Systems and methods related to optical nanosensors comprising photoluminescent nanostructures
Systems and methods related to optical nanosensors comprising photoluminescent nanostructures are generally described.
1. A method of determining an analyte, comprising:
exposing a first nanosensor comprising a first photoluminescent carbon-based nanostructure and a first polymer interacting with the first photoluminescent carbon-based nanostructure to a first analyte, the first analyte including at least one NO 2 group, wherein:
the first analyte interacts with the first nanosensor to produce a first emission of electromagnetic radiation, and
determining the first analyte based at least in part upon the first emission of electromagnetic radiation.
2. The method of claim 1 , further comprising exposing the first nanosensor to a second analyte, wherein the second analyte interacts with the first nanosensor to produce a second emission of electromagnetic radiation, distinguishable from the first emission.
3. The method of claim 2 , wherein the first emission of electromagnetic radiation has a first average intensity, and the second emission of electromagnetic radiation has a second average intensity, wherein the first and second average intensities are different.
4. The method of claim 2 , wherein the first emission of electromagnetic radiation has at least one peak wavelength, and the second emission of electromagnetic radiation has a second peak wavelength, wherein the first and second peak wavelengths are different.
5. The method of claim 2 , wherein the first emission of electromagnetic radiation occurs at a first wavelength with a first intensity, and the second emission of electromagnetic radiation occurs at the first wavelength at a second intensity that is different from the first intensity.
6. The method of claim 1 , further comprising:
exposing a second nanosensor comprising a second photoluminescent carbon-based nanostructure and a second polymer interacting with the second photoluminescent carbon-based nanostructure to the first analyte;
wherein the first analyte interacts with the second nanosensor to produce a second emission of electromagnetic radiation, distinguishable from the first emission.
7. The method of claim 6 , further comprising exposing the first nanosensor and the second nanosensor to a second analyte, wherein
the second analyte interacts with the first nanosensor to produce a third emission of electromagnetic radiation, and the second analyte interacts with the second nanosensor to produce a fourth emission of electromagnetic radiation, distinguishable from the third emission, and
determining the second analyte based at least in part upon the third or fourth emissions of electromagnetic radiation.
8. The method of claim 7 , wherein the first nanosensor, the second nanosensor, or both, are simultaneously exposed to the first and second analytes.
9. The method of claim 8 , wherein determining the first analyte, determining the second analyte, or both, includes using principal component analysis.
10. The method of claim 1 , wherein determining the analyte comprises determining the concentration of the analyte.
11. The method of claim 1 , wherein the first polymer comprises a polypeptide.
12. The method of claim 11 , wherein the first polymer comprises a polypeptide selected from the group consisting of: an amphiphilic helical polypeptide; a polypeptide including between about 5 and about 50 amino acid residues; and a polypeptide with a molecular weight of between about 400 g/mol and about 10,000 g/mol.
13. The method of claim 1 , wherein the first polymer comprises a polypeptide sequence, or derivative thereof, observed in the venom of a member of the Insecta class; a member of the Hymenoptera order; or a member of the Vespidae or Apidae families.
14. The method of claim 1 , wherein the first polymer comprises a polypeptide, or derivative thereof, from the Mastoparan or Bombolitin peptide families.
15. The method of claim 1 , wherein the first polymer comprises a polypeptide comprising at least one of KKAAA VLLPVLLAAP, EEEECCCCHSSYWY AFNNKT, INLKALAALAKKIL, INLKALAALAKALL, INWKGIAAMAKKLL, IKIMDILAKLGKVLAHV, INIKDILAKL VKVLGHV, IKITTMLAKLGKVLAHV, or SKITDILAKLGKVLAHV.
16. The method of claim 1 , wherein the first polymer comprises polyvinylpyrrolidone, polyvinyl alcohol, collagen, or phenylated dextran.
17. The method of claim 1 , wherein the first polymer comprises an oligonucleotide.
18. The method of claim 1 , wherein the first polymer comprises a single-stranded DNA oligonucleotide.
19. The method of claim 18 , wherein the single-stranded DNA oligonucleotide comprises at least 5 repeating units, in succession, of at least one of (GT), (AT), (AAAAT), or (GGGGT), at least 10 repeating units, in succession, of at least one of (GT) or (AT), at least 15 repeating units, in succession, of at least one of (GT) or (AT).
20. The method of claim 2 , wherein the nanosensor emits a third emission of electromagnetic radiation, distinguishable from the first emission and the second emission, upon interacting with a second analyte.
21. The method of claim 1 , wherein the photoluminescent nanostructure comprises a carbon nanotube, a single-walled carbon nanotube, or a semiconducting single-walled carbon nanotube.
22. The method of claim 1 , wherein the analyte comprises a nitro aryl group.
23. The method of claim 1 , wherein the analyte comprises at least one of a pesticide or an explosive.
24. The method of claim 1 , wherein the analyte comprises at least one of 2,4-dinitrophenol, 4-nitro-3-(trifluoromethyl)phenol, picric acid, trinitrotoluene, or cyclotrimethylenetrinitramine.