Yang Chao, Su Chao, Zou Jie, Zhong Binru, Wang Lin, Chen Bailang, Li Jianmo, Wei Minxin
Research and Development (R&D) Department, Konee Biomedical (Shenzhen) Co., Ltd., Shenzhen, Guangdong, China.
Division of Cardiovascular Surgery, Cardiac and Vascular Center, The University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong, China.
Front Bioeng Biotechnol. 2024 Nov 20;12:1418259. doi: 10.3389/fbioe.2024.1418259. eCollection 2024.
This study evaluates the efficacy of uncrosslinked porcine collagen coated vascular grafts (UPCCVG) in facilitating neointima formation and endothelialization.
Prior to coating, the uncrosslinked porcine collagen underwent comprehensive characterization employing SDS-PAGE, image analysis, circular dichroism and immunogenicity. The PET substrate of the vascular graft was coated with collagen solution utilizing the dip-coating method. Water permeability, blood leakage resistance, radial compliance, hemolysis, cytotoxicity and cell proliferation of UPCCVG were studied. Subsequent evaluation involved the implantation of UPCCVG as a substitute for the porcine abdominal aorta. Digital subtraction angiography (DSA) was employed to evaluate UPCCVG patency post-implantation, while histology, immunohistochemistry, and scanning electron microscopy were utilized to assess neointima formation and endothelialization. The thrombosis of UPCCVG was analyzed simultaneously to further characterize its blood compatibility.
The uncrosslinked collagen demonstrated high purity, maintaining its triple helix structure and molecular weight akin to the type I bovine collagen standard substrate, indicative of preserved biological activity and low immunogenicity. UPCCVG exhibited water permeability, blood leakage resistance, radial compliance and blood compatibility comparable to commercial grafts. DSA revealed satisfactory patency of UPCCVG without evidence of stenosis or swelling at the 3-week post-implantation mark. Histological analysis illustrated well-developed neointima with appropriate thickness and controlled proliferation. Immunohistochemistry confirmed the presence of endothelial cells (VWF positive) and smooth muscle cells (α-SMA positive) within the neointima, indicating successful endothelialization. Moreover, the morphology of the neointima surface closely resembled that of the natural artery tunica intima, oriented along the direction of blood flow.
UPCCVG, composed of uncrosslinked porcine collagen, demonstrates promising potential in fostering neointima formation and endothelialization while mitigating intimal hyperplasia. This biocompatible uncrosslinked porcine collagen merits further investigation for its clinical applications in vascular reconstruction.
本研究评估了未交联猪胶原蛋白涂层血管移植物(UPCCVG)在促进新生内膜形成和内皮化方面的疗效。
在涂层之前,采用SDS-PAGE、图像分析、圆二色性和免疫原性对未交联猪胶原蛋白进行了全面表征。血管移植物的PET基材采用浸涂法用胶原蛋白溶液进行涂层。研究了UPCCVG的透水性、抗血液渗漏性、径向顺应性、溶血、细胞毒性和细胞增殖。随后的评估包括植入UPCCVG作为猪腹主动脉的替代品。采用数字减影血管造影(DSA)评估植入后UPCCVG的通畅性,同时利用组织学、免疫组织化学和扫描电子显微镜评估新生内膜形成和内皮化。同时分析了UPCCVG的血栓形成情况,以进一步表征其血液相容性。
未交联胶原蛋白显示出高纯度,保持了其三螺旋结构和与I型牛胶原蛋白标准底物相似的分子量,表明其生物活性得以保留且免疫原性较低。UPCCVG表现出与商业移植物相当的透水性、抗血液渗漏性、径向顺应性和血液相容性。DSA显示UPCCVG在植入后3周时通畅情况良好,无狭窄或肿胀迹象。组织学分析表明新生内膜发育良好,厚度合适且增殖得到控制。免疫组织化学证实新生内膜内存在内皮细胞(VWF阳性)和平滑肌细胞(α-SMA阳性),表明内皮化成功。此外,新生内膜表面的形态与天然动脉内膜极为相似,沿血流方向排列。
由未交联猪胶原蛋白组成的UPCCVG在促进新生内膜形成和内皮化同时减轻内膜增生方面显示出有前景的潜力。这种具有生物相容性的未交联猪胶原蛋白在血管重建的临床应用方面值得进一步研究。