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Anticancer effect of docetaxel/hydroxypropyl-beta-cyclodextrin complex without histamine release

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dc.contributor.authorKim, Tae Kon-
dc.contributor.authorYoo, Hye Hyun-
dc.date.accessioned2021-06-22T18:42:08Z-
dc.date.available2021-06-22T18:42:08Z-
dc.date.created2021-01-21-
dc.date.issued2015-12-
dc.identifier.issn1388-3127-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/16474-
dc.description.abstractIn this study, the anticancer effect and improved safety for hypesensitivity reactions of docetaxel/hydroxypropyl-beta-cyclodextrin complex (DCX-CD) were investigated. The preparation of DCX-CD was confirmed by using differential scanning calorimetry, X-ray powder diffraction analysis, and scanning electron microscope. The anticancer activity was tested in human lung cancer A549 cell-transplanted mice and the hypersensitivity was tested in Beagle dogs after intravenous administration of DCX-CD, Taxotere, and their respective vehicles. In the hypersensitivity test, plasma histamine levels were determined using an ELISA method. Our results showed that DCX-CD was pharmacologically equivalent to Taxotere. Furthermore, DCX-CD did not cause the release of histamines or any significant symptoms associated with hypersensitivity. These results suggested that DCX-CD could be a promising alternative to Taxotere for cancer chemotherapy with reduced side effects.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER-
dc.titleAnticancer effect of docetaxel/hydroxypropyl-beta-cyclodextrin complex without histamine release-
dc.typeArticle-
dc.contributor.affiliatedAuthorYoo, Hye Hyun-
dc.identifier.doi10.1007/s10847-015-0571-2-
dc.identifier.scopusid2-s2.0-84958777098-
dc.identifier.wosid000364225300015-
dc.identifier.bibliographicCitationJournal of Inclusion Phenomena and Macrocyclic Chemistry , v.83, no.3-4, pp.355 - 361-
dc.relation.isPartOfJournal of Inclusion Phenomena and Macrocyclic Chemistry-
dc.citation.titleJournal of Inclusion Phenomena and Macrocyclic Chemistry-
dc.citation.volume83-
dc.citation.number3-4-
dc.citation.startPage355-
dc.citation.endPage361-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusDOCETAXEL FORMULATION-
dc.subject.keywordPlusTAXOTERE-
dc.subject.keywordPlusSID530-
dc.subject.keywordPlusPHARMACOKINETICS-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusSAFETY-
dc.subject.keywordPlusPLASMA-
dc.subject.keywordAuthorDocetaxel-
dc.subject.keywordAuthorHP-beta-CD-
dc.subject.keywordAuthorAnticancer activity-
dc.subject.keywordAuthorHypersensitivity-
dc.identifier.urlhttps://link.springer.com/article/10.1007%2Fs10847-015-0571-2-
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