4.8 Review

Nano delivery systems to the rescue of ciprofloxacin against resistant bacteria ?E. coli; P. aeruginosa; Saureus; and MRSA? and their infections

Journal

JOURNAL OF CONTROLLED RELEASE
Volume 349, Issue -, Pages 338-353

Publisher

ELSEVIER
DOI: 10.1016/j.jconrel.2022.07.003

Keywords

Ciprofloxacin; Antimicrobial agents; Antibiotics; Nano -drug delivery systems; Antibacterial

Funding

  1. College of Health Sciences of the University of KwaZulu-Natal (UKZN)
  2. UKZN Novel Drug Delivery Research Group
  3. National Research Foundation (NRF) South Africa [106040, 103664, 116652]
  4. Medical Research Council (MRC) of South Africa

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This review provides an overview of the resistance mechanisms, causes, and approaches to overcome resistance to CIP. It critically evaluates various nano delivery systems for the delivery of CIP against infections caused by E. coli, P. aeruginosa, S. aureus, and MRSA. Future research directions for optimizing nano delivery systems are also highlighted.
Ciprofloxacin (CIP) a broad-spectrum antibiotic, is used extensively for the treatment of diverse infections and diseases of bacteria origin, and this includes infections caused by E. coli; P. aeruginosa; S. aureus; and MRSA. This extensive use of CIP has therefore led to an increase in resistance by these infection causing organisms. Nano delivery systems has recently proven to be a possible solution to resistance to these organisms. They have been applied as a strategy to improve the target specificity of CIP against infections and diseases caused by these organisms, thereby maximising the efficacy of CIP to overcome the resistance. Herein, we proffer a brief over-view of the mechanisms of resistance; the causes of resistance; and the various approaches employed to overcome this resistance. The review then proceeds to critically evaluate various nano delivery systems including inorganic based nanoparticles; lipid-based nanoparticles; capsules, dendrimers, hydrogels, micelles, and polymeric nano -particles; and others; that have been applied for the delivery of CIP against E. coli; P. aeruginosa; S. aureus; and MRSA infections. Finally, the review highlights future areas of research, for the optimisation of various nano delivery systems, to maximise the therapeutic efficacy of CIP against these organisms. This review confirms the potential of nano delivery systems, for addressing the challenges of resistance to caused by E. coli; P. aeruginosa; S. aureus; and MRSA to CIP.

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