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M I Walters

Publications and source records attributed to M I Walters.

10 recordsLinked to original sources

Gentamicin/heparin interactions: effects on two immunoassays and on protein binding.

Heparin has been reported to have two different effects on gentamicin. One is the interference by heparin with the quantitation of gentamicin; the other is an increase in the bound fraction of gentamicin in the presence of serum. The reports conflict regarding what concentration of heparin causes these effects. The main objective of this study was to determine what effect heparin had on the determination of gentamicin using an enzyme immunoassay (EIA) or a fluorescence polarization immunoassay (FPIA). Heparin concentrations studied simulated the amounts that would be found in plasma when blood samples are collected with an evacuated heparinized tube (less than 30 U/ml), or the greater amounts that might be present when blood is collected from indwelling lines (100-200 U/ml). Heparin had no effect on the quantitation of gentamicin by FPIA. In measurements done by EIA, heparin had no effect at 28 U/ml but did significantly inhibit the reaction by 10-20% when its concentration was 100-200 U/ml. We studied the effects of heparin on the distribution equilibrium of gentamicin by measuring free gentamicin produced in an ultrafiltrate. It was found that the bound fraction increased as the heparin concentration increased. Our results with aqueous and serum-based samples suggest that the increased binding was the result of a direct binding of gentamicin to heparin, as well as a more complex interaction involving heparin, gentamicin, and proteins.

Drug Interactions

Changes in calcium distribution during therapeutic plasmapheresis.

Observations of normal persons indicated that there was a net shift of serum calcium from the ionized and protein-bound fractions to the anion-bound fraction when these persons received citrate during donor plasmapheresis. To confirm these findings and to extend them to diseased persons, we measured total, ionized, and ultrafilterable Ca concentrations in 11 patients who were undergoing therapeutic plasmapheresis. Anticoagulation was achieved with anticoagulant citrate dextrose solution. Mean concentrations of total, ionized, and protein-bound Ca decreased, whereas the ultrafilterable and anion-bound fractions increased. Our results suggest that protein-bound Ca may be relatively labile and may help to maintain constant levels of ionized Ca. Also, the observed increase in the anion-bound Ca level with citrate infusion suggests a shift from the protein-bound and ionized Ca fractions to this pool.

Adult

Rapid colorimetric assay for acetaminophen without salicylate or phenylephrine interference.

A simple rapid, and economical procedure is presented for the quantitative determination of acetaminophen in serum. Acetaminophen is extracted into solvent, and, when back-extracted into base, is simultaneously reacted with Folin-Ciocalteau reagent to form a colored complex. The potential interference of bilirubin is eliminated by treatment with p-diazobenzene sulfonic acid. Results obtained with this method agree with those obtained by "high-pressure" liquid chromatography.

Acetaminophen

Phenothiazines.

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Antipsychotic Agents

A simple and rapid method for the determination of thiocyanate in serum.

Studies were performed to evaluate ultrafiltration as a means for isolating thiocyanate from serum prior to its colorimetric determination as a ferric chloride complex. Recovery of thiocyanate from serum was enhanced by addition of alkali prior to preparation of the ultrafiltrate, and averaged 96.8%. The reproducibility (CV) of test was 2.3%, within-day; and 3.3%, between-day. The colorimetric reaction was linear to 100 micrograms/mL. The method was tested by determining thiocyanate concentrations in samples collected from smoking and nonsmoking individuals. Thiocyanate concentrations in patient samples, collected after IV-infusion of nitroprusside, were scattered around those of the general population, and ranged from 0.3 to 20 micrograms/mL.

Colorimetry