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Optimal temperature control in fractional precipitation for paclitaxel pre-purification

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dc.contributor.authorJeon, Sun Im-
dc.contributor.authorMun, Sung yong-
dc.contributor.authorKim, Jin-Hyun-
dc.date.accessioned2022-12-21T12:02:46Z-
dc.date.available2022-12-21T12:02:46Z-
dc.date.created2022-08-26-
dc.date.issued2006-02-
dc.identifier.issn1359-5113-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/181781-
dc.description.abstractFractional precipitation is a simple, efficient method for pre-purifying paclitaxel from plant cell cultures. The storage temperature of fractional precipitation was optimized in terms of the yield and purity of paclitaxel with a fixed methanol concentration in water (61.5%, v/v), paclitaxel content in the crude extract (0.5%, w/v), and storage time (3 days). The greatest yield (similar to 84%) was obtained with storage at a constant temperature (0 degrees C) for 3 days. Conversely, the highest purity (similar to 79%) was obtained with stepwise reduction in temperature over 3 days. For a constant storage temperature, the maximum purity (similar to 67%) was obtained at 0 degrees C. There was little difference in the yield of paclitaxel between -20 and 12 degrees C. At a constant storage temperature (0 degrees C), both the precipitate yield and purity increased rapidly up to 18 h, and then increased more slowly. This pre-purification process serves to minimize solvent usage, and the size and complexity of the high-performance liquid chromatography (HPLC) operation required for paclitaxel purification.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.titleOptimal temperature control in fractional precipitation for paclitaxel pre-purification-
dc.typeArticle-
dc.contributor.affiliatedAuthorMun, Sung yong-
dc.identifier.doi10.1016/j.procbio.2005.07.016-
dc.identifier.scopusid2-s2.0-29244488578-
dc.identifier.wosid000234624200005-
dc.identifier.bibliographicCitationPROCESS BIOCHEMISTRY, v.41, no.2, pp.276 - 280-
dc.relation.isPartOfPROCESS BIOCHEMISTRY-
dc.citation.titlePROCESS BIOCHEMISTRY-
dc.citation.volume41-
dc.citation.number2-
dc.citation.startPage276-
dc.citation.endPage280-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.subject.keywordPlusCELL-CULTURES-
dc.subject.keywordPlusTAXUS-BREVIFOLIA-
dc.subject.keywordPlusTAXOL-
dc.subject.keywordPlusCHROMATOGRAPHY-
dc.subject.keywordPlusSEPARATION-
dc.subject.keywordPlusCHINENSIS-
dc.subject.keywordPlusNEEDLES-
dc.subject.keywordAuthorpaclitaxel-
dc.subject.keywordAuthorfractional precipitation-
dc.subject.keywordAuthortemperature-
dc.subject.keywordAuthorpre-purification-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1359511305003223?via%3Dihub-
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