Nanoemulsion delivery systems for enhanced efficacy of antimicrobials and essential oils.

Biomater Sci

Department of Pharmacological and Pharmaceutical Sciences, University of Houston, Houston, TX, 77204, USA.

Published: February 2022

AI Article Synopsis

  • The rise of infectious diseases and antimicrobial resistance necessitates innovative drug delivery methods to improve treatment efficacy and minimize side effects.
  • Nanoemulsions (NE) are small droplet systems that enhance the delivery of antimicrobials by improving drug solubility and targeting, making them a suitable option to combat infections and resistance.
  • The use of NE can either deliver drugs effectively or utilize essential oils for antimicrobial effects, with potential for various administration routes, and there are ongoing advancements in their clinical application for infectious disease therapy.

Article Abstract

The ever-growing threat of new and existing infectious diseases in combination with antimicrobial resistance requires the need for innovative and effective forms of drug delivery. Optimal drug delivery systems for existing and newly developed antimicrobials can enhance drug bioavailability, enable site-specific drug targeting, and overcome current limitations of drug formulations such as short elimination half-lives, poor drug solubility, and undesirable side effects. Nanoemulsions (NE) consist of nanometer-sized droplets stabilized by emulsifiers and are typically more stable and permeable due to their smaller particle sizes and higher surface area compared to conventional emulsions. NE have been identified as a promising means of antimicrobial delivery due to their intrinsic antimicrobial properties, ability to increase drug solubility, stability, bioavailability, organ and cellular targeting potentials, capability of targeting biofilms, and potential to overcome antimicrobial resistance. Herein, we discuss non-drug loaded essential oil-based NE that can confer antimicrobial actions through predominantly physical or biochemical mechanisms without drug payloads. We also describe drug-loaded NE for enhanced antimicrobial efficacy by augmenting the potency of existing antimicrobials. We highlight the versatility of NE to be administered through multiple different routes (oral, parenteral, dermal, transdermal, pulmonary, nasal, ocular, and rectal). We summarize recent advances in the clinical translation of antimicrobial NE and shed light on future development of effective antimicrobial therapy to combat infectious diseases.

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Source
http://dx.doi.org/10.1039/d1bm01537kDOI Listing

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