EP0510030A1 - Übergangsmetallkomplexe für die mr-diagnostik - Google Patents

Übergangsmetallkomplexe für die mr-diagnostik

Info

Publication number
EP0510030A1
EP0510030A1 EP19910901732 EP91901732A EP0510030A1 EP 0510030 A1 EP0510030 A1 EP 0510030A1 EP 19910901732 EP19910901732 EP 19910901732 EP 91901732 A EP91901732 A EP 91901732A EP 0510030 A1 EP0510030 A1 EP 0510030A1
Authority
EP
European Patent Office
Prior art keywords
complexes
transition metal
cooh
diagnostics
general formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP19910901732
Other languages
German (de)
English (en)
French (fr)
Inventor
Uwe Krüger
Herbert Rupp
Klaus-Dieter Beller
Hans-Peter Kley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Takeda GmbH
Original Assignee
Byk Gulden Lomberg Chemische Fabrik GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Byk Gulden Lomberg Chemische Fabrik GmbH filed Critical Byk Gulden Lomberg Chemische Fabrik GmbH
Publication of EP0510030A1 publication Critical patent/EP0510030A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K49/00Preparations for testing in vivo
    • A61K49/06Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations

Definitions

  • the invention relates to new contrast media for MR diagnostics.
  • EP-A-0303555 discloses complexes of ethanolamine phosphoric acid with iron (III) and manganese (II) which are intended for prophylaxis and therapy.
  • EP-A-0173163 proposes the use of metal complexes with phosphonylorganophosphates for MR diagnostics.
  • EP-A-0290047 describes measurement tall complexes of dipyridoxyl phosphoric acids as MR contrast agents.
  • EP-A 0284549 proposes the use of magnetic liquids to increase the relaxivity in MR-diagnostic examinations. Due to the strongly relaxing effect of the superparamagnetic particles contained in the magnetic liquids, a so-called negative contrast can also be achieved by signal cancellation.
  • EP-A 0190676 discloses all-cis-1,3,5-triamino-2,4,6-cyclohexanetriol derivatives which are suitable for complexing metal cations, in particular iron (III).
  • the object of the present invention is to provide new contrast media for MR diagnostics, which are characterized by high complex stability, good water solubility at physiological pH values, strong relaxivity and by a pronounced organ specificity combined with reduced side effects and distinguish faster excretion.
  • the invention relates to the use of complexes of the compounds of the general formula I,
  • Rl, R2, R3, R4, R5 and R6 are the same or different and
  • R7 represents hydrogen, COOH and PO (OH), with paramagnetic transition metal cations and their salts with cations of strong bases for the production of agents for MR diagnostics.
  • R7 represent hydrogen, COOH and PO (OH).
  • R2, R4 and R6 C (0) CH, C (0) C H, CH COOH, CH CH COOH, CH P (0) (OH),
  • Suitable transition metal cations are the cations of the transition metals of atomic numbers 21 to 29, 42 and 44 and the cations of the lanthanide elements of atomic numbers 57 to 70, gadolinium being preferred by the lanthanide elements.
  • iron (III) -all-cis-1,3,5-tris is particularly preferred.
  • the first preferred complex shows a longitudinal relaxivity TR of 2J058 [sec mmol] and a transverse relaxivity TR of 1.945 [sec mmol].
  • the second complex shows values of 4,113 (TR) and 4,340 (TR).
  • the sodium and N-methylglucamine salts are preferred as salts of the complexes used according to the invention.
  • Si show a strong relaxivity with regard to both T1 and T2, so that they can also be used for signal extinction similar to magnetite particles.
  • Contrast agents for MR diagnostics contain one or more of the complexes of the general formula I and, if desired, customary additives.
  • the complexes are prepared in a manner known per se by adding salts of paramagnetic transition metal ions in water and / or alcohol, such as
  • Methanol, ethanol, etc. dissolves and, if necessary, with the appropriate amount of ligand, while stirring at 50 ° C. to 120 ° C., until the reaction is complete. If the complex formed is insoluble in the solvent used, it crystallizes and can be filtered off. If the complex is soluble in the solvent used, it can be isolated by evaporating the solution to dryness. The complex compound obtained is then dissolved or suspended in water and mixed with the desired inorganic or organic base until the neutral point is reached. After filtration of undissolved portions, the solution is evaporated and the desired complex salt is obtained as residue. The salts of the complexes are obtained, for example, by reaction with strong bases.
  • the new contrast media are prepared in a manner known per se by dissolving the complexes and / or their salts in water or physiological salt solution and, if desired, additives customary in galenics, such as, for example, physiologically compatible buffer solutions (for example sodium dihydro gene phosphate solution), albumin and the like, and the solution is sterilized.
  • physiologically compatible buffer solutions for example sodium dihydro gene phosphate solution
  • albumin for example, albumin and the like
  • the solutions can be filled as such into ampoules or freeze-dried to a soluble powder.
  • the aqueous solutions are adjusted to a pH with sufficient local tissue tolerance, for example to a pH of 7 to 9.
  • the aqueous solutions are administered orally or parenterally, in particular intravascularly.
  • aqueous solutions which contain the paramagnetic complex in a concentration of 30 to 200 mmol / liter. Approximately 1 to 100 ⁇ mol of the complex is administered per kg body weight per application. For an adult, a dose of 1 to 50 mmol proves to be appropriate for IV use.

Landscapes

  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Radiology & Medical Imaging (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
EP19910901732 1990-01-09 1991-01-08 Übergangsmetallkomplexe für die mr-diagnostik Withdrawn EP0510030A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH62/90 1990-01-09
CH6290A CH679742A5 (es) 1990-01-09 1990-01-09

Publications (1)

Publication Number Publication Date
EP0510030A1 true EP0510030A1 (de) 1992-10-28

Family

ID=4178448

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19910901732 Withdrawn EP0510030A1 (de) 1990-01-09 1991-01-08 Übergangsmetallkomplexe für die mr-diagnostik

Country Status (5)

Country Link
EP (1) EP0510030A1 (es)
JP (1) JPH05504343A (es)
AU (1) AU7044791A (es)
CH (1) CH679742A5 (es)
WO (1) WO1991010454A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4028139A1 (de) * 1990-09-05 1992-03-12 Hausmann Ag Labor Verwendung der komplexe radioaktiver metallionen mit all-cis-1,3,5-triamino-2,4,6-cyclohexantriol und seinen derivaten fuer roentgendiagnostische zwecke und in der tumortherapie sowie zur herstellung von mitteln fuer roentgendiagnostische zwecke und fuer die tumortherapie
JP2894879B2 (ja) * 1991-10-04 1999-05-24 日本メジフィジックス株式会社 診断用造影剤
JP5172162B2 (ja) 2006-08-25 2013-03-27 株式会社日立ハイテクノロジーズ 欠陥検査装置
EP2849804A1 (en) 2012-05-18 2015-03-25 Bayer Pharma Aktiengesellschaft Bis azainositol heavy metal complexes for x-ray imaging
EP2796152A1 (en) * 2013-04-25 2014-10-29 Bayer Pharma Aktiengesellschaft Unsymmetrical Bis Azainositol Hafnium Complexes for X-Ray Imaging
EP2873670A1 (en) 2013-11-14 2015-05-20 Bayer Pharma Aktiengesellschaft Bis azainositol zirconium complexes for X-ray imaging

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3129906C3 (de) * 1981-07-24 1996-12-19 Schering Ag Paramagnetische Komplexsalze, deren Herstellung und Mittel zur Verwendung bei der NMR-Diagnostik
DE3503614A1 (de) * 1985-02-02 1986-08-07 Laboratorien Hausmann AG, St. Gallen All-cis-1,3,5-triamino-2,4,6-cyclohexantriol-derivate, verfahren zu ihrer herstellung und sie enthaltende pharmazeutische praeparate
DE3625417C2 (de) * 1986-07-28 1998-10-08 Schering Ag Tetraazacyclododecan-Derivate

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9110454A1 *

Also Published As

Publication number Publication date
AU7044791A (en) 1991-08-05
CH679742A5 (es) 1992-04-15
JPH05504343A (ja) 1993-07-08
WO1991010454A1 (de) 1991-07-25

Similar Documents

Publication Publication Date Title
EP0071564B1 (de) Paramagnetische Komplexsalze, deren Herstellung und Verwendung bei der NMR-Diagnostik
DE3751829T2 (de) Anwendung von Chelat-Komplexen
EP0124766B1 (de) Enterales Kontrastmittel für die Kernspintomographie und dessen Herstellung
US5087440A (en) Heterocyclic derivatives of DTPA used for magnetic resonance imaging
DE3650572T2 (de) Kontrastmittel zur darstellung des leber-gallensystems mittels nmr-kontrastmittel
DE69032761T2 (de) Hydroxy-aryl metallchelate für bildformung zur nmr diagnose
EP0270483B1 (de) Verbesserte metallhaltige Pharmazeutika
DE3401052C2 (de) Diagnostische Mittel
DE68908185T2 (de) Chelat-zusammensetzung.
DE2628517C2 (de) Dicarbonsäure-bis(3,5-dicarbamoyl-2,4,6-trijodanilid)-Verbindungen, Verfahren zu ihrer Herstellung und Röntgenkontrastmittel
US5077037A (en) Novel compositions for magnetic resonance imaging
DE69212630T2 (de) Bilderzeugungsmittel für Diagnose
EP0130934A1 (de) Neue Komplexbildner, Komplexe und Komplexsalze
DE69314613T3 (de) Neues chelatisierungsmittel, komplexverbindungen, die aus diesem mittel und metallatomen aufgebaut sind, und diagnostische mittel, die diese verbindungen enthalten
DE69432418T2 (de) Phosphonate- und nicht-phosphonate einheiten enthaltende polyamino-paramagnetische-chelate fuer anwendung in mri
DE69226022T2 (de) Hydroxamat- und hydrazidderivate von polyaminen und ihre medizinische verwendung als chelatierende wirkstoffe
DE69116637T2 (de) Mittel zur magnetischen Resonanzabbildung
DE68922218T2 (de) Kontrastmittel für magnetische resonanzabbildung des kleinen darms und des hepatobiliaren systems.
DE69009758T2 (de) Mittel für magnetische resonanzbilderzeugung.
EP0510030A1 (de) Übergangsmetallkomplexe für die mr-diagnostik
EP1307237B9 (de) Perfluoralkylhaltige komplexe mit polaren resten, verfahren zu deren herstellung und ihre verwendung
DE3324236A1 (de) Neue komplexbildner
EP3813887B1 (de) Verfahren zur herstellung eines fe-tcdta-kontrastmittels und nach dem verfahren erhältliches produkt
US5616312A (en) Thiol ligands and complexes for X-ray imaging
DE2909355A1 (de) Albumin-mikroaggregate zur radioaktiven darstellung von retikulo-endothelialen systemen

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19920708

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 19950801