Menze Roman, Hesse Bernhard, Kusmierczuk Maciej, Chen Duote, Weitkamp Timm, Bettink Stephanie, Scheller Bruno
MeKo Manufacturing e.K., Im Kirchenfelde 12-14, 31157, Sarstedt, Germany.
Xploraytion GmbH, Bismarckstr. 10-12, 10625, Berlin, Germany.
Bioact Mater. 2023 Sep 23;32:1-11. doi: 10.1016/j.bioactmat.2023.09.008. eCollection 2024 Feb.
Bioresorbable magnesium scaffolds are a promising future treatment option for coronary artery stenosis, especially for young adults. Due to the degradation of these scaffolds (<1 year), long-term device-related clinical events could be reduced compared to treatments with conventional drug eluting stents. First clinical trials indicate a return of vasomotion after one year, which may be associated with improved long-term clinical outcomes. However, even after decades of development, the degradation process, ideal degradation time and biological response in vivo are still not fully understood. The present study investigates the in vivo degradation of magnesium scaffolds in the coronary arteries of pigs influenced by different strut thicknesses and the presence of antiproliferative drugs. Due to high 3D image contrast of synchrotron-based micro-CT with phase contrast (SR-μCT), a qualitative and quantitative evaluation of the degradation morphology of magnesium scaffolds was obtained. For the segmentation of the μCT images a convolutional network architecture (U-net) was exploited, demonstrating the huge potential of merging high resolution SR-μCT with deep learning (DL) supported data analysis. In total, 30 scaffolds, made of the rare earth alloy Resoloy®, with different strut designs were implanted into the coronary arteries of 10 domestic pigs for 28 days using drug-coated or uncoated angioplasty balloons for post-dilatation. The degradation morphology was analyzed using scanning electron microscopy, energy dispersive x-ray spectroscopy and SR-μCT. The data from these methods were then related to data from angiography, optical coherence tomography and histology. A thinner strut size (95 vs. 130 μm) and the presence of paclitaxel indicated a slower degradation rate at 28 d in vivo, which positively influences the late lumen loss (0.5 and 0.6 mm vs. 1.0 and 1.1 mm) and recoil values (0 and 1.7% vs. 6.1 and 22%).
生物可吸收镁支架是冠状动脉狭窄未来一种很有前景的治疗选择,尤其对于年轻人。由于这些支架的降解(<1年),与使用传统药物洗脱支架治疗相比,与器械相关的长期临床事件可能会减少。首次临床试验表明,一年后血管运动恢复,这可能与改善的长期临床结果相关。然而,即使经过数十年的发展,降解过程、理想的降解时间和体内生物学反应仍未完全了解。本研究调查了不同支柱厚度和抗增殖药物存在情况下,镁支架在猪冠状动脉中的体内降解情况。由于基于同步加速器的相位对比微CT(SR-μCT)具有高3D图像对比度,因此对镁支架的降解形态进行了定性和定量评估。对于μCT图像的分割,采用了卷积网络架构(U-net),证明了将高分辨率SR-μCT与深度学习(DL)支持的数据分析相结合的巨大潜力。总共将30个由稀土合金Resoloy®制成、具有不同支柱设计的支架,使用药物涂层或未涂层的血管成形术球囊进行后扩张,植入10头家猪的冠状动脉中28天。使用扫描电子显微镜、能量色散X射线光谱和SR-μCT分析降解形态。然后将这些方法获得的数据与血管造影、光学相干断层扫描和组织学数据相关联。较薄的支柱尺寸(95 vs. 130μm)和紫杉醇的存在表明在体内28天时降解速率较慢,这对晚期管腔丢失(0.5和0.6mm vs. 1.0和1.1mm)和回缩值(0和1.7% vs. 6.1和22%)有积极影响。