NO302797B1 - Kontrastmedier og anvendelse - Google Patents
Kontrastmedier og anvendelse Download PDFInfo
- Publication number
- NO302797B1 NO302797B1 NO920261A NO920261A NO302797B1 NO 302797 B1 NO302797 B1 NO 302797B1 NO 920261 A NO920261 A NO 920261A NO 920261 A NO920261 A NO 920261A NO 302797 B1 NO302797 B1 NO 302797B1
- Authority
- NO
- Norway
- Prior art keywords
- contrast medium
- paramagnetic metal
- contrast
- medium according
- ray
- Prior art date
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- 239000002872 contrast media Substances 0.000 title claims abstract description 72
- 229940039231 contrast media Drugs 0.000 title description 12
- 230000005298 paramagnetic effect Effects 0.000 claims abstract description 36
- 229910052751 metal Inorganic materials 0.000 claims abstract description 22
- 239000002184 metal Substances 0.000 claims abstract description 22
- 239000000126 substance Substances 0.000 claims abstract description 22
- 210000001035 gastrointestinal tract Anatomy 0.000 claims description 10
- -1 iodecimole Chemical compound 0.000 claims description 9
- 229910052688 Gadolinium Inorganic materials 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 239000013522 chelant Substances 0.000 claims description 4
- 238000002059 diagnostic imaging Methods 0.000 claims description 4
- 238000009472 formulation Methods 0.000 claims description 4
- 229960001025 iohexol Drugs 0.000 claims description 4
- NTHXOOBQLCIOLC-UHFFFAOYSA-N iohexol Chemical compound OCC(O)CN(C(=O)C)C1=C(I)C(C(=O)NCC(O)CO)=C(I)C(C(=O)NCC(O)CO)=C1I NTHXOOBQLCIOLC-UHFFFAOYSA-N 0.000 claims description 4
- UXIGWFXRQKWHHA-UHFFFAOYSA-N Iotalamic acid Chemical compound CNC(=O)C1=C(I)C(NC(C)=O)=C(I)C(C(O)=O)=C1I UXIGWFXRQKWHHA-UHFFFAOYSA-N 0.000 claims description 3
- 239000012876 carrier material Substances 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- VVDGWALACJEJKG-UHFFFAOYSA-N iodamide Chemical group CC(=O)NCC1=C(I)C(NC(C)=O)=C(I)C(C(O)=O)=C1I VVDGWALACJEJKG-UHFFFAOYSA-N 0.000 claims description 3
- 229960004647 iopamidol Drugs 0.000 claims description 3
- XQZXYNRDCRIARQ-LURJTMIESA-N iopamidol Chemical compound C[C@H](O)C(=O)NC1=C(I)C(C(=O)NC(CO)CO)=C(I)C(C(=O)NC(CO)CO)=C1I XQZXYNRDCRIARQ-LURJTMIESA-N 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- GGGDNPWHMNJRFN-UHFFFAOYSA-N metrizoic acid Chemical class CC(=O)N(C)C1=C(I)C(NC(C)=O)=C(I)C(C(O)=O)=C1I GGGDNPWHMNJRFN-UHFFFAOYSA-N 0.000 claims description 3
- DFDJVFYYDGMDTB-BIYVAJLZSA-N 1-n,3-n-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-5-[[(3s,4r,5s)-3,4,5,6-tetrahydroxy-2-oxohexanoyl]amino]benzene-1,3-dicarboxamide Chemical compound OCC(O)CNC(=O)C1=C(I)C(NC(=O)C(=O)[C@@H](O)[C@H](O)[C@@H](O)CO)=C(I)C(C(=O)NCC(O)CO)=C1I DFDJVFYYDGMDTB-BIYVAJLZSA-N 0.000 claims description 2
- ASFIRRNYUOVVLY-JVOWFEOISA-N 2,4,6-triiodo-n-methyl-3,5-bis[[(2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanoyl]amino]benzamide Chemical compound CNC(=O)C1=C(I)C(NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)=C(I)C(NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)=C1I ASFIRRNYUOVVLY-JVOWFEOISA-N 0.000 claims description 2
- MKMHLTWTZQIVCH-SFNQMWQSSA-N 3-[acetyl(2-hydroxyethyl)amino]-2,4,6-triiodo-n-methyl-5-[[(2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanoyl]amino]benzamide Chemical compound CNC(=O)C1=C(I)C(NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)=C(I)C(N(CCO)C(C)=O)=C1I MKMHLTWTZQIVCH-SFNQMWQSSA-N 0.000 claims description 2
- OQHLOKBHRXMXLD-UHFFFAOYSA-N 5-[3-[3-[3,5-bis[2,3-dihydroxypropyl(methyl)carbamoyl]-2,4,6-triiodoanilino]-3-oxopropyl]sulfanylpropanoylamino]-1-n,3-n-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-1-n,3-n-dimethylbenzene-1,3-dicarboxamide Chemical compound OCC(O)CN(C)C(=O)C1=C(I)C(C(=O)N(CC(O)CO)C)=C(I)C(NC(=O)CCSCCC(=O)NC=2C(=C(C(=O)N(C)CC(O)CO)C(I)=C(C(=O)N(C)CC(O)CO)C=2I)I)=C1I OQHLOKBHRXMXLD-UHFFFAOYSA-N 0.000 claims description 2
- BAQCROVBDNBEEB-UBYUBLNFSA-N Metrizamide Chemical compound CC(=O)N(C)C1=C(I)C(NC(C)=O)=C(I)C(C(=O)N[C@@H]2[C@H]([C@H](O)[C@@H](CO)OC2O)O)=C1I BAQCROVBDNBEEB-UBYUBLNFSA-N 0.000 claims description 2
- YVPYQUNUQOZFHG-UHFFFAOYSA-N amidotrizoic acid Chemical compound CC(=O)NC1=C(I)C(NC(C)=O)=C(I)C(C(O)=O)=C1I YVPYQUNUQOZFHG-UHFFFAOYSA-N 0.000 claims description 2
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- NBQNWMBBSKPBAY-UHFFFAOYSA-N iodixanol Chemical compound IC=1C(C(=O)NCC(O)CO)=C(I)C(C(=O)NCC(O)CO)=C(I)C=1N(C(=O)C)CC(O)CN(C(C)=O)C1=C(I)C(C(=O)NCC(O)CO)=C(I)C(C(=O)NCC(O)CO)=C1I NBQNWMBBSKPBAY-UHFFFAOYSA-N 0.000 claims description 2
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- DGAIEPBNLOQYER-UHFFFAOYSA-N iopromide Chemical compound COCC(=O)NC1=C(I)C(C(=O)NCC(O)CO)=C(I)C(C(=O)N(C)CC(O)CO)=C1I DGAIEPBNLOQYER-UHFFFAOYSA-N 0.000 claims description 2
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- IWLIBARWYNRYQO-OCPVLIPCSA-N 3,5-diacetamido-2,4,6-triiodo-n-methyl-n-[2-[methyl-[(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl]amino]-2-oxoethyl]benzamide Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)CN(C)C(=O)CN(C)C(=O)C1=C(I)C(NC(C)=O)=C(I)C(NC(C)=O)=C1I IWLIBARWYNRYQO-OCPVLIPCSA-N 0.000 claims 1
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- 239000003153 chemical reaction reagent Substances 0.000 claims 1
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- SQORATIMOBOFKR-UHFFFAOYSA-H gadolinium(3+);oxalate Chemical compound [Gd+3].[Gd+3].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O SQORATIMOBOFKR-UHFFFAOYSA-H 0.000 description 1
- LGMLJQFQKXPRGA-VPVMAENOSA-K gadopentetate dimeglumine Chemical compound [Gd+3].CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.OC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O LGMLJQFQKXPRGA-VPVMAENOSA-K 0.000 description 1
- KJZYNXUDTRRSPN-UHFFFAOYSA-N holmium atom Chemical compound [Ho] KJZYNXUDTRRSPN-UHFFFAOYSA-N 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 229950002407 iodecimol Drugs 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- HHFIATHHSBFCBY-UHFFFAOYSA-N ioglicic acid Chemical compound CNC(=O)CNC(=O)C1=C(I)C(NC(C)=O)=C(I)C(C(O)=O)=C1I HHFIATHHSBFCBY-UHFFFAOYSA-N 0.000 description 1
- OLAOYPRJVHUHCF-UHFFFAOYSA-N iooxitalamic acid Chemical compound CC(=O)NC1=C(I)C(C(O)=O)=C(I)C(C(=O)NCCO)=C1I OLAOYPRJVHUHCF-UHFFFAOYSA-N 0.000 description 1
- 229960002603 iopromide Drugs 0.000 description 1
- YMFIJXDFAPHJIN-UHFFFAOYSA-N iopronic acid Chemical compound CCC(C(O)=O)COCCOC1=C(I)C=C(I)C(NC(C)=O)=C1I YMFIJXDFAPHJIN-UHFFFAOYSA-N 0.000 description 1
- RXUVYYAWLAIABB-UHFFFAOYSA-N iosefamic acid Chemical compound OC(=O)C1=C(I)C(C(=O)NC)=C(I)C(NC(=O)CCCCCCCCC(=O)NC=2C(=C(C(=O)NC)C(I)=C(C(O)=O)C=2I)I)=C1I RXUVYYAWLAIABB-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000005291 magnetic effect Effects 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229960003194 meglumine Drugs 0.000 description 1
- MIKKOBKEXMRYFQ-WZTVWXICSA-N meglumine amidotrizoate Chemical compound C[NH2+]C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.CC(=O)NC1=C(I)C(NC(C)=O)=C(I)C(C([O-])=O)=C1I MIKKOBKEXMRYFQ-WZTVWXICSA-N 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 230000003232 mucoadhesive effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000001208 nuclear magnetic resonance pulse sequence Methods 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000003204 osmotic effect Effects 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 230000010412 perfusion Effects 0.000 description 1
- IKYIXZSIKOYSLD-UHFFFAOYSA-N pheniodol sodium Chemical compound C=1C=CC=CC=1C(C(=O)O)CC1=CC(I)=C(O)C(I)=C1 IKYIXZSIKOYSLD-UHFFFAOYSA-N 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 229940085605 saccharin sodium Drugs 0.000 description 1
- 210000000813 small intestine Anatomy 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 230000009747 swallowing Effects 0.000 description 1
- 231100000057 systemic toxicity Toxicity 0.000 description 1
- 210000003932 urinary bladder Anatomy 0.000 description 1
- 210000004291 uterus Anatomy 0.000 description 1
- 210000001215 vagina Anatomy 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
- A61K49/08—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
- A61K49/10—Organic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/04—X-ray contrast preparations
- A61K49/0433—X-ray contrast preparations containing an organic halogenated X-ray contrast-enhancing agent
- A61K49/0447—Physical forms of mixtures of two different X-ray contrast-enhancing agents, containing at least one X-ray contrast-enhancing agent which is a halogenated organic compound
- A61K49/0495—Physical forms of mixtures of two different X-ray contrast-enhancing agents, containing at least one X-ray contrast-enhancing agent which is a halogenated organic compound intended for oral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K49/00—Preparations for testing in vivo
- A61K49/06—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations
- A61K49/08—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
- A61K49/085—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier conjugated systems
-
- 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
- Y10S436/806—Electrical property or magnetic property
-
- 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
- Y10T436/24—Nuclear magnetic resonance, electron spin resonance or other spin effects or mass spectrometry
Landscapes
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Radiology & Medical Imaging (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
- Liquid Crystal (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
- Steroid Compounds (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB898916781A GB8916781D0 (en) | 1989-07-21 | 1989-07-21 | Compositions |
| PCT/EP1990/001197 WO1991001149A1 (fr) | 1989-07-21 | 1990-07-19 | Substances de contraste |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO920261L NO920261L (no) | 1992-01-20 |
| NO920261D0 NO920261D0 (no) | 1992-01-20 |
| NO302797B1 true NO302797B1 (no) | 1998-04-27 |
Family
ID=10660460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO920261A NO302797B1 (no) | 1989-07-21 | 1992-01-20 | Kontrastmedier og anvendelse |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US5242683A (fr) |
| EP (2) | EP0473729A1 (fr) |
| JP (1) | JP3054660B2 (fr) |
| AT (1) | ATE103183T1 (fr) |
| AU (1) | AU641422B2 (fr) |
| CA (1) | CA2055604A1 (fr) |
| DE (1) | DE69007575T2 (fr) |
| DK (1) | DK0414288T3 (fr) |
| ES (1) | ES2052161T3 (fr) |
| FI (1) | FI98988C (fr) |
| GB (1) | GB8916781D0 (fr) |
| NO (1) | NO302797B1 (fr) |
| WO (1) | WO1991001149A1 (fr) |
Families Citing this family (54)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5114703A (en) * | 1989-05-30 | 1992-05-19 | Alliance Pharmaceutical Corp. | Percutaneous lymphography using particulate fluorocarbon emulsions |
| GB8916782D0 (en) * | 1989-07-21 | 1989-09-06 | Nycomed As | Compositions |
| US5547682A (en) * | 1989-12-22 | 1996-08-20 | Bioquest, Incorporated | Preparation and use of novel injectable RES avoiding inorganic particles for medical application |
| DE4115789A1 (de) * | 1991-05-10 | 1992-11-12 | Schering Ag | Makrocyclische polymer-komplexbildner, deren komplexe, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische mittel |
| AU6996594A (en) * | 1993-06-02 | 1994-12-20 | Bracco S.P.A. | Iodinated paramagnetic chelates, and their use as contrast agents |
| US6183497B1 (en) | 1998-05-01 | 2001-02-06 | Sub-Q, Inc. | Absorbable sponge with contrasting agent |
| US6071301A (en) | 1998-05-01 | 2000-06-06 | Sub Q., Inc. | Device and method for facilitating hemostasis of a biopsy tract |
| US6162192A (en) | 1998-05-01 | 2000-12-19 | Sub Q, Inc. | System and method for facilitating hemostasis of blood vessel punctures with absorbable sponge |
| US6071300A (en) | 1995-09-15 | 2000-06-06 | Sub-Q Inc. | Apparatus and method for percutaneous sealing of blood vessel punctures |
| DE19641197C2 (de) * | 1996-09-24 | 1999-02-18 | Schering Ag | Ionenpaare und ihre Verwendung als Kontrastmittel |
| FR2772025B1 (fr) * | 1997-12-10 | 2000-03-03 | Guerbet Sa | Chelates metalliques de macrocycles polyaminocarboxyliques et leur application a l'imagerie par resonance magnetique |
| US6315753B1 (en) | 1998-05-01 | 2001-11-13 | Sub-Q, Inc. | System and method for facilitating hemostasis of blood vessel punctures with absorbable sponge |
| US7625352B1 (en) | 1998-05-01 | 2009-12-01 | Sub-Q, Inc. | Depth and puncture control for system for hemostasis of blood vessel |
| US20010045575A1 (en) | 1998-05-01 | 2001-11-29 | Mark Ashby | Device and method for facilitating hemostasis of a biopsy tract |
| US6610026B2 (en) | 1998-05-01 | 2003-08-26 | Sub-Q, Inc. | Method of hydrating a sponge material for delivery to a body |
| US6200328B1 (en) | 1998-05-01 | 2001-03-13 | Sub Q, Incorporated | Device and method for facilitating hemostasis of a biopsy tract |
| WO2000047115A1 (fr) | 1999-02-10 | 2000-08-17 | Sub-Q, Inc. | Dispositif et procede pour faciliter l'hemostase d'une voie de biopsie |
| US6984219B2 (en) | 1999-09-23 | 2006-01-10 | Mark Ashby | Depth and puncture control for blood vessel hemostasis system |
| US7695492B1 (en) | 1999-09-23 | 2010-04-13 | Boston Scientific Scimed, Inc. | Enhanced bleed back system |
| US6540735B1 (en) | 2000-05-12 | 2003-04-01 | Sub-Q, Inc. | System and method for facilitating hemostasis of blood vessel punctures with absorbable sponge |
| US7201725B1 (en) | 2000-09-25 | 2007-04-10 | Sub-Q, Inc. | Device and method for determining a depth of an incision |
| US8187625B2 (en) | 2001-03-12 | 2012-05-29 | Boston Scientific Scimed, Inc. | Cross-linked gelatin composition comprising a wetting agent |
| WO2002087636A1 (fr) | 2001-03-12 | 2002-11-07 | Sub-Q, Inc. | Procedes permettant de steriliser des compositions de gelatine reticulee |
| US6584355B2 (en) * | 2001-04-10 | 2003-06-24 | Cardiac Pacemakers, Inc. | System and method for measuring battery current |
| US7008440B2 (en) | 2001-11-08 | 2006-03-07 | Sub-Q, Inc. | System and method for delivering hemostasis promoting material to a blood vessel puncture site by fluid pressure |
| US7029489B1 (en) | 2001-05-18 | 2006-04-18 | Sub-Q, Inc. | System and method for delivering hemostasis promoting material to a blood vessel puncture site |
| US6863680B2 (en) * | 2001-11-08 | 2005-03-08 | Sub-Q, Inc. | System and method for delivering hemostasis promoting material to a blood vessel puncture site by fluid pressure |
| US7037323B2 (en) | 2001-11-08 | 2006-05-02 | Sub-Q, Inc. | Pledget-handling system and method for delivering hemostasis promoting material to a blood vessel puncture site by fluid pressure |
| US7037322B1 (en) | 2001-11-08 | 2006-05-02 | Sub-Q, Inc. | System and method for delivering hemostasis promoting material to a blood vessel puncture with a staging tube |
| US7192436B2 (en) | 2001-11-08 | 2007-03-20 | Sub-Q, Inc. | Pledget-handling system and method for delivering hemostasis promoting material to a blood vessel puncture site by fluid pressure |
| CA2493041C (fr) * | 2002-07-19 | 2011-08-16 | Dominik Meyer | Composition pharmaceutique injectable pour le traitement des douleurs articulaires post-operatoires qui comprend un anesthesique local du groupe amide |
| US20040102730A1 (en) * | 2002-10-22 | 2004-05-27 | Davis Thomas P. | System and method for facilitating hemostasis of blood vessel punctures with absorbable sponge |
| US7455680B1 (en) | 2002-11-04 | 2008-11-25 | Boston Scientific Scimed, Inc. | Apparatus and method for inhibiting blood loss |
| US8317821B1 (en) | 2002-11-04 | 2012-11-27 | Boston Scientific Scimed, Inc. | Release mechanism |
| US7955353B1 (en) | 2002-11-04 | 2011-06-07 | Sub-Q, Inc. | Dissolvable closure device |
| US7378081B2 (en) * | 2003-01-29 | 2008-05-27 | Vincon Research Enterprises, Llc | Composition and method for direct visualization of the human appendix |
| US20050180920A1 (en) * | 2003-01-29 | 2005-08-18 | Vincenzo Giuliano | Oral contrast media composition for computerized axial tomographic examinations and method |
| US20040265235A1 (en) * | 2003-06-26 | 2004-12-30 | Uzgiris Egidijus Edward | Magnetic resonance contrast-enhancing agents and method for detecting and imaging artherosclerotic plaque |
| US7875043B1 (en) | 2003-12-09 | 2011-01-25 | Sub-Q, Inc. | Cinching loop |
| WO2006068639A1 (fr) * | 2004-12-21 | 2006-06-29 | Vincenzo Giuliano | Composition de produit de contraste administrable par voie orale pour tomodensitometrie axiale et procede d'utilisation |
| US7384624B2 (en) * | 2004-12-27 | 2008-06-10 | James Raines | Oral contrast and method of producing the oral contrast |
| EP1830902A2 (fr) * | 2004-12-30 | 2007-09-12 | Cinvention Ag | Ensemble comprenant un agent produisant un signal, un implant et un medicament |
| EA011516B1 (ru) * | 2005-01-13 | 2009-04-28 | Синвеншен Аг | Композиционный материал и способ его изготовления |
| WO2006084382A1 (fr) * | 2005-02-11 | 2006-08-17 | University Health Network | Compositions et procedes d'imagerie multimodale |
| WO2006097503A2 (fr) * | 2005-03-18 | 2006-09-21 | Cinvention Ag | Procede de preparation de materiaux metalliques frittes poreux |
| CA2612195A1 (fr) * | 2005-07-01 | 2007-01-11 | Cinvention Ag | Dispositifs medicaux comprenant une matiere composite reticulee |
| EP1937753A1 (fr) * | 2005-10-18 | 2008-07-02 | Cinvention Ag | Particules thermodurcies et procédés pour la production de celles-ci |
| DE602007012693D1 (de) | 2006-05-26 | 2011-04-07 | Baxter Healthcare Sa | Injizierbare fibrin-zusammensetzung zur knochenverstärkung |
| ES2359526T3 (es) * | 2006-05-26 | 2011-05-24 | Baxter International Inc. | Agente inyectable para el relleno de huecos óseos. |
| US8601223B1 (en) | 2006-09-19 | 2013-12-03 | Nvidia Corporation | Techniques for servicing fetch requests utilizing coalesing page table entries |
| JP5385257B2 (ja) * | 2007-03-26 | 2014-01-08 | バクスター・インターナショナル・インコーポレイテッド | 軟部組織増強のための注入可能な空隙の充填剤 |
| KR101585751B1 (ko) * | 2010-07-12 | 2016-01-14 | 지이 헬스케어 에이에스 | 저농도의 조영제 및/또는 저방사선량의 x-선 영상화 |
| NZ626988A (en) | 2012-01-11 | 2015-10-30 | Ge Healthcare As | X-ray imaging contrast media with low iodine concentration and x-ray imaging process |
| KR20160119060A (ko) * | 2013-12-04 | 2016-10-12 | 호비온 사이언티아 리미티드 | 조영매 맛 차폐 제제 |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2387735A (en) * | 1941-07-03 | 1945-10-30 | Martin Dennis Company | Method of forming carboxylic amino acids |
| US2407645A (en) * | 1943-06-21 | 1946-09-17 | Martin Dennis Company | Aliphatic polycarboxylic amino acids and process of making them |
| US4647447A (en) * | 1981-07-24 | 1987-03-03 | Schering Aktiengesellschaft | Diagnostic media |
| DE3316703A1 (de) * | 1983-05-04 | 1984-11-08 | Schering AG, 1000 Berlin und 4709 Bergkamen | Orales kontrastmittel fuer die kernspintomographie und dessen herstellung |
| DE3324235A1 (de) * | 1983-07-01 | 1985-01-10 | Schering AG, 1000 Berlin und 4709 Bergkamen | Neue komplexbildner, komplexe und komplexsalze |
| US4615879A (en) * | 1983-11-14 | 1986-10-07 | Vanderbilt University | Particulate NMR contrast agents for gastrointestinal application |
| US5013831A (en) * | 1984-01-30 | 1991-05-07 | Enzo Biochem, Inc. | Detectable molecules, method of preparation and use |
| GB8413772D0 (en) * | 1984-05-30 | 1984-07-04 | Nyegaard & Co As | Chemical compounds |
| US4639365A (en) * | 1984-10-18 | 1987-01-27 | The Board Of Regents, The University Of Texas System | Gadolinium chelates as NMR contrast agents |
| DE3577185D1 (de) * | 1984-11-01 | 1990-05-23 | Nycomed As | Paramagnetische kontrastmittel fuer die anwendung in "in vivo" nmr-diagnostischen methoden und die herstellung davon. |
| SE465907B (sv) * | 1984-11-01 | 1991-11-18 | Nyegaard & Co As | Diagnosticeringsmedel innehaallande en paramagnetisk metall |
| US4826673A (en) * | 1985-01-09 | 1989-05-02 | Mallinckrodt, Inc. | Methods and compositions for enhancing magnetic resonance imaging |
| US4880008A (en) * | 1985-05-08 | 1989-11-14 | The General Hospital Corporation | Vivo enhancement of NMR relaxivity |
| NZ212437A (en) * | 1985-06-17 | 1992-06-25 | Mark Philip Best | Site-directed antibody conjugates, and their preparation |
| JPS62153229A (ja) * | 1985-12-27 | 1987-07-08 | Nippon Oil Co Ltd | 皮膚マ−カ− |
| US4885363A (en) * | 1987-04-24 | 1989-12-05 | E. R. Squibb & Sons, Inc. | 1-substituted-1,4,7-triscarboxymethyl-1,4,7,10-tetraazacyclododecane and analogs |
| IT1213029B (it) * | 1986-01-30 | 1989-12-07 | Bracco Ind Chimica Spa | Chelati di ioni metallici paramagnetici. |
| US5104641A (en) * | 1986-03-07 | 1992-04-14 | M.R.I., Inc. | Nitroxide NMR contrast enhancing agents and their use in NMR imaging |
| AU608759B2 (en) * | 1986-08-04 | 1991-04-18 | Amersham Health Salutar Inc | NMR imaging with paramagnetic polyvalents metal salts of poly-(acid-alkylene-amido)-alkanes |
| IL83966A (en) * | 1986-09-26 | 1992-03-29 | Schering Ag | Amides of aminopolycarboxylic acids and pharmaceutical compositions containing them |
| DE3701665A1 (de) * | 1987-01-19 | 1988-07-28 | Schering Ag | Polymer-komplexe, verfahren zu deren herstellung und diese enthaltende pharmazeutische mittel |
| DE3709851A1 (de) * | 1987-03-24 | 1988-10-06 | Silica Gel Gmbh Adsorptions Te | Nmr-diagnostische fluessigkeitszusammensetzungen |
| US5198208A (en) * | 1987-07-16 | 1993-03-30 | Nycomed Imaging As | Aminopolycarboxylic acids and derivatives thereof |
| US5114703A (en) * | 1989-05-30 | 1992-05-19 | Alliance Pharmaceutical Corp. | Percutaneous lymphography using particulate fluorocarbon emulsions |
-
1989
- 1989-07-21 GB GB898916781A patent/GB8916781D0/en active Pending
-
1990
- 1990-07-19 DE DE69007575T patent/DE69007575T2/de not_active Expired - Fee Related
- 1990-07-19 JP JP2510854A patent/JP3054660B2/ja not_active Expired - Fee Related
- 1990-07-19 EP EP90911456A patent/EP0473729A1/fr active Pending
- 1990-07-19 ES ES90201964T patent/ES2052161T3/es not_active Expired - Lifetime
- 1990-07-19 CA CA002055604A patent/CA2055604A1/fr not_active Abandoned
- 1990-07-19 AT AT90201964T patent/ATE103183T1/de active
- 1990-07-19 WO PCT/EP1990/001197 patent/WO1991001149A1/fr active IP Right Grant
- 1990-07-19 EP EP90201964A patent/EP0414288B1/fr not_active Expired - Lifetime
- 1990-07-19 AU AU61438/90A patent/AU641422B2/en not_active Ceased
- 1990-07-19 DK DK90201964.5T patent/DK0414288T3/da active
- 1990-07-19 US US07/778,054 patent/US5242683A/en not_active Expired - Lifetime
-
1992
- 1992-01-20 FI FI920238A patent/FI98988C/fi not_active IP Right Cessation
- 1992-01-20 NO NO920261A patent/NO302797B1/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE69007575D1 (de) | 1994-04-28 |
| US5242683A (en) | 1993-09-07 |
| NO920261L (no) | 1992-01-20 |
| FI920238A0 (fi) | 1992-01-20 |
| DK0414288T3 (da) | 1994-04-11 |
| FI98988C (fi) | 1997-09-25 |
| JP3054660B2 (ja) | 2000-06-19 |
| NO920261D0 (no) | 1992-01-20 |
| EP0414288A1 (fr) | 1991-02-27 |
| FI98988B (fi) | 1997-06-13 |
| EP0414288B1 (fr) | 1994-03-23 |
| CA2055604A1 (fr) | 1991-01-22 |
| GB8916781D0 (en) | 1989-09-06 |
| EP0473729A1 (fr) | 1992-03-11 |
| WO1991001149A1 (fr) | 1991-02-07 |
| ES2052161T3 (es) | 1994-07-01 |
| AU641422B2 (en) | 1993-09-23 |
| AU6143890A (en) | 1991-02-22 |
| ATE103183T1 (de) | 1994-04-15 |
| DE69007575T2 (de) | 1994-07-21 |
| JPH04506807A (ja) | 1992-11-26 |
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