Cefotaxime Mediated Synthesis of Gold Nanoparticles: Characterization and Antibacterial Activity

Turki Al Hagbani1, Syed Mohd Danish Rizvi1, Talib Hussain2

  • 1Department of Pharmaceutics, College of Pharmacy, University of Ha'il, Ha'il 81442, Saudi Arabia.

Polymers
|February 26, 2022
PubMed

Insights

Researchers developed cefotaxime-loaded gold nanoparticles (C-AuNPs) to combat antibiotic resistance. These nanoparticles show enhanced antibacterial activity against resistant bacteria, offering a promising nanotechnology approach to overcome multidrug-resistant pathogens.

Area of Science:

  • Nanotechnology and Materials Science
  • Microbiology and Infectious Diseases
  • Pharmacology and Drug Delivery

Background:

  • Third-generation cephalosporin antibiotics like cefotaxime (CTX) face declining efficacy due to rising multidrug-resistant (MDR) pathogens.
  • Nanotechnology presents a viable strategy to overcome microbial resistance challenges.

Purpose of the Study:

  • To synthesize and characterize cefotaxime-loaded gold nanoparticles (C-AuNPs) using cefotaxime sodium as a reducing and capping agent.
  • To evaluate the in vitro antibacterial efficacy of C-AuNPs against Gram-positive and Gram-negative bacteria, particularly MDR strains.

Main Methods:

  • Synthesis of gold nanoparticles (AuNPs) using cefotaxime sodium.
  • Characterization of C-AuNPs using UV-Visible spectroscopy, FTIR, Transmission Electron Microscopy (TEM), and Dynamic Light Scattering (DLS).
  • Assessment of in vitro antibacterial activity and determination of minimum inhibitory concentration (MIC) values.

Main Results:

  • Successful synthesis of stable, nano-sized spherical C-AuNPs confirmed by spectroscopic and microscopic techniques.
  • C-AuNPs demonstrated enhanced antibacterial activity and lower MIC values compared to pure cefotaxime against tested Gram-negative (Escherichia coli, Klebsiella oxytoca, Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus) bacteria.
  • The colloidal stability of C-AuNPs was attributed to their higher net negative surface charge.

Conclusions:

  • Cefotaxime can be effectively utilized as a reducing and capping agent for synthesizing stable C-AuNPs.
  • Loading cefotaxime onto gold nanoparticles significantly enhances its antibacterial potency against multidrug-resistant bacteria.
  • C-AuNPs represent a promising nanomedicine approach to restore and boost the efficacy of existing antibiotics against resistant pathogens.

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