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The type of polyurethane influenced biocompatibility of titaniumcarboxonitride layers created by a plasma-activated chemical vapour deposition process
Lehle, Karla, Li, Jing, Zimmermann, H. und Schmid, Christof (2014) The type of polyurethane influenced biocompatibility of titaniumcarboxonitride layers created by a plasma-activated chemical vapour deposition process. Materials 7, S. 623-636.Veröffentlichungsdatum dieses Volltextes: 17 Feb 2020 09:00
Artikel
DOI zum Zitieren dieses Dokuments: 10.5283/epub.41620
Zusammenfassung
Polycarbonateurethanes (PCU) and polyetherurethanes (PEU) are used for medical devices, however their bio- and haemocompatibility is limited. In this study, the effect of titaniferous upgrading of different polyurethanes on the bio-and haemocompatibility was investigated by endothelial cell (EC) adhesion/proliferation and platelet adhesion (scanning electron microscopy), respectively. There was ...
Polycarbonateurethanes (PCU) and polyetherurethanes (PEU) are used for medical devices, however their bio- and haemocompatibility is limited. In this study, the effect of titaniferous upgrading of different polyurethanes on the bio-and haemocompatibility was investigated by endothelial cell (EC) adhesion/proliferation and platelet adhesion (scanning electron microscopy), respectively. There was no EC adhesion/proliferation and only minor platelet adhesion on upgraded and pure PCU (Desmopan). PEUs (Texin 985, Tecothane 1085, Elastollan 1180A) differed in their cyto-and haemocompatibility. While EC adhesion depended on the type of PEU, any proliferative activity was inhibited. Additional titaniferous upgrading of PEU induced EC proliferation and increased metabolic activity. However, adherent ECs were significantly activated. While Texin was highly thrombotic, only small amounts of platelets adhered onto Tecothane and Elastollan. Additional titaniferous upgrading reduced thrombogenicity of Texin, preserved haemocompatibility of Elastollan, and increased platelet activation/aggregation on Tecothane. In conclusion, none of the PUs was cytocompatible; only titaniferous upgrading allowed EC proliferation and metabolism on PEUs. Haemocompatibility depended on the type of PU.
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| Dokumentenart | Artikel | ||||
| Titel eines Journals oder einer Zeitschrift | Materials | ||||
| Verlag: | MDPI AG | ||||
|---|---|---|---|---|---|
| Ort der Veröffentlichung: | BASEL | ||||
| Band: | 7 | ||||
| Seitenbereich: | S. 623-636 | ||||
| Datum | 2014 | ||||
| Institutionen | Medizin > Lehrstuhl für Herz-, Thorax- und herznahe Gefäßchirurgie | ||||
| Identifikationsnummer |
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| Stichwörter / Keywords | HARD-SEGMENT CHEMISTRY; HUMAN VASCULAR CELLS; TITANIUM; BIOCOMPATIBILITY; STABILITY; STRESS; TITANIUMCARBOXONITRIDE; BIOMATERIALS; EXPRESSION; RESISTANCE; endothelial cell seeding; cytocompatibility; haemocompatibility; platelet adhesion; cardiovascular tissue engineering; titanium | ||||
| Dewey-Dezimal-Klassifikation | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin | ||||
| Status | Veröffentlicht | ||||
| Begutachtet | Ja, diese Version wurde begutachtet | ||||
| An der Universität Regensburg entstanden | Ja | ||||
| URN der UB Regensburg | urn:nbn:de:bvb:355-epub-416202 | ||||
| Dokumenten-ID | 41620 |
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