A novel stent flow chamber system demonstrates reduced thrombogenicity of bioresorbable magnesium scaffolds

Coronary artery disease (CAD) is characterized by narrowing and subsequent blockade of coronary arteries, and imposes a significant health and economic burden. Stent and scaffold devices are introduced in advanced CAD to improve vascular stability and restore blood flow. Although in vitro flow syste...

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Published inScientific reports Vol. 14; no. 1; pp. 26691 - 8
Main Authors Müller, Monja, Ludwig, Lars, Englert, Hanna, Riedl, Katharina A., Müller, May Cathleen, Hemkemeyer, Sandra A., Beerens, Manu, Mailer, Reiner K., Renné, Thomas, Lang, Sabine, Baumann-Zumstein, Philine, Frye, Maike
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 04.11.2024
Nature Publishing Group
Nature Portfolio
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Summary:Coronary artery disease (CAD) is characterized by narrowing and subsequent blockade of coronary arteries, and imposes a significant health and economic burden. Stent and scaffold devices are introduced in advanced CAD to improve vascular stability and restore blood flow. Although in vitro flow systems like the Chandler loop have been developed to enhance the understanding of interactions between device materials, their coatings, and vascular cells, imaging-based in vitro analysis of device performance is limited. In this study, we established a novel stent flow chamber system designed to assess the thrombogenicity of bioresorbable magnesium scaffold (RMS) and stent materials in vitro. Additionally, we compared the thrombogenicity – an important clinical parameter in stent performance – of the Magmaris-316 L stainless steel stent with its predecessors, Magmaris RMS and a prototype of the third-generation RMS (DREAMS 3G). Analysis of platelet adhesion and coverage of the different devices under flow conditions demonstrated that the Magmaris RMS exhibits reduced thrombogenicity compared to the Magmaris-316 L stainless steel stent. Moreover, thrombogenicity of the DREAMS 3G prototype, composed of BIOmag material, is further decreased compared to its predecessors. The observed reduction in thrombogenicity of the DREAMS 3G prototype in vitro suggests additional improvements in clinical safety and efficacy, highlighting its promise for treating CAD. Future research on this prototype may thus open avenues for analyzing other blood components and patient-derived endothelial cells. In line with the 3R principles, this approach may also help reduce the need for animal testing.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-024-77266-0