4.8 Article

High-Density Three-Dimensional Network of Covalently Linked Nitric Oxide Donors to Achieve Antibacterial and Antibiofilm Surfaces

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 29, 页码 33745-33755

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c00340

关键词

healthcare-associated infections; biomedical device; antibacterial; antibiofilm; NOno release; nonleachable coating; biocompatibility

资金

  1. Ministry of Education, Singapore, under its MOE AcRF Tier 3 Awards [MOE2018-T3-1-003, MOE2013-T3-1-002]
  2. Singapore Ministry of Health Industry Alignment Fund [NMRC/MOHIAFCAT2/003/2014]
  3. ASTAR RIE2020 Advanced Manufacturing and Engineering (AME) IAP-PP Specialty Chemicals Programme (SERC Grant) [A1786a0032]
  4. NTU

向作者/读者索取更多资源

A novel pretreatment chemistry was developed to create a high-density 3-D RSNO network coating on biomedical device surfaces, effectively inhibiting biofilm formation with good biocompatibility and antibacterial activity. The high-density RSNO coating showed nearly 99% reduction of P. aeruginosa and MRSA in vivo, demonstrating potential for application in various biomedical devices.
Bacterial colonization on biomedical devices often leads to biofilms that are recalcitrant to antibiotic treatment and the leading cause of hospital-acquired infections. We have invented a novel pretreatment chemistry for device surfaces to produce a high-density three-dimensional (3-D) network of covalently linked S-nitrosothiol (RSNO), which is a nitric oxide (NO) donor. Poly(polyethylene glycol-hydroxyl-terminated) (i.e., PPEG-OH) brushes were grafted from an ozone-pretreated polyurethane (PU) surface. The high-density hydroxyl groups on the dangling PPEG-OH brushes then underwent condensation with a mercapto-silane (i.e., MPS, mercaptopropyl trimethoxysilane) followed by S-nitrosylation to produce a 3-D network of NO-releasing RSNO to form the PU/PPEG-OH-MPS-NO coating. This 3-D coating produces NO flux of up to 7 nmol/(cm(2) min), which is nearly 3 orders of magnitude higher than the picomole/(cm(2) min) levels of other NO-releasing biomedical implants previously reported. The covalent immobilization of RSNO avoids donor leaching and reduces the risks of cytotoxicity arising from leachable RSNO. Our coated PU surfaces display good biocompatibility and exhibit excellent antibiofilm formation activity in vitro (up to 99.99%) against a broad spectrum of Gram-positive and Gram-negative bacteria. Further, the high-density RSNO achieves nearly 99% and 99.9% in vivo reduction of Pseudomonas aeruginosa (P. aeruginosa) and methicillin-resistant Staphylococcus aureus (MRSA) in a murine subcutaneous implantation infection model. Our surface chemistry to create high NO payload without NO-donor leaching can be applied to many biomedical devices.

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