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An in vitro study of the elastic property loss of poly(L-lactic acid), PLLA, filaments undergoing hydrolysis in tissue engineering applications.

机译:在组织工程应用中进行水解的聚L-乳酸PLLA长丝的弹性损失的体外研究。

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The objective of the investigation was to describe the elastic property loss in a stressed PLLA filament in a scaffold for soft tissue ingrowth undergoing hydrolysis. A tissue-engineered scaffold for the liver was the theoretical example. This was a construct located in the upper mid-abdomen region able to withstand the elastic forces associated with sitting, standing, and minimal activities. For this study, fibers were melt-spun from PLLA, aged according to ASTM F 1635-95, and sterilized with gamma irradiation. Samples were mechanically tested (ASTM D 3822-96 and ASTM D 1774-94). In addition, the changes in molecular weight were followed by intrinsic viscosity (ASTM D 2857-93).; In general, the longer that most samples were aged, the lower the molecular weight. The elastic recovery did not change significantly. The breaking tenacity remained stable at least for the time of this study. In the 5.0 DR sample, the crystallinity was low (26%). Gamma irradiation severely degraded the specimens (94% molecular weight loss). Therefore, the amount and location of the amorphous regions in the filament cross section is important in determining the rate of the degradation and the subsequent mechanical property loss.; While these define the minimal stresses on the filaments, more study on how strong the filaments are when bonded together in scaffold or fabric are required. Also, elastic and tensile testing of the samples while they are in the physiological soaking solution would keep the samples viable and as close to in vivo conditions as possible.
机译:研究的目的是描述在经受水解的软组织向内生长的支架中,受应力的PLLA丝的弹性损失。肝脏的组织工程支架是理论上的例子。这是位于上腹部中部区域的结构,能够承受与坐,站立和最少活动相关的弹力。在本研究中,纤维是从PLLA熔纺而成的,根据ASTM F 1635-95进行时效处理,并用伽马射线辐照灭菌。对样品进行机械测试(ASTM D 3822-96和ASTM D 1774-94)。另外,分子量变化后是特性粘度(ASTM D 2857-93)。通常,大多数样品的老化时间越长,分子量越低。弹性回复没有明显变化。断裂韧性至少在本研究期间保持稳定。在5.0 D R 样品中,结晶度低(26%)。伽玛射线严重降解了样品(94%的分子量损失)。因此,长丝横截面中非晶区域的数量和位置对于确定降解速率和随后的机械性能损失很重要。尽管这些定义了细丝上的最小应力,但需要进一步研究当在脚手架或织物中粘结在一起时细丝的强度。而且,在将样品置于生理浸液中时进行弹性和拉伸测试将使样品保持活力,并尽可能接近体内的条件。

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