Enhanced osteogenic differentiation of mesenchymal stem cells on metal–organic framework based on copper, zinc, and imidazole coated poly‐l‐lactic acid nanofiber scaffolds

The presence of inorganic bioactive minerals with polymers can accelerate and promote several processes including: bone cell joining, proliferation, differentiation, and expression of osteogenic proteins. In this study, zinc (Zn), copper (Cu), and imidazole metal–organic framework (MOF) nanoparticle...

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Published in:Journal of biomedical materials research. Part A Vol. 107; no. 8; pp. 1841 - 1848
Main Authors: Telgerd, M. D., Sadeghinia, Mohammad, Birhanu, Gebremariam, Daryasari, M. P., Zandi‐Karimi, Ali, Sadeghinia, Ali, Akbarijavar, Hamid, Karami, M. H., Seyedjafari, Ehsan
Format: Journal Article
Language:English
Published: Hoboken, USA John Wiley & Sons, Inc 01-08-2019
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Summary:The presence of inorganic bioactive minerals with polymers can accelerate and promote several processes including: bone cell joining, proliferation, differentiation, and expression of osteogenic proteins. In this study, zinc (Zn), copper (Cu), and imidazole metal–organic framework (MOF) nanoparticles were synthesized and coated over poly‐l‐lactic acid (PLLA) nanofibrous scaffolds for bone tissue engineering application. The surface and bioactive features of the scaffolds were characterized. The osteogenic potential of the scaffolds on human adipose tissue‐derived mesenchymal stem cells (MSCs) was evaluated. Zn–Cu imidazole MOF coated PLLA scaffolds (PLLA@MOF) showed a comparable rate of MSC proliferation with the pure PLLA scaffolds and tissue culture plate (TCP). However, the PLLA@MOF potential of osteogenic differentiation was significantly greater than either pristine PLLA scaffolds or TCP. Hence, coating Zn–Cu imidazole MOF has a significant effect on the osteogenesis of MSC. Therefore, PLLA@MOF is novel scaffolds with bioactive components which are crucial for osteoconductivity and also able to provoke the osteogenesis and angiogenesis.
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University of Tehran
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ISSN:1549-3296
1552-4965
DOI:10.1002/jbm.a.36707