Electrochemical method for detecting water born pathogens
View Patent ↗A novel, surface immobilization electrochemical assay allows for rapid, accurate and highly sensitive detection of microorganisms and biological molecules. Known surface immobilization methods are utilized to bind an analyte to a surface. A binding material with a covalently attached electroactive complex generates electrical current in the presence of analyte. An electrode is used to detect the current, that is directly related to the concentration of analyte. The invention is especially suitable for detection of Cryptospiridium parvum.
1. A method for analyzing at least one microorganism in a solution, comprising the steps of:
heat shocking said microorganism causing said microorganism to release heat shock polynucleotides;
allowing said heat shock polynucleotides to transfer to a self-contained microassay structure having at least one integrated, individually addressable electrode and an assay surface, wherein said at least one integrated, individually addressable electrode is a detecting electrode constructed adjacent to or within a diffusion layer of said assay surface, said assay surface having a primary polynucleotide probe complementary to a portion of said heat shock polynucleotides;
addition of a secondary polynucleotide probe complementary to a portion of said heat shock polynucleotides and having an electroactive complex covalently attached, wherein said electroactive complex may be activated such that an electric current is generated within said microassay structure, and wherein said electroactive complex does not transfer electrons directly to said detecting electrode for generation of said electric current;
allowing said secondary polynucleotide probe and said electroactive complex to bind to said heat shock polynucleotides;
activating said electroactive complex attached to said secondary polynucleotide probe;
measuring said electric current generated by said activation of said electroactive complex at said detecting electrode.
2. The method of claim 1 further comprising applying a polymerase chain reaction subsequent to said heat shocking of said microorganism.
3. The method of claim 1 wherein said at least one integrated, individually addressable electrode of said microassay structure further comprises a solid capture electrode integrated on a solid substrate, an additional detecting electrode, and an auxiliary electrode.
4. The method of claim 3 wherein said solid substrate is fabricated using ceramic tape.
5. The method of claim 1 wherein said microassay structure is comprised of low temperature co-fired ceramic tape and metallic ink.
6. The method of claim 5 wherein said ceramic tapes serves as a substrate for said at least one integrated, individually addressable electrode.
7. The method of claim 1 wherein said microassay structure is comprised of a dip-chip and/or a microcavity array chip, said chip being integrated with at least one individually addressable electrode.
8. The method of claim 1 wherein said activating said electroactive complex is selected from the group consisting of changing temperature, changing pH, application of electrical currents, exposure to electromagnetic radiation, denaturation and addition of an activating compound.
9. The method of claim 1 wherein said at least one microassay structure is comprised of a plurality of microassay structures.
10. The method of claim 1 wherein said analyte is a bacteria, protozoa, or other microorganism.
11. The method of claim 1 wherein said at least one microorganism is selected from the group consisting of Cryptosporidium parvum, Escherichia coli, Campylobacter lari, Giardia lamblia, Listeria monocytogenes, Bacillus anthracis, Plasmodium species, Staphylococcus species and Salmonella typhi.
12. The method of claim 1 wherein said electroactive complex is selected from the group consisting of a metalloprotein, a synthetic dendrimer, a redox enzyme, a chelating agent, an enzyme, a polymer and an inorganic species.
13. The method of claim 1 wherein said microassay structure is formed by photolithographic means.
14. The method of claim 1 wherein said microassay structure is formed by photolithographic means on ceramic tape, polymeric materials, silicon wafer, or glass.
15. The method of claim 1 wherein said at least one integrated, individually addressable electrode is fabricated using ceramic tape.
16. The method of claim 1 wherein said secondary polynucleotide probe does not include nanoparticle labels attached to oligonucleotides.
17. The method of claim 1 wherein said transferring said heat shock polynucleotides includes allowing said heat shock polynucleotides to diffuse into said second microassay structure.
18. A method for analyzing at least one microorganism in a solution, comprising the steps of:
heat shocking said microorganism causing said microorganism to release heat shock polynucleotides;
allowing said heat shock polynucleotides to transfer to a self-contained microassay structure having at least one integrated, individually addressable electrode and an assay surface, wherein said at least one integrated, individually addressable electrode is a detecting electrode constructed adjacent to or within a diffusion layer of said assay surface, said assay surface having a primary polynucleotide probe complementary to a portion of said heat shock polynucleotides;
addition of a secondary polynucleotide probe complementary to a portion of said heat shock polynucleotides and having an electroactive complex covalently attached, wherein said electroactive complex may be activated such that an electric current is generated within said microassay structure, and wherein said electroactive complex does not transfer electrons directly to said detecting electrode for generation of said electric current;
allowing said secondary polynucleotide probe and said electroactive complex to bind to said heat shock polynucleotides;
activating said electroactive complex attached to said secondary polynucleotide probe;
measuring said electric current generated by said activation of said electroactive complex at said detecting electrode; and
wherein said microorganism is selected from the group consisting of Cryptosporidium parvum, Escherichia coli, Campylobacter lari, Giardia lamblia, Listeria monocytogenes, Bacillus anthracis, Plasmodium species, Staphylococcus species and Salmonella typhi.