Tj. Sigurdsson et al., PERIODONTAL REPAIR IN DOGS - EVALUATION OF RHBMP-2 CARRIERS, The International journal of periodontics & restorative dentistry, 16(6), 1996, pp. 525-537
This study evaluated candidate carriers for recombinant human bone mor
phogenetic protein-2 (rhBMP-2)-driven periodontal regeneration. Previo
us experiments indicated the ability of rhBMP-2 in a particulate deliv
ery system to result in substantial regeneration of bone and periodont
al attachment. In the present study, canine demineralized bone matrix
(DBM), bovine deorganified crystalline bone matrix (Bio-Oss), an absor
bable collagen sponge (ACS) of type I bovine collagen, poly(D, L-lacti
de-co-glycolide) microparticles (PLGA), and polylactic acid granules (
Drilac) were tested for their ability to support rhBMP-2 (0.2 mg/mL im
plant volume)-driven periodontal regeneration. The implants were teste
d in routine critical size canine supra-alveolar periodontal defects w
ith transgingival tooth positioning. Contralateral defects in six beag
le dogs were semirandomly assigned to receive: DBM/rhBMP-2, DBM (no rh
BMP-2), Bio-Oss/rhBMP-2, ACS/rhBMP-2, PLGA/rhBMP-2, or Drilac/rhBMP-2.
Animals were sacrificed 8 weeks postsurgery, and block sections of th
e defects were processed for light microscopy. Substantial bone regene
ration was observed in all defects implanted with rhBMP-2. Other measu
res of periodontal healing, including cementum regeneration and presen
ce of ankylosis, were more variable between the implants. DBM and Bio-
Oss performed well as carriers for rhBMP-2-driven periodontal regenera
tion, although other impediments to their clinical use exist. This stu
dy indicates that qualities of the carrier system, including its space
-maintaining capacity, can affect the ability of rhBMP-2 to regenerate
both alveolar bone and periodontal attachment.