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In Vivo Biological Behavior of Polymer Scaffolds of Natural Origin in the Bone Repair Process.

Authors :
Cunha FB
Pomini KT
Plepis AMG
Martins VDCA
Machado EG
de Moraes R
Munhoz MAES
Machado MVR
Duarte MAH
Alcalde MP
Buchaim DV
Buchaim RL
Fernandes VAR
Pereira ESBM
Pelegrine AA
Cunha MRD
Source :
Molecules (Basel, Switzerland) [Molecules] 2021 Mar 13; Vol. 26 (6). Date of Electronic Publication: 2021 Mar 13.
Publication Year :
2021

Abstract

Autologous bone grafts, used mainly in extensive bone loss, are considered the gold standard treatment in regenerative medicine, but still have limitations mainly in relation to the amount of bone available, donor area, morbidity and creation of additional surgical area. This fact encourages tissue engineering in relation to the need to develop new biomaterials, from sources other than the individual himself. Therefore, the present study aimed to investigate the effects of an elastin and collagen matrix on the bone repair process in critical size defects in rat calvaria. The animals (Wistar rats, n = 30) were submitted to a surgical procedure to create the bone defect and were divided into three groups: Control Group (CG, n = 10), defects filled with blood clot; E24/37 Group (E24/37, n = 10), defects filled with bovine elastin matrix hydrolyzed for 24 h at 37 °C and C24/25 Group (C24/25, n = 10), defects filled with porcine collagen matrix hydrolyzed for 24 h at 25 °C. Macroscopic and radiographic analyses demonstrated the absence of inflammatory signs and infection. Microtomographical 2D and 3D images showed centripetal bone growth and restricted margins of the bone defect. Histologically, the images confirmed the pattern of bone deposition at the margins of the remaining bone and without complete closure by bone tissue. In the morphometric analysis, the groups E24/37 and C24/25 (13.68 ± 1.44; 53.20 ± 4.47, respectively) showed statistically significant differences in relation to the CG (5.86 ± 2.87). It was concluded that the matrices used as scaffolds are biocompatible and increase the formation of new bone in a critical size defect, with greater formation in the polymer derived from the intestinal serous layer of porcine origin (C24/25).

Details

Language :
English
ISSN :
1420-3049
Volume :
26
Issue :
6
Database :
MEDLINE
Journal :
Molecules (Basel, Switzerland)
Publication Type :
Academic Journal
Accession number :
33805847
Full Text :
https://doi.org/10.3390/molecules26061598