Determination of sequestering agents in cosmetics and synthetic detergents by high-performance liquid chromatography with ultraviolet detection

被引:18
作者
Kemmei, Tomoko
Kodama, Shuji
Yamamoto, Atsushi
Inoue, Yoshinori
Hayakawa, Kazuichi
机构
[1] Toyama Inst Hlth, Toyama 9390363, Japan
[2] Chubu Univ, Coll Biosci & Biotechnol, Dept Biol Chem, Kasugai, Aichi 4878501, Japan
[3] Osaka City Univ, Sch Med, Dept Prevent Med & Environm Hlth, Abeno Ku, Osaka 5458585, Japan
[4] Kanazawa Univ, Grad Sch Nat Sci & Technol, Kanazawa, Ishikawa 9201192, Japan
基金
日本学术振兴会;
关键词
high-performance liquid chromatography; cosmetics; synthetic detergents; sequestering agents;
D O I
10.1016/j.chroma.2007.09.037
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Using a fast reversible reaction of aminopolycarboxylic acids (APCAs) into Fe(III)-APCA complexes in the presence of Fe(III) ions, seven kinds of APCAs [nitrilotriacetate (NTA), N-(2-hydroxyethyl)ethylenediamine-triacetate (HEDTA), ethylenediamine-tetraacetate (EDTA), 1,3-propanediamine-tetraacetate (PDTA), diethylenetriamine-pentaacetate (DTPA), 1,2-diaminopropane-tetraacetate (MeEDTA), and O,O'-bis(2aminoethyl)ethyleneglycol-tetraacetate (GEDTA)] in cosmetics and synthetic detergents were separated on two reversed-phase C30 columns connected in series and detected with ultraviolet detection. Simple pretreatment, consisted of thousand times dilution of samples and addition of 100 mu l of the Fe(III) solution containing 10 mM Fe(III) chloride and 0.5 M sulfuric acid to 10 ml of diluted samples, permitted the determination of APCAs in cosmetics and synthetic detergents at concentration level of 0.1 mM, except 0.3 mM for GEDTA. APCAs except GEDTA could be detected at concentration level of 0.03 mM and GEDTA could be detected at concentration level of 0.09 mM. Good recoveries (95-110%) were obtained for each APCA by the standard addition method on two diluted samples with high accuracy (RSD 0.2-9.1 %). Three APCAs (EDTA, HEDTA and NTA) were detected in various concentrations in cosmetics and synthetic detergents and the other APCAs were not detected in any of the samples. This method requires no tedious pretreatment and takes only 15 min for one analysis, so it is useful for determination of APCAs. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 68
页数:6
相关论文
共 22 条
[1]   BEHAVIOR OF NTA AND EDTA IN BIOLOGICAL WASTE-WATER TREATMENT [J].
ALDER, AC ;
SIEGRIST, H ;
GUJER, W ;
GIGER, W .
WATER RESEARCH, 1990, 24 (06) :733-742
[2]   Determination of strong binding chelators and their metal complexes by anion-exchange chromatography and inductively coupled plasma mass spectrometry [J].
Ammann, AA .
JOURNAL OF CHROMATOGRAPHY A, 2002, 947 (02) :205-216
[3]   Analysis of polar organic micropollutants in water with ion chromatography electrospray mass spectrometry [J].
Bauer, KH ;
Knepper, TP ;
Maes, A ;
Schatz, V ;
Voihsel, M .
JOURNAL OF CHROMATOGRAPHY A, 1999, 837 (1-2) :117-128
[4]   Determination of metal complexes of ethylenediaminetetraacetate in the presence of organic matter by high-performance liquid chromatography [J].
Bedsworth, WW ;
Sedlak, DL .
JOURNAL OF CHROMATOGRAPHY A, 2001, 905 (1-2) :157-162
[5]   THE ANALYSIS OF EDTA IN WATER BY HPLC [J].
BERGERS, PJM ;
DEGROOT, AC .
WATER RESEARCH, 1994, 28 (03) :639-642
[6]   BIODEGRADATION OF SYNTHETIC CHELATES IN SUBSURFACE SEDIMENTS FROM THE SOUTHEAST COASTAL-PLAIN [J].
BOLTON, H ;
LI, SW ;
WORKMAN, DJ ;
GIRVIN, DC .
JOURNAL OF ENVIRONMENTAL QUALITY, 1993, 22 (01) :125-132
[7]   EFFECT OF THE SOLIDS RETENTION TIME ON THE RATE OF BIODEGRADATION OF ORGANIC-COMPOUNDS [J].
CECH, JS ;
CHUDOBA, J .
ACTA HYDROCHIMICA ET HYDROBIOLOGICA, 1988, 16 (03) :313-323
[8]   Determination of ethylenediaminetetraacetic acid at very low concentrations by high-performance liquid chromatography coupled with electrospray mass spectrometry [J].
Dodi, A ;
Monnier, V .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1032 (1-2) :87-92
[9]  
Dodi A, 2006, LC GC EUR, V19, P542
[10]   COMPLEXATION OF TRACE-METALS BY ETHYLENEDIAMINETETRAACETIC ACID (EDTA) IN NATURAL-WATERS [J].
GARDINER, J .
WATER RESEARCH, 1976, 10 (06) :507-514