American Monitor Corporation

Jerry W Denney

Robert L Long

Mark C Outcalt

An improved assay method and reagent composition for the determination of magnesium in a fluid sample by reaction with an alkaline buffered solution of calmagite, in which caffeine and preferably also thiourea have been included, thereby achieving parity between protein-free and protein-containing samples while eliminating the need for cyanide.

Assay method and reagent composition for the determination of magnesium

A colorimetric assay method and stabilized working reagents for the determination of magnesium in which an alkaline reagent containing a dye to complex magnesium reacts directly with the sample, requiring no protein-removal steps and no addition of substances to artificially correct for absorption differences of the metallized and free dye due to the presence of protein. The dye is either Calmagite or Eriochrome Black T. The reagent is buffered so that the pH is greater than about 9.0; the relative Van Slyke buffer value .beta.' of the reagent is greater than 1.

Magnesium assay with calmagite or eriochrome black T reagents

An improved triglyceride assay and reagent system which provides the introduction of iron into a reaction mixture in which glycerol from hydrolyzed triglycerides is coupled to a NAD/NADH indicator system, and measuring the resultant change of the oxidation state of the iron by use of an iron chelator, thereby improving the sensitivity and performance of the assay.

Triglycerides assay and reagents therefor

The discovery of 9-(2-pyridyl)-acenaphtho[1,2-e]-as-triazine and its sulfonated form, having particular advantages when used as both a chelator and indicator of ferrous ions in organic or aqueous mediums; a process for the synthesis of those compounds in which hydrazine is used as both a reactant and as a solvent in production of intermediate compounds, eliminating the need of ethanol and the disadvantageous ether-extraction step; the use of N,N-dimethylformamide as a reaction solvent in the production of triazines; the use of the new triazine compounds to measure iron, transferrin, and UIBC/TIBC in biological systems; the use of dimethylsulfoxide and certain processes to eliminate the interferences commonly encountered in these assays; and the use of the triazine compounds to measure both total and/or reduced iron in a variety of matrices.

Assay of iron and iron binding protein reagents and methods

The discovery of 9-(2-pyridyl)-acenaphtho[ 1,2-e]-as-triazine and its sulfonated form, having particular advantages when used as both a chelator and indicator of ferrous ions in organic or aqueous mediums; a process for the synthesis of those compounds in which hydrazine is used as both a reactant and as a solvent in production of intermediate compounds, eliminating the need of ethanol and the disadvantageous ether-extraction step; the use of N,N-dimethylformamide as a reaction solvent in the production of triazines; the use of the new triazine compounds to measure iron, transferrin, and UIBC/TIBC in biological systems; the use of dimethylsulfoxide and certain processes to eliminate interferences commonly encountered in these assays; and the use of the triazine compounds to measure both total and/or reduced iron in a variety of matrices.

9-(2-Pyridyl)-acenaphtho[1,2-e]-as-triazines

Urea assay or analysis process and reagents therefor, in which the assay involves a reaction between a sample of biological fluid and an acidic reagent solution of o-phthaldehyde and a chromogenic compound; the chromogenic compounds include certain substituted benzene compounds, certain substituted naphthalene compounds, certain aminopyrimidines, certain substituted quinolines, certain morpholino substituted quinolines and certain morpholino substituted naphthalenes.

Urea assay

An alkaline picrate reagent system useful for the quantitation of creatinine in biological fluids. Interference from constituents normally found in serum or urine is eliminated by the use of dimethylsulfoxide with preferably an aralkane detergent in combination with a kinetic or reaction rate analysis mode. It obviates the need for any pretreatment of the sample, and avoids the need of other chemicals in the system which if allowed to contaminate glassware would have a deleterious effect on other analyses performed in the laboratory.

Creatinine assay and reagent system

A urea assay or analysis process and reagents therefor, in which the assay involves a reaction between a sample of biological fluid and an acidic reagent solution of o-phthaldehyde and a chromogenic compound; the chromogenic compounds include certain substituted benzene compounds, certain substituted naphthalene compounds, certain aminopyrimidines, certain substituted quinolines, certain morpholino substituted quinolines and certain morpholino substituted naphthalenes.

Growing community of inventors

Carmel, IN, United States of America

Jerry W Denney