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聚富马酸丙二醇酯聚合物网络以及交联大分子单体聚富马酸丙二醇酯 - 二丙烯酸酯的体外降解

In vitro degradation of polymeric networks of poly(propylene fumarate) and the crosslinking macromer poly(propylene fumarate)-diacrylate.

作者信息

Timmer Mark D, Ambrose Catherine G, Mikos Antonios G

机构信息

Department of Bioengineering, Institute of Biosciences and Bioengineering, Rice University, P.O. Box 1892, MS-142, Houston, TX 77251-1892, USA.

出版信息

Biomaterials. 2003 Feb;24(4):571-7. doi: 10.1016/s0142-9612(02)00368-x.

DOI:10.1016/s0142-9612(02)00368-x
PMID:12437951
Abstract

Polymeric networks of poly(propylene fumarate) (PPF) crosslinked with poly(propylene fumarate)-diacrylate (PPF-DA) are currently being investigated as an injectable, biodegradable bone cement. This study examined the effect of crosslinking density, medium pH, and the incorporation of a beta-tricalcium phosphate (beta-TCP) filler on the in vitro degradation of PPF/PPF-DA. Cylindrical specimens were submerged in buffered saline at 37 degrees C and the change in weight, geometry, and compressive mechanical properties were monitored over a 52-week period. All formulations showed an initial increase in modulus and yield strength over the first 12 weeks, achieving maxima of 1307+/-101 and 51+/-3MPa, respectively, for the beta-TCP composite. PPF/PPF-DA networks with the lower crosslinking density demonstrated the greatest degradation with a 17% mass loss. Samples in the lower buffer pH 5.0 compared to physiological pH 7.4 did not show any differences in mass loss, but exhibited a faster decrease in the compressive strength over time. The beta-TCP composites maintained their mechanical properties at the level following their initial increase. These results show that the degradation of PPF/PPF-DA networks can be controlled by the crosslinking density, accelerated at a lower pH, and prolonged with the incorporation of the beta-TCP filler.

摘要

用聚富马酸丙二醇酯二丙烯酸酯(PPF - DA)交联的聚富马酸丙二醇酯(PPF)聚合物网络目前正作为一种可注射的、可生物降解的骨水泥进行研究。本研究考察了交联密度、介质pH值以及β - 磷酸三钙(β - TCP)填料的加入对PPF/PPF - DA体外降解的影响。将圆柱形试样浸没在37℃的缓冲盐水中,在52周的时间内监测其重量、几何形状和压缩力学性能的变化。所有配方在最初的12周内模量和屈服强度均呈现初始增加,β - TCP复合材料的模量和屈服强度分别达到最大值1307±101MPa和51±3MPa。交联密度较低的PPF/PPF - DA网络降解最为显著,质量损失达17%。与生理pH值7.4相比,缓冲pH值为5.0的样品在质量损失方面没有任何差异,但随着时间的推移,其抗压强度下降得更快。β - TCP复合材料在初始增加后的水平上保持其力学性能。这些结果表明,PPF/PPF - DA网络的降解可通过交联密度来控制,在较低pH值下加速降解,而加入β - TCP填料则可延长降解时间。

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