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用于治疗慢性伤口感染的生物膜靶向抗菌伤口敷料的研发。

Development of biofilm-targeted antimicrobial wound dressing for the treatment of chronic wound infections.

作者信息

Ng Shiow-Fern, Leow Hon-Lunn

机构信息

a Faculty of Pharmacy , Centre for Drug Delivery Research, Universiti Kebangsaan Malaysia , Kuala Lumpur , Malaysia.

出版信息

Drug Dev Ind Pharm. 2015;41(11):1902-9. doi: 10.3109/03639045.2015.1019888. Epub 2015 Mar 11.

Abstract

It has been established that microbial biofilms are largely responsible for the recalcitrance of many wound infections to conventional antibiotics. It was proposed that the efficacy of antibiotics could be optimized via the inhibition of bacterial biofilm growth in wounds. The combination of antibiofilm agent and antibiotics into a wound dressing may be a plausible strategy in wound infection management. Xylitol is an antibiofilm agent that has been shown to inhibit the biofilm formation. The purpose of this study was to develop an alginate film containing xylitol and gentamicin for the treatment of wound infection. Three films, i.e. blank alginate film (SA), alginate film with xylitol (F5) and alginate film with xylitol and gentamicin (AG), were prepared. The films were studied for their physical properties, swelling ratio, moisture absorption, moisture vapor transmission rate (MVTR), mechanical and rheology properties, drug content uniformity as well as in vitro drug release properties. Antimicrobial and antibiofilm in vitro studies on Staphylococcus aureus and Pseudomonas aeruginosa were also performed. The results showed that AG demonstrates superior mechanical properties, rheological properties and a higher MVTR compared with SA and F5. The drug flux of AG was higher than that of commercial gentamicin cream. Furthermore, antimicrobial studies showed that AG is effective against both S. aureus and P. aeruginosa, and the antibiofilm assays demonstrated that the combination was effective against biofilm bacteria. In summary, alginate films containing xylitol and gentamicin may potentially be used as new dressings for the treatment of wound infection.

摘要

已经证实,微生物生物膜在很大程度上导致了许多伤口感染对传统抗生素具有耐药性。有人提出,通过抑制伤口中细菌生物膜的生长,可以优化抗生素的疗效。将抗生物膜剂和抗生素组合到伤口敷料中可能是伤口感染管理中的一种可行策略。木糖醇是一种已被证明能抑制生物膜形成的抗生物膜剂。本研究的目的是开发一种含有木糖醇和庆大霉素的藻酸盐膜用于治疗伤口感染。制备了三种膜,即空白藻酸盐膜(SA)、含木糖醇的藻酸盐膜(F5)和含木糖醇和庆大霉素的藻酸盐膜(AG)。对这些膜的物理性质、膨胀率、吸湿性、透湿率(MVTR)、机械和流变学性质、药物含量均匀性以及体外药物释放性质进行了研究。还对金黄色葡萄球菌和铜绿假单胞菌进行了体外抗菌和抗生物膜研究。结果表明,与SA和F5相比,AG表现出优异的机械性能、流变学性能和更高的MVTR。AG的药物通量高于市售庆大霉素乳膏。此外,抗菌研究表明AG对金黄色葡萄球菌和铜绿假单胞菌均有效,抗生物膜试验表明该组合对生物膜细菌有效。总之,含有木糖醇和庆大霉素的藻酸盐膜可能潜在地用作治疗伤口感染的新型敷料。

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