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Proceedings ArticleDOI

Electrochemical impedance sensor for Levobupivacaine using conducting polypyrrole doped with SWCNTs as sensing material

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TLDR
An electrochemical impedance method to detect concentrations of the local anesthetics Levobupivacaine was implemented and the concentration could be detected to 1 ppm as mentioned in this paper, which is the highest concentration known to date.
Abstract
An electrochemical impedance method to detect concentrations of the local anesthetics Levobupivacaine was implemented and the concentration could be detected to 1 ppm. Electropolymerized pyrrole to polypyrrole (Ppy) and Carbon nanotube (CNT) was fabricated on gold electrodes and used as sensors. Various concentrations of Levobupivacaine from 1 to 500 ppm were prepared in DI water as the test samples.

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References
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Journal ArticleDOI

Use of conducting polypyrrole blends as gas sensors

TL;DR: In this paper, the use of polymeric blends formed by the controlled growth of doped polypyrrole chains in the interior of films of different dielectric polymers as sensors of the presence of representative examples of volatile organic compounds was discussed.
Journal ArticleDOI

Simultaneous determination of bupivacaine, mepivacain, prilocaine and ropivacain in human serum by liquid chromatography-tandem mass spectrometry.

TL;DR: A liquid chromatography-tandem mass spectrometric method with a rapid and simple sample preparation was developed and validated for the simultaneous determination of the local anesthetics bupivacaine, mepivicaine, prilocaine and ropavacaine in human serum.
Journal ArticleDOI

Stability of sufentanil and levobupivacaine solutions and a mixture in a 0.9% sodium chloride infusion stored in polypropylene syringes.

TL;DR: According to the chemical and microbiological stability studies, the sufentanil-levobupivacaine mixture in PP syringes could be stored for 28 days at 4 and 21 degrees C.
Journal ArticleDOI

Studies directed towards asymmetric synthesis of levobupivacaine

TL;DR: In this article, the first catalytic asymmetric synthesis of levobupivacaine was reported, where the key step involves the asymmetric alkylation of N-benzylimine glycinamide (2b).
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