Literature DB >> 33418649

Understanding the Role of Polymer Surface Nanoscale Topography on Inhibiting Bacteria Adhesion and Growth.

Luting Liu, Batur Ercan1, Linlin Sun2, Katherine S Ziemer, Thomas J Webster3,2.   

Abstract

Catheter-associated infections, most of which are caused by microbial biofilms, are still a serious issue in healthcare and are associated with significant morbidity, mortality, and excessive medical costs. Currently, the use of nanostructured materials, especially materials with nanofeatured topographies, which have more surface area, altered surface energy, enhanced select protein adsorption, and selectively increased desirable cell functions while simultaneously decreasing competitive cell functions, seem to be among the most promising ways for reducing initial bacteria attachment, biofilm formation, and infections. In this study, polydimethylsiloxane (PDMS), a commonly used polymeric catheter material, was formulated to mimic the nanopatterned topography of natural tissue by using a template method with nanotubular anodized titanium. Results showed that increased PDMS surface nanoscale roughness alone can inhibit both Gram-negative (Escherichia coli) and Gram-positive (Staphylococcus aureus) bacteria adhesion and growth for up to 2 days, the time length of the current study. Additionally, increased fibroblast and endothelial cell adhesion on nano-PDMS indicated that this nanoscale topography had no toxic effects toward mammalian cells. Mechanistically, this study also developed a model for the first time to correlate bacteria responses to nanoscale roughness with initial protein and biomolecule adsorption (specifically, casein protein and glucose, which are unique biomolecules that mediate bacteria functions). Data revealed that the increase in nanoscale roughness and associated energy contributed to greater select casein adsorption during the first several minutes of culture, which is critical for decreasing bacteria attachment and growth. In contrast, no significant differences for glucose adsorption between samples before and after nanofabrication were identified. These results together indicated that the present biomimetic nanopatterned PDMS surface without any chemical or antibiotic modification has the potential to combat catheter-associated infections and should be further investigated.

Entities:  

Keywords:  antibacterial; catheter-associated infections; cell adhesion; nanotechnology; protein adsorption

Year:  2015        PMID: 33418649     DOI: 10.1021/acsbiomaterials.5b00431

Source DB:  PubMed          Journal:  ACS Biomater Sci Eng        ISSN: 2373-9878


  4 in total

1.  Physiochemically Distinct Surface Properties of SU-8 Polymer Modulate Bacterial Cell-Surface Holdfast and Colonization.

Authors:  Silambarasan Anbumani; Aldeliane M da Silva; Andrei Alaferdov; Marcos V Puydinger Dos Santos; Isis G B Carvalho; Mariana de Souza E Silva; Stanislav Moshkalev; Hernandes F Carvalho; Alessandra A de Souza; Monica A Cotta
Journal:  ACS Appl Bio Mater       Date:  2022-09-26

2.  Protein-coated nanostructured surfaces affect the adhesion of Escherichia coli.

Authors:  Pawel Kallas; Håkon Valen; Mats Hulander; Nikolaj Gadegaard; John Stormonth-Darling; Padraic O'Reilly; Bernd Thiede; Martin Andersson; Håvard Jostein Haugen
Journal:  Nanoscale       Date:  2022-05-26       Impact factor: 8.307

3.  Engineering multifunctional bactericidal nanofibers for abdominal hernia repair.

Authors:  Samson Afewerki; Nicole Bassous; Samarah Vargas Harb; Marcus Alexandre F Corat; Sushila Maharjan; Guillermo U Ruiz-Esparza; Mirian M M de Paula; Thomas J Webster; Carla Roberta Tim; Bartolomeu Cruz Viana; Danquan Wang; Xichi Wang; Fernanda Roberta Marciano; Anderson Oliveira Lobo
Journal:  Commun Biol       Date:  2021-02-19

Review 4.  Use of Nanotechnology to Mitigate Biofouling in Stainless Steel Devices Used in Food Processing, Healthcare, and Marine Environments.

Authors:  Hugo Pérez; Gregorio Vargas; Rodolfo Silva
Journal:  Toxics       Date:  2022-01-12
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.