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논문 기본 정보
- 자료유형
- 학술대회자료
- 저자정보
- 저널정보
- 대한약학회 대한약학회 학술대회 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
- 발행연도
- 2003.1
- 수록면
- 2,251 - 2,251 (1page)
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Purpose. Paclitaxel has demonstrated significant activity in clinical trials against a wide variety of tumors. The clinical application of Taxol$\^$\ulcorner/, a commercial product of solubilized paclitaxel with co solvents of ethanol and Cremophor, however, has been limited largely by hypersensitivity of the excipient. The aim of this study was to formulate paclitaxel-loaded lipid nanodispersions (Px-LN) for i.v. administration without toxic excipients, and to evaluate in vitro characteristics and in vivo pharmacokinetic behaviors. (omitted)
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Pharmacokinetics of the Paclitaxel of New Micelle Formulation
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Pharmacokinetics of New Solubilizer in Intravenous Micelle Formulation of Paclitaxel in Mice
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Mass Production of Paclitaxel by Plant Cell Culture
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프라본과 파크리탁셀과의 약물상호작용
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Lipid nanodispersion for parenteral drug delivery: in vitro characterization
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Enhanced Bioavailability of Paclitaxel by Bamboo Concentrate Administration
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pharmacokinetics of paclitaxel in rabbits with carbon tetrachloride-induced hepatic failure
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