PE20211471A1 - Formulacion de medios de contraste y proceso para prepararlos - Google Patents

Formulacion de medios de contraste y proceso para prepararlos

Info

Publication number
PE20211471A1
PE20211471A1 PE2021000733A PE2021000733A PE20211471A1 PE 20211471 A1 PE20211471 A1 PE 20211471A1 PE 2021000733 A PE2021000733 A PE 2021000733A PE 2021000733 A PE2021000733 A PE 2021000733A PE 20211471 A1 PE20211471 A1 PE 20211471A1
Authority
PE
Peru
Prior art keywords
metal ion
paramagnetic metal
alkyl
formulation
group
Prior art date
Application number
PE2021000733A
Other languages
English (en)
Inventor
Stephan Holzschuh
Thomas Frenzel
Gregor Jost
Jessica Lohrke
Wolfgang Ebert
Thomas Brumby
Wolfgang Halfbrodt
Original Assignee
Bayer Ag
Bayer Pharma AG
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 Bayer Ag, Bayer Pharma AG filed Critical Bayer Ag
Publication of PE20211471A1 publication Critical patent/PE20211471A1/es

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
    • A61K49/08Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
    • A61K49/10Organic compounds
    • A61K49/101Organic compounds the carrier being a complex-forming compound able to form MRI-active complexes with paramagnetic metals
    • A61K49/106Organic compounds the carrier being a complex-forming compound able to form MRI-active complexes with paramagnetic metals the complex-forming compound being cyclic, e.g. DOTA
    • A61K49/108Organic compounds the carrier being a complex-forming compound able to form MRI-active complexes with paramagnetic metals the complex-forming compound being cyclic, e.g. DOTA the metal complex being Gd-DOTA
    • 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
    • A61K49/08Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
    • A61K49/085Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier conjugated systems
    • 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
    • A61K49/08Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
    • A61K49/10Organic compounds
    • A61K49/101Organic compounds the carrier being a complex-forming compound able to form MRI-active complexes with paramagnetic metals
    • A61K49/106Organic compounds the carrier being a complex-forming compound able to form MRI-active complexes with paramagnetic metals the complex-forming compound being cyclic, e.g. DOTA
    • 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
    • A61K49/08Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by the carrier
    • A61K49/10Organic compounds
    • A61K49/12Macromolecular compounds
    • A61K49/124Macromolecular compounds dendrimers, dendrons, hyperbranched compounds
    • 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
    • A61K49/18Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes

Landscapes

  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Radiology & Medical Imaging (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Magnetic Resonance Imaging Apparatus (AREA)

Abstract

La presente divulgacion se refiere a una formulacion farmaceutica liquida que comprende un tetra-quelato derivado de DO3A de la formula general (I), donde R1 representa un grupo seleccionado de a), b) o c); indica el punto de union de dicho grupo con el resto de la molecula; R2, R3 y R4 son hidrogeno, alquilo-C1-C6, cicloalquilo-C3-C6, (alcoxi-C1-C2)-(alquil-C2-C3)-, fenilo; entre otros; R5 es alquilo-C1-C6, cicloalquilo-C3-C6, (alcoxi-C1-C2)-(alquil-C2-C3)-, fenilo, entre otros; X representa un grupo C(=O)OH o C(=O)O- y M representa un ion de un metal paramagnetico. El tetra-quelato derivado de DO3A tiene una concentracion en la formulacion en un intervalo de 1 a 1000 mmol de ion metalico paramagnetico/L y el ion del metal paramagnetico no es Gd3+, y en un intervalo de 60 a 750 mmol de ion metalico paramagnetico/L, en donde el ion del metal paramagnetico tambien puede ser Gd3+. Dichas formulaciones son utiles como agentes de contraste, en particular para imagenes de resonancia magnetica.
PE2021000733A 2018-11-23 2019-11-21 Formulacion de medios de contraste y proceso para prepararlos PE20211471A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP18208090 2018-11-23
PCT/EP2019/082117 WO2020104602A1 (en) 2018-11-23 2019-11-21 Formulation of contrast media and process of preparation thereof

Publications (1)

Publication Number Publication Date
PE20211471A1 true PE20211471A1 (es) 2021-08-05

Family

ID=64456867

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2021000733A PE20211471A1 (es) 2018-11-23 2019-11-21 Formulacion de medios de contraste y proceso para prepararlos

Country Status (16)

Country Link
US (1) US11944690B2 (es)
EP (1) EP3883613A1 (es)
JP (1) JP2022508185A (es)
KR (1) KR20210095168A (es)
CN (1) CN113164628A (es)
AU (1) AU2019382881A1 (es)
BR (1) BR112021007707A2 (es)
CA (1) CA3120665A1 (es)
CL (2) CL2021001331A1 (es)
CO (1) CO2021006034A2 (es)
IL (1) IL283281A (es)
JO (1) JOP20210114A1 (es)
MX (1) MX2021006024A (es)
PE (1) PE20211471A1 (es)
SG (1) SG11202104657RA (es)
WO (1) WO2020104602A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4335461A1 (en) * 2022-09-09 2024-03-13 Bayer AG Combinations of contrast agents
EP4360660A1 (en) * 2022-10-24 2024-05-01 Bayer AG Process for the preparation of a gadolinium contrast agent

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