Selective Focusing of Catecholamines and Weakly Acidic Compounds by Capillary Electrophoresis Using a Dynamic pH Junction

Селективное фокусирование катехоламинов и слабо кислотных соединений в капиллярном электрофорезе с использованием динамического pH-перехода
Philip Britz‐McKibbin, David D. Y. Chen
2000-02-19

capillary electrophoresiscatecholaminesdynamic pH junctionepinephrine limit of detectionvelocity-difference induced focusing
A systematic study of selective analyte focusing in a multisection electrolyte system by capillary electrophoresis (CE) is presented. It was found that a dynamic pH junction between sample and background electrolyte zones can be used to focus zwitterionic catecholamines and weakly acidic compounds without the use of special ampholytes. Differences in pH and concentration of complexing agents, such as borate, in the sample and background electrolyte zones were determined to cause focusing through changes in the local velocity of the analyte in two different segments of the capillary. Velocity-difference induced focusing (V-DIF) of analytes using a dynamic pH junction allowed the injection of large sample volumes and significantly improved the concentration sensitivity of CE. Under optimized conditions, the limit of detection for epinephrine was determined to be about 4 x 10(-8) M (the original sample) with conventional UV absorbance detection. Moreover, separation efficiencies greater than a million theoretical plates can be achieved by focusing such large sample volumes into narrow zones. Multisection electrolyte systems, which lead to the formation of a dynamic pH junction, can be tuned toward improving the concentration sensitivity of specific analytes if their chemical properties are known.
1
A dynamic pH junction between sample and background electrolyte zones can focus zwitterionic catecholamines and weakly acidic compounds without special ampholytes.
2
Differences in pH and concentration of complexing agents (e.g., borate) cause focusing by changing local analyte velocity in two capillary segments.
3
Focusing large sample volumes via this method yields separation efficiencies exceeding one million theoretical plates.
4
Multisection electrolyte systems forming a dynamic pH junction can be tuned to enhance concentration sensitivity for specific analytes based on their chemical properties.
5
Under optimized conditions, the limit of detection for epinephrine was about 4 × 10⁻⁸ M using conventional UV absorbance detection.
6
Velocity-difference induced focusing (V-DIF) with a dynamic pH junction permits large sample volume injection and significantly improves CE concentration sensitivity.

Zwitterionic catecholamines and weakly acidic analytes in a capillary electrophoresis multisection electrolyte system using a dynamic pH junction

Selective focusing (velocity-difference induced focusing) and concentration-sensitivity enhancement of these analytes via a dynamic pH junction caused by pH and complexing-agent differences between sample and background electrolyte zones

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2000-02-19
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Philip Britz‐McKibbin
David D. Y. Chen
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