WO1978000005A1 - Magnetic polymer particles - Google Patents
Magnetic polymer particles Download PDFInfo
- Publication number
- WO1978000005A1 WO1978000005A1 PCT/SE1978/000001 SE7800001W WO7800005A1 WO 1978000005 A1 WO1978000005 A1 WO 1978000005A1 SE 7800001 W SE7800001 W SE 7800001W WO 7800005 A1 WO7800005 A1 WO 7800005A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- magnetic
- particles
- active substance
- polymer
- polymer particles
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 95
- 239000002245 particle Substances 0.000 title claims abstract description 87
- 230000005291 magnetic effect Effects 0.000 title claims abstract description 79
- 239000000696 magnetic material Substances 0.000 claims abstract description 38
- 239000013543 active substance Substances 0.000 claims abstract description 32
- 238000000034 method Methods 0.000 claims abstract description 32
- 239000000126 substance Substances 0.000 claims abstract description 25
- 239000000178 monomer Substances 0.000 claims abstract description 17
- 239000000969 carrier Substances 0.000 claims abstract description 14
- 239000011148 porous material Substances 0.000 claims abstract description 9
- 230000000717 retained effect Effects 0.000 claims abstract description 6
- 239000003814 drug Substances 0.000 claims abstract 3
- 229940088623 biologically active substance Drugs 0.000 claims description 19
- 102000004190 Enzymes Human genes 0.000 claims description 16
- 108090000790 Enzymes Proteins 0.000 claims description 16
- 229910000859 α-Fe Inorganic materials 0.000 claims description 14
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 claims description 10
- 229920000936 Agarose Polymers 0.000 claims description 9
- 229920002472 Starch Polymers 0.000 claims description 9
- 235000019698 starch Nutrition 0.000 claims description 9
- 239000008107 starch Substances 0.000 claims description 9
- 150000004676 glycans Chemical class 0.000 claims description 8
- 239000005017 polysaccharide Substances 0.000 claims description 8
- 229920000058 polyacrylate Polymers 0.000 claims description 7
- 229920001282 polysaccharide Polymers 0.000 claims description 7
- 102000035195 Peptidases Human genes 0.000 claims description 6
- 108091005804 Peptidases Proteins 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 102000004877 Insulin Human genes 0.000 claims description 5
- 108090001061 Insulin Proteins 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 229940125396 insulin Drugs 0.000 claims description 5
- 239000002502 liposome Substances 0.000 claims description 5
- 150000003431 steroids Chemical class 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 4
- 101001091385 Homo sapiens Kallikrein-6 Proteins 0.000 claims description 3
- 102100034866 Kallikrein-6 Human genes 0.000 claims description 3
- -1 agarose or starch Chemical class 0.000 claims description 3
- 238000010348 incorporation Methods 0.000 claims 6
- NOVZFMNCTCKLPF-UHFFFAOYSA-N 2,5-bis(aziridin-1-yl)-3,6-dipropoxycyclohexa-2,5-diene-1,4-dione Chemical compound O=C1C(OCCC)=C(N2CC2)C(=O)C(OCCC)=C1N1CC1 NOVZFMNCTCKLPF-UHFFFAOYSA-N 0.000 claims 4
- 239000000824 cytostatic agent Substances 0.000 claims 4
- 229940125532 enzyme inhibitor Drugs 0.000 claims 3
- 239000002532 enzyme inhibitor Substances 0.000 claims 3
- 238000006116 polymerization reaction Methods 0.000 abstract description 4
- 238000001042 affinity chromatography Methods 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 238000002965 ELISA Methods 0.000 abstract 1
- 230000008021 deposition Effects 0.000 abstract 1
- 238000003018 immunoassay Methods 0.000 abstract 1
- 230000005415 magnetization Effects 0.000 abstract 1
- 229940088598 enzyme Drugs 0.000 description 11
- 239000003112 inhibitor Substances 0.000 description 11
- 239000011554 ferrofluid Substances 0.000 description 4
- 239000000499 gel Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 108091006905 Human Serum Albumin Proteins 0.000 description 2
- 102000008100 Human Serum Albumin Human genes 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229920002684 Sepharose Polymers 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- OIRDTQYFTABQOQ-KQYNXXCUSA-N adenosine Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O OIRDTQYFTABQOQ-KQYNXXCUSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000006249 magnetic particle Substances 0.000 description 2
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 2
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 2
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 1
- XTWYTFMLZFPYCI-KQYNXXCUSA-N 5'-adenylphosphoric acid Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O XTWYTFMLZFPYCI-KQYNXXCUSA-N 0.000 description 1
- 102100031126 6-phosphogluconolactonase Human genes 0.000 description 1
- 108010029731 6-phosphogluconolactonase Proteins 0.000 description 1
- XTWYTFMLZFPYCI-UHFFFAOYSA-N Adenosine diphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(O)=O)C(O)C1O XTWYTFMLZFPYCI-UHFFFAOYSA-N 0.000 description 1
- 241000234282 Allium Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 1
- 230000005653 Brownian motion process Effects 0.000 description 1
- 239000002126 C01EB10 - Adenosine Substances 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102000009123 Fibrin Human genes 0.000 description 1
- 108010073385 Fibrin Proteins 0.000 description 1
- BWGVNKXGVNDBDI-UHFFFAOYSA-N Fibrin monomer Chemical compound CNC(=O)CNC(=O)CN BWGVNKXGVNDBDI-UHFFFAOYSA-N 0.000 description 1
- 108010018962 Glucosephosphate Dehydrogenase Proteins 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 102000004142 Trypsin Human genes 0.000 description 1
- 108090000631 Trypsin Proteins 0.000 description 1
- 229960005305 adenosine Drugs 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940098773 bovine serum albumin Drugs 0.000 description 1
- 238000005537 brownian motion Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229950003499 fibrin Drugs 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000000266 injurious effect Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 150000004804 polysaccharides Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012064 sodium phosphate buffer Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5094—Microcapsules containing magnetic carrier material, e.g. ferrite for drug targeting
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2446/00—Magnetic particle immunoreagent carriers
- G01N2446/10—Magnetic particle immunoreagent carriers the magnetic material being used to coat a pre-existing polymer particle but not being present in the particle core
Definitions
- This invention relates to magnetic polymer particles and the process for their production and utilization.
- the invention relates to magnetic polymer particles as carriers of biologically, preferably pharmaceutically, active substances, the utilization of the magnetic polymer particles, the method of retaining a biologically active substance, preferably a pharmaceuti- ⁇ ally active substance within a restricted area, and the method of treating diseased tissue with the use of the magnetic polymer particles.
- Magnetic polymer particles as carriers of biological ⁇ ly active substances, preferably pharmaceutically active substances, should be useful within many technical and medicinal fields because they can be concentrated by the application of a magnetic field.
- the present invention provides magnetic polymer par ⁇ ticles as carriers of biologically, preferably pharmaceu ⁇ tically active substance, said particles being particles of a preferably porous polymer in the pores or lattice of which magnetic material is deposited, and the biologi ⁇ cally active substance being associated with the polymer.
- the invention comprises a method of produ ⁇ cing magnetic polymer particles as carriers of biological ⁇ ly, preferably pharmaceutically active substance, in which method particles of a preferably porous polymer, which may carry the biologically active substance, and/or polymeri- zable monomers are contacted with a colloidal solution of a magnetic material and, optionally, non-associated biolo ⁇ gically active substance, the optionally present monomers are polymerized, the solvent is optionally removed, the magnetic material and the optionally present, non-associ ⁇ ated biologically active substance being deposited in the pores or lattice of the polymer particles, and the resul ⁇ ting magnetic polymer particles are then associated with the pharmaceutically active substance unless said substan ⁇ ce is already associated with the polymer particles.
- the invention also comprises the utilization of the magnetic polymer particles as carriers of biologically, preferably pharmaceutically active substance, the substan ⁇ ce being associated with particles of a preferably porous polymer and magnetical properties being imparted to said particles by treatment with a magnetic material in the form of particles or colloidal solution.
- the invention in addition provides a method of ' re ⁇ taining a biologically, preferably pharmaceutically acti ⁇ ve substance within a restricted area, in which method the substance is associated with a carrier in the form of pre ⁇ ferably porous polymer particles to which magnetic proper- ties are imparted by treatmentwith amagnetic material in the form of particles or a colloidal solution, and the magne ⁇ tic carrier with the substance associated therewith is then retained within the restricted area by application of a magnetic field.
- the invention provides a method of treating a diseased tissue, in which an effective amount of a phar ⁇ maceutically active substance is concentrated in said tis ⁇ sue by the substance being supplied to the tissue associ ⁇ ated with a carrier in the form of magnetic, preferably porous polymer particles and concentrated to the diseased tissue by application of a magnetic field.
- polystyrene resin As polymer use can be made for instance of a poly- saccharide, preferably agarose or starch. Another suit ⁇ able polymer is acrylic polymer.
- the polymer should be biocompatible. A particular advantage, when used in the treatment of mammals, is gained if the polymer is biode ⁇ gradable, such as starch which is enzymatically degraded in the organism. Polymers forming too small lattices are unsuitable.
- the magnetic material is used in the form of par ⁇ ticles or a colloidal solution, preferably colloidal fer- rite. Colloidal ferrite is commercially available as ul- tramicroscopical (about 100 A) ferrite particles surroun- ded by a thin layer (about 25 A) of a polymer.
- partic ⁇ les are prevented by said polymer layer from adhering to each other in a magnetic field. Random collisions (Brow- nian motion) with the molecules of the carrier liquid re- tain the particles in colloidal solution.
- particulate magnetic material can also be incor ⁇ porated with the polymer particles according to the inven ⁇ tion.
- a suitable material is particulate ferrite, Fe Q . or nickel.
- the magnetic poly ⁇ mer particles which contain colloidal magnetic material are produced in a very advantageous manner by contacting already formed, preferably porous polymer which may have associated biological ligands, with a colloidal solution of magnetic material.
- said magnetic material After optional removal of the solvent of the magnetic material, said magnetic material remains in the polymer, probably by precipitation in the pores or lattice of the polymer, whereby the polymer obtains mag ⁇ netic properties.
- polymer particles al- ready produced can be made magnetical afterwards.
- Polymers which are already substituted with biological ligands are commercially available, which makes this method extremely advantageous. If the polymer which has thus been made mag ⁇ netic does not already have associated ligands, said poly- mer is then contacted with a biologically active substance which is thereby associated with the polymer serving as a carrier of the substance.
- magnetic polymer particles are pro- prised by polymerization of say acrylic monomers in pre ⁇ sence of a colloidal solution of magnetic material, said magnetic material remaining in the resulting polymeric lat ⁇ tice.
- Another way is to contact say acrylic monomers simul ⁇ taneously with the colloidal solution of magnetic material and agarose, the acrylic monomers being polymerized.
- biological li ⁇ gands can be associated for instance by the so-called BrCN-method.
- the polymer particles are pro ⁇ substituted by polymerization of a monomer in the simultaneous presence of a crosslinking agent, the colloidal solution of magnetic material and the pharmaceutically active sub ⁇ stance.
- a crosslinking agent such as trypsin
- Ferrofluid columnloidal solution of ferrite particles, trademark
- Magnetic polymer particles can also be produced in that a particulate magnetic material is contacted with po— lymerizable monomers or a solution of a polysaccharide, such as agarose or starch, in which case the magnetic po ⁇ lymers will be incorporated with the lattice of the poly- mer. These magnetic polymer particles are then contacted with the biologically active substance, whereby said bio ⁇ logically active substance will be associated with the magnetic polymer particles.
- the magnetic polymeric particles according to the invention which contain colloidal magnetic material, can be used for instance at so-called affinity chromatography, for instance to separate enzymes from a mixture of seve ⁇ ral different enzymes.
- an en ⁇ zyme inhibitor which may be either a specific inhibitor or a general inhibitor or cofactor, is associated with the magnetic polymer particles.
- specific inhibitor is meant an inhibitor specific to but one enzyme, and this is the case with most inhibitors, whereas a general inhibitor can inhibit several different enzymes.
- glucose-6-phosphate dehydrogenase which has been adsorbed to postmagnetized 2' ,5'-ADP-Sepha- rose (from Pharmacia, Sweden) , have been successfully em ⁇ ployed.
- the magnetic polymer particles according to the in- vention can further be used in immuno adsorbance.
- Anti ⁇ bodies against human serum albumin are thereby associated with Sepharose (from Pharmacia, Sweden) and are postmagne ⁇ tized by treatment with a colloidal solution of magnetic material. With the aid of the antibodies thus supported on a magnetic carrier human serum albumin can be collected.
- the magnetic material can be used either in the form of particles or a colloi ⁇ dal solution according to what is suitable in various uses. Particular advantages are, however, gained with the use of a colloidal solution, int. al. because - as has also been mentioned in the foregoing - polymers already formed can be postmagnetized.
- the present invention also provides a very advant ⁇ ageous method of retaining a biologically, preferably pharmaceutically active substance within a restricted area, it being necessary to utilize a much smaller amount of the active substance than would have been the case with the same substance without application of the method of the invention.
- thrombi Proteolytic enzymes, such as plas- mine, are known by their ability to dissolve different substrates, among them fibrin (thrombi) .
- the enzymes can be enriched and retained in posi ⁇ tion in vivo with the aid of an outer or an inner magnetic field.
- the active substance for instance a cytosta- ticu , being either coupled via a reversable weak bond to the carrier and being then released on the spot where it shall become active, or be fixedly coupled to the carrier, being active in a bound state.
- a further field in which the magnetic particles ac ⁇ cording to the present invention can be employed is in general chemical, particularly organo-chemical reactions in which the substances to be reacted are first associ ⁇ ated with a magnetic carrier according to the present in ⁇ vention, whereupon a very intimate contact is realized between the substances associated with the carrier by the application of a magnetic field.
- This will produce a high specific reaction without any secondary reactions, that is, very high efficiency, and it is possible to work at low concentrations.
- an interaction between two or more components can be forced by the application of a magnetic field.
- live microbes have been successfully baked into gels of polymeric materials such as polysaccharides, to- gether with a colloidal ferrite solution (Ferrofluid) .
- a colloidal ferrite solution Ferrofluid
- the ferrite particles simply adsorb t the gel or precipitate out in the interior of the beads re ⁇ mains to be established.
- the magnetic properties of the gel remain unchanged after extensive washing with buffer (even washing with, for example, ethanol or 40% ethylene glycol did not remove the ferrite particles) and repeated use in magnetic fields; they are strong enough to allow rapid sedimentation even when applying weak permanent magnets.
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Preparation (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE7706431A SE431214B (sv) | 1977-06-02 | 1977-06-02 | Sett att framstella magnetiska polymerpartiklar som berare av en foretredesvis biologiskt aktiv substans |
SE7706431 | 1977-06-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1978000005A1 true WO1978000005A1 (en) | 1978-12-07 |
Family
ID=20331500
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/SE1978/000001 WO1978000005A1 (en) | 1977-06-02 | 1978-06-01 | Magnetic polymer particles |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0007932B1 (en, 2012) |
JP (1) | JPS5417110A (en, 2012) |
DE (1) | DE2853480C2 (en, 2012) |
GB (1) | GB2035798B (en, 2012) |
SE (2) | SE431214B (en, 2012) |
WO (1) | WO1978000005A1 (en, 2012) |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2828941A1 (de) * | 1978-06-30 | 1980-01-10 | Robert Thomas Gordon | Mittel zur behandlung von krebs |
EP0042249A3 (en) * | 1980-06-13 | 1982-09-22 | Eli Lilly And Company | Magnetically-localizable, biodegradable lipid microspheres |
WO1983001738A1 (en) * | 1981-11-12 | 1983-05-26 | SCHRÖDER, Ulf | Intravascularly administrable, magnetically responsive nanosphere or manoparticle, a process for the production thereof, and the use thereof |
EP0184899A1 (en) * | 1984-11-01 | 1986-06-18 | Nycomed As | Paramagnetic contrast agents for use in "in vivo" diagnostic methods using NMR, and their preparation |
EP0186947A1 (en) * | 1984-11-01 | 1986-07-09 | Nycomed As | Paramagnetic contrast agents for use in "in vivo" diagnostic methods using NMR, and their preparation |
US4770183A (en) * | 1986-07-03 | 1988-09-13 | Advanced Magnetics Incorporated | Biologically degradable superparamagnetic particles for use as nuclear magnetic resonance imaging agents |
DE3709851A1 (de) * | 1987-03-24 | 1988-10-06 | Silica Gel Gmbh Adsorptions Te | Nmr-diagnostische fluessigkeitszusammensetzungen |
US4863715A (en) * | 1984-03-29 | 1989-09-05 | Nycomed As | Method of NMK imaging using a contrast agent comprising particles of a ferromagnetic material |
GB2184015B (en) * | 1985-12-11 | 1990-07-11 | Ceskoslovenska Akademie Ved | Preparation for the diagnostics of the transport function of salpinx and a method for preparation thereof |
US4951675A (en) * | 1986-07-03 | 1990-08-28 | Advanced Magnetics, Incorporated | Biodegradable superparamagnetic metal oxides as contrast agents for MR imaging |
FR2656317A1 (fr) * | 1989-12-27 | 1991-06-28 | Rhone Poulenc Chimie | Microspheres magnetisables a base de polysilsesquioxane, leur procede de preparation et leur application en biologie. |
US5162037A (en) * | 1988-04-01 | 1992-11-10 | Whitson Laboratories, Inc. | Magnetically influenced homeopathic pharmaceutical formulations, methods of their preparation and methods of their administration |
AU632481B2 (en) * | 1988-04-01 | 1993-01-07 | Whitson-Fischman, Nancy | Magnetically influenced homeopathic pharmaceutical formulations, methods of their preparation and methods of their administration |
EP0516198A3 (en) * | 1985-10-04 | 1993-03-03 | Immunicon Corporation | Magnetic-polymer particles |
US5618514A (en) * | 1983-12-21 | 1997-04-08 | Nycomed Imaging As | Diagnostic and contrast agent |
US5720939A (en) * | 1985-08-15 | 1998-02-24 | Nycomed Imaging As | Method of contrast enhanced magnetic resonance imaging using magnetically responsive-particles |
EP1306128A1 (en) * | 2001-10-29 | 2003-05-02 | Tenaxis Gmbh | Sorptive composite materials |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4297337A (en) * | 1979-04-13 | 1981-10-27 | Corning Glass Works | Solid-phase immunoassays using magnetic glass |
JPS6336171Y2 (en, 2012) * | 1981-03-12 | 1988-09-26 | ||
JPS57204318A (en) * | 1981-06-06 | 1982-12-15 | Aisin Seiki Co Ltd | Clutch disc |
DE3227809A1 (de) * | 1982-07-24 | 1984-01-26 | LuK Lamellen und Kupplungsbau GmbH, 7580 Bühl | Drehschwingungsdaempfer, insbesondere fuer mit drehmomentenwandlern ausgeruestete kraftfahrzeugantriebe |
DE3230664A1 (de) * | 1982-08-18 | 1984-02-23 | Fichtel & Sachs Ag, 8720 Schweinfurt | Torsionsschwingungsdaempfer mit axialer steuerblech-abstuetzung |
JPS59140923A (ja) * | 1983-01-31 | 1984-08-13 | Atsugi Motor Parts Co Ltd | クラッチディスク |
JPS6124533U (ja) * | 1984-07-19 | 1986-02-13 | 株式会社 大金製作所 | ダンパ−デイスク |
JPS6152422A (ja) * | 1984-08-21 | 1986-03-15 | Mitsubishi Motors Corp | ダンパ−デイスク |
JPS61117923U (en, 2012) * | 1985-01-11 | 1986-07-25 | ||
SU1722256A3 (ru) * | 1989-11-02 | 1992-03-23 | Viktor A Volkonskij | Cпocoб пoлучehия maгhиtoупpabляemoй диcпepcии |
EP0963832B1 (en) * | 1997-02-28 | 2002-09-25 | Idemitsu Petrochemical Co., Ltd. | Soft transparent polyethylene resin sheet |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1467974A1 (de) * | 1964-06-08 | 1969-01-23 | Tsukamoto Kenkichi | Verfahren zur Verbesserung der Wirksamkeit von Eisenpraeparaten und Vorrichtung zur Durchfuehrung des Verfahrens |
FR7403M (en, 2012) * | 1967-04-18 | 1969-11-03 | ||
DE2150581A1 (de) * | 1970-10-12 | 1972-04-13 | Technicon Instr | Verfahren und Vorrichtung zum Trennen der Lymphozyten von einer Blutprobe |
DE2217266A1 (de) * | 1971-04-13 | 1972-10-26 | Technicon Instr | Verfahren und vorrichtung zum trennen der lymphozyten von einer blutprobe |
US4018886A (en) * | 1975-07-01 | 1977-04-19 | General Electric Company | Diagnostic method and device employing protein-coated magnetic particles |
DE2654723A1 (de) * | 1975-12-02 | 1977-06-23 | Pasteur Institut | Magnetisches gel fuer immunoenzymatische bestimmungen |
-
1977
- 1977-06-02 SE SE7706431A patent/SE431214B/xx not_active IP Right Cessation
-
1978
- 1978-06-01 WO PCT/SE1978/000001 patent/WO1978000005A1/en unknown
- 1978-06-01 GB GB7903109A patent/GB2035798B/en not_active Expired
- 1978-06-01 DE DE19782853480 patent/DE2853480C2/de not_active Expired
- 1978-06-02 JP JP6660178A patent/JPS5417110A/ja active Granted
- 1978-12-08 EP EP78900004A patent/EP0007932B1/en not_active Expired
-
1979
- 1979-01-26 SE SE7900712A patent/SE441802B/sv not_active IP Right Cessation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1467974A1 (de) * | 1964-06-08 | 1969-01-23 | Tsukamoto Kenkichi | Verfahren zur Verbesserung der Wirksamkeit von Eisenpraeparaten und Vorrichtung zur Durchfuehrung des Verfahrens |
FR7403M (en, 2012) * | 1967-04-18 | 1969-11-03 | ||
DE2150581A1 (de) * | 1970-10-12 | 1972-04-13 | Technicon Instr | Verfahren und Vorrichtung zum Trennen der Lymphozyten von einer Blutprobe |
DE2217266A1 (de) * | 1971-04-13 | 1972-10-26 | Technicon Instr | Verfahren und vorrichtung zum trennen der lymphozyten von einer blutprobe |
US4018886A (en) * | 1975-07-01 | 1977-04-19 | General Electric Company | Diagnostic method and device employing protein-coated magnetic particles |
DE2654723A1 (de) * | 1975-12-02 | 1977-06-23 | Pasteur Institut | Magnetisches gel fuer immunoenzymatische bestimmungen |
Non-Patent Citations (1)
Title |
---|
Methods in Enzymology, Volume XLIV, 1976, "Immobilized Enzymes", p. 216, 278, 324-326. * |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2828941A1 (de) * | 1978-06-30 | 1980-01-10 | Robert Thomas Gordon | Mittel zur behandlung von krebs |
EP0042249A3 (en) * | 1980-06-13 | 1982-09-22 | Eli Lilly And Company | Magnetically-localizable, biodegradable lipid microspheres |
WO1983001738A1 (en) * | 1981-11-12 | 1983-05-26 | SCHRÖDER, Ulf | Intravascularly administrable, magnetically responsive nanosphere or manoparticle, a process for the production thereof, and the use thereof |
US6544496B1 (en) | 1983-12-21 | 2003-04-08 | Amersham Health As | Diagnostic and contrast agent |
US5670135A (en) * | 1983-12-21 | 1997-09-23 | Nycomed Imaging As | Ultrasonic contrast agent comprising carbohydrate particles |
US5618514A (en) * | 1983-12-21 | 1997-04-08 | Nycomed Imaging As | Diagnostic and contrast agent |
US5817291A (en) * | 1983-12-21 | 1998-10-06 | Nycomed Imaging As | Method of ultrasonic imaging comprising administering biocompatible spheres or particles |
US4863715A (en) * | 1984-03-29 | 1989-09-05 | Nycomed As | Method of NMK imaging using a contrast agent comprising particles of a ferromagnetic material |
EP0186947A1 (en) * | 1984-11-01 | 1986-07-09 | Nycomed As | Paramagnetic contrast agents for use in "in vivo" diagnostic methods using NMR, and their preparation |
US4985233A (en) * | 1984-11-01 | 1991-01-15 | Nycomed /As | A diagnostic agent containing a non-radioactive paramagnetic metal species in a macromolecular carrier |
US4986980A (en) * | 1984-11-01 | 1991-01-22 | Nycomed As | Water-soluble, carrier-bound paramagnetic metal containing diagnostic agents |
EP0184899A1 (en) * | 1984-11-01 | 1986-06-18 | Nycomed As | Paramagnetic contrast agents for use in "in vivo" diagnostic methods using NMR, and their preparation |
US5720939A (en) * | 1985-08-15 | 1998-02-24 | Nycomed Imaging As | Method of contrast enhanced magnetic resonance imaging using magnetically responsive-particles |
EP0516198A3 (en) * | 1985-10-04 | 1993-03-03 | Immunicon Corporation | Magnetic-polymer particles |
GB2184015B (en) * | 1985-12-11 | 1990-07-11 | Ceskoslovenska Akademie Ved | Preparation for the diagnostics of the transport function of salpinx and a method for preparation thereof |
US4951675A (en) * | 1986-07-03 | 1990-08-28 | Advanced Magnetics, Incorporated | Biodegradable superparamagnetic metal oxides as contrast agents for MR imaging |
US4770183A (en) * | 1986-07-03 | 1988-09-13 | Advanced Magnetics Incorporated | Biologically degradable superparamagnetic particles for use as nuclear magnetic resonance imaging agents |
DE3709851A1 (de) * | 1987-03-24 | 1988-10-06 | Silica Gel Gmbh Adsorptions Te | Nmr-diagnostische fluessigkeitszusammensetzungen |
AU632481B2 (en) * | 1988-04-01 | 1993-01-07 | Whitson-Fischman, Nancy | Magnetically influenced homeopathic pharmaceutical formulations, methods of their preparation and methods of their administration |
US5162037A (en) * | 1988-04-01 | 1992-11-10 | Whitson Laboratories, Inc. | Magnetically influenced homeopathic pharmaceutical formulations, methods of their preparation and methods of their administration |
EP0436449A1 (fr) * | 1989-12-27 | 1991-07-10 | Societe Prolabo | Microsphères magnétisables à base de polysilsesquioxane, leur procédé de préparation et leur application en biologie |
FR2656317A1 (fr) * | 1989-12-27 | 1991-06-28 | Rhone Poulenc Chimie | Microspheres magnetisables a base de polysilsesquioxane, leur procede de preparation et leur application en biologie. |
EP1306128A1 (en) * | 2001-10-29 | 2003-05-02 | Tenaxis Gmbh | Sorptive composite materials |
WO2003037505A1 (en) * | 2001-10-29 | 2003-05-08 | Preentec Ag | Sorptive composite materials |
Also Published As
Publication number | Publication date |
---|---|
EP0007932B1 (en) | 1983-08-24 |
SE431214B (sv) | 1984-01-23 |
GB2035798B (en) | 1982-11-03 |
GB2035798A (en) | 1980-06-25 |
JPS6360726B2 (en, 2012) | 1988-11-25 |
EP0007932A1 (en) | 1980-02-20 |
SE7706431L (sv) | 1978-12-03 |
JPS5417110A (en) | 1979-02-08 |
SE441802B (sv) | 1985-11-11 |
DE2853480T1 (en, 2012) | 1980-12-11 |
DE2853480C2 (en, 2012) | 1987-08-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO1978000005A1 (en) | Magnetic polymer particles | |
US4335094A (en) | Magnetic polymer particles | |
US4495288A (en) | Method of culturing anchorage dependent cells | |
US4737533A (en) | Dry material which can be hydrated into an aqueous gel, containing dispersed polymer particles, process for the preparation thereof and use thereof in biological applications | |
US4210722A (en) | Protein immobilizer | |
US3711574A (en) | Copolymers of acrylamide gas | |
DE2633259A1 (de) | Verfahren zur herstellung von unbeweglich gemachten enzymen | |
JP2005537342A (ja) | 生化学分析、診断および治療のために変更可能な物理構造を有する、感熱性ポリマーキャリア | |
JPS59225064A (ja) | 生理活性物質固定化用担体 | |
Nordling et al. | On the intracellular uptake of neuraminidase | |
Bernfeld et al. | Water-insoluble enzymes: arrangement of aldolase within an insoluble carrier | |
US5942463A (en) | Alkali resistant protein adsorbent | |
Inada et al. | Fibrinolysis by urokinase endowed with magnetic property | |
JPS6128375B2 (en, 2012) | ||
RU2068703C1 (ru) | Способ получения магноиммуносорбентов | |
Abdel‐Hay et al. | The use of acrylic acid‐co‐nylon substrates for immobilizing enzymes | |
EP0040238A1 (en) | PLASMINOGENIC ACTIVATORS USEFUL AS THERAPEUTIC AND DIAGNOSTIC AGENTS AND THEIR INSULATION. | |
JPH0516164B2 (en, 2012) | ||
RU2123860C1 (ru) | Аффинный сорбент для удаления фактора некроза опухоли и способ его получения | |
US4246350A (en) | Protein immobilization on chelating resins | |
KR910004208A (ko) | 안정성인자 viii의 제조방법 | |
JPS61181376A (ja) | 固定化された生物学的活性化合物の製造方法 | |
JPS63304000A (ja) | 生体由来物質の固定化方法 | |
Landman et al. | Activation of immobilized acetyl-Coenzyme A carboxylase | |
Nakagawa et al. | Comparison of the Properties of Tomato β-Fructofuranosidase Embedded within a Polyacrylamide Gel and Adsorbed on CM-cellulose |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Designated state(s): DE GB SE US Kind code of ref document: A1 Designated state(s): DE GB SE US |
|
AL | Designated countries for regional patents |
Designated state(s): FR Kind code of ref document: A1 Designated state(s): FR |
|
RET | De translation (de og part 6b) |
Ref country code: DE Ref document number: 2853480 Date of ref document: 19801211 Format of ref document f/p: P |