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Pericardial tissue for cardiovascular application: an in-vitro evaluation of established and advanced production processes

机译:用于心血管应用的心包组织:对既定和先进生产工艺的体外评估

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摘要

Pericardial tissue is widely used as a biomaterial, especially for cardiovascular application. Tissue processing plays a key role in developing future scaffolds derived from biological material, yet standardized evaluation is still pending. This study presents a comprehensive assessment of different treatment protocols of bovine pericardium and compares those findings to commercially available decellularized bovine (CAB) and equine (CAE) pericardial patches. Native samples were fixed with glutaraldehyde (GA) or decellularized. These decellularized samples were subsequently either treated with GA (DEC-GA) or sterilized (DEC). Treatment effects were assessed by histological evaluation of structural and biomechanical properties. Furthermore, decellularization efficacy and accuracy of the applied sterilization protocol were evaluated. Cell seeding of processed pericardial samples with human endothelial cells constituted as biocompatibility test.GA-fixed tissue revealed structural deterioration, cytotoxicity and opposed to popular believe, GA-treatment did not lead to sterility of the samples. Biomechanical assessment revealed an increase in tensile strength of GA and a decrease of DEC and DEC-GA. DEC samples were successfully sterilized and showed good decellularization results, with a significant decrease in residual DNA. Comparative assessment revealed overall good results of CAE, yet results of CAB varied largely, e.g. decellularization efficacy or tissue thickness. Biocompatibility of DEC, CAB and CAE was confirmed by successful cell adhesion. Substantial differences of native tissue properties were observed, resulting in varying treatment efficacies. This study provides a first overview describing consequential variations among biomaterials and illustrates the necessity of multidimensional assessment and tissue quality management for biological scaffold development.[GRAPHICS].
机译:心包组织被广泛用作生物材料,尤其是在心血管方面。组织加工在开发源自生物材料的未来支架中起着关键作用,但是标准化评估仍在进行中。这项研究对牛心包的不同治疗方案进行了全面评估,并将这些发现与市售的脱细胞牛(CAB)和马(CAE)心包贴片进行了比较。天然样品用戊二醛(GA)固定或脱细胞。这些脱细胞的样品随后用GA(DEC-GA)或灭菌(DEC)处理。通过组织学和结构力学性能评估来评估治疗效果。此外,评估了脱细胞功效和所应用灭菌方案的准确性。经处理的心包样品与人内皮细胞的细胞接种构成了生物相容性测试。GA固定的组织显示出结构恶化,细胞毒性,并且与普遍的看法相反,GA处理并未导致样品的无菌性。生物力学评估显示,GA的拉伸强度增加,DEC和DEC-GA降低。 DEC样品已成功灭菌,并显示出良好的脱细胞效果,残留DNA明显减少。比较评估显示CAE总体上良好的结果,但CAB的结果差异很大,例如,脱细胞功效或组织厚度。 DEC,CAB和CAE的生物相容性通过成功的细胞粘附得到证实。观察到天然组织性质的实质性差异,导致不同的治疗效果。这项研究提供了描述生物材料之间相应变化的第一篇综述,并阐明了进行生物支架开发的多维评估和组织质量管理的必要性。[GRAPHICS]

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  • 来源
    《Journal of materials science》 |2018年第11期|172.1-172.13|共13页
  • 作者单位

    Ludwig Maximilian Univ Munich Grosshadern Med Ctr Dept Cardiac Surg Lab Tissue Engn Munich Germany;

    Ludwig Maximilian Univ Munich Grosshadern Med Ctr Dept Cardiac Surg Lab Tissue Engn Munich Germany|Tech Univ Inst Med & Polymer Engn Munich Germany;

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