Osteogenic protein 1 device stimulates bone healing to hydroxyapaptite-coated and titanium implants

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Osteogenic protein 1 device stimulates bone healing to hydroxyapaptite-coated and titanium implants. / Lind, M; Overgaard, S; Song, Y; Goodman, S B; Bünger, C; Søballe, K.

In: Journal of Arthroplasty, Vol. 15, No. 3, 04.2000, p. 339-46.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Lind, M, Overgaard, S, Song, Y, Goodman, SB, Bünger, C & Søballe, K 2000, 'Osteogenic protein 1 device stimulates bone healing to hydroxyapaptite-coated and titanium implants', Journal of Arthroplasty, vol. 15, no. 3, pp. 339-46.

APA

Lind, M., Overgaard, S., Song, Y., Goodman, S. B., Bünger, C., & Søballe, K. (2000). Osteogenic protein 1 device stimulates bone healing to hydroxyapaptite-coated and titanium implants. Journal of Arthroplasty, 15(3), 339-46.

Vancouver

Lind M, Overgaard S, Song Y, Goodman SB, Bünger C, Søballe K. Osteogenic protein 1 device stimulates bone healing to hydroxyapaptite-coated and titanium implants. Journal of Arthroplasty. 2000 Apr;15(3):339-46.

Author

Lind, M ; Overgaard, S ; Song, Y ; Goodman, S B ; Bünger, C ; Søballe, K. / Osteogenic protein 1 device stimulates bone healing to hydroxyapaptite-coated and titanium implants. In: Journal of Arthroplasty. 2000 ; Vol. 15, No. 3. pp. 339-46.

Bibtex

@article{f442cafa2a8d49f8ad34ae457b291d4e,
title = "Osteogenic protein 1 device stimulates bone healing to hydroxyapaptite-coated and titanium implants",
abstract = "This study evaluated the effects of osteogenic protein 1 (OP-1) placed in a gap around uncoated and hydroxyapatite (HA)-coated implants. Unloaded cylindrical titanium alloy implants were inserted in the femoral condyles of 16 skeletally mature dogs surrounded by a 3-mm gap. The gap around the implants was filled with 325 microg OP-1 in 130 mg bovine collagen type I as carrier (OP-1 device) or collagen carrier alone or left empty. All groups were tested with both HA-coated and uncoated implants, and the animals were sacrificed after 6 weeks. Implant fixation was determined by push-out test. Bone ongrowth and bone formation were evaluated by quantitative histomorphometry. OP-1 device enhanced mechanical fixation of uncoated and HA-coated implants, resulting in a higher shear strength than implants with collagen matrix and control implants. Bone ingrowth and bone formation in the gap were also stimulated 3-fold for OP-1 groups when compared with empty controls, but no difference was found between OP-1 groups and collagen matrix groups. This study suggests that the OP-1 device placed in a gap around uncoated and HA-coated implants is capable of enhancing mechanical fixation and periimplant bone formation. The collagen carrier alone also enhanced bone ongrowth and fixation significantly.",
author = "M Lind and S Overgaard and Y Song and Goodman, {S B} and C B{\"u}nger and K S{\o}balle",
year = "2000",
month = apr,
language = "English",
volume = "15",
pages = "339--46",
journal = "Journal of Arthroplasty",
issn = "0883-5403",
publisher = "Churchill Livingstone",
number = "3",

}

RIS

TY - JOUR

T1 - Osteogenic protein 1 device stimulates bone healing to hydroxyapaptite-coated and titanium implants

AU - Lind, M

AU - Overgaard, S

AU - Song, Y

AU - Goodman, S B

AU - Bünger, C

AU - Søballe, K

PY - 2000/4

Y1 - 2000/4

N2 - This study evaluated the effects of osteogenic protein 1 (OP-1) placed in a gap around uncoated and hydroxyapatite (HA)-coated implants. Unloaded cylindrical titanium alloy implants were inserted in the femoral condyles of 16 skeletally mature dogs surrounded by a 3-mm gap. The gap around the implants was filled with 325 microg OP-1 in 130 mg bovine collagen type I as carrier (OP-1 device) or collagen carrier alone or left empty. All groups were tested with both HA-coated and uncoated implants, and the animals were sacrificed after 6 weeks. Implant fixation was determined by push-out test. Bone ongrowth and bone formation were evaluated by quantitative histomorphometry. OP-1 device enhanced mechanical fixation of uncoated and HA-coated implants, resulting in a higher shear strength than implants with collagen matrix and control implants. Bone ingrowth and bone formation in the gap were also stimulated 3-fold for OP-1 groups when compared with empty controls, but no difference was found between OP-1 groups and collagen matrix groups. This study suggests that the OP-1 device placed in a gap around uncoated and HA-coated implants is capable of enhancing mechanical fixation and periimplant bone formation. The collagen carrier alone also enhanced bone ongrowth and fixation significantly.

AB - This study evaluated the effects of osteogenic protein 1 (OP-1) placed in a gap around uncoated and hydroxyapatite (HA)-coated implants. Unloaded cylindrical titanium alloy implants were inserted in the femoral condyles of 16 skeletally mature dogs surrounded by a 3-mm gap. The gap around the implants was filled with 325 microg OP-1 in 130 mg bovine collagen type I as carrier (OP-1 device) or collagen carrier alone or left empty. All groups were tested with both HA-coated and uncoated implants, and the animals were sacrificed after 6 weeks. Implant fixation was determined by push-out test. Bone ongrowth and bone formation were evaluated by quantitative histomorphometry. OP-1 device enhanced mechanical fixation of uncoated and HA-coated implants, resulting in a higher shear strength than implants with collagen matrix and control implants. Bone ingrowth and bone formation in the gap were also stimulated 3-fold for OP-1 groups when compared with empty controls, but no difference was found between OP-1 groups and collagen matrix groups. This study suggests that the OP-1 device placed in a gap around uncoated and HA-coated implants is capable of enhancing mechanical fixation and periimplant bone formation. The collagen carrier alone also enhanced bone ongrowth and fixation significantly.

M3 - Journal article

C2 - 10794230

VL - 15

SP - 339

EP - 346

JO - Journal of Arthroplasty

JF - Journal of Arthroplasty

SN - 0883-5403

IS - 3

ER -

ID: 252054801