Fast, Simple and Accurate Method for Simultaneous Determination of α-Lipoic Acid and Selected Thiols in Human Saliva by Capillary Electrophoresis with UV Detection and pH-Mediated Sample Stacking
2025
Urszula Sudomir | Justyna Piechocka | Rafał Głowacki | Paweł Kubalczyk
This report presents the first method for simultaneous determination of the 2-S-lepidinium derivatives of total &alpha:-lipoic acid (LA), homocysteine (Hcy), cysteinylglycine (CysGly), and cysteine (Cys) in human saliva, using capillary electrophoresis with pH-mediated sample stacking and ultraviolet detection (CE-UV) at 355 nm. Electrophoretic separation is carried out at 20 kV and 25 °:C using a standard fused silica capillary (effective length 91.5 cm, inner diameter 75 µ:m). The background electrolyte consists of 0.5 mol/L lithium acetate buffer, adjusted to pH 3.5 with 0.5 mol/L acetic acid. The limit of quantification was determined to be 1 µ:mol/L for LA and 0.17 µ:mol/L for Hcy, 0.11 µ:mol/L for CysGly, and 0.10 µ:mol/L for Cys in saliva samples. Calibration curves demonstrated linearity over the concentration range of 3 to 30 µ:mol/L for all analytes. Method precision did not exceed 4.7%, and accuracy ranged from 87.9% to 114.0%. The developed method was successfully applied to saliva samples from eleven apparently healthy volunteers to determine the content of LA, Hcy, CysGly, and Cys. The Hcy, CysGly, and Cys concentrations ranged from 0.55 to 13.76 µ:mol/L, 0.89 to 9.29 µ:mol/L, and 1.73 to 12.99 µ:mol/L, respectively. No LA-derived peaks were detected in the native saliva samples.
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