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An Overview of Biofilm Formation-Combating Strategies and Mechanisms of Action of Antibiofilm Agents

期刊

LIFE-BASEL
卷 12, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/life12081110

关键词

biofilms; antibiotic resistance; combating strategies; antibiofilm agents; natural products; antibodies; nanomaterials

资金

  1. US National Science Foundation [1736255, 2036867, 2125083]
  2. US Department of Energy-Bioenergy Technology Office [DE-EE0009273]
  3. Direct For Biological Sciences
  4. Emerging Frontiers [2125083] Funding Source: National Science Foundation
  5. Div Of Civil, Mechanical, & Manufact Inn
  6. Directorate For Engineering [2036867] Funding Source: National Science Foundation

向作者/读者索取更多资源

Biofilm formation on surfaces by microbial colonization is a global health issue that causes infections and provides resistance to treatment. Effective anti-biofilm strategies are necessary to reduce healthcare problems associated with biofilms.
Biofilm formation on surfaces via microbial colonization causes infections and has become a major health issue globally. The biofilm lifestyle provides resistance to environmental stresses and antimicrobial therapies. Biofilms can cause several chronic conditions, and effective treatment has become a challenge due to increased antimicrobial resistance. Antibiotics available for treating biofilm-associated infections are generally not very effective and require high doses that may cause toxicity in the host. Therefore, it is essential to study and develop efficient anti-biofilm strategies that can significantly reduce the rate of biofilm-associated healthcare problems. In this context, some effective combating strategies with potential anti-biofilm agents, including plant extracts, peptides, enzymes, lantibiotics, chelating agents, biosurfactants, polysaccharides, organic, inorganic, and metal nanoparticles, etc., have been reviewed to overcome biofilm-associated healthcare problems. From their extensive literature survey, it can be concluded that these molecules with considerable structural alterations might be applied to the treatment of biofilm-associated infections, by evaluating their significant delivery to the target site of the host. To design effective anti-biofilm molecules, it must be assured that the minimum inhibitory concentrations of these anti-biofilm compounds can eradicate biofilm-associated infections without causing toxic effects at a significant rate.

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