PLGA公司
磷酸钙骨水泥
材料科学
生物活性玻璃
降级(电信)
背景(考古学)
生物医学工程
复合材料
水泥
纳米技术
纳米颗粒
医学
计算机科学
电信
生物
古生物学
作者
Ana Cláudia Muniz Rennó,M. Reza Nejadnik,Floor C. J. van de Watering,Murilo C. Crovace,Edgar D. Zanotto,J.P.M. Hoefnagels,Joop G.C. Wolke,John A. Jansen,Jeroen J.J.P. van den Beucken
摘要
Abstract Calcium phosphate cements (CPCs) have been widely used as an alternative to biological grafts due to their excellent osteoconductive properties. Although degradation has been improved by using poly( D,L ‐lactic‐ co ‐glycolic) acid (PLGA) microspheres as porogens, the biological performance of CPC/PLGA composites is insufficient to stimulate bone healing in large bone defects. In this context, the aim of this study was to investigate the effect of incorporating osteopromotive bioactive glass (BG; up to 50 wt %) on setting properties, in vitro degradation behavior and morphological characteristics of CPC/BG and CPC/PLGA/BG. The results revealed that the initial and final setting time of the composites increased with increasing amounts of incorporated BG. The degradation test showed a BG‐dependent increasing effect on pH of CPC/BG and CPC/PLGA/BG pre‐set scaffolds immersed in PBS compared to CPC and CPC/PLGA equivalents. Whereas no effects on mass loss were observed for CPC and CPC/BG pre‐set scaffolds, CPC/PLGA/BG pre‐set scaffolds showed an accelerated mass loss compared with CPC/PLGA equivalents. Morphologically, no changes were observed for CPC and CPC/BG pre‐set scaffolds. In contrast, CPC/PLGA and CPC/PLGA/BG showed apparent degradation of PLGA microspheres and faster loss of integrity for CPC/PLGA/BG pre‐set scaffolds compared with CPC/PLGA equivalents. Based on the present in vitro results, it can be concluded that BG can be successfully introduced into CPC and CPC/PLGA without exceeding the setting time beyond clinically acceptable values. All injectable composites containing BG had suitable handling properties and specifically CPC/PLGA/BG showed an increased rate of mass loss. Future investigations should focus on translating these findings to in vivo applications. © 2013 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2013.
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