Evaluation of the Bioinductive Effects of a Novel Antibiotic Eluting Cardiac Implantable Electronic Device Envelope.

IF 5 3区 医学 Q1 ENGINEERING, BIOMEDICAL
Sun Woo Kim, Nathan W Fedak, Eleanor Love, Alexander Tam, Ali Fatehi Hassanabad, Jeannine Turnbull, Guoqi Teng, Darrell Belke, Justin Deniset, Paul W M Fedak
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Abstract

Background: Subcutaneous pocket infection is a common morbidity associated with the integration of cardiac implantable electronic devices (CIEDs). A new antibiotic-eluting CIED bioenvelope has been developed as a prophylactic measure to mitigate infection and skin erosion caused by device migration. This study investigated the envelope's regulatory properties in scar formation and vascularization.

Methods: Fibroblasts were seeded on either plastic (n = 6) or small intestine submucosal extracellular matrix (SIS-ECM) (n = 6) for 24 h. The culture media were analyzed for proangiogenic and proinflammatory proteins with multiplex. Sham (n = 8) or SIS-ECM (n = 8) was randomly implanted into the dorsal subcutaneous pocket of mice. The implants were excised on day 7, cultured for 24 h, and the media analyzed. Rabbit models were implanted with either synthetic polymer HDPE (n = 12) or SIS-ECM (n = 11). The treatments were excised at weeks 2, 10, and 26 and then stained for analysis.

Results: SIS-ECM significantly increased the fibroblasts' paracrine release of proangiogenic and proinflammatory factors like VEGF-A (p < 0.05) and IL-6 (p < 0.05) compared with plastic. The murine tissue interacting with SIS-ECM released significantly more angiogenic proteins like VEGF-A (p < 0.05) than the sham. The histology analysis of rabbit subcutaneous tissue revealed a decreasing level of inflammation and fibrosis over time with SIS-ECM.

Conclusions: The CIED bioenvelope elicited proangiogenic paracrine signaling and reduced fibrotic response in fibroblasts and animal models. Clinical translation of the CIED bioenvelope as an adjunct to regular prophylactic practice may be warranted in the future.

一种新型抗生素洗脱心脏植入式电子装置包膜的生物诱导效应评价。
背景:皮下袋感染是与心脏植入式电子装置(cied)整合相关的常见疾病。一种新的抗生素洗脱CIED生物包膜已被开发作为一种预防措施,以减轻感染和皮肤侵蚀引起的设备迁移。本研究探讨了包膜在疤痕形成和血管形成中的调控特性。方法:将成纤维细胞分别在塑料(n = 6)或小肠粘膜下细胞外基质(SIS-ECM) (n = 6)上培养24 h。分析培养基中促血管生成和促炎症蛋白的多样性。将Sham (n = 8)或SIS-ECM (n = 8)随机植入小鼠背部皮下袋。第7天切除植入物,培养24 h,分析培养基。兔模型分别植入合成聚合物HDPE (n = 12)和SIS-ECM (n = 11)。在第2周、第10周和第26周切除,然后染色分析。结果:与塑料相比,SIS-ECM显著增加成纤维细胞旁分泌促血管生成和促炎症因子VEGF-A (p < 0.05)和IL-6 (p < 0.05)的释放。与sham相比,与SIS-ECM相互作用的小鼠组织释放了更多的血管生成蛋白,如VEGF-A (p < 0.05)。兔皮下组织的组织学分析显示,随着时间的推移,SIS-ECM的炎症和纤维化水平降低。结论:在成纤维细胞和动物模型中,CIED生物包膜诱导了促血管生成旁分泌信号,并降低了纤维化反应。临床翻译CIED生物包膜作为常规预防实践的辅助可能在未来得到保证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Functional Biomaterials
Journal of Functional Biomaterials Engineering-Biomedical Engineering
CiteScore
4.60
自引率
4.20%
发文量
226
审稿时长
11 weeks
期刊介绍: Journal of Functional Biomaterials (JFB, ISSN 2079-4983) is an international and interdisciplinary scientific journal that publishes regular research papers (articles), reviews and short communications about applications of materials for biomedical use. JFB covers subjects from chemistry, pharmacy, biology, physics over to engineering. The journal focuses on the preparation, performance and use of functional biomaterials in biomedical devices and their behaviour in physiological environments. Our aim is to encourage scientists to publish their results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Several topical special issues will be published. Scope: adhesion, adsorption, biocompatibility, biohybrid materials, bio-inert materials, biomaterials, biomedical devices, biomimetic materials, bone repair, cardiovascular devices, ceramics, composite materials, dental implants, dental materials, drug delivery systems, functional biopolymers, glasses, hyper branched polymers, molecularly imprinted polymers (MIPs), nanomedicine, nanoparticles, nanotechnology, natural materials, self-assembly smart materials, stimuli responsive materials, surface modification, tissue devices, tissue engineering, tissue-derived materials, urological devices.
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