Dataset Information

Nitric oxide permselectivity in electropolymerized films for sensing applications.

ABSTRACT: The presence of biological interferents in physiological media necessitates chemical modification of the working electrode to facilitate accurate electrochemical measurement of nitric oxide (NO). In this study, we evaluated a series of self-terminating electropolymerized films prepared from one of three isomers of phenylenediamine (PD), phenol, eugenol, or 5-amino-1-naphthol (5A1N) to improve the NO selectivity of a platinum working electrode. The electrodeposition procedure for each monomer was individually optimized using cyclic voltammetry (CV) or constant potential amperometry (CPA). Cyclic voltammetry deposition parameters favoring slower film formation generally yielded films with improved selectivity for NO over nitrite and l-ascorbate. Nitric oxide sensors were fabricated and compared using the optimized deposition procedure for each monomer. Sensors prepared using poly-phenol and poly-5A1N film-modified platinum working electrodes demonstrated the most ideal analytical performance, with the former demonstrating the best selectivity. In simulated wound fluid, platinum electrodes modified with poly-5A1N films proved superior with respect to the NO sensitivity and detection limit.

SUBMITTER: Brown MD

PROVIDER: S-EPMC6929558 | biostudies-literature | 2016 Dec

REPOSITORIES: biostudies-literature

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Nitric oxide permselectivity in electropolymerized films for sensing applications.

Brown Micah D MD Schoenfisch Mark H MH

ACS sensors 20161116 12

The presence of biological interferents in physiological media necessitates chemical modification of the working electrode to facilitate accurate electrochemical measurement of nitric oxide (NO). In this study, we evaluated a series of self-terminating electropolymerized films prepared from one of three isomers of phenylenediamine (PD), phenol, eugenol, or 5-amino-1-naphthol (5A1N) to improve the NO selectivity of a platinum working electrode. The electrodeposition procedure for each monomer was ...[more]

PMID: 31875180

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Project description:Nitric oxide (NO) releasing polymers have been widely applied as biomaterials for a variety of biomedical implants and devices. However, the chemical leaching of NO donors and their byproduct species is almost always observed during the application of polymers doped with NO donors, unless the donor is covalently linked to the polymer. Herein, we report the first NO releasing poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) fluorinated copolymer prepared by incorporating a fluorinated S-nitrosothiol as the NO donor. Under physiological conditions, the resulting polymeric films can release NO for 16?days. Importantly, due to both fluorine-fluorine and electrostatic charge interactions between the fluorinated NO donor and the PVDF-HFP copolymer, the total chemical leaching of the fluorinated NO donor and its disulfide product after 9?day was only 0.6% (mol%) of the initial amount of NO donor loaded into the film. These new NO release PVDF-HFP films exhibit antimicrobial and anti-biofilm activities against both Gram positive S. aureus and Gram negative P. aeruginosa strains. The NO-releasing PVDF-HFP polymer can also be coated on Teflon tubing to release NO under physiological conditions for extended time periods. This NO-releasing PVDF-HFP copolymer with greatly reduced chemical leaching could help enhance the biocompatibility and antimicrobial activity of various biomedical devices. STATEMENT OF SIGNIFICANCE: Fluoropolymers have been widely used in creating various biomedical implants and devices. However, nitric oxide (NO) release fluoropolymers have not been well studied to date. Additionally, in the application of biomaterials doped with NO donors, a significant amount of NO donors and their byproducts almost always leach into aqueous environment. We now report an NO releasing poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) fluoropolymer by incorporating a new fluorinated S-nitrosothiol. The NO release can last for 16?days under physiological conditions. The total chemical leaching was determined to be only 0.6?mol% of the initial S-nitrosothiol loaded. As expected, significant antimicrobial/anti-biofilm activities of the NO release PVDF-HFP film were observed against Gram positive S. aureus and Gram negative P. aeruginosa bacterial strains.

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Nitric oxide permselectivity in electropolymerized films for sensing applications.

Publications

Nitric oxide permselectivity in electropolymerized films for sensing applications.

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