Test device and kit for detecting helicobacter pylori

• US 5,420,016 A
• Filed: 02/18/1994
• Issued: 05/30/1995
• Est. Priority Date: 03/24/1992
• Status: Expired due to Fees

• Current Assignee: Serim Research Corporation
• Original Assignee: Serim Research Corporation
• Inventors: Boguslaski, Robert C., Carrico, Robert J.
• Primary Examiner(s): Beisner, William H.
• Assistant Examiner(s): GITOMER, RALPH J
• Application Number:
  US08/198,236
• Time in Patent Office: 466 Days
• Field of Search: 422/56, 422/57, 422/58, 422/60, 422/61, 435/10, 435/12, 435/34, 435/805, 435/810, 436/169, 436/808, 436/810
• US Class Current: 435/12
• CPC Class Codes: C12Q 1/04 Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor C12Q1/6897 takes precedence
• CPC Class Codes: C12Q 1/58 involving urea or urease
• CPC Class Codes: G01N 2333/205 from Campylobacter (G)
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10S 436/811 Test for named disease, body condition or organ function

Abstract

A rapid method and easy to use unitized test device is disclosed for determining the presence of Helicobacter pylori in a biological tissue specimen by detecting the presence of urease in the tissue. The system basically utilizes a multilayer test device for separating and optimizing the various reactions involved, i.e. the urease in the specimen with a substrate and the ammonia generated thereby with an indicator element.

Claims

1. A multilayer test device for detecting urease in biological tissue specimens comprising:

A. a substrate element comprising a matrix containing a substrate for urease;

B. a diffusion element comprising a membrane permeable to ammonia and impermeable to water;

C. an indicator element comprising a matrix containing a means for detecting ammonia, the indicator element being in contiguous relationship with the diffusion element;

D. wherein a predetermined quantity of sulfamic acid sufficient to react with ammonia to produce a desired sensitivity is present in the indicator element or the diffusion element; and

E. means for placing and maintaining a biological tissue specimen between the substrate element and the diffusion element.

2. The device of claim 1 wherein the substrate element contains urea.

3. The device of claim 2 wherein the substrate element matrix is absorbent paper.

4. The device of claim 1 wherein the substrate element includes a buffer to maintain the pH of the matrix in a pH range of from about 7.0 to 9.0.

5. The device of claim 1 wherein the means for placing and maintaining a biological tissue specimen between the substrate element matrix and the diffusion element is a support member comprising a clear plastic foil on which the substrate element matrix and the diffusion element are placed in a side by side relationship such that when a biological tissue specimen is placed on the diffusion element, the substrate element may be folded over including the specimen therebetween.

6. The device of claim 1 wherein the means for detecting ammonia is a pH sensitive dye having a pKa of about from 2.0 to 8.0.

7. The device of claim 1 wherein the diffusion element is a membrane having a pore size of about from 0.05 to 10 microns.

8. The device of claim 1 wherein a predetermined amount of urease is placed on the diffusion element and acts as a positive control for the test device.

9. A test kit for detecting urease in biological tissue specimens comprising:

A. an aqueous rehydrating solution;

B. a buffer having a pH of about from 7.0 to 9.0;

C. a substrate element comprising a matrix having therein a dried residue of urea;

D. a diffusion element comprising a membrane permeable to ammonia and impermeable to water;

E. an indicator element comprising a matrix containing a dried residue of a pH indicator having a pKa of about from 2.0 to 6.0 for detecting ammonia, the indicator element being in contiguous relationship with the diffusion element;

F. wherein a predetermined quantity of sulfamic acid sufficient to react with ammonia to produce a desired sensitivity is present in the indicator element or the diffusion element; and

G. means for placing and maintaining a biological specimen between the substrate element and the diffusion element whereby any urease in the biological specimen will react with the urea to generate ammonia which will permeate the diffusion membrane and be detected by the indicator element.

10. A test kit as in claim 9 wherein the substrate element matrix and the indicator element are attached to a common support member in a side by side relationship allowing one to be folded over onto the other.

11. A test kit as in claim 10 wherein the kit contains a holder or clamp for the common support member to be retained in a folded position.

12. A test kit as in claim 9 wherein urease is positioned on the diffusion element apart from the biological specimen position which urease acts as a positive control for the test kit.

13. A test kit as in claim 9 wherein the aqueous rehydrating solution and the buffer are combined to form a common solution.

14. A test kit as in claim 9 wherein the buffer is contained in the substrate element.

15. A test kit as in claim 9 wherein a predetermined amount of urease is placed on the diffusion element and acts as a positive control for the test kit.