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壳聚糖基水凝胶的制备及其在创伤愈合中的应用。

Enhancement of Inhibition of the sp. Biofilm Formation on Bacterial Cellulose-Based Wound Dressing by the Combined Action of Alginate Lyase and Gentamicin.

机构信息

Department of Microbiology and Biotechnology, Faculty of Biotechnology and Animal Husbandry, West Pomeranian University of Technology in Szczecin, 45 Piastów Avenue, 71-311 Szczecin, Poland.

Department of Laboratory Medicine, Pomeranian Medical University in Szczecin, Powstańców Wielkopolskich 72, 70-111 Szczecin, Poland.

出版信息

Int J Mol Sci. 2023 Mar 1;24(5):4740. doi: 10.3390/ijms24054740.

Abstract

Bacterial biofilms generally contribute to chronic infections, including wound infections. Due to the antibiotic resistance mechanisms protecting bacteria living in the biofilm, they are a serious problem in the wound healing process. To accelerate the wound healing process and avoid bacterial infection, it is necessary to select the appropriate dressing material. In this study, the promising therapeutic properties of alginate lyase (AlgL) immobilised on BC membranes for protecting wounds from infection were investigated. The AlgL was immobilised on never dried BC pellicles via physical adsorption. The maximum adsorption capacity of AlgL was 6.0 mg/g of dry BC, and the equilibrium was reached after 2 h. The adsorption kinetics was studied, and it has been proven that the adsorption was consistent with Langmuir isotherm. In addition, the impact of enzyme immobilisation on bacterial biofilm stability and the effect of simultaneous immobilisation of AlgL and gentamicin on the viability of bacterial cells was investigated. The obtained results showed that the AlgL immobilisation significantly reduced the amount of polysaccharides component of the biofilm. Moreover, the biofilm disruption by AlgL immobilised on BC membranes exhibited synergism with the gentamicin, resulting in 86.5% more dead PAO-1 cells.

摘要

细菌生物膜通常会导致慢性感染,包括伤口感染。由于保护生活在生物膜中的细菌的抗生素耐药机制,它们是伤口愈合过程中的一个严重问题。为了加速伤口愈合过程并避免细菌感染,有必要选择合适的敷料材料。在这项研究中,研究了固定在 BC 膜上的海藻酸盐裂解酶 (AlgL) 用于保护伤口免受感染的有前途的治疗特性。AlgL 通过物理吸附固定在从未干燥的 BC 膜上。AlgL 的最大吸附容量为 6.0mg/g 干燥的 BC,2 小时后达到平衡。研究了吸附动力学,证明吸附符合朗缪尔等温线。此外,还研究了酶固定化对细菌生物膜稳定性的影响以及同时固定 AlgL 和庆大霉素对细菌细胞活力的影响。所得结果表明,AlgL 固定化显著降低了生物膜中多糖成分的含量。此外,BC 膜上固定的 AlgL 对生物膜的破坏与庆大霉素表现出协同作用,导致 PAO-1 细胞死亡 86.5%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf0f/10002595/062aabc343b6/ijms-24-04740-g001.jpg

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