Abstract
Nearly 80% of global bacterial infections are associated with biofilm bacteria (Joo, Otto, Chem Biol 19:1503–1513, 2012). In contrast to planktonic bacteria, biofilms are a complex, organized bacterial community possessing a sophisticated protective armor, in the form of the extracellular polymeric substance (EPS), which acts as a robust defense mechanism against eradication. Chronic biofilm infections affect 17 million people annually, and approximately 550,000 people die as a result of their chronic infections (Wolcott et al J Wound Care 19:45–50, 2010). The challenge with biofilm-related infections is that they cannot be adequately confirmed via diagnostic tests in the clinical setting, and, more importantly, they are intrinsically resistant to host immunity, antibiotics, and biocides. This renders current therapeutic options inadequate to successfully eradicate the infection. Next Science™ has applied novel material science methods to combat biofilm through its innovative Xbio™ technology. Xbio technology, which includes the proprietary product, BlastX™, works by disrupting the biofilm matrix and creating an environment that compromises the biofilm’s structural integrity. In doing so, the EPS can be broken down and removed, thereby allowing the pathogens within the environment to be targeted and preventing the biofilm’s reformation.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Joo, H. S., & Otto, M. (2012). Molecular basis of in-vivo biofilm formation by bacterial. Chemistry & Biology, 19(12), 1503–1513.
Wolcott, R., Rhoads, D., Bennett, M., Wolcott, B., Gogokhia, L., Costerton, J., & Dowd, S. (2010). Chronic wounds and the medical biofilm paradigm. Journal of Wound Care, 19(2), p45–p50.
Landén, N. X., & Li, D. (2016). Mona Ståhle.Transition from inflammation to proliferation: a critical step during wound healing. Cellular and Molecular Life Sciences, 73(20), 3861–3885.
Attinger, C., & Wolcott, R. (2012). Clinically addressing biofilm in chronic wounds. Advances in Wound Care, 1(3), 127–132.
Aziz-Abdel, M. S. (2014). Bacterial biofilm: Dispersal and inhibition strategies. SAJ Biotechnology, 1, 105. https://doi.org/10.18875/2375-6713.1.105.
Frykberg, R. G., & Banks, J. (2015). Challenges in the Treatment of Chronic Wounds. Advances in Wound Care, 4(9), 560–582. https://doi.org/10.1089/wound.2015.0635.
Flemming, H. C., & Wingender, J. (2010). The Biofilm Matrix. Nature Reviews Microbiology, 8, 623–633.
Performance of the Massachusetts Health Care System Series: A focus on provider quality. CHIA Center for Health Information and Analysis, chiamass.gov.
Bjarnsholt, T., Kirketerp-Møller, K., Jensen, P. Ø., et al. (2008). Why chronic wounds will not heal: a novel hypothesis. Wound Repair and Regeneration, 16(10), 2–10.
Sen, C., Gordillo, G., Roy, S., Kirsner, R., Lambert, L., Hunt, T., Gottrup, F., Gurtner, G., & Longaker, M. (2009). Human skin wounds: A major and snowballing threat to public health and economy. Wound Repair and Regeneration, 17(6), 763–771.
Hall-Stoodley, L., & Stoodley, P. (2009). Evolving concepts in biofilm infections. Cell Microbiol, 11(7), 1034–1043.
Brooun, A., Liu, S., & Lewis, K. (2000). A dose response study of antibiotic resistance in Pseudomonas aeruginosa biofilms. Antimicrobial Agents and Chemotherapy, 44(3), 640–646.
Lewis, K. (2007). Persister cells, dormancy and infectious disease. Nature Reviews. Microbiology, 5(1), 48–56.31.
Davies, D. G., Parsek, M. R., Pearson, J. P., et al. (1998). The involvement of cell-to-cell signals in the development of a bacterial biofilm. Science, 280(5361), 295–298.
Carroll, K., Hobden, J., Miller, S., Morse, S., Mietzner, T., Detrick, B., Mitchell, T., McKerrow, J., & Sakanari, J. (2016). Jawetz, Melnick, & Adelbergs medical microbiology (27th ed.). Shenzen: McGraw-Hill.
Kim et al. (2018). Wounds, 30(5), 114–119. Epub 2018 February 23 (Biofilms Made Easy (wounds international) – Phillips; Skin and Wound Care 2013 – Kevin Wu; Wound Education Update Feb 2014 – Wounds UK Best Practice Statement)
Snyder, R. J., Bohn, G., Hanft, J., Harkless, L., Kim, P., Lavery, L., Schultz, G., & Wolcott, R. (2017). Wound bioflm: current perspectives and strategies on biofilm disruption and treatments. Wounds, 29(6), S1–S17.
Snyder, R. J., Bohn, G., Hanft, J., Harkless, L., Kim, P., Lavery, L., Schultz, G., & Wolcott, R. (2017). Wound Biofilm: Current Perspectives and Strategies on Biofilm Disruption and Treatments. Wounds, 29(6), S1–S17.
Ryder, M. (2005). Catheter related infections – It’s all about biofilms. Topics in Advanced Practice Nursing eJournal, 5(3), 1–6.
Data on file. Center for Biofilm Engineering at Montana State University. Next Science Report TR-10-12-004.
Mallefet, P., & Dweck, A. C. (2008). Mechanisms involved in wound healing. Biomedical Scientist, 52(7), 609.
Next Science website. http://www.nextscience.com
Code of Federal Regulations. https://www.fda.gov/medicaldevices/deviceregulationandguidance/overview/default.htm
FDA.gov https://www.fda.gov/combinationproducts/aboutcombinationproducts/ucm101496.htm#CP
Evaluation of Automatic Class III Designation (De Novo). FDA.gov https://www.fda.gov/medicaldevices/deviceregulationandguidance/howtomarketyourdevice/premarketsubmissions/ucm462775.htm
Disclaimer
Dr. Myntti has financial interest in Next Science and the technologies discussed.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Myntti, M. (2019). Translation of Antibiofilm Technologies to Wounds and Other Clinical Care. In: Williams, D. (eds) Targeting Biofilms in Translational Research, Device Development, and Industrial Sectors. Springer, Cham. https://doi.org/10.1007/978-3-030-30667-0_6
Download citation
DOI: https://doi.org/10.1007/978-3-030-30667-0_6
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-30666-3
Online ISBN: 978-3-030-30667-0
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)