Mechanically Tunable Bone Scaffolds: In Vivo Hardening of 3D-Printed Calcium Phosphate/Polycaprolactone Inks
Metadatos
Mostrar el registro completo del ítemAutor
Mateu Sanz, Miguel; Varela, Pablo; del-Mazo-Barbara, Laura; Lodoso-Torrecilla, Irene; Jiménez-Piqué, Emilio; Franch, Jordi; Alaminos Mingorance, Miguel; Ginebra, María PauEditorial
Wiley-VCH
Fecha
2025-09-19Referencia bibliográfica
M. Mateu-Sanz, P. Varela, L. del-Mazo-Barbara, et al. “ Mechanically Tunable Bone Scaffolds: In Vivo Hardening of 3D-Printed Calcium Phosphate/Polycaprolactone Inks.” Adv. Funct. Mater. (2025): e09357. https://doi.org/10.1002/adfm.202509357
Patrocinador
Spanish Ministry of Science and Innovation through project (Grant Number: PDC2022-133143-I00); Departament d'Innovació, Universitats i Empresa, Generalitat de Catalunya (ICREA Academia Award); Ministerio de Ciencia e Innovación (Grant Number: CEX2023-001300-M); HORIZON EUROPE European Research Council (Grant Number: 101055053)Resumen
Calcium phosphate 3D printing has revolutionized customized bone grafting.
However, its inherent fragility limits clinical applicability. In this work, this
problem is overcome by designing a composite scaffold able to harden in vivo.
An α-tricalcium phosphate/polycaprolactone scaffold is developed that is
ductile and tough when freshly printed and undergoes a transformation to
hydroxyapatite following implantation in the body, resulting in its hardening.
The hardening reaction, that takes place under physiological conditions and
its impact on the biological response and osteogenic capacity of the material
are investigated, both in vitro and in vivo, by comparing the in vivo hardening
scaffolds with 3D printed hydroxyapatite and hydroxyapatite/polycaprolactone
counterparts. In vitro results confirm the bioactivity, osteogenicity, and
immunomodulatory potential of the polycaprolactone-based scaffolds. MG-63
cells increase the expression of osteogenic markers, while a downregulation
of proinflammatory cytokines is observed in RAW246.7 cells. In vivo
evaluation in a rabbit model confirms progressive bone infiltration and
maturation, while osteoclast-mediated scaffold degradation is observed, being
gradually resorbed and replaced by newly formed bone. Overall, in vivo
hardening α-tricalcium phosphate/polycaprolactone scaffolds achieve
mechanical properties comparable to human trabecular bone while retaining
the biocompatibility and osteogenic potential of biomimetic hydroxyapatite.





