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首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >Co-immobilization of cellobiose dehydrogenase and deoxyribonuclease I on chitosan nanoparticles against fungal/bacterial polymicrobial biofilms targeting both biofilm matrix and microorganisms.
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Co-immobilization of cellobiose dehydrogenase and deoxyribonuclease I on chitosan nanoparticles against fungal/bacterial polymicrobial biofilms targeting both biofilm matrix and microorganisms.

机译:对壳聚糖纳米粒子对针对生物膜基质和微生物靶向壳聚糖纳米粒子的Celobiose脱氢酶和脱氧糖核酸酶的共固定。

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摘要

Polymicrobial biofilm related infections have been a major threat in health care. In this study, the co-immobilization of cellobiose dehydrogenase (CDH) and deoxyribonuclease I (DNase) on positively charged chitosan nanoparticles (CSNPs) resulted in a bi-functional nanoparticle (CSNP-DNase-CDH) targeting both biofilm matrix and microorganisms. The in-vitro antibiofilm activities of CSNPs against monomicrobial and polymicrobial biofilms of Candida albicans and Staphylococcus aureus were evaluated. The results showed that CSNPs were able to penetrate across the matrix of biofilms and interfere with embedded microbial cells. CSNP-DNase-CDH exhibited a higher activity than CSNPs loaded with only DNase or CDH for inhibiting monomicrobial and polymicrobial biofilm formation as well as for disrupting pre-formed biofilms. Furthermore, CSNP-DNase-CDH could disrupt the biofilm formation through degradation of eDNA, reduce biofilm thickness, and kill microbial cells on silicone. The bi-functional CSNP is applicable for the protection of medical devices from polymicrobial biofilms or the treatment of device associated infections.
机译:多发性生物膜相关感染是医疗保健的主要威胁。在该研究中,纤维二糖脱氢酶(CDH)和脱氧氧脲核酸酶I(DNase)的共固化在带正电带电的壳聚糖纳米粒子(CSNP)中导致靶向生物膜基质和微生物的双官能纳米颗粒(CSNP-DNase-CDH)。评估了CSNP对单体癌和金黄色葡萄球菌的单体细胞和金黄色葡萄球菌的体外抗菌菌活性。结果表明,CSNP能够穿过生物膜的基质并干扰嵌入的微生物细胞。 CSNP-DNase-CDH表现出比仅由DNA酶或CDH的CSNPS的活性呈现更高的活性,用于抑制单体血管和多种细胞生物膜形成以及破坏预形成的生物膜。此外,CSNP-DNase-CDH可以通过edna的降解来破坏生物膜形成,降低生物膜厚度,并在硅氧烷上杀死微生物细胞。双功能CSNP适用于保护来自多发性生物膜的医疗装置或治疗装置相关感染。

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