Photodynamic, UV-curable and fibre-forming polyvinyl alcohol derivative with broad processability and staining-free antibacterial capability

IF 6.3 2区 化学 Q1 POLYMER SCIENCE European Polymer Journal Pub Date : 2025-03-19 Epub Date: 2025-02-04 DOI:10.1016/j.eurpolymj.2025.113794
Man Li , Charles Brooker , Rucha Ambike , Ziyu Gao , Paul Thornton , Thuy Do , Giuseppe Tronci
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Abstract

Antimicrobial photodynamic therapy (APDT) is a promising antibiotic-free strategy for broad-spectrum infection control in chronic wounds, minimising bacterial resistance risks. However, rapid photosensitiser diffusion, tissue staining, side toxicity, and short-lived antimicrobial effects present significant clinical limitations for integrating APDT into wound dressings. To address these challenges, we present the design of a bespoke polyvinyl alcohol (PVA) derivative conjugated with both phenothiazine and methacrylate functionalities, enabling staining-free antibacterial photodynamic effects, cellular tolerability and processability into various wound dressing formats, including films, textile fibres and nanoscale coatings. Tosylation of PVA is leveraged for the covalent coupling of toluidine blue ([TB]: 0.69 ± 0.03–0.81 ± 0.05 mg per gram of polymer), as confirmed by UV–Vis spectroscopy and the minimal average release of TB (≤ 3 wt%, < 0.4 µg) following 96-hour incubation in vitro. UV-induced network formation is demonstrated by complete solution gelation, rheology, and a high gel content ( > 95 wt%), and exploited to accomplish cast films and nanoscale integrated wound dressing coatings. UV curing is also successfully coupled with an in-house wet spinning process to realise individual, water-insoluble fibres as the building blocks of fibrous wound dressings. A fluorometric assay supports the generation of reactive oxygen species when the UV-cured samples are exposed to work, but not UV, light, yielding a mean log10 reduction of up to 2.13 in S. aureus, and the complete eradication of P. aeruginosa. Direct and extract cytotoxicity tests with UV-cured films and fibres demonstrate the viability of L929 fibroblasts following 60-min light irradiation and 72-hour cell culture. The bespoke molecular architecture, broad processability and cellular tolerability of this PVA derivative are highly attractive aiming to integrate durable staining-free photodynamic capability in a wide range of healthcare technologies, from chronic wound dressings up to minimally invasive localised therapy.

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光动力,紫外光固化和纤维形成聚乙烯醇衍生物,具有广泛的加工性和无染色的抗菌能力
抗菌光动力疗法(APDT)是一种很有前途的无抗生素策略,用于控制慢性伤口的广谱感染,最大限度地减少细菌耐药风险。然而,光敏剂的快速扩散、组织染色、副作用和短暂的抗菌作用是将APDT整合到伤口敷料中的重大临床局限性。为了解决这些挑战,我们设计了一种定制的聚乙烯醇(PVA)衍生物,具有吩噻嗪和甲基丙烯酸酯的功能,具有无染色的抗菌光动力效应,细胞耐受性和可加工性,可用于各种伤口敷料格式,包括薄膜,纺织纤维和纳米级涂层。PVA的甲苯胺蓝([TB]: 0.69±0.03-0.81±0.05 mg / g聚合物)的共价偶联被利用,正如紫外可见光谱和TB的最小平均释放(≤3 wt%, <;0.4µg),体外培养96小时。紫外线诱导的网络形成通过完全的溶液凝胶化、流变性和高凝胶含量来证明(Ḡ >;95% wt%),并开发完成铸膜和纳米级集成伤口敷料涂层。紫外线固化也成功地与内部湿纺丝工艺相结合,实现了单个的、不溶于水的纤维作为纤维伤口敷料的基石。当紫外固化的样品暴露在工作环境中而不是紫外线下时,荧光测定法支持活性氧的产生,金黄色葡萄球菌的平均log10减少高达2.13,铜绿假单胞菌完全根除。用紫外光固化膜和纤维进行的直接和提取细胞毒性试验表明,经过60分钟的光照射和72小时的细胞培养,L929成纤维细胞具有活力。这种PVA衍生物的定制分子结构、广泛的可加工性和细胞耐受性非常有吸引力,旨在将耐用的无染色光动力能力整合到广泛的医疗保健技术中,从慢性伤口敷料到微创局部治疗。
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来源期刊
European Polymer Journal
European Polymer Journal 化学-高分子科学
CiteScore
9.90
自引率
10.00%
发文量
691
审稿时长
23 days
期刊介绍: European Polymer Journal is dedicated to publishing work on fundamental and applied polymer chemistry and macromolecular materials. The journal covers all aspects of polymer synthesis, including polymerization mechanisms and chemical functional transformations, with a focus on novel polymers and the relationships between molecular structure and polymer properties. In addition, we welcome submissions on bio-based or renewable polymers, stimuli-responsive systems and polymer bio-hybrids. European Polymer Journal also publishes research on the biomedical application of polymers, including drug delivery and regenerative medicine. The main scope is covered but not limited to the following core research areas: Polymer synthesis and functionalization • Novel synthetic routes for polymerization, functional modification, controlled/living polymerization and precision polymers. Stimuli-responsive polymers • Including shape memory and self-healing polymers. Supramolecular polymers and self-assembly • Molecular recognition and higher order polymer structures. Renewable and sustainable polymers • Bio-based, biodegradable and anti-microbial polymers and polymeric bio-nanocomposites. Polymers at interfaces and surfaces • Chemistry and engineering of surfaces with biological relevance, including patterning, antifouling polymers and polymers for membrane applications. Biomedical applications and nanomedicine • Polymers for regenerative medicine, drug delivery molecular release and gene therapy The scope of European Polymer Journal no longer includes Polymer Physics.
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