Photo-crosslinked networks based on panthenol-derived polyesters: degradable materials for biomedical applications

Tissue engineering has an increasing demand for safe materials that can support complex architectures in tissue regeneration. The development of new biodegradable polymers is a challenge that needs to be constantly addressed to drive the advancements towards biomedical applications. In this study, a new polyester based on D,L-panthenol, poly(D,L-4,3′-panthenyl adipate) (PPA), was successfully synthesized, modified, and photo-crosslinked. While panthenol (also called provitamin B5, a cofactor present in a plethora of metabolic reactions) is widely used in the cosmetic industry due to its moisturizing and wound-healing properties, to the best of our knowledge, no previous records of panthenol-derived polycondensation exist in the literature. The synthesized PPA, a polyol, was modified by introducing acryloyl moieties, yielding an amorphous PPA acrylate with around 67 % of double bonds. The acrylate system allows the incorporation of a wide range of co-crosslinkers with diverse reactivities and functional groups, enabling straightforward tuning of network properties. Various co-monomers or co-crosslinkers were incorporated, including N-isopropylacrylamide, N-vinylpyrrolidone, 1-vinylimidazole, 1,6-hexanediol diacrylate, and divinyl adipate, yielding exceptional efficiency in photo-curing, achieving high network densities with rapid gelation kinetics, and full double bond conversion. The systems have proven to be hydrolytically degradable with tunable degradation rates and non-cytotoxic towards NIH-3T3 cell lines. These photo-curable systems are promising candidates for light-based scaffold biofabrication techniques. Moreover, the potential for panthenol-derived polymer functionalization with different unsaturated groups unlocks exciting possibilities for biomedical applications. • Panthenol was used for the first time as a monomer in step-growth polymerization. • Poly(panthenyl adipate), PPA, was acrylated to produce the photo-curable PPA-AC. • PPA-AC was combined with vinylic monomers to produce tailorable materials. • PPA-AC materials are degradable and suitable for light-based biofabrication. • Panthenol-based polymers allow diverse functionalization for biomedical use.

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Journal
Materials Today Advances
Published
2026-01-08
DOI
https://doi.org/10.1016/j.mtadv.2026.100686
Primary Topic
Polymer composites and self-healing
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article
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article

Photo-crosslinked networks based on panthenol-derived polyesters: degradable materials for biomedical applications

S. Van Vlierberghe, Denisse Esther Mallaupoma Camarena, Anna Szabó, Luiz Henrique Catalani et al.
Materials Today Advances
Polymer composites and self-healing
article

Photo-crosslinked networks based on panthenol-derived polyesters: degradable materials for biomedical applications

S. Van Vlierberghe, Denisse Esther Mallaupoma Camarena, Anna Szabó, Luiz Henrique Catalani, Isabela Lima Autran Dourado, Flávia Gonçalves, Daniel Franco Minatelli
article en

Abstract

Tissue engineering has an increasing demand for safe materials that can support complex architectures in tissue regeneration. The development of new biodegradable polymers is a challenge that needs to be constantly addressed to drive the advancements towards biomedical applications. In this study, a new polyester based on D,L-panthenol, poly(D,L-4,3′-panthenyl adipate) (PPA), was successfully synthesized, modified, and photo-crosslinked. While panthenol (also called provitamin B5, a cofactor present in a plethora of metabolic reactions) is widely used in the cosmetic industry due to its moisturizing and wound-healing properties, to the best of our knowledge, no previous records of panthenol-derived polycondensation exist in the literature. The synthesized PPA, a polyol, was modified by introducing acryloyl moieties, yielding an amorphous PPA acrylate with around 67 % of double bonds. The acrylate system allows the incorporation of a wide range of co-crosslinkers with diverse reactivities and functional groups, enabling straightforward tuning of network properties. Various co-monomers or co-crosslinkers were incorporated, including N-isopropylacrylamide, N-vinylpyrrolidone, 1-vinylimidazole, 1,6-hexanediol diacrylate, and divinyl adipate, yielding exceptional efficiency in photo-curing, achieving high network densities with rapid gelation kinetics, and full double bond conversion. The systems have proven to be hydrolytically degradable with tunable degradation rates and non-cytotoxic towards NIH-3T3 cell lines. These photo-curable systems are promising candidates for light-based scaffold biofabrication techniques. Moreover, the potential for panthenol-derived polymer functionalization with different unsaturated groups unlocks exciting possibilities for biomedical applications. • Panthenol was used for the first time as a monomer in step-growth polymerization. • Poly(panthenyl adipate), PPA, was acrylated to produce the photo-curable PPA-AC. • PPA-AC was combined with vinylic monomers to produce tailorable materials. • PPA-AC materials are degradable and suitable for light-based biofabrication. • Panthenol-based polymers allow diverse functionalization for biomedical use.

Materials Today AdvancesVol. 29
Universidade de São Paulo (BR), Ghent University (BE), Institute of Macromolecular Chemistry (UA), Universidade de Santo Amaro (BR)
Industry, innovation and infrastructure
Openalex Percentile: Top 93%
Polymer composites and self-healing
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