1978
DOI: 10.1016/s0003-2670(01)83284-0
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Voltammetric determination of morphine on stationary platinum and graphite electrodes

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Cited by 39 publications
(12 citation statements)
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“…The oxidation of codeine or ethylmorphine which have methoxy and ethoxy groups, respectively, instead of a phenolic group in the 3-position, was studied and the first peak was obtained only at potentials higher than 1.0 V (data not shown). The oxidation of the phenolic group leads to the formation of pseudomorphine as the main product, as already suggested [3,5] (Scheme 1). This product, obtained from oxidation of the phenolic group, is, according to the literature [5], responsible for the poorly defined peak occurring at 0.8 V for morphine, since the structure of pseudomorphine (Fig.…”
Section: Electrochemical Oxidationmentioning
confidence: 53%
“…The oxidation of codeine or ethylmorphine which have methoxy and ethoxy groups, respectively, instead of a phenolic group in the 3-position, was studied and the first peak was obtained only at potentials higher than 1.0 V (data not shown). The oxidation of the phenolic group leads to the formation of pseudomorphine as the main product, as already suggested [3,5] (Scheme 1). This product, obtained from oxidation of the phenolic group, is, according to the literature [5], responsible for the poorly defined peak occurring at 0.8 V for morphine, since the structure of pseudomorphine (Fig.…”
Section: Electrochemical Oxidationmentioning
confidence: 53%
“…Although the first studies involving the oxidation of morphine occurred in the early 1960s, [15] its boom only happened at the end of the 1970s. [16,17] The study of the oxidative electroactivity of morphine and analogs showed that the phenolic group present in the structure of these compounds was the electroactive centre. The oxidative mechanism proposed involved one electron oxidation of morphine followed by dimerization of the free radical to pseudomorphine.…”
Section: Morphinementioning
confidence: 99%
“…The oxidative mechanism proposed involved one electron oxidation of morphine followed by dimerization of the free radical to pseudomorphine. [16] While morphine is easily oxidized at relatively low potentials, most of the other opiates are not oxidizable except at high potentials. This is due to the fact that these opiates contain a phenol ether or ester instead of a hydroxyl group at the 3-position of morphine (Fig.…”
Section: Morphinementioning
confidence: 99%
“…Confirming this, it was observed that MIP binding sites reached a near saturation state at for higher CMQ concentrations. [34]. Values of K D for MIP/4-VP and NIP/4-VP sensors were, respectively, 0.939 and 0.483 mM.…”
Section: Binding Properties Of Mip and Nip Were Investigated By Meansmentioning
confidence: 88%