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Development of hydroxyapatite/poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate)/gelatin composite nanofibers to improve bone‐forming cell proliferation and mineral deposition.

Authors :
Al‐Senani, Ghadah M.
Abu Al‐Ola, Khulood A.
Al‐Qahtani, Salhah D.
Source :
Polymer Engineering & Science; Nov2024, Vol. 64 Issue 11, p5831-5841, 11p
Publication Year :
2024

Abstract

Calcium phosphate hydroxyapatite (HA) was successfully incorporated into poly(3‐hydroxybutyrate‐co‐3‐hydroxyvalerate)/gelatin (PHBV/GEL) nanofibers through an electrospinning process in a hexafluoroisopropanol solvent (HFIP). The PHBV/GEL was electrospun and collected using a rotating metallic network to develop highly ordered nonwoven mats. The effects of HA addition on the morphologies of the obtained fibers were investigated using SEM. The average diameter of the fibers ranged around 700–900 nm, depending on the HA content. From a mechanical perspective, the addition of HA nanoparticles showed variations in tensile strength and elastic modulus values. The lowest tensile strength measured for neat PHBV/GEL was 0.37 ± 0.08 MPa with an elastic modulus of 9.45 ± 0.65 MPa, whereas the highest tensile strength reported for 5% HA‐loaded PHBV/GEL mats was 1.1 ± 0.4 MPa with an elastic modulus of 16.9 ± 0.39 MPa. In addition, cell viability, and mineral deposition were also studied using MC3T3‐E1 pre‐osteoblasts. The in vitro experiment results showed that the HA loaded‐PHBV/GEL mats provide optimal conditions for cell growth and osteogenic differentiation of MC3T3‐E1 cells. This study reveals the potential of PHBV/GEL/HA matrices in the development of novel guided bone‐regeneration (GBR) membranes for orthopedic and craniomaxillofacial surgery, by providing favorable structural features for attachment, growth, and differentiation of osteoblast cells. Highlights: Simple and cheap electrospinning strategy toward network‐like fibrous mats.Microstructure, mechanical, and biological features were evaluated.Electrospun PHBV/GEL/HA promoted calcium phosphate deposition by MC3T3‐E1 cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00323888
Volume :
64
Issue :
11
Database :
Complementary Index
Journal :
Polymer Engineering & Science
Publication Type :
Academic Journal
Accession number :
180737304
Full Text :
https://doi.org/10.1002/pen.26955