TY - JOUR
T1 - Surface enhancements accelerate bone bonding to CPC-coated strain gauges
AU - Cordaro, Nicholas M.
AU - Szivek, John A.
AU - DeYoung, Don W.
PY - 2001
Y1 - 2001
N2 - Calcium phosphate ceramic (CPC)-coated strain gauges have been used for in vivo bone strain measurements for up to 18 weeks, but they require 6 to 9 weeks for sufficient bonding. Osteogenic protein-1 (OP-1), PepTite™ (a proprietary ligand), calcium sulfate dihydrate (CSD), transforming growth factor β-1 (TGF-β1), and an endothelial cell layer with and without TGF-β1 were used as surface enhancements to accelerate bone-to-CPC bonding. Young male Sprague-Dawley rats were implanted with unenhanced and enhanced CPC-coated gauges. Animals were allowed normal activity for 3 weeks and then calcein labeled. Femurs were explanted following euthanasia. A gauge was attached with cyanoacrylate to the opposite femur in the same position as the CPC-coated gauge. Bones were cantilever-loaded to assess strain transfer. They were sectioned and stained with mineralized bone stain (MIBS) and examined with transmitted and ultraviolet light. Mechanical testing indicated increased sensing accuracy for TGF-β1 and OP-1 enhancements to 105 ± 14% and 92 ± 12% versus 52 ± 44% for the unenhanced gauges. The PepTite™ and the endothelial-cell-layer-enhanced gauges showed lower sensing accuracy, and histology revealed a vascular layer near CPC particles. TGF-β1 increased bone formation when used prior to endothelial cell sodding. CSD prevented strain transfer to the femur. TGF-β1 and OP-1 surface enhancements produced accurate in vivo strain sensing on the rat femur after 3 weeks.
AB - Calcium phosphate ceramic (CPC)-coated strain gauges have been used for in vivo bone strain measurements for up to 18 weeks, but they require 6 to 9 weeks for sufficient bonding. Osteogenic protein-1 (OP-1), PepTite™ (a proprietary ligand), calcium sulfate dihydrate (CSD), transforming growth factor β-1 (TGF-β1), and an endothelial cell layer with and without TGF-β1 were used as surface enhancements to accelerate bone-to-CPC bonding. Young male Sprague-Dawley rats were implanted with unenhanced and enhanced CPC-coated gauges. Animals were allowed normal activity for 3 weeks and then calcein labeled. Femurs were explanted following euthanasia. A gauge was attached with cyanoacrylate to the opposite femur in the same position as the CPC-coated gauge. Bones were cantilever-loaded to assess strain transfer. They were sectioned and stained with mineralized bone stain (MIBS) and examined with transmitted and ultraviolet light. Mechanical testing indicated increased sensing accuracy for TGF-β1 and OP-1 enhancements to 105 ± 14% and 92 ± 12% versus 52 ± 44% for the unenhanced gauges. The PepTite™ and the endothelial-cell-layer-enhanced gauges showed lower sensing accuracy, and histology revealed a vascular layer near CPC particles. TGF-β1 increased bone formation when used prior to endothelial cell sodding. CSD prevented strain transfer to the femur. TGF-β1 and OP-1 surface enhancements produced accurate in vivo strain sensing on the rat femur after 3 weeks.
KW - Calcium phosphate ceramics
KW - Endothelial cells
KW - Osteogenic protein-1
KW - Strain gauge
KW - Transforming growth factor β-1
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U2 - 10.1002/1097-4636(200107)56:1<109::AID-JBM1075>3.0.CO;2-W
DO - 10.1002/1097-4636(200107)56:1<109::AID-JBM1075>3.0.CO;2-W
M3 - Article
C2 - 11309797
AN - SCOPUS:0035003071
SN - 0021-9304
VL - 56
SP - 109
EP - 119
JO - Journal of Biomedical Materials Research
JF - Journal of Biomedical Materials Research
IS - 1
ER -