Liquid Chromatographic Determination of Carhadox in Complete Feeds, Premixes, and Concentrates: Interlaboratory Study

1988 ◽  
Vol 71 (3) ◽  
pp. 484-490
Author(s):  
René M L Aerts ◽  
Geziena A Werdmuller

Abstract A liquid chromatographic (LC) method previously published for the determination of carbadox in finished feeds and premixes was slightly modified and tested in an interlaboratory study. The feed samples are extracted with methanol-acetonitrile (50 + 50) after wetting with water. The extracts are purified over a short alumina column. An aliquot of the eluate is analyzed with reverse phase liquid chromatography with ultraviolet detection. Before the actual interlaboratory study, a prestudy with 2 familiarization feed samples was performed. For the interlaboratory study, 2 series of meal and pelleted samples were prepared with carbadox from different suppliers. Eight collaborating laboratories received 6 feed samples previously milled and ground and 4 pelleted samples which had to be ground by the collaborator's in-house method. Collaborators also received 3 carbadox concentrates (about 10% w/w) and 4 premix samples derived from the concentrates (about 1% w/w). Coefficients of variation under reproducibility conditions were 8.3% for meal samples and 4.9% for pellets. A minor but significant effect was noted for the influence of pelleting temperature on the carbadox content. A minor and insignificant effect was observed for the influence of the milling and grinding procedure on the carbadox content. Alumina cleanup of 1% premixes was not essential, although the resulting chromatograms were cleaner. A slight difference in reproducibility was observed with concentrates (10%) when 0.2 or 0.5 g sample size was used, although the average carbadox concentration found was the same. For premixes and concentrates, coefficients of variation under reproducibility conditions were low, ranging from 2.9 to 7.5%.

1988 ◽  
Vol 71 (5) ◽  
pp. 1054-1056 ◽  
Author(s):  
Joel E Houglum ◽  
Richard D Larson ◽  
Rose M Neal

Abstract A reverse-phase liquid chromatographic method for the assay of sulfamethazine (SMZ) in feeds is described. Feed samples are extracted with 50% methanol solution, centrifuged, filtered, and diluted when necessary, and chromatographed on a C-18 column. Samples are eluted with a mobile phase of 20% methanol and 80% of a solution containing acetic acid and tetramethylammonium chloride. The average recovery from spiked samples was 97.2% with a coefficient of variation of 1.2%. Linearity was very good (correlation coefficient 0.9997). Within-day and between-day coefficients of variation averaged 1.3 and 2.6%, respectively. The results for samples assayed by this method compared closely with the results from the same extracts assayed by the AOAC colorimetric method


1980 ◽  
Vol 63 (1) ◽  
pp. 37-42 ◽  
Author(s):  
Ross J Norstrom ◽  
Henry T Won ◽  
Micheline Van Hove Holdrinet ◽  
Patrick G Calway ◽  
Caroline D Naftel

Abstract Mirex and photomirex (8-monohydromirex) were separated from polychlorinated biphenyls (PCBs) and other aromatic compounds by nitration with fuming nitric acid-concentrated sulfuric acid and removal of nitro-PCBs on an alumina microcolumn; the compounds were then determined by gas-liquid chromatography. Recoveries of Mirex and photomirex were 102±8 and 104±5%, respectively, from standard solutions which had a PCB-to-Mirex and photomirex ratio of 1000. Recoveries from fortified, uncontaminated samples of sediment, fish, and eggs averaged 93±7 and 92±3% for Mirex and photomirex, respectively. The coefficients of variation for repeatability and reproducibility averaged 8 and 15%, respectively, in an interlaboratory study conducted by 4 laboratories using extracts of naturally contaminated substrates (sediment, carp, eel, and gull egg). Levels of Mirex in the samples ranged from 0.1 to 8 mg/kg, and levels of PCB ranged from 0.5 to 166 mg/kg.


1997 ◽  
Vol 80 (6) ◽  
pp. 1156-1160
Author(s):  
Robin S Readnour ◽  
Mark R Coleman ◽  
Mary G Leadbetter ◽  
F Armstrong ◽  
H Campbell ◽  
...  

Abstract An analytical method for the determination of tilmicosin at 200–400 mg/kg, the intended use concentration range, was evaluated in an interlaboratory study involving 5 laboratories, including the sponsor. The interlaboratory study evaluated the intra- and interlaboratory precision and accuracy of a tilmicosin feed method. The method procedure involved extracting tilmicosin from feed by adding 200 mL extractant to 20 g feed and shaking for 1 h. The extract is filtered and analyzed by gradient liquid chromatography which separates tilmicosin from feed matrix in 30 min. Each laboratory assayed 5 replicates of fortified feed at concentrations of 0,100, 200, 400, and 600 mg/kg. The mean recovery among fortified samples ranged from 81.4 to 98.8%, with a percent coefficient of variation (%CV) ranging from 0.3 to 4.0%. For all blank control feed samples no significant interferences were observed. In addition, each laboratory assayed 5 replicates of medicated feed samples prepared at 2 levels (200 and 400 mg/kg) with either a horizontal or vertical mixer. Along with the medicated feed samples were included 5 replicates of a blank control feed. The identities of the medicated and blank control feed samples were blinded to the analysts. The results for the medicated feed samples ranged from 95.8 to 106% of label claim, with a %CV ranging from 2.1 to 6.7%.


1985 ◽  
Vol 68 (6) ◽  
pp. 1134-1136 ◽  
Author(s):  
Rodney J Bushway

Abstract A liquid chromatographic method has been developed to quantitate pyrethrins in pesticide formulations. Samples were dissolved in tetrahydrofuran (THF) and injected onto an amino column with a solvent system of hexane-nonstabilized THF (90 + 10) at a flow rate of 1.5 mL/min. Detection was monitored at 240 nm and 0.4 AUFS. Total elution time was 7 min. Twelve products varying in concentration from 0.05 to 3.75% and formulated with numerous other ingredients were analyzed. Percent coefficients of variation ranged from 1.39 to 9.68 with the majority less than 5.00. Although piperonyl butoxide and Noctyl bicycloheptene dicarboximide (MGK 264) were not quantitated, neither interfered with the pyrethrin analysis


1993 ◽  
Vol 76 (6) ◽  
pp. 1248-1254 ◽  
Author(s):  
Louis G M Th Tuinstra ◽  
Arie H Roos ◽  
John M P Van Trijp ◽  
◽  
P A Burdaspal ◽  
...  

Abstract A liquid chromatographic method for determining low aflatoxin M1 concentrations in milk was evaluated in an International Dairy Federation (IDF) interlaboratory study. The study involved 16 participants from 11 countries. The method, chosen after a comparison of several methods by a preparatory group, uses an immunoaffinity column for cleanup. As the sample passes through the column, antibodies selectively bind with aflatoxin M1 (antigen) present and form an antibody-antigen complex. All other components of the sample matrix are washed off the column with water. Then, aflatoxin M1 is eluted from the column with acetonitrile, which is collected. Final determination is carried out by reversed-phase liquid chromatography with fluorescence detection. Over the tested range (80-600 ng aflatoxin M1/kg milk powder), an RSDR ranging from 11 to 23% was obtained by analyzing 24 samples (blind duplicates), 2 samples of which were blanks.


1988 ◽  
Vol 71 (6) ◽  
pp. 1115-1117
Author(s):  
Jorge I CastaÑo ◽  
Francisco J Palacio ◽  
Luis R Vargas

Abstract A liquid chromatographic method for the quantitative determination of propyl paraben in cigarette tobacco filler has been developed. Propyl paraben is extracted from cigarette tobacco filler with acetonitrile and further purified using a silica Sep-Pak® cartridge and ethyl acetate-petroleum ether (1 + 4) as eluting solvent. The purified extracts are analyzed by reverse-phase liquid chromatography using buffered water (pH 4)-acetonitrile (65 + 35) as mobile phase, with UV detection at 254 nm. Cut tobacco samples were fortified with 100 and 200 ppm propyl paraben. Average recoveries (N = 5) of propyl paraben were 98 and 94%, respectively, with coefficients of variation less than 4%.


1984 ◽  
Vol 67 (2) ◽  
pp. 218-221 ◽  
Author(s):  
Milda J Walters ◽  
◽  
N Falcone ◽  
K G Hanel ◽  
E H Jefferson ◽  
...  

Abstract A normal phase liquid chromatographic (LC) method for determining the hydrocortisone content of bulk drug substance, tablet composites, and individual tablets was subjected to a collaborative study by 6 laboratories. The results showed a mean recovery of 98.5% for an authentic tablet formulation and reproducibility coefficients of variation of 0.97, 1.6, and 2.7% for bulk drug substance, tablet composites, and individual tablets, respectively. Infrared (IR) and thin layer chromatographic (TLC) identification tests, also included in the collaborative study, were satisfactory. The LC method for determining hydrocortisone in bulk drug substance, tablet composites, and individual tablets, with IR and TLC identification, has been adopted official first action.


1992 ◽  
Vol 75 (4) ◽  
pp. 747-750 ◽  
Author(s):  
Philip James Kijak

Abstract A laboratory trial was completed for an analytical method that can quantitate the marker residue of ivermectin, 22,23-dihydroavermectin B1a, in bovine milk at 1 ng/mL Currently, ivermectin is not approved for use in lactating dairy cows. In this method, the ivermectin residues are isolated from the milk matrix by a series of liquid-liquid extractions. A fluorescent derivative of the marker compound is prepared and then quantified by liquid chromatography with fluorescence detection. The interlaboratory study was successfully completed by using dosed milk and milk fortified with marker residue at 1,2, and 4 ng/mL. The average recoveries by the 3 participating laboratories were 87,59, and 95% at 1 ng/mL; 90,61, and 96% at 2 ng/mL; and 90,73, and 99% at 4 ng/mL. The concentrations of the marker residue in the dosed milk were 4.3, 3.7, and 4.7 ng/mL; coefficients of variation were 4.0,24.8, and 5.9%, respectively.


1986 ◽  
Vol 69 (5) ◽  
pp. 760-762
Author(s):  
Krystyna Tyczkowska ◽  
Arthur L Aronson

Abstract A sensitive liquid chromatographic method has been developed for the simultaneous determination of oxytetracycline, minocycline, tetracycline, and doxycycline in serum. A serum sample is vortex-mixed with a solution of mobile phase for tetracyclines and 2% (v/v) phosphoric acid. The mixture is filtered using a 30 000 molecular weight cutoff microseparation tube which separates high-molecular-weight solutes following low-speed centrifugation. Tetracyclines are separated from other serum components by reverse phase liquid chromatography (LC) with buffered methanol mobile phase. Ultraviolet absorbance of the column effluent is monitored at 267 nm. Concentrations as low as 0.2 μg/mL of tetracyclines in serum are quantitatable, with recoveries from 76.2 to 102.6% and coefficients of variation from 2.69 to 5.36%. The method has been tested in bovine, porcine, equine, caprine, ovine, canine, feline, and avian (turkey) serum.


1984 ◽  
Vol 67 (4) ◽  
pp. 674-676
Author(s):  
James F Brower

Abstract A normal phase liquid chromatographic (LC) method for the determination of prednisolone in tablets and bulk drugs was studied by 7 analysts. An LC system, consisting of a methanol-water-ethylene dichloride- acetic acid mobile phase and a silica column, was used to analyze bulk drugs, individual tablets, and composite samples. Analysts were supplied with 16 samples, including simulated formulations, composites of commercial tablets, intact tablets, and bulk drug substances. Results agreed with those obtained by the author. The coefficients of variation of the analysts' results ranged from 1.34% for bulk drugs to 2.14% for tablet composites. The LC method is suggested as an alternative to the official AOAC and USP XX blue tetrazolium colorimetric methods.


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