Coated flow path components for chromatographic effects

Patent metadata

Field	Value
Publication number	US-2024302333-A1
Application number	US-202418645498-A
Country	US
Kind code	A1
Filing date	Apr 25, 2024
Priority date	Feb 27, 2019
Publication date	Sep 12, 2024
Grant date	—

Abstract

The present disclosure relates to the determination of analytes in a sample using chromatography. The present disclosure provides methods of separating an analyte from a sample. The method includes introducing a sample comprising the analytes into a chromatographic system. The chromatographic system has a flow path disposed in an interior of the chromatographic system, at least a portion of the flow path having an active coating, and a chromatographic column having a stationary phase material in an interior of the chromatographic column that facilitates separation of the analytes in the sample through interaction with at least one analyte in the sample. The active coating is selected to interact with at least one analyte in the sample through (1) a repulsive force, (2) a secondary interaction, or (3) a retention mechanism distinct from the interaction with the stationary phase material.

First claim

1 .- 8 . (canceled)

9 . A chromatographic device for separating analytes in a sample, the chromatographic device comprising:
a sample injector having a sample injection needle for injecting the sample into the mobile phase; a sample reservoir container in fluid communication with the sample injector; a chromatography column downstream of the sample injector, the chromatography column having fluid connectors; and fluid conduits connecting the sample injector and the chromatography column; wherein interior surfaces of the fluid conduits, sample injector, sample reservoir container, and chromatography column form a fluidic flow path having wetted surfaces; and wherein at least a portion of the wetted surfaces of the fluidic flow path are coated with an alkylsilyl coating having the Formula I:

wherein each X is independently selected from (C 1 -C 6 )alkoxy, —NH(C 1 -C 6 )alkyl, —N((C 1 -C 6 )alkyl) 2 , OH, OR A , R B , R C , R D and halo;
R A represents a point of attachment to the interior surfaces of the fluidic system and at least one X is OR A ;
R B is absent or represents a hydrophobicity modifier;
R C represents a charge modifier and at least one X is R C ;
R D is absent, a chelator, or a crown ether; and
Y is a bridging moiety selected from (C 1 -C 20 )alkyl, —O[(CH 2 ) 2 O] 1-20 —, —(C 1 -C 10 )[NH(CO)NH(C 1 -C 10 )] 1-20 —, or —(C 1 -C 10 )[alkylphenyl(C 1 -C 10 )alkyl] 1-20 -.

10 . The chromatographic device of claim 9 , wherein the charge modifier has the same charge as at least one analyte in the sample.

11 . The chromatographic device of claim 9 , wherein the charge modifier (R C ) is attached to Formula I by a silyl ether moiety and has a composition selected from the group consisting of n-cyclohexylaminomethyl silyl , n-(2-aminoethyl)-3-aminopropyl silyl , n-cyclohexyl-3-aminopropyl silyl, n-(2-aminoethyl)-3-aminopropylmethyl silyl, n-cyclohexylaminomethyl silyl, bis (silylpropyl)-n-methylamine, 3-aminopropyl diisopropyl silyl, (3-aminopropyl) silyl, n,n-diethyl-3-aminopropyl silyl, propanesulfonic acid silyl, N-(hydroxyethyl)-N,N-bis(silyl propyl)amine, 2-(4-pyridylethyl) silyl, tris (silylmethyl) amine, carboxyethyl silyl , and silyl propyl methyl phosphonate.

12 . The chromatographic device of claim 11 , wherein the charge modifier (R C ) is

wherein Z is independently selected from (C 1 -C 6 )alkoxy, —NH(C 1 -C 6 )alkyl, —N((C 1 -C 6 )alkyl) 2 , OH, halo, or an attachment point to Formula I; and
wherein at least one Z is the attachment point to Formula I.

13 . (canceled)

14 . The chromatographic device of claim 9 , wherein the charge modifier (R C ) is a quaternary amine.

15 . (canceled)

16 . (canceled)

17 . (canceled)

18 . The chromatographic device of claim 9 , wherein the hydrophobicity modifier (R B ) is present.

19 . (canceled)

20 . The chromatographic device of claim 18 , wherein the hydrophobicity modifier (R B ) is attached to Formula I by a silyl ether moiety and has a composition selected from the group consisting of n-decyl silyl, trimethyl silyl, n-propyl silyl, t-butyl dimethyl silyl, 4-phenylbutyl silyl, n-octadecyl diisobutyl silyl, 6-phenylhexyl silyl, n-octadecyl silyl, n-methyl-O-methyl carbamate silyl, phenyl silyl, diphenyl methyl silyl, sulfobetaine silyl, carboxybetaine silyl, glycidoxy propyl silyl, hydrolyzed glycidoxypropyl silyl, and N-(propyl) gluconamide silyl.

21 . The chromatographic device of claim 20 , wherein the hydrophobicity modifier (R B ) is

wherein Z is independently selected from (C 1 -C 6 )alkoxy, —NH(C 1 -C 6 )alkyl, —N((C 1 -C 6 )alkyl) 2 , OH, halo, or an attachment point to Formula I; and
wherein at least one Z is the attachment point to Formula I.

22 . (canceled)

23 . The chromatographic device of claim 18 , wherein the alkylsilyl coating of Formula I is

at least one X is the charge modifier (R C ), wherein R C is

and at least one X is the hydrophobicity modifier (R B ), wherein R B is

wherein Z is independently selected from (C 1 -C 6 )alkoxy, —NH(C 1 -C 6 )alkyl, —N((C 1 -C 6 )alkyl) 2 , OH, halo, or an attachment point to Formula I; and
wherein at least one Z is the attachment point to Formula I.

24 . The chromatographic device of claim 18 , wherein the alkylsilyl coating of Formula I is

at least one X is the charge modifier (R C ), wherein R C is

and at least one X is the hydrophobicity modifier (R B ), wherein R B is

wherein Z is independently selected from (C 1 -C 6 )alkoxy, —NH(C 1 -C 6 )alkyl, —N((C 1 -C 6 )alkyl) 2 , OH, halo, or an attachment point to Formula I; and
wherein at least one Z is the attachment point to Formula I.

25 . The chromatographic device of claim 18 , wherein the alkylsilyl coating of Formula I is

at least one X is the charge modifier (R C ), wherein R C is

and at least one X is the hydrophobicity modifier (R B ), wherein R B is

wherein Z is independently selected from (C 1 -C 6 )alkoxy, —NH(C 1 -C 6 )alkyl, —N((C 1 -C 6 )alkyl) 2 , OH, halo, or an attachment point to Formula I; and
wherein at least one Z is the attachment point to Formula I.

26 . (canceled)

27 . (canceled)

28 . (canceled)

29 . The chromatographic device of claim 9 , wherein the chromatography column includes a frit having a wetted surface coated with the alkylsilyl coating of Formula I.

30 . The chromatographic device of claim 29 , wherein the hydrophobicity modifier (R B ) is present.

31 . The chromatographic device of claim 29 , wherein the frit is positioned at an outlet of the chromatography column.

32 . The chromatographic device of claim 29 , wherein the frit is positioned at an inlet of the chromatography column.

33 . The chromatographic device of claim 9 , further comprising a detector downstream of the chromatography column, wherein the fluidic flow path further comprises the detector.

34 . The chromatographic device of claim 33 , wherein the detector is a mass spectrometer and the fluidic

Assignees

• Waters Technologies Corp

Inventors

• Lauber Matthew A
• Gilar Martin
• Delano Mathew H
• Donegan Michael

Classifications

• G01N2030/027

  Liquid chromatography · CPC title

• B01D15/3847

  Multimodal interactions · CPC title

• B01D15/361

  Ion-exchange · CPC title

• B01D15/22

  relating to the construction of the column · CPC title

• B01D15/1878

  for multi-dimensional chromatography · CPC title