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使用XRD sin(2)ψ技术对裸金属支架和聚乳酸涂层支架扩张过程中的应力状况进行原位研究。

In-situ investigation of stress conditions during expansion of bare metal stents and PLLA-coated stents using the XRD sin(2)ψ-technique.

作者信息

Kowalski Wolfgang, Dammer Markus, Bakczewitz Frank, Schmitz Klaus-Peter, Grabow Niels, Kessler Olaf

机构信息

University of Rostock, Faculty of Mechanical Engineering and Marine Technology, Chair of Materials Science, 18051 Rostock, Germany.

Cortronik GmbH, 18119 Rostock-Warnemünde, Germany.

出版信息

J Mech Behav Biomed Mater. 2015 Sep;49:23-9. doi: 10.1016/j.jmbbm.2015.04.020. Epub 2015 Apr 24.

DOI:10.1016/j.jmbbm.2015.04.020
PMID:25974098
Abstract

Drug eluting stents (DES) consist of platform, coating and drug. The platform often is a balloon-expandable bare metal stent made of the CoCr alloy L-605 or stainless steel 316 L. The function of the coating, typically a permanent polymer, is to hold and release the drug, which should improve therapeutic outcome. Before implantation, DES are compressed (crimped) to allow implantation in the human body. During implantation, DES are expanded by balloon inflation. Crimping, as well as expansion, causes high stresses and high strains locally in the DES struts, as well as in the polymer coating. These stresses and strains are important design criteria of DES. Usually, they are calculated numerically by finite element analysis (FEA), but experimental results for validation are hardly available. In this work, the X-ray diffraction (XRD) sin(2)ψ-technique is applied to in-situ determination of stress conditions of bare metal L-605 stents, and Poly-(L-lactide) (PLLA) coated stents. This provides a realistic characterization of the near-surface stress state and a validation option of the numerical FEA. XRD-results from terminal stent struts of the bare metal stent show an increasing compressive load stress in tangential direction with increasing stent expansion. These findings correlate with numerical FEA results. The PLLA-coating also bears increasing compressive load stress during expansion.

摘要

药物洗脱支架(DES)由平台、涂层和药物组成。平台通常是由钴铬合金L-605或不锈钢316L制成的球囊扩张式裸金属支架。涂层(通常是一种永久性聚合物)的作用是容纳和释放药物,这应能改善治疗效果。在植入前,DES被压缩(卷曲)以便植入人体。在植入过程中,DES通过球囊充气而扩张。卷曲以及扩张会在DES支架以及聚合物涂层中局部产生高应力和高应变。这些应力和应变是DES的重要设计标准。通常,它们通过有限元分析(FEA)进行数值计算,但几乎没有用于验证的实验结果。在这项工作中,X射线衍射(XRD)sin(2)ψ技术被应用于原位测定裸金属L-605支架和聚(L-丙交酯)(PLLA)涂层支架的应力状况。这提供了近表面应力状态的实际表征以及数值FEA的验证选项。裸金属支架末端支架的XRD结果表明,随着支架扩张,切向方向的压缩载荷应力增加。这些发现与数值FEA结果相关。PLLA涂层在扩张过程中也承受着不断增加的压缩载荷应力。

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