In situ incorporation of heparin/bivalirudin into a phytic acid coating on biodegradable magnesium with improved anticorrosion and biocompatible properties. Issue 22 (17th May 2017)
- Record Type:
- Journal Article
- Title:
- In situ incorporation of heparin/bivalirudin into a phytic acid coating on biodegradable magnesium with improved anticorrosion and biocompatible properties. Issue 22 (17th May 2017)
- Main Title:
- In situ incorporation of heparin/bivalirudin into a phytic acid coating on biodegradable magnesium with improved anticorrosion and biocompatible properties
- Authors:
- Chen, Yingqi
Zhang, Xuan
Zhao, Sheng
Maitz, Manfred F.
Zhang, Wentai
Yang, Su
Mao, Jinlong
Huang, Nan
Wan, Guojiang - Abstract:
- Abstract : Drugs were incorporated into a phytic acid coating on Mg by an in situ chemical route for corrosion control and biocompatibility. Abstract : Heparin (Hep) or bivalirudin (BVLD) were immobilized in an organic phytic acid (PA) coating on Mg by an in situ chemical route. Such a drug-loaded PA coating was designed to enhance both corrosion control and biocompatibility. It was found that both Hep- and BVLD-loaded PA coatings exhibited a dual role in effectively controlling corrosion as well as providing a biofunctional effect. Experiments involving electrochemical corrosion and in vitro degradation by immersion revealed that PA&Hep- and PA&BVLD-coated Mg had the same effect or even slower corrosion/degradation in phosphate buffered saline compared to PA-coated Mg, and it degraded significantly slower than untreated Mg. Moreover, Hep- or BVLD-loaded PA coatings showed relatively good hemocompatibility, with a prolonged clotting time, inhibited platelets adhesion as well as reduced hemolysis compared to untreated Mg. In addition, both PA&Hep and PA&BVLD coatings promoted endothelial cells growth and restrained the proliferation of smooth muscle cells. In vivo assays indicated that PA&Hep-coated Mg exhibited a significant difference in mass loss compared to untreated Mg, as well as better histocompatibility than other samples. These results demonstrate that our coating strategy shows a great potential in surface modification of biodegradable Mg. Finally, the mechanism forAbstract : Drugs were incorporated into a phytic acid coating on Mg by an in situ chemical route for corrosion control and biocompatibility. Abstract : Heparin (Hep) or bivalirudin (BVLD) were immobilized in an organic phytic acid (PA) coating on Mg by an in situ chemical route. Such a drug-loaded PA coating was designed to enhance both corrosion control and biocompatibility. It was found that both Hep- and BVLD-loaded PA coatings exhibited a dual role in effectively controlling corrosion as well as providing a biofunctional effect. Experiments involving electrochemical corrosion and in vitro degradation by immersion revealed that PA&Hep- and PA&BVLD-coated Mg had the same effect or even slower corrosion/degradation in phosphate buffered saline compared to PA-coated Mg, and it degraded significantly slower than untreated Mg. Moreover, Hep- or BVLD-loaded PA coatings showed relatively good hemocompatibility, with a prolonged clotting time, inhibited platelets adhesion as well as reduced hemolysis compared to untreated Mg. In addition, both PA&Hep and PA&BVLD coatings promoted endothelial cells growth and restrained the proliferation of smooth muscle cells. In vivo assays indicated that PA&Hep-coated Mg exhibited a significant difference in mass loss compared to untreated Mg, as well as better histocompatibility than other samples. These results demonstrate that our coating strategy shows a great potential in surface modification of biodegradable Mg. Finally, the mechanism for the incorporation of the drugs into the PA coating is discussed from both theoretical and practical perspectives. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 5:Issue 22(2017)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 5:Issue 22(2017)
- Issue Display:
- Volume 5, Issue 22 (2017)
- Year:
- 2017
- Volume:
- 5
- Issue:
- 22
- Issue Sort Value:
- 2017-0005-0022-0000
- Page Start:
- 4162
- Page End:
- 4176
- Publication Date:
- 2017-05-17
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Biomedical materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tb# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6tb03157a ↗
- Languages:
- English
- ISSNs:
- 2050-750X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205200
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1874.xml