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Electroformed pure iron as a new biomaterial for degradable stents: In vitro degradation and preliminary cell viability studies
In the search for a metallic material showing moderate and uniform degradation for application as degradable cardiovascular stents, electroformed iron (E-Fe) was evaluated by in vitro degradation and cell viability tests. Static immersion and dynamic degradation were used to evaluate degradation rat...
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Published in: | Acta biomaterialia 2010-05, Vol.6 (5), p.1843-1851 |
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creator | Moravej, M. Purnama, A. Fiset, M. Couet, J. Mantovani, D. |
description | In the search for a metallic material showing moderate and uniform degradation for application as degradable cardiovascular stents, electroformed iron (E-Fe) was evaluated by
in vitro degradation and cell viability tests. Static immersion and dynamic degradation were used to evaluate degradation rate and mechanism, while cell viability assay was used to assess cytotoxicity. The results were compared with those of iron fabricated by casting and thermomechanical treatment previously investigated as a stent material. Electroformed iron showed faster degradation than iron fabricated by casting (0.25 vs. 0.14
mm
year
−1), with a uniform degradation mechanism. Cell viability results showed that E-Fe did not result in a decrease in metabolic activity when exposed to primary rat smooth muscle cells. However, it caused a decrease in cell proliferation activity which could be beneficial for the inhibition of in-stent restenosis. |
doi_str_mv | 10.1016/j.actbio.2010.01.008 |
format | article |
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in vitro degradation and cell viability tests. Static immersion and dynamic degradation were used to evaluate degradation rate and mechanism, while cell viability assay was used to assess cytotoxicity. The results were compared with those of iron fabricated by casting and thermomechanical treatment previously investigated as a stent material. Electroformed iron showed faster degradation than iron fabricated by casting (0.25 vs. 0.14
mm
year
−1), with a uniform degradation mechanism. Cell viability results showed that E-Fe did not result in a decrease in metabolic activity when exposed to primary rat smooth muscle cells. However, it caused a decrease in cell proliferation activity which could be beneficial for the inhibition of in-stent restenosis.</description><identifier>ISSN: 1742-7061</identifier><identifier>EISSN: 1878-7568</identifier><identifier>DOI: 10.1016/j.actbio.2010.01.008</identifier><identifier>PMID: 20080213</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Absorbable Implants ; Animals ; Biocompatible Materials - pharmacology ; Cell Survival - drug effects ; Cell viability ; Degradable materials ; Electrochemistry - methods ; Electroforming ; In vitro degradation ; Iron - pharmacology ; Materials Testing - methods ; Myocytes, Smooth Muscle - cytology ; Myocytes, Smooth Muscle - drug effects ; Rats ; Stainless Steel - pharmacology ; Stents ; X-Ray Diffraction</subject><ispartof>Acta biomaterialia, 2010-05, Vol.6 (5), p.1843-1851</ispartof><rights>2010 Acta Materialia Inc.</rights><rights>Copyright (c) 2010 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-8363a99a5c3c300d3faa6ef30de5cf433b2a6af653ca20880423f21dbae22d5b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20080213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moravej, M.</creatorcontrib><creatorcontrib>Purnama, A.</creatorcontrib><creatorcontrib>Fiset, M.</creatorcontrib><creatorcontrib>Couet, J.</creatorcontrib><creatorcontrib>Mantovani, D.</creatorcontrib><title>Electroformed pure iron as a new biomaterial for degradable stents: In vitro degradation and preliminary cell viability studies</title><title>Acta biomaterialia</title><addtitle>Acta Biomater</addtitle><description>In the search for a metallic material showing moderate and uniform degradation for application as degradable cardiovascular stents, electroformed iron (E-Fe) was evaluated by
in vitro degradation and cell viability tests. Static immersion and dynamic degradation were used to evaluate degradation rate and mechanism, while cell viability assay was used to assess cytotoxicity. The results were compared with those of iron fabricated by casting and thermomechanical treatment previously investigated as a stent material. Electroformed iron showed faster degradation than iron fabricated by casting (0.25 vs. 0.14
mm
year
−1), with a uniform degradation mechanism. Cell viability results showed that E-Fe did not result in a decrease in metabolic activity when exposed to primary rat smooth muscle cells. 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in vitro degradation and cell viability tests. Static immersion and dynamic degradation were used to evaluate degradation rate and mechanism, while cell viability assay was used to assess cytotoxicity. The results were compared with those of iron fabricated by casting and thermomechanical treatment previously investigated as a stent material. Electroformed iron showed faster degradation than iron fabricated by casting (0.25 vs. 0.14
mm
year
−1), with a uniform degradation mechanism. Cell viability results showed that E-Fe did not result in a decrease in metabolic activity when exposed to primary rat smooth muscle cells. However, it caused a decrease in cell proliferation activity which could be beneficial for the inhibition of in-stent restenosis.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>20080213</pmid><doi>10.1016/j.actbio.2010.01.008</doi><tpages>9</tpages></addata></record> |
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subjects | Absorbable Implants Animals Biocompatible Materials - pharmacology Cell Survival - drug effects Cell viability Degradable materials Electrochemistry - methods Electroforming In vitro degradation Iron - pharmacology Materials Testing - methods Myocytes, Smooth Muscle - cytology Myocytes, Smooth Muscle - drug effects Rats Stainless Steel - pharmacology Stents X-Ray Diffraction |
title | Electroformed pure iron as a new biomaterial for degradable stents: In vitro degradation and preliminary cell viability studies |
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