WO2005120589A3 - Contrast agent comprising alginate and an isotope or paramagnetic ion - Google Patents

Contrast agent comprising alginate and an isotope or paramagnetic ion Download PDF

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Publication number
WO2005120589A3
WO2005120589A3 PCT/NO2005/000205 NO2005000205W WO2005120589A3 WO 2005120589 A3 WO2005120589 A3 WO 2005120589A3 NO 2005000205 W NO2005000205 W NO 2005000205W WO 2005120589 A3 WO2005120589 A3 WO 2005120589A3
Authority
WO
WIPO (PCT)
Prior art keywords
manganese
alginate
ions
compound
isotope
Prior art date
Application number
PCT/NO2005/000205
Other languages
French (fr)
Other versions
WO2005120589A2 (en
Inventor
Christian Brekken
Yrr Moerch
Original Assignee
Ntnu Technology Transfer
Christian Brekken
Yrr Moerch
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 Ntnu Technology Transfer, Christian Brekken, Yrr Moerch filed Critical Ntnu Technology Transfer
Publication of WO2005120589A2 publication Critical patent/WO2005120589A2/en
Publication of WO2005120589A3 publication Critical patent/WO2005120589A3/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K51/00Preparations containing radioactive substances for use in therapy or testing in vivo
    • A61K51/02Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
    • A61K51/04Organic compounds
    • A61K51/06Macromolecular compounds, carriers being organic macromolecular compounds, i.e. organic oligomeric, polymeric, dendrimeric molecules
    • A61K51/065Macromolecular compounds, carriers being organic macromolecular compounds, i.e. organic oligomeric, polymeric, dendrimeric molecules conjugates with carriers being macromolecules
    • 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
    • A61K49/126Linear polymers, e.g. dextran, inulin, PEG
    • A61K49/128Linear polymers, e.g. dextran, inulin, PEG comprising multiple complex or complex-forming groups, being either part of the linear polymeric backbone or being pending groups covalently linked to the linear polymeric backbone
    • 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
    • A61K49/1803Semi-solid preparations, e.g. ointments, gels, hydrogels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K51/00Preparations containing radioactive substances for use in therapy or testing in vivo
    • A61K51/12Preparations containing radioactive substances for use in therapy or testing in vivo characterised by a special physical form, e.g. emulsion, microcapsules, liposomes, characterized by a special physical form, e.g. emulsions, dispersions, microcapsules
    • A61K51/1213Semi-solid forms, gels, hydrogels, ointments, fats and waxes that are solid at room temperature

Abstract

A system for the delivery of contrast agents such as manganese (MR-active Mn2+ or other manganese isotopes) into extravascular body compartments in living subjects (mammals, amphibians, fish etc.) is described. The compound consists of alginate, manganese ions and other stabilizing ions (Ba2+, Ca2+ etc.) in a gel, formed by mixing of alginate and solutions of the ions mentioned above. The primary alginate used in production of the compound can be adjusted in structure (M- and G-block content and sequence), molecular weight and concentration. In addition, the salt solution and concentration can be varied in order to produce alginate gels of variable manganese amount (dose) and local manganese release rate (dose-rate). When injected or implanted into extravascular body compartments manganese ions will be released from the gel by ion exchange with body fluids and passive diffusion. Once released the manganese ions shortens the longitudinal MR relaxation time of water molecules in their vicinity amounting to positive image contrast in T1-weighted MR images. Furthermore, the compound may also act as slow release agent for positron emission tomography scanning, provided the manganese-isotope is emitting positrons (m52mMn).
PCT/NO2005/000205 2004-06-14 2005-06-13 Contrast agent comprising alginate and an isotope or paramagnetic ion WO2005120589A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
NO20042486 2004-06-14
NO20042486A NO320691B1 (en) 2004-06-14 2004-06-14 New contrast release system.

Publications (2)

Publication Number Publication Date
WO2005120589A2 WO2005120589A2 (en) 2005-12-22
WO2005120589A3 true WO2005120589A3 (en) 2006-06-15

Family

ID=35005930

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/NO2005/000205 WO2005120589A2 (en) 2004-06-14 2005-06-13 Contrast agent comprising alginate and an isotope or paramagnetic ion

Country Status (2)

Country Link
NO (1) NO320691B1 (en)
WO (1) WO2005120589A2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9156189B2 (en) * 2010-10-01 2015-10-13 The Johns Hopkins University Systems and methods for high-throughput microfluidic bead production

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986003781A1 (en) * 1984-12-17 1986-07-03 Sintef Process for producing alginates having improved physical properties, and the use of said alginates
WO1993010440A1 (en) * 1991-11-19 1993-05-27 Unger Evan C Gel particle contrast media for improved diagnostic imaging
WO2003045457A2 (en) * 2001-11-27 2003-06-05 Scimed Life Systems, Inc. Medical devices visible under magnetic resonance imaging
WO2003086474A2 (en) * 2002-04-11 2003-10-23 Carbomer, Inc Fluorinated or paramagnetic alginate polymer, annexin paramagnetic conjugate, and their use as contrasting agent in mri

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986003781A1 (en) * 1984-12-17 1986-07-03 Sintef Process for producing alginates having improved physical properties, and the use of said alginates
WO1993010440A1 (en) * 1991-11-19 1993-05-27 Unger Evan C Gel particle contrast media for improved diagnostic imaging
WO2003045457A2 (en) * 2001-11-27 2003-06-05 Scimed Life Systems, Inc. Medical devices visible under magnetic resonance imaging
WO2003086474A2 (en) * 2002-04-11 2003-10-23 Carbomer, Inc Fluorinated or paramagnetic alginate polymer, annexin paramagnetic conjugate, and their use as contrasting agent in mri

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
EMMERICHS N.: "Interaction between alginates and manganese cations: identification of preferred cation binding sites", INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, vol. 34, 2004, pages 73 - 79, XP008060943 *
GOTOH T. ET AL: "Adsorption of Cu and Mn on covalently cross-linked alginate beads", CHEMOSPHERE, vol. 55, 2004, pages 57 - 64, XP008060940 *
KLÖCH G. ET AL: "Production of purified alginates suitable for use in immunoisolated trasplantation", APPL MICROBIOL BIOTECHNOL, vol. 40, 1994, XP008061137 *
NOETH U ET AL: "19F-MRI IN VIVO DETERMINATION OF THE PARTIAL OXYGEN PRESSURE IN PERFLUOROCARBON-LOADED ALGINATE CAPSULES IMPLANTED INTO THE PERITONEAL CAVITY AND DIFFERENT TISSUES", MAGNETIC RESONANCE IN MEDICINE, ACADEMIC PRESS, DULUTH, MN, US, vol. 42, no. 6, 1999, pages 1039 - 1047, XP001162703, ISSN: 0740-3194 *
ZIMMERMANN H ET AL: "Fabrication of homogeneously cross-linked, functional alginate microcapsules validated by NMR-, CLSM- and AFM-imaging", BIOMATERIALS, ELSEVIER SCIENCE PUBLISHERS BV., BARKING, GB, vol. 24, no. 12, May 2003 (2003-05-01), pages 2083 - 2096, XP004413509, ISSN: 0142-9612 *

Also Published As

Publication number Publication date
NO20042486L (en) 2005-12-15
NO320691B1 (en) 2006-01-16
WO2005120589A2 (en) 2005-12-22
NO20042486D0 (en) 2004-06-14

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