Polyurethane nanofiber scaffolds for future bone tissue applications: Using β‐cyclodextrin and zinc oxide nanoparticles to improve the properties

Author:

Khan Rumysa Saleem1ORCID,Rather Anjum Hamid1ORCID,Rafiq Muheeb1ORCID,Wani Taha Umair123ORCID,Jadhav Arvind H.4ORCID,Abdal‐hay Abdalla56ORCID,Kanjwal Muzafar A.7ORCID,Ahmad Syed Mudasir8ORCID,Sheikh Faheem A.1ORCID

Affiliation:

1. Nanostructured and Biomimetic Lab, Department of Nanotechnology University of Kashmir Hazratbal Srinagar India

2. Non‐Clinical Evaluation Center Biomedical Research Institute, Jeonbuk National University Hospital Jeonju South Korea

3. College of Pharmacy and Research Institute of Pharmaceutical Sciences Gyeongsang National University Jinju South Korea

4. Centre for Nano and Material Science (CNMS) Jain University, Jain Global Campus Bangalore India

5. School of Dentistry, Oral Health Centre Herston The University of Queensland Herston Queensland Australia

6. Department of Mechanical Engineering Faculty of Engineering, South Valley University Qena Egypt

7. Mechanical Engineering Department Khalifa University Abu Dhabi United Arab Emirates

8. Division of Animal Biotechnology, Faculty of Veterinary Sciences & Animal Husbandry SKUAST‐Kashmir Srinagar India

Abstract

AbstractNumerous strategies exist to design a suitable bone graft made from polyurethane (PU) nanofibers. However, using PU nanofibers is impractical owing to their hydrophobicity. This work transforms the hydrophobicity of PU nanofibers using β‐cyclodextrin (β‐CD) and zinc oxide (ZnO) nanoparticles (NPs). Transmission and scanning electron microscopy (SEM) indicated the size of ~100 to 200 nm for ZnO NPs, and these NPs could finely harmonize inside nanofibers. The phenolphthalein absorbance test confirmed the inclusion of ZnO and β‐CD. Fourier transform infrared, X‐ray diffraction, and photoelectron spectroscopy showed that synthesized composites have intermolecular hydrogen interactions between the PU, β‐CD, and ZnO NPs. These embellishments improved the hydrophilicity from a contact angle of 60.2 ± 0.2° to 0°. The tensile strength of modified fibers increased from 2.16 ± 0.14 to 6.65 ± 6.0 MPa. The incorporation of ZnO NPs caused the mineralization of the nanofibers and the maximum number of hydroxyapatite NPs in the composite, which had the highest concentration of ZnO NPs. These nanofiber mats boosted the proliferation of Human Embryonic Kidney 293 T cells till 6 days of culture for the nanofiber with 5% β‐CD and 75 mg ZnO NPs combination. Cell fixation studies indicated the successful attachment of cells onto nanofibers. Consequently, our multifunctional scaffolds could be osteoproductive and osteoinductive biomaterials for future bone tissue engineering.

Publisher

Wiley

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