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Development of a micelle-fractional precipitation hybrid process for the pre-purification of paclitaxel from plant cell cultures

Authors
Han, Min-GyeongJeon, Keum-YoungMun, SungyongKim, Jin-Hyun
Issue Date
Aug-2010
Publisher
ELSEVIER SCI LTD
Keywords
Paclitaxel; Micelle-fractional precipitation hybrid process; Pre-purification; Surface area per working volume (S/V); Ion exchange resin
Citation
PROCESS BIOCHEMISTRY, v.45, no.8, pp.1368 - 1374
Indexed
SCIE
SCOPUS
Journal Title
PROCESS BIOCHEMISTRY
Volume
45
Number
8
Start Page
1368
End Page
1374
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/174342
DOI
10.1016/j.procbio.2010.05.010
ISSN
1359-5113
Abstract
A micelle-fractional precipitation hybrid process was developed for the effective pre-purification of the anticancer agent paclitaxel extracted from plant cell cultures. First, it was found that the efficiency of such a developed process could be remarkably enhanced by removing waxy substances originating from plant cells using the adsorbent sylopute. Paclitaxel yield was improved and the fractional precipitation time was shortened by increasing the surface area per working volume (Sly) of the reacting solution through the addition of a cation exchange resin (Amberlite IR120 or Amberlite 200), an anion exchange resin (Amberlite IRA400 or Amberlite IRA96), or glass beads. Most of the paclitaxel (>98%) could be obtained after about 12 h of fractional precipitation using Amberlite 200. Purity increased with increasing fractional precipitation time up to 9h to about 85%, after which it showed little change. On the other hand, no paclitaxel precipitate was formed using either of the nonionic exchange resins because paclitaxel, which is hydrophobic, was strongly adsorbed on the hydrophobic resin surface. Since high-purity paclitaxel can be obtained in high yield and the precipitation time can be reduced by combining micelle formation with fractional precipitation, this hybrid method is expected to significantly enhance the final purification process.
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