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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received August 11, 2003
Accepted January 26, 2004
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Chromatographic Separation of Bupivacaine Racemate by Mathematical Model with Competitive Langmuir Isotherm

Center for Advanced Bioseparation Technology, Dept. of Chem. Eng., Inha University, 253 Yonghyun-Dong, Nam-Ku, Incheon 402-751, Korea
rowkho@inha.ac.kr
Korean Journal of Chemical Engineering, July 2004, 21(4), 829-835(7), 10.1007/BF02705528
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Abstract

HPLC (High Performance Liquid Chromatography) was utilized for the chiral separation of racemic bupivacaine, and mathematical modeling with competitive Langmuir isotherm was performed to determine the optimum feed condition. For each racemic compound, the isotherm parameters a, b and mass transfer coefficients k were obtained by parameter estimation and maximum likelihood method. The agreement of elution profiles between the experimental data and the calculated values was fairly good. In order to find the optimum separation condition, simulations were carried out to determine the feed conditions such as concentration and injection volume. To preparatively separate racemic bupivacaine, the desirable injection volumes were 0.05 ml at 2.0 mg/ml of the concentration of racemic mixture or 0.01 ml at 20 mg/ml.

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