally. Wounds infection caused by Pseudomonas aeruginosa present significant challenges due to their resistance to multiple antimicrobial drugs. The Gram-negative bacteria secretes endotoxin lipopolysaccharide (LPS), which impede wound healing and may lead to severe complications, including life-threatening sepsis. Previously, our laboratory has successfully developed a new hydrogel containing a synthetic antimicrobial peptide as an alternative therapy to conventional antibiotics. This hydrogel contains LL37 microspheres embedded into activated carbon-chitosan hydrogel (LL37-AC-CS). LL37-AC-CS has shown desirable physicochemical properties as well as promising antimicrobial and antitoxin activities in vitro. This current study has two main objectives. The first is to evaluate the in vivo antimicrobial efficacy of LL37-AC-CS hydrogel in full-thickness rat wounds infected with P. aeruginosa. The second objective is to investigate the antitoxin efficacy on the rat wound models treated with E. coli endotoxins LPS. The wound healing efficacy was assessed in terms of the macroscopic appearance, wound contraction rate, histology, and wound tissue biochemical markers. As a result, the LL37-AC-CS hydrogel exhibited remarkable antimicrobial and antitoxin efficacy as compared to the controls. The wound healing efficacy was evident in increased wound closure rate and decrease in bacterial bioburden, and favourable changes in wound healing biomarkers namely the myeloperoxidase, interleukin-6 and tumour necrosis factor α. The elevation of hydroxyproline levels in the LPS-treated wound model indicates there was collagen synthesis. In conclusion, the results presented in this study have significantly enhanced our comprehension of the LL37-AC-CS hydrogel's potential in wound healing. Specifically, the research highlights its effectiveness in eliminating endotoxins and preventing bacterial growth.

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负载LL37微球的活性炭-壳聚糖水凝胶敷料治疗感染伤口:体内抗菌和抗毒素评估。
伤口愈合是一个复杂的过程,对恢复至关重要。由病原体引起的伤口愈合延迟已对全球数百万患者造成重大临床影响。由于铜绿假单胞菌对多种抗菌药物具有耐药性,因此对伤口感染提出了重大挑战。革兰氏阴性菌分泌内毒素脂多糖(LPS),阻碍伤口愈合并可能导致严重并发症,包括危及生命的败血症。此前,我们的实验室已经成功开发了一种含有合成抗菌肽的新型水凝胶,作为传统抗生素的替代疗法。该水凝胶含有嵌入活性炭-壳聚糖水凝胶(LL37- ac - cs)的LL37微球。LL37-AC-CS在体外具有良好的理化性质和抗菌抗毒素活性。目前的研究有两个主要目标。首先是评价LL37-AC-CS水凝胶对铜绿假单胞菌感染大鼠全层创面的体内抗菌效果。二是探讨大肠杆菌内毒素LPS对大鼠创面模型的抗毒素作用。从宏观外观、创面收缩率、组织学、创面组织生化指标等方面评价创面愈合效果。结果表明,与对照组相比,LL37-AC-CS水凝胶具有显著的抗菌和抗毒素功效。伤口愈合效果表现为伤口愈合率的提高和细菌生物负荷的减少,以及伤口愈合生物标志物,即髓过氧化物酶、白细胞介素-6和肿瘤坏死因子α的有利变化。lps处理的创面模型中羟脯氨酸水平升高表明存在胶原合成。总之,本研究结果显著增强了我们对LL37-AC-CS水凝胶在伤口愈合中的潜力的理解。具体来说,研究强调了它在消除内毒素和防止细菌生长方面的有效性。
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来源期刊
Drug Delivery and Translational Research
Drug Delivery and Translational Research MEDICINE, RESEARCH & EXPERIMENTALPHARMACOL-PHARMACOLOGY & PHARMACY
CiteScore
11.70
自引率
1.90%
发文量
160
期刊介绍: The journal provides a unique forum for scientific publication of high-quality research that is exclusively focused on translational aspects of drug delivery. Rationally developed, effective delivery systems can potentially affect clinical outcome in different disease conditions. Research focused on the following areas of translational drug delivery research will be considered for publication in the journal. Designing and developing novel drug delivery systems, with a focus on their application to disease conditions; Preclinical and clinical data related to drug delivery systems; Drug distribution, pharmacokinetics, clearance, with drug delivery systems as compared to traditional dosing to demonstrate beneficial outcomes Short-term and long-term biocompatibility of drug delivery systems, host response; Biomaterials with growth factors for stem-cell differentiation in regenerative medicine and tissue engineering; Image-guided drug therapy, Nanomedicine; Devices for drug delivery and drug/device combination products. In addition to original full-length papers, communications, and reviews, the journal includes editorials, reports of future meetings, research highlights, and announcements pertaining to the activities of the Controlled Release Society.
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