Assessment of ion transfer amperometry at liquid–liquid interfaces for detection in CE

In this research, ion transfer across the interface between two immiscible electrolytesolutions (ITIES) was used as a method of detection in a CE separation system. Thismethod allows for the electrochemical detection of ionic analytes that cannot be easilyoxidized or reduced. Method development reve...

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Bibliographic Details
Main Authors: Sisk, G., Herzog, G., Glennon, J., Arrigan, Damien
Format: Journal Article
Published: Wiley-VCH Verlag 2009
Subjects:
Online Access:http://hdl.handle.net/20.500.11937/17665
Description
Summary:In this research, ion transfer across the interface between two immiscible electrolytesolutions (ITIES) was used as a method of detection in a CE separation system. Thismethod allows for the electrochemical detection of ionic analytes that cannot be easilyoxidized or reduced. Method development revealed that the optimal separation conditionsfor three model ions (tetraethylammonium, tetrabutylammonium, and benzensulfonate)were found to be 5mM sodium tetraborate buffer pH 9.2 with a separationvoltage of 20 kV using a 40 cm, 50 mm id fused silica capillary. Constant potentialamperometry and pulsed amperometric detection were applied at the ITIES in which theorganic phase was gelled. A miniaturized ITIES within a pipette tip was investigated,which resulted in improved separation efficiency and LOD. To demonstrate the ability ofthe system to detect substances of bioanalytical interest, the b-adrenergic receptorblockers timolol and propranolol were detected. The simplicity of the detection platformmeans that it may be useful for analytical situations not requiring trace or ultratracedetection capabilities.