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Elucidating the role of multivalency, shape, size and functional group density on antibacterial activity of diversified supramolecular nanostructures enabled by templated assembly.
Sikder, Amrita; Pearce, Amanda K; Kumar, C M Santosh; O'Reilly, Rachel K.
Afiliación
  • Sikder A; School of Chemistry, University of Birmingham, Birmingham, B15 2TT, UK. r.oreilly@bham.ac.uk.
  • Pearce AK; School of Chemistry, University of Birmingham, Birmingham, B15 2TT, UK. r.oreilly@bham.ac.uk.
  • Kumar CMS; Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, B15 2TT, UK.
  • O'Reilly RK; School of Chemistry, University of Birmingham, Birmingham, B15 2TT, UK. r.oreilly@bham.ac.uk.
Mater Horiz ; 10(1): 171-178, 2023 01 03.
Article en En | MEDLINE | ID: mdl-36321619
ABSTRACT
With the increased prevalence of antibiotic-resistant infections, there is an urgent need to develop novel antibacterial materials. In addition, gaining a complete understanding of the structural features that impart activity toward target microorganisms is essential to enable materials optimisation. Here we have reported a rational design to fabricate antibacterial supramolecular nanoparticles with variable shape, size and cationic group density, by exploiting noncovalent interactions between a shape determining template amphiphile and a cationic amphiphile to introduce charge on the nanoparticle surface. We have shown that the monomeric cationic amphiphile alone showed poor antibacterial activity, whereas nanostructures formed by co-assembling the complementary units showed significantly enhanced antibacterial efficiency. Further, the systematic variation of several structural parameters such as shape, spacing between the cationic groups and size of these nanostructures allowed us to elicit the role of each parameter on the overall antibacterial properties. Finally, we investigated the origin of the differing antibacterial activity of these nanoparticles having different shape and size but with the same molecular composition, by comparing the thermodynamic parameters of their binding interactions with a bacterial membrane mimic.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nanoestructuras / Nanopartículas Tipo de estudio: Risk_factors_studies Idioma: En Revista: Mater Horiz Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Nanoestructuras / Nanopartículas Tipo de estudio: Risk_factors_studies Idioma: En Revista: Mater Horiz Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido