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采用电喷技术开发具有生物活性的聚合物药物洗脱冠状动脉支架涂层。

Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying.

机构信息

Department of Biomedical Engineering, University of Strathclyde, Graham Hills Building, 40 George Street, Glasgow, G1 1QE, UK.

出版信息

Ann Biomed Eng. 2020 Jan;48(1):271-281. doi: 10.1007/s10439-019-02346-6. Epub 2019 Aug 22.

Abstract

Drug-eluting stents are now routinely used in the treatment of acute coronary syndromes caused by coronary artery disease. Whilst the sustained release of anti-proliferative drugs from these devices has greatly reduced the need for repeat revascularisation procedures, this approach is not suitable for all patients and appears to delay regrowth of the endothelium, necessitating the use of prolonged dual anti-platelet therapy. Although the development of more advanced stent platforms and drug coatings has produced modest improvements in performance, these devices have not fully addressed the limitations experienced with their first-generation counterparts. In the present study, we developed a novel stent coating that provides controlled sirolimus release from a bioactive polymer (accelerate™ AT) that has previously been shown to support endothelial cell growth in vitro. A bespoke electrospray deposition process provided control over the coating thickness, surface roughness, drug load, and release kinetics. The resultant optimised coating combines rapid release of an anti-proliferative agent from a bioactive polymer coating that promotes re-endothelialisation, thereby offering potential protection against in-stent restenosis and thrombosis. This novel, dual-action coating therefore has significant therapeutic potential, with the enhanced control of drug load and release kinetics offered by electrospray deposition also opening up opportunities for more personalised treatment approaches. Further development and evaluation of these technologies in vitro and in vivo is therefore warranted.

摘要

药物洗脱支架目前已常规用于治疗由冠状动脉疾病引起的急性冠状动脉综合征。虽然这些器械中抗增殖药物的持续释放大大降低了重复血运重建的需求,但这种方法并不适用于所有患者,而且似乎会延迟内皮细胞的再生,因此需要长期使用双联抗血小板治疗。尽管更先进的支架平台和药物涂层的发展在性能上有了适度的提高,但这些器械并没有完全解决第一代支架存在的局限性。在本研究中,我们开发了一种新型支架涂层,该涂层可从生物活性聚合物(accelerate™ AT)中控制释放西罗莫司,该聚合物先前已被证明可在体外支持内皮细胞生长。定制的电喷沉积工艺可控制涂层厚度、表面粗糙度、药物负载和释放动力学。所得的优化涂层结合了生物活性聚合物涂层中抗增殖剂的快速释放,可促进再内皮化,从而提供对支架内再狭窄和血栓形成的潜在保护。因此,这种新型双重作用涂层具有显著的治疗潜力,电喷沉积提供的药物负载和释放动力学的增强控制也为更个性化的治疗方法开辟了机会。因此,有必要在体外和体内进一步开发和评估这些技术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f22e/6928095/36246ca30b9e/10439_2019_2346_Fig1_HTML.jpg

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