Polydopamine –aminoglycoside nanoconjugates: Synthesis, characterization, antimicrobial evaluation and cytocompatibility

https://doi.org/10.1016/j.msec.2019.110284Get rights and content

Highlights

  • Polydopamine nanoparticles have been synthesized by oxidative self-polymerization.

  • Aminoglycoside-conjugation yielded nanoconjugates.

  • These exhibited excellent antimicrobial activity with high cyto-compatibility.

  • Nanoconjugates also showed activity against resistant pathogens.

Abstract

Development of nanoparticle- and self-assembled nanomaterial-based therapeutics has become a rapidly growing area in the field of nanotechnology. One of the natural compounds, dopamine, presents as a neurotransmitter in the human brain serving as a messenger and deals with the behavioural responses, has provided an ideal platform through self-polymerization under aerobic conditions leading to the formation of a beneficial organic biopolymer, polydopamine (PDA). This polymer provides sufficient reactive functionalities, which can further be use to attach amine- or thiol-containing ligands to obtain conjugates. In the present study, self-polymerized polydopamine nanoparticles have been synthesized and tethered to aminoglycosides (AGs: Gentamicin, Kanamycin and Neomycin) through amino moieties to obtain PDA-AG nanoconjugates. These nanoconjugates are characterized by physicochemical techniques and evaluated for their antimicrobial potency against various bacterial strains including resistant ones. Simultaneously, cytocompatibility was also assessed for PDA-AG nanoconjugates. Of these three nanoconjugates (PDA-Gentamicin, PDA-Kanamycin and PDA-Neomycin), PDA-Kanamycin (PDA-K) nanoconjugate exhibited the highest activity against potent pathogens, least toxicity in human embryonic kidney (HEK 293) cells and intense toxic effects on human glioblastoma (U87) cells. Together, these results advocate the promising potential of these nanoconjugates to be used as potent antimicrobials in future applications.

Keywords

Polydopamine
Aminoglycosides
Nanoconjugates
Antimicrobial activity
Cytotoxicity

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