EP0991943A1 - Magnetic particles with biologically active receptors - Google Patents
Magnetic particles with biologically active receptorsInfo
- Publication number
- EP0991943A1 EP0991943A1 EP97929133A EP97929133A EP0991943A1 EP 0991943 A1 EP0991943 A1 EP 0991943A1 EP 97929133 A EP97929133 A EP 97929133A EP 97929133 A EP97929133 A EP 97929133A EP 0991943 A1 EP0991943 A1 EP 0991943A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- magnetic particles
- particles according
- protein
- magnetic
- color pigments
- 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- Withdrawn
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54313—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals the carrier being characterised by its particulate form
- G01N33/54326—Magnetic particles
- G01N33/5434—Magnetic particles using magnetic particle immunoreagent carriers which constitute new materials per se
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2446/00—Magnetic particle immunoreagent carriers
- G01N2446/20—Magnetic particle immunoreagent carriers the magnetic material being present in the particle core
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/824—Immunological separation techniques
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/10—Composition for standardization, calibration, simulation, stabilization, preparation or preservation; processes of use in preparation for chemical testing
Definitions
- the invention relates to magnetic particles for separating biological mixtures, a process for their production and use of the magnetic particles.
- US 4,795,698 discloses a method for producing suspendable magnetic particles coated with a biological material.
- the coprecipitate is resuspended, washed and then processed into a magnetic polymer material.
- the method has the disadvantage that iron ions are released ⁇ .
- the object of the present invention is to eliminate the disadvantages of the prior art.
- simple and inexpensive to produce magnetic particles for separating biological mixtures are to be provided.
- magnetic particles are provided for separating biological mixtures, which have pearlescent color pigments with magnetic properties and a co-polymer coating.
- Pearlescent color pigments are oily raw materials that are produced in particle form for the coating industry on a large scale. These are mica sheets that can be coated with various metal oxides, such as hamatite or titanium oxide.
- black pigment In the case of magnetic pearlescent color pigments, a core made of mica is first coated with titanium oxide and then with magnetite. This so-called black pigment has ferromagnetic properties. It is available in m particle size distributions of usually 10-60 ⁇ m, preferably in m particle sizes of 1-30 ⁇ m.
- the black pigment usually has the following composition:
- the black pigment can surprisingly be coated directly with biological polymers. In this form it is suitable for separating biological mixtures.
- magnétique pearlescent color pigments Another surprising property of the magnetic pearlescent color pigments is their resistance to acids, such as glacial acetic acid, alkalis, such as sodium hydroxide, and to inorganic and organic solvents, such as dimethyl sulfoxide / water mixtures, acetone, alcohols, nitro thinners, methylene chloride u. the like
- acids such as glacial acetic acid, alkalis, such as sodium hydroxide
- inorganic and organic solvents such as dimethyl sulfoxide / water mixtures, acetone, alcohols, nitro thinners, methylene chloride u. the like
- the magnetic behavior of the particles according to the invention is not influenced by the aforementioned substances.
- the particles according to the invention are preferably used in combinatorial chemistry and in high throughput screening. They can be used in particular as solid phase carriers for organic reactions.
- the biological polymer coating is not resistant to reactions requiring extreme solvents. It has surprisingly been found that black pigments can be used as solid phase carriers in combinatorial chemistry or in high throughput screening. They can also be used as a catalyst.
- R-IgG For the production of biotmylated Rmder immunoglobulin, 0.5 ml of an R-IgG solution, the 2 mg of R-IgG (Boeh ⁇ nger Mannneim) is dissolved, and 1 ml of phosphate-buffered saline solution, pH 7.25 (2.76 g / 1 NaH PO HO ; 3.56 g / 1 Na HPO 2H 0; 8 g / 1
- the particles are then washed 3 times with 100 ml of Milli-Q water, the solid and liquid phase being separated between the washing steps by sedimentation or centrifugation.
- the particles are then taken up again in 40 ml of phosphate-buffered sodium chloride solution, pH 7.25.
Landscapes
- Health & Medical Sciences (AREA)
- Immunology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Cell Biology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Peptides Or Proteins (AREA)
- Treatment Of Liquids With Adsorbents In General (AREA)
Abstract
Magnetic particles for separating biological mixtures consist of nacreous lustre pigments with magnetic properties coated with a biological polymer.
Description
Magnetische Partikel mit biologisch aktiven RezeptorenMagnetic particles with biologically active receptors
Die Erfindung betrifft magnetische Partikel zum Trennen von biologischen Gemischen, ein Verfahren zu deren Herstellung sowie eine Verwendung der magnetischen Partikel.The invention relates to magnetic particles for separating biological mixtures, a process for their production and use of the magnetic particles.
Aus der US 3,970,518 ist es bekannt, magnetische Partikel mit verschiedenartigen magnetischen Eigenschaften als Festphase zum Trennen von oiologischen Gemischen zu verwenden. Die Par- tikel sind mit einem biologiscnen Material überzogen. Sie eignen sich bsp. zum Abtrennen bestimmter Zellpopulationen aus einem Gemisch verschiedenartiger Zellpopulationen.From US 3,970,518 it is known to use magnetic particles with different magnetic properties as a solid phase for separating oiological mixtures. The particles are coated with a biological material. They are suitable, for example. for separating certain cell populations from a mixture of different cell populations.
Die US 4,795,698 offenbart ein Verfahren zur Herstellung suspendierbarer, mit einem biologischen Material überzogener magnetischer Partikel. Dabei wird eine Koprazipitation aus einer Fe (III) -Ionen und ein Polymer, bsp. ein Protein, enthaltenden Losung durch Zugabe bei einer starken Base, wie NH_OH, durchgeführt. Das Koprazipitat wird resuspendiert, gewaschen und dann zu einem magnetischen Polymermaterial weiterverarbeitet. Das Verfahren hat den Nachteil, daß Eisenionen frei¬ gesetzt werden.US 4,795,698 discloses a method for producing suspendable magnetic particles coated with a biological material. A coprecipitation from an Fe (III) ion and a polymer, e.g. a protein containing solution by adding a strong base such as NH_OH. The coprecipitate is resuspended, washed and then processed into a magnetic polymer material. The method has the disadvantage that iron ions are released ¬.
Aufgabe der vorliegenden Erfindung ist es, die Nachteile des Stands der Technik zu beseitigen. Insbesondere sollen einfach und kostengünstig herstellbare magnetische Partikel zum Trennen biologischer Gemische bereitgestellt werden.The object of the present invention is to eliminate the disadvantages of the prior art. In particular, simple and inexpensive to produce magnetic particles for separating biological mixtures are to be provided.
Diese Aufgabe wird durch die Merkmale der Ansprüche 1 und 11 bis 18 gelost. Zweckmäßige Ausgestaltungen ergeben sich aus den Merkmalen der Ansprüche 2 bis 10.
Nach Maßgabe der Erfindung sind magnetische Partikel zum Trennen von biologischen Gemischen vorgesehen, die Perlglanzfarbpigmente mit magnetischen Eigenschaften und einem cαolo- gischen Polymeruberzug aufweisen. Perlglanzfarbpigmente sind oillige Ausgangsrohstoffe, die m Partikelform für die Lack- mdustrie m großem Maßstab hergestellt werden. Dabei handelt es sich um Glimmerblattchen, die mit verschiedenen Metalloxi- den, wie Hamatit oder Titanoxid, belegt sein können.This object is achieved by the features of claims 1 and 11 to 18. Appropriate configurations result from the features of claims 2 to 10. According to the invention, magnetic particles are provided for separating biological mixtures, which have pearlescent color pigments with magnetic properties and a co-polymer coating. Pearlescent color pigments are oily raw materials that are produced in particle form for the coating industry on a large scale. These are mica sheets that can be coated with various metal oxides, such as hamatite or titanium oxide.
Bei magnetischen Perlglanzfarbpigmenten ist ein Kern aus Glimmer zunächst mit Titanoxid und dann mit Magnetit umman- tel. Dieses sogenannte Schwarzpigment besitzt ferromagneti- sche Eigenschaften. Es ist m Partikelgroßenverteilungen von üblicherweise 10 - 60 μm, vorzugsweise m Partikelgroßen von 1 - 30 μm, verfugbar. Das Schwarzpigment hat üblicherweise die folgenαe Zusammensetzung:In the case of magnetic pearlescent color pigments, a core made of mica is first coated with titanium oxide and then with magnetite. This so-called black pigment has ferromagnetic properties. It is available in m particle size distributions of usually 10-60 μm, preferably in m particle sizes of 1-30 μm. The black pigment usually has the following composition:
Glimmer 38 - 48 Gew.MMica 38 - 48 wt
Titandioxid 5 - 9 Gew. Magnetit 47 - 53 Gew.Titanium dioxide 5 - 9 wt. Magnetite 47 - 53 wt.
Das Schwarzpigment kann überraschenderweise direkt mit biologischen Polymeren überzogen werden. Es eignet sich in dieser Form zum Trennen von biologischen Gemischen.The black pigment can surprisingly be coated directly with biological polymers. In this form it is suitable for separating biological mixtures.
Eine weitere überraschende Eigenschaft der magnetischen Perlglanzfarbpigmente ist deren Resistenz gegen Sauren, wie Eisessig, Laugen, wie Natriumhydroxid, sowie gegen anorganische und organische Losungsmittel, wie Dι-methyl-sulfoxιd/ Wasser- Gemische, Aceton, Alkohole, Nitro-Verdunnungen, Methylenchlo- rid u. dgl . Das magnetische Verhalten der erfmdungsgemaßen Partikel wird durch die vorgenannten Substanzen nicht beeinflußt.
Die erfmdungsgemaßen Partikel finden vorzugsweise m der kombinatorischen Chemie und im High Throughput Screenmg Anwendung. Sie können insbesondere als Festphasentrager für or- ganische Reaktionen eingesetzt werden.Another surprising property of the magnetic pearlescent color pigments is their resistance to acids, such as glacial acetic acid, alkalis, such as sodium hydroxide, and to inorganic and organic solvents, such as dimethyl sulfoxide / water mixtures, acetone, alcohols, nitro thinners, methylene chloride u. the like The magnetic behavior of the particles according to the invention is not influenced by the aforementioned substances. The particles according to the invention are preferably used in combinatorial chemistry and in high throughput screening. They can be used in particular as solid phase carriers for organic reactions.
Bei extreme Losungsmittel erfordernden Reaktionen ist der biologische Poly eruberzug nicht resistent. Es wurde überraschenderweise gefunden, daß Schwarzpigmente als Festphasen- trager m der kombinatorischen Chemie oder im High Throughput Screenmg verwendbar sind. Sie können ferner als Katalysator eingesetzt werden.The biological polymer coating is not resistant to reactions requiring extreme solvents. It has surprisingly been found that black pigments can be used as solid phase carriers in combinatorial chemistry or in high throughput screening. They can also be used as a catalyst.
Nachfolgend wird die Erfindung anhand eines Ausfuhrungsbei- spiels naher erläutert.The invention is explained in more detail below on the basis of an exemplary embodiment.
1. Herstellung von biotmyliertem Rinder-Immunglobulm G (R- igG)1. Production of biotmylated cattle immunoglobulin G (R-igG)
Zur Herstellung von biotmyliertem Rmder-Immunglobulm werden 0,5 ml einer R-IgG-Losung, die 2 mg R-IgG (Boehπnger Mannneim) gelost m 1 ml phosphatgepufferter Kochsalzlosung, pH 7,25 (2,76 g/1 NaH PO H O; 3,56 g/1 Na HPO 2H 0; 8 g/1For the production of biotmylated Rmder immunoglobulin, 0.5 ml of an R-IgG solution, the 2 mg of R-IgG (Boehπnger Mannneim) is dissolved, and 1 ml of phosphate-buffered saline solution, pH 7.25 (2.76 g / 1 NaH PO HO ; 3.56 g / 1 Na HPO 2H 0; 8 g / 1
NaCl) enthalt, mit einer 6 μl D-Biotmoyl-ε-ammocapronsaure- N-hy roxysuccmimid-ester-Losung m phospnatgepufferter Kochsalzlosung, pH 7,25, und DMSO (Biotm Labelmg Kit von Beoh- ringer Mannneim) vermischt. Die Mischung wird 2,5 h bei Raumtemperatur mittels eines Magnetruhrers gerührt und anschließend über Nacht stehengelassen. Das molare Verhältnis von Biotin zu R-IgG entspricht 20 : 1.
2. Beschichtung von Magnetpartikeln mit biotiyliertem R-IgGNaCl), mixed with a 6 μl D-biotmoyl-ε-ammocaproic acid-N-hy roxysuccmimid-ester solution in phosphate-buffered saline, pH 7.25, and DMSO (Biotm Labelmg Kit from Behringer Mannneim). The mixture is stirred for 2.5 hours at room temperature using a magnetic stirrer and then left to stand overnight. The molar ratio of biotin to R-IgG corresponds to 20: 1. 2. Coating of magnetic particles with biotiylated R-IgG
2 g "4898 Iπodm® Black Mica" (Merck Katalog Nr. 4898.00050) werden einer Losung von 40 ml Beschichtungspuffer (NaHCC , 4,2 g/1, pH 9,6) und 6 μl R-IgG-Biotm-Losung gemäß Ziffer 1 suspendiert und unter Verwendung eines mechanischen Ruhrwerks über Nacht so mkubiert, daß die Suspension durch gelindes Bewegen erhalten bleibt.2 g "4898 Iπodm® Black Mica" (Merck Catalog No. 4898.00050) are a solution of 40 ml coating buffer (NaHCC, 4.2 g / 1, pH 9.6) and 6 μl R-IgG-Biotm solution according to number 1 suspended and incubated overnight using a mechanical stirrer so that the suspension is retained by gentle movement.
Anschließend werden die Partikel 3 x mit je 100 ml Milli-Q- Wasser gewaschen, wobei jeweils zwischen den Waschschritten durch Sedimentation oder Zentπfugation die Trennung von fester und flussiger Phase erfolgt. Anschließend werden die Partikel m 40 ml phosphatgepufferter Kochsalzlosung, pH 7,25, wieder aufgenommen.The particles are then washed 3 times with 100 ml of Milli-Q water, the solid and liquid phase being separated between the washing steps by sedimentation or centrifugation. The particles are then taken up again in 40 ml of phosphate-buffered sodium chloride solution, pH 7.25.
3. Beschichtung von Magnetpartikeln mit R-IgG3. Coating of magnetic particles with R-IgG
Zur Kontrolle wird ein Ansatz mit nicht biotmyliertem R-IgG unter identischen Konzentrationsbedingungen wie bei Ziffer 2 durchgeführt .As a control, an approach with non-biotmylated R-IgG is carried out under the same concentration conditions as in number 2.
4. Austesten der Bmdefahigkeit4. Testing for fitness
Zum Austesten der Bmdefahigkeit werden 200 μl der vollständig suspendierten Magnetpartikel gemäß Ziffer 2 mit 200 μl einer Streptavidm-Peroxidase-Konjugatlosung (Boehr ger Mannheim Katalog Nr.: 1089 153) 1 : 20.000 Verdünnung in phosphatgepufferter Kochsalzlosung, pH 7,25, gemischt und un- ter Schuttein 45 mm. mkubiert. Anschließend werden mittelsTo test the ability to absorb chemicals, 200 μl of the completely suspended magnetic particles according to number 2 are mixed with 200 μl of a streptavidm-peroxidase conjugate solution (Boehr ger Mannheim catalog no .: 1089 153) 1: 20,000 dilution in phosphate-buffered saline solution, pH 7.25, and uns - rubble 45 mm. mcubated. Then use
Magnetseparator (Boehrmger Mannheim Best. Nr. 1 641 794) dieMagnetic separator (Boehrmger Mannheim Order No. 1 641 794)
Partikel abgetrennt und der Überstand verworfen. Das wird wiederholt. /Anschließend werden 220 μl ABTS©-LosungParticles separated and the supernatant discarded. That is repeated. / Then add 220 μl ABTS © solution
(Boehrmger Mannheim Katalog Nr. 1 204 530 und 1 112 422) zu-
gegeben und nach Resuspension 15 mm. mkubiert. Mittels Magnetseparator werden die Partikel abgetrennt. 200 μl_ des Uberstands werden m eine Mikrotitrationsplatte (Innova GmbH) überfuhrt und bei 405 nm rransmissionsphotometrisch gemessen.(Boehrmger Mannheim Catalog No. 1 204 530 and 1 112 422) given and after resuspension 15 mm. mcubated. The particles are separated using a magnetic separator. 200 μl of the supernatant are transferred to a microtitration plate (Innova GmbH) and measured at 405 nm using transmission photometry.
ErgebnisResult
Magnetpartikel mit R-IgG Biotin 850 mE (gemäß Ziffer 2)Magnetic particles with R-IgG Biotin 850 mE (according to number 2)
Kontrolle mit R-IgG (gemäß Ziffer 3; 210 mE
Control with R-IgG (according to number 3; 210 mE
Claims
1. Magnetische Partikel zum Trennen von biologischen Gemischen, die Perlglanzfarbpigmente mit magnetischen Eigenschaf- ten und einen biologischen Polymeruberzug aufweisen.1. Magnetic particles for separating biological mixtures, which have pearlescent color pigments with magnetic properties and a biological polymer coating.
2. Magnetische Partikel nach Anspruch 1, wobei der Polymeruberzug ein Protein ist.2. Magnetic particles according to claim 1, wherein the polymer coating is a protein.
3. Magnetische Partikel nach Anspruch 2, wobei das Protein ein bmdefahiges Protein ist.3. Magnetic particles according to claim 2, wherein the protein is a bmdefahiges protein.
4. Magnetische Partikel nach einem der vorhergehenden Ansprüche, wobei das Protein einen bmdefahigen Rezeptor tragt.4. Magnetic particles according to one of the preceding claims, wherein the protein carries an bmdefahigen receptor.
5. Magnetische Partikel nach einem der vorhergehenden Ansprüche, wobei das Protein ein Rezeptor ist.5. Magnetic particles according to one of the preceding claims, wherein the protein is a receptor.
6. Magnetische Partikel nach einem der vorhergehenden Anspru- ehe, wobei das bmdefahige Protein ein Antikörper ist.6. Magnetic particles according to one of the preceding claims, wherein the bmdefahigen protein is an antibody.
7. Magnetische Partikel naen einem der vorhergehenden /Ansprüche, wobei das bmdefahige Protein ein Antigen ist.7. Magnetic particles according to any one of the preceding / claims, wherein the bmdefahigen protein is an antigen.
8. Magnetische Partikel nach einem der vorhergehenden Ansprüche, wobei das bmdefahige Protein eine Komponente des Li- gand-Rezeptor-Paares von Streptavid oder Biotm ist.8. Magnetic particles according to one of the preceding claims, wherein the bmde-capable protein is a component of the ligand-receptor pair of streptavid or biotm.
9. Magnetische Partikel nach einem der vorhergehenden Anspru- ehe, wobei die Perlglanzfarbpigmente einen Kern aus Glimmer aufweisen, der mit mindestens einem Metalloxid umgeben ist, das magnetische Eigenschaften aufweist.9. Magnetic particles according to one of the preceding claims, wherein the pearlescent color pigments have a core of mica which is surrounded by at least one metal oxide which has magnetic properties.
10. Magnetische Partikel nach einem der vorhergehenden An- spruche, wobei die Perlglanzfarbpigmente einer Korngroßen-
Verteilung von 0,1 - 500 μm, vorzugsweise von 1 - 100 μm, vorliegen.10. Magnetic particles according to one of the preceding claims, the pearlescent color pigments of a grain size Distribution from 0.1 to 500 μm, preferably from 1 to 100 μm, are present.
11. Verfahren zum Herstellen von magnetischen Partikeln zum Trennen von biologischen Gemischen, wobei die Partikel Perlglanzfarbpigmente mit magnetischen Eigenschaften sind und direkt mit einem Überzug aus biologischem Material bescnichtet werden.11. A method for producing magnetic particles for separating biological mixtures, the particles being pearlescent color pigments with magnetic properties and directly coated with a coating of biological material.
12. Verwendung von magnetischen Partikeln nach einem αer Ansprüche 1 bis 10 zum Abtrennen der Festphase tei Immunoas- says .12. Use of magnetic particles according to an αer claims 1 to 10 for separating the solid phase tei Immunoas- says.
13. Verwendung von magnetischen Partikeln nach einem der An- spruche 1 bis 10 als Bestandteil eines analytiscnen Reagenzansatzes .13. Use of magnetic particles according to one of claims 1 to 10 as part of an analytical reagent batch.
14. Verwendung von magnetischen Partikeln nach einem der Ansprüche 1 bis 10 als Bestandteil eines Analysesystems, beste- hend aus Reagenz und Partikeln.14. Use of magnetic particles according to one of claims 1 to 10 as part of an analysis system, consisting of reagent and particles.
15. Verwendung von magnetischen Partikeln nach einem αer Ansprüche 1 bis 10 als Bestandteil eines Analysesystems, bestehenden aus Geraten, Reagenzien und Partikeln.15. Use of magnetic particles according to an αer claims 1 to 10 as part of an analysis system, consisting of devices, reagents and particles.
16. Verwendung der magnetischen Partikel nach einem der Ansprüche 1 bis 10 für die kombinatorische Chemie und/oder das High Throughput Screenmg.16. Use of the magnetic particles according to one of claims 1 to 10 for combinatorial chemistry and / or high throughput screenmg.
17. Verwendung nach Anspruch 16, wobei die magnetischen Partikel stark saurem oder basischen Milieu oder m einem organischen Losungsmittel eingesetzt werden.
17. Use according to claim 16, wherein the magnetic particles are used in a strongly acidic or basic medium or in an organic solvent.
18. Verwendung von magnetischen Perlglanzfarbpigmenten für die kombinatorische Chemie und/oder das High Throughput Screenmg.
18. Use of magnetic pearlescent color pigments for combinatorial chemistry and / or high throughput screenmg.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/DE1997/001300 WO1998058257A1 (en) | 1997-06-18 | 1997-06-18 | Magnetic particles with biologically active receptors |
Publications (1)
Publication Number | Publication Date |
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EP0991943A1 true EP0991943A1 (en) | 2000-04-12 |
Family
ID=6918506
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP97929133A Withdrawn EP0991943A1 (en) | 1997-06-18 | 1997-06-18 | Magnetic particles with biologically active receptors |
Country Status (4)
Country | Link |
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US (1) | US6372517B1 (en) |
EP (1) | EP0991943A1 (en) |
JP (1) | JP2002511141A (en) |
WO (1) | WO1998058257A1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10355409A1 (en) | 2003-11-25 | 2005-06-30 | Magnamedics Gmbh | Spherical, magnetic silica gel carriers with increased surface area for the purification of nucleic acids |
JP3922648B2 (en) | 2004-05-24 | 2007-05-30 | 株式会社資生堂 | Affinity particles and affinity separation method |
US7850775B2 (en) * | 2006-11-09 | 2010-12-14 | Sun Chemical Corporation | Multi-colored lustrous pearlescent pigments |
US8349067B2 (en) | 2006-11-09 | 2013-01-08 | Sun Chemical Corp. | Multi-colored lustrous pearlescent pigments |
US8906154B2 (en) * | 2006-11-09 | 2014-12-09 | Sun Chemical Corporation | Coating, ink, or article comprising multi-colored lustrous pearlescent pigments |
US8221536B2 (en) | 2006-11-09 | 2012-07-17 | Sun Chemical Corp. | Cosmetic comprising multi-colored lustrous pearlescent pigments |
US8211224B2 (en) * | 2006-11-09 | 2012-07-03 | Sun Chemical Corp. | Multi-colored lustrous pearlescent pigments and process for making |
US8323396B2 (en) * | 2006-11-09 | 2012-12-04 | Sun Chemical Corp. | Orange pearlescent pigments |
US8211225B2 (en) | 2008-04-09 | 2012-07-03 | Sun Chemical Corp. | Magnetic pigments and process of enhancing magnetic properties |
DE102010014840B4 (en) | 2010-04-13 | 2015-12-10 | Magnamedics Gmbh | DNase-coated magnetic particles |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4038099A (en) * | 1971-08-30 | 1977-07-26 | The Mearl Corporation | Rutile-coated mica nacreous pigments and process for the preparation thereof |
US3861946A (en) * | 1972-07-21 | 1975-01-21 | Mearl Corp | Titanium dioxide nacreous pigments and process for the preparation thereof |
DE2313331C2 (en) * | 1973-03-17 | 1986-11-13 | Merck Patent Gmbh, 6100 Darmstadt | Mica flake pigments containing iron oxide |
US3970518A (en) | 1975-07-01 | 1976-07-20 | General Electric Company | Magnetic separation of biological particles |
GB1556272A (en) * | 1976-05-26 | 1979-11-21 | Mearl Corp | Iron oxide coated mica nacreous pigments |
US4055377A (en) * | 1976-08-03 | 1977-10-25 | Minnesota Mining And Manufacturing Company | Magnetically orientable retroreflectorization particles |
US4192691A (en) * | 1978-10-26 | 1980-03-11 | The Mearl Corporation | Metal oxide platelets as nacreous pigments |
DE3030056A1 (en) * | 1980-08-08 | 1982-03-25 | Basf Ag, 6700 Ludwigshafen | METHOD FOR THE PRODUCTION OF SCALE-SHAPED Mica Pigments Coated With Metal Oxides |
US4725499A (en) * | 1982-06-24 | 1988-02-16 | Mitsui Toatsu Chemicals, Inc. | Polymer-coated solid materials |
US4795698A (en) | 1985-10-04 | 1989-01-03 | Immunicon Corporation | Magnetic-polymer particles |
US4868106A (en) * | 1985-10-17 | 1989-09-19 | Konishiroku Photo Industry Co., Ltd. | Analytical element and method for determining a component in a test sample |
US5705265A (en) * | 1986-03-24 | 1998-01-06 | Emsci Inc. | Coated substrates useful as catalysts |
DE3617430A1 (en) * | 1986-05-23 | 1987-11-26 | Merck Patent Gmbh | PEARL PIGMENT |
DE3709217A1 (en) * | 1987-03-20 | 1988-09-29 | Basf Ag | LABEL-SHAPED PIGMENTS BASED ON IRON OXIDE |
FI77881C (en) * | 1987-04-14 | 1989-05-10 | Kemira Oy | YTBELAGDA SILIKATPARTIKLAR. |
FI78924C (en) * | 1988-01-22 | 1989-10-10 | Kemira Oy | Dye or color pigment containing pearl pigment and a process for its preparation |
CA1329867C (en) * | 1988-07-20 | 1994-05-31 | Hiroshi Ito | Pigment |
JP2979414B2 (en) * | 1989-09-29 | 1999-11-15 | 富士レビオ株式会社 | Magnetic particles and immunoassay using the same |
DE3938055A1 (en) * | 1989-11-16 | 1991-05-23 | Merck Patent Gmbh | MATERIALS COATED WITH PLAIN-SHAPED PIGMENTS |
US5935866A (en) * | 1989-12-22 | 1999-08-10 | Binax Nh, Inc. | Preparation of sub 100 A magnetic particles and magnetic molecular switches |
AU8951191A (en) * | 1990-10-29 | 1992-05-26 | Dekalb Plant Genetics | Isolation of biological materials using magnetic particles |
CA2114913C (en) * | 1993-02-05 | 2003-12-09 | Takafumi Atarashi | Powder having at least one layer and process for preparing the same |
US5855790A (en) * | 1994-02-07 | 1999-01-05 | Selective Environmental Technologies, Inc. | Magnetic particles, a method for the preparation thereof and their use in the purification of solutions |
US5643721A (en) * | 1994-02-09 | 1997-07-01 | Abbott Laboratories | Bioreagent immobilization medium |
US5576185A (en) * | 1994-04-15 | 1996-11-19 | Coulter Corporation | Method of positive or negative selection of a population or subpopulation of a sample utilizing particles and gravity sedimentation |
US5698839A (en) * | 1995-04-07 | 1997-12-16 | Eastman Kodak Company | Magnetically encodable card having magnetic pigment uniformly dispersed in plastic |
DE19606598C1 (en) * | 1996-02-22 | 1997-11-13 | Innova Gmbh | Magnetic particles for separating biological mixtures |
US6045914A (en) * | 1996-06-03 | 2000-04-04 | Engelhard Corporation | Pearlescent glass pigment |
EP1029244A4 (en) * | 1997-10-02 | 2003-07-23 | Aclara Biosciences Inc | Capillary assays involving separation of free and bound species |
US6001526A (en) * | 1998-03-24 | 1999-12-14 | Minolta Co., Ltd. | Binder carrier containing ethylenic unsaturated nitrile copolymer as binder resin |
US6165260A (en) * | 1999-03-30 | 2000-12-26 | Engelhard Corporation | Pearlescent pigments exhibiting color travel |
-
1997
- 1997-06-18 EP EP97929133A patent/EP0991943A1/en not_active Withdrawn
- 1997-06-18 JP JP50349899A patent/JP2002511141A/en active Pending
- 1997-06-18 US US09/445,984 patent/US6372517B1/en not_active Expired - Fee Related
- 1997-06-18 WO PCT/DE1997/001300 patent/WO1998058257A1/en not_active Application Discontinuation
Non-Patent Citations (1)
Title |
---|
See references of WO9858257A1 * |
Also Published As
Publication number | Publication date |
---|---|
US6372517B1 (en) | 2002-04-16 |
WO1998058257A1 (en) | 1998-12-23 |
JP2002511141A (en) | 2002-04-09 |
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