Surface enhanced Raman spectroscopy (SERS) systems for the detection of viruses and methods of use thereof

1. A method of detecting at least one biomolecule in a sample, comprising:

attaching at least one first biomolecule to an array of nanorods on a substrate, wherein a tilt angle (β) between an individual nanorod and the substrate surface is about 0° to about 90°;

exposing the substrate including the first biomolecule to the sample containing at least one of a second biomolecule and a third biomolecule, wherein the second biomolecule is a first strain of human immunodeficiency virus (HIV) and the third biomolecule is a second strain of human immunodeficiency virus (HIV); and

measuring a surface enhanced Raman spectroscopy (SERS) spectrum, wherein a SERS spectrum of the array of nanorods and the first biomolecule is detectably different than a SERS spectrum of the array of nanorods, the first biomolecule, and the second biomolecule and a SERS spectrum of the array of nanorods, the first biomolecule, and the third biomolecule, and wherein the SERS spectrum of the array of nanorods, the first biomolecule, and the second biomolecule is detectably different than the SERS spectrum of the array of nanorods, the first biomolecule, and the third biomolecule.

2. The method of claim 1 , wherein the nanorods are selected from one of the following materials: a metal, a metal oxide, a metal nitride, a metal oxynitride, a polymer, a multicomponent material, or combinations thereof.

3. The method of claim 2 , wherein the material is selected from: silver, nickel, aluminum, silicon, gold, platinum, palladium, titanium, cobalt, copper, zinc, oxides of each, nitrides of each, oxynitrides of each, carbides of each, or combinations thereof.

4. The method of claim 1 , wherein the first biomolecule is selected from: a polynucleotide, a protein, a polypeptide, a glycoprotein, lipid, a carbohydrate, a fatty acid, a fatty ester, a macromolecular polypeptide complex, or combinations thereof.

5. The method of claim 1 , wherein the first biomolecule is an antibody of the second biomolecule and the third biomolecule.

6. The method of claim 1 , wherein the sample is selected from: blood, saliva, tears, phlegm, sweat, urine, plasma, lymph, spinal fluid, cells, microorganisms, a combination thereof or aqueous dilutions thereof.

7. A method of detecting at least one virus in a sample, comprising:

exposing a substrate having an array of nanorods on the substrate to the sample, wherein a tilt angle (β) between an individual nanorod and the substrate surface is about 0° to about 90°, and wherein the sample includes at least one of a first virus and a second virus, wherein the first virus and the second virus are each a different strain of human immunodeficiency virus (HIV); and

measuring a surface enhanced Raman spectroscopy (SERS) spectrum, wherein a SERS spectrum of the array of nanorods and the first virus is detectably different than a SERS spectrum of the array of nanorods and the second virus.

8. The method of claim 7 , wherein the array of nanorods has a first biomolecule disposed on each of the nanorods, and wherein the first biomolecule has an affinity for at least one of the first virus and the second virus.

9. The method of claim 7 , wherein the first virus and the second virus comprise different strains of HIV, wherein the first viral strain has a first measurable surface-enhance Raman spectroscopic signature, wherein the second viral strain has a second measurable surface-enhanced Raman spectroscopic signature, and wherein the first measurable surface-enhanced spectroscopic signature and the second measurable surface-enhanced Raman spectroscopic signature are distinguishable.

10. The method of claim 7 , wherein the strains of human immunodeficiency virus (HIV) are selected from: BaL, LAV, or NL4-3.

11. The method of claim 7 , further comprising analyzing the measurable surface-enhanced Raman spectroscopic spectrum for each virus by the use of an analysis method selected from at least one of Principal component analysis (PCA) or K-means Clustering Algorithm analysis.

12. The method of claim 7 , wherein the first virus and the second virus comprise the same strands of the same virus, wherein one or both strands include a mutation.

13. The method of claim 12 , further comprising analyzing the SERS spectra of two or more nucleic acid strands of the same virus, wherein one or both strands include a mutation.

14. The method of claim 7 , wherein the first virus and the second virus comprise different portions of the same strand of the same virus.

15. A method of detecting at least one virus in a sample, comprising:

exposing a substrate having an array of nanorods on the substrate to the sample, wherein a tilt angle (β) between an individual nanorod and the substrate surface is about 0° to about 90°, and wherein the sample includes at least one of a first virus and a second virus; and

measuring a surface enhanced Raman spectroscopy (SERS) spectrum, wherein a SERS spectrum of the array of nanorods and the first virus is detectably different than a SERS spectrum of the array of nanorods and the second virus.