Controlling the structure of supramolecular fibre formation for benzothiazole based hydrogels with antimicrobial activity against methicillin resistant Staphylococcus aureus .
Kira L F HiltonAntonis A KaramalegkosNyasha AllenLauren GwynneBree StreatherLisa J WhiteKaren B BakerSamantha A HenryGeorge T WilliamsHelena J ShepherdMark ShepherdCharlotte K HindMark J SuttonToby A JenkinsDaniel P MulvihillJennifer M A TulletMarina EzcurraJennifer R HiscockPublished in: Journal of materials chemistry. B (2023)
Antimicrobial resistance is one of the greatest threats to human health. Gram-positive methicillin resistant Staphylococcus aureus (MRSA), in both its planktonic and biofilm form, is of particular concern. Herein we identify the hydrogelation properties for a series of intrinsically fluorescent, structurally related supramolecular self-associating amphiphiles and determine their efficacy against both planktonic and biofilm forms of MRSA. To further explore the potential translation of this hydrogel technology for real-world applications, the toxicity of the amphiphiles was determined against the eukaryotic multicellular model organism, Caenorhabditis elegans . Due to the intrinsic fluorescent nature of these supramolecular amphiphiles, material characterisation of their molecular self-associating properties included; comparative optical density plate reader assays, rheometry and widefield fluorescence microscopy. This enabled determination of amphiphile structure and hydrogel sol dependence on resultant fibre formation.
Keyphrases
- methicillin resistant staphylococcus aureus
- human health
- staphylococcus aureus
- antimicrobial resistance
- energy transfer
- quantum dots
- drug delivery
- single molecule
- risk assessment
- living cells
- hyaluronic acid
- pseudomonas aeruginosa
- tissue engineering
- wound healing
- high resolution
- label free
- biofilm formation
- water soluble
- climate change
- candida albicans
- high throughput
- high speed
- oxidative stress
- gram negative
- fluorescent probe
- optical coherence tomography
- drug release
- escherichia coli
- solid phase extraction
- mass spectrometry