Pharmacokinetics of 11-hydroxyaclacinomycin X (ID-6105), a novel anthracycline, after i.v. bolus multiple administration in rats

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dc.contributor.authorB I Yoo-
dc.contributor.authorK B Ahan-
dc.contributor.authorM H Kang-
dc.contributor.authorO S Kwon-
dc.contributor.authorYoung-Soo Hong-
dc.contributor.authorJung Joon Lee-
dc.contributor.authorH S Lee-
dc.contributor.authorJ S Ryu-
dc.contributor.authorT Y Kim-
dc.contributor.authorD C Moon-
dc.contributor.authorS Song-
dc.contributor.authorY B Chung-
dc.date.accessioned2017-04-19T09:02:58Z-
dc.date.available2017-04-19T09:02:58Z-
dc.date.issued2005-
dc.identifier.issn0253-6269-
dc.identifier.uri10.1007/BF02977679ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/6997-
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 t1/2α, t 1/2β, Vdss, 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.publisherPharmaceutical Soc Korea-
dc.titlePharmacokinetics of 11-hydroxyaclacinomycin X (ID-6105), a novel anthracycline, after i.v. bolus multiple administration in rats-
dc.title.alternativePharmacokinetics of 11-hydroxyaclacinomycin X (ID-6105), a novel anthracycline, after i.v. bolus multiple administration in rats-
dc.typeArticle-
dc.citation.titleArchives of Pharmacal Research-
dc.citation.number4-
dc.citation.endPage482-
dc.citation.startPage476-
dc.citation.volume28-
dc.contributor.affiliatedAuthorYoung-Soo Hong-
dc.contributor.affiliatedAuthorJung Joon Lee-
dc.contributor.alternativeName유보임-
dc.contributor.alternativeName안광복-
dc.contributor.alternativeName강민희-
dc.contributor.alternativeName권오승-
dc.contributor.alternativeName홍영수-
dc.contributor.alternativeName이정준-
dc.contributor.alternativeName이홍섭-
dc.contributor.alternativeName류정수-
dc.contributor.alternativeName김태용-
dc.contributor.alternativeName문동철-
dc.contributor.alternativeName송석길-
dc.contributor.alternativeName정윤복-
dc.identifier.bibliographicCitationArchives of Pharmacal Research, vol. 28, no. 4, pp. 476-482-
dc.identifier.doi10.1007/BF02977679-
dc.subject.keyword11-Hydroxyaclacinomycin X (ID-6105)-
dc.subject.keywordExcretion-
dc.subject.keywordMultiple administration-
dc.subject.keywordPharmacokinetics-
dc.subject.keywordTissue distribution-
dc.subject.local11-Hydroxyaclacinomycin X (ID-6105)-
dc.subject.localExcretion-
dc.subject.localexcretion-
dc.subject.localMultiple administration-
dc.subject.localpharmacokinetics-
dc.subject.localPharmacokinetics-
dc.subject.localTissue distribution-
dc.subject.localtissue distribution-
dc.description.journalClassY-
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