PubMed Health⌕ Search

Biomedical subjects

M C Bowman

Publications and source records attributed to M C Bowman.

At least 37 records · Page 2Linked to original sources
PubMed1981

Trace analysis of sulfamethazine in animal feed, human urine, and wastewater by electron capture gas chromatography.

Sulfamethazine, a widely used antibacterial drug additive in feeds for swine, chickens, and cattle, was scheduled for toxicological evaluation because of potential human health hazards associated with its residues in edible animal tissues. Analytical chemical procedures that would ensure proper concentration, homogeneity, and stability of the drug in dosed feed and its safe usage during the animal studies were prerequisites for such toxicological tests. Electron capture gas chromatographic (EC/GC) methods were therefore devised for the analysis of sulfamethazine residues in animal feed, human urine, and wastewater at levels as low as 100, 10, and 10 ppb, respectively. Sample extracts were cleaned up by using liquid/liquid partitioning, and the extracts were subjected to two derivatizations followed by cleanup on a silica gel column. The derivatizations of sulfamethazine consisted of methylation followed by trifluoroacetylation of the primary amine function. Ancillary data concerning stability of the compound in animal feed, water, and as a dry residue on glass, extraction efficiencies, partition values with various solvents, and the analysis of residues in feed by high pressure liquid chromatography (HPLC) at levels as low as 1.0 ppm are presented.

Animal Feed↗
PubMed1980

A toxicological risk assessment procedure: a proposal for a surveillance index for hazardous chemicals.

Health-oriented government agencies responsible for the protection of the public from possible adverse effects, such as that posed by chemical residues in the food supply, must establish priorities on regulatory action as well as for manpower to conduct monitoring programs. A new procedure entitled Surveillance Index (SI) is presented as a technique to evaluate toxic materials that are potential candidates as residues in food supplies and to assign an index number that identifies a relative hazard to the public among the various residues. The SI numbers can be used as criteria by which chemical residues should be monitored whenever conditions such as time and available resources are limiting factors.

Chemical Industry↗
PubMed1980

Chemical monitoring of urine from workers potentially exposed to benzidine-derived azo dyes.

Benzidine (Bzd) and monoacetylbenzidine (MoAcBzd) were found in the urine of workers exposed to benzidine-based azo dyes. A colorimetric screening method, based on the reaction of extracted free aromatic amines with 2,4,6-trinitrobenzene-sulfonic acid (TNBS), was used with a specific electron-capture gas chromatographic (EC-GC) method. Alkaline hydrolyzable conjugates of Bzd and 2,4-diaminoazobenzene (DiAmAzBz) were found together with free DiAmAzBz and traces of 3,3'-dimethylbenzidine (DiMeBzd) and 3,3'-dimethoxybenzidine (DiMxBzd). The presence of a known human bladder carcinogen (Bzd) and its metabolites in the urine of workers exposed to benzidine-based azo dyes is a cause for concern.

Azo Compounds↗
PubMed1980

Determination of sodium saccharin in animal feed, wastewater and human urine by high-pressure liquid chromatography.

Analytical methods are described for sodium saccharin in animal feed, wastewater and human urine at levels as low as 10, 0.1 and 10 ppm, respectively. Samples of animal feed and wastewater are subjected to liquid-liquid partitioning then the feed is further cleaned up on a column of silica gel prior to analysis by high-pressure liquid chromatography (HPLC) using a paired-ion mobile phase and an ultraviolet detector set at 230 nm. Samples of human urine require a cleanpu on a column of XAD-2 prior to the partitioning and silica gel steps as well as an adjustment in the composition of the mobile phase to quantify saccharin. Data concerning partition values and the stability of sodium saccharin in animal feed are also presented.

Animal Feed↗
PubMed1980

Trace analysis of potentially carcinogenic metabolites of an azo dye and pigment in hamster and human urine as determined by two chromatographic procedures.

Analytical chemical procedures are described for determining traces of possible metabolites of two azo compounds. Direct Black 38 and Pigment Yellow 12, in hamster urine and to monitor the urine from workers who may be occupationally exposed during the manufacture or use of the dye and pigment. These methods were required for metabolism studies designed to assess the hazards that may occur if the two compounds are converted by in vivo mechanisms to potential carcinogens. Salient elements of the procedure are: extraction of the free aromatic amines and neutral compounds; alkaline hydrolysis of the aqueous phase and extraction of any hydrolyzed conjugates as free amines, and the analysis of the free amines and acetylated metabolites directly by high pressure liquid chromatography or by electron capture gas chromatography after conversion of the amines to heptafluorobutyryl derivatives. Residues of metabolites in hamster and human urine were determined at levels as low as 1 ppb. Ancillary data concerning hydrolysis of diacetylated metabolites and partition values for possible metabolites in various solvent systems are also presented.

Animals↗
PubMed1980

Determination of gentian violet in animal feed, human urine, and wastewater by high pressure liquid chromatography.

Sensitive and specific procedures are described for the analysis of residues of gentian violet in animal feed, human urine, and wastewater at levels of 1000 ppm down to 10 ppb, 1 ppb, and 10 ppb, respectively. The cleaned-up extracts were analyzed by reverse-phase high pressure liquid chromatography by using an absorption detector at 588 nm. Recoveries of the compound from animal feed, human urine, and wastewater at the 10 ppb level were 79%, 58%, and 60%, respectively. Information concerning the stability of the compound in animal feed and the efficiency of extracting the residues is presented. Ancillary information is also reported concerning the separation and analysis of six related triphenylmethane dyes.

Animal Feed↗
PubMed1979

Trenbolone acetate and trenbolone: trace analysis in animal chow, wastewater and human urine by high pressure liquid chromatography and electron capture gas chromatography.

Analytical methodology is described for determining residues of the synthetic anabolic steroid trenbolone acetate (TBA) and its hydrolysis product trenbolone (TBOH) in admixture in animal chow, human urine, and wastewater. Benzene extracts of the substrates are subjected to liquid-liquid partitioning, further cleanup on a column of silica gel, and direct analysis by high pressure liquid chromotography or derivatization with pentafluoropropionic anhydride and analysis by electron capture gas chromatography. Satisfactory recoveries were obtained with both compounds from all three substrates. Residue levels of TBA and TBOH as low as 0.32 and 0.04 ppm, respectively, could be detected in chow; about 0.6 ppb of each compound could be detected in urine and wastewater. Thin layer chromatographic behavior of the two compounds in 7 solvent systems and other ancillary analytical data are also presented.

Acetates↗
PubMed1979

Control of test substances.

The efficient control of chemicals during a nonclinical laboratory study is of the utmost importance from three main points of view: (1) integrity of the experiment, (2) safety of personnel, and (3) protection of the environment. While the general principles involved in chemical control may be set forth in formal GLPs, detailed problems concerning individual test substances can only be resolved by utilizing the competency and judgment of a researcher who possesses adequate analytical chemical methods. Integrity of an experiment requires knowledge of the identity, purity, and stability of the test substance, as well as its proper handling and storage and a knowledge of its chemical properties. Assurance of homogeneity, stability, and proper concentration of the chemical in the dosage form is also of primary importance. The development and use of adequate analytical chemical procedures for determining the test agent in human samples, air, clothing, and on work surfaces is necessary for the initiation of surveillance procedures to assure safety of personnel from exposure to the test substances. The environment must be protected from hazardous test substances by using adequate disposal techniques for the chemical and all contaminated materials. This usually involves development of wastewater cleanup systems and continuous monitoring of the effluent to prevent discharge of hazardous substances. Incineration is the most useful method for disposal of solids and highly contaminated liquids. Work from our laboratory, done during the past 5 years, provides an illustration of the important principles, problems, and pitfalls encountered in chemical control.

Environmental Exposure↗
PubMed1978

Carcinogens and analogs: trace analysis of thirteen compounds in admixture in wastewater and human urine.

A gas chromatographic method is described for determining traces of 13 carcinogens and related compounds (aromatic amines and estrogens) in admixture in wastewater and human urine. This method was developed for use in toxicological research for monitoring the safe disposal of wastewater and to signal any accidental exposure of personnel to hazardous test substances. Salient elements of the procedure are: extraction of phenolic and neutral residues from the acidified sample, liquid--liquid partitioning cleanup and separation of neutral from phenolic residues at pH 14 and 10.2, acid hydrolysis of the neutral component, subsequent alkalinization of the sample and extraction of the basic residues as the free amines, conversion of all residues to the corresponding pentafluoropropionyl (PFP) derivatives and quantification by electron-capture gas chromatography. Residues were detectable in wastewater and urine at the 0.1 and 1 ppb levels, respectively. Additional information is provided concerning partition values for all PFP derivatives in five solvent systems, structure verification of the derivatives by mass spectrometry and the adaption of this method to the monitoring of surfaces and air in potentially contaminated work areas.

Amines↗
PubMed1978

Determination of sodium phenobarbital in animal chow by high-pressure liquid chromatography.

An analytical procedure is described for determining residues of sodium phenobarbital in animal chow at levels as low as 0.14 ppm. The methanol extract is subjected to a liquid-liquid cleanup at pH 13 and 1, further cleaned up on a silica gel column and assayed by high-pressure liquid chromatography by using an ultraviolet absorption detector at 210 nm. Data concerning extraction efficiency, partition values and stability of the chemical in animal chow are also presented.

Animal Feed↗
PubMed1978

High pressure liquid chromatographic determination of rotenone and degradation products in animal chow and tissues.

An analytical procedure is described for determining residues of rotenone, rotenolone, dehydrotenone, and rotenone in admixture in animal chow and tissues. The methanol or ethyl ether extracts from samples of chow and tissues, respectively, are subjected to a liquid-liquid partitioning cleanup with hexane-acetonitrile, further cleanup on a column of silica gel, and subsequent analysis by high pressure liquid chromatography using an ultraviolet absorption detector set at 295 nm. Animal chow, mouse fetuses, and gastrointestinal tracts spiked with 0.5 ppm of each compound in admixture yielded average recoveries of 92, 51, and 79%, respectively; minimum quantities of the 4 compounds detectable in the 3 substrates averaged 0.12, 0.04, ajd 0.14 ppm, respectively. Stability studies indicate that rotenone reacts with animal chow with a half-life of 7--8 days and is photodegraded in incandescent light with a half-life of 0.65 day. No transplacental transfer of rotenone or its products was observed in fetuses from mice receiving 7 consecutive daily doses of rotenone at levels up to 25 mg/kg.

Animal Feed↗
PubMed1977

Trace analysis of estradiol in animal chow by electron-capture gas chromatography.

A gas chromatographic method is described for trace analysis of the natural steroidal hormone estradiol in animal chow at levels as low as 3 ppb. Salient elements of the method include extraction of the estradiol with methanol, an initial clean-up on a column of Sepadex LH-20, liquid-liquid partitioning at pH 14 and 10.2, additional cleanup on a slilica gel column, conversion of the estradiol to the pentafluoropropionly (PFP) derivative and analysis by electron-capture gas chromatography on a column of OV-25. Samples containing less than ppb of estradiol are subjected to further clean-up on silica gel after derivatization and prior to analysis.

Animal Feed↗