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dc.contributor.authorLee, C.H.-
dc.contributor.authorSohn, D.W.-
dc.contributor.authorKim, H.S.-
dc.contributor.authorLee, S.-J.-
dc.contributor.authorCho, Y.-H.-
dc.contributor.authorYoon, M.S.-
dc.contributor.authorChung, H.-
dc.contributor.authorPark, T.Y.-
dc.contributor.authorChoi, Y.W.-
dc.contributor.authorKim, S.W.-
dc.date.accessioned2024-01-21T05:02:23Z-
dc.date.available2024-01-21T05:02:23Z-
dc.date.created2021-09-02-
dc.date.issued2005-06-
dc.identifier.issn0494-4747-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136443-
dc.description.abstractPurpose: Paclitaxel is an anticancer drug that blocks cell division by stabilizing microtubules. Even though paclitaxel has been shown to be effective in killing bladder cancer cell lines in vitro, the in vivo absorption was extremely low. A paclitaxel formulation was prepared in solution only, which was bioadhesive, and its effects evaluated in the MBT-2 cell line and in C3H2 bladder cancer mice. In addition, the toxicity of the paclitaxel formulation was also evaluated. Materials and methods: A muco-adhesive oily paclitaxel formulation was made by the combining of monoolein, tricaprylin, Tween 80 and paclitaxel. MBT-2 cells were cultivated in different concentration of taxol, and the tumoricidal activity measured by the indirect methylthiazol-2-yl-2, 5-diphenyl tetrazolium bromide (MTT) assay. In an in vivo study, the treatment regimen for the s.c. C3H2 mice was five consecutive once daily administrations, beginning on day 4 post tumor implant. The length and width of the tumors were measured twice a week, and the tumor volume calculated. On day 21, the tumor volume change and toxicity were evaluated. Results: The average particle size of paclitaxel-loaded lipid nanoparticle was about 600nm, with a polydispersity of 1,000. Only 2.6% of the MBT-2 cells were viable after 24 hour of treatment with the formulation at a paclitaxel concentration of 10 μg/ml, while showing minimal toxicity of the formulation without paclitaxel. Paclitaxel-loaded lipid nanoparticles, administered orally, allowed significant antitumor activity in C3H2 mice (p<0.05). Conclusions: Paclitaxel-loaded lipid nanoparticles have a remarkable cytotoxic effect against MBT-2 cells, in a dose dependent manner, and the oral paclitaxel-loaded lipid nanoparticle therapy had an inhibitory effect on bladder tumors in a MBT-2 model, but without systemic toxicity. Therefore, oral paclitaxel-loaded lipid nanoparticles may be used for advanced bladder cancer patients.-
dc.languageKorean-
dc.subjectbromine derivative-
dc.subjectglycerol oleate-
dc.subjectlipid-
dc.subjectnanoparticle-
dc.subjectpaclitaxel-
dc.subjectpolysorbate 80-
dc.subjecttrioctanoin-
dc.subjectanimal experiment-
dc.subjectanimal model-
dc.subjectantineoplastic activity-
dc.subjectarticle-
dc.subjectbioassay-
dc.subjectbladder cancer-
dc.subjectcell culture-
dc.subjectcell strain-
dc.subjectcontrolled study-
dc.subjectculture medium-
dc.subjectcytotoxicity-
dc.subjectdose response-
dc.subjectdrug binding-
dc.subjectdrug dose regimen-
dc.subjectdrug efficacy-
dc.subjectdrug formulation-
dc.subjectdrug mechanism-
dc.subjectdrug response-
dc.subjectin vivo study-
dc.subjectmouse-
dc.subjectnonhuman-
dc.subjectparticle size-
dc.subjecttumor volume-
dc.titleThe anticancer efficacy and toxicity of oral paclitaxel-loaded lipid nanoparticle in a C3H2 bladder cancer mice-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationKorean Journal of Urology, v.46, no.8, pp.854 - 860-
dc.citation.titleKorean Journal of Urology-
dc.citation.volume46-
dc.citation.number8-
dc.citation.startPage854-
dc.citation.endPage860-
dc.description.journalRegisteredClassscopus-
dc.identifier.kciidART001104718-
dc.identifier.scopusid2-s2.0-23944501968-
dc.type.docTypeArticle-
dc.subject.keywordPlusbromine derivative-
dc.subject.keywordPlusglycerol oleate-
dc.subject.keywordPluslipid-
dc.subject.keywordPlusnanoparticle-
dc.subject.keywordPluspaclitaxel-
dc.subject.keywordPluspolysorbate 80-
dc.subject.keywordPlustrioctanoin-
dc.subject.keywordPlusanimal experiment-
dc.subject.keywordPlusanimal model-
dc.subject.keywordPlusantineoplastic activity-
dc.subject.keywordPlusarticle-
dc.subject.keywordPlusbioassay-
dc.subject.keywordPlusbladder cancer-
dc.subject.keywordPluscell culture-
dc.subject.keywordPluscell strain-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusculture medium-
dc.subject.keywordPluscytotoxicity-
dc.subject.keywordPlusdose response-
dc.subject.keywordPlusdrug binding-
dc.subject.keywordPlusdrug dose regimen-
dc.subject.keywordPlusdrug efficacy-
dc.subject.keywordPlusdrug formulation-
dc.subject.keywordPlusdrug mechanism-
dc.subject.keywordPlusdrug response-
dc.subject.keywordPlusin vivo study-
dc.subject.keywordPlusmouse-
dc.subject.keywordPlusnonhuman-
dc.subject.keywordPlusparticle size-
dc.subject.keywordPlustumor volume-
dc.subject.keywordAuthorBladder cancer-
dc.subject.keywordAuthorMice-
dc.subject.keywordAuthorNanoparticle-
dc.subject.keywordAuthorPaclitaxel-
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KIST Article > 2005
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