Simultaneous determination of phenylenediamine isomers and dihydroxybenzene isomers in hair dyes by capillary zone electrophoresis coupled with amperometric detection

  • Shuqing Dong
  • , Langzhu Chi
  • , Shan Zhang
  • , Pingang He
  • , Qingjiang Wang*
  • , Yuzhi Fang
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

70 Scopus citations

Abstract

The simultaneous determination of three isomers of phenylenediamines (o, m, and p-phenylenediamine) and two isomers of dihydroxybenzenes (catechol and resorcinol) in hair dyes was performed by capillary zone electrophoresis coupled with amperometric detection (CZE-AD). The effects of working electrode potential, pH and concentration of running buffer, separation voltage, and injection time on CZE-AD were investigated. Under the optimum conditions the five analytes could be perfectly separated in 0.30 mol L-1 borate-0.40 mol L-1 phosphate buffer (pH 5.8) within 15 min. A 300 μm diameter platinum electrode had good responses at +0.85 V (versus SCE) for the five analytes. Their linear ranges were from 1.0∈×∈10 -6 to 1.0∈×∈10-4 mol L-1 and the detection limits were as low as 10-7 mol L-1 (S/N∈=∈3). This working electrode was successfully used to analyze eight kinds of hair dye sample with recoveries in the range 91.0-108.0% and RSDs less than 5.0%. These results demonstrated that capillary zone electrophoresis coupled with electrochemical detection using a platinum working electrode as detector was convenient, highly sensitive, highly repeatable and could be used in the rapid determination of practical samples. [Figure not available: see fulltext.]

Original languageEnglish
Pages (from-to)653-659
Number of pages7
JournalAnalytical and Bioanalytical Chemistry
Volume391
Issue number2
DOIs
StatePublished - May 2008

Keywords

  • Amperometric detection
  • Capillary zone electrophoresis
  • Hair dyes
  • Isomers
  • Platinum working electrode

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