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Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices
Design of blood compatible surfaces is obligatory to minimize platelet surface interactions and improve the thromboresistance of foreign surfaces when they are utilized as biomaterials particularly for blood contacting devices. Pure metallocene polyethylene (mPE) and nitric acid (HNO(3)) treated mPE...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727976/ https://www.ncbi.nlm.nih.gov/pubmed/26819837 http://dx.doi.org/10.7717/peerj.1388 |
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author | Vellayappan, Muthu Vignesh Jaganathan, Saravana Kumar Muhamad, Ida Idayu |
author_facet | Vellayappan, Muthu Vignesh Jaganathan, Saravana Kumar Muhamad, Ida Idayu |
author_sort | Vellayappan, Muthu Vignesh |
collection | PubMed |
description | Design of blood compatible surfaces is obligatory to minimize platelet surface interactions and improve the thromboresistance of foreign surfaces when they are utilized as biomaterials particularly for blood contacting devices. Pure metallocene polyethylene (mPE) and nitric acid (HNO(3)) treated mPE antithrombogenicity and hydrophilicity were investigated. The contact angle of the mPE treated with HNO(3) decreased. Surface of mPE and HNO(3) treated mPE investigated with FTIR revealed no major changes in its functional groups. 3D Hirox digital microscopy, SEM and AFM images show increased porosity and surface roughness. Blood coagulation assays prothrombin time (PT) and activated partial thromboplastin time (APTT) were delayed significantly (P < 0.05) for HNO(3) treated mPE. Hemolysis assay and platelet adhesion of the treated surface resulted in the lysis of red blood cells and platelet adherence, respectively indicating improved hemocompatibility of HNO(3) treated mPE. To determine that HNO(3) does not deteriorate elastic modulus of mPE, the elastic modulus of mPE and HNO(3) treated mPE was compared and the result shows no significant difference. Hence, the overall observation suggests that the novel HNO(3) treated mPE may hold great promises to be exploited for blood contacting devices like grafts, catheters, and etc. |
format | Online Article Text |
id | pubmed-4727976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47279762016-01-27 Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices Vellayappan, Muthu Vignesh Jaganathan, Saravana Kumar Muhamad, Ida Idayu PeerJ Biochemistry Design of blood compatible surfaces is obligatory to minimize platelet surface interactions and improve the thromboresistance of foreign surfaces when they are utilized as biomaterials particularly for blood contacting devices. Pure metallocene polyethylene (mPE) and nitric acid (HNO(3)) treated mPE antithrombogenicity and hydrophilicity were investigated. The contact angle of the mPE treated with HNO(3) decreased. Surface of mPE and HNO(3) treated mPE investigated with FTIR revealed no major changes in its functional groups. 3D Hirox digital microscopy, SEM and AFM images show increased porosity and surface roughness. Blood coagulation assays prothrombin time (PT) and activated partial thromboplastin time (APTT) were delayed significantly (P < 0.05) for HNO(3) treated mPE. Hemolysis assay and platelet adhesion of the treated surface resulted in the lysis of red blood cells and platelet adherence, respectively indicating improved hemocompatibility of HNO(3) treated mPE. To determine that HNO(3) does not deteriorate elastic modulus of mPE, the elastic modulus of mPE and HNO(3) treated mPE was compared and the result shows no significant difference. Hence, the overall observation suggests that the novel HNO(3) treated mPE may hold great promises to be exploited for blood contacting devices like grafts, catheters, and etc. PeerJ Inc. 2016-01-19 /pmc/articles/PMC4727976/ /pubmed/26819837 http://dx.doi.org/10.7717/peerj.1388 Text en ©2016 Vellayappan et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Biochemistry Vellayappan, Muthu Vignesh Jaganathan, Saravana Kumar Muhamad, Ida Idayu Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices |
title | Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices |
title_full | Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices |
title_fullStr | Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices |
title_full_unstemmed | Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices |
title_short | Unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices |
title_sort | unravelling the potential of nitric acid as a surface modifier for improving the hemocompatibility of metallocene polyethylene for blood contacting devices |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727976/ https://www.ncbi.nlm.nih.gov/pubmed/26819837 http://dx.doi.org/10.7717/peerj.1388 |
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