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Inhibition of biofilms by glucose oxidase lactoperoxidase and guaiacol: the active antibacterial component in an enzyme alginogel

机译:通过葡萄糖氧化酶乳酰氧化酶和愈菌酚的抑制生物膜:酶Alginogel中的活性抗菌组分

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摘要

The association of biofilms with wound chronicity has prompted a search for antimicrobial interventions that are effective against biofilms. A patented preparation of glucose oxidase, lactoperoxidase and guaiacol (GLG), which is the antibacterial component of Flaminal®, has been shown to inhibit a wide range of bacteria, but it has not yet been tested on biofilms. This study aims to determine the effect of GLG on biofilms of Staphylococcus aureus, methicillin‐resistant S. aureus and Pseudomonas aeruginosa. Static biofilms were grown in microtitre plates and on coverslips and treated with a range of concentrations of GLG. Effects were monitored by estimating biofilm biomass by staining with crystal violet, biofilm activity by staining with either resazurin or fluorescein diacetate and biofilm viability by staining with LIVE/DEAD® BacLight™ Bacterial Viability Kit. GLG was able to prevent the formation of biofilms at concentration ≤0·5% (w/v) and higher concentrations were required to inhibit established biofilms. GLG did not disrupt biofilm biomass. Staphylococci were more susceptible to GLG than P. aeruginosa. These in vitro findings must be verified by in vivo studies.
机译:生物膜与伤口慢性的关联促使寻找对生物膜有效的抗微生物干预措施。已经显示出专利制备葡萄糖氧化酶,乳酰氧化酶和Guaiacol(Guaiacol(Guaiacol(Guaiacol(Guaiacol),其是Flaminal®的抗菌组分,以抑制各种细菌,但尚未在生物膜上进行测试。本研究旨在确定GLG对金黄色葡萄球菌的生物膜的影响,耐甲氧胞素抗性S. aureus和假单胞菌铜绿假单胞菌。静电生物膜在微量滴定板和盖玻片上生长,并用一系列浓度的GLG处理。通过用晶体紫,生物膜活性染色通过染色通过Resazurin或荧光素二乙酸酯和生物膜活力染色来估计生物膜生物量来监测生物膜生物量。通过用Live /Dead®Bacllow™细菌活力试剂盒染色,通过染色。 GLG能够防止浓度≤0·5%(W / V)的生物膜形成,并且需要更高的浓度来抑制已建立的生物膜。 GLG没有破坏生物膜生物量。葡萄球菌比铜绿假单胞菌更容易受到GLG的影响。这些体外发现必须通过体内研究来验证。

著录项

  • 期刊名称 International Wound Journal
  • 作者

    Rose A Cooper;

  • 作者单位
  • 年(卷),期 2013(10),6
  • 年度 2013
  • 页码 630–637
  • 总页数 8
  • 原文格式 PDF
  • 正文语种
  • 中图分类
  • 关键词

    机译:氟胺;葡萄糖氧化酶;愈菌醇;乳酰氧化酶;伤口;

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