Synthesis of antimicrobial gallium anoparticles using the hot injection method

Christina Limantoro, Theerthankar Das, Meng He, Dmitry Dirin, Jim Manos, Maksym V. Kovalenko, Wojciech Chrzanowski

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)
3 Downloads (Pure)

Abstract

Antibiotic resistance continues to be an ongoing problem in global public health despite interventions to reduce antibiotic overuse. Furthermore, it threatens to undo the achievements and progress of modern medicine. To address these issues, the development of new alternative treatments is needed. Metallic nanoparticles have become an increasingly attractive alternative due to their unique physicochemical properties that allow for different applications and their various mechanisms of action. In this study, gallium nanoparticles (Ga NPs) were tested against several clinical strains of Pseudomonas aeruginosa (DFU53, 364077, and 365707) and multi-drug-resistant Acinetobacter baumannii (MRAB). The results showed that Ga NPs did not inhibit bacterial growth when tested against the bacterial strains using a broth microdilution assay, but they exhibited effects in biofilm production in P. aeruginosa DFU53. Furthermore, as captured by atomic force microscopy imaging, P. aeruginosa DFU53 and MRAB biofilms underwent morphological changes, appearing rough and irregular when they were treated with Ga NPs. Although Ga NPs did not affect planktonic bacterial growth, their effects on both biofilm formation and established biofilm demonstrate their potential role in the race to combat antibiotic resistance, especially in biofilm-related infections.
Original languageEnglish
Pages (from-to)310-320
Number of pages11
JournalACS Materials Au
Volume3
Issue number4
DOIs
Publication statusPublished - Jul 2023
Externally publishedYes

Keywords

  • antibiotic-resistant bacteria
  • antimicrobial
  • biofilm
  • gallium
  • nanoparticles

Fingerprint

Dive into the research topics of 'Synthesis of antimicrobial gallium anoparticles using the hot injection method'. Together they form a unique fingerprint.

Cite this