SAMPLING AND ASSAY DEVICE TOGETHER WITH METHODS FOR USE THEREOF

• US 20100055717A1
• Filed: 09/10/2009
• Published: 03/04/2010
• Est. Priority Date: 02/18/2004
• Status: Abandoned Application

• Current Assignee: ANI Biotech OY
• Original Assignee: ANI Biotech OY
• Inventors: Saramaki, Mika, Niskanen, Aimo
• Application Number:
  US12/557,248
• Publication Number:
  US 20100055717A1
• Time in Patent Office: Days
• US Class Current: 435/7.900
• CPC Class Codes: B01L 3/5029 using swabs
• CPC Class Codes: G01N 2001/028 Sampling from a surface, swabbing, vaporising
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387

Abstract

An immunochemical sampling device, kits including the sampling device, processes for production of the sampling device, and methods for use of the sampling device in lateral flow immunoassays. The sampling device comprises a solid support that is partially wrapped in a porous carrier, then covered in a hydrophobic cover. At its distal end, the porous carrier comprises a labeled binding reagent that is retained in the solid support until released into controlled flow with the liquid sample when the sampling device is brought into contact with a test strip.

Claims

1. An immunochemical method for use of a test strip having a test zone to determine the presence or absence of an analyte in a saliva sample which avoids saturation or contamination of the test zone by direct application of the sample thereto, the method comprising:

a) collecting saliva onto a sampling device, wherein the sampling device comprises;

i) a porous carrier disposed around a solid support under a wrapping torque from 0.05 and 0.5 Nm, wherein the carrier has a distal end containing a labeled binding reagent releasably bound to the porous carrier; and

ii) a hydrophobic cover disposed on and around the labeled binding reagent bound to the porous carrier, leaving the proximal end of the carrier exposed, wherein the hydrophobic cover includes vents of 0.1 to 0.5 mm in diameter that prevent the washing out of labeled binding reagent away from the covered portion of the carrier into the sample, but are sufficient in number and distribution across the cover to equalize the pressure within and without the porous carrier as sample fluid is applied thereto to control;

b) pressing the proximal end of the sampling device into fluid communicative contact with a test strip having immobilized binding reagents in a test zone, wherein the saliva sample is retained in the porous carrier until such contact is established, and released after it is established;

c) allowing sufficient time for the sample admixed with labeled binding reagent to migrate from the sampling device to the test zone; and

d) observing the test result at the test zone.

2. The method of claim 1, wherein the labeled binding reagent is bound to 1% to 50% of the surface area of the porous carrier.

3. The method of claim 1, wherein the labeled binding reagent is bound to 20% to 40% of the surface area of the porous carrier.

4. The method of claim 1, wherein the analyte is selected from the group consisting of antibodies, antigens, lectins, receptors, ligands, fragments thereof or combinations thereof.

5. The method of claim 1, wherein the label of the labeled binding reagent is selected from comprising colored latex, gold, metal, dye, fluorogenic substances, superparamagnetic substances, chromogenic substances, fluorochromogens or enzymatic labels.

6. An immunochemical method for use of a test strip having a test zone to determine the presence or absence of an analyte in a saliva sample which avoids saturation or contamination of the test zone by direct application of the sample thereto, the method comprising:

a) collecting saliva onto a sampling device, wherein the sampling device comprises;

i) a porous carrier disposed around a solid support under a wrapping torque from 0.05 and 0.5 Nm, wherein the carrier has a distal end containing a labeled binding reagent releasably bound to the porous carrier; and

ii) a hydrophobic cover disposed on and around the labeled binding reagent bound to the porous carrier, leaving the proximal end of the carrier exposed, wherein the hydrophobic cover includes vents of 0.1 to 0.5 mm in diameter that prevent the washing out of labeled binding reagent away from the covered portion of the carrier into the sample, but are sufficient in number and distribution across the cover to equalize the pressure within and without the porous carrier as sample fluid is applied thereto to control;

b) pressing the proximal end of the sampling device into fluid communicative contact with a test strip having immobilized binding reagents in a test zone, wherein the saliva sample is retained in the porous carrier until such contact is established, and released after it is established;

c) allowing sufficient time for the sample admixed with labeled binding reagent to migrate from the sampling device to the test zone; and

d) observing the test result at the test zone.

7. The method of claim 6, wherein the labeled binding reagent is bound to 1% to 50% of the surface area of the porous carrier.

8. The method of claim 6, wherein the labeled binding reagent is bound to 20% to 40% of the surface area of the porous carrier.

9. The method of claim 6, wherein the analyte is selected from the group consisting of antibodies, antigens, lectins, receptors, ligands, fragments thereof or combinations thereof.

10. The method of claim 6, wherein the label of the labeled binding reagent is selected from comprising colored latex, gold, metal, dye, fluorogenic substances, superparamagnetic substances, chromogenic substances, fluorochromogens or enzymatic labels.