DETERMINATION OF ARSANILIC ACID IN LIVESTOCK FEEDS BY HPLC USING AN ANION EXCHANGE COLUMN AND ULTRAVIOLET DETECTION

2010 ◽  
Vol 33 (3) ◽  
pp. 405-412 ◽  
Author(s):  
Jinrong Wang ◽  
Linghong Nie ◽  
Zuolong Fu ◽  
Jinjin Wang
2013 ◽  
Vol 96 (5) ◽  
pp. 1103-1108 ◽  
Author(s):  
Benjamin S Liao ◽  
Jacqueline C Sram ◽  
Darin J Files

Abstract A simple and effective anion ion chromatography (IC) method with anion exchange column and conductivity detector has been developed to determine free sulfites (SO3–2) in dried fruits processed with sulfur dioxide. No oxidation agent, such as hydrogen peroxide, is used to convert sulfites to sulfates for IC analysis. In addition, no stabilizing agent, such as formaldehyde, fructose or EDTA, is required during the sample extraction. This method uses aqueous 0.2 N NaOH as the solvent for standard preparation and sample extraction. The sulfites, either prepared from standard sodium sulfite powder or extracted from food samples, are presumed to be unbound SO3–2 in aqueous 0.2 N NaOH (pH > 13), because the bound sulfites in the sample matrix are released at pH > 10. In this study, sulfites in the standard solutions were stable at room temperature (i.e., 15–25°C) for up to 12 days. The lowest standard of the linear calibration curve is set at 1.59 μg/mL SO3–2 (equivalent to 6.36 μg/g sample with no dilution) for analysis of processed dried fruits that would contain high levels (>1000 μg/g) of sulfites. As a consequence, this method typically requires significant dilution of the sample extract. Samples are prepared with a simple procedure of sample compositing, extraction with aqueous 0.2 N NaOH, centrifugation, dilution as needed, and filtration prior to IC. The sulfites in these sample extracts are stable at room temperature for up to 20 h. Using anion IC, the sulfites are eluted under isocratic conditions with 10 mM aqueous sodium carbonate solution as the mobile phase passing through an anion exchange column. The sulfites are easily separated, with an analysis run time of 18 min, regardless of the dried fruit matrix. Recoveries from samples spiked with sodium sulfites were demonstrated to be between 81 and 105% for five different fruit matrixes (apricot, golden grape, white peach, fig, and mango). Overall, this method is simple to perform and effective for the determination of high levels of sulfites in dried fruits.


1971 ◽  
Vol 17 (9) ◽  
pp. 867-871 ◽  
Author(s):  
J I Routh ◽  
R E Bannow ◽  
R W Fincham ◽  
J L Stoll

Abstract L-Dopa and its major metabolites were separated from daily 24-h urines from patients with Parkinson’s disease, who were being treated with increasing doses of the drug, up to 4 g per day. An aliquot of each sample was passed through three different ion-exchange columns. Catecholamines (dopamine, epinephrine, norepinephrine, metanephrine, and normetanephrine) were retained on a cation-exchange column, eluted with boric acid, and quantitated by fluorometric analysis. Catechol acids, present in the effluent of the cation-exchange column, were retained on an anion-exchange column. An aliquot of the eluate of the anion-exchange column was used for colorimetric determination of 3,4-dihydroxyphenylacetic acid, while the effluent from this column was used for colorimetric determination of dopa. A second aliquot of the eluate from this column was passed over a column of alumina, which retained all the acidic metabolites except homovanillic acid, which was measured fluorometrically in the effluent from the alumina column. Vanilmandelic acid was determined in another aliquot of each urine sample by use of paper electrophoresis. The excretion pattern elicited suggests a major metabolic pathway for the L-dopa administered to patients with Parkinson's disease.


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