IP Library Granted Patent US 7,547,526
Granted Patent B2
US 7,547,526 · App. 11/081,378 · Granted Jun 16, 2009

Cell concentration and pathogen recovery

Assignee: Purdue Research Foundation
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Quick Facts
Patent No.
US 7,547,526
App. No.
11/081,378
Granted
Jun 16, 2009
Kind
B2
Abstract

Methods and kits for the isolation of organisms. Such methods and kits are particularly useful for concentrating and recovering viable organisms from food material. The recovered organisms are of sufficient number and purity to allow detection using a biochip device.

Claims (29)

1. A method of rapid concentration and recovery of viable microorganisms from a sample, the method comprising:

(a) providing a microorganism-containing sample, the sample comprising a liquid component having a first volume;

(b) providing a hollow fiber filter comprising at least one hollow fiber strand, wherein the hollow fiber filter comprises fibers having a length between 1 cm and 25 cm;

(c) reducing the first volume of the liquid component by applying the sample to the hollow fiber filter, wherein the volume is reduced by at least 1000 times;

(d) back flushing the microorganisms from the hollow fiber filter to remove the microorganisms from the hollow fiber filter without vortexing and in a buffer having a second volume;

(e) delivering the second volume and the microorganisms from the hollow fiber filter to a biochip device; and

(f) detecting the presence of viable microorganisms using the biochip device.

2. The method of claim 1 comprising culturing the microorganisms in the biochip to detect the presence of viable microorganisms.

3. The method of claim 1 wherein detecting the viable microorganisms comprises measuring the change in impedance in the biochip device.

4. The method of claim 1 wherein the hollow fiber filter comprises fibers having an average pore size of less than 0.5 μm.

5. The method of claim 1 further comprising flowing the sample through a first filter.

6. The method of claim 5 wherein the first filter comprises an average pore size of 2 μm to 20 μm.

7. The method of claim 6 , wherein the first filter comprises a rolled stationary phase filter or a membrane.

8. The method of claim 1 , wherein (a) to (d) are performed in less than 60 minutes.

9. The method of claim 1 , wherein (a) to (d) are performed in 30 minutes or less.

10. The method of claim 1 , wherein the microorganisms are selected from the group of bacteria, fungi and protozoans.

11. The method of claim 1 , further comprising treating the sample to provide the liquid component using one or more of the treatments selected from the group consisting of diluting, blending, chopping, centrifuging, filtering, enzyme treating, massaging and contacting the sample with a positively-charged or negatively-charged membrane or particles.

12. The method of claim 1 wherein the hollow fiber filter comprises fibers comprising polysulfone.

13. The method of claim 1 , further comprising treating the hollow fiber filter with a blocking solution prior to reducing the volume of the liquid component.

14. The method of claim 13 , wherein the blocking solution comprises a concentration of polyoxyethylene sorbitan monolaureate between 0.001 percent and 1.0 percent.

15. The method of claim 1 , wherein the concentration and recovery of the viable micro-organisms is manually performed.

16. A method of rapid concentration and recovery of viable microorganisms from a sample, the method comprising:

(a) providing a microorganism-containing sample, the sample comprising a liquid component;

(b) providing a hollow fiber filter, comprising at least one hollow fiber strand, the fiber having an average pore size of less than 0.5 μm and a length of between 1 cm and 25 cm;

(c) reducing a volume of the liquid component by flowing the sample through the hollow fiber filter, wherein the volume is reduced by at least 1000 times;

(d) recovering viable microorganisms from the hollow fiber filter without vortexing by back flushing the microorganisms from the hollow fiber filter in a buffer having a reduced volume, the buffer being suitable for delivery to a biochip device;

(e) flowing the buffer containing the recovered viable microorganisms into the biochip device; and

(f) detecting the presence of the viable microorganisms using the biochip device.

17. The method of claim 16 , wherein (a) to (f) are performed in less than 8 hours.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2006
From: PURDUE UNIVERSITY
To: PURDUE RESEARCH FOUNDATION
Reel/Frame 018491/0450 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2005
From: LADISCH, MICHAEL R.; LIU, XINGYA; STEWART, AMANDA C.; CHEN, WAN-TZU; MOSIER, NATHAN S.; HUANG, THOMAS; BWATWA, JEREMIAH; HENDRICKSON, RICHARD
To: PURDUE UNIVERSITY
Reel/Frame 016774/0087 →
Continuity (2)
Provisional Application 6055323500 · Mar 15, 2004
Related Publication 20050244943A1 · Nov 3, 2005