TY - GEN
T1 - Novel biodegradable poly(lactic-co-glycolic acid) foam for bone regeneration
AU - Thomson, Robert C.
AU - Yaszemski, Michael J.
AU - Powers, John M.
AU - Mikos, Antonios G.
PY - 1994/1/1
Y1 - 1994/1/1
N2 - We present a novel method for manufacturing three-dimensional, biodegradable poly(DL-lactic-co-glycolic acid) (PLGA) foam scaffolds for use in bone regeneration. The technique involves the formation of a composite material consisting of gelatin microspheres surrounded by a PLGA matrix. The gelatin microspheres are leached out leaving an open-cell foam with a pore size and morphology defined by a gelatin microspheres. The foam porosity can be controlled by altering the volume fraction of gelatin used to make composite material. PLGA 50:50 was used as a model degradable polymer to establish the effect of porosity, pore size, and degradation on foam mechanical properties. The compressive strengths and moduli of PLGA 50:50 foams were found to decrease with increasing porosity but were largely unaffected by pore size. Foams with compressive strengths up to 2.5 MPa were manufactured. From in vitro degradation studies we established that for PLGA 50:50 foams the mechanical properties declined in parallel with the decrease in molecular weight. Below a weight average molecular weight of 10,000 the foam had very little mechanical strength (0.02 MPa). These result indicates that PLGA would not be suitable as a scaffold material for bone regeneration. However, the dependence of mechanical properties on porosity, pore size,and degree of degradation which we have determined will aid us in designing a PLGA foam (with a comonomer ratio other than 50:50) suitable for bone regeneration.
AB - We present a novel method for manufacturing three-dimensional, biodegradable poly(DL-lactic-co-glycolic acid) (PLGA) foam scaffolds for use in bone regeneration. The technique involves the formation of a composite material consisting of gelatin microspheres surrounded by a PLGA matrix. The gelatin microspheres are leached out leaving an open-cell foam with a pore size and morphology defined by a gelatin microspheres. The foam porosity can be controlled by altering the volume fraction of gelatin used to make composite material. PLGA 50:50 was used as a model degradable polymer to establish the effect of porosity, pore size, and degradation on foam mechanical properties. The compressive strengths and moduli of PLGA 50:50 foams were found to decrease with increasing porosity but were largely unaffected by pore size. Foams with compressive strengths up to 2.5 MPa were manufactured. From in vitro degradation studies we established that for PLGA 50:50 foams the mechanical properties declined in parallel with the decrease in molecular weight. Below a weight average molecular weight of 10,000 the foam had very little mechanical strength (0.02 MPa). These result indicates that PLGA would not be suitable as a scaffold material for bone regeneration. However, the dependence of mechanical properties on porosity, pore size,and degree of degradation which we have determined will aid us in designing a PLGA foam (with a comonomer ratio other than 50:50) suitable for bone regeneration.
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M3 - Conference contribution
AN - SCOPUS:0028098948
SN - 1558992308
T3 - Materials Research Society Symposium Proceedings
SP - 33
EP - 39
BT - Materials Research Society Symposium Proceedings
PB - Publ by Materials Research Society
T2 - Proceedings of the Biomaterials for Drug and Cell Delivery
Y2 - 29 November 1993 through 1 December 1993
ER -