TY - JOUR
T1 - Multimodal pore formation in calcium phosphate cements
AU - Lodoso-Torrecilla, I.
AU - van Gestel, N.A.P.
AU - Diaz-Gomez, L.
AU - Grosfeld, E.C.
AU - Laperre, K.
AU - Wolke, J.G.C.
AU - Smith, B.T.
AU - Arts, J.J.
AU - Mikos, A.G.
AU - Jansen, J.A.
AU - Hofmann, S.
AU - van den Beucken, J.J.J.P.
N1 - © 2017 Wiley Periodicals, Inc.
PY - 2018/2/1
Y1 - 2018/2/1
N2 - Calcium phosphate cements (CPCs) are commonly used as bone substitute materials. However, their slow degradation rate and lack of macroporosity hinders new bone formation. Poly(dl-lactic-co-glycolic acid) (PLGA) incorporation is of great interest as, upon degradation, produces acidic by-products that enhance CPC degradation. Yet, new bone formation is delayed until PLGA degradation occurs a few weeks after implantation. Therefore, the aim of this study was to accelerate the early stage pore formation within CPCs in vitro. With that purpose, we incorporated the water-soluble porogen sucrose at different weight percentages (10 or 20 wt %) to CPC and CPC/PLGA composites. The results revealed that incorporation of sucrose porogens increased mass loss within the first week of in vitro degradation in groups containing sucrose compared to control groups. After week 1, a further mass loss was observed related to PLGA and CPC degradation. Macroporosity analysis confirmed that macroporosity formation is influenced by the dissolution of sucrose at an early stage and by the degradation of PLGA and CPC at a later stage. We concluded that the combination of sucrose and PLGA porogens in CPC is a promising approach to promote early stage bone tissue ingrowth and complete replacement of CPC through multimodal pore formation.
AB - Calcium phosphate cements (CPCs) are commonly used as bone substitute materials. However, their slow degradation rate and lack of macroporosity hinders new bone formation. Poly(dl-lactic-co-glycolic acid) (PLGA) incorporation is of great interest as, upon degradation, produces acidic by-products that enhance CPC degradation. Yet, new bone formation is delayed until PLGA degradation occurs a few weeks after implantation. Therefore, the aim of this study was to accelerate the early stage pore formation within CPCs in vitro. With that purpose, we incorporated the water-soluble porogen sucrose at different weight percentages (10 or 20 wt %) to CPC and CPC/PLGA composites. The results revealed that incorporation of sucrose porogens increased mass loss within the first week of in vitro degradation in groups containing sucrose compared to control groups. After week 1, a further mass loss was observed related to PLGA and CPC degradation. Macroporosity analysis confirmed that macroporosity formation is influenced by the dissolution of sucrose at an early stage and by the degradation of PLGA and CPC at a later stage. We concluded that the combination of sucrose and PLGA porogens in CPC is a promising approach to promote early stage bone tissue ingrowth and complete replacement of CPC through multimodal pore formation.
KW - calcium phosphate cement
KW - PLGA
KW - sucrose
KW - degradation
KW - porosity
KW - Time Factors
KW - Porosity
KW - X-Ray Microtomography
KW - Bone Cements/chemistry
KW - Calcium Phosphates/chemistry
UR - http://www.scopus.com/inward/record.url?scp=85039848587&partnerID=8YFLogxK
U2 - 10.1002/jbm.a.36245
DO - 10.1002/jbm.a.36245
M3 - Article
C2 - 28940662
SN - 1549-3296
VL - 106
SP - 500
EP - 509
JO - Journal of Biomedical Materials Research, Part A
JF - Journal of Biomedical Materials Research, Part A
IS - 2
ER -