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Characterization of Anti-Adhesion Properties of Alginate/Polyethylene Oxide Film to Reduce Postsurgical Peritoneal Adhesions

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dc.contributor.authorKim, Duckil-
dc.contributor.authorChoi, Geun Joo-
dc.contributor.authorBaek, Seungho-
dc.contributor.authorAbdullah, Abdullah-
dc.contributor.authorJang, Soohyun-
dc.contributor.authorHong, Soon Auck-
dc.contributor.authorKim, Beom Gyu-
dc.contributor.authorLee, Joonhee-
dc.contributor.authorKang, Hyun-
dc.contributor.authorLee, Donghyun-
dc.date.available2019-03-08T07:58:12Z-
dc.date.issued2017-09-
dc.identifier.issn1947-2935-
dc.identifier.issn1947-2943-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/4028-
dc.description.abstractPostsurgical peritoneal adhesions lead to severe complications including chronic abdominal pain, female infertility, and small bowel obstruction. Adhesions can be minimized by introducing a physical barrier film between the tissues after surgery. We newly developed an anti-adhesive barrier film using alginate and polyethylene oxide (PEO). We determined the anti-adhesive properties of our alginate/PEO film through in vitro and in vivo studies. Alginate fibrous films were synthesized using electrospinning technique. PEO was added to alginate at 1:9 to minimize the repulsive forces within highly anionic alginate to make the fibrous film synthesis reproducible. The alginate/PEO film was then characterized for its morphology using atomic force microscopy (AFM) and Fourier transform infrared (FTIR) spectroscopy. For the in vitro study, NIH-3T3 cells were selected and cytotoxicity analysis was performed additionally. In the in vivo study, an intra-abdominal adhesion rat model was used. Sixty rats underwent laparotomy and cecal abrasion, and then, the alginate/PEO film was applied to the adhesion induction site. Peritoneal adhesion was assessed macroscopically and microscopically 2 weeks after surgery. In the in vitro study, alginate/PEO film exhibited enhanced anti-adhesive and cell repellent properties. In addition, the cytotoxicity analysis showed that the alginate/PEO film was non-toxic to mammalian cells. In the in vivo study, the alginate/PEO film showed significant adhesion reduction in both macroscopic and microscopic evaluations. The observed results suggest that the alginate/PEO film can be used as an effective physical barrier between tissues for reduced postsurgical peritoneal adhesions.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER SCIENTIFIC PUBLISHERS-
dc.titleCharacterization of Anti-Adhesion Properties of Alginate/Polyethylene Oxide Film to Reduce Postsurgical Peritoneal Adhesions-
dc.typeArticle-
dc.identifier.doi10.1166/sam.2017.3166-
dc.identifier.bibliographicCitationSCIENCE OF ADVANCED MATERIALS, v.9, no.9, pp 1669 - 1677-
dc.description.isOpenAccessN-
dc.identifier.wosid000412929100036-
dc.identifier.scopusid2-s2.0-85030834113-
dc.citation.endPage1677-
dc.citation.number9-
dc.citation.startPage1669-
dc.citation.titleSCIENCE OF ADVANCED MATERIALS-
dc.citation.volume9-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorAlginate/Polyethylene Oxide Film-
dc.subject.keywordAuthorPeritoneal Adhesion-
dc.subject.keywordAuthorAnti-Adhesion-
dc.subject.keywordAuthorNIH-3T3-
dc.subject.keywordAuthorAnimal Model-
dc.subject.keywordPlusIN-VITRO-
dc.subject.keywordPlusPREVENTION-
dc.subject.keywordPlusALGINATE-
dc.subject.keywordPlusCHITOSAN-
dc.subject.keywordPlusSURGERY-
dc.subject.keywordPlusBARRIER-
dc.subject.keywordPlusPATHOPHYSIOLOGY-
dc.subject.keywordPlusBIOAVAILABILITY-
dc.subject.keywordPlusMEMBRANES-
dc.subject.keywordPlusSCAFFOLD-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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