Title of article :
Shear assay measurements of cell adhesion on biomaterials surfaces
Author/Authors :
Fu، نويسنده , , G. and Milburn، نويسنده , , C. J. Mwenifumbo، نويسنده , , S. and Cao، نويسنده , , Y. and Oparinde، نويسنده , , G.M. and Adeoye، نويسنده , , M.O. and Therialt، نويسنده , , C. and Beye، نويسنده , , A.C. and Soboyejo، نويسنده , , W.O.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
9
From page :
1293
To page :
1301
Abstract :
The paper examines the adhesion of human osterosarcoma (HOS) cells to selected biomaterials surfaces that are relevant to implantable biomedical systems and bio-micro-electro-mechanical systems (BioMEMS). The four biomaterials that were explored include: silicon, silicon coated with a nanoscale layer of titanium, Ti–6Al–4V, and poly-di-methy-siloxane (PDMS). The interfacial strengths between the HOS cells and the biomaterials surfaces were determined using a shear assay technique. The adhesion forces were determined using a combination of confocal microscopy images of the three-dimensional cell structure, and computational fluid dynamics (CFD) simulations that coupled actual cell morphologies and non-Newtonian fluid properties in the computation of the adhesion forces. After cell detachment by the shear assay, immunofluorescence staining of the biomedical surfaces was used to reveal the proteins associated with cell detachment. These revealed that the nano-scale Ti coating increases the cell/surface adhesion strength. Silicon with Ti coating has the strongest adhesion strength, while the other surfaces had similar adhesion strength. The measured strengths are shown to be largely associated with the detachment of focal adhesion proteins from extra-cellular matrix (ECM) proteins.
Keywords :
Cell/surface interfacial strengths , Shear assay technique , Computational fluid dynamics , Biomedical systems , BioMEMS surfaces
Journal title :
Materials Science and Engineering C
Serial Year :
2009
Journal title :
Materials Science and Engineering C
Record number :
2100264
Link To Document :
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