Please use this identifier to cite or link to this item: https://doi.org/10.1007/s11095-005-4585-0
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dc.titleSt. John's wort modulates the toxicities and pharmacokinetics of CPT-11 (Irinotecan) in rats
dc.contributor.authorHu, Z.
dc.contributor.authorYang, X.
dc.contributor.authorHo, P.C.-L.
dc.contributor.authorChan, E.
dc.contributor.authorSui, Y.C.
dc.contributor.authorXu, C.
dc.contributor.authorLi, X.
dc.contributor.authorZhu, Y.-Z.
dc.contributor.authorDuan, W.
dc.contributor.authorChen, X.
dc.contributor.authorHuang, M.
dc.contributor.authorYang, H.
dc.contributor.authorZhou, S.
dc.date.accessioned2014-10-29T01:58:46Z
dc.date.available2014-10-29T01:58:46Z
dc.date.issued2005-06
dc.identifier.citationHu, Z., Yang, X., Ho, P.C.-L., Chan, E., Sui, Y.C., Xu, C., Li, X., Zhu, Y.-Z., Duan, W., Chen, X., Huang, M., Yang, H., Zhou, S. (2005-06). St. John's wort modulates the toxicities and pharmacokinetics of CPT-11 (Irinotecan) in rats. Pharmaceutical Research 22 (6) : 902-914. ScholarBank@NUS Repository. https://doi.org/10.1007/s11095-005-4585-0
dc.identifier.issn07248741
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/106355
dc.description.abstractPurpose. CPT-11 is a DNA topoisomerase I inhibitor for the therapy of colorectal cancer, whereas St. John's Wort (Hypericum perforatum, SJW) is a widely used herbal anti-depressant. This study aimed to investigate the effects of co-administered SJW on the toxicities and pharmacokinetics of CPT-11 and the underlying mechanisms. Methods. The body weight loss, gastrointestinal and hematological toxicities induced by CPT-11, and the pharmacokinetic parameters of CPT-11 were evaluated in rats pretreated with SJW or vehicle. Results. Rats treated with CPT-11 alone experienced rapid decrease in body weight, whereas co-administration of SJW with CPT-11 resulted in lesser body weight loss. The gastrointestinal and hematological toxicities following CPT-11 injection were both alleviated in the presence of SJW. The rat pharmacokinetics of both CPT-11 and its metabolite SN-38 were significantly altered in presence of SJW. Conclusions. In conclusion, co-administered SJW significantly ameliorated the toxicities induced by CPT-11. The protective effect of SJW may be partially due to pharmacokinetic interaction between CPT-11 and SJW. © 2005 Springer Science + Business Media, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s11095-005-4585-0
dc.sourceScopus
dc.subjectCPT-11
dc.subjectPharmacokinetics
dc.subjectSt. John's wort
dc.subjectToxicity
dc.typeArticle
dc.contributor.departmentPHARMACY
dc.description.doi10.1007/s11095-005-4585-0
dc.description.sourcetitlePharmaceutical Research
dc.description.volume22
dc.description.issue6
dc.description.page902-914
dc.description.codenPHREE
dc.identifier.isiut000229730800009
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