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1.
Eur J Vasc Endovasc Surg ; 59(4): 643-652, 2020 04.
Article in English | MEDLINE | ID: mdl-31874809

ABSTRACT

OBJECTIVE: Biodegradable materials for in situ vascular tissue engineering could meet the increasing clinical demand for sufficient synthetic small diameter vascular substitutes in aortocoronary bypass and peripheral vascular surgery. The aim of this study was to design a new degradable thermoplastic polycarbonate urethane (dPCU) with improved biocompatibility and optimal biomechanical properties. Electrospun conduits made from dPCU were evaluated in short and long term follow up and compared with expanded polytetrafluoroethylene (ePTFE) controls. METHODS: Both conduits were investigated prior to implantation to assess their biocompatibility and inflammatory potential via real time polymerase chain reaction using a macrophage culture. dPCU grafts (n = 28) and ePTFE controls (n = 28) were then implanted into the infrarenal abdominal aorta of Sprague-Dawley rats. After seven days, one, six, and 12 months, grafts were analysed by histology and immunohistochemistry (IHC) and assessed biomechanically. RESULTS: Anti-inflammatory signalling was upregulated in dPCU conduits and increased significantly over time in vitro. dPCU and ePTFE grafts offered excellent long and short term patency rates (92.9% in both groups at 12 months) in the rat model without dilatation or aneurysm formation. In comparison to ePTFE, dPCU grafts showed transmural ingrowth of vascular specific cells resulting in a structured neovessel formation around the graft. The graft material was slowly reduced, while the compliance of the neovessel increased over time. CONCLUSION: The newly designed dPCU grafts have the potential to be safely applied for in situ vascular tissue engineering applications. The degradable substitutes showed good in vivo performance and revealed desirable characteristics such as biomechanical stability, non-thrombogenicity, and minimal inflammatory response after long term implantation.


Subject(s)
Absorbable Implants , Nanofibers/therapeutic use , Polycarboxylate Cement/pharmacology , Time , Absorbable Implants/adverse effects , Animals , Biocompatible Materials/metabolism , Blood Vessel Prosthesis Implantation , Polytetrafluoroethylene/pharmacology , Rats, Sprague-Dawley , Replantation/methods , Urethane/pharmacology , Vascular Patency/drug effects
2.
Biomacromolecules ; 21(2): 376-387, 2020 02 10.
Article in English | MEDLINE | ID: mdl-31718163

ABSTRACT

We report biodegradable thermoplastic polyurethanes for soft tissue engineering applications, where frequently used carboxylic acid ester degradation motifs were substituted with carbonate moieties to achieve superior degradation properties. While the use of carbonates in soft blocks has been reported, their use in hard blocks of thermoplastic polyurethanes is unprecedented. Soft blocks consist of poly(hexamethylene carbonate), and hard blocks combine hexamethylene diisocyanate with the newly synthesized cleavable carbonate chain extender bis(3-hydroxypropylene)carbonate (BHPC), mimicking the motif of poly(trimethylene carbonate) with highly regarded degradation properties. Simultaneously, the mechanical benefits of segmented polyurethanes are exploited. A lower hard block concentration in BHPC-based polymers was more suitable for vascular grafts. Nonacidic degradation products and hard block dependent degradation rates were found. Implantation of BHPC-based electrospun degradable vascular prostheses in a small animal model revealed high patency rates and no signs of aneurysm formations. Specific vascular graft remodeling and only minimal signs of inflammatory reactions were observed.


Subject(s)
Biocompatible Materials/chemistry , Blood Vessel Prosthesis , Polycarboxylate Cement/chemistry , Polyurethanes/chemistry , Animals , Aorta/pathology , Aorta/surgery , Biomechanical Phenomena , Isocyanates/chemistry , Magnetic Resonance Spectroscopy , Materials Testing , Microscopy, Electron, Scanning , Prosthesis Implantation , Rats, Sprague-Dawley , Spectroscopy, Fourier Transform Infrared
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