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Development of a background electrolyte for the determination of inorganic cations in high ionic strength samples by capillary electrophoresis with indirect UV-absorption detection
被引:4
作者:
Lancioni, Carlina
[1
]
Aspromonte, Juan
[1
,2
]
Tascon, Marcos
[3
]
Gagliardi, Leonardo G.
[1
]
机构:
[1] Univ Nacl La Plata, Lab Invest & Desarrollo Metodos Analit, LIDMA, CONICET,CIC PBA,Fac Ciencias Exactas, Calle 47 Esq 115, RA-1900 La Plata, Argentina
[2] Univ Leuven, KU Leuven, Dept Pharmaceut & Pharmacol Sci, Pharmaceut Anal, Herestr 49 PB923, B-3000 Leuven, Belgium
[3] Univ Nacl San Martin, Inst Invest & Ingn Ambiental IIIA CONICET UNSAM, 25 Mayo & Francia,B1650, San Martin, Argentina
关键词:
Inorganic cations;
High ionic strength samples;
Capillary electrophoresis;
Indirect UV-absorption detection;
ZONE-ELECTROPHORESIS;
CONDUCTIVITY DETECTION;
AMINO-ACIDS;
CHROMATOGRAPHY;
SEPARATION;
SELECTIVITY;
MIXTURES;
ANIONS;
WATER;
D O I:
10.1016/j.chroma.2021.462091
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
In this study, a background electrolyte capable to separate and quantify inorganic cations in high ionic strength samples by UV-absorption indirect detection was designed. In this regard, the four most abundant monovalent and divalent cations in earth crust (K+, Na+, Ca+2, Mg+2) were selected as model compounds. A group of small carboxylic acids and, several toluidines and pyridines were evaluated as mild strength complexing agents and chromophoric probes, respectively. The optimized background electrolyte was composed of 200 mM 2,4,6-trimethylpyridine as the chromophoric probe, 250 mM lactic acid as the weak complexing agent and pH buffering reagent (adjusted to pH 4.5), and 5% v/v methanol as organic solvent modifier. Based on a minimum number of components, it provided outstanding separation performance in less than 4 min in a wide linear dynamic range (10 - 2500 mu g.mL(-1)). Performances were contrasted against a reference method based on conductometric detection. Furthermore, studies of separation efficiency and peak shape were carried out at different analyte concentrations in high electric conductivity solutions. The herein developed method demonstrated exceptional features in terms of limits of detection (similar to 10 mu g.mL(-1)), resolution, speed of analysis, sensitivity and peak capacity in high electric conductivity samples. Moreover, the method was successfully applied to high ionic strength samples such as rock digest, sea water, soy sauce and isotonic drinks. (C) 2021 Published by Elsevier B.V.
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