Palladium nanoparticles synthesis, characterization using glucosamine as the reductant and stabilizing agent to explore their antibacterial & catalytic applications

Microb Pathog. 2018 Dec:125:150-157. doi: 10.1016/j.micpath.2018.09.020. Epub 2018 Sep 12.

Abstract

Low cost and an easy technique for the synthesis of palladium nanoparticles (PdNPs) was developed. Glucosamine was used to stabilize palladium precursor (PdCl2) into palladium nanoparticles. Several analytical techniques were used for the determination of morphology, crystalline structure; size, capping, and composition of synthesize palladium nanoparticles. The UV-visible spectroscopy SPR peak (Surface Plasmon Resonance) at 284 nm revealed synthesis of PdNPs. Energy dispersive X-ray (EDX) and X-ray diffraction (XRD) studies proved the elemental composition and crystalline structure of the synthesized palladium nanoparticles respectively. The average particle sizes (5.5 nm) were obtained by using the 1 M glucosamine solution, with a fixed amount of PdCl2 (4 mM). Moreover, the as synthesized PdNPs was evaluated against Gram negative bacterial E. which shows tremendous antibacterial activity as compare to tobramycin standard antibiotics. It's mechanistically found that PdNPs damage cell membrane and caused imbalance of metabolism system of the cell as a result production of reactive oxygen species (ROS). Thus, these finding revealed that cells become leaky and all organelles come out from cells, finally caused death of the E. coli. Addition, the as prepared PdNPs also showed excellent catalytic activities toward reduction of methylene blue and 4-nitrophenol.Thus, glucosamine mediated PdNPs having dual functions biomedical as well as intoxicating catalyst for industries.

Keywords: Antibacterial activity; Catalytic activities; Characterization; Green synthesis; Palladium nanoparticles.

MeSH terms

  • Anti-Bacterial Agents / metabolism*
  • Cell Membrane / drug effects
  • Escherichia coli / drug effects
  • Excipients / metabolism
  • Glucosamine / metabolism*
  • Metabolic Networks and Pathways / drug effects
  • Metal Nanoparticles / chemistry
  • Metal Nanoparticles / ultrastructure*
  • Palladium / metabolism*
  • Reactive Oxygen Species / metabolism
  • Reducing Agents / metabolism*
  • Spectrometry, X-Ray Emission
  • Spectrum Analysis
  • Surface Plasmon Resonance
  • X-Ray Diffraction

Substances

  • Anti-Bacterial Agents
  • Excipients
  • Reactive Oxygen Species
  • Reducing Agents
  • Palladium
  • Glucosamine