IP Library › Granted Patent US 10,881,986
Granted Patent B2
US 10,881,986 · App. 16/282,626 · Granted Jan 5, 2021

Liquid chromatography technique

Inventors: Jesse Bischof (State College, PA); Lucas D. Patterson (Altoona, PA); Gary Barone (State College, PA); Min Yuan (State College, PA); David A. Smith (Bellefonte, PA)
Assignee: SILCOTEK CORP.
B01D15/3828B01D15/161B01D15/163B01D15/22G01N30/30G01N30/36G01N30/56B01J20/3265G01N30/60G01N2030/567
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Quick Facts
Patent No.
US 10,881,986
App. No.
16/282,626
Granted
Jan 5, 2021
Kind
B2
Abstract

Liquid chromatography techniques are disclosed. Specifically, the liquid chromatography technique includes providing a liquid chromatography system having a coated metallic fluid-contacting element, and transporting a fluid to contact the coated metallic fluid-contacting element. Conditions for the transporting of the fluid are selected from the group consisting of the temperature of the fluid being greater than 150° C., pressure urging the fluid being greater than 60 MPa, the fluid having a protein-containing analyte incompatible with one or both of titanium and polyether ether ketone, the fluid having a chelating agent incompatible with the one or both of the titanium or the polyether ether ketone, and combinations thereof.

Claims (27)

1. A liquid chromatography technique, comprising:

providing a liquid chromatography system having a coated metallic fluid-contacting element; and

transporting a fluid to contact the coated metallic fluid-contacting element;

wherein the fluid has a protein-containing analyte incompatible with one or both of titanium and polyether ether ketone, and the fluid has a chelating agent incompatible with the one or both of the titanium or the polyether ether ketone, and wherein the fluid includes an analyte selected from the group consisting of tetracycline, N-hydroxypyridine-2-on, adenosine triphosphate, and deoxynucleotide monophosphate.

2. The liquid chromatography technique of claim 1 , wherein the coated metallic fluid-contacting element has a coating including carbon, silicon, oxygen, and hydrogen, and a stainless steel substrate.

3. The liquid chromatography technique of claim 1 , wherein the coated metallic fluid-contacting element has a coating including carbon, silicon, oxygen, hydrogen, and fluorine, and a stainless steel substrate.

4. The liquid chromatography technique of claim 1 , wherein the coated metallic fluid-contacting element has a coating including carbon, silicon, oxygen, hydrogen, and nitrogen, and a stainless steel substrate.

5. The technique of claim 1 , wherein the pressure for the urging of the fluid is greater than 120 MPa.

6. The technique of claim 1 , wherein the temperature of the fluid is greater than 400° C.

7. The technique of claim 1 , wherein the pH of the fluid is less than 2.

8. The technique of claim 1 , wherein the coated metallic fluid-contacting element is a coated metallic column has a diameter of less than 2.1 mm.

9. The technique of claim 1 , wherein the coated metallic fluid-contacting element has a length of less than 20 cm.

10. The technique of claim 1 , wherein the transporting of the fluid through the coated metallic fluid-contacting element is at a linear velocity of at least 8 mm per second.

11. The technique of claim 1 , wherein the fluid includes a solvent selected from the group consisting of water, acetonitrile, methanol, formic acid, phosphoric acid, tetrahydrofuran, trifluoroacetic acid, and combinations thereof.

12. The technique of claim 1 , wherein the liquid chromatography system comprises a stationary phase positioned within the coated metallic fluid-contacting element, the stationary phase including particles having a size of less than 3 micrometers, and the coated metallic column having a length of between 10 cm and 20 cm.

13. The technique of claim 1 , wherein the liquid chromatography system comprises a stationary phase positioned within the coated metallic fluid-contacting element, the stationary phase including particles having a size of less than 1.5 micrometers.

14. The technique of claim 1 , wherein the coated metallic fluid-contacting element is bioinert.

15. The technique of claim 1 , wherein the coated metallic fluid-contacting element is resistant to protein stiction.

16. The technique of claim 1 , wherein the coated metallic fluid-contacting element has a coating having a thickness of at least 400 nm.

17. The technique of claim 1 , wherein the coated metallic fluid-contacting element has a coating having a thickness of between 1,000 nm and 1,600 nm.

18. A liquid chromatography technique, comprising:

providing a liquid chromatography system having a coated metallic column, a stationary phase being positioned within the coated metallic column, the stationary phase including particles having a size of less than 1.5 micrometers

transporting a fluid through the coated metallic column, wherein conditions for the transporting of the fluid include the temperature of the fluid being greater than 150° C., pressure urging the fluid within the coated metallic column being greater than 60 MPa, the fluid having a protein-containing analyte incompatible with one or both of titanium and polyether ether ketone, the fluid having a chelating agent incompatible with the one or both of the titanium or the polyether ether ketone, or combinations thereof;

wherein the coated metallic column has a coating including carbon, silicon, oxygen, and hydrogen, and a stainless steel substrate, the pH of the fluid is less than 2, the coated metallic column has a diameter of less than 2.1 mm, the coated metallic column has a length of less than 20 cm, and the coated metallic component has a coating having a thickness of at least 400 nm;

wherein the transporting of the fluid through the coated metallic column is at a linear velocity of at least 8 mm per second;

wherein the fluid includes a solvent selected from the group consisting of water, acetonitrile, methanol, formic acid, phosphoric acid, tetrahydrofuran, trifluoroacetic acid, and combinations thereof; and

wherein the fluid includes an analyte selected from the group consisting of tetracycline, N-hydroxypyridine-2-on, adenosine triphosphate, and deoxynucleotide monophosphate.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 22, 2019
From: BISCHOF, JESSE; PATTERSON, LUCAS D.; BARONE, GARY; YUAN, MIN; SMITH, DAVID A.
To: SILCOTEK CORP.
Reel/Frame 048413/0457 →
Continuity (2)
Provisional Application 62634299 · Feb 23, 2018
Related Publication 20190262745A1 · Aug 29, 2019
Cited By (1)
US 12,216,034