Granted Patent B2

US 12,416,607 · App. 18/206,989 · Granted Sep 16, 2025

Inventors: Matthew A Lauber (North Smithfield, RI); Mathew H. DeLano (Needham, MA); Scott A. McCall (Smithfield, RI); Jonathan Belanger (Whitinsville, MA); Theodore A. Dourdeville (Falmouth, MA); Kerri Smith (Marlborough, MA); Paul Rainville (Princeton, MA); Dimple Shah (Medway, MA); Stephen J. Shiner (Holden, MA); Catalin Doneanu (Franklin, MA); Michael Donegan (Charlton, MA)

Assignee: Waters Technologies Corporation

G01N30/56B01J20/291B01J20/3272B05D1/60C23C14/046C23C14/12C23C14/24C23C16/045C23C16/30G01N30/6052B05D2518/10G01N2030/567G01N30/7266

Abstract

Claims (25)

1. A chromatographic device for separating analytes in a liquid sample comprising:

a sample injector having a sample injection needle for injecting the liquid sample into a mobile phase;

a sample reservoir container in fluid communication with the sample injector;

a liquid chromatography column downstream of the sample injector, the liquid chromatography column having fluid connectors; and

fluid conduits connecting the sample injector and the liquid chromatography column;

wherein interior surfaces of the fluid conduits, sample injector, sample reservoir container, and liquid chromatography column form a fluidic flow path having wetted surfaces; and

wherein a bioinert coating is deposited on at least a portion of the wetted surfaces by infiltrating vaporized bis(trichlorosilyl)ethane or bis(trismethoxysilyl)ethane through the fluidic flow path to form the bioinert coating.

2. The chromatographic device of claim 1 , wherein at least portion of the fluidic flow path is formed of metal components.

3. The chromatographic device of claim 1 , wherein the bioinert coating consists of a product of the silane hydrolysis reaction of vapor deposited bis(trichlorosilyl)ethane and water vapor or a product of the silane hydrolysis reaction of vapor deposited bis(trismethoxysilyl)ethane and water vapor.

4. The chromatographic device of claim 1 , wherein the bioinert coating has a contact angle of at least about 15°.

5. The chromatographic device of claim 1 , wherein the bioinert coating has a contact angle less than about 50°.

6. The chromatographic device of claim 1 further comprising a detector downstream of the liquid chromatography column and wherein the fluidic flow path further comprises the detector.

7. The chromatographic device of claim 6 , wherein the detector is a mass spectrometer and the fluidic flow path includes wetted surfaces of an electrospray needle.

8. The chromatographic device of claim 1 , wherein the fluidic flow path has a length to diameter ratio of at least 20.

9. The chromatographic device of claim 1 , wherein the bioinert coating has a thickness of at least 100 Å.

10. The chromatographic device of claim 9 , wherein the bioinert coating has a total thickness of about 500 Å.

11. The chromatographic device of claim 1 , wherein the chromatographic device is characterized such that, when the analytes comprise phosphoglycans, phosphopeptides, glycans, or proteins, chromatographic separation of the analytes has improved recovery and peak shape relative to an uncoated wetted surface as measured in increased chromatographic peak area and reduced peak width.

12. A method of tailoring a metallic fluidic flow path for separation of a liquid sample comprising an analyte, the method comprising:

(a) infiltrating vaporized bis(trichlorosilyl)ethane or bis(trismethoxysilyl)ethane into a metallic fluidic flow path; and

(b) controlling temperature and pressure to deposit a bioinert coating on wetted surfaces of the metallic fluidic flow path, the bioinert coating having a thickness of at least 100 Å and a contact angle of at least 15°.

13. The method of claim 12 , further comprising pretreating the wetted surfaces of the metallic fluidic flow path with a plasma prior to depositing the bioinert coating.

14. The method of claim 12 , further comprising delivering water vapor to the metallic fluidic flow path for silane hydrolysis of the vaporized bis(trichlorosilyl)ethane or bis(trismethoxysilyl)ethane on the wetted surfaces.

15. The method of claim 12 , further comprising modifying the bioinert coating with a silanizing reagent to functionalize the bioinert coating with a different silane than the vaporized bis(trichlorosilyl)ethane or bis(trismethoxysilyl)ethane.

16. The method of claim 15 , wherein the silanizing reagent is a non-volatile zwitterion or an acidic or basic silane.

17. The method of claim 16 , wherein the non-volatile zwitterion is sulfobetaine or carboxybetaine.

Assignments (1)

Continuity (3)

References Cited (400)