4.8 Article

Diatom Microbubbler for Active Biofilm Removal in Confined Spaces

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 10, Issue 42, Pages 35685-35692

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b08643

Keywords

MnO2 nanosheets; diatom; microbubble; self-locomotion; biofilm

Funding

  1. National Institutes of Health [1R01 HL109192, 1R21 HL131469]
  2. National Science Foundation (STC-EBICS Grant) [CBET-0939511]
  3. Korea Institute of Industrial Technology [JE140004]
  4. A*STAR Graduate Scholarship (Overseas) from the Agency for Science, Technology, and Research
  5. Institute of Bioengineering and Nanotechnology (A*STAR), Singapore
  6. National Research Council of Science & Technology (NST), Republic of Korea [JE140004] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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 micro bubbles 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.

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