Abstract
AbstractThis work describes a local induced near‐surface pH effect (pHS) arising from the presence of one analyte, leading to an influence or even suppression of redox signals of a second analyte present in solution. This concept and its impact on voltammetric sensing is illustrated by focusing on the detection of cocaine in the presence of the common adulterant benzocaine. An in‐depth study on the observed interference mechanism and its specificity for benzocaine and not for other adulterants was performed through the use of multiple electrochemical strategies. It was concluded that the potential shift and loss of intensity of the square‐wave voltammetric cocaine signal in the presence of benzocaine was caused by a local pHS effect. A cathodic pretreatment strategy was developed to nonetheless allow accurate cocaine detection. These insights are useful for explaining unidentified phenomena involving compounds with properties similar to benzocaine in voltammetric electroanalysis.
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