Method of making a test device

• US 7,419,796 B2
• Filed: 10/02/2002
• Issued: 09/02/2008
• Est. Priority Date: 06/23/1999
• Status: Expired due to Fees

• Current Assignee: Cornell Research Foundation Incorporated (Cornell University)
• Original Assignee: Cornell Research Foundation Incorporated (Cornell University)
• Inventors: Siebert, Sui Ti Atienza, Martorell-Pena, Daniel, Durst, Richard A.
• Primary Examiner(s): NGUYEN, BAO THUY L
• Application Number:
  US10/264,159
• Publication Number:
  US 20030104506A1
• Time in Patent Office: 2,162 Days
• Field of Search: 436/518, 436/532, 436/829, 436/810, 424/9.321
• US Class Current: 435/7.92
• CPC Class Codes: G01N 33/54388 based on lateral flow
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: G01N 33/586 Liposomes, microcapsules or cells
• CPC Class Codes: Y10S 436/829 Liposomes, e.g. encapsulation

Abstract

The present invention relates to a method for making a test device for detecting or quantifying an analyte in a sample. This method involves contacting a membrane with a mixture including derivatized, marker-loaded liposomes, and substantially dehydrating the mixture on the membrane under vacuum pressure at a temperature of from about 4° C. to about 80° C., wherein said mixture further includes one or more sugars in an amount sufficient to promote the stability of the liposomes during dehydration and rehydration. The present invention also relates to a test device and method for detecting or quantifying an analyte in a sample. The test device includes a membrane which includes an immobilized liposome zone, wherein the immobilized liposome zone has bound thereto dehydrated, derivatized, marker-loaded liposomes dehydrated under vacuum pressure at a temperature of from about 4° C. to about 80° C. from a mixture which includes one or more sugars in an amount sufficient to promote the stability of the liposomes during dehydration and rehydration.

Claims

1. A method for making a test device for detecting or quantifying an analyte in a sample comprising:

providing a membrane with a sugar glaze on its outer surface,

contacting the sugar glazed membrane with a mixture comprising derivatized, marker-loaded liposomes,

substantially dehydrating the mixture on the membrane under vacuum pressure at a temperature of from about 4°

C. to about 80°

C., and

immobilizing a first binding material specific for the analyte in a capture zone on the membrane.

2. The method according to claim 1, wherein the derivatized, marker-loaded liposomes are derivatized with an analyte analog.

3. The method according to claim 1, wherein the marker is a fluorescent dye, a visible dye, a bioluminescent material, a chemiluminescent material, an enzymatic substrate, a radioactive material, or an electrochemical marker.

4. The method according to claim 1, wherein the membrane is an absorbent material.

5. The method according to claim 4, wherein the absorbent material is nitrocellulose, glass fiber, woven fabric, nylon, nonwoven material, polyester fabric, rayon, cellulose rayon blend, mixed fiber of cellulose and glass, or polyethersulfone.

6. The method according to claim 1, further comprising:

blocking the membrane in its entirety with one or more blocking agents at a concentration that prevents lysis of derivatized, marker-loaded liposomes during dehydration and rehydration.

7. The method according to claim 6, wherein the blocking agent is selected from the group consisting of polyvinylpyrrolidone, gelatin, non-fat dry milk, bovine serum albumin, casein, gum arabic, and mixtures thereof.

8. The method according to claim 1, wherein the dehydrating is carried out at a temperature of from about 4°

C. to about 50°

C.

9. The method according to claim 1, wherein the sugar is selected from the group consisting of sucrose, trehalose, maltose, glucose, lactose, and mixtures thereof.

10. A test device for detecting or quantifying an analyte in a sample comprising:

a sugar glazed membrane which comprises an immobilized liposome zone, wherein the immobilized liposome zone has bound thereto dehydrated, derivatized, marker-loaded liposomes and a capture zone having a first binding material specific for the analyte bound thereto.

11. The test device according to claim 10, wherein the marker is a fluorescent dye, a visible dye, a bioluminescent material, a chemiluminescent material, an enzymatic substrate, a radioactive material, or an electrochemical marker.

12. The test device according to claim 10, wherein the membrane is an absorbent material.

13. The test device according to claim 12, wherein the absorbent material is nitrocellulose, glass fiber, woven fabric, nylon, nonwoven material, polyester fabric, rayon, cellulose rayon blend, mixed fiber of cellulose and glass, or polyethersulfone.

14. The test device according to claim 10, wherein sugar is selected from the group consisting of sucrose, trehalose, maltose, glucose, lactose, and mixtures thereof.

15. A test device according to claim 10, further comprising:

one or more blocking agents blocking the membrane in its entirety at a concentration that prevents lysis of derivatized, marker-loaded liposomes during dehydration and rehydration.