Romina Berger , Alina Rahtz , Alexander Schweigerdt , Daniel D. Stöbener , Andrea Cosimi , Wibke Dempwolf , Henning Menzel , Sonja Johannsmeier , Marie Weinhart
{"title":"稳定的,生物活性的水凝胶涂层在有机硅表面的非侵入性净化通过光化学处理","authors":"Romina Berger , Alina Rahtz , Alexander Schweigerdt , Daniel D. Stöbener , Andrea Cosimi , Wibke Dempwolf , Henning Menzel , Sonja Johannsmeier , Marie Weinhart","doi":"10.1016/j.bioactmat.2025.07.052","DOIUrl":null,"url":null,"abstract":"<div><div>Polydimethylsiloxane (PDMS) is widely used in biomedical applications due to its biocompatibility, chemical stability, flexibility, and resistance to degradation in physiological environments. However, its intrinsic inertness limits further (bio)functionalization, and its hydrophobic recovery compromises the longevity of conventional surface modifications. To address these challenges, we developed a nanoprecipitation method for the straightforward colloidal deposition, covalent thermal crosslinking, and surface anchoring of a chemically tunable, biocompatible polyacrylamide with reactive hydroxyl groups, enabling further surface modifications. This polymer incorporates ∼6 % bioinspired catechol units, introduced via an elegant one-pot Kabachnik-Fields reaction, to facilitate thermally induced network formation and enhance adhesion to plasma-activated PDMS. The resulting uniform coatings exhibited tunable dry layer thicknesses up to 44 ± 7 nm and effectively suppressed PDMS chain rearrangement even after steam autoclaving, ensuring long-term stability in aqueous and ambient environments for at least 90 days.</div><div>The bioactive post-modification potential was demonstrated in a proof-of-concept study by immobilizing the photosensitizer <em>rose bengal</em> at surface concentrations of 20 or 40 μg cm<sup>−2</sup>. The coating exhibited antimicrobial activity against <em>S. aureus</em>, achieving a 4-log reduction (99.99 %) in colony-forming units after 30 min of irradiation at 554 nm (342 J cm<sup>−2</sup>), even when bacteria were suspended in liquid, without direct surface contact. In contrast, antimicrobial activity against <em>E. coli</em> was only observed with minimized liquid volume, bringing the motile bacteria into close contact with the surface.</div><div>This work established a straightforward and versatile strategy for the stable and bioactive functionalization of PDMS surfaces for application in non-invasive surface decontamination.</div></div>","PeriodicalId":8762,"journal":{"name":"Bioactive Materials","volume":"54 ","pages":"Pages 86-102"},"PeriodicalIF":18.0000,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Stable, bioactive hydrogel coating on silicone surfaces for non-invasive decontamination via photochemical treatment\",\"authors\":\"Romina Berger , Alina Rahtz , Alexander Schweigerdt , Daniel D. 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This polymer incorporates ∼6 % bioinspired catechol units, introduced via an elegant one-pot Kabachnik-Fields reaction, to facilitate thermally induced network formation and enhance adhesion to plasma-activated PDMS. The resulting uniform coatings exhibited tunable dry layer thicknesses up to 44 ± 7 nm and effectively suppressed PDMS chain rearrangement even after steam autoclaving, ensuring long-term stability in aqueous and ambient environments for at least 90 days.</div><div>The bioactive post-modification potential was demonstrated in a proof-of-concept study by immobilizing the photosensitizer <em>rose bengal</em> at surface concentrations of 20 or 40 μg cm<sup>−2</sup>. The coating exhibited antimicrobial activity against <em>S. aureus</em>, achieving a 4-log reduction (99.99 %) in colony-forming units after 30 min of irradiation at 554 nm (342 J cm<sup>−2</sup>), even when bacteria were suspended in liquid, without direct surface contact. 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Stable, bioactive hydrogel coating on silicone surfaces for non-invasive decontamination via photochemical treatment
Polydimethylsiloxane (PDMS) is widely used in biomedical applications due to its biocompatibility, chemical stability, flexibility, and resistance to degradation in physiological environments. However, its intrinsic inertness limits further (bio)functionalization, and its hydrophobic recovery compromises the longevity of conventional surface modifications. To address these challenges, we developed a nanoprecipitation method for the straightforward colloidal deposition, covalent thermal crosslinking, and surface anchoring of a chemically tunable, biocompatible polyacrylamide with reactive hydroxyl groups, enabling further surface modifications. This polymer incorporates ∼6 % bioinspired catechol units, introduced via an elegant one-pot Kabachnik-Fields reaction, to facilitate thermally induced network formation and enhance adhesion to plasma-activated PDMS. The resulting uniform coatings exhibited tunable dry layer thicknesses up to 44 ± 7 nm and effectively suppressed PDMS chain rearrangement even after steam autoclaving, ensuring long-term stability in aqueous and ambient environments for at least 90 days.
The bioactive post-modification potential was demonstrated in a proof-of-concept study by immobilizing the photosensitizer rose bengal at surface concentrations of 20 or 40 μg cm−2. The coating exhibited antimicrobial activity against S. aureus, achieving a 4-log reduction (99.99 %) in colony-forming units after 30 min of irradiation at 554 nm (342 J cm−2), even when bacteria were suspended in liquid, without direct surface contact. In contrast, antimicrobial activity against E. coli was only observed with minimized liquid volume, bringing the motile bacteria into close contact with the surface.
This work established a straightforward and versatile strategy for the stable and bioactive functionalization of PDMS surfaces for application in non-invasive surface decontamination.
Bioactive MaterialsBiochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
28.00
自引率
6.30%
发文量
436
审稿时长
20 days
期刊介绍:
Bioactive Materials is a peer-reviewed research publication that focuses on advancements in bioactive materials. The journal accepts research papers, reviews, and rapid communications in the field of next-generation biomaterials that interact with cells, tissues, and organs in various living organisms.
The primary goal of Bioactive Materials is to promote the science and engineering of biomaterials that exhibit adaptiveness to the biological environment. These materials are specifically designed to stimulate or direct appropriate cell and tissue responses or regulate interactions with microorganisms.
The journal covers a wide range of bioactive materials, including those that are engineered or designed in terms of their physical form (e.g. particulate, fiber), topology (e.g. porosity, surface roughness), or dimensions (ranging from macro to nano-scales). Contributions are sought from the following categories of bioactive materials:
Bioactive metals and alloys
Bioactive inorganics: ceramics, glasses, and carbon-based materials
Bioactive polymers and gels
Bioactive materials derived from natural sources
Bioactive composites
These materials find applications in human and veterinary medicine, such as implants, tissue engineering scaffolds, cell/drug/gene carriers, as well as imaging and sensing devices.