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 comprising the steps of:
(a) forming liquid crystal microdomains having one or more defects from a liquid crystal, wherein the liquid crystal microdomains are capable of scattering light;
(b) contacting the liquid crystal with a test sample that may contain the analyte;
(c) obtaining measurements of the scattering of light by other liquid crystal microdomains that do not include the analyte;
(d) exposing the liquid crystal microdomains formed from the liquid crystal contacted with the test sample to light;
(e) measuring the scattering of light by the liquid crystal microdomains formed from the liquid crystal contacted with the test sample,
wherein a difference between the resulting light scattering measurements as compared to the light scattering measurements exhibited by other liquid crystal microdomains that do not include the analyte indicates the presence of the analyte in the test sample, and wherein no difference between the resulting light scattering measurements as compared to the light scattering measurements exhibited by other liquid crystal microdomains that do not include the analyte indicates the absence of the analyte in the test sample.
2. The method of claim 1 , wherein the step of forming liquid crystal microdomains having one or more defects from a liquid crystal is performed before the step of contacting the liquid crystal with a test sample that may contain the analyte.
3. The method of claim 1 , wherein the test sample comprises the analyte.
4. The method of claim 3 , further comprising purifying the analyte in the test sample from a mixture.
5. The method of claim 1 , wherein the step of measuring the scattering of light by the liquid crystal microdomains occurs as the liquid crystal microdomains are passing through a flow channel.
6. The method of claim 1 , wherein the step of measuring the scattering of light by the liquid crystal microdomains comprises measuring forward scatter of light by the liquid crystal microdomains.
7. The method of claim 6 , wherein the step of measuring the scattering of light by the liquid crystal microdomains further comprises measuring side scatter of light by the liquid crystal microdomain.
8. The method of claim 1 , wherein the step of measuring the scattering of light by the liquid crystal microdomains is performed using a flow cytometer.
9. The method of claim 1 , wherein the liquid crystal microdomains have a minor axis of between about 0.5 μm and about 200 μm.
10. The method of claim 1 , wherein the liquid crystal microdomains are dispersed liquid crystal droplets within a liquid crystal emulsion.
11. The method of claim 10 , wherein the dispersed liquid crystal droplets have a minor axis of between about 1 μm and about 10 μm.
12. The method of claim 1 , further comprising determining the number of defects within the microdomains using the light scattering measurements.
13. The method of claim 12 , wherein a reduction in the number of defects within the microdomains is determined by the difference between the light scattering measurements.
14. The method of claim 1 , wherein the analyte comprises a lipid.
15. The method of claim 14 , wherein the lipid is a phospholipid.