Rotation-assisted wet-spinning of UV-cured gelatin fibres and nonwovens
Jessica Rickman, Giuseppe Tronci, He Liang, Stephen J. Russell

TL;DR
This paper introduces a scalable wet-spinning and UV-curing method for producing mechanically robust, water-insoluble gelatin fibres and nonwovens with tunable properties, advancing biomedical material design.
Contribution
It presents a novel multiscale approach combining functionalized gelatin synthesis with a voltage-free spinning and UV-curing process, enabling scalable production of customizable gelatin fibres and nonwovens.
Findings
Achieved tensile strength up to ~80 MPa in UV-cured Gel-4VBC fibres.
Demonstrated one-step spunlaid formation of fibroblast-friendly nonwovens.
Controlled mechanical properties through coagulation conditions.
Abstract
Photoinduced network formation is an attractive strategy for designing water-insoluble gelatin fibres as medical device building blocks and for enabling late-stage property customisation. However, mechanically-competent, long-lasting filaments are still hard to realise with current photoactive, e.g. methacrylated, gelatin systems due to inherent spinning instability and restricted coagulation capability. To explore this challenge, we present a multiscale approach combining the synthesis of 4-vinylbenzyl chloride (4VBC)-functionalised gelatin (Gel-4VBC) with a voltage-free spinning and UV-curing process so that biopolymer networks in the form of either individual fibres or nonwovens could be successfully manufactured. In comparison to state-of-the-art methacrylated gelatin, the mechanical properties of UV-cured Gel-4VBC fibres were readily modulated by adjustment of coagulation…
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