Effects of Oxygen on Determination of Thiocholine by 5,5'-Dithiobis (2-Nitrobenzoic Acid) .

1966 ◽  
Vol 122 (1) ◽  
pp. 50-55
Author(s):  
M. C. Vaughan ◽  
R. P. Smith ◽  
R. E. Gosselin
Keyword(s):  
1983 ◽  
Vol 130 (2) ◽  
pp. 257-261 ◽  
Author(s):  
Gian Marco Ghiggeri ◽  
Giovanni Candiano ◽  
Gerolamo Delfino ◽  
Carlo Queirolo

1989 ◽  
Vol 72 (6) ◽  
pp. 903-906
Author(s):  
Gracia A Perfetti ◽  
Frank L Joe ◽  
Gregory W Diachenko

Abstract A liquid chromatographic (LC) method is described for the determination of sulfite in grapes and certain grape products. Sulfite is extracted from grapes with aqueous formaldehyde solution buffered at pH 5; free sulfite is converted to hydroxymethylsulfonate (HMS), which is extremely stable at pH 3-7. Subsequent heating to 80°C for 30 min converts reversibly bound forms of sulfite to HMS. The extract is then analyzed by reverse-phase ion-pairing liquid chromatography, using a Cjg column and a mobile phase of aqueous 0.005M tetrabutylammonium ion in 0.05M acetate, pH 4.7, and a flow rate of 1 mL/min. Aqueous KOH is added to the eluate to convert HMS to free sulfite, which is then treated with 5,5'-dithiobis[2-nitrobenzoic acid]. This reaction produces the 3-carboxy-4-nitrothiophenolate anion, which is determined by measurement of electronic absorption at 450 nm. For grapes spiked with HMS at 5-20 ppm (as S02), recoveries ranged from 92 to 112%, with a coefficient of variation of 4.6%. The method was also used to determine sulfite in various grape products. Results were comparable to those obtained by the AOAC official Monier-Williams method.


1978 ◽  
Vol 24 (7) ◽  
pp. 1140-1143 ◽  
Author(s):  
D L Rabenstein ◽  
R Saetre

Abstract A high-performance liquid chromatographic method is presented for determination of glutathione in whole blood. Sample preparation involves hemolysis, protein precipitation, centrifugation, and filtration. The glutathione in the filtrate is then separated from other sulfhydryl-containing molecules by liquid chromatography with Zipax SCX cation-exchanger followed by detection with a mercury-based electrochemical detector. The liquid-chromatographic analysis time is approximately 5 min. Because of the chromatographic separation and the selectivity of the detector, the detection step is free from interferences from other components of blood. The method has been checked by comparison with the colorimetric assay based on reaction with 5,5'-dithiobis(2-nitrobenzoic acid). The chromatographic results are consistently slightly lower, presumably because of the greater selectivity of this method.


1982 ◽  
Vol 54 (7) ◽  
pp. 1082-1087 ◽  
Author(s):  
Kazuhiro. Kuwata ◽  
Michiko. Uebori ◽  
Kazuhiko. Yamada ◽  
Yoshiaki. Yamazaki

2013 ◽  
Vol 52 (6) ◽  
pp. 526-531
Author(s):  
M. B. de Freitas ◽  
E. B. Lages ◽  
I. M. B. Goncalves ◽  
R. B. de Oliveira ◽  
C. D. Vianna-Soares

1996 ◽  
Vol 79 (3) ◽  
pp. 757-763 ◽  
Author(s):  
Jose J Cerón ◽  
María J Fernandez Del Palacio ◽  
Luis J Bernal ◽  
Cándido Gutierrez

Abstract An automated method using 2,2’-dithiodipyridine (2-PDS) as chromophore for determination of wholeblood cholinesterase activity was developed. Assay procedures, optimal concentrations of chromophore and substrate, detection limit, precision, backgrounds, and sensitivity of the method were compared with those of an earlier automated method based on the Eilman method and using 5,5’-dithiobis(2-nitrobenzoic acid) (DTNB) as chromophore. The new method has the advantages of automation (resulting in increase throughput rate and decrease in amount of reagents used) and good precision and sensitivity. Sample dilutions also are reduced in the new method because hemoglobin interference is less.


1975 ◽  
Vol 149 (1) ◽  
pp. 281-283 ◽  
Author(s):  
P. D. J. Weitzman

Thionitrobenzoate was prepared from 5,5′-dithiobis-(2-nitrobenzoic acid), and its reaction with several disulphide-containing proteins was examined under various conditions. No evidence for any cleavage of disulphide bonds was obtained. The claim by Robyt et al. [Arch. Biochem. Biophys. (1971) 147, 262–269] that thionitrobenzoate allows the quantitative determination of disulphide bonds in proteins is not substantiated.


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