Samenvatting
For in situ tissue engineering (TE) applications it is important that implant degradation proceeds in concord with neo-tissue formation to avoid graft failure. It will therefore be valuable to have an imaging contrast agent (CA) available that can report on the degrading implant. For this purpose, a biodegradable radiopaque biomaterial is presented, modularly composed of a bisurea chain-extended polycaprolactone (PCL2000-U4U) elastomer and a novel iodinated bisurea-modified CA additive (I-U4U). Supramolecular hydrogen bonding interactions between the components ensure their intimate mixing. Porous implant TE-grafts are prepared by simply electrospinning a solution containing PCL2000-U4U and I-U4U. Rats receive an aortic interposition graft, either composed of only PCL2000-U4U (control) or of PCL2000-U4U and I-U4U (test). The grafts are explanted for analysis at three time points over a 1-month period. Computed tomography imaging of the test group implants prior to explantation shows a decrease in iodide volume and density over time. Explant analysis also indicates scaffold degradation. (Immuno)histochemistry shows comparable cellular contents and a similar neo-tissue formation process for test and control group, demonstrating that the CA does not have apparent adverse effects. A supramolecular approach to create solid radiopaque biomaterials can therefore be used to noninvasively monitor the biodegradation of synthetic implants.
Originele taal-2 | Engels |
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Artikelnummer | 2000024 |
Aantal pagina's | 14 |
Tijdschrift | Macromolecular Bioscience |
Volume | 20 |
Nummer van het tijdschrift | 7 |
Vroegere onlinedatum | 17 jun. 2020 |
DOI's | |
Status | Gepubliceerd - 1 jul. 2020 |
Bibliografische nota
© 2020 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.Financiering
This research formed part of the iValve project of the research program of the BioMedical Materials institute, co-founded by the Dutch Ministry of Economic Affairs, Agriculture and Innovation. The financial contribution of the Nederlandse Hartstichting is most gratefully acknowledged. All members of the iValve project are thanked for valuable discussions. Joost L.J. van Dongen, Xianwen Lou (from the Macromolecular and Organic Chemistry group at the TU/e Eindhoven, the Netherlands) and Michel Fransen (SyMO-Chem BV) are thanked for their contributions and help on MS (HRMS, MALDI-TOF-MS, HPLC-MS and GC-MS) and GPC measurements. This research formed part of the iValve project of the research program of the BioMedical Materials institute, co‐founded by the Dutch Ministry of Economic Affairs, Agriculture and Innovation. The financial contribution of the Nederlandse Hartstichting is most gratefully acknowledged. All members of the iValve project are thanked for valuable discussions. Joost L.J. van Dongen, Xianwen Lou (from the Macromolecular and Organic Chemistry group at the TU/e Eindhoven, the Netherlands) and Michel Fransen (SyMO‐Chem BV) are thanked for their contributions and help on MS (HRMS, MALDI‐TOF‐MS, HPLC‐MS and GC‐MS) and GPC measurements.
Financiers | Financiernummer |
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BioMedical Materials institute | |
Dutch Ministry of Economic Affairs, Agriculture and Innovation | |
Ministerie van Economische Zaken en Klimaat |