TY - JOUR
T1 - Simultaneous determination of phenylenediamine isomers and dihydroxybenzene isomers in hair dyes by capillary zone electrophoresis coupled with amperometric detection
AU - Dong, Shuqing
AU - Chi, Langzhu
AU - Zhang, Shan
AU - He, Pingang
AU - Wang, Qingjiang
AU - Fang, Yuzhi
PY - 2008/5
Y1 - 2008/5
N2 - 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.]
AB - 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.]
KW - Amperometric detection
KW - Capillary zone electrophoresis
KW - Hair dyes
KW - Isomers
KW - Platinum working electrode
UR - https://www.scopus.com/pages/publications/43049090792
U2 - 10.1007/s00216-008-2053-5
DO - 10.1007/s00216-008-2053-5
M3 - 文章
AN - SCOPUS:43049090792
SN - 1618-2642
VL - 391
SP - 653
EP - 659
JO - Analytical and Bioanalytical Chemistry
JF - Analytical and Bioanalytical Chemistry
IS - 2
ER -