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A method for collecting a microbiological substance utilizes a micro fabricated biochip having a collection chamber. A fluid sample containing a microbiological entity of interest is delivered to the collection chamber in the biochip. Then a non-uniform electric field is generated in the collection

A method for collecting a microbiological substance utilizes a micro fabricated biochip having a collection chamber. A fluid sample containing a microbiological entity of interest is delivered to the collection chamber in the biochip. Then a non-uniform electric field is generated in the collection chamber, to retain the microbiological entity of interest in the collection chamber. The microbiological entity is retained through dielectrophoresis induced by the energization of the electrodes by a periodically applied, alternating current.

대표청구항 ▼

What is claimed is: 1. A method for collecting and rapidly concentrating a microbiological substance, comprising: providing a microfabricated boichip having a collection chamber; delivering a fluid sample to said collection chamber in said biochip, said fluid sample containing a microbiological ent

What is claimed is: 1. A method for collecting and rapidly concentrating a microbiological substance, comprising: providing a microfabricated boichip having a collection chamber; delivering a fluid sample to said collection chamber in said biochip, said fluid sample containing a microbiological entity of interest; generating a spatially non-uniform electric field in said collection chamber in a pulsed mode so that successive intervals of application of said non-uniform electric field are spaced from one another by periods of time; retaining said microbiological entity of interest in said collection chamber during the successive intervals of application of said non-urn form electric field at least partially by virtue of said non-uniform electric field; and retaining said microbiological entity of interest in said collection chamber during said periods of time. 2. The method defined in claim 1,: wherein the retaining of said microbiological entity of interest in said collection chamber during said periods of time is accomplished by attaching said microbiological entity of interest to said collection chamber during said intervals of application of said non-uniform electric field, further comprising: removing at least some contaminants from said fluid sample in said collection chamber during said periods between successive intervals of application of said non-uniform electric field while retaining said microbiological entity of interest in said collection chamber during the successive intervals of application of said non-uniform electric field and during said periods of time, the removing of said contaminants being performed by flowing said fluid sample out of said chamber. 3. The method defined in claim 2 wherein attaching said microbiological entity of interest to said collection chamber includes attaching antibodies to at least one fixed or permanent surface of said collection chamber and attaching said microbiological entity of interest to said surface via said antibodies. 4. The method defined in claim 1 wherein the retaining of said microbiological entity of interest in said collection chamber includes adding to said fluid sample, prior to the delivering thereof to said collection chamber, a plurality of microscopic carrier elements each provided with a multiplicity of binding agents for. coupling said microbiological material to said carrier elements. 5. The method defined in claim 4 wherein said carrier elements are beads or microspheres. 6. The method defined in claim 4, further comprising separating contaminants from said fluid sample in said collection chamber, wherein the separating of said contaminants includes trapping said carrier elements with the coupled microbiological entity of interest in said collection chamber while flushing remaining portions of said fluid sample from said collection chamber. 7. The method defined in claim 1 wherein said microbiological entity of interest is a pathogenic strain of bacteria, further comprising measuring an electrical parameter of fluid in said collection chamber to detect metabolic activity of said microbiological entity of interest, thereby determining viability of said microbiological entity of interest. 8. The method defined in claim 1, further comprising extracting said fluid sample from a food product prior to delivering of said fluid sample to said biochip. 9. A method for collecting and rapidly concentrating a microbiological substance, comprising: providing a microfabricated boichip having a collection chamber; delivering a fluid sample to said collection chamber in said biochip, said fluid sample containing a microbiological entity of interest; generating a spatially non-uniform electric field in said collection chamber in a pulsed mode so that successive intervals of application of said non-uniform electric field are spaced from one another by periods of time; retaining said microbiological entity of interest in said collection chamber during the successive intervals of application of said non-uniform electric field, at least partially by virtue of said non-uniform electric field; retaining said microbiological entities of interest in said collection chamber during said periods of time, by attaching said microbiological entity of interest to at least one fixed or permanent surface of said collection chamber via antibodies disposed on said surface; and removing at some contaminants from said fluid sample in said collection chamber by flowing said fluid sample through and out of said chamber. 10. The method defined in claim 9, further comprising after the removing of contaminants from said fluid sample, operating detection elements in said collection chamber repeatedly over time to measure an electrical parameter of said fluid sample to detect changes in electrical impedance: of said fluid sample arising from metabolic activity of said microbiological entity of interest in said fluid sample to determine whether the fluid sample contains said microbiological entity of interest in a viable form. 11. A method for testing for he presence of a viable microorganism, comprising: flowing a fluid sample possibly containing a microorganism of a preselected type to a collection chamber having a volume less than approximately 1 microliter; at least temporarily retaining said microorganism in said collection chamber by dielectrophoresis applied in a pulsed mode so that successive intervals of application of a non-uniform electric field are spaced from one another by periods of time; retaining said microorganism in said collection chamber during the successive intervals of application of said non-uniform electric field and during, at least partially by virtue of said non-uniform electric field; retaining said microbiological entity of interest in said collection chamber during said periods of time; terminating the flowing of said fluid sample to said collection chamber; after the terminating of flow to said collection chamber, periodically making measurements of an electrical parameter of an electrical circuit incorporating said collection chamber and a fixed amount of fluid therein; retaining said microorganism in said collection chamber during the making of said measurements; and automatically using said measurements to detect changes in electrical impedance of said fixed amount of fluid arising from metabolic activity of the microorganism, thereby determining viability of the microorganism. 12. The method defined in claim 11 wherein the preparing of said fluid sample includes attaching said microorganism to carrier elements, the retaining of said microorganism in said collection chamber includes retaining said carrier elements therein. 13. A method for testing for the presence of a viable microorganism, comprising: delivering a fluid sample possibly containing a microorganism of a preselected type to a collection chamber having a volume less than approximately 1 microliter; applying a dielectrophoresis field to at least temporarily retain said microorganism in said collection chamber; periodically turning off said dielectrophoresis field; retaining said microorganism in said collection chamber during the application of said dielectrophoresis field and when said dielectrophoresis field is turned off; when said dielectrophoresis field is turned off, periodically making measurements of an electrical parameter of an electrical circuit incorporating said collection chamber and a fixed amount of fluid therein; and automatically using said measurements to detect changes in electrical impedance of said fixed amount of fluid arising from metabolic activity of the microorganism, thereby determining viability of the microorganism. 14. A method for testing for the presence of a viable microorganism, comprising: flowing a fluid sample possibly containing a microorganism of a preselected type to a collection chamber having a volume less than approximately 1 microliter; applying a dielectrophoresis field to the fluid sample in said collection chamber to at least temporarily retain said microorganism in said collection chamber; turning off said dielectrophoresis field; after the turning off said dielectrophoresis field, introducing a nutrient solution into said collection chamber; retaining said microorganism in said collection chamber during application of said dielectrophoresis field and when said dielectrophoresis field is turned off; after the introducing of said nutrient solution into said collection chamber and while said dielectrophoresis field is turned off and said microorganism is retained in said collection chamber, periodically making measurements of an electrical parameter of an electrical circuit incorporating said collection chamber and a fixed amount of nutrient containing fluid therein; and automatically using said measurements to detect changes in electrical impedance of said fixed amount of nutrient containing fluid arising from metabolic activity of the microorganism, thereby determining viability of the microorganism.