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dc.contributor.authorYoo, BI-
dc.contributor.authorAhan, KB-
dc.contributor.authorKang, MH-
dc.contributor.authorKwon, OS-
dc.contributor.authorHong, YS-
dc.contributor.authorLee, JJ-
dc.contributor.authorLee, HS-
dc.contributor.authorRyu, JS-
dc.contributor.authorKim, TY-
dc.contributor.authorMoon, DC-
dc.contributor.authorSong, S-
dc.contributor.authorChung, YB-
dc.date.accessioned2024-01-21T05:12:05Z-
dc.date.available2024-01-21T05:12:05Z-
dc.date.created2021-09-03-
dc.date.issued2005-04-
dc.identifier.issn0253-6269-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/136620-
dc.description.abstractWe investigated the pharmacokinetics of 11-hydroxyaclacinomycin X (ID-6105), a novel anthracycline, after intravenous (i.v.) bolus administration at a multiple dose every 24 h for 5 days in rats. To analyze ID-6105 levels in biological samples, we used an HPLC-based method which was validated in a pharmacokinetic study by suitable criteria. The concentrations of ID-6105 after the multiple administration for 5 days were not significantly different from the results after the single administration. The t(1/2 alpha), t(1/2 beta), V-dss and CLt after the multiple administration were not significantly different from the values after the single administration. Moreover, the concentrations of ID-6105 1 min at day 1-5 after i.v. bolus multiple administration did not show the significant difference. Of the various tissues, ID-6105 mainly distributed to the kidney, lung, spleen, adrenal gland, and liver after i.v. bolus multiple administration. ID-6105 concentrations in the kidney or lung 2 h after i.v. bolus administration were comparable to the plasma concentration shortly after i.v. bolus administration. However, the ID-6105 concentrations in various tissues 48 h after i.v. bolus administration decreased to low levels. ID-6105 was excreted largely in the bile after i.v. bolus multiple administration at the dose of 3 mg/kg. The amounts of ID-6105 found in the bile by 12 h or in the urine by 48 h after the administration were calculated to be 14.1% or 4.55% of the initial dose, respectively, indicating that ID-6105 is mostly excreted in the bile. In conclusion, ID-6105 was rapidly cleared from the blood and transferred to tissues, suggesting that ID-6105 might not be accumulated in the blood following i.v. bolus multiple dosages of 3 mg/kg every 24 h for 5 days. By 48 h after i.v. bolus administration, ID-6105 concentrations in various tissues had decreased to very low levels. The majority of ID-6105 appears to be excreted in the bile.-
dc.languageEnglish-
dc.publisherPHARMACEUTICAL SOC KOREA-
dc.titlePharmacokinetics of 11-hydroxyaclacinomycin X (ID-6105), a novel anthracycline, after iv bolus multiple administration in rats-
dc.typeArticle-
dc.identifier.doi10.1007/BF02977679-
dc.description.journalClass1-
dc.identifier.bibliographicCitationARCHIVES OF PHARMACAL RESEARCH, v.28, no.4, pp.476 - 482-
dc.citation.titleARCHIVES OF PHARMACAL RESEARCH-
dc.citation.volume28-
dc.citation.number4-
dc.citation.startPage476-
dc.citation.endPage482-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.identifier.kciidART001086635-
dc.identifier.wosid000228809700016-
dc.identifier.scopusid2-s2.0-22844433404-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusSTREPTOMYCES-GALILAEUS ATCC-31133-
dc.subject.keywordPlusAKLAVINONE 11-HYDROXYLASE GENE-
dc.subject.keywordPlusBLOCKED MUTANT-
dc.subject.keywordPlusACLACINOMYCIN-
dc.subject.keywordPlusANTIBIOTICS-
dc.subject.keywordPlusMETABOLITES-
dc.subject.keywordPlusCAESIUS-
dc.subject.keywordAuthor11-hydroxyaclacinomycin X (ID-6105)-
dc.subject.keywordAuthorpharmacokinetics-
dc.subject.keywordAuthormultiple administration-
dc.subject.keywordAuthortissue distribution-
dc.subject.keywordAuthorexcretion-
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