2016
DOI: 10.1002/elps.201500328
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Development and validation of a micellar electrokinetic capillary chromatography method for the determination of goserelin and related substances

Abstract: An MEKC method for the analysis of goserelin and related substances has been developed using a combination of additives including CTAB, β-CD, and sodium hexanesulfonate. For this assay, the running buffer (pH and additives) and separation conditions (voltage and temperature) were optimized. The optimized system was the following: 200 mM 6-aminocaproic acid buffer (pH 4.2) supplemented with 175 mM CTAB, 3.0% w/v β-CD, and 20 mM sodium hexanesulfonate; the voltage was 10 kV in reverse polarity mode, the temperat… Show more

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Cited by 7 publications
(3 citation statements)
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“…Combination of three additives, cationic detergent CTAB, anionic sodium hexanesulfonate, and stereoselector β‐CD, have been employed for MEKC analysis of goserelin and its related substances . The optimized system was composed of 200 mM 6‐aminocaproic acid buffer, pH 4.2, 175 mM CTAB, 20 mM sodium hexanesulfonate, and 3% m/v β‐CD, and was able to separate GSH and its eight analogs within ca 30 min in 50 μm id capillary, 48.5/40 cm total/effective length, at –10 kV separation voltage, 20°C and 220 nm detection wavelength.…”
Section: Separations By the Particular Ce And Cec Methodsmentioning
confidence: 99%
“…Combination of three additives, cationic detergent CTAB, anionic sodium hexanesulfonate, and stereoselector β‐CD, have been employed for MEKC analysis of goserelin and its related substances . The optimized system was composed of 200 mM 6‐aminocaproic acid buffer, pH 4.2, 175 mM CTAB, 20 mM sodium hexanesulfonate, and 3% m/v β‐CD, and was able to separate GSH and its eight analogs within ca 30 min in 50 μm id capillary, 48.5/40 cm total/effective length, at –10 kV separation voltage, 20°C and 220 nm detection wavelength.…”
Section: Separations By the Particular Ce And Cec Methodsmentioning
confidence: 99%
“…An alternative approach for detecting protein prenylation inside mammalian systems that is not reliant on membrane localization as proxy endpoint, is called Protein Lipidation Quantification (PLQ). This method is derived from an established method of Micellar Electro-Kinetic Chromatography (MEKC) that allows selective partition of prenylated proteins into detergent micelles (using SDS) during capillary electrophoresis ( 169 , 170 ). Detergent micelles serve as pseudo-stationary phase and exhibit differential electrophoretic migration compared to unprenylated free analyte.…”
Section: Techniques To Investigate Prenylated Proteomementioning
confidence: 99%
“…Electrokinetic chromatography (EKC) has been widely applied in separation science . With micelles as pseudostationary phase (PSP), the EKC separation is based on electrophoresis combined with chromatography, which makes it possible to separate neutral and charged analytes simultaneously.…”
Section: Introductionmentioning
confidence: 99%