These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Simultaneous monitoring of inorganic cations, amines and amino acids in human sweat by capillary electrophoresis.
    Author: Hirokawa T, Okamoto H, Gosyo Y, Tsuda T, Timerbaev AR.
    Journal: Anal Chim Acta; 2007 Jan 02; 581(1):83-8. PubMed ID: 17386429.
    Abstract:
    The determination of cationic constituents of sweat is widely recognized as a difficult analytical task due to its complex composition and minute sample volumes available for the individual analysis. Capillary electrophoresis (CE) has been evaluated as a simple routine method to measure sweat metal cations, biogenic amines, and amino acids using a sampling procedure previously developed in one of collaborative teams. The carrier electrolyte, which consisted of 10 mM 4-methylbenzylamine, 6.5 mM alpha-hydroxyisobutyric acid, and 2 mM 18-crown-6 at pH 4.25, allowed the separation of five cations (NH(4)(+), K(+), Ca(2+), Na(+), Mg(2+)) and four amino acids (ornithine, histidine, lysine, arginine) to be completed in about 13 min with a positive polarity of the applied voltage (30 kV). By increasing the sample volume (due to employing hydrodynamic instead of hydrostatic injection mode), it was also possible to detect indirect UV signals of Zn(2+), diethanolamine, and trithanolamine. Sweat samples were collected from the fingers and forearms of three healthy male volunteers and analyzed by CE. A good repeatability and reproducibility of peak area responses based on five intraday and three inter-day assays (average %R.S.D. less than 3.5 and 2.5, respectively) were obtained. The limits of detection were in the range of 3.2-5.8 microM for alkali and alkaline-earth cations (hydrostatic injection) and 0.27-0.79 microM for other target analytes (hydrodynamic injection). The analytical results for particular analytes were found to vary, depending on the sampling spot and individual, but in general correspond well to clinical concentration ranges.
    [Abstract] [Full Text] [Related] [New Search]