Potentiometric sensor for hydroxyzine determination
A Bouklouze, M Elbouzekraoui… - … Journal Devoted to …, 2002 - Wiley Online Library
A Bouklouze, M Elbouzekraoui, Y Cherrah, M Hassar, JM Kauffmann
Electroanalysis: An International Journal Devoted to Fundamental …, 2002•Wiley Online LibraryA new polymeric membrane electrode has been developed for the determination of
hydroxyzine. The electrode was constructed by solubilizing the hydroxyzine silicotungstate
ion pair into a polyvinylchloride matrix plasticized by nitrophenyloctylether. The electrode
exhibited a near‐Nernstian response (57 mV/decade) in the concentration range comprised
between 1× 10− 2 M and 6× 10− 7 M with a lower limit of detection of 2.5× 10− 7 M. The
electrode response was not sensitive to pH changes between 2.8 and 6.9 and not affected …
hydroxyzine. The electrode was constructed by solubilizing the hydroxyzine silicotungstate
ion pair into a polyvinylchloride matrix plasticized by nitrophenyloctylether. The electrode
exhibited a near‐Nernstian response (57 mV/decade) in the concentration range comprised
between 1× 10− 2 M and 6× 10− 7 M with a lower limit of detection of 2.5× 10− 7 M. The
electrode response was not sensitive to pH changes between 2.8 and 6.9 and not affected …
Abstract
A new polymeric membrane electrode has been developed for the determination of hydroxyzine. The electrode was constructed by solubilizing the hydroxyzine silicotungstate ion pair into a polyvinylchloride matrix plasticized by nitrophenyloctylether. The electrode exhibited a near‐Nernstian response (57 mV/decade) in the concentration range comprised between 1×10−2 M and 6×10−7 M with a lower limit of detection of 2.5×10−7 M. The electrode response was not sensitive to pH changes between 2.8 and 6.9 and not affected by possible interfering species such as cetirizine and pharmaceutical excipients. The electrode was successfully applied to the determination of hydroxyzine in pharmaceuticals and in a dissolution profile study of tablets. The results were validated by comparison with LC and spectrophotometric assays according to the USP Pharmacopoeia methods.
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