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首页> 外文期刊>Materials science & engineering >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:将纤维二糖脱氢酶和脱氧核糖核酸酶I共同固定在壳聚糖纳米颗粒上,针对同时针对生物膜基质和微生物的真菌/细菌微生物生物膜

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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:与微生物生物膜有关的感染已成为卫生保健的主要威胁。在这项研究中,纤维二糖脱氢酶(CDH)和脱氧核糖核酸酶I(DNase)共同固定在带正电荷的壳聚糖纳米颗粒(CSNPs)上,从而产生了针对生物膜基质和微生物的双功能纳米颗粒(CSNP-DNase-CDH)。评估了CSNPs对白色念珠菌和金黄色葡萄球菌的单微生物和多微生物生物膜的体外抗生物膜活性。结果表明,CSNPs能够穿透生物膜的基质并干扰嵌入的微生物细胞。与仅装载DNase或CDH的CSNP相比,CSNP-DNase-CDH在抑制单微生物和多微生物生物膜形成以及破坏预先形成的生物膜方面表现出更高的活性。此外,CSNP-DNase-CDH可以通过降解eDNA破坏生物膜的形成,降低生物膜的厚度,并杀死有机硅上的微生物细胞。双功能CSNP适用于保护医疗器械免受微生物生物膜的侵害或治疗与器械相关的感染。

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