US20130306563A1 - Chromatography column support - Google Patents

Chromatography column support Download PDF

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Publication number
US20130306563A1
US20130306563A1 US13/980,985 US201213980985A US2013306563A1 US 20130306563 A1 US20130306563 A1 US 20130306563A1 US 201213980985 A US201213980985 A US 201213980985A US 2013306563 A1 US2013306563 A1 US 2013306563A1
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United States
Prior art keywords
support
legs
column
chromatography column
chromatography
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Abandoned
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US13/980,985
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English (en)
Inventor
Andreas Blaschyk
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Hoffmann La Roche Inc
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Hoffmann La Roche Inc
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Assigned to ROCHE DIAGNOSTICS GMBH reassignment ROCHE DIAGNOSTICS GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: BLASCHYK, ANDREAS
Assigned to F. HOFFMANN-LA ROCHE AG reassignment F. HOFFMANN-LA ROCHE AG ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ROCHE DIAGNOSTICS GMBH
Assigned to HOFFMANN-LA ROCHE INC. reassignment HOFFMANN-LA ROCHE INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: F. HOFFMANN-LA ROCHE AG
Publication of US20130306563A1 publication Critical patent/US20130306563A1/en
Abandoned legal-status Critical Current

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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/60Construction of the column
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D15/00Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • B01D15/08Selective adsorption, e.g. chromatography
    • B01D15/10Selective adsorption, e.g. chromatography characterised by constructional or operational features
    • B01D15/22Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to the construction of the column
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/50Conditioning of the sorbent material or stationary liquid
    • G01N30/56Packing methods or coating methods
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/60Construction of the column
    • G01N30/6047Construction of the column with supporting means; Holders
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/60Construction of the column
    • G01N30/6052Construction of the column body
    • G01N30/6069Construction of the column body with compartments or bed substructure
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/50Conditioning of the sorbent material or stationary liquid
    • G01N30/56Packing methods or coating methods
    • G01N2030/562Packing methods or coating methods packing
    • G01N2030/565Packing methods or coating methods packing slurry packing
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/60Construction of the column
    • G01N30/6004Construction of the column end pieces
    • G01N30/6021Adjustable pistons
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/60Construction of the column
    • G01N30/6004Construction of the column end pieces
    • G01N30/603Construction of the column end pieces retaining the stationary phase, e.g. Frits

Definitions

  • a chromatography column support which allows a movable frit to be positioned within a chromatography column at a desired position.
  • the support comprises a multitude of legs and a multitude of connectors connected to the upper end of the legs providing a support over the entire diameter of the column for a movable frit.
  • a chromatographic column is reported.
  • the chromatography apparatus as reported therein comprises a column of the type having a gas inlet, a gas outlet, at least one column wall interconnecting the gas inlet and gas outlet and confining solid particulate packing material, and means for preventing and reducing component profile distortion by straightening or reshaping component profiles after they have sustained distortion.
  • the legs are plates comprising a multitude of holes.
  • the support comprises three legs and one connector, whereby the connector is Y-shaped.
  • the support comprises at least four legs and at most sixteen legs and comprises four connectors.
  • At least one of the connectors and one of the legs are combined in one unit. In one embodiment each of the connectors is combined with a leg in a unit.
  • the chromatography column support comprises more legs than connectors.
  • the chromatography column support is a single entity.
  • the chromatography column support comprises multiple entities.
  • the connectors have a width of less than 8.0 mm.
  • the chromatography column support has a diameter of less than 12.5 cm.
  • the chromatography column support is made of stainless steel, or silicone, or polytetrafluoroethylene, or glass.
  • Another aspect as reported herein is a device comprising
  • Another aspect as reported herein is the use of a chromatography column support as reported herein for the stabilization of a chromatography column packing from inside the packing.
  • the chromatography column support is constructed in a way to minimize the disturbance of the chromatography material during the column packing process. Additionally it is constructed in a way to minimize the disturbance of the mobile phase flowing though the chromatography material during a chromatographic separation process.
  • the chromatography column support as reported herein can be made as a single piece (e.g. by casting the molded material in a casting mold) or from multiple pieces (e.g. by connecting the pieces together, such as screwing or bonding).
  • the chromatography column support as reported herein is not affixed to the chromatography column. It can be removed from the column without the need to first detach it from the column.
  • the chromatography column support as reported herein supports the chromatography column packing inside the packing.
  • chromatography columns as well as top and/or bottom plates inside the chromatography column support the chromatography column packing from the outside.
  • the chromatography column support as reported herein forms a framework inside the chromatography column packing. This framework supports the stability and homogeneity of the chromatography material packing from inside the packing.
  • a common chromatography column supports the chromatography material packing only from the outside.
  • a chromatography column packing comprising a chromatography column support as reported herein has improved stability compared to a chromatography column packing in a conventional chromatography column without the chromatography column support as reported herein.
  • one connector and one leg are combined in one unit denotes that the presence of an additional connector is obsolete as the leg has the same length as the connector and is connected to other legs/connectors at or around the axis of symmetry.
  • the chromatography material is located within a column housing (chromatography column) and denoted as “stationary phase”.
  • stationary phase To enable a stationary phase to interact with substances/polypeptides in a solution applied to it, the stationary phase is surrounded by/embedded in a “mobile phase”.
  • mobile phase denotes a liquid, e.g. a buffered, aqueous solution, a mixture of water and an organic solvent, or an organic solvent, which is used in the chromatographic purification method in which a stationary phase is employed.
  • affinity chromatography with microbial proteins (e.g. protein A or protein G affinity chromatography), ion exchange chromatography (e.g. cation exchange (carboxymethyl resins), anion exchange (amino ethyl resins) and mixed-mode exchange), thiophilic adsorption (e.g. with beta-mercaptoethanol and other SH ligands), hydrophobic interaction or aromatic adsorption chromatography (e.g. with phenyl-sepharose, aza-arenophilic resins, or m-aminophenylboronic acid), metal chelate affinity chromatography (e.g.
  • microbial proteins e.g. protein A or protein G affinity chromatography
  • ion exchange chromatography e.g. cation exchange (carboxymethyl resins), anion exchange (amino ethyl resins) and mixed-mode exchange
  • thiophilic adsorption e.g. with beta-mercaptoethanol and other SH
  • Ni(II)- and Cu(II)-affinity material size exclusion chromatography
  • electrophoretical methods such as gel electrophoresis, capillary electrophoresis
  • a chromatography column comprising a chromatography material and a mobile phase is employed.
  • the mobile phase is forced through the chromatography column and therewith through the chromatography material by applying pressure to the mobile phase.
  • Mediated by the mobile phase the pressure is also applied to the chromatography material whereby a pressure drop from the inlet of the chromatography column to the outlet of the chromatography column is established.
  • the pressure has dropped to the outside atmospheric pressure.
  • the highest pressure force is applied to the upper fraction of the chromatography material in the chromatography column.
  • the applied pressure normally depends on the one hand on the particle size of the chromatography material as well as on the viscosity of the mobile phase as a constant flow through the chromatography column is set but not a constant pressure. Generally the pressure increases with decreasing chromatography material particle size. At a constant flow rate through the chromatography material a change in viscosity of the mobile phase, e.g. during the regeneration or cleaning of the chromatography material, results in a change of the pressure applied to the chromatography material.
  • the chromatography material in general is not a pressure insensitive material, i.e. it can be compressed and expands after a compression.
  • the chromatography material is compressed and the height of the chromatography material inside the chromatography column, i.e. the bed height, is reduced.
  • the chromatography material expands again and the height of the chromatography material inside the chromatography column increases at most to the height before the application of the pressure.
  • This compression and expansion of the chromatography material is at the same time a macroscopic process of the entire chromatography material and a microscopic process of the individual particles of the chromatography material. With increasing numbers of such compression-expansion-cycles the particles of the chromatography material break down into smaller particles.
  • the chromatography material packing gets more compact and, therewith, at the same time the pressure required for maintaining a constant liquid phase flow through the chromatography column, i.e. the chromatography material, increases. This in turn again results in a further break down of the chromatography material particles resulting again in an increased pressure and so on.
  • a chromatography column separation generally can be operated up to a maximum pressure. When this upper pressure limit is reached the chromatography column packing has to be replaced in its entirety.
  • the support as reported herein is movable within the column, i.e. it can be placed anywhere along the axis of the column.
  • the height of the support and therewith the height of the corresponding horizontal section of the chromatography column is variable and can be adjusted to the properties of the chromatography material used with the support. Additionally, as the support is movable within the column damage to the inner wall of the chromatography column is prevented.
  • the support as reported herein can be made of any material that can be used in column chromatography, such as Teflon (polytetrafluoroethylene), stainless steel, silicone, or glass.
  • the chromatography column support as reported herein is made of polytetrafluoroethylene or stainless steel or silicone or glass. This allows for the provision of an inert support that does not interfere or interact with the chromatography material (column packing) as well as the substances to be separated.
  • the chromatography column support is made of a chromatographically inert material.
  • the support as reported herein is not affixed to the chromatography column the support can be applied to and also removed from the column in an easy way. Additionally because the support is removable from the column it can be easily and efficiently cleaned and sanitized.
  • the chromatography column support in the device as reported herein is freely moveable within the chromatography column. In one embodiment the chromatography column support in the device as reported herein is within the chromatography column but not affixed to the inner wall of the chromatography column.
  • the support as reported herein can be provided in many different variations in diameter and height and is therewith applicable to a multitude of different chromatography columns. But the diameter of the chromatography column support as reported herein is always less than the inner diameter of the chromatography column in order to ensure a free movability inside the column either during the packing of the column and/or the use of the column.
  • the legs of the support are in the form of a plate an additional stabilization effect of the chromatographic material can be provided.
  • the legs and the connectors form a single unit and, thus, the chromatography column support comprises at least three legs that are connected to each other at or around the axis of symmetry.
  • the support as reported herein can be used in combination with a movable frit.
  • the support can provide a stabilizing effect throughout the entire chromatography material inside the column.
  • the support as provided herein improves the packing process as a homogeneous packing of the chromatography material can be effected already prior to the application of the support. After the use of the column (single-use column) or when the chromatography material has to be replaced (multi-use column) the support can easily be removed with the chromatography material, just as with a column not comprising a support as reported herein. It is also possible to make the packing process with the support as reported herein already introduced into the respective horizontal section of the chromatography column.
  • one aspect as reported herein is the use of a chromatography column support as reported herein for supporting chromatography material in a chromatography column.
  • the support made of stainless steel, or silicone, or polytetrafluoroethylene, or glass.
  • the legs are plates and that the connectors and the legs form a unit in which the upper edge of the respective leg is the connector.
  • the legs are perforated plates.
  • the support comprises one or more circular legs that have different radii with respect to each other and with respect to the axis of symmetry.
  • a lateral flow between the sections defined by the legs of the support is possible.
  • the chromatography material is provided with an inner structure without introducing compartments that are tightly closed to other compartments inside the column.
  • the packing of the chromatography material can be obtained in a more homogeneous form, (ii) the formation of tension inside the packing can be prevented, (iii) flow and mass transport is ensured over the entire cross-section of the chromatography column, (iv) an easy packing and de-packing process is possible.
  • one aspect as reported herein is the use of a chromatography column support as reported herein for providing an inner structure to a chromatography material in a chromatography column.
  • the supported packing region can be from the bottom of the column up to the top without any non-supported areas in between or above or below the chromatography material packing.
  • each of the horizontal sections provided by a combination of a support as reported herein and a movable frit can be packed individually enabling the packing of a chromatography column from the bottom to the top.
  • a different chromatography material can be introduced, thus, providing a means for a so called hybrid-chromatography.
  • the support as reported herein provides for a vertical as well as horizontal supportation of the chromatography material inside the chromatography column.
  • one aspect as reported herein is the use of a chromatography column support as reported herein for providing vertical and horizontal support of the chromatography material inside a chromatography column.
  • the support as reported herein provides a means for using the currently used chromatography columns in a more flexible way and at the same time minimizing the costs associated with flexibility as only the novel support has to be added.
  • FIG. 1 In the upper part of FIG. 1 one embodiment of the support as reported herein which has four legs in the form of planes (full areas) is shown.
  • the legs and the connectors are combined in a single unit and the support does not comprise additional connectors.
  • the upper edge of the leg corresponds to the connector.
  • the planes of the legs are in a 90° angle to each other and to the plane defined by the upper edges of the legs (i.e. the connectors).
  • the diameter of the support and the outer area of the legs i.e.
  • the outer edge of the legs which is the edge in the direction of the column and perpendicular to the plane defined by the upper edges/connectors) can be adapted to any column diameter, so that the support can be introduced and removed into any column without friction and damaging the inner surface of the column.
  • the height of the support as reported herein is variable and can be adjusted to the specific application.
  • the bottom area of the support can be adapted to the base on which the support is to be placed.
  • the base is a frit in most cases. The base supports the support and carries his weight without the column wall being involved.
  • the upper area of the chromatography column support is formed in a way that either it is suitable as a base for a moveable column fit (moveably chromatography column separator) or the upper adapter of the column can be put thereon. It is therefore ensured that the complete packing is stabilized by the support as reported herein.
  • one aspect as reported herein is the use of a support as reported herein to stabilize the packing of a chromatography column. If a moveable column separator is used, another support, optionally in a different form, can be put on the separator at most until the maximum column length reached. However, it also possible that only a part of the chromatography column packing is equipped with the support as reported herein.
  • FIG. 1 In the lower part of FIG. 1 one embodiment of the support as reported herein is shown.
  • This support comprises six legs each in form of a plane which are divided up symmetrically.
  • the upper edge of each of the six legs represents the six connectors with which the legs form a unit in this embodiment.
  • the legs are attached to each other at a circle around the axis of symmetry of the support.
  • the pressure expected inside a column and the function of the support which is demanded determines the number of legs. These are dependent on the used chromatography medium and the process conditions.
  • FIG. 2 In the upper part of FIG. 2 one embodiment of the support as reported herein is shown.
  • the legs are in the form of a plane and form a unit together with the connectors which are represented by the upper edges of each of the legs.
  • Characteristic for this embodiment are the longish openings in the planes of the legs of the support.
  • This form offers an improved support for the chromatographic material and is especially suited for soft gels.
  • one aspect as reported herein is the use of a chromatography column support as reported in this embodiment for stabilizing the packing of soft chromatography gels. Without being bound by theory it is assumed that the chromatographic material can find more support/contact area in the narrow rooms. The load and the pressure are absorbed by the support and passed on to the lower layers of the column packing in reduced form.
  • one aspect as reported herein is the use of a chromatography column support as reported herein for adsorbing pressure inside a chromatography column packing.
  • Another characteristic of this embodiment is the crossways networking which is obtained. A lateral flow between the individual sections made up by the legs of the support is therefore possible.
  • a lateral flow between the individual sections defined by the legs of the support and the axis of symmetry of the support is possible. This should provide an improved mass transfer and column performance.
  • the homogeneity of the packet during the column life also remains unchanged. The appearing tensions spread out better in column bed, which is only partly interrupted.
  • each of the connectors forms a single unit with the individual legs.
  • some of the legs are connected to each other at the axis of symmetry of the support.
  • the support comprises additional legs that are not connected to each other around or at the axis of symmetry.
  • This support is characterized by the fact that holes inside the planes of the legs of the support provide the crossways networking.
  • the legs are made of perforated plates.
  • the support further comprises at least two, especially three, circular legs (and round connectors) that all have different radii with respect to the axis of symmetry of the support.
  • a first number of legs is connected to each other at the axis of symmetry of the support and all legs (connectors) are connected to each other by the circular legs (round connectors) of the support.
  • the support comprises three circular legs (round connectors), whereby the first circular leg (round connector) has a radius with respect to the axis of symmetry of the support of one sixth of the total diameter of the support, the second circular leg (round connector) has a radius of one third of the total diameter of the support, and the third circular leg (round connector) has a radius of half the total diameter of the support. All legs are also connected to each other with the further round connectors.
  • a connector comprising circular legs and perforated plates as legs for stabilizing the column packing of large diameter chromatography columns.
  • large diameter chromatography column denotes a chromatography column with an inner diameter of 15 cm or more.
  • FIG. 2 In the lower part of FIG. 2 one exemplary embodiment of the support as reported herein is shown.
  • the support is shown inside a chromatographic column.
  • the column comprises a support as reported herein and a moveably chromatography column fit placed thereon. These elements are flexible and not permanently connected to the column wall or other column components or to each other.
  • the support comprises three legs in form of a rod and three connectors connected to each other at the axis of symmetry of the support.
  • FIG. 3 an exemplarily chromatographic column which is equipped with several different supports as reported herein is shown.
  • the column in addition comprises a number of moveable chromatography column separators.
  • the column wall offers only the guidance for the supports and the moveable column separators which glide along the chromatography column wall while they are moved.
  • the column wall does not have to be modified. None of the elements is permanently connected or affixed to the column wall.
  • Such a column can also be packed with different chromatographic materials in the individual horizontal sections made up of a pair of support and separator.
  • one aspect as reported herein is the use of a support as reported herein and a moveable frit to define horizontal sections in a chromatography column.
  • the composition of all the used elements can be changed very simple and every time. Unpacking the column can be carried out in a conventional way.
  • the used supports and moveable chromatography column separators can simply be removed from the column together with the column packing. All used equipment parts can independently of each other be cleaned or partly
  • FIG. 4 a pressure flow diagram of a chromatography column comprising a DEAE-Sepharose chromatographic material is shown.
  • the left curve shows the typical behavior of a DEAE-Sepharose chromatographic material in columns which are packed in a conventional way.
  • the right curve the behavior of a column equipped with two supports as reported herein and two chromatographic column separators is shown. It can be seen that the maximum flow rate of the conventionally packed column is less than half of the flow rate which has been achieved with the column comprising a support as reported herein (24 l/h instead of 55 l/h).
  • FIG. 5 a pressure flow diagram of a chromatography column comprising an HA-Ultrogel chromatographic material is shown.
  • the left curve shows the typical behavior of HA-Ultrogel in columns which are operated without a support as reported herein.
  • the right curve the behavior of a column comprising two supports as reported herein and two moveable chromatographic column separators is shown.
  • the maximum flow of the column without the support as reported herein is less than the flow rate of the column comprising a support as reported herein (8 l/h instead of 15 l/h) (details of the column without a support as reported herein: 4 l slurry of HA-Ultrogel, bed height: 24 cm; used eluent: 0.0005 mol (conductivity 5 mS) KCl solution; details of the column comprising a support as reported herein: height of the used support: 8 cm, strength of the used separator: 5 mm, 4 l slurry of DEAE Sepharose distributed on three compartments, bed height: 24 cm, used eluent: 0.0005 mol (conductivity 5 mS) KCl solution).
  • the device comprises two chromatography column separators and two supports as reported herein.
  • the device comprises three chromatography column separators and three supports as reported herein.
  • the separator and the support both have an outer diameter that is less than the inner diameter of the chromatography column.
  • the diameter of the support and the separator is of from 90% to 99% of the inner diameter of the chromatography column. All the embodiments of the support as reported herein and outlined above are also embodiments of the supports comprised in the device as reported herein. Specific embodiments of the separators comprised in the device as reported herein are outlined below.
  • the presence of one chromatography column separator divides the chromatography column in an upper chromatography column chamber and a lower chromatography column chamber.
  • the separator has a variable position within the chromatography column. This “movability” is provided for by a guide ring. Thus, the separator can slide vertically within the column and the separator is embedded in the chromatography material.
  • a chromatography column separator consisting of a guide ring and a fit mounted therein does not interfere with the chromatographical separation process.
  • the separator allows e.g. that only a fraction of the chromatography material has to be exchanged when the maximum operating pressure is reached, without the need to replace the entire chromatography column packing. That is, the chromatography column separator permits that the chromatography material in an upper chromatography column chamber can be exchanged without interfering with the chromatography material in a lower chromatography column chamber.
  • the partial removal of the chromatography material is possible as the separator on the one hand divides the total chromatography material in the chromatography column in distinct fractions and on the other hand prevents the packed chromatography material in the lower chromatography column chamber from being perturbed upon the removal of the chromatography material in the upper chromatography column chamber.
  • the separator on the one hand divides the total chromatography material in the chromatography column in distinct fractions and on the other hand prevents the packed chromatography material in the lower chromatography column chamber from being perturbed upon the removal of the chromatography material in the upper chromatography column chamber.
  • the chromatography column separator comprises a guide ring into which a fit made of any inert material can be mounted.
  • An “inert material” is a material that does not interfere with the chromatography separation process, i.e. a chromatogram obtained with a chromatography column containing one or more chromatography column separators as reported herein is identical to a chromatogram obtained with a chromatography column containing no chromatography column separators under/with otherwise identical conditions.
  • inert materials are e.g. metal, especially stainless steel, silicone, polypropylene, polyethylene, polytetrafluoroethylene, sintered materials or combinations thereof, especially polytetrafluoroethylene coated stainless steel.
  • FIG. 6 exemplary chromatography column separators are shown.
  • a separator with a single frit is depicted comprising a frit ( 1 ) and a fitting ( 2 ).
  • a separator with an upper frit ( 3 ) and a lower frit ( 4 ) and a fitting ( 2 ) is shown.
  • FIG. 6 a a separator with a single frit is depicted comprising a frit ( 1 ) and a fitting ( 2 ).
  • FIG. 6 b a separator with an upper frit ( 3 ) and a lower frit ( 4 ) and a fitting ( 2 ) is shown.
  • each of the axially symmetric cross-section areas has a) a tapering structure, wherein the tapering is from the outside to the inside of the guide ring, and b) a notch ( 8 ) with an opening directed to the inside of the guide ring for mounting a frit.
  • the chromatography column separator comprises a guide ring and a fit mounted into the guide ring.
  • the guide ring is of circular shape and for use in a liquid chromatography column.
  • the guide ring has a vertical cross-section comprising two axially symmetric cross-section areas ( 5 and 6 ), wherein each of the axially symmetric cross-section areas has
  • the notch is a rectangular notch.
  • each of the cross-section areas has a triangular shape and the longest side ( 7 ) has a length of at least 1.5 times the diameter of the notch ( 8 ).
  • the ring is made of rubber, plastic, silicone, polytetrafluoroethylene, polyethylene, or polypropylene.
  • the frit has a pore size of from 1 ⁇ m to 20 ⁇ m, or b) each of the frits has a pore size of from 1 ⁇ m to 20 ⁇ m independently of each other whereby the pore size of the upper frit is smaller than the pore size of the lower frit.
  • the frit is made of metal, silicone, polypropylene, polyethylene, polytetrafluoroethylene, sintered materials or combinations thereof.
  • the separator comprises distance holders all attached to one side of the separator.
  • the chromatography column separator comprises one frit, in another embodiment the separator comprises an upper fit and a lower frit. In a further embodiment the chromatography column separator or the upper fit or the lower fit has a pore size of from 1 ⁇ m to 20 ⁇ m, whereby the pore size of the upper frit is smaller than the pore size of the lower frit. In another embodiment the frit is made of metal, silicone, polypropylene, polyethylene, polytetrafluoroethylene, sintered materials or combinations thereof.
  • the fitting or guide ring has a circular shape with a cross-section that can have any shape as long as it has a rectangular notch for taking up the frit.
  • the cross-section of the fitting has the shape of a triangle with a rectangular notch for taking up the frit in the corner of the triangle with the biggest inside angle.
  • the fitting or guide ring has the cross-section or provides cross-sectional areas in form of a triangle, in another embodiment of a rectangular triangle, wherein the frit is attached to the corner of the triangle with an inner angle of 90°.
  • the cross-section area of the guide ring has a trapezoid from with the rectangular notch for taking up the frit being at the shorter side of the parallel sides.
  • the fitting has the form of a rectangle, in another embodiment of a rectangle with inner angles of 90°, 90°, 80° and 100°. In one embodiment are the inner angles of 80° and 100° are at the upper side or at the bottom side of the rectangle.
  • the longest side of the guide ring is the outer edge of the separator and has contact to the chromatography column wall when the separator is placed inside a chromatography column. In another embodiment the longest side has a vertical orientation.
  • the cross-section areas of the fitting or guide ring have the form of a rectangle with inner angles of 90° with the rectangular notch for taking up the frit in one of the shorter sides or in case of a square in one of the sides.
  • the side with the notch is the side of the fitting directing to the center of the separator and likewise the chromatography column or in other words the notch is in the side of the fitting or guide ring that is parallel to the flow direction of the mobile phase and that has a diameter smaller than the outer diameter of the frit.
  • the guide ring has besides the preventing of liquid phase and chromatography material particles passing the separator beside frit the function to prevent the canting and therewith stalling of the entire separator in the chromatography column during the compression and expansion of the chromatography material upon the applying of the outside pressure.
  • the separator is placed inside the chromatography material packed into a chromatography column. The separator can be moved freely and placed exactly inside the column as it can slide along the inner wall of the chromatography column.
  • the vertical cross-sectional areas of the guide ring have the form of a triangle or trapezoid in which the guide ring has a tapering structure, wherein the tapering is from the outside to the inside of the guide ring, that is the guide ring is at its outer edge higher than at its inner edge or at the notch, respectively.
  • the outer edge of the guide ring has a height that is at least 1.5 times the height of the notch. In another embodiment the outer edge of the guide ring has a height that is at least 1.5 times, or two times, or three times, or more than three times the height of the notch.
  • the separator comprises an upper frit and a lower frit
  • the fitting or guide ring is a single fitting or ring and in another embodiment the fitting or guide ring is made of an upper fitting or ring and a lower fitting or ring.
  • the two fittings or rings have in one embodiment a contact-area comprising the lower side of the upper fitting or ring and the upper side of the lower fitting or ring, whereby the contact sides are flat, i.e. have no notch or groove, and are in line with the lower side of the upper fit and the upper side of the lower frit, i.e. the lower side of the upper fitting and the lower side of the upper frit form a single surface without offset and likewise the upper side of the lower fitting or ring and the upper side of the lower frit form a single surface without offset whereby both surfaces are parallel.
  • the smallest inner diameter of the fitting or guide ring or of the upper fitting and of the lower fitting is smaller than the outer diameter of the frit, i.e. the fitting or guide ring extends over the outer perimeter of the fit towards the center of the chromatography column.
  • the packing of a chromatography column with a chromatography material with a support and/or an embedded chromatography column separator can be split up into two packing phases.
  • the packing can be started with the packing of a first fraction of the chromatography material into the column according to general procedures. Afterwards the support and the chromatography column separator can be placed in and on top of the first fraction of the chromatography material. Finally the second fraction of the chromatography material can be packed into the column on top of the separator according to general procedures.
  • This packing method is a packing from the bottom to the top. In contrast columns not containing a support and a separator are packed from the top requiring among other things higher packing pressure.
  • the chromatography column support as reported herein provides a means for packing a chromatography column in two sequential steps if one support and one separator are used, or in three or more sequential steps if two or more supports and separators are used.
  • the column can be divided in an upper chamber and a lower chamber (one support and one separator) or a lower chamber, a middle chamber, and an upper chamber (two supports and two separators) whereof each itself is equivalent to a chromatography column with reduced chromatography material bed height.
  • the volume (of the chromatography material in one chamber) to surface (of the chamber) ratio is changed, i.e. lowered, and the stability of the chromatography material packing is increased.
  • the connectors are plates.
  • the legs are plates and the connectors are the upper edge of the respective plate.
  • At least one of the connectors and one of the legs form a single unit, whereby the legs are plates and the connector is the upper edge of the plate. I.e. the connector is defined by the upper edge of the plate.
  • each of the connectors forms a single unit with an individual leg.
  • each of the connectors forms a single unit with a leg.
  • each of the legs forms a single unit with a connector and, thus, the chromatography column support comprises units that are connected to each other at or around the axis of symmetry.
  • some of the legs are connected to each other at the axis of symmetry of the support.
  • the plates are perforated plates.
  • the support comprises additional legs that are not connected to each other at or around the axis of symmetry.
  • the support comprises one or more circular legs having different radii with respect to the axis of symmetry of the support.
  • a lateral flow between the sections defined by the legs of the support and the axis of symmetry of the support is possible.
  • the support comprises three legs and one connector, whereby the connector is Y-shaped and the legs are in form of rods.
  • the support consists of three legs in form of rods and a Y-shaped connector.
  • the support consists of three legs in form of plates that are connected to each other at or around the axis of symmetry.
  • the support consists of four legs in form of rods and an X-shaped connector.
  • the support consists of four legs in form of plates that are connected to each other at or around the axis of symmetry.
  • the support consists of six legs in form of rods and an X-shaped connector.
  • the support consists of six legs in form of plates that are connected to each other at or around the axis of symmetry.
  • the plates are perforated plates.
  • the support comprises at least four legs and at most sixteen legs and comprises four connectors.
  • the chromatography column support comprises more legs than connectors.
  • the chromatography column support is a single entity.
  • the chromatography column support comprises multiple entities.
  • the connectors have a width of less than 8.0 mm.
  • the chromatography column support has a diameter of less than 12.5 cm.
  • the chromatography column support is made of a chromatographically inert material.
  • the chromatography column support is made of stainless steel, or silicone, or polytetrafluoroethylene, or glass.
  • One aspect as reported herein is a device comprising
  • the chromatography column support is freely moveable within the chromatography column.
  • the chromatography column support in the device as reported herein is within the chromatography column but not affixed to the inner wall of the chromatography column.
  • One aspect as reported herein is the use of a chromatography column support as reported herein for the stabilization of a chromatography column packing from inside the packing.
  • One aspect as reported herein is the use of a chromatography column support as reported herein for supporting chromatography material inside a chromatography column.
  • One aspect as reported herein is the use of a chromatography column support as reported herein for providing an inner structure to a chromatography material in a chromatography column.
  • One aspect as reported herein is the use of a chromatography column support as reported herein for providing vertical and horizontal support of the chromatography material inside a chromatography column.
  • One aspect as reported herein is the use of a support as reported herein to stabilize the packing of a chromatography column.
  • chromatography column support comprising perforated plates as combined legs and connectors or comprising plates as legs which comprise longish openings for stabilizing the packing of soft chromatography gels.
  • One aspect as reported herein is the use of a chromatography column support for adsorbing pressure inside a chromatography column packing.
  • One aspect as reported herein is the use of a connector comprising circular legs and perforated plates as legs for stabilizing the column packing of large diameter chromatography columns.
  • One aspect as reported herein is the use of a support as reported herein and a moveable frit to define horizontal sections in a chromatography column.
  • FIG. 1 Exemplary embodiments of the support as reported herein: upper: element which has four legs in the form of full areas, these in 90° angles stand to each; lower: element which has six legs.
  • FIG. 2 Exemplary embodiments of the support as reported herein: upper: element with four legs comprising longish openings in the leg areas; middle: element with round holes in the legs providing crossways networking; lower: element which has three legs inside a chromatography column
  • FIG. 3 Scheme of a chromatographic column comprising several different supports as reported herein and several chromatography column separators.
  • FIG. 4 Flow diagram of a DEAE-Sepharose chromatography column: left curve: column without a support as reported herein; right curve: column with a support as reported herein.
  • FIG. 5 Flow diagram of a HA-Ultrogel chromatography column: left curve: column without a support as reported herein; right curve: column with a support as reported herein.
  • FIG. 6 Exemplary chromatography column separators: a) separator with a single frit comprising a frit ( 1 ) and a fitting ( 2 ); b) separator with an upper frit ( 1 ) and a lower frit ( 3 ) and an upper fitting ( 2 ) and a lower fitting ( 4 ); c) vertical cross-section of the guide ring of the separator comprising two axially symmetric cross-section areas ( 5 and 6 ) each having i) a tapering structure, wherein the tapering is from the outside to the inside of the guide ring, and i) a notch ( 8 ) with an opening directed to the inside of the guide ring for mounting a frit.
  • FIG. 7 Pressure values during the regenerations and cycle numbers of a chromatography column not comprising the support as reported herein.
  • FIG. 8 Pressure values during the regenerations and cycle numbers of a chromatography column comprising the support as reported herein.
  • the homogeneous inserting and distribution of the chromatography medium is very important.
  • the first is to put the flexible bed support element in the column first and inserting the slurry afterwards. In this case the slurry must homogeneously be brought in into the column.
  • the other possibility is bringing in the slurry into the column first, homogenizing it in the column and afterwards introducing the bed support element by putting it directly into the slurry in the column.
  • a homogeneous column bed forms and encloses the element. After the specified settling time can either an intermediate column fit be put on the bed support element or the column can be locked with an adapter. If an intermediate column frit is used, another flexible bed support element can be put on top and the packing of the next column compartment can be started. The process can be repeated until the complete column height is filled/packed.
  • Pressure values during the regenerations and cycle numbers are shown in FIG. 7 .
  • Pressure values during the regenerations and cycle numbers are shown in FIG. 8 .

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  • General Physics & Mathematics (AREA)
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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20200360837A1 (en) * 2017-11-17 2020-11-19 Bio-Rad Laboratories, Inc. Chromatography plug
US10935524B2 (en) 2017-07-27 2021-03-02 CEM Corporation, Lucidity Division Gas chromatograph device with inductively heated column and method of use thereof
US10955393B2 (en) 2017-07-27 2021-03-23 CEM Corporation, Lucidity Division Gas chromatograph device with removable column holder and method of use thereof
EP3668585A4 (en) * 2017-08-15 2021-10-06 Fluid Management Systems, Inc. SYSTEMS AND METHODS FOR VACUUM EXTRACTION AND PURIFICATION OF LIQUID
US11435328B2 (en) * 2020-02-28 2022-09-06 Agilent Technologies, Inc. Unions and couplers

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11395980B2 (en) 2010-01-25 2022-07-26 Spf Technologies Llc Chromatographic cassette
US10507409B2 (en) 2016-03-12 2019-12-17 Spf Technologies, Llc Hyper-productive chromatography system and process
US11219844B2 (en) 2010-01-25 2022-01-11 Spf Technologies Llc Stackable planar adsorptive devices
US10391423B2 (en) 2010-01-25 2019-08-27 Spf Technologies Llc Stackable planar adsorptive devices
CN107261556B (zh) * 2013-08-12 2019-08-16 Spf技术有限责任公司 可堆叠的平面吸附装置
JP6745501B2 (ja) 2014-04-12 2020-08-26 サイティバ・スウェーデン・アクチボラグ クロマトグラフィーカラム用の持ち上げおよび保持システム
MX2020005699A (es) * 2017-12-13 2020-10-16 Regeneron Pharma Dispositivos y sistemas para manipulacion de soportes de lecho de columna para cromatografia y metodos relacionados.
WO2023023032A1 (en) * 2021-08-16 2023-02-23 Jsr Corporation Chromatographic bed insert

Family Cites Families (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3374606A (en) 1965-09-10 1968-03-26 Abcor Inc Method of and apparatus for chromatographic separations
US3298527A (en) 1965-05-17 1967-01-17 Wright John Lemon Chromatographic flow column
DE1598049B2 (de) 1965-06-03 1972-04-06 Boehringer Mannheim Gmbh, 6800 Mannheim Verfahren und vorrichtung zur technischen durchfuehrung der saeulenchromatographie
US3398512A (en) 1966-04-18 1968-08-27 Continental Oil Co Chromatography apparatus
GB1203439A (en) 1966-11-08 1970-08-26 Pharmacia Fine Chemicals Ab Improvements in or relating to gel filtration columns
US3453811A (en) 1968-05-03 1969-07-08 Abcor Inc Chromatographic columns with partition elements therein
US3657864A (en) * 1970-04-03 1972-04-25 Texaco Inc Separation system for the resolving of volatile mixtures
FR2207740B1 (ja) 1972-11-24 1976-04-30 Rhone Poulenc Ind
DE2808154C3 (de) * 1978-02-25 1980-09-11 Roehm Gmbh, 6100 Darmstadt Verfahren und Kolonne zur Gelfiltration
EP0008921A1 (en) 1978-09-08 1980-03-19 Wright Scientific Limited Column chromatography and like processes and apparatus for the practice thereof
US4351621A (en) * 1979-12-19 1982-09-28 Liou Jin S Connector for combination furniture
DE3436095A1 (de) 1984-10-02 1986-04-10 Merck Patent Gmbh, 6100 Darmstadt Chromatographiesaeule
US4719011A (en) 1985-03-22 1988-01-12 H. T. Chemicals, Inc. High pressure liquid chromatography columns
JPS6242051A (ja) * 1985-08-19 1987-02-24 Kurita Water Ind Ltd クロマトグラフイ−装置
US5124133A (en) * 1985-10-31 1992-06-23 Wilmer Schoenrock Apparatus and method for providing a uniform flow profile through large diameter, low-pressure vessels
DE3606474A1 (de) 1986-02-28 1987-09-17 Merck Patent Gmbh Chromatographievorsaeule
JPH0638904B2 (ja) * 1987-07-14 1994-05-25 キッコーマン株式会社 連続移動式充填層装置
WO1991014490A1 (en) 1990-03-29 1991-10-03 Ht Chemicals Inc. Slurry compressor, apparatus for guiding compressor, and method for packing slurry in column
JPH0687984B2 (ja) * 1990-11-28 1994-11-09 雪印乳業株式会社 イオン交換樹脂内蔵回転型カラムイオン交換器およびそれを用いたイオン交換処理方法
RU2009482C1 (ru) * 1991-12-28 1994-03-15 Малое научно-производственное предприятие "Элсико" Колонка для жидкостной хроматографии
FR2690444B1 (fr) 1992-04-22 1995-07-13 Rucheton Marcel Procede de preparation d'une solution d'albumine plasmatique purifiee.
FI97277C (fi) * 1993-01-25 1996-11-25 Suomen Sokeri Oy Kromatografinen erotuskolonni, sen sisärakenteet ja kromatografinen erotusmenetelmä
JP3348256B2 (ja) * 1993-02-22 2002-11-20 エヌイーシートーキン株式会社 奪熱雰囲気検出装置
JP3159609B2 (ja) 1994-08-18 2001-04-23 住友林業株式会社 引戸用引手具
GB9419888D0 (en) 1994-10-03 1994-11-16 Davis John Apparatus and techiques for separation
US5667676A (en) 1996-05-01 1997-09-16 Alaska; Andrew B. Side-packed chromatographic column
US5866008A (en) 1997-02-11 1999-02-02 Shalon; Yehuda Method for packing and sealing chromatographic columns
US6281336B1 (en) 1998-06-09 2001-08-28 Statens Serum Institut Process for producing immunoglobulins for intravenous administration and other immunoglobulin products
AU5213999A (en) 1998-08-20 2000-03-14 Dyax Corporation Segmented chromatography column
US6352266B1 (en) 1998-10-22 2002-03-05 Michael J. Rigoli Seal for a liquid chromatography column
US6458273B1 (en) 1999-10-29 2002-10-01 Ontogen Corporation Sample separation apparatus and method for multiple channel high throughput purification
CZ299516B6 (cs) 1999-07-02 2008-08-20 F. Hoffmann-La Roche Ag Konjugát erythropoetinového glykoproteinu, zpusobjeho výroby a použití a farmaceutická kompozice sjeho obsahem
JP2001330598A (ja) 2000-05-22 2001-11-30 Fuji Chemical Industries Ltd 多層充填剤充填カラム
US6440301B1 (en) 2000-09-29 2002-08-27 Westinghouse Savannah River Company, Llc Chromatography resin support
US6565745B2 (en) 2001-08-01 2003-05-20 Isco, Inc. Disposable chromatographic columns
US20030146159A1 (en) * 2002-02-06 2003-08-07 Guiochon Georges A. Method and apparatus to pack high efficiency columns for chromatography
CN2531388Y (zh) * 2002-04-10 2003-01-15 中国石油天然气总公司石油勘探开发科学研究院 快速石油烃分布分析仪
GB0230265D0 (en) * 2002-12-30 2003-02-05 Amersham Biosciences Ab Piston and scraper assembly
US6942794B2 (en) 2003-03-21 2005-09-13 Millipore Corporation High velocity chromatography column flow distributor
CA2584372A1 (en) 2004-11-04 2006-05-11 Bio-Rad Pasteur Stackable chromatography module and chromatography column comprising a stack of such modules
US7314551B2 (en) * 2004-11-19 2008-01-01 Uop Llc Flow distribution apparatus
TW200902555A (en) 2005-01-03 2009-01-16 Hoffmann La Roche Antibodies against IL-13 receptor alpha 1 and uses thereof
JP4604817B2 (ja) 2005-04-28 2011-01-05 マツダ株式会社 自動変速機のバンドブレーキ装置
JP3957078B1 (ja) 2005-05-24 2007-08-08 ヘラマンタイトン株式会社 カートリッジカラム
JP4972329B2 (ja) 2006-03-27 2012-07-11 株式会社日立ハイテクノロジーズ 高速液体クロマトグラフ用カラム及び高速液体クロマトグラフ装置
EP1916522A1 (en) 2006-10-25 2008-04-30 Agilent Technologies, Inc. Column having separated sections of stationary phase
JP4861217B2 (ja) * 2007-03-07 2012-01-25 日本碍子株式会社 分離カラム
JP4840218B2 (ja) * 2007-03-28 2011-12-21 栗田工業株式会社 クロマトグラフィカラム用の液導入ユニット、整流部材およびクロマトグラフィ装置
US7780853B2 (en) 2007-06-15 2010-08-24 Ge Healthcare Bio-Sciences Ab Method for conducting maintenance on a chromatography column
KR101477871B1 (ko) 2009-07-30 2014-12-30 에프. 호프만-라 로슈 아게 이동식 크로마토그래피 컬럼 세퍼레이터

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10935524B2 (en) 2017-07-27 2021-03-02 CEM Corporation, Lucidity Division Gas chromatograph device with inductively heated column and method of use thereof
US10955393B2 (en) 2017-07-27 2021-03-23 CEM Corporation, Lucidity Division Gas chromatograph device with removable column holder and method of use thereof
EP3668585A4 (en) * 2017-08-15 2021-10-06 Fluid Management Systems, Inc. SYSTEMS AND METHODS FOR VACUUM EXTRACTION AND PURIFICATION OF LIQUID
US20200360837A1 (en) * 2017-11-17 2020-11-19 Bio-Rad Laboratories, Inc. Chromatography plug
US11839836B2 (en) * 2017-11-17 2023-12-12 Bio-Rad Laboratories, Inc. Chromatography plug
US11435328B2 (en) * 2020-02-28 2022-09-06 Agilent Technologies, Inc. Unions and couplers

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MX347297B (es) 2017-04-21
JP6389285B2 (ja) 2018-09-12
RU2584176C2 (ru) 2016-05-20
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HK1189269A1 (zh) 2014-05-30
BR112013017573B1 (pt) 2021-05-18
CN103339502B (zh) 2016-02-17
US11241638B2 (en) 2022-02-08
CN103339502A (zh) 2013-10-02
JP2017083471A (ja) 2017-05-18
EP2671074A1 (en) 2013-12-11
MX2013008354A (es) 2013-08-27
CA2824218C (en) 2019-12-03
JP6073811B2 (ja) 2017-02-01
JP2014508924A (ja) 2014-04-10
WO2012104278A1 (en) 2012-08-09
KR101951965B1 (ko) 2019-02-25
US20190255462A1 (en) 2019-08-22
BR112013017573A2 (pt) 2016-10-18
KR20140008340A (ko) 2014-01-21

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