Preparative separation of multicomponent mixtures by simulated moving bed liquid chromatography
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abstract
Direct racemic resolution of enantiomers by means of liquid chromatography using chiral
stationary phases is nowadays a very popular technique. This popularity is mainly due to
development of new chiral stationary phases and also by exploring and developing new and
more efficient modes of operation. The use of chiral liquid chromatography through the
simulated moving bed (SMB} technology has gained a renewed interest as an alternative
technique for the production of fme chemicals and pharmaceuticals.
The classic SMB process is a continuous process to separate binary (or pseudo-binary)
mixtures or to recover one single component from a multicomponent mixture. Several
modified SMB processes have been introduced to separate multicomponent mixtures. Among
then, the cascade SMB, the intermittent SMB, the JO processes and other complex multi-zone
SMB related techniques, are often applied to the separation of multicomponent mixtures. The
JO technology allows the separation of ternary mixtures through a cyclic process constituted
by two discrete steps [1 ].
Nadolol is a pharmaceutical drug marketed as a mixture of four stereoisomers, used to treat
cardiovascular diseases. However, its prescription is also related with some severe risks such
as heart failure. It is well known that pure enantiomer separation is important to control chiral
drugs safety. Recently, our research group reported the pseudo-binary separation of nadolol
by SMB chromatography [2]. Using the classic SMB mode of operation, the complete
separation of nadolol stereoisomers was achieved using Chiralpa.k AD chiral stationary phase
(CSP). The more retained stereoisomer was collected 100% pure in the extract and a mixture
of the other three stereoisomers was collected in the raffmate. In this work, we will present
different strategies for multicomponent separation, using different solvent compositions, other
CSP and SMB related techniques. Namely, (a) The use of Chiralpak lA, that comparing to
AD CSP, allows the use of a wider range of solvents and therefore better separation
performances; (b) The use of the JO process to achieve a final ternary separation, using the
mixture of the three stereoisomers that eo-eluted in the raffinate in the separation previously
referred and (c) The separation ofthe two pairs ofnadolol enantiomers using an achiral C18
material, followed by two parallel classic SMB binary enantioseparation processes.
Financial support by the Portuguese R&D foundation FCf (Fundação para a Ciência e a Tecnologia) and
European Community through FEDER (project PTDC/EQU-EQU/119025/2010) is gratefully acknowledged.
This work was co-financed by FCTIMEC and FEDER under Program PT2020 (Project UID/EQU/50020/2013)
and by QREN, ON2 and FEDER (Project NORTE-07-0162-FEDER-000050).