Determination of Dimetridazole and Ipronidazole in Feeds at Cross-Contamination Levels

1988 ◽  
Vol 71 (3) ◽  
pp. 474-477 ◽  
Author(s):  
Duane D Hughes

Abstract A rapid method for the determination of dimetridazole and ipronidazole in feeds is described. The compounds are extracted from a borate buffer (pH 8.65) with benzene, partitioned into IN HC1, and then partitioned back into benzene from a basic aqueous phase. The benzene extract is concentrated and injected onto a nonpolar (Apiezon L) gas chromatographic column for determination by 63Ni electroncapture detection. Recoveries from feeds of various composition, spiked at 0.2 ppm with both dimetridazole and ipronidazole, ranged from 70 to 115%; for the same feeds spiked at 1 ppm or more, the recoveries were greater than 80%. Carbadox, furazolidone, levamisole, oxytetracycline, chlortetracycline, sulfamethazine, sulfaquinoxaline, arsanilic acid, piperazine, penicillin, and commonly added vitamins and minerals do not interfere. A 2-dimensional thin layer chromatographic system is presented as a means of additional identification.

1981 ◽  
Vol 64 (6) ◽  
pp. 1312-1314
Author(s):  
Sana Udaya Bhaskar ◽  
Nanguneri V Nanda Kumar

Abstract A simple, sensitive, and rapid method is described for the quantitative estimation of nanogram amounts of methyl parathion (O,O-dimethyl O-p-nitrophenyl phosphorothioate) as methyl paraoxon (O,O-dimethyl O-p-nitrophenyl phosphate) on thin layer chromatograms. Methyl paraoxon is detected by pig liver acetone powder cholinesterase inhibition, using p-nitrobenzenediazoniumfluoroborate as the chromogenic reagent. Commercial pig liver acetone powder is more advantageous than raw liver sources because it is readily available and can be preserved indefinitely. About 0.1 ng methyl parathion can be detected, and amounts from 5 to 50 ng can be quantitatively estimated.


1964 ◽  
Vol 47 (5) ◽  
pp. 894-897
Author(s):  
C Genest ◽  
D M Smith

Abstract Benzo[a]pyrene can be used as an index of carcinogens in smoke. A simple and rapid method has been developed for determining this substance. The dried food was extracted with ra-hexane, the hexane was then extracted with dimethyl sulfoxide, and the polynuclear hydrocarbon was displaced from this solvent into benzene by water. The benzene extract was reduced to a small volume and an aliquot was spotted on a thin-layer chromatographic plate beside spots of a standard benzo[a]pyrene solution. The plate was chroma tographed with 2,2,4-trimethyl pentane:benzene (97:3). When observed under ultraviolet light at 3660 Å, 0.002 μg of pure benzo[a]pyrene could be found and the addition of 0.01—0.05 ppm to unsmoked foods could be detected. No smoked food examined contained this level of benzo-[a]pyrene.


1994 ◽  
Vol 77 (3) ◽  
pp. 637-646 ◽  
Author(s):  
Douglas L Park ◽  
Mary W Trucksess ◽  
Stanley Nesheem ◽  
Michael Stack ◽  
Richard F Newell

Abstract An interlaboratory study of a solvent-efficient thin-layer chromatographic (TLC) method for the determination of aflatoxins B1, B2, G1, and G2 was conducted in laboratories located in the United States, France, Tunisia, and Denmark. Eighteen artificially contaminated samples plus blanks of raw peanuts and peanut butter and corn containing varying amounts of aflatoxins B1, B2, G1, and G2 were distributed to participating laboratories. The method consists of elements of the U.S. Food and Drug Administration (FDA), Contaminants Branch (CB) (AOAC Method 968.22) and FDA, Best Foods (BF) (AOAC Method 970.45) methods with reduced requirements for solvents. Participating laboratories used either visual or densitometric techniques during the final determinative step. Statistical analysis of the data was performed to determine or confirm outliers and to compute repeatability and reproducibility of the method using either visual or densitometric techniques for the determinative step. Reported results from laboratories using a densitometer showed that, for corn, the relative standard deviation for repeatability (RSDr) for aflatoxin Bi ranged from 56.6 to 41.7% for contamination levels ranging from 5 to 50 ng/g. For raw peanuts and peanut butter, the RSDr values for aflatoxin Bi ranged from 21.3 to 37.3% and 65.9 to 42.1%, respectively, for the contamination levels ranging from 5 to 25 ng/g. RSDr ranges for anatoxins B2, Gi, and G2 were similar. For reproducibility (R), the RSDr ranges for aflatoxin Bi were 41.7-56.6%, 56.6-84.8%, and 26.4-37.3% for corn, peanut butter, and raw peanuts, respectively. Average re-coveries for all aflatoxins at all levels were 95.3, 139.0, and 95.6% for corn, peanut butter, and raw peanuts, respectively. When analysts determined af latoxin concentrations in corn by visual comparison to standards, the RSDr values for aflatoxin Bi were 47.8-11.4% for contamination levels ranging from 5 to 50 ng/g. For raw peanuts and peanut butter, the RSDr values for aflatoxin Bi were 76.3-12.6% and 33.4-8.8%, respectively, for the contamination levels ranging from 5 to 25 ng/g. RSDr values for aflatoxins B2, G1, and G2 were similar. The RSDr values for aflatoxin Bi were 34.6-90.2%, 45.5-59.3%, and 31.8-78.3% for corn, peanut butter, and raw peanuts, respectively. Average recoveries for all anatoxins at all levels were 111.0,157.6, and 92.3% for corn, peanut butter, and raw peanuts, respectively. High recoveries were noted for anatoxins in peanut butter determined by either a densitometer or comparison to standards. Generally, increased precision was observed with the method at higher contamination levels. On the basis of the results obtained in this AOAC/IUPAC collaborative study, the solvent-efficient TLC method using densitometry for the quantitative step was adopted first action by AOAC for the determination of aflatoxins B1, B2, G1, and G2 in corn at levels within the range of 5-50 ng/g, 3-15 ng/g, 10-50 ng/g, and 3- 15 ng/g, respectively, by densitometry; for anatoxins B1 and B2 in raw peanuts at levels ranging from 5 to 25 ng/g and from 1.5 to 7.5 ng/g, respectively, by densitometry; and for aflatoxins B1 and G1 in corn at 10-50 and 50 ng/g, respectively, and aflatoxins B1, B2, and G1 in raw peanuts at 10-25 ng/g, 7.5 ng/g, and 10-25 ng/g, respectively. Because of high recovery values, additional study is recommended for peanut butter. The solvent-efficient TLC method for determination of aflatoxins B1, B2, G1, and G2 in corn and peanuts has been adopted first action by AOAC INTERNATIONAL.


1981 ◽  
Vol 64 (3) ◽  
pp. 729-732
Author(s):  
Nanguneri V Nanda Kumar ◽  
Yalavarthi Prameela Devi

Abstract A new simple, sensitive, and rapid method is described for the qualitative and quantitative determination of mercuric chloride by paper chromatographic-enzymatic and micro thin layer chromatographic-enzymatic methods. Mercuric chloride is detected by succinate dehydrogenase inhibition using 2-(4-iodophenyl)-3-(4-nitrophenyl) 5-phenyltetrazolium chloride and N-methylphenazonium methosulfate as the chromogenic reagent. From 0.5 to 5μg mercuric chloride may be estimated, and 50 ng may be detected. The method can be used for the quantitative determination of mercuric chloride in fresh and sea water without cleanup and for the detection of copper sulfate.


1974 ◽  
Vol 57 (3) ◽  
pp. 621-625 ◽  
Author(s):  
Peter M Scott

Abstract Collaborators in 20 laboratories studied a method for the determination of patulin in apple juice. The collaborators mixed patulin solutions with the apple juice to obtain 9 spiked samples (of which 2 were blanks) and 1 practice sample. After column chromatography of the apple juice extract, patulin was estimated visually by thin layer chromatography, using 3-methyl-2-benzothiazolinone hydrazone.HCl as the spray reagent. Mean recoveries of patulin ranged from 69.8 to 98.3% for 3 contamination levels. The method has been adopted as official first action for the determination of patulin in apple juice.


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