TY - JOUR
T1 - Mesoporous silicon-PLGA composite microspheres for the double controlled release of biomolecules for orthopedic tissue engineering
AU - Fan, Dongmei
AU - De Rosa, Enrica
AU - Murphy, Matthew B.
AU - Peng, Yang
AU - Smid, Christine A.
AU - Chiappini, Ciro
AU - Liu, Xuewu
AU - Simmons, Paul
AU - Weiner, Bradley K.
AU - Ferrari, Mauro
AU - Tasciotti, Ennio
PY - 2012/1/25
Y1 - 2012/1/25
N2 - In this study, poly(dl-lactide-co-glycolide)/porous silicon (PLGA/pSi) composite microspheres, synthesized by a solid-in-oil-in-water (S/O/W) emulsion method, are developed for the long-term controlled delivery of biomolecules for orthopedic tissue engineering applications. Confocal and fluorescent microscopy, together with material analysis, show that each composite microsphere contained multiple pSi particles embedded within the PLGA matrix. The release profiles of fluorescein isothiocyanate (FITC)-labeled bovine serum albumin (FITC-BSA), loaded inside the pSi within the PLGA matrix, indicate that both PLGA and pSi contribute to the control of the release rate of the payload. Protein stability studies show that PLGA/pSi composite can protect BSA from degradation during the long term release. We find that during the degradation of the composite material, the presence of the pSi particles neutralizes the acidic pH due to the PLGA degradation by-products, thus minimizing the risk of inducing inflammatory responses in the exposed cells while stimulating the mineralization in osteogenic growth media. Confocal studies show that the cellular uptake of the composite microspheres is avoided, while the fluorescent payload is detectable intracellularly after 7 days of co-incubation. In conclusion, the PLGA/pSi composite microspheres offer an additional level of controlled release and could be ideal candidates as drug delivery vehicles for orthopedic tissue engineering applications. Poly(dl-lactide-co-glycolide)/porous silicon (PLGA/pSi) composite microspheres are synthesized by a solid-in-oil-in-water (S/O/W) emulsion method. These composite microspheres can exhibit sustained protein release, preserve protein bioactivity, stimulate mineralization, neutralize the acidic pH due to the PLGA degradation by-products, and avoid uptake by cells. These microspheres are developed for the long-term controlled delivery of biomolecules for orthopedic tissue engineering applications.
AB - In this study, poly(dl-lactide-co-glycolide)/porous silicon (PLGA/pSi) composite microspheres, synthesized by a solid-in-oil-in-water (S/O/W) emulsion method, are developed for the long-term controlled delivery of biomolecules for orthopedic tissue engineering applications. Confocal and fluorescent microscopy, together with material analysis, show that each composite microsphere contained multiple pSi particles embedded within the PLGA matrix. The release profiles of fluorescein isothiocyanate (FITC)-labeled bovine serum albumin (FITC-BSA), loaded inside the pSi within the PLGA matrix, indicate that both PLGA and pSi contribute to the control of the release rate of the payload. Protein stability studies show that PLGA/pSi composite can protect BSA from degradation during the long term release. We find that during the degradation of the composite material, the presence of the pSi particles neutralizes the acidic pH due to the PLGA degradation by-products, thus minimizing the risk of inducing inflammatory responses in the exposed cells while stimulating the mineralization in osteogenic growth media. Confocal studies show that the cellular uptake of the composite microspheres is avoided, while the fluorescent payload is detectable intracellularly after 7 days of co-incubation. In conclusion, the PLGA/pSi composite microspheres offer an additional level of controlled release and could be ideal candidates as drug delivery vehicles for orthopedic tissue engineering applications. Poly(dl-lactide-co-glycolide)/porous silicon (PLGA/pSi) composite microspheres are synthesized by a solid-in-oil-in-water (S/O/W) emulsion method. These composite microspheres can exhibit sustained protein release, preserve protein bioactivity, stimulate mineralization, neutralize the acidic pH due to the PLGA degradation by-products, and avoid uptake by cells. These microspheres are developed for the long-term controlled delivery of biomolecules for orthopedic tissue engineering applications.
KW - controlled release
KW - mesoporous silicon (pSi)
KW - microemulsion
KW - orthopedic tissue engineering
KW - poly(dl -lactide-co-glycolide) (PLGA)
UR - http://www.scopus.com/inward/record.url?scp=84862955512&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84862955512&partnerID=8YFLogxK
U2 - 10.1002/adfm.201100403
DO - 10.1002/adfm.201100403
M3 - Article
AN - SCOPUS:84862955512
VL - 22
SP - 282
EP - 293
JO - Advanced Functional Materials
JF - Advanced Functional Materials
SN - 1616-301X
IS - 2
ER -