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Establishment of an Experimental System for Intraperitoneal Chemotherapy in a Rat Model

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dc.contributor.authorPark, Sunwoo-
dc.contributor.authorPark, Soo Jin-
dc.contributor.authorLee, Hee Su-
dc.contributor.authorHam, Jiyeon-
dc.contributor.authorLee, Eun Ji-
dc.contributor.authorKim, Junsik-
dc.contributor.authorRyu, Soomin-
dc.contributor.authorSeol, Aeran-
dc.contributor.authorLim, Whasun-
dc.contributor.authorLee, Jung Chan-
dc.contributor.authorSong, Gwonhwa-
dc.contributor.authorKim, Hee seung-
dc.date.accessioned2022-02-24T11:41:20Z-
dc.date.available2022-02-24T11:41:20Z-
dc.date.created2022-02-07-
dc.date.issued2021-09-
dc.identifier.issn0258-851X-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/136738-
dc.description.abstractAim: To establish an experimental system for comparing different methods of intraperitoneal chemotherapy in a rat model. Materials and Methods: We used six-week-old Sprague-Dawley rats, and created an early postoperative intraperitoneal chemotherapy (EPIC) system using 18-gauge syringes and evacuators, and a hyperthermic intraperitoneal chemotherapy (HIPEC) system using two peristaltic pumps which controlled the flow rate and temperature. Pressurized intraperitoneal aerosol chemotherapy (PIPAC) was achieved using a nozzle for dispersing aerosols at a flow rate up to 41.5 ml/min. The distribution and intensity of 0.2% trypan blue dye was compared among three methods. Results: The distribution was limited and the intensity was weak after EPIC, and the dye stained moderately in gravity-dependent regions after HIPEC. On the other hand, the distribution was the most comprehensive, and the intensity was the greatest after PIPAC. Conclusion: This experimental system in a rat model may reflect the comparative effect among EPIC, HIPEC and PIPAC in humans.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherINT INST ANTICANCER RESEARCH-
dc.subjectPERITONEAL CARCINOMATOSIS-
dc.subjectAEROSOL CHEMOTHERAPY-
dc.subjectOVARIAN-CANCER-
dc.subjectCYTOREDUCTIVE SURGERY-
dc.subjectTISSUE DISTRIBUTION-
dc.subjectPHARMACOKINETICS-
dc.subjectHYPERTHERMIA-
dc.subjectCHEMOPERFUSION-
dc.subjectDOXORUBICIN-
dc.subjectPACLITAXEL-
dc.titleEstablishment of an Experimental System for Intraperitoneal Chemotherapy in a Rat Model-
dc.typeArticle-
dc.contributor.affiliatedAuthorSong, Gwonhwa-
dc.identifier.doi10.21873/invivo.12554-
dc.identifier.scopusid2-s2.0-85113824455-
dc.identifier.wosid000686259500013-
dc.identifier.bibliographicCitationIN VIVO, v.35, no.5, pp.2703 - 2710-
dc.relation.isPartOfIN VIVO-
dc.citation.titleIN VIVO-
dc.citation.volume35-
dc.citation.number5-
dc.citation.startPage2703-
dc.citation.endPage2710-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordPlusAEROSOL CHEMOTHERAPY-
dc.subject.keywordPlusCHEMOPERFUSION-
dc.subject.keywordPlusCYTOREDUCTIVE SURGERY-
dc.subject.keywordPlusDOXORUBICIN-
dc.subject.keywordPlusHYPERTHERMIA-
dc.subject.keywordPlusOVARIAN-CANCER-
dc.subject.keywordPlusPACLITAXEL-
dc.subject.keywordPlusPERITONEAL CARCINOMATOSIS-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.subject.keywordPlusTISSUE DISTRIBUTION-
dc.subject.keywordAuthorExperimental system-
dc.subject.keywordAuthorintraperitoneal chemotherapy-
dc.subject.keywordAuthorrat-
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