Systems and methods for two-dimensional chromatography

US2016238573A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016238573-A1
Application numberUS-201514923273-A
CountryUS
Kind codeA1
Filing dateOct 26, 2015
Priority dateOct 27, 2014
Publication dateAug 18, 2016
Grant date

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

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Provided are two-dimensional chromatography systems and methods for separating and/or analyzing complex mixtures of organic compounds. In particularly, a two-dimensional reversed-phase liquid chromatography (RPLC)-supercritical fluid chromatography (SFC) system is described including a trapping column at the interface which collects the analytes eluted from the first dimension chromatography while letting the RPLC mobile phase pass through. The peaks of interest from the RPLC dimension column are effectively focused as sharp concentration pulses on the trapping column, which is subsequently injected onto the second dimension SFC column. The system can be used for simultaneous achiral and chiral analysis of pharmaceutical compounds. The first dimension RPLC separation provides the achiral purity result, and the second dimension SFC separation provides the chiral purity result (enantiomeric excess).

First claim

Opening claim text (preview).

1 . A chromatography system for separating a sample comprising: a first separation unit comprising: a) a first pump assembly for driving a first mobile phase through the first separation unit, b) a sample injector for introducing a sample to the first separation unit; and c) a reversed-phase liquid chromatography (RPLC) column; a second separation unit comprising: a) a second pump assembly for driving a second mobile phase through the second separation unit, and b) a supercritical fluid chromatography (SFC) column; and, a first fluidic routing unit comprising a plurality of sample loops, said first fluidic routing unit is connected to the first separation unit and the second separation unit, wherein at least one of the plurality of sample loops comprises a trapping column, said trapping column comprising a stationary phase; and wherein the chromatography system is configured for first separating the sample in the first separation unit and subsequently introducing at least a portion of the sample eluted from the RPLC column of the first separation unit to the second separation unit. 2 . The chromatography system of claim 1 , wherein the first fluidic routing unit comprises two sample loops; wherein one of the two sample loops is in fluidic communication with the first separation unit and the other one of the two sample loops is in fluidic communication with the second separation unit. 3 . The chromatography system of claim 1 , wherein the first fluidic routing unit comprises at least three sample loops, and wherein at least one of the sample loops is in fluidic isolation from the first separation unit and the second separation unit. 4 . The chromatography system of claim 3 , wherein at least one sample loop comprising a stationary phase material is in fluidic isolation from the first separation unit and the second separation unit. 5 . The chromatography system of claim 1 , wherein the first fluidic routing unit comprises a plurality of trapping columns each positioned in a sample loop. 6 . The chromatography system of claim 1 , wherein the first fluidic routing unit is configured to allow fluid flow through a sample loop in a first direction when said sample loop is positioned in fluidic communication with the first separation unit and to allow fluid flow through said sample loop in a direction opposite to the first direction when said sample loop is positioned in fluidic communication with the second separation unit. 7 . The chromatography system of claim 1 , wherein the first fluidic routing unit is configured to allow fluid flow through a sample loop in a first direction when said sample loop is positioned in fluidic communication with the first separation unit and to allow fluid flow through said sample loop in a direction same as the first direction when said sample loop is positioned in fluidic communication with the second separation unit. 8 . The chromatography system of claim 1 , wherein the RPLC column comprises a reversed-phase stationary phase. 9 . The chromatography system of claim 8 , wherein the reversed-phase stationary phase comprises a C-18 phase. 10 . The chromatography system of claim 8 , wherein the stationary phase in the trapping column comprises a reversed-phase material. 11 . The chromatography system of claim 9 , wherein the reversed-phase material comprises a C-18 phase. 12 . The chromatography system of claim 1 , wherein the second separation unit comprises one SFC column. 13 . The chromatography system of claim 12 , wherein the SFC column comprises a normal phase stationary phase. 14 . The chromatography system of claim 13 , wherein the normal phase stationary phase comprises a silica gel. 15 . The chromatography system of claim 1 , wherein the second separation unit further comprises a focus column located upstream of the SFC column. 16 . The chromatography system of claim 15 , wherein the focus column comprises a reversed-phase material. 17 . The chromatography system of claim 1 , wherein the second separation unit comprises: a) an array of SFC columns, wherein the SFC columns in the array are arranged in a parallel configuration; and b) a second fluidic routing unit for directing flow of the second mobile phase to a pre-identified SFC column in the array. 18 . The chromatography system of claim 17 , wherein the second separation unit further comprises a focus column located upstream of each SFC column in the array of SFC columns. 19 . The chromatography system of claim 1 , further comprising a first detector positioned downstream of the RPLC column. 20 . The chromatography system of claim 1 , further comprising a second detector positioned downstream of the SFC column. 21 . The chromatography system of claim 1 , further comprising at least one control device operably connected to one or more of: a) the first pump assembly; b) the sample injector; c) the first detector; d) the first fluidic routing unit; e) the second pump assembly; and f) the second detector. 22 . A method for separating a sample comprising the steps of: (i) capturing at least a portion of a sample on a trapping column, said portion is obtained by separating the sample by reversed-phase liquid chromatography (RPLC), said trapping column comprising a stationary phase; and (ii) subjecting the portion of the sample captured on the trapping column to further separation by supercritical fluid chromatography (SFC). 23 . The method of claim 22 , further comprising separating the sample with a reversed-phase liquid chromatography comprising: (i) introducing the sample into a first mobile phase; (ii) driving the first mobile phase containing the sample through a RPLC column; and (iii) separating the sample on the RPLC column. 24 . The method of claim 23 , further comprising detecting the presence of a component of the sample in the first mobile phase after passing through the RPLC column. 25 . The method of claim 22 , further comprising eluting the portion of the sample captured on the trapping column off the trapping column. 26 . The method of claim 22 , further comprising detecting a component of the sample after further separation by SFC. 27 . The method of claim 22 , further comprising positioning the trapping column in a flow path of the first mobile phase downstream of the RPLC column for capturing at least a portion of the sample separated by the RPLC column. 28 . The method of claim 27 , further comprising switching the trapping column carrying the captured portion to a flow path of a second mobile phase for eluting the captured portion off the trapping column. 29 . The method of claim 28 , wherein the step of positioning the trapping column in the flow path of the first mobile phase or the step of switching the trapping column to the flow path of the second mobile phase is performed in a fluidic routing unit interfacing a fluidic path of the PRLC and a fluidic path of the SFC. 30 . The method of claim 22 , further comprising re-capturing at least a portion of the sample eluted off the trapping column on a focus column prior to further separation by SFC. 31 . The method of claim 22 , wherein the first mobile phase flows through the trapping column in a first direction, and the portion of the sample captured on the trapping

Assignees

Inventors

Classifications

  • optical isomers · CPC title

  • Optical detectors {(measurement of intensity, velocity, spectral content, polarisation, or phase of infrared, visible or ultraviolet light G01J)} · CPC title

  • Chiral chromatography · CPC title

  • B01D15/14Primary

    relating to the introduction of the feed to the apparatus · CPC title

  • using supercritical fluid as mobile phase or eluent · CPC title

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What does patent US2016238573A1 cover?
Provided are two-dimensional chromatography systems and methods for separating and/or analyzing complex mixtures of organic compounds. In particularly, a two-dimensional reversed-phase liquid chromatography (RPLC)-supercritical fluid chromatography (SFC) system is described including a trapping column at the interface which collects the analytes eluted from the first dimension chromatography wh…
Who is the assignee on this patent?
Genentech Inc
What technology area does this patent fall under?
Primary CPC classification B01D15/14. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Thu Aug 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).