The determination of mimosine and 3,4-dihydroxypyridine in biological material

1964 ◽  
Vol 15 (1) ◽  
pp. 168 ◽  
Author(s):  
MP Hegarty ◽  
RD Court ◽  
PM Thorne

A simple, specific method is described for the determination of mimosine and 3,4-dihydroxypyridine (DHP) in extracts of leaves and seeds of Leucaena glauca Benth. and in urine. Plant material is extracted with cold 0.1 N hydrochloric acid, and interfering substances are removed by chromatography on a cation-exchange resin. Organic cations are displaced from the resin with 2N ammonium hydroxide and the concentrated eluate chromatographed in one direction with the use of mesityl oxide : formic acid : water (41 : 7 : 6 by volume). The spots of mimosine and DHP, revealed with a ferric chloride spray, are cut out and the colour fully developed and measured. Urines are analysed in the same way except for a preliminary hydrolysis of the conjugated DHP. The method is satisfactory for estimating amounts of mimosine and DHP in the range 10–160 µg applied to the paper. Recoveries of these substances added to various extracts and to urine have varied between 98–102%. Appreciable destruction of mimosine, with the formation of some DHP, occurred when fresh L. glauca leaves were dried even under mild conditions. In fresh material no loss of mimosine occurred when it was placed immediately in 0.1 N hydrochloric acid. The ready hydrolysis of mimosine to DHP by boiling 0. I N hydrochloric acid has been demonstrated for the first time.

1968 ◽  
Vol 51 (5) ◽  
pp. 1013-1016
Author(s):  
Sura J P Agarwal ◽  
Martin I Blake

Abstract A simple, nonaqueous titration procedure is described for the determination of sodium diphenylhydantoin and phenobarbital combinations. Preliminary separation of the components is unnecessary. The phenobarbital content is determined by direct titration in tert.-butyl alcohol, using sodium methoxide or triethyl n-butyl ammonium hydroxide as the titrant. The total acidity is determined by titration of the sample after passage through a cation exchange resin (Amberlite IRC-50). The sodium diphenylhydantoin content is obtained by difference. Quantitative recoveries were obtained for synthetic mixtures and commercially available dosage forms


1964 ◽  
Vol 47 (2) ◽  
pp. 203-208
Author(s):  
Stanley E Katz ◽  
Joseph Spock

Abstract The fluorometric procedure for chlortetracycline in mixed feeds is based upon the degradation of chlortetracycline in alkaline solution to isochlortetracycline. The fluorescence of the isochlortetracycline is directly proportional to the concentration of chlortetracycline present prior to alkaline degradation. Chlortetracycline is extracted from mixed feeds with an acidmethanol solvent system, separated from the feed extract by adsorption on a Dowex 50 ion exchange resin, and eluted from the resin by ammonium hydroxide after conversion to isochlortetracycline. The isochlortetracycline is measured fluorometrically. Recoveries from known feeds are generally greater than 90% and agreements with microbiological assays are very close.


1961 ◽  
Vol 82 (12) ◽  
pp. 1650-1653
Author(s):  
Hiroyuki TSUBOT ◽  
Hidetake KAKIHANA

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