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Biphasic Calcium Phosphate and Activated Carbon Microparticles in a Plasma Clot for Bone Reconstruction and In Situ Drug Delivery: A Feasibility Study.
Rekima, Samah; Gautier, Nadine; Bonnamy, Sylvie; Rochet, Nathalie; Olivier, Florian.
Afiliación
  • Rekima S; INSERM, CNRS, iBV, Université Côte d'Azur, 06107 Nice, France.
  • Gautier N; INSERM, CNRS, iBV, Université Côte d'Azur, 06107 Nice, France.
  • Bonnamy S; CNRS, Université d'Orléans, ICMN UMR 7374, 45071 Orléans, France.
  • Rochet N; INSERM, CNRS, iBV, Université Côte d'Azur, 06107 Nice, France.
  • Olivier F; CNRS, Université d'Orléans, ICMN UMR 7374, 45071 Orléans, France.
Materials (Basel) ; 17(8)2024 Apr 11.
Article en En | MEDLINE | ID: mdl-38673106
ABSTRACT
The development of bone-filling biomaterials capable of delivering in situ bone growth promoters or therapeutic agents is a key area of research. We previously developed a biomaterial constituting biphasic calcium phosphate (BCP) microparticles embedded in an autologous blood or plasma clot, which induced bone-like tissue formation in ectopic sites and mature bone formation in orthotopic sites, in small and large animals. More recently, we showed that activated carbon (AC) fiber cloth is a biocompatible material that can be used, due to its multiscale porosity, as therapeutic drug delivery system. The present work aimed first to assess the feasibility of preparing calibrated AC microparticles, and second to investigate the properties of a BCP/AC microparticle combination embedded in a plasma clot. We show here, for the first time, after subcutaneous (SC) implantation in mice, that the addition of AC microparticles to a BCP/plasma clot does not impair bone-like tissue formation and has a beneficial effect on the vascularization of the newly formed tissue. Our results also confirm, in this SC model, the ability of AC in particle form to adsorb and deliver large molecules at an implantation site. Altogether, these results demonstrate the feasibility of using this BCP/AC/plasma clot composite for bone reconstruction and drug delivery.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Materials (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Materials (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Francia