In vitro evaluation of marrow clot enrichment on microstructure decoration, cell delivery and proliferation of porous titanium scaffolds by selective laser melting three‐dimensional printing

• Published in: Journal of biomedical materials research. Part B, Applied biomaterials Vol. 106; no. 6; pp. 2245 - 2253
• Main Authors: Yao, Qing‐qiang, Hu, Jun, Zheng, Peng‐fei, Li, Jia‐yi, Zhou, Jin, Tian, Shu‐chang, Wei, Bo, Xu, Yan, Wang, Li‐ming
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.08.2018
• Subjects: Alkaline phosphatase; Biocompatibility; Biomechanics; Biomedical materials; Bone marrow; Cell culture; Cell number; Cell proliferation; Collagen (type I); Decoration; Deoxyribonucleic acid; Differentiation (biology); DNA; Enrichment; Erythrocytes; Fabrication; Fibrin; Laser beam melting; Materials research; Materials science; Materials substitution; Melting; Mesenchyme; Microstructure; Modulus of elasticity; Osseointegration; Osteocalcin; Pores; Scaffolds; Stem cells; Surgical implants; Titanium; Titanium alloys; Titanium base alloys; bone marrow clot; microstructure decoration; titanium scaffolds; porous scaffolds
• ISSN: 1552-4973; 1552-4981; 1552-4981
• DOI: 10.1002/jbm.b.34032

Titanium alloy is a clinically approved material for bone substitution. Although three‐dimensional printing (3DP) fabrication technique can build up porous Ti scaffolds with the designed shape and microstructure, the biomechanical performance of 3DP Ti scaffolds still need to be improved to increase the reliability of osseointegration capacity. To address this issue, rabbit bone marrow clot (MC) is used to modify 3DP Ti scaffolds by stem cell delivery and microenvironment decoration inside the pores of these scaffolds. Moreover, 3DP Ti scaffolds were built up using selective laser melting, and 3DP MC‐Ti scaffolds were constructed through the enrichment of MC with Ti scaffolds in vitro . Results demonstrated that the obtained 3DP Ti scaffolds in current study has an average modulus of elasticity (ME) at 1294.48 MPa with average yield strength of 33.154 MPa. For MC‐Ti scaffolds, MC enrichment obstructs the pores of 3DP scaffolds due to the large amount of fibrin and erythrocytes and leads to a decrease in ratio of live cells at 1‐week culture. Cell proliferation and osteogenic differentiation performance of MC‐Ti scaffolds were promoted with porous recanalization in the later 3 weeks. After 2 weeks in vitro culture, fivefold of cell number in MC‐Ti scaffolds were observed than bone marrow‐derived mesenchymal stem cell‐seeded Ti scaffolds. Compared to Ti scaffolds, fourfold of deoxyribonucleic acid content, type I collagen‐α1, osteocalcin, and alkaline phosphatase expression in MC‐Ti scaffolds were observed after 4 weeks in vitro culture. Results suggested that the combination with MC is a highly efficient method that improves the biological performance of Ti scaffolds. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 2245–2253, 2018.