0 603

Cited 0 times in

Improved calcification resistance and biocompatibility of tissue patch grafted with sulfonated PEO or heparin after glutaraldehyde fixation

DC Field Value Language
dc.contributor.author박종철-
dc.contributor.author서활-
dc.date.accessioned2016-02-19T11:26:56Z-
dc.date.available2016-02-19T11:26:56Z-
dc.date.issued2001-
dc.identifier.issn0021-9304-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/143166-
dc.description.abstractA novel chemical modification of biological tissues was developed aimed at improving biocompatibility and calcification resistance. This method involved the additional grafting of sulfonated PEO (PEO-SO3) or heparin after conventional glutaraldehyde (GA) fixation of bovine pericardium (BP). The amino groups of PEO-SO3 or heparin were utilized to react to the GA residues to block them. The PEO-SO3 or heparin grafted tissues demonstrated a slightly higher shrinkage temperature and tensile strength, but greater resistance to collagenase digestion, than GA treated ones. These results suggest that modified tissues have improved durability due to the grafting and filling effect of PEO-SO3 or heparin in addition to the GA cross-linking. At the direct contact cytotoxicity test in vitro, PEO-SO3 or heparin grafted tissue was shown to be nontoxic, while relatively significant cytotoxicity was observed for the GA treated tissues, possibly due to the release of GA. From the in vivo calcification study, calcium contents deposited on the modified tissues were much less than those on GA treated tissues. Such a decreased calcification might be explained by the decrease of residual GA groups during the additional treatment, and the space-filling effect and the nonadhesive property and/or the blood compatiblility of PEO-SO3 or heparin grafted covalently. The newly modified tissue patch was observed to show improved pathological assessibility including less inflammation and tissue reactions. This simple modification method may be useful for calcification-resistant and blood-compatible tissue patches for cardiovascular implants.-
dc.description.statementOfResponsibilityopen-
dc.format.extent27~35-
dc.relation.isPartOfJOURNAL OF BIOMEDICAL MATERIALS RESEARCH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHAorta, Thoracic/pathology-
dc.subject.MESHAorta, Thoracic/surgery-
dc.subject.MESHBiocompatible Materials/chemistry-
dc.subject.MESHBiocompatible Materials/toxicity-
dc.subject.MESHBioprosthesis*-
dc.subject.MESHBorohydrides/pharmacology-
dc.subject.MESHCalcinosis/prevention & control*-
dc.subject.MESHCattle-
dc.subject.MESHCollagenases/pharmacology-
dc.subject.MESHCross-Linking Reagents/chemistry-
dc.subject.MESHCross-Linking Reagents/pharmacology*-
dc.subject.MESHCross-Linking Reagents/toxicity-
dc.subject.MESHDermatologic Surgical Procedures-
dc.subject.MESHDogs-
dc.subject.MESHFixatives/chemistry-
dc.subject.MESHFixatives/pharmacology*-
dc.subject.MESHFixatives/toxicity-
dc.subject.MESHGlutaral/chemistry-
dc.subject.MESHGlutaral/pharmacology*-
dc.subject.MESHGlutaral/toxicity-
dc.subject.MESHHeparin/chemistry-
dc.subject.MESHHeparin/pharmacology*-
dc.subject.MESHHeparin/toxicity-
dc.subject.MESHL Cells (Cell Line)/drug effects-
dc.subject.MESHMale-
dc.subject.MESHMaterials Testing-
dc.subject.MESHMice-
dc.subject.MESHOxidation-Reduction-
dc.subject.MESHPericardium/chemistry-
dc.subject.MESHPericardium/drug effects*-
dc.subject.MESHPolyethylene Glycols/chemistry-
dc.subject.MESHPolyethylene Glycols/pharmacology*-
dc.subject.MESHPulmonary Artery/pathology-
dc.subject.MESHPulmonary Artery/surgery-
dc.subject.MESHRats-
dc.subject.MESHRats, Sprague-Dawley-
dc.subject.MESHSkin/pathology-
dc.subject.MESHSpecimen Handling-
dc.subject.MESHSulfonic Acids/chemistry-
dc.subject.MESHSulfonic Acids/pharmacology*-
dc.subject.MESHTemperature-
dc.subject.MESHTensile Strength-
dc.titleImproved calcification resistance and biocompatibility of tissue patch grafted with sulfonated PEO or heparin after glutaraldehyde fixation-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Medical Engineering (의학공학)-
dc.contributor.googleauthorWon Kyu Lee-
dc.contributor.googleauthorKi Dong Park-
dc.contributor.googleauthorYoung Ha Kim-
dc.contributor.googleauthorHwal Suh-
dc.contributor.googleauthorJong Chul Park-
dc.contributor.googleauthorJong Eun Lee-
dc.contributor.googleauthorKyung Sun-
dc.contributor.googleauthorMan Jong Baek-
dc.contributor.googleauthorHyung-Mook Kim-
dc.contributor.googleauthorSoo Hyun Kim-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA01662-
dc.contributor.localIdA01924-
dc.relation.journalcodeJ01265-
dc.identifier.eissn1097-4636-
dc.identifier.pmid11152994-
dc.identifier.urlhttp://onlinelibrary.wiley.com/doi/10.1002/1097-4636(2001)58:1%3C27::AID-JBM40%3E3.0.CO;2-2/abstract-
dc.subject.keywordbovine pericardium tissue patch-
dc.subject.keywordsulfonated PEO or heparin grafting-
dc.subject.keywordstability-
dc.subject.keywordcytotoxicity-
dc.subject.keywordcalcification-
dc.contributor.alternativeNamePark, Jong Chul-
dc.contributor.alternativeNameSuh, Hwal-
dc.contributor.affiliatedAuthorPark, Jong Chul-
dc.contributor.affiliatedAuthorSuh, Hwal-
dc.rights.accessRightsnot free-
dc.citation.volume58-
dc.citation.number1-
dc.citation.startPage27-
dc.citation.endPage35-
dc.identifier.bibliographicCitationJOURNAL OF BIOMEDICAL MATERIALS RESEARCH , Vol.58(1) : 27-35, 2001-
dc.identifier.rimsid39104-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Medical Engineering (의학공학교실) > 1. Journal Papers

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.