Antibacterial Liquid Metals: Biofilm Treatment via Magnetic Activation.
Aaron James ElbourneSamuel CheesemanPaul AtkinNghia Phuoc TruongNitu SyedAli ZavabetiMd MohiuddinDorna EsrafilzadehDaniel CozzolinoChris F McConvilleMichael D DickeyRussell J CrawfordKourosh Kalantar-ZadehJames ChapmanTorben DaenekeVi Khanh TruongPublished in: ACS nano (2020)
Antibiotic resistance has made the treatment of biofilm-related infections challenging. As such, the quest for next-generation antimicrobial technologies must focus on targeted therapies to which pathogenic bacteria cannot develop resistance. Stimuli-responsive therapies represent an alternative technological focus due to their capability of delivering targeted treatment. This study provides a proof-of-concept investigation into the use of magneto-responsive gallium-based liquid metal (LM) droplets as antibacterial materials, which can physically damage, disintegrate, and kill pathogens within a mature biofilm. Once exposed to a low-intensity rotating magnetic field, the LM droplets become physically actuated and transform their shape, developing sharp edges. When placed in contact with a bacterial biofilm, the movement of the particles resulting from the magnetic field, coupled with the presence of nanosharp edges, physically ruptures the bacterial cells and the dense biofilm matrix is broken down. The antibacterial efficacy of the magnetically activated LM particles was assessed against both Gram-positive and Gram-negative bacterial biofilms. After 90 min over 99% of both bacterial species became nonviable, and the destruction of the biofilms was observed. These results will impact the design of next-generation, LM-based biofilm treatments.
Keyphrases
- candida albicans
- staphylococcus aureus
- pseudomonas aeruginosa
- gram negative
- biofilm formation
- multidrug resistant
- cancer therapy
- induced apoptosis
- oxidative stress
- escherichia coli
- mass spectrometry
- drug delivery
- anti inflammatory
- cell death
- endoplasmic reticulum stress
- cell proliferation
- cell cycle arrest
- heavy metals
- liquid chromatography
- molecularly imprinted
- drug induced