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Updated: Sep 20, 2025

Microfluidic-based Electrotaxis for On-demand Quantitative Analysis of Caenorhabditis elegans' Locomotion
Published on: May 2, 2013
Determination of ions in Caenorhabditis elegans by ion chromatography
Alexandre Varão Moura1, Alex Aparecido Rosini Silva2, José Domingos Santo da Silva3
1MS(4) Life Laboratory of Mass Spectrometry, Health Sciences Postgraduate Program, São Francisco University, Bragança Paulista, São Paulo, CEP 12916-900, Brazil; Graduate Program in Pure and Applied Chemistry (POSQUIPA) Federal University of Western Bahia, Rua Bertioga, 892, Morada Nobre II, Barreiras, Bahia, CEP 47810-059, Brazil.
Abstract:
The Caenorhabditis elegans (C. elegans) is a model organism that has been increasingly used in health and environmental toxicity assessments. The quantification of such elements in vivo can assist in studies that seek to relate the exposure concentration to possible biological effects. Therefore, this study is the first to propose a method of quantitative analysis of 21 ions by ion chromatography (IC), which can be applied in different toxicity studies in C. elegans. The developed method was validated for 12 anionic species (fluoride, acetate, chloride, nitrite, bromide, nitrate, sulfate, oxalate, molybdate, dichromate, phosphate, and perchlorate), and 9 cationic species (lithium, sodium, ammonium, thallium, potassium, magnesium, manganese, calcium, and barium). The method did not present the presence of interfering species, with R2 varying between 0.9991 and 0.9999, with a linear range from 1 to 100 µg L-1. Limits of detection (LOD) and limits of quantification (LOQ) values ranged from 0.2319 μg L-1 to 1.7160 μg L-1 and 0.7028 μg L-1 to 5.1999 μg L-1, respectively. The intraday and interday precision tests showed an Relative Standard Deviation (RSD) below 10.0 % and recovery ranging from 71.0 % to 118.0 % with a maximum RSD of 5.5 %. The method was applied to real samples of C. elegans treated with 200 uM of thallium acetate solution, determining the uptake and bioaccumulated Tl+ content during acute exposure.

