isooctane/dichloromethane

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Analysis of [3H]estradiol-17beta metabolites in calf perirenal fat.

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Residues of estradiol-17 beta (E2 beta) in the kidney fat of one milk-fed calf were studies using radiometric methodologies. A three-month old Friesian male veal calf was injected intramuscularly daily for 3 d with 333 mg of [6,7(n)-3H]-E2 beta (specific activity: 7.55 MBq mmol-1) dissolved in 2 ml

Studies on the positive-ion mass spectra from atmospheric pressure chemical ionization of gases and solvents used in liquid chromatography and direct liquid injection.

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Detailed studies have been made using different source gases and solvents in a Micromass Quattro mass spectrometer under positive ion atmospheric pressure chemical ionization conditions. The major background ions from nitrogen, air, or carbon dioxide were investigated by tandem mass spectrometry,

Development of a harmonized method for the profiling of amphetamines. II. Stability of impurities in organic solvents.

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The present study focused on the stability of 22 amphetamine impurities dissolved in six organic solvents: isooctane, toluene, ethanol, dichloromethane, ethyl acetate, and diethyl ether. The aim was to find the most inert, and thereby most suitable, solvent for amphetamine profiling. Mixtures of the

Liquid chromatographic determination of vitamin K1 trans- and cis-isomers in infant formula.

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The normal phase liquid chromatographic (LC) method for determination of trans- and cis-isomers of vitamin K1 (phylloquinone) in infant formula described here uses an Apex silica column, isocratic elution, and UV absorption detection at 254 nm. Vitamin K1 is extracted quantitatively from the product

Rapid ion-pair liquid chromatographic method for the determination of fenbendazole in cows' milk.

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A simple and rapid methodology for the analysis of fenbendazole residues in cows' milk, at levels down to 3 ng ml-1, has been developed. Samples are extracted with acetonitrile and centrifuged. The supernatant is de-fatted with isooctane, and mixed with dichloromethane. The separated aqueous layer

Determination of vitamin E in animal feeds by normal phase high pressure liquid chromatography.

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A simple and rapid quantitative method for the determination of vitamin E in animal feeds is described. The method involves direct extraction with a mixture of isooctane--1,4-dioxane (80 + 20) followed by saponification. Additional purification was achieved by using a silica gel Sep-Pak. Elution

The determination of plasma corticosterone of chickens by high pressure liquid chromatography.

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A simple method for separating and measuring chicken plasma corticosterone by high pressure liquid chromatography (HPLC) is described. Plasma was extracted twice, first, with isooctane to remove nonpolar steroids and, second, the polar steroids were extracted with dichloromethane. Analytical

Evaluation of a hypercrosslinked polystyrene, MN-200, as a sorbent for the preconcentration of volatile organic compounds in air.

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Breakthrough volumes, average percentage recoveries, and storage stabilities were obtained for vapors of 8 volatile organic compounds (pentane, octane, undecane, isooctane, cyclohexane, toluene, methanol, and dichloromethane) on a new adsorbent material, Hypersol-Macronet, MN-200. Breakthrough

Simplified cleanup and liquid chromatographic ultraviolet determination of linuron and three metabolites in potatoes.

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A simple and efficient method is presented for the extraction, cleanup, and liquid chromatographic (LC) determination of linuron and 3 of its metabolites, 3-(3,4-dichlorophenyl)-1-methyl urea (DCPMU), 3-(3,4-dichlorophenyl) urea (DCPU), and 3,4-dichloroaniline (DCA), in potatoes. Samples are

Development of a gas chromatography-mass spectrometry method for the determination of pesticides in gaseous and particulate phases in the atmosphere.

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A reliable multi-residue method for determining gaseous and particulate phase pesticides in atmospheric samples has been developed. This method, based on full scan gas chromatography-mass spectrometry (GC-MS), allowed the proper determination of sixteen relevant pesticides, in a wide range of

Determination of polycyclic aromatic hydrocarbons (PAHs) in seafood using gas chromatography-mass spectrometry: collaborative study.

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A collaborative study was conducted to determine selected polycyclic aromatic hydrocarbons (PAHs) and their relevant alkyl homologs in seafood matrixes using a fast sample preparation method followed by analysis with GC/MS. The sample preparation method involves addition of (13)C-PAH surrogate

Acanthamoebicidal activity of Fusarium sp. Tlau3, an endophytic fungus from Thunbergia laurifolia Lindl.

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A fungal endophyte identified as Fusarium sp. Tlau3 was isolated from fresh twig of Thunbergia laurifolia Lindl., a Thai medicinal plant collected from the forest of Chiang Mai Province, Northern Thailand. The fungus was grown on a medium containing yeast extracts and sucrose. The fungal metabolites

Ultra-high pressure LC for astaxanthin determination in shrimp by-products and active food packaging.

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Nowadays, there is increasing interest in natural antioxidants from food by-products. Astaxanthin is a potent antioxidant and one of the major carotenoids in crustaceans and salmonids. An ultra-high pressure liquid chromatographic method was developed and validated for the determination of

Dialkylketones in Paperboard Food Contact Materials-Method of Analysis in Fatty Foods and Comparative Migration into Liquid Simulants Versus Foodstuffs.

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Dialkyl diketene dimers are used as sizing agents in the manufacture of paper and board for food contact applications to increase wetting stability. Unbound residues can hydrolyze and decarboxylate into dialkylketones. These non-intentionally added substances (NIAS) have potential to migrate to

Synthesis of 81Br-labeled polybrominated diphenyl ethers and their characterization using GC(EI)MS and GC(ICP)MS.

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A mixture of different (81)Br-labeled polybrominated diphenyl ethers (PBDEs) was prepared and characterized for its future use as spike for the isotope dilution analysis of PBDEs. The synthesis was carried out by direct bromination of diphenyl ether using (81)Br enriched Br(2) obtained after aqueous

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