EP0419568A1 - Austausch-chromatographievorrichtung - Google Patents

Austausch-chromatographievorrichtung

Info

Publication number
EP0419568A1
EP0419568A1 EP89907585A EP89907585A EP0419568A1 EP 0419568 A1 EP0419568 A1 EP 0419568A1 EP 89907585 A EP89907585 A EP 89907585A EP 89907585 A EP89907585 A EP 89907585A EP 0419568 A1 EP0419568 A1 EP 0419568A1
Authority
EP
European Patent Office
Prior art keywords
column
channel
face
segment
tube
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP89907585A
Other languages
English (en)
French (fr)
Other versions
EP0419568A4 (en
Inventor
Thomas A. Snyder
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of EP0419568A1 publication Critical patent/EP0419568A1/de
Publication of EP0419568A4 publication Critical patent/EP0419568A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • 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
    • G01N30/26Conditioning of the fluid carrier; Flow patterns
    • G01N30/38Flow patterns
    • G01N2030/381Flow patterns centrifugal chromatography
    • 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
    • G01N30/04Preparation or injection of sample to be analysed
    • G01N30/16Injection
    • G01N30/18Injection using a septum or microsyringe

Definitions

  • the present invention relates to apparatus for column chromatography, specifically high-performance liquid chromatography. More particularly, the present invention is directed to keyed chromatography columns, complementary keyed collecting tubes, complementary racks, and methods of using the same for column chromatography.
  • Chromatography comprises a group of methods for separating a mixture of substances into their component parts. "Chromatography” is, however, a misnomer for these methods because the color of components is rarely the basis used for identifying and isolating component parts in modern techniques.
  • chromatographic techniques include gas chromatography (GC) or gas- liquid chromatography (GLC) , thin layer chromatography (TLC) , and column chromatography, frequently called high-performance liquid chromatography (HPLC) .
  • Column chromatography may be used to separate and identify a variety of substances, including pharmaceutical drugs, hormones, and cell constituents including deoxyribonucleic acid (DNA) and ribonuclei ⁇ acid (RNA) .
  • column chromatography is a selective filtration or elution process whereby a substance or species to be chro atographed is dissolved or suspended in an eluant and passed through a porous or semi-porous bed or column of chromatographic separation material, from which an eluate may be collected.
  • the chromatographic separation material is typically chosen dependent upon the substances to be chromatographed. Such separation material may be generally categorized into five types: (1) size-exclusion; (2) affinity; (3) ion-exchange; (4) reversed-phase; and (5) ion pairing. See generally J. A. Thompson, "A Review of High Performance Liquid Chromatography in Nucleic Acids Research," BioChromatography, 1:16 (1986).
  • pressure may be required (or desired in the interest of time) to force the eluants and substances through the separation material.
  • Conventional techniques include positive pressure, such as a pump or syringe, and negative pressure, such as gravity, vacuum withdrawal or centrifugation. With such a variety of techniques, versatile column chromatography apparatus is often required.
  • Supelco, Inc. manufactures Supelclean Disposal SPE Tubes, which contain silica gel-based bonded phase packings. Solutions may be passed through these tubes into collecting tubes using negative pressure by a vacuum or centrifugation, or by positive pressure by an air pump or syringe.
  • the Supelco tube requires a tube adapter to be fitted for a syringe or other positive pressure source using only friction to hold the adapter and positive pressure source in communication with the tube containing the chromatographic material and eluant.
  • Negative pressure by centrifugation is achieved by inserting the column or tube into a collecting tube and inserting this combined unit into a centrifugation device. No locking devices are present.
  • Microvette* columns which may be inserted into a collecting tube adapted to receive the Microvette* columns using friction to hold the columns in place.
  • the Microvette* column is, however, capable of being twisted even after being inserted into the collecting tube and thus provides no secure means for coupling or uncoupling the Microvette* columns to insertion apparatus.
  • Gelman Sciences Inc. manufactures filtration products for high-pressure liquid chromatography adapted to receive substances suspended in an eluant from an insertion device, such as a syringe.
  • the Gelman devices use filters which also function as a coupling between the collecting tube and the insertion source, typically a syringe. The coupling is achieved by friction, but may be locked in place by means of an additional, external clamping device.
  • CooperBiomedical, Inc. manufactures a mini-spin column comprising a separation material- filled column and a collecting tube adapted to receive and hold in place the column by friction means.
  • the column is not, however, adapted for coupling to an insertion means, such as a syringe. Further, nothing prohibits the column once inserted into the receiving collecting tube from rotating.
  • the column contains one fibrous filter packed into the lower, tapered end of the column on top of which the bed of separation material is packed.
  • Apparatus made by companies including those listed above are used to chromatograph a variety of substances, including highly toxic or virulent substances.
  • Conventional apparatus generally require that the operator or technician employing the chromatography apparatus come in contact with the apparatus during use. For example, to remove a chromatography column from a collecting tube normally requires one to pull the tube out by hand or by using clamp-like instruments.
  • to place a conventional chromatography column coupled to a syringe, for example, into a collecting tube uncouple the syringe and leave the column in the tube, one must normally hold the chromatography colum n in place to prevent the column from twisting or pulling out while the syringe is removed.
  • the present invention comprises a chromatography column comprising a polymer body having a channel extending therethrough, means for coupling the column to insertion apparatus having complementary coupling means, and keying means on the outer surface of the column.
  • the present invention further comprises a collecting tube having one end having an aperture therethrough being adapted to receive complementary keying means and having keying means on the outer surface of the tube.
  • the present invention further comprises a rack for receiving generally cylindrical bodies having complementary keying means.
  • the present invention comprises a kit for column chromatography comprising a chromatography column, a collecting tube and a rack for receiving the chromatography column and the collecting tube, all as described above.
  • the present invention comprises a method of filtering fluids, which comprises drawing a fluid into an insertion apparatus having coupling means and coupling the insertion apparatus to the chromatography column described above, inserting the fluid into the inlet end of the chromatography column, inserting the chromatography column into a collecting tube having one end with an aperture therethrough adapted to receive the complementary keying means of the chromatography column, and applying pressure to the species and eluant.
  • Figure 1 is a front elevational view of a keyed chromatography column in accordance with the present invention shown inserted into a collecting tube in accordance with the present invention and attached to an insertion device (here a medical syringe) and Figure 1 also contains a partial cross-sectional view showing coupling means on the chromatography column in accordance with the present invention and complementary coupling means on the insertion device;
  • an insertion device here a medical syringe
  • Figure 2 is a cross-sectional view of the keyed chromatography column along line 2-2 in Figure 6;
  • Figure 3 is a front elevational view of a keyed chromatography column having a cap inserted thereinto showing the chromatography column as inserted into a collecting tube in accordance with the present invention
  • Figure 4 is a cross-sectional view of the keyed chromatography column along line 4-4 in Figure 6;
  • Figure 5 is a top plan view of the collecting tube along line 5-5 in Figure 6;
  • Figure 6 is an exploded diagram showing a front elevational view of a cap which may be inserted into the chromatography column, which is shown as a partial cross-sectional view of a front elevational view of the chromatography column, which, in turn, may be inserted into the collecting tube, which is shown as a front elevational view of the collecting tube having a removable top end in accordance with the present invention;
  • Figure 7 is an isometric view showing a stand and illustrating keyed apertures adapted to receive the keyed chromatography column and collecting tube shown in Figure 6;
  • FIG 8 is a top plan view of a keyed stand having therein a keyed chromatography column according to the present invention.
  • keyed column chromatography apparatus comprises a chromatography column 30 comprising a polymer body, which has an open top end face 31 and an open bottom end face 33 and a channel 37 extending therethrough from the top end face 31 to the bottom end__f ce 3-3, where the channel 37 is generally circular and tapered from the top end face 31 to the bottom end face 33, the diameter of the channel 37 at the bottom end face 33 being smaller than the diameter of the channel 37 at the top end face 31.
  • the outer surface of the chromatography column 30 generally defines four segments.
  • the first segment 44 has a generally circular shape in cross-section and is generally uniform in cross- section along..the length thereof.
  • the second segment 46 is generally circular in, cross-section and is tapered from one end of the second segment 46 to the other end of the second segment 46.
  • the third segment 48 is generally circular in shape in cross-section and has a generally uniform shape in cross-section along the length thereof.
  • the diameter of the outer surface of the third segment 48 is generally smaller than the diameter of the outer surface of the first segment 44.
  • the fourth segment 49 of the chromatography column 30 according to the present invention has a generally circular shape in cross- section and is substantially tapered from one end of the fourth segment 49 to the other end of the fourth segment 49.
  • the polymer body comprises polypropylene, polyethylene, polyethylene terephalthane glycol (PETG) , nylon, polycarbonate, Barex, polyester, polypropinate, polytetrafluoroethylene (Teflon) , polyvinyl chloride, polysulfone and polystyrene. More preferably, the polymer body comprises polypropylene.
  • the polymer should be resistant to chemical action and thermal degradation and, preferably, should be fairly resistant to pressure exerted on the polymer body, specifically pressure from within the channel 37 of the polymer body.
  • PETG polyethylene terephalthane glycol
  • nylon nylon
  • polycarbonate Barex
  • polyester polypropinate
  • Teflon polytetrafluoroethylene
  • Teflon polyvinyl chloride
  • polysulfone polysulfone
  • polystyrene More preferably, the polymer body comprises polypropylene.
  • the polymer should be resistant to chemical action and thermal degradation and, preferably, should be
  • the polymer body of the chromatography column 30 may be formed using methods and techniques known in the art for molding polymer bodies.
  • the polymer body is formed by injection molding.
  • One skilled in the art will appreciate, however, that other methods and techniques for forming polymer bodies may be used in accordance with the present invention.
  • the channel 37 of the chromatography column 30 is adapted to receive at least one porous filter 36 which is securely positioned within the channel 37.
  • the filter 36 is circular or disk-shaped to conform to the cross-sectional shape of the channel 37 through the column 30 and preferably comprises plastic selected from the group consisting of polyvinylidene difluoride, cellulose, polysul one, polypropylene, nylon and polytetrafluoroethylene.
  • the porous filter 36 comprises porous plastic.
  • filters 36 include FP Vericel, GN Metricel, HT Tuffryn, Metricel, Polypropylene, Nylaflo, Versapor and glass fiber filters, all known in the art and described generally in "Separation Products for Molecular Biology", The Filter Book, at 153-55 (Gelman Science: 1988) .
  • the type and density or porosity of the porous filter 36 depends on the type and viscosity of the fluid to be filtered (discussed below) and the desired filtration to be performed.
  • One skilled in the art may readily determine the type and porosity of the porous filter 36., based on the filtration or chromatograph to be performed using the chromatography column 30 in accordance with the present invention.
  • the porous filter 36 may be securely positioned within the channel 37 of the chromatography column 30 by positioning the filter 36 in engagement with a retaining ring 38 inwardly protruding into the channel 37 of the chromatography column 30.
  • a retaining ring 38 may be, for example, an integral part of the polymer body, formed during the molding of the polymer body as described above.
  • a pair of retaining rings 38 may be positioned in the channel 37 so that the filter 36 is intermediate and in engagement with the pair of retaining rings 38.
  • the filter 36 may also be securely positioned by placing a filter 36 having a predetermined diameter into the tapered channel until the filter 36 becomes wedged at a point where the diameter of the channel 37 is smaller than the diameter of the filter 36 and can move no further, and positioning a retaining ring 38 in engagement with the side of the filter 36 toward the channel 37 having a larger diameter (i.e., distal the smaller diameter channel 37 proximal to the bottom end face 33) .
  • retaining rings 38 may be heat welded into the channel 37 of the chromatography column 30.
  • a porous filter disk 36 may have a diameter larger than the diameter of the channel 37 in the chromatography column 30 and a circular groove may be cut into the channel 37 to securely receive such a porous filter disk 36.
  • the channel 37 of the chromatography column 30 is further adapted to receive a bed of chromatographic separation material 40 positioned within the channel 37 adjacent the porous filter 36.
  • the separation material 40 comprises silica, cellulose, dextran, agarose, sepharose, sephadex, hydroxyapatite and paired-ion chromatography system resin. More preferably, the separation material 40 comprises paired-ion chromatography system resin.
  • the separation material 40 comprises paired-ion chromatography system resin.
  • the column 30 has a porous filter 36 and a bed of separation material 40 in the channel 37.
  • the separation material 40 is generally held in place by the porous filter 36, which is preferably placed proximal to the bottom end face 33 of the chromatography column 30 and securely positioned thereat.
  • the column 30 has a pair of porous filters 36, which are securely positioned in the channel 37, and a bed of separation material 40 positioned intermediate the pair of filters 36 in the channel 37 of the column 30.
  • the separation material 40 is positioned between two securely fastened filters 36, the material 40 will be held in place more securely and uniformly, resistant to any positive and/or negative forces exerted on the separation material 40 and any fluids passed therethrough.
  • the separation material 40 and at least one porous filter 36 is substantially present in the channel through the third segment 48.
  • the amount and type of separation material is purely dependent upon the desired chromatographic separation to be performed and may be readily determined by one skilled in the art.
  • the column 30 has means positioned at the top end face 31 of the column 30 for coupling the column 30 to insertion apparatus, such as the syringe 10 illustrated in Figures 1 and 6, which has complementary or reciprocal coupling means. It will be understood, however, that other insertion apparatus having complemental coupling means may be used in accordance with the present invention.
  • means for coupling the column 30 to insertion apparatus comprises at least one lug 32 protruding from the periphery of the top end face 31 of the column 30. More preferably, means for coupling the column 30 to insertion apparatus comprises two lugs 32 opposingly protruding from the periphery of the top end face 31 of the column 30. More preferably still, means for coupling the column 30 to insertion apparatus comprises a female luer lock.
  • Luer locks are known in the art as effective coupling means.
  • the American National Standard Institute (ANSI) describes such luer locks for use in, for example, connecting two medical devices, such as a syringe and a needle, as a liquid leak-proof and mechanically secure method which permits the two devices to be readily separated.
  • a luer lock comprises two mating tapered fittings, commonly called a luer slip, that are slip-fitted into each other with sufficient force to effect a leak-proof connection.
  • the channel 37 through the chromatography column 30 is formed so that the channel 37*proximal to the top end face 31 of the column 30 forms a female luer taper.
  • coupling means may be used in accordance with the present invention.
  • Complemental coupling means on an insertion apparatus such as a syringe 10 preferably comprises a male luer lock 12 as illustrated in the partial sectional view of Figure 1.
  • a male luer taper may be used as complemental coupling means in accordance with the present invention.
  • One example of device having a male luer taper is illustrated in Figures 3 and 6 showing a cap 42 comprising a male luer taper which may be firmly inserted into the channel 37 having a complemental female luer taper, thereby securely engaging the walls of the channel 37 and sealing the channel -Q7 proximal to the top end face 31.
  • the chromatography column 30 has at least one keying means on the outer surface of the column 30, which interrupts the generally circular shape of the outer surface thereof, and is positioned between the two end faces (31 and 33) of the column 30.
  • keying means are means which prevent the column 30 from being twisted about its. longitudinal axis when a torquing force is applied along such axis and when the column 30 is inserted or keyed into apparatus adapted to receive said keying means.
  • the keying means comprises a generally flat, planar surface 34 formed on the outer surface of the second segment 46 of the chromatography column 30. In another embodiment of the present invention, the keying means comprises two opposing generally flat, planar surfaces 34 formed on the outer surface of the second segment 46 of the column 30.
  • keying means may be used in accordance with the present invention.
  • a chromatography column 30 may be formed having protruding ridges longitudinally extending along the outer surface thereof; generally flat, planar surfaces 34, such as those described above, may be formed on the outer surface of the first segment 44 or the third segment 38; longitudinally extending grooves may be formed on the outer surface of the column 30; a chromatography column 30 may have lugs protruding outwardly from the outer surface thereof.
  • a generally flat, planar surface 34 formed on the outer surface of the column 30 is effective and relatively easy to manufacture.
  • keying means comprising a planar surface 34 is adapted to form a stop 35 at the end of said keying means proximal to the top end face 31 of the column 30.
  • stop 3.5 may be used to halt the insertion of the column 30 into an apparatus adapted to receive the column 30 having keying means, at a predetermined interval,. i.e., the point at which the stop 35 is located on the outer surface of the column 30.
  • FIGS 3, 5 and 6 illustrate a collecting tube 14 in accordance with the present invention.
  • a collecting tube 14 comprises a hollow body having a closed bottom end face 21 and a top end face 19 having an aperture 18 therethrough.
  • the hollow body of the Sollecting tube 14 has a circular hollow therein having a diameter large enough to receive, for example, the chromatography column 30 therein.
  • the aperture 18 is adapted to receive complemental keying means, in particular, the keying means present on the outer surface of the chromatography column 30 described above.
  • the outer surface of the collecting tube 14 defines a first tube segment 24 having a generally circular shape in cross-section which is generally uniform in cross-section along the length thereof.
  • the outer surface of the collecting tube 14 defines a second tube segment 26 having a generally circular shape in cross-section, which may be generally uniform in cross-section along the length thereof or tapered from the end of the second tube segment 26 proximal to the top end face 19 to the end of the second tube segment 26 distal to the top end face 19.
  • the outer surface of the collecting tube 14 also defines a third tube segment 28 having a generally circular shape in cross-section and tapered from the end of the third tube segment 28 proximal to the top end face 19 to the end of the third tube segment 28 distal to the top end face 19.
  • the collecting tube 14 has at least one keying means on the outer surface of the tube 14, which interrupts the generally circular shape thereof which is positioned between the two end faces (19 and 21) of the collecting tube 14.
  • the keying means on the outer surface of the collecting tube 14 comprises at least one flat, planar surface 20 formed on the outer surface of the second tube segment 26 of the tube 14.
  • the keying means on the outer surface of the collecting tube 14 may be provided in the same manner as the keying means positioned on the outer surface of the chromatography column 30 described above. It will be further understood that similar parameters, methods and materials may be employed to position keying means on the outer surface of the collecting tube 14 as were employed to position keying means on the outer surface of the chromatography column 30 described above.
  • the body of the collecting tube 14 comprises polymer or glass. More preferably, the body comprises polymer.
  • polymers which may be used to form the body of the collecting tube 14 in accordance with the present invention include polyvinylidene difluoride, cellulose, polysulfone, polypropylene, nylon and polytetrafluoroethylene. It is particularly preferred that the body of the collecting tube comprises polypropylene.
  • the body of the collecting tube 14 may be comprised of other suitable materials, such as metal.
  • Suitable materials preferably include those materials capable of resisting chemical action and withstanding relatively high forces typically downwardly directed within the hollow body occurring, for example, where a collecting tube 14 containing fluid is used in centrifugation apparatus.
  • a collecting tube 14 containing fluid is used in centrifugation apparatus.
  • One skilled in the art may readily determine the material desired to be used to form the body of the collecting tube 14 in accordance with the present invention.
  • the aperture 18 through the top end face 19 of the collecting tube 14 preferably has a generally circular shape, interrupted by at least one flat, planar surface, which corresponds and is adapted to receive complemental generally cylindrical configurations having keying means as described above.
  • the aperture 18 is preferably adapted to receive the complementary keying means present on the outer surface of the chromatography column 30 described above.
  • the aperture 18 through the top end face of the collecting tube 14 preferably has a generally circular shape interrupted by two opposing flat, planar surfaces corresponding in relative shape and relative position to the complemental flat, planar surfaces 34 formed on the outer surface of the chromatography column 30.
  • the configuration of the aperture 18 through the top end face 19 of the collecting tube 14 corresponds to the complemental configuration of a cross- section through the chromatography column 30 at a point where the keying means is positioned (as, for example, along line 4-4 in Figure 6) .
  • One skilled in the art may readily determine the desired configurations of the aperture 18 through the top end face 19 of the collecting tube 14 in accordance with the present invention.
  • top end face 19 of the collecting tube 14 having an aperture 18 therethrough is adapted to be removable.
  • a removable top end face 19 may facilitate recovery of any fluid present in the collecting tube 14 during or after use of the collecting tube 14 with, for example, a chromatography column 30, especially where the aperture 18 has a diameter substantially smaller than the inner diameter of the hollow body of the collecting tube 14.
  • a removable top end face 19 comprises a collecting tube cap 16 as illustrated in Figures 3, 5 and 6.
  • the collecting tube cap 16 preferably comprises a polymer selected from the group described above for the body of the collecting tube 14 and may be the same as or different than the material used to form the collecting tube 14. It is preferred that the cap 16 is adapted to securely fasten to the body of the collecting tube 14.
  • a top end face comprising a collecting tube cap 16 having an aperture 18 therethrough as described above, comprises a male fitting which inserts into the hollow body of the collecting tube 14 and further comprises pressure ribs 17 outwardly protruding from the portion of the cap 16 that inserts into the collecting tube 14, as illustrated in Figure 6. It may be further desired to form a lip 22 outwardly protruding from the cap 16 to facilitate removal of the cap 16 from the collecting tube 14.
  • Such collecting tube caps 16 are, without an aperture 18 therethrough as described above, known in the art and available from manufacturers including Sarstedt, Inc.
  • other removable top end faces 19 may be used in accordance with the present invention.
  • the present invention further provides a rack 50 for receiving generally cylindrical bodies having keying means on the outer surfaces thereof.
  • Figures 7 and 8 illustrate a rack 50 comprising a top surface 58 having a plurality of apertures therethrough, said apertures being adapted to receive keying means, and a plurality of legs 56 sufficient to support the surface of the rack.
  • some of the apertures 52 through the surface 58 of the rack 50 are adapted to receive the keying means of the chromatography column 30 described above.
  • it is preferred that some apertures 54 through the surface 58 of the rack 50 are adapted to receive the keying means of the collecting tube 14 described above.
  • apertures 60 through the surface 58 of the rack 50 which are not adapted to receive keying means but are merely adapted to receive generally cylindrical bodies.
  • One skilled in the art may readily determine the number and location of apertures, some of which may be designed to receive keying means.
  • a rack 50 having means for positioning the rack 50 over complementary positioned collecting means (not shown) .
  • collecting means is a tray for collecting fluid.
  • the rack 50 may have positioning means comprising a plurality of lugs (not shown) downwardly protruding from the legs of the rack so that the lugs may be received by complementary apertures through the collecting means. It will be understood that other, similar positioning means may be used on a rack 50 in accordance with the present invention.
  • the apparatus of the present invention may be used individually or in combination to filter fluids.
  • a fluid may be filtered by drawing the fluid to be filtered into an insertion apparatus having coupling means, such as a syringe 10 having a male luer lock 12, and coupling the insertion apparatus to the chromatography column 30 described above.
  • the chromatography column 30 preferably has at least one porous filter 36 securely positioned within the channel 37 of the column 30.
  • the chromatography column 30 has a pair of porous filters 36 securely positioned in a spaced relation to one another within the channel 37 of the column 30 and a bed of chromatographic separation material 40 intermediate the pair of porous filters 36 within the channel 37 of the column 30.
  • the chromatography column 30 is inserted into the collecting tube 14 described above and pressure is applied to the fluid to force the fluid through the chromatography column 30.
  • the pressure may be applied using, for example, the insertion apparatus or, preferably, the insertion apparatus may be removed, said removal being facilitated by the keying means of the column 30 being received through the aperture 18 of the collecting tube 14, placing the collecting tube 14 having the chromatography column 30 inserted therethrough into a centrifugation device, for example, and applying, through centrifugal force, negative pressure to the fluid.
  • a centrifugation device for example, and applying, through centrifugal force, negative pressure to the fluid.
  • kit including a chromatography column 30, a cap 42, a collecting tube 14 and a rack 50, all as described above.
  • a kit may be individually designed to include some or all of the above as may be desired for a particular use.
  • One skilled in the art may determine the desired composition of a kit including the apparatus and methods of the present invention.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)
EP19890907585 1988-06-17 1989-06-13 Keyed column chromatography apparatus Withdrawn EP0419568A4 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US20832088A 1988-06-17 1988-06-17
US208320 1988-06-17

Publications (2)

Publication Number Publication Date
EP0419568A1 true EP0419568A1 (de) 1991-04-03
EP0419568A4 EP0419568A4 (en) 1991-09-11

Family

ID=22774151

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19890907585 Withdrawn EP0419568A4 (en) 1988-06-17 1989-06-13 Keyed column chromatography apparatus

Country Status (3)

Country Link
EP (1) EP0419568A4 (de)
AU (1) AU3847689A (de)
WO (1) WO1989012491A1 (de)

Families Citing this family (3)

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Publication number Priority date Publication date Assignee Title
CN1040690C (zh) * 1992-09-03 1998-11-11 惠普公司 一种色谱用的固相提取柱
CA2719787C (en) * 2008-03-28 2017-03-07 Biotix Inc. Sample preparation devices and methods for processing analytes
CN115078615B (zh) * 2022-08-22 2022-12-02 湖南德米特仪器有限公司 一种用于液相色谱的萃取柱

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US2979210A (en) * 1960-04-19 1961-04-11 Arthur H Thomas Company Test tube rack
US4476016A (en) * 1976-10-06 1984-10-09 Kiyasu John Y Heart attack screening method, apparatus and kit for same
US4214993A (en) * 1978-04-03 1980-07-29 E. I. Du Pont De Nemours And Company Apparatus for separating fluids
US4270921A (en) * 1979-09-24 1981-06-02 Graas Joseph E Microchromatographic device and method for rapid determination of a desired substance
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Title
No further relevant documents have been disclosed. *
See also references of WO8912491A1 *

Also Published As

Publication number Publication date
EP0419568A4 (en) 1991-09-11
WO1989012491A1 (en) 1989-12-28
AU3847689A (en) 1990-01-12

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