SUBSTRATE WITH MATRIX-FREE NANOSTRUCTURED HYDROPHILIC ANALYTE SPOTS FOR USE IN MASS SPECTROMETRY

• US 20190323139A1
• Filed: 07/01/2019
• Published: 10/24/2019
• Est. Priority Date: 12/30/2016
• Status: Active Application

• Current Assignee: Inredox LLC
• Original Assignee: Inredox LLC
• Inventors: Carpenter, Frank Howland, Routkevitch, Dmitri, Stowell, Michael H.B.
• Application Number:
  US16/458,208
• Publication Number:
  US 20190323139A1
• Time in Patent Office: Days
• CPC Class Codes: C25D 11/022 Anodisation on selected surface areas
• CPC Class Codes: C25D 11/04 of aluminium or alloys based thereon
• CPC Class Codes: C25D 11/045 for forming AAO templates
• CPC Class Codes: C25D 11/06 characterised by the electrolytes used
• CPC Class Codes: C25D 11/12 Anodising more than once, e.g. in different baths
• CPC Class Codes: C25D 11/18 After-treatment, e.g. pore-sealing
• CPC Class Codes: C25D 11/20 Electrolytic after-treatment
• CPC Class Codes: C25D 11/24 Chemical after-treatment
• CPC Class Codes: C25D 11/26 of refractory metals or alloys based thereon
• CPC Class Codes: C25D 11/32 of semiconducting materials
• CPC Class Codes: H01J 49/0418 for laser desorption, e.g. matrix-assisted laser desorption/ionisation [MALDI] plates or surface enhanced laser desorption/ionisation [SELDI] plates
• CPC Class Codes: H01J 49/164 Laser desorption/ionisation, e.g. matrix-assisted laser desorption/ionisation [MALDI] sample holders H01J49/0418

Abstract

The present disclosure describes a matrix-free nanostructured substrate for use in mass spectrometry. The substrate may preferably include one or more localized analyte spots for placement of an analyte, where each analyte spot may comprise a nanostructured metal oxide or semiconductor containing nanotubes or nanopores. The substrate may further include unstructured metal, metal oxide, or semiconductor that is not nanotubular or nanoporous in the part of the substrate that surrounds each of the analyte spots. In some embodiments, the nanostructured metal oxide or semiconductor may be chemically or structurally modified, and the analyte spots may additionally or alternatively include secondary nanostructures such as nanorods, nanoparticles, nanocoatings, or nanotubes. This may facilitate energy transfer to the analyte for matrix-free laser desorption/ionization. The analyte spots may preferably be more hydrophilic than the surrounding part of the substrate to ensure concentration of the analyte at the analyte spots.

Claims

1. A substrate configured to receive one or more samples for analysis using laser desorption/ionization mass spectrometry comprising:

a. one or more localized analyte spots; and

b. a substrate base;

wherein the one or more analyte spots comprise primary nanostructures comprising at least one nanoporous or nanotubular metal oxide or semiconductor;

wherein the one or more analyte spots have a diameter of between about 0.1 mm and 10 mm;

wherein the substrate base comprises a non-nanoporous and non-nanotubular metal, metal oxide, or semiconductor; and

wherein the one or more analyte spots are more hydrophilic than the substrate base.

2. The substrate of claim 1, wherein the nanoporous or nanotubular metal oxide or semiconductor is selected from the group consisting of nanoporous aluminum oxide, nanotubular titanium oxide, and nanoporous silicon, and wherein the one or more analyte spots have a diameter of between about 0.2 mm and 5 mm.

3. The substrate of claim 1, wherein the nanoporous or nanotubular metal oxide or semiconductor is selected from the group consisting of nanoporous aluminum oxide, nanotubular titanium oxide, and nanoporous silicon, and wherein the nanoporous or nanotubular metal oxide or semiconductor comprises nanopores or nanotubes with a diameter of between about 1 nm and 1000 nm and a length of between about 10 nm and 10 μ

m.

4. The substrate of claim 2, wherein the nanoporous or nanotubular metal oxide or semiconductor comprises nanopores or nanotubes with a diameter of between about 1 nm and 1000 nm and a length of between about 10 nm and 10 μ

m.

5. The substrate of claim 3, wherein the nanoporous or nanotubular metal oxide or semiconductor comprises nanopores or nanotubes with a diameter of between about 10 nm and 250 nm.

6. The substrate of claim 5, wherein the nanoporous or nanotubular metal oxide or semiconductor comprises nanopores or nanotubes with a length of between about 250 nm and 2 μ

m.

7. The substrate of claim 4, wherein the nanoporous or nanotubular metal oxide or semiconductor comprises nanopores or nanotubes with a diameter of between about 10 nm and 250 nm.

8. The substrate of claim 7, wherein the nanoporous or nanotubular metal oxide or semiconductor comprises nanopores or nanotubes with a length of between about 250 nm and 2 μ

m.

9. The substrate of claim 1, wherein the analyte spots are coated with a thin surface of a deposit selected from the group consisting of metals and semiconductors.

10. The substrate of claim 3, wherein the primary nanostructures are partially or completely filled with secondary nanostructures comprising nanorods, nanoparticles, nanocoatings, or secondary nanotubes comprising one or more deposits selected from the group consisting of metals, metal alloys, metal oxides, and semiconductors.

11. The substrate of claim 10, wherein the primary nanostructures are partially or completely filled with nanorods, and wherein the diameter of the nanorods is substantially equal to or less than the diameter of the primary nanostructures.

12. The substrate of claim 10, wherein the primary nanostructures are partially or completely filled with nanoparticles.

13. The substrate of claim 10, wherein the primary nanostructures are partially or completely filled with secondary nanotubes.

14. The substrate of claim 10, wherein the nanorods, nanoparticles, nanocoatings, or secondary nanotubes comprise one or more deposits selected from the group consisting of copper, gold, silver, cobalt, and nickel, and alloys thereof.

15. The substrate of claim 3, wherein the primary nanostructures are conformally coated with one or more deposits selected from the group consisting of metals, metal alloys, metal oxides, and semiconductors to generate a conformal nanocoating, wherein the conformal coating may be continuous or discontinuous.

16. The substrate of claim 15, wherein the conformally coated primary nanostructures are partially or completely filled with nanoparticles comprising one or more deposits selected from the group consisting of metals, metal alloys, metal oxides, and semiconductors.

17. The substrate of claim 10, wherein the one or more analyte spots comprise two or more sections, wherein one or more sections are partially or completely filled with secondary nanostructures comprising nanorods, nanoparticles, nanocoatings, or secondary nanotubes and one or more sections are not filled with secondary nanostructures.

18. The substrate of claim 10 comprising two or more analyte spots comprising a first analyte spot and a second analyte spot;

wherein the first analyte spot comprises primary nanostructures that are partially or completely filled with a first set of secondary nanostructures comprising nanorods, nanoparticles, nanocoatings, or secondary nanotubes; and

wherein the second analyte spot comprises primary nanostructures that are not filled with secondary nanostructures or are partially or completely filled with a second set of secondary nanostructures having a different composition than the first set of secondary nanostructures.

19. A method of generating the substrate of claim 1 comprising the steps of:

a. obtaining a substrate base;

b. patterning the substrate base using a mask to define analyte spots of a desired shape and size to generate a patterned substrate;

c. anodizing the patterned substrate to form localized nanostructured analyte spots to generate a patterned and anodized substrate; and

d. removing the mask.

20. A method of analyzing a sample comprising one or more analytes using mass spectrometry, wherein the method comprises the steps of:

a. placing the one or more analytes in the one or more analyte spots of the substrate of claim 1;

b. ionizing at least one of the one or more analytes using a laser to generate one or more ionized analytes;

c. introducing the one or more ionized analytes into a mass spectrometer; and

d. obtaining a mass spectrum of the one or more ionized analytes.