2001
DOI: 10.1016/s0021-9673(01)01279-1
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Tris(2,2′-bipyridyl)ruthenium(III)-based electrochemiluminescence detector with indium/tin oxide working electrode for capillary electrophoresis

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Cited by 78 publications
(59 citation statements)
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“…When the buffer concentration was changed from 10 to tion limits under the optimized conditions are listed in Table 1. The limit of detection for proline was about 2 µmol/L, this value being about two-fold higher than that reported by Chiang and Whang (16), and about 10-fold higher than that reported in Wang and Bobbit's work (15). Since the optimization was made according to the conditions in the biological matrix, the detection limit was still acceptable.…”
Section: Factors Influencing Ce Separationmentioning
confidence: 57%
“…When the buffer concentration was changed from 10 to tion limits under the optimized conditions are listed in Table 1. The limit of detection for proline was about 2 µmol/L, this value being about two-fold higher than that reported by Chiang and Whang (16), and about 10-fold higher than that reported in Wang and Bobbit's work (15). Since the optimization was made according to the conditions in the biological matrix, the detection limit was still acceptable.…”
Section: Factors Influencing Ce Separationmentioning
confidence: 57%
“…It has been found that, in general, electrochemical reaction of many organic molecules such as dopamine [15], ascorbic acid [16], tripropal amine [17] and oxalic acid [18] on ITO is significantly slower than metal and carbon electrodes. This has been attributed to the lack of catalytic sites on ITO, although the exact mechanism is still not clear.…”
Section: Resultsmentioning
confidence: 99%
“…Electrochemical reaction of many organic molecules such as dopamine [15], ascorbic acid [16], tripropal amine [17] and oxalic acid [18] on ITO is significantly slower than metal and carbon electrodes, likely due to the lack of catalytic sites on ITO. Specifically, ascorbic acid exhibits an apparent electrooxidation response at 0.5 V on metal electrodes [19,20] and at 0.6 V on glassy carbon electrode [21], whereas the oxidation reaction is inhibited and thereby results in a large overpotential on ITO [16].…”
Section: Introductionmentioning
confidence: 99%
“…According to the reports on the CL detection in capillary electrophoresis [14,15,21,26,27], there were two key points that decided whether the experiment could be done successfully. One was the reaction dynamics of the CL systems.…”
Section: Analytical Performancementioning
confidence: 99%