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Merck

Application of dual cyclodextrin systems in capillary electrophoresis enantioseparations.

Methods in molecular biology (Clifton, N.J.) (2013-01-04)
Anne-Catherine Servais, Marianne Fillet
ABSTRAKT

The enantioseparation of acidic and neutral compounds can be successfully achieved in capillary electrophoresis (CE) using dual cyclodextrin (CD) systems. This chapter describes how to separate the enantiomers of acidic or neutral substances using dual CD systems made up of a negatively charged CD derivative, i.e., sulfobutyl-β-CD (SB-β-CD) or carboxymethyl-β-CD (CM-β-CD), in combination with a neutral one, namely, heptakis(2,3,6-tri-O-methyl)-β-CD (TM-β-CD). An acidic compound (carprofen) and a weakly acidic drug (pentobarbital) were selected as model compounds.

MATERIAŁY
Numer produktu
Marka
Opis produktu

Supelco
Pentobarbital solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
Sigma-Aldrich
β-Cyclodextrin, powder, BioReagent, suitable for cell culture, ≥97%
Sigma-Aldrich
β-Cyclodextrin, Wacker Chemie AG, ≥98.0% (HPLC)
Sigma-Aldrich
β-Cyclodextrin, Wacker Chemie AG, ≥95.0% (HPLC)
Sigma-Aldrich
β-Cyclodextrin, ≥97%
Sigma-Aldrich
β-Cyclodextrin, Wacker Chemie AG
Sigma-Aldrich
Heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin, ≥98.0%
Sigma-Aldrich
Heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin, ≥90%
Supelco
Carprofen, VETRANAL®, analytical standard