Separation of nadolol racemates by fixed-bed and continuous preparative liquid chromatography using C18 columns
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abstract
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. Its chemical structure has three stereogenic centers which allows for eight possible stereoisomers. However, the two hydroxyl substituents on the cyclohexane ring are fixed in the cis-configuration, which precludes four stereoisomers. Nadolol is presently marketed as an equal mixture of the four stereoisomers.
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 simulated moving bed (SMB) chromatography using both coated Chiralpak AD and Chiralpak IA immobilized chiral stationary phases (CSP).1,2 This technology is generally based on the use of chiral adsorbents which must have enough recognition for all the chiral species.
In this work it is proposed an alternative strategy, implementing a first achiral separation step, to be followed by two subsequent parallel chiral separation steps.3,4 In this first achiral step, C18 columns are used to perform the separation of the two pairs of nadolol enantiomers (“racemate A” from “racemate B”) under reversed-phase mode. The C18 achiral adsorbent allows the separation of the two pairs of nadolol diastereomers, i.e., the first racemate (composed by the nadolol compounds 2 and 3) co-eluting in the raffinate, and the second racemate (composed by the nadolol compounds 1 and 4) to be obtained in the extract SMB stream. After this preliminary achiral separation step, two parallel SMB runs must be carried out using a chiral stationary phase to achieve the complete separation of all the four nadolol stereoisomers.
Extensive experimental and simulation results will be presented including solvent screening, measurement of equilibrium and kinetic data, and both fixed-bed and SMB preparative separations.
This work was financially supported by Project POCI-01-0145-FEDER-006984 - Associate Laboratory LSRE-LCM - funded by FEDER funds through COMPETE2020 - Programa Operacional Competitividade e Internacionalização (POCI) – and by national funds through FCT - Fundação para a Ciência e a Tecnologia. This work was also co-financed by QREN, ON2 and FEDER through Project NORTE-07-0162-FEDER-000050.
