J. Hollinger et al., POLY(ALPHA-HYDROXY ACID) CARRIER FOR DELIVERING RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2 FOR BONE REGENERATION, Journal of controlled release, 39(2-3), 1996, pp. 287-304
Autografting is the most common treatment to correct osseous defects,
with donor sites of calvarium, iliac crest, and rib used most often [1
]. While varying degrees of 'success' have been reported with this the
rapy, a universal concern is donor site morbidity, Allogeneic bank bon
e is an alternative to the autograft and while donor site morbidity is
not an issue, bank bone has liabilities that make it less effective t
han the autograft. Therefore, an off-the-shelf product to replace thes
e therapies would improve the quality of care for patients. Towards th
e development of such a product, we report on two studies that assesse
d a combination of recombinant human bone morphogenetic protein-2 deli
vered to osseous wound sites with a poly(alpha-hydroxy acid) carrier:
poly(lactide-co-glycolide). Results from these studies indicate bone r
epair can be accomplished with this combination. However, despite a ri
ch therapeutic promise, clinical utility must be amplified. Therefore,
the focus of our attention in the future will be the delivery system.