Diatom Microbubbler for Active Biofilm Removal in Confined Spaces.
Yongbeom SeoJiayu LeongJun Dong ParkYu-Tong HongSang-Hyon ChuCheol ParkDong Hyun KimYu-Heng DengVitaliy DushnovJoonghui SohSimon RogersYi Yan YangHyunjoon KongPublished in: ACS applied materials & interfaces (2018)
Bacterial biofilms form on and within many living tissues, medical devices, and engineered materials, threatening human health and sustainability. Removing biofilms remains a grand challenge despite tremendous efforts made so far, particularly when they are formed in confined spaces. One primary cause is the limited transport of antibacterial agents into extracellular polymeric substances (EPS) of the biofilm. In this study, we hypothesized that a microparticle engineered to be self-locomotive with microbubbles would clean a structure fouled by biofilm by fracturing the EPS and subsequently improving transports of the antiseptic reagent. We examined this hypothesis by doping a hollow cylinder-shaped diatom biosilica with manganese oxide (MnO2) nanosheets. In an antiseptic H2O2 solution, the diatoms doped by MnO2 nanosheets, denoted as diatom bubbler, discharged oxygen gas bubbles continuously and became self-motile. Subsequently, the diatoms infiltrated the bacterial biofilm formed on either flat or microgrooved silicon substrates and continued to generate microbubbles. The resulting microbubbles merged and converted surface energy to mechanical energy high enough to fracture the matrix of biofilm. Consequently, H2O2 molecules diffused into the biofilm and killed most bacterial cells. Overall, this study provides a unique and powerful tool that can significantly impact current efforts to clean a wide array of biofouled products and devices.
Keyphrases
- candida albicans
- pseudomonas aeruginosa
- staphylococcus aureus
- biofilm formation
- human health
- quantum dots
- risk assessment
- cystic fibrosis
- highly efficient
- induced apoptosis
- gene expression
- drug delivery
- quality improvement
- high resolution
- escherichia coli
- oxidative stress
- drug release
- cell proliferation
- cell cycle arrest
- drinking water
- endoplasmic reticulum stress
- cancer therapy
- ionic liquid
- high density