Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cheng, Bill | en_US |
dc.contributor.author | Xing, Yue-Min | en_US |
dc.contributor.author | Shih, Nai-Chia | en_US |
dc.contributor.author | Weng, Jen-Po | en_US |
dc.contributor.author | Lin, Hsin-Chieh | en_US |
dc.date.accessioned | 2018-08-21T05:53:38Z | - |
dc.date.available | 2018-08-21T05:53:38Z | - |
dc.date.issued | 2018-01-01 | en_US |
dc.identifier.issn | 2046-2069 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1039/c8ra01583j | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/144961 | - |
dc.description.abstract | Arteriovenous graft (AVG) failure continues to be a life-threatening problem in haemodialysis. Graft failure can occur if the implanted graft is not well-matched to the vasculature of the patient. Likewise, stenosis often develops at the vein-graft anastomosis, contributing to thrombosis and early graft failure. To address this clinical need, a novel ink formulation comprised of ACMO/TMPTA/TMETA for 3D printing a AVG was developed (ACMO-AVG), in which the printed AVG was biocompatible and did not induce cytotoxicity. The ease of customizing the ACMO-AVG according to different requirements was demonstrated. Furthermore, the AVG displayed similar mechanical properties to the commercially available arteriovenous ePTFE graft (ePTFE-AVG). Unlike ePTFE-AVG, the ACMO-AVG displayed excellent anti-fouling characteristics because no plasma protein adsorption and platelet adhesion were detected on the luminal surfaces after 2 h of incubation. Similarly, exposure to human endothelial cells and human vascular smooth muscle cells did not result in any cell detection on the surfaces of the ACMO-AVG. Thus, the present study demonstrates a newly developed 3D printing ink formulation that can be successfully 3D printed into a clinically applicable vascular access used for haemodialysis. | en_US |
dc.language.iso | en_US | en_US |
dc.title | The formulation and characterization of 3D printed grafts as vascular access for potential use in hemodialysis | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1039/c8ra01583j | en_US |
dc.identifier.journal | RSC ADVANCES | en_US |
dc.citation.volume | 8 | en_US |
dc.citation.spage | 15471 | en_US |
dc.citation.epage | 15479 | en_US |
dc.contributor.department | 材料科學與工程學系 | zh_TW |
dc.contributor.department | Department of Materials Science and Engineering | en_US |
dc.identifier.wosnumber | WOS:000431813800025 | en_US |
Appears in Collections: | Articles |