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Tube Expansion Deformation Enables In Situ Synchrotron X-ray Scattering Measurements during Extensional Flow-Induced Crystallization of Poly l-Lactide Near the Glass Transition

机译:管膨胀变形使得在玻璃化转变附近的聚l-丙交酯的拉伸流致结晶过程中能够进行同步加速器X射线散射测量

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摘要

Coronary Heart Disease (CHD) is one of the leading causes of death worldwide, claiming over seven million lives each year. Permanent metal stents, the current standard of care for CHD, inhibit arterial vasomotion and induce serious complications such as late stent thrombosis. Bioresorbable vascular scaffolds (BVSs) made from poly l-lactide (PLLA) overcome these complications by supporting the occluded artery for 3–6 months and then being completely resorbed in 2–3 years, leaving behind a healthy artery. The BVS that recently received clinical approval is, however, relatively thick (~150 µm, approximately twice as thick as metal stents ~80 µm). Thinner scaffolds would facilitate implantation and enable treatment of smaller arteries. The key to a thinner scaffold is careful control of the PLLA microstructure during processing to confer greater strength in a thinner profile. However, the rapid time scales of processing (~1 s) defy prediction due to a lack of structural information. Here, we present a custom-designed instrument that connects the strain-field imposed on PLLA during processing to in situ development of microstructure observed using synchrotron X-ray scattering. The connection between deformation, structure and strength enables processing–structure–property relationships to guide the design of thinner yet stronger BVSs.
机译:冠心病(CHD)是全球主要的死亡原因之一,每年夺走700万条生命。永久性金属支架是目前冠心病的标准治疗方法,可抑制动脉血管运动并引起严重的并发症,如晚期支架血栓形成。由聚l-丙交酯(PLLA)制成的可生物吸收的血管支架(BVS)通过支撑被阻塞的动脉3-6个月,然后在2-3年内被完全吸收,从而留下一条健康的动脉,从而克服了这些并发症。但是,最近获得临床批准的BVS相对较厚(〜150 µm,大约是〜80 µm金属支架的两倍)。较薄的支架将有助于植入并能够治疗较小的动脉。支架更薄的关键是在加工过程中仔细控制PLLA的微观结构,以在更薄的轮廓上赋予更大的强度。但是,由于缺乏结构信息,处理的快速时标(〜1 s)无法预测。在这里,我们介绍了一种定制设计的仪器,该仪器将在处理过程中施加在PLLA上的应变场连接到使用同步加速器X射线散射观察到的微观结构的原位显影。变形,结构和强度之间的联系使加工,结构,性能之间的关系可以指导更薄但更坚固的BVS的设计。

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