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Incorporation of Antibiotics into Solid Lipid Nanoparticles: A Promising Approach to Reduce Antibiotic Resistance Emergence

期刊

NANOMATERIALS
卷 11, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/nano11051251

关键词

antibiotics; antimicrobial resistance; multidrug-resistant bacteria; drug delivery systems; solid lipid nanoparticles

资金

  1. University of the Basque Country [GIU18/229, COLAB19/08]
  2. Industry Department of the Basque Government [ELKARTEK2020 KK-2020/00007]

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Solid lipid nanoparticles show promise as a drug delivery system to improve antibiotic characteristics and increase treatment efficiency in the face of antimicrobial resistance. By analyzing the role and advantages of SLNs, as well as their potential drawbacks, this review helps to better understand the application of these new formulations in tackling antibiotic resistance.
Antimicrobial resistance is one of the biggest threats to global health as current antibiotics are becoming useless against resistant infectious pathogens. Consequently, new antimicrobial strategies are urgently required. Drug delivery systems represent a potential solution to improve current antibiotic properties and reverse resistance mechanisms. Among different drug delivery systems, solid lipid nanoparticles represent a highly interesting option as they offer many advantages for nontoxic targeted drug delivery. Several publications have demonstrated the capacity of SLNs to significantly improve antibiotic characteristics increasing treatment efficiency. In this review article, antibiotic-loaded solid lipid nanoparticle-related works are analyzed to summarize all information associated with applying these new formulations to tackle the antibiotic resistance problem. The main antimicrobial resistance mechanisms and relevant solid lipid nanoparticle characteristics are presented to later discuss the potential of these nanoparticles to improve current antibiotic treatment characteristics and overcome antimicrobial resistance mechanisms. Moreover, solid lipid nanoparticles also offer new possibilities for other antimicrobial agents that cannot be administrated as free drugs. The advantages and disadvantages of these new formulations are also discussed in this review. Finally, given the progress of the studies carried out to date, future directions are discussed.

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