Reinforcement of interfacial adhesion of a coated polymer layer on a cobalt-chromium surface for drug-eluting stents

During the balloon expansion of several commercially available drug-eluting stents, various types of defects in the polymer layer have been observed. The aim of this study is to prevent these defects by increasing the interfacial adhesion between the metal substrate and the drug-in-polymer matrix us...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 30(2014), 27 vom: 15. Juli, Seite 8020-8
1. Verfasser: Bedair, Tarek M (VerfasserIn)
Weitere Verfasser: Cho, Youngjin, Kim, Tae Jung, Kim, Young Dong, Park, Bang Ju, Joung, Yoon Ki, Han, Dong Keun
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Chromium Alloys Coated Materials, Biocompatible Polyesters polycaprolactone 24980-41-4
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245 1 0 |a Reinforcement of interfacial adhesion of a coated polymer layer on a cobalt-chromium surface for drug-eluting stents 
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520 |a During the balloon expansion of several commercially available drug-eluting stents, various types of defects in the polymer layer have been observed. The aim of this study is to prevent these defects by increasing the interfacial adhesion between the metal substrate and the drug-in-polymer matrix using poly(caprolactone) (PCL) brushes onto a cobalt-chromium (Co-Cr or CC) alloy surface. The chemical modification of the Co-Cr surface was accomplished by grafting ricinoleic acid (RA) onto the metal substrate followed by surface-initiated ring opening polymerization of ε-caprolactone. The unmodified, RA-grafted (CC-RA), and PCL-grafted Co-Cr substrates (CC-RA-PCL3D and CC-RA-PCL6D) were characterized by various surface analyses. Poly(d,l-lactide) containing sirolimus was spray coated onto the unmodified and modified substrates. The adhesion property of the polymer coating on the PCL-grafted surfaces was improved compared to those of other samples. Among all of the drug-in-polymer coated samples, both CC-RA-PCL3D and CC-RA-PCL6D exhibited a stabilized drug release profile over 49 days. It was also revealed that CC-RA-PCL6D showed the slowest drug release of all the samples. On the basis of these results, the proposed nanocoupling method has shown not only improved adhesion of the drug-in-polymer matrix to the Co-Cr substrate but also controlled drug release 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
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650 7 |a Coated Materials, Biocompatible  |2 NLM 
650 7 |a Polyesters  |2 NLM 
650 7 |a polycaprolactone  |2 NLM 
650 7 |a 24980-41-4  |2 NLM 
700 1 |a Cho, Youngjin  |e verfasserin  |4 aut 
700 1 |a Kim, Tae Jung  |e verfasserin  |4 aut 
700 1 |a Kim, Young Dong  |e verfasserin  |4 aut 
700 1 |a Park, Bang Ju  |e verfasserin  |4 aut 
700 1 |a Joung, Yoon Ki  |e verfasserin  |4 aut 
700 1 |a Han, Dong Keun  |e verfasserin  |4 aut 
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