Sampling devices and methods for concentrating microorganisms

US9328325B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9328325-B2
Application numberUS-200913142288-A
CountryUS
Kind codeB2
Filing dateDec 30, 2009
Priority dateDec 31, 2008
Publication dateMay 3, 2016
Grant dateMay 3, 2016

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present disclosure describes methods for concentrating microorganisms with concentration agents in a sampling device and the sampling device described herein. More specifically, methods for concentrating microorganisms from large volume samples with concentration agents in a sampling device can provide for rapid, low cost, simple (involving no complex equipment or procedures), and/or effective processes under a variety of conditions.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for concentrating microorganisms comprising the steps of: providing a sampling device comprising: a body comprising a first opening at a first end a second opening at a second end opposite the first end; a first reservoir disposed between the first end and the second end; and a rotatable feature disposed in the body between the reservoir and the second opening; wherein the rotatable feature comprises a second reservoir; wherein the rotatable feature is configured to place the second reservoir into liquid communication with the first reservoir or with the second opening; wherein the second reservoir is configured such that it cannot be in simultaneous liquid communication with both the first reservoir and the second opening; mixing a concentration agent with a sample comprising a microorganism in the first reservoir to provide a microorganism bound composition; and isolating the microorganism bound composition from the first reservoir by rotating the rotatable feature. 2. The method of claim 1 , wherein mixing a concentration agent with a sample comprises mixing a concentration agent selected from the group consisting of particles with affinity ligands, particles without affinity ligands, antibodies or antigen binding fragments, receptors and combinations thereof. 3. The method of claim 1 , wherein mixing a concentration agent with a sample further comprises mixing a buffer with the concentration agent and the sample. 4. The method of claim 1 , wherein the mixing step further comprises mixing a detection agent and a growth medium with the concentration agent and the sample. 5. A sampling device comprising: a body comprising a first opening at a first end a second opening at a second end opposite the first end; a first reservoir disposed between the first end and the second end; and a rotatable feature disposed in the body between the reservoir and the second opening; wherein the rotatable feature comprises a second reservoir; wherein the rotatable feature is configured to place the second reservoir into liquid communication with the first reservoir or with the second opening; wherein the second reservoir is configured such that it cannot be in simultaneous liquid communication with both the first reservoir and the second opening. 6. The sampling device of claim 5 , wherein the first reservoir further comprises a first volume and the second reservoir further comprises a second volume, wherein a ratio of the first volume to the second volume is in a range of about 10:1 to about 1000:1. 7. The sampling device of claim 5 , further comprising a concentration agent disposed in the first reservoir, wherein the concentration agent is selected from the group consisting of particles with affinity ligands, particles without affinity ligands, antibodies or antigen binding fragments, receptors and combinations thereof. 8. The sampling device of claim 5 , further comprising a detection agent and a growth medium. 9. The sampling device of claim 7 , wherein the concentration agent comprises a dispersible or particulate agent. 10. The sampling device of claim 7 , wherein the concentration agent comprises gamma-FeO(OH). 11. The sampling device of claim 7 , wherein the concentration agent comprises metal silicates. 12. The sampling device of claim 7 , wherein the concentration agent comprises diatomaceous earth. 13. The sampling device of claim 7 , wherein the concentration agent comprises surface treated diatomaceous earth, the surface treatment selected from the group consisting of titanium dioxide, nanoscale gold, nanoscale platinum and combinations thereof.

Assignees

Inventors

Classifications

  • by adsorption or absorption · CPC title

  • C12M47/02Primary

    Separating microorganisms from the culture medium; Concentration of biomass (separating microorganisms from their culture media C12N1/02) · CPC title

  • filtration · CPC title

  • G01N1/40Primary

    Concentrating samples · CPC title

  • C12Q1/24Primary

    Methods of sampling, or inoculating or spreading a sample; Methods of physically isolating an intact microorganisms · CPC title

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What does patent US9328325B2 cover?
The present disclosure describes methods for concentrating microorganisms with concentration agents in a sampling device and the sampling device described herein. More specifically, methods for concentrating microorganisms from large volume samples with concentration agents in a sampling device can provide for rapid, low cost, simple (involving no complex equipment or procedures), and/or effect…
Who is the assignee on this patent?
Kshirsagar Manjiri T, Halverson Kurt J, Percy Neil, and 2 more
What technology area does this patent fall under?
Primary CPC classification C12M47/02. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 03 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).