Literature DB >> 2296757

Osseous wound healing with xenogeneic bone implants with a biodegradable carrier.

J O Hollinger1, J P Schmitz, D E Mark, A E Seyfer.   

Abstract

Human antigen-extracted, autolyzed (AA) bone and a bovine bone morphogenetic protein were prepared as implants within biodegradable carriers and compared with autogenous bone grafts and controls in the healing of critical-size bony defects in nonhuman primates. The treated craniotomy sites were studied 3 and 6 months after surgery; radiodensity and volume of newly deposited trabecular bone were assessed by radiomorphometric and histomorphometric methods, respectively. There was no evidence of adverse immunologic response to the experimental implants. The autografts resulted in the greatest volume of new bone formation (p less than 0.01), but the AA implants elicited a significantly greater response than either the bovine bone morphogenetic protein derivatives or the controls (p less than 0.05). By 6 months, the AA derivatives had healed with actively coalescing islands of new bone, displaying normal-appearing outer and inner tables along with well-developed marrow cavities. It appears that xenogeneic AA implants have the ability to elicit an excellent osseous response in critical-size calvarial wounds. In addition, the carrier polymer for the implants acted as an effective soft-tissue spacer before being absorbed.

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Year:  1990        PMID: 2296757

Source DB:  PubMed          Journal:  Surgery        ISSN: 0039-6060            Impact factor:   3.982


  5 in total

1.  The influence of polymer glass transition temperature and molecular weight on drug release from tablets containing poly(DL-lactic acid).

Authors:  M O Omelczuk; J W McGinity
Journal:  Pharm Res       Date:  1992-01       Impact factor: 4.200

Review 2.  Biotechnology and bone graft substitutes.

Authors:  R A Kenley; K Yim; J Abrams; E Ron; T Turek; L J Marden; J O Hollinger
Journal:  Pharm Res       Date:  1993-10       Impact factor: 4.200

3.  Platelet-derived growth factor inhibits bone regeneration induced by osteogenin, a bone morphogenetic protein, in rat craniotomy defects.

Authors:  L J Marden; R S Fan; G F Pierce; A H Reddi; J O Hollinger
Journal:  J Clin Invest       Date:  1993-12       Impact factor: 14.808

Review 4.  Craniofacial Bone Tissue Engineering: Current Approaches and Potential Therapy.

Authors:  Arbi Aghali
Journal:  Cells       Date:  2021-11-03       Impact factor: 6.600

Review 5.  Evaluation of bone morphogenic proteins in periodontal practice.

Authors:  Supreet Kaur; Vishakha Grover; Harkiran Kaur; Ranjan Malhotra
Journal:  Indian J Dent       Date:  2016 Jan-Mar
  5 in total

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