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Effect of nanocoating with rhamnogalacturonan-I on surface properties and osteoblasts response
Long‐term stability of titanium implants are dependent on a variety of factors. Nanocoating with organic molecules is one of the methods used to improve osseointegration. Therefore, the aim of this study is to evaluate the in vitro effect of nanocoating with pectic rhamnogalacturonan‐I (RG‐I) on sur...
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Published in: | Journal of biomedical materials research. Part A 2012-03, Vol.100A (3), p.654-664 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Long‐term stability of titanium implants are dependent on a variety of factors. Nanocoating with organic molecules is one of the methods used to improve osseointegration. Therefore, the aim of this study is to evaluate the in vitro effect of nanocoating with pectic rhamnogalacturonan‐I (RG‐I) on surface properties and osteoblasts response. Three different RG‐Is from apple and lupin pectins were modified and coated on amino‐functionalized tissue culture polystyrene plates (aminated TCPS). Surface properties were evaluated by scanning electron microscopy, contact angle measurement, atomic force microscopy, and X‐ray photoelectron spectroscopy. The effects of nanocoating on proliferation, matrix formation and mineralization, and expression of genes (real‐time PCR) related to osteoblast differentiation and activity were tested using human osteoblast‐like SaOS‐2 cells. It was shown that RG‐I coatings affected the surface properties. All three RG‐I induced bone matrix formation and mineralization, which was also supported by the finding that gene expression levels of alkaline phosphatase, osteocalcin, and collagen type‐1 were increased in cells cultured on the RG‐I coated surface, indicating a more differentiated osteoblastic phenotype. This makes RG‐I coating a promising and novel candidate for nanocoatings of implants. © 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012. |
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ISSN: | 1549-3296 1552-4965 |
DOI: | 10.1002/jbm.a.33311 |