Development of 3D Printed pNIPAM-Chitosan Scaffolds for Dentoalveolar Tissue Engineering

Author:

Salar Amoli Mehdi12,Anand Resmi13,EzEldeen Mostafa24ORCID,Geris Liesbet356ORCID,Jacobs Reinhilde27,Bloemen Veerle13ORCID

Affiliation:

1. Surface and Interface Engineered Materials (SIEM), Campus Group T, KU Leuven, Andreas Vesaliusstraat 13, 3000 Leuven, Belgium

2. OMFS IMPATH Research Group, Faculty of Medicine, Department of Imaging and Pathology, KU Leuven and Oral and Maxillofacial Surgery, University Hospitals Leuven, Kapucijnenvoer 33, 3000 Leuven, Belgium

3. Prometheus, Division of Skeletal Tissue Engineering Leuven, KU Leuven, 3000 Leuven, Belgium

4. Department of Oral Health Sciences, KU Leuven and Paediatric Dentistry and Special Dental Care, University Hospitals Leuven, Kapucijnenvoer 33, 3000 Leuven, Belgium

5. Biomechanics Research Unit, GIGA-R In Silico Medicine, University of Liège, Quartier Hôpital, Avenue de l’Hôpital 11, 4000 Liège, Belgium

6. Biomechanics Section, KU Leuven, Celestijnenlaan 300C (2419), 3000 Leuven, Belgium

7. Department of Dental Medicine, Karolinska Institutet, 171 77 Stockholm, Sweden

Abstract

While available treatments have addressed a variety of complications in the dentoalveolar region, associated challenges have resulted in exploration of tissue engineering techniques. Often, scaffold biomaterials with specific properties are required for such strategies to be successful, development of which is an active area of research. This study focuses on the development of a copolymer of poly (N-isopropylacrylamide) (pNIPAM) and chitosan, used for 3D printing of scaffolds for dentoalveolar regeneration. The synthesized material was characterized by Fourier transform infrared spectroscopy, and the possibility of printing was evaluated through various printability tests. The rate of degradation and swelling was analyzed through gravimetry, and surface morphology was characterized by scanning electron microscopy. Viability of dental pulp stem cells seeded on the scaffolds was evaluated by live/dead analysis and DNA quantification. The results demonstrated successful copolymerization, and three formulations among various synthesized formulations were successfully 3D printed. Up to 35% degradability was confirmed within 7 days, and a maximum swelling of approximately 1200% was achieved. Furthermore, initial assessment of cell viability demonstrated biocompatibility of the developed scaffolds. While further studies are required to achieve the tissue engineering goals, the present results tend to indicate that the proposed hydrogel might be a valid candidate for scaffold fabrication serving dentoalveolar tissue engineering through 3D printing.

Funder

Research Council of KU Leuven

European Research Council

Publisher

MDPI AG

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