A quantitative procedure for the analysis of volatile organic acids and lactic acid in silage is described. The samples were extracted with diethyl ether, derivatized by t-butyldimethylsilylation, and then separated by capillary gas chromatography. The same procedure was useful for the identification by gas chromatography/mass spectrometry of organic acids in samples such as the metabolic fermentation products of anaerobic bacteria.
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) is shown to give inaccurate results for the analysis of low molecular weight ethoxylate polymers. It is demonstrated that when the degree of ethoxylation is low (n < 9), MALDI-TOFMS produces substantially higher values for the number-average molecular weight (M n ) than obtained with more classical methods such as NMR spectrometry and a wet chemical method to determine the hydroxyl number. Apparently, this is the result of discrimination of the former technique against lower molecular weight ethoxylates in a polymer distribution. The results presented in this paper demonstrate this discrimination through the analysis of a series of ethoxylates with progressively lower M n values. It was also found that by derivatization of the polymer with phthalic anhydride, to produce the carboxylate derivative, the discrimination is reduced and data obtained with MALDI-TOFMS match more precisely the results obtained with the other methods.
Indicine-N-oxide was analyzed by gas chromatography mass spectrometry with nanogram sensitivity after trimethylsilylation. Two different products were produced by altering the conditions of this reaction. Mass spectral evidence is presented to show that one of these was the expected trisubstituted pyrrolizidine product while the other was a trisubstituted pyrrole. The latter derivative is useful for distinguishing between indicine-N-oxide and indicine which dies not form this novel product under the same conditions. Analogous pyrrole and pyrrolizidine products were formed from heliotrine-N-oxide, a compound that can serve as an internal standard from measuring indicine-N-oxide and its metabolites in biological samples. A method for purifying such samples by strong cation exchange chromatography prior to derivatization is also discussed.
Phenytoin pharmacokinetics and biotransformation were studied with stable isotope tracer techniques in six patients before and after addition of phenobarbital. No significant (p less than 0.05) changes in phenytoin serum concentration, clearance, elimination half-life, volume of distribution, or clearance via production of p-hydroxyphenyl-phenylhydantoin or phenytoin dihydrodiol occurred after addition of phenobarbital. Thus, frequent phenytoin serum concentration determinations or a change in phenytoin dosing rate are probably not necessary after adding phenobarbital.
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