Analyte detection using liquid crystals
Devices and methods for using changes in the defects in micrometer sized dispersed liquid crystal domains to detect or quantify analytes in a test sample, including endotoxin lipopolysaccharide (LPS), are disclosed. The dispersed liquid crystal microdomains are exposed to the test sample, and any changes in the number of defects in the liquid crystal microdomains are detected by detecting changes in the anchoring configuration of the microdomains. Such changes in anchoring configuration indicate the presence of analyte in the test sample.
1. A method for detecting an analyte in a test sample having an analyte concentration of less than 1 μg/ml, comprising:
(a) contacting one or more liquid crystal microdomains having two point defects and a minor axis of between about 0.5 mm and about 200 mm with a test sample having an analyte concentration of less than 1 μg/ml; and
(b) determining the number of point defects in the one or more liquid crystal microdomains after performing the contacting step (a);
wherein a reduction in the number of point defects from two to one in at least one of the one or more liquid crystal microdomains indicates the presence of the analyte in the test sample.
2. The method of claim 1 , wherein the number of point defects in the one or more liquid crystal microdomains is determined by detecting an anchoring configuration of the one or more liquid crystal microdomains.
3. The method of claim 1 , wherein the test sample is an aqueous test sample.
4. The method of claim 1 , wherein the analyte is endotoxin lipopolysaccharide (LPS) or lipid A.
5. The method of claim 2 , wherein the step of detecting an anchoring configuration of the one or more liquid crystal microdomains is performed by one or more of the group consisting of optical imaging, fluorescence imaging, optical imaging using polarized light, polarized light microscopy, bright field microscopy, fluorescence microscopy, light scattering measurement, flow cytometry, fluorescence flow cytometry, microelectrophoresis, dielectrophoresis, measurement of electrical capacitance, measurement of magnetic properties, measuring turbidity, detecting optical reflection, detecting transmittance of light, visual inspection, using a plate reader, using microwell plates, and using a cuvette in a detector.
6. The method of claim 1 , wherein the one or more liquid crystal microdomains having two point defects include a plurality of dispersed liquid crystal microdomains.
7. The method of claim 6 , further comprising using the determined number of point defects in the plurality of liquid crystal microdomains to quantify the analyte present in the sample.
8. The method of claim 7 , wherein the analyte is endotoxin lipopolysaccharide (LPS) or lipid A.
9. The method of claim 6 , wherein the plurality of dispersed liquid crystal microdomains are liquid crystal droplets dispersed within a water emulsion.
10. A method for quantifying an analyte in a test sample comprising:
(a) contacting a plurality of dispersed liquid crystal microdomains having two point defects and a minor axis of between about 0.5 mm and about 200 mm with a test sample; and
(b) determining the number of point defects in the plurality of dispersed liquid crystal microdomains after performing the contacting step (a);
wherein the extent of reduction in the number of point defects from two to one in the plurality of dispersed liquid crystal microdomains is used to quantify the analyte present in the test sample.
11. The method of claim 10 , wherein the test sample has an analyte concentration of less than 1 μg/ml.
12. The method of claim 10 , wherein the number of point defects in the plurality of liquid crystal microdomains is determined by detecting an anchoring configuration of the plurality of liquid crystal microdomains.
13. The method of claim 10 , wherein the test sample is an aqueous test sample.
14. The method of claim 10 , wherein the analyte is endotoxin lipopolysaccharide (LPS) or lipid A.
15. The method of claim 12 , wherein the step of detecting an anchoring configuration of the plurality of liquid crystal microdomains is performed by one or more of the group consisting of optical imaging, fluorescence imaging, optical imaging using polarized light, polarized light microscopy, bright field microscopy, fluorescence microscopy, light scattering measurement, flow cytometry, fluorescence flow cytometry, microelectrophoresis, dielectrophoresis, measurement of electrical capacitance, measurement of magnetic properties, measuring turbidity, detecting optical reflection, detecting transmittance of light, visual inspection, using a plate reader, using microwell plates, and using a cuvette in a detector.
16. The method of claim 10 , wherein the plurality of dispersed liquid crystal microdomains are liquid crystal droplets in a water emulsion.
17. The method of claim 16 , wherein the test sample is an aqueous test sample.
18. The method of claim 17 , wherein the volume ratio of the aqueous test sample to the liquid crystal contained within the water emulsion is greater than or equal to about 1,000 to 1.
19. The method of claim 18 , wherein the volume ratio of the aqueous sample to the liquid crystal contained within the liquid crystal emulsion of greater than or equal to about 40,000 to 1.
20. A method for detecting endotoxin lipopolysaccharide (LPS) in a test sample having an LPS concentration of less than 1 μg/ml, comprising:
(a) contacting one or more liquid crystal microdomains having two point defects and a minor axis of between about 0.5 mm and about 200 mm with a test sample having an LPS concentration of less than 1 μg/ml; and
(b) determining the number of point defects in the one or more liquid crystal microdomains after performing the contacting step (a), wherein a reduction in the number of point defects from two to one in at least one of the one or more liquid crystal microdomains indicates the presence of the LPS in the test sample.