Abstract

This article presents data related to the research article entitled “The effect of coating type on mechanical properties and controlled drug release of PCL/zein coated 45S5 bioactive glass scaffolds for bone tissue engineering” [1]. We provide data on mechanical properties, in vitro bioactivity and drug release of bioactive glass (BG) scaffolds coated by poly (ε-caprolactone) (PCL) and zein used as a controlled release device for tetracycline hydrochloride (TCH). By coating the BG scaffolds with PCL or PCL/zein blend the mechanical properties of the scaffolds were substantially improved, i.e., the compressive strength increased from 0.004±0.001 MPa (uncoated BG scaffolds) to 0.15±0.02 MPa (PCL/zein coated BG scaffolds). A dense bone-like apatite layer formed on the surface of PCL/zein coated scaffolds immersed for 14 days in simulated body fluid (SBF). The data describe control of drug release and in vitro degradation behavior of coating by engineering the concentration of zein. Thus, the developed scaffolds exhibit attractive properties for application in bone tissue engineering research.

Highlights

  • Mechanical properties and drug release behavior of PCL/zein coated 45S5 bioactive glass scaffolds for bone tissue engineering application

  • This article presents data related to the research article entitled “The effect of coating type on mechanical properties and controlled drug release of PCL/zein coated 45S5 bioactive glass scaffolds for bone tissue engineering” [1]

  • We provide data on mechanical properties, in vitro bioactivity and drug release of bioactive glass (BG) scaffolds coated by poly (ε-caprolactone) (PCL) and zein used as a controlled release device for tetracycline hydrochloride (TCH)

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Summary

Fabrication of bioglass-based scaffolds

Reticulated polyurethane (PU) foams (45 ppi, Eurofoam, Germany) and 45S5 BG powder (composition in wt%: 45% SiO2, 24.5% Na2O, 24.4% CaO and 6% P2O5) of particle size $ 5 mm have been used to fabricate the scaffolds. The scaffolds were fabricated by the foam replication method, following a similar process as described elsewhere [2]

Polymer coating procedure and drug loading
Findings
Drug release analysis
Full Text
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