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The 3<sup>rd</sup> International Conference on Drug Discovery & Therapy: Dubai, February 7 - 11, 2011

Pharmaceutical Research & Development (Track)

Enantioselective Extraction Of Racemic Amlodipine Using Tartaric Acid Derivatives And B-Cyclodextrin Derivatives As Chiral Selectors

Hairul Nazirahmiddle Abdul Halim
School Of Bioprocess Engineering Universiti Malaysia Perlis (Unimap) 02600 Arau Perlis Malaysia

Abstract:

The distribution behavior of amlodipine enantiomers was examined in a two-phase system containing tartaric acid derivatives in organic phase and beta-cyclodextrin derivatives in aqueous phase. The effect of extraction equilibrium time, influence of different alkyl chain of tartaric acids, types of beta-cyclodextrin derivatives and organic solvent were investigated, respectively. It was found that the chiral extraction reaches equilibrium after 6 hours. Solvents showed a large influence on enantioselectivity and partition coefficients.

Keywords: Chiral Drug, Racemic Amldipine, Enantioselective Extraction