JOHN PALMER
Barber in Philadelphia, PA

5032506, Jul 16, 1991

Dec 16, 1986

6/942414

John L. Palmer - Philadelphia PA
Marsha W. Timmerman - Allentown PA

Enzymatics, Inc. - Horsham PA

C12Q 132, C12Q 126, C12N 1112

435 26

An assay system useful for the determination of NAD(P)H, NAD(P), or a substrate of an enzyme which reacts with the formation or comsumption of NAD(P)H. Concentrations of organic substrates for example alcohol, cholesterol, uric acid, in a biological fluid such as saliva, blood or urine may be determined. The system includes a diaphorase which catalyzes a NAD(P)H-dependent reduction of a chromogen to cause a visible color change; this color change is indicative of the concentration sought to be determined. The system includes a chromogen which is a first substrate for the diaphorase which causes a color change when reduced by NAD(P)H, and a second substrate which is a competing substrate for the diaphorase; the competing substrate is irreversibly reduced by the diaphorase. The system is capable of measuring colorimetrically without dilution concentrations of organic compounds in biological fluids which previously could not be measured in such concentration. The system provides a convenient, practical sobriety test.

5278079, Jan 11, 1994

Sep 2, 1992

7/939707

Julian Gubinski - Jamison PA
John L. Palmer - Philadelphia PA

Enzymatics, Inc. - Horsham PA

G01N 3122, B01L 1100

436165

A channel or chamber device having means for inhibiting flow of aqueous medium therein after the channel or chamber has been filled with aqueous medium. The device has a channel or chamber with a sample intake port at one end and an exhaust port at the other end. A restricted or reduced size chamber portion having reduced dimension (height, cross-sectional area or diameter) toward the exhaust port is provided with a water-expandable polymer in the restricted or reduced size chamber portion. The water-expandable polymer inhibits flow or forms a seal in the exhaust port when the polymer is contacted with an aqueous medium. The channel or chamber device having means for inhibiting flow of aqueous medium therein is especially adaptable to capillaries used in medical diagnostic measuring devices which contain an analytical reagent for biological fluids, such as saliva and plasma.

5036000, Jul 30, 1991

Jul 20, 1987

7/075817

John L. Palmer - Philadelphia PA
Marsha W. Timmerman - Allentown PA

Enzymatics, Inc. - Horsham PA

C12Q 132, C12Q 154, C12M 140

435 26

A system for quantitative colorimetric analysis of biological fluids or organic compounds, including NAD(P)H, or a substrate of an enzyme which reacts with the formation or consumption of NAD(P)H. Concentrations of organic substrates for example alcohol, cholesterol, uric acid, in a biological fluid such as saliva, blood or urine may be determined. The system gives a digital reading of the organic material the concentration which is sought to be determined; the concentration of NAD(P)H is determined by a color change or color "signal" when the NAD(P)H is above a threshold concentration and by the absence of a color signal when the concentration of NAD(P)H is below the threshold concentration. The system includes a chromogen, an electron-accepting reactant which, until exhausted, prevents a visible color change due to accumulation of reduced chromogen, and a catalyst. The system is capable of measuring colorimetrically without dilution concentrations of organic compounds in biological fluids which previously could not be measured in such concentration.

5112741, May 12, 1992

Jul 7, 1988

7/216008

John L. Palmer - Philadelphia PA
Marsha W. Timmerman - Allentown PA
Stephan D. Daubney - Allentown PA

Enzymatics, Inc. - Horsham PA

C12Q 126

435 25

The invention provides a reagent system for the enzymatic determination of an oxidizable substrate in a fluid sample; the system includes an active amine trap for inactivating high concentrations of aldehyde and ketone oxidation products comprising a combination of at least one primary amine and at least one alpha-effect amine. An example of the oxidizable substrate is alcohol.