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Formulation and Characterization of a New Injectable Bone Substitute Composed PVA/Borax/CaCO3 and Demineralized Bone Matrix.
Medrano-David, Daniela; Lopera, Aura María; Londoño, Martha Elena; Araque-Marín, Pedronel.
Afiliación
  • Medrano-David D; Research Group GIBEC, Life Sciences Faculty, EIA University, Envigado 055420, Colombia.
  • Lopera AM; Research Group GIBEC, Life Sciences Faculty, EIA University, Envigado 055420, Colombia.
  • Londoño ME; Research Group GIBEC, Life Sciences Faculty, EIA University, Envigado 055420, Colombia.
  • Araque-Marín P; Research and Innovation Group in Chemical Formulations, Life Sciences Faculty, EIA University, Envigado 055420, Colombia.
J Funct Biomater ; 12(3)2021 Aug 11.
Article en En | MEDLINE | ID: mdl-34449632
ABSTRACT
The occurrence of bone-related disorders and diseases has dramatically increased in recent years around the world. Demineralized bone matrix (DBM) has been widely used as a bone implant due to its osteoinduction and bioactivity. However, the use of DBM is limited because it is a particulate material, which makes it difficult to manipulate and implant with precision. In addition, these particles are susceptible to migration to other sites. To address this situation, DBM is commonly incorporated into a variety of carriers. An injectable scaffold has advantages over bone grafts or preformed scaffolds, such as the ability to flow and fill a bone defect. The aim of this research was to develop a DBM carrier with such viscoelastic properties in order to obtain an injectable bone substitute (IBS). The developed DBM carrier consisted of a PVA/glycerol network cross-linked with borax and reinforced with CaCO3 as a pH neutralizer, porosity generator, and source of Ca. The physicochemical properties were determined by an injectability test, FTIR, SEM, and TGA. Porosity, degradation, bioactivity, possible cytotoxic effect, and proliferation in osteoblasts were also determined. The results showed that the developed material has great potential to be used in bone tissue regeneration.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Funct Biomater Año: 2021 Tipo del documento: Article País de afiliación: Colombia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Funct Biomater Año: 2021 Tipo del documento: Article País de afiliación: Colombia