IP Library › Patent Application 16405056
Patent Application
App. No. 16/405,056

RAPID MICROBIAL DETECTION

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Quick Facts
Patent No.
US None
App. No.
16/405,056
Abstract

Devices and methods are provided to detect the presence of bacteria and small microorganisms, and to identify various microbial attributes rapidly.

Claims (33)

1 . A method of processing within a microfluidic device a sample that includes microorganisms and non-microbial cells, the method comprising:

selectively lysing material including non-microbial cells to form lysed debris within the sample while leaving intact microorganisms within the sample.

2 . The method of claim 1 , further comprising:

separating and removing lysed debris from non-lysed and intact microorganisms within the sample.

3 . The method of claim 1 , further comprising:

identifying the intact microorganisms within the sample.

4 . The method of claim 2 , further comprising:

identifying the intact microorganisms within the sample.

5 . The method of claim 2 , further comprising collecting lysed debris separated from the sample in a waste collection stage of the microfluidic device.

6 . The method of claim 2 , wherein the separating and removing lysed debris from non-lysed and intact microorganisms within the sample occurs without using a nucleotide, an antibody, or other ligand or reagent that specifically recognizes and binds to a microorganism.

7 . The method of claim 1 , wherein the microorganisms are selected from the group consisting of bacteria, fungi, and small unicellular and multicellular organisms.

8 . The method of claim 1 , wherein the microorganisms are selected from the group of genera consisting of Staphylococcus, Escherichia, Listeria, Salmonella, Streptococcus, Klebsiella and Campylobacter.

9 . The method of claim 1 , wherein the sample is a liquid selected from the group consisting of whole blood, plasma, serum, saliva, urine, cerebrospinal fluid, water, and fruit and vegetable juices.

10 . The method of claim 1 , wherein the sample is selected from the group consisting of meat, produce, processed food, dairy products, poultry products, pharmaceutical process streams, bulk drug substance, and final drug product.

11 . The method of claim 1 , wherein the sample has a volume ranging from about 0.1 mL to about 10 mL.

12 . The method of claim 3 , wherein the identifying intact microorganisms within the sample comprises:

subjecting the sample to infrared spectrometric analysis utilizing a detector; and

determining a presence of intact microorganisms within the sample based upon the infrared spectrometric analysis.

13 . The method of claim 12 , wherein the identifying intact microorganisms within the sample further comprises:

determining a species of one or more intact microorganisms within the sample based upon the infrared spectrometric analysis.

14 . The method of claim 12 , wherein the determining a species of one or more intact microorganisms within the sample further comprises:

providing data associated with the infrared spectrometric analysis to a computer device for determination of the species of the one or more intact microorganisms.

15 . The method of claim 12 , wherein the determining a species of one or more intact microorganisms within the sample further comprises:

comparing spectral data obtained from the infrared spectrometric analysis with spectral data from a database; and

identifying the species of the microorganism based upon the comparing.

16 . The method of claim 3 , further comprising:

prior to identifying the intact microorganisms within the sample, concentrating the microorganisms in the sample via reducing a volume of the sample and/or filtration of the sample.

17 . The method of claim 1 , wherein the selective lysing is achieved by passing the sample through stationary microporous surfaces.

18 . The method of claim 17 , wherein the microporous surfaces include pores having diameters from 1 micrometer to 10 micrometers.

19 . The method of claim 1 , wherein the selective lysing is achieved by passing the sample through a porous monolithic structure including microporous surfaces.

20 . The method of claim 1 , further comprising, prior to the selective lysing, separating and removing from the sample components that are larger in size than microorganisms within the sample.

21 . The method of claim 20 , wherein the separation and removal from the sample components that are larger in size than microorganisms within the sample comprises passing the sample through a channel having a spiral path within the microfluidic device.

22 . The method of claim 20 , wherein the separation of lysed debris from non-lysed and intact microorganisms within the sample comprises passing the sample through a linear array of posts within the microfluidic device to separate, via deterministic lateral displacement (DLD), lysed debris from the sample while maintaining the microbial cells of interest within the sample.