{"title":"Bilayer and clickable electrospun membrane from tailored polyurethanes: a versatile platform for easy surface functionalization.","authors":"Stefano Torresi , Unai Montejo , Ana Alonso-Varona , Nagore Gabilondo , Arantxa Eceiza","doi":"10.1016/j.jsamd.2025.100884","DOIUrl":null,"url":null,"abstract":"<div><div>Two biobased linear polyurethanes were synthesized and electrospun to produce a final bilayer nanofibrous membrane. On one side, it was used a thiol-containing composition, PU-SH, while on the other was employed a non-functionalized polyurethane, PU-PD. The bilayer membrane was conceived to be easily functionalized in water, taking advantage of the high reactivity of thiols. The accessibility and reactivity of the PU-SH layer was corroborated by labelling it with a maleimide-functionalized fluorescent molecule, through a thiol-maleimide click reaction. Furthermore, considering the high hydrophobicity and the mechanical strength of PU-PD and the possible functionalization of the PU-SH layer with Ag nanoparticles (AgNPs), preliminary biocompatibility and antimicrobial studies were conducted for its application as wound dressing. The work demonstrated that accurate control of the polymeric backbone chemistry led to customizable membranes by the rapid, green and homogeneous post-functionalization of the nanofibers with surface clickable groups.</div></div>","PeriodicalId":17219,"journal":{"name":"Journal of Science: Advanced Materials and Devices","volume":"10 2","pages":"Article 100884"},"PeriodicalIF":6.7000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Science: Advanced Materials and Devices","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468217925000371","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Two biobased linear polyurethanes were synthesized and electrospun to produce a final bilayer nanofibrous membrane. On one side, it was used a thiol-containing composition, PU-SH, while on the other was employed a non-functionalized polyurethane, PU-PD. The bilayer membrane was conceived to be easily functionalized in water, taking advantage of the high reactivity of thiols. The accessibility and reactivity of the PU-SH layer was corroborated by labelling it with a maleimide-functionalized fluorescent molecule, through a thiol-maleimide click reaction. Furthermore, considering the high hydrophobicity and the mechanical strength of PU-PD and the possible functionalization of the PU-SH layer with Ag nanoparticles (AgNPs), preliminary biocompatibility and antimicrobial studies were conducted for its application as wound dressing. The work demonstrated that accurate control of the polymeric backbone chemistry led to customizable membranes by the rapid, green and homogeneous post-functionalization of the nanofibers with surface clickable groups.
期刊介绍:
In 1985, the Journal of Science was founded as a platform for publishing national and international research papers across various disciplines, including natural sciences, technology, social sciences, and humanities. Over the years, the journal has experienced remarkable growth in terms of quality, size, and scope. Today, it encompasses a diverse range of publications dedicated to academic research.
Considering the rapid expansion of materials science, we are pleased to introduce the Journal of Science: Advanced Materials and Devices. This new addition to our journal series offers researchers an exciting opportunity to publish their work on all aspects of materials science and technology within the esteemed Journal of Science.
With this development, we aim to revolutionize the way research in materials science is expressed and organized, further strengthening our commitment to promoting outstanding research across various scientific and technological fields.