Full description
Attached file provides supplementary data for linked article. Antimicrobial action of nanomaterials is typically assigned to the nanomaterial composition, size and/or shape, whereas influence of complex corona stabilizing the nanoparticle surface is often neglected. We demonstrate sequential surface functionalization of tyrosine-reduced gold nanoparticles (AuNPsTyr) with polyoxometalates (POMs) and lysine to explore controlled chemical functionality-driven antimicrobial activity. Our investigations reveal that highly biocompatible gold nanoparticles can be tuned to be a strong antibacterial agent by fine-tuning their surface properties in a controllable manner. The observation from the antimicrobial studies on a gram negative bacterium Escherichia coli were further validated by investigating the anticancer properties of these step-wise surface-controlled materials against A549 human lung carcinoma cells, which showed a similar toxicity pattern. These studies highlight that the nanomaterial toxicity and biological applicability are strongly governed by their surface corona. Subjects
Gold nanoparticle |
Lysine |
Nanotechnology |
Nanobiotechnology |
Polymer |
Polyoxometalate derivative |
Technology |
Unclassified drug |
User Contributed Tags
Login to tag this record with meaningful keywords to make it easier to discover
Identifiers
- Local : e9a9578fb8249974cbe3192bf26b4e12
