Endocultivation the influence of delayed vs. simultaneous application of BMP-2 onto individually formed hydroxyapatite matrices for heterotopic bone induction
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Endocultivation the influence of delayed vs. simultaneous application of BMP-2 onto individually formed hydroxyapatite matrices for heterotopic bone induction. / Becker, S T; Bolte, H; Schünemann, K; Seitz, H; Bara, J J; Beck-Broichsitter, B E; Russo, P A J; Wiltfang, J; Warnke, P H.
in: INT J ORAL MAX SURG, Jahrgang 41, Nr. 9, 01.09.2012, S. 1153-60.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Endocultivation the influence of delayed vs. simultaneous application of BMP-2 onto individually formed hydroxyapatite matrices for heterotopic bone induction
AU - Becker, S T
AU - Bolte, H
AU - Schünemann, K
AU - Seitz, H
AU - Bara, J J
AU - Beck-Broichsitter, B E
AU - Russo, P A J
AU - Wiltfang, J
AU - Warnke, P H
N1 - Copyright © 2012 International Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.
PY - 2012/9/1
Y1 - 2012/9/1
N2 - When bone morphogenetic protein (BMP) is delivered to matrices in vivo may affect tissue engineered bone constructs for jaw reconstruction after cancer surgery. This study compared the effects of BMP application at different times after matrix implantation for heterotopic bone induction in a rat model. Hydroxyapatite blocks were implanted unilaterally onto the surface of the latissimus dorsi muscle. A second block was implanted onto the contralateral muscle after 1, 2 or 4 weeks and 200 μg rhBMP-2 was injected into the blocks on both sides. Bone formation and density inside the blocks was analysed by CT and histology. 8 weeks after BMP application increases in bone density within the scaffolds were most pronounced in the simultaneous application group (179 HU). Less pronounced increases were observed for the 1 (65 HU), 2 (58 HU) and 4 (31 HU; p<0.0001) week delay group. Homogeneous bone induction started from the central channel of the blocks. Capillaries and larger vessels were seen in all constructs, samples receiving delayed BMP treatment demonstrated significantly greater neovascularization. Delayed application of BMP was less effective for heterotopic bone formation than simultaneous application. A central channel allows homogeneous bone induction directly from the centre of the blocks.
AB - When bone morphogenetic protein (BMP) is delivered to matrices in vivo may affect tissue engineered bone constructs for jaw reconstruction after cancer surgery. This study compared the effects of BMP application at different times after matrix implantation for heterotopic bone induction in a rat model. Hydroxyapatite blocks were implanted unilaterally onto the surface of the latissimus dorsi muscle. A second block was implanted onto the contralateral muscle after 1, 2 or 4 weeks and 200 μg rhBMP-2 was injected into the blocks on both sides. Bone formation and density inside the blocks was analysed by CT and histology. 8 weeks after BMP application increases in bone density within the scaffolds were most pronounced in the simultaneous application group (179 HU). Less pronounced increases were observed for the 1 (65 HU), 2 (58 HU) and 4 (31 HU; p<0.0001) week delay group. Homogeneous bone induction started from the central channel of the blocks. Capillaries and larger vessels were seen in all constructs, samples receiving delayed BMP treatment demonstrated significantly greater neovascularization. Delayed application of BMP was less effective for heterotopic bone formation than simultaneous application. A central channel allows homogeneous bone induction directly from the centre of the blocks.
KW - Absorbable Implants
KW - Animals
KW - Bone Matrix
KW - Bone Morphogenetic Protein 2
KW - Bone Substitutes
KW - Drug Administration Schedule
KW - Drug Delivery Systems
KW - Female
KW - Hydroxyapatites
KW - Implants, Experimental
KW - Osseointegration
KW - Osteogenesis
KW - Rats
KW - Rats, Inbred Lew
KW - Time Factors
KW - Tissue Engineering
KW - Tissue Scaffolds
U2 - 10.1016/j.ijom.2012.03.031
DO - 10.1016/j.ijom.2012.03.031
M3 - SCORING: Journal article
C2 - 22652448
VL - 41
SP - 1153
EP - 1160
JO - INT J ORAL MAX SURG
JF - INT J ORAL MAX SURG
SN - 0901-5027
IS - 9
ER -