Multilayer analytical element containing primary amine buffer and method for the determination of ethanol

• US 5,416,004 A
• Filed: 01/19/1993
• Issued: 05/16/1995
• Est. Priority Date: 01/19/1993
• Status: Expired due to Term

• Current Assignee: Clinical Diagnostic Systems Inc.
• Original Assignee: Clinical Diagnostic Systems Inc.
• Inventors: Detwiler, Richard L.
• Primary Examiner(s): Wityshyn, Michael G.
• Assistant Examiner(s): Leary, Louise N.
• Application Number:
  US08/005,683
• Time in Patent Office: 847 Days
• Field of Search: 435/26, 435/25, 435/16, 435/17, 435/14, 435/4, 436/170, 436/132, 436/131, 436/164, 422/56, 422/60, 422/68.1
• US Class Current: 435/26
• CPC Class Codes: G01N 2800/307 Drug dependency, e.g. alcoholism
• CPC Class Codes: G01N 33/4972 Determining alcohol content for vehicle safety devices B60K28/06
• CPC Class Codes: G01N 33/526 the element being adapted for a specific analyte
• CPC Class Codes: G01N 33/98 involving alcohol, e.g. ethanol in breath
• CPC Class Codes: Y10T 436/203332 Hydroxyl containing
• CPC Class Codes: Y10T 436/204165 Ethanol

Abstract

A multilayer analytical element has been prepared for accurate and rapid colorimetric determination of ethanol in aqueous specimens using alcohol dehydogenase and an oxidized nicotinamide coenzyme. The element includes three reagent layers beneath a porous spreading layer. The middle reagent layer has a crosslinked hydrophilic binder, while the other two reagent layers have uncrosslinked binders. In addition, both uncrosslinked reagent layers include a relatively high amount of a buffer having a primary amine, which buffer maintains the layer pH at from about 8 to about 10. Alcohol dehydrogenase is in the reagent layer next to the porous spreading layer.

Claims

1. An analytical element for the determination of ethanol comprising a support having thereon, in order and in fluid contact:

a) a first reagent layer containing a buffer having a primary amine mixed with an uncrosslinked hydrophilic binder, said buffer maintaining the pH at from about 8 to about 10 during an assay for ethanol and being present in an amount of at least about 25 mmoles/m²,

b) a second reagent layer comprising a crosslinked hydrophilic binder,

c) a third reagent layer comprising alcohol dehydrogenase and a buffer present in an amount of at least about 25 mmoles/m² mixed with an uncrosslinked hydrophilic binder, said buffer being the same as that in said first reagent layer and maintaining the pH at from about 8 to about 10, and

d) a porous spreading layer containing an oxidized nicotinamide coenzyme.

2. The element of claim 1 wherein said hydrophilic binder in each of said reagent layers is gelatin.

3. The element of claim 1 wherein said buffer in said first and third reagent layers is tris(hydroxymethyl)aminomethane, tris(methyl)aminomethane and their acid forms or tris(hydroxymethyl)aminomethane glutamate.

4. The element of claim 1 wherein said buffer in said first and third reagent layers is tris(hydroxymethyl)aminomethane or tris(hydroxymethyl)aminomethane hydrofluoride.

5. The element of claim 1 wherein said porous spreading layer is formed from a blush polymer.

6. The element of claim 1 further comprising a subbing layer between said third reagent layer and said porous spreading layer.

7. The element of claim 1 wherein said nicotinamide coenzyme is nicotinamide adenine dinucleotide.

8. The element of claim 1 wherein the amount of buffer in each of said first and third reagent layers is from about 30 to about 50 mmoles/m².

9. A method for the detection of ethanol comprising:

A) contacting an aqueous fluid suspected of containing ethanol with an analytical element comprising a support having thereon, in order and in fluid contact;

a) a first reagent layer containing a buffer having a primary amine mixed with an uncrosslinked hydrophilic binder, said buffer maintaining the pH at from about 8 to about 10 during an assay for ethanol and being present in an amount of at least about 25 mmoles/m²,

b) a second reagent layer comprising a crosslinked hydrophilic binder,

c) a third reagent layer comprising alcohol dehydrogenase and a buffer present in an amount of at least about 25 mmoles/m² mixed with an uncrosslinked hydrophilic binder, said buffer being the same as that in said first reagent layer and maintaining the pH at from about 8 to about 10, and

d) a porous spreading layer containing an oxidized nicotinamide coenzyme, and

B) detecting the absorbance of the reduced form of said nicotinamide coenzyme as an indication of the presence of ethanol in said aqueous fluid.

10. The method of claim 9 wherein the detecting step B) is carried out within about 5 minutes of the contacting step A).

11. The method of claim 9 wherein said aqueous fluid is human whole blood, serum or plasma.

12. The method of claim 9 wherein ethanol is detected from measuring the absorbance of the reduced form of nicotinamide adenine dinucleotide.

13. The method of claim 9 wherein during which said element is maintained at a pH of from about 8.5 to about 9.