Alginate-hydrogel versus alginate-solid system. Efficacy in bone regeneration in osteoporosis.


Journal

Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 22 11 2019
revised: 01 04 2020
accepted: 21 04 2020
entrez: 1 7 2020
pubmed: 1 7 2020
medline: 31 3 2021
Statut: ppublish

Résumé

In the present study, two different PLGA-Alginate scaffolds, a hydrogel (HY) and a solid sponge (SS), were developed for β-estradiol and BMP-2 sustained delivery for bone regeneration in osteoporosis. β-Estradiol and BMP-2 were encapsulated in PLGA and PLGA-Alginate microspheres respectively. Scaffolds were characterized in vitro in terms of porosity, water uptake, release rate and HY rheological properties. BMP-2 release profiles were also analysed in vivo. The bone regeneration induced by both HY and SS was evaluated using a critical-sized bone defect in an osteoporotic (OP) rat model. Compared to HY, SS presented 30% higher porosity, more than double water absorption capacity and almost negligible mass loss compared to the 40% of HY. Both systems were flexible and fit well the defect shape, however, HY has the advantage of being injectable. Despite both delivery systems had similar composition and release profile, bone repair was around 30% higher with SS than with HY, possibly due to its longer residence time at the defect site. The incorporation of mesenchymal stem cells obtained from OP rats did not result in any improvement or synergistic effect on bone repair.

Identifiants

pubmed: 32600680
pii: S0928-4931(19)34237-7
doi: 10.1016/j.msec.2020.111009
pii:
doi:

Substances chimiques

Alginates 0
Bone Morphogenetic Protein 2 0
Delayed-Action Preparations 0
Hydrogels 0
Estradiol 4TI98Z838E

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

111009

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no conflict of interest.

Auteurs

Patricia García-García (P)

Department of Chemical Engineering and Pharmaceutical Technology, Universidad de La Laguna, 38200 La Laguna, Spain.

Ricardo Reyes (R)

Department of Biochemistry, Microbiology, Cell Biology and Genetics, Universidad de La Laguna, 38200 La Laguna, Spain; Institute of Biomedical Technologies (ITB), Center for Biomedical Research of the Canary Islands (CIBICAN), Universidad de La Laguna, 38200 La Laguna, Spain.

Edgar Pérez-Herrero (E)

Department of Chemical Engineering and Pharmaceutical Technology, Universidad de La Laguna, 38200 La Laguna, Spain; Institute of Biomedical Technologies (ITB), Center for Biomedical Research of the Canary Islands (CIBICAN), Universidad de La Laguna, 38200 La Laguna, Spain.

María Rosa Arnau (MR)

Servicio de Estabulario, Universidad de La Laguna, 38200 La Laguna, Spain; Institute of Biomedical Technologies (ITB), Center for Biomedical Research of the Canary Islands (CIBICAN), Universidad de La Laguna, 38200 La Laguna, Spain.

Carmen Évora (C)

Department of Chemical Engineering and Pharmaceutical Technology, Universidad de La Laguna, 38200 La Laguna, Spain; Institute of Biomedical Technologies (ITB), Center for Biomedical Research of the Canary Islands (CIBICAN), Universidad de La Laguna, 38200 La Laguna, Spain. Electronic address: cevora@ull.edu.es.

Araceli Delgado (A)

Department of Chemical Engineering and Pharmaceutical Technology, Universidad de La Laguna, 38200 La Laguna, Spain; Institute of Biomedical Technologies (ITB), Center for Biomedical Research of the Canary Islands (CIBICAN), Universidad de La Laguna, 38200 La Laguna, Spain. Electronic address: adelgado@ull.edu.es.

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Classifications MeSH