IP Library Granted Patent US 7,419,796
Granted Patent B2
US 7,419,796 · App. 10/264,159 · Granted Sep 2, 2008

Method of making a test device

Assignee: Cornell Research Foundation
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,419,796
App. No.
10/264,159
Granted
Sep 2, 2008
Kind
B2
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 (22)

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.

Continuity (3)
Continuation 0960312600 · Jun 23, 2000
Provisional Application 6014057200 · Jun 23, 1999
Related Publication 20030104506A1 · Jun 5, 2003