低聚碳酸三亚甲基对丙烯酸骨水泥刚度的影响

C. Persson, Alejandro López, H. Fathali, A. Hoess, R. Rojas, M. Ott, J. Hilborn, H. Engqvist
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引用次数: 6

摘要

随着老年人口的增加,骨质疏松症等与年龄相关疾病相关的骨折数量也随之增加。在这些患者中使用的丙烯酸骨水泥相对较高的刚度被认为会导致体内骨水泥周围的负荷分布不理想,从而导致临床并发症,例如额外的骨折。本研究的目的是开发一种低模量骨水泥,基于目前使用的,市售的用于椎体成形术的聚甲基丙烯酸甲酯(PMMA)水泥。为此,将丙烯酸酯端功能化低聚(三亚甲基碳酸酯)(oTMC)掺入水泥中,并评估了所选配方的压缩力学性能,以及细胞毒性和处理性能。椎体成形性骨水泥V需要16%的oTMC才能达到1063 MPa (SD 74)的弹性模量,相应的抗压强度为46.1 MPa (SD 1.9)。在大多数情况下,1小时和12小时服用的水泥提取物会降低MG-63细胞的活力,而24小时服用的提取物对细胞行为没有显著影响。改性还使固化时间从14.7 min (SD 1.7)增加到18.0 min (SD 0.9),最大聚合温度从41.5℃(SD 3.4)降低到30.7℃(SD 1.4)。虽然其他相关性能的进一步评估,如可注射性和体内生物相容性,仍有待完成,但本文提出的结果在接近临床应用的低刚度骨水泥方面是有希望的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of oligo(trimethylene carbonate) addition on the stiffness of acrylic bone cement
ABSTRACT With the increasing elderly population an increase in the number of bony fractures associated to age-related diseases such as osteoporosis also follows. The relatively high stiffness of the acrylic bone cements used in these patients has been suggested to give raise to a suboptimal load distribution surrounding the cement in vivo, and hence contribute to clinical complications, such as additional fractures. The aim of this study was to develop a low-modulus bone cement, based on currently used, commercially available poly(methyl methacrylate) (PMMA) cements for vertebroplasty. To this end, acrylate end-functionalized oligo(trimethylene carbonate) (oTMC) was incorporated into the cements, and the resulting compressive mechanical properties were evaluated, as well as the cytotoxic and handling properties of selected formulations. Sixteen wt%oTMC was needed in the vertebroplastic cement Osteopal V to achieve an elastic modulus of 1063 MPa (SD 74), which gave a corresponding compressive strength of 46.1 MPa (SD 1.9). Cement extracts taken at 1 and 12 hours gave a reduced MG-63 cell viability in most cases, while extracts taken at 24 hours had no significant effect on cell behavior. The modification also gave an increase in setting time, from 14.7 min (SD 1.7) to 18.0 min (SD 0.9), and a decrease in maximum polymerization temperature, from 41.5°C (SD 3.4) to 30.7°C (SD 1.4). While further evaluation of other relevant properties, such as injectability and in vivo biocompatibility, remains to be done, the results presented herein are promising in terms of approaching clinically applicable bone cements with a lower stiffness.
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