WO1998011922A2 - Method - Google Patents
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- Publication number
- WO1998011922A2 WO1998011922A2 PCT/GB1997/002073 GB9702073W WO9811922A2 WO 1998011922 A2 WO1998011922 A2 WO 1998011922A2 GB 9702073 W GB9702073 W GB 9702073W WO 9811922 A2 WO9811922 A2 WO 9811922A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- manganese
- imaging
- contrast
- contrast agent
- human
- Prior art date
Links
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
- A61K49/18—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes
- A61K49/1818—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles
-
- 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
-
- 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
- A61K49/18—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes
- A61K49/1818—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles
- A61K49/1821—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles
- A61K49/1824—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles coated or functionalised nanoparticles
- A61K49/1827—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles coated or functionalised nanoparticles having a (super)(para)magnetic core, being a solid MRI-active material, e.g. magnetite, or composed of a plurality of MRI-active, organic agents, e.g. Gd-chelates, or nuclei, e.g. Eu3+, encapsulated or entrapped in the core of the coated or functionalised nanoparticle
- A61K49/1833—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles coated or functionalised nanoparticles having a (super)(para)magnetic core, being a solid MRI-active material, e.g. magnetite, or composed of a plurality of MRI-active, organic agents, e.g. Gd-chelates, or nuclei, e.g. Eu3+, encapsulated or entrapped in the core of the coated or functionalised nanoparticle having a (super)(para)magnetic core coated or functionalised with a small organic molecule
- A61K49/1848—Nuclear magnetic resonance [NMR] contrast preparations; Magnetic resonance imaging [MRI] contrast preparations characterised by a special physical form, e.g. emulsions, microcapsules, liposomes particles, e.g. uncoated or non-functionalised microparticles or nanoparticles coated or functionalised microparticles or nanoparticles coated or functionalised nanoparticles having a (super)(para)magnetic core, being a solid MRI-active material, e.g. magnetite, or composed of a plurality of MRI-active, organic agents, e.g. Gd-chelates, or nuclei, e.g. Eu3+, encapsulated or entrapped in the core of the coated or functionalised nanoparticle having a (super)(para)magnetic core coated or functionalised with a small organic molecule the small organic molecule being a silane
Definitions
- the present invention relates to improvements in and relating to magnetic resonance imaging (MRI) , in particular to the use of manganese compounds in the preparation of contrast media for imaging of the gastrointestinal tract .
- MRI magnetic resonance imaging
- MRI Magnetic resonance Imaging
- imaging nuclei generally water protons in body fluids and tissues
- MR magnetic resonance
- contrast agents raise the signal level of the target site relative to that of its surroundings are termed “positive” contrast agents whilst those lowering the signal level relative to surroundings are termed “negative” contrast agents.
- Paramagnetic contrast agents may be either positive or negative MRI contrast agents.
- the effect of paramagnetic substances on magnetic resonance signal intensities is dependent on many factors, the most important of which are the concentration of the paramagnetic substance at the imaged site, the nature of the paramagnetic substance itself and the pulse sequence and magnetic field strength used in the imaging routine.
- paramagnetic contrast agents are positive MRI contrast agents at low concentrations where their T : lowering effect dominates and negative MRI contrast agents at higher concentrations where their T, (or T 2 *) lowering effect is dominant.
- An example of a physiologically tolerable paramagnetic material known for use as an MRI contrast agent is manganese ion, which may conveniently be used in the form of its salts or chelates .
- Manganese when administered intravenously as a contrast agent, may be teratogenic at clinical dosages. Administered intravenously, manganese is also known to interfere with the normal functioning of the heart by replacement of calcium in the calcium pump of the heart .
- US-A-5143716 concerns methods of imaging of the gastrointestinal region to detect the presence of tumorous tissue.
- the contrast medium described comprises a combination of at least one polyphosphorylated compound and at least one paramagnetic ion, including Mn 2t . Whilst it is suggested that such a contrast medium is capable of providing images showing any diseased tissue in the g.i. tract, this does not permit the detection of regions of the gut, in particular the gut wall, which may be functioning abnormally.
- the invention provides the use of a physiologically tolerable manganese compound or a salt thereof, in combination with a second contrast agent, preferably one which is retained within the gut and there exhibits a negative contrast effect, in the manufacture of an enterally, e.g. orally or rectally, administrable MRI contrast medium composition for use in a method of functional imaging of the gastrointestinal tract of a human or non-human animal body.
- the imaging technique provides clear delineation of those portions of the gut wall in which manganese uptake is occurring.
- the method in accordance with the invention not only enables the detection of tumors within the gut, but also enables the identification of regions of the gut which may be functioning abnormally, for example areas which may be the site of infection or areas in which the gut wall may be damaged or diseased.
- the manganese may conveniently be administered as a combined preparation with the second contrast agent.
- the second contrast agent may be administered separately, prior to, during or subsequent to administration of the manganese-containing contrast medium.
- the invention thus provides the use of a physiologically tolerable manganese compound, or a salt thereof, together with a second contrast agent, in the manufacture of MRI contrast medium compositions for simultaneous, separate or sequential administration in a method of functional imaging of the gastrointestinal tract of a human or non- human animal body .
- the invention also provides an MRI contrast agent kit comprising a physiologically tolerable manganese compound, or a salt thereof, and separately a second contrast agent for simultaneous, separate or sequential administration in a method of functional imaging of the gastrointestinal tract of a human or non-human animal body.
- the kit in accordance with the invention may be used for the separate administration of the contrast agents or, alternatively, the contrast agents from the kit may be mixed and administered together.
- paramagnetic materials such as manganese ions may act as either positive or negative MRI contrast agents depending upon a number of factors, including the concentration of the ions at the imaging site and the magnetic field strength used in the imaging procedure. Depending upon the resulting manganese ion concentration within the g.i. tract, this may be such as to create a signal suppressing or enhancing effect there .
- the manganese- containing contrast agent will function outside the gut contents as a positive contrast agent.
- the second contrast agent is therefore conveniently a negative contrast agent and may be any negative MRI contrast agent suitable for enteral administration.
- AMI 227 known ferromagnetic and superparamagnetic species
- SINEREM from Advanced Magnetics
- magnetic iron oxide particles either free or enclosed within or bound to a non-magnetic matrix material
- LUMIREM Guerbet SA
- ABDOSCAN Ned Imaging AS
- a second contrast agent for use in accordance with the method of the invention include Gd and Dy ions bound to a polymeric matrix, for example the materials available under the trade name GADOLITE (Gadolinium alumina silicate oral suspension) , available from Pharmacyclics .
- GADOLITE Gadolinium alumina silicate oral suspension
- Other examples include known susceptibility agents such as insoluble barium compounds, e.g. barium sulphate, and other agents commonly used in barium meals or barium enemas in X-ray investigations of the gut.
- negative contrast agents suitable for use in accordance with the invention include gases, gas generating agents or gas filled particles.
- the second contrast agent may comprise a gas generating agent capable of releasing a gas, such as C0 2 or N 2 , following oral administration.
- gas generating agents are those capable of releasing C0 2 or N 2 on contact with the gastric juices in the stomach.
- this can be achieved by providing the gas generating agent with a coating which does not dissolve on contact with the gastric juices.
- suitable gas generating agents for use in accordance with the invention include MnC0 3 , Na 2 C0 3 and NaHC0 3 .
- the manganese compound which for oral administration is preferably soluble in gastrointestinal fluid may for example be a chelate or a salt, or may be a mixture of different salts and/or chelates .
- Particularly preferred are metal chelates and salts in which the manganese is present as Mn(II) rather than Mn(III) since the former has a higher magnetic moment and thus is more effective as an MR contrast agent.
- manganese compounds particularly suitable for use in accordance with the invention include manganese chloride, ascorbate, kojate, salicylate and gluconate .
- Diagnostically effective levels of uptake of manganese may conveniently be achieved by ensuring that no food or hydrophilic polymer components containing a significant amount of a Mn 7+ - chelating unit are simultaneously present in the gut, e.g. by administering the manganese compound following a period of fasting.
- significant amount is meant that the amount of Mn + - chelating unit is sufficiently high so as to influence the uptake of manganese .
- the manganese compound is itself substantially free from hydrophilic polymer components containing a significant amount of a Mn 2+ - chelating unit and is administered to a human or non- human animal body which has fasted for a period of at least 6, preferably at least 10, more preferably at least 12 hours before enteral administration of the manganese composition.
- fasting it is meant that no solid food which may contain hydrophilic polymer components containing a significant amount of a Mn 2t - chelating unit, in particular soluble or fibrous hydrophilic polymers, has been consumed within the stated period. Water or sugar containing fluids may be taken during the fasting period.
- the invention provides a method of obtaining enhanced images of the liver and the lower gut by means of rectal administration of the contrast medium. Due to the vascularisation of the lower gut, rectally administered manganese passes directly to the heart following absorption, without first passing through the liver. We have, however, surprisingly found that effective uptake of manganese in the lower gut can be achieved using lower doses of rectally administered manganese, resulting in particularly enhanced images of the lower gut. This is of particular value in detecting tumours in the lower gut, e.g. in the diagnosis of colorectal cancer.
- the contrast agents are rectally administered to the g.i. tract of a human or non-human animal body which is substantially free from hydrophilic polymer components containing a significant amount of a Mn 2t - chelating unit at the time of imaging.
- the contrast agents may be administered to a human or non-human animal body which has fasted for a period of at least 6, preferably at least 10, more preferably at least 12 hours.
- Maximum uptake of the rectally administered contrast agents may, however, be achieved by prior irrigation of the colon, thereby ensuring that this is substantially free from any hydrophilic polymer components containing a significant amount of a Mn 2+ - chelating unit.
- Rectal administration may be via rectally inserted tubes which enable administration of the contrast medium to a selected region of the gut. Rectal administration may be advantageous and is known to introduce less nausea than a similar dose administered orally.
- rectal administration of the manganese contrast agent may be combined with insufflation of the lower g.i. tract to obtain a particularly enhanced double contrast effect. Insufflation may conveniently be achieved by blowing a gas, such as air, preferably C0 2 or N 2 , into the lower colon either simultaneously or subsequent to administration of the manganese contrast agent. In this way, the bulk of the lower colon is filled with gas and the manganese contrast agent is present inside and in connection with the walls of the gut. In the resulting MR images, the bulk of the colon is blackened out and the gut walls are highlighted.
- a gas such as air
- the manganese compounds may conveniently be used in combination with one or more uptake promoters capable of enhancing manganese transport across the membranes of the g.i. tract. Examples of such uptake promoters are described in WO-A-96/05867. Alternatively, the manganese compound is administered substantially free from such uptake promoter.
- Suitable uptake promoters include reducing compounds containing an ⁇ -hydroxy ketone group (-CH (OH) -CO-) , acids containing - and/or ⁇ -hydroxy or amino groups, vitamin D and mixtures thereof.
- reducing nature of the uptake promoter is important since normal uptake of manganese by the gut tends to favour Mn(II) rather than Mn(III) .
- acids containing ⁇ - and/or ⁇ -hydroxy or amino groups is intended to include aromatic acids containing ortho-hydroxy or ortho-amino groups .
- Preferred uptake promoters include those in which the reducing compound further contains an oxygen atom in a heterocyclic ring structure.
- uptake promoters are ascorbic and kojic acids. Ascorbic acid has been found to increase the uptake of manganese in the g.i. tract
- the concentration of manganese is conveniently greater than lOmM, preferably in the range of from lOmM to 50mM.
- the manganese concentration is conveniently in the range of from 0. ImM to lOmM, preferably from ImM to 6mM.
- the quantity of the second contrast agent necessary to achieve negative contrast within the gut may be significantly lower, e.g. 1/5 to 1/2 the quantity required in the absence of the manganese.
- the contrast media When using the contrast media to obtain images of the gut, in order to avoid image artefacts resulting from pockets of the gut being contrast agent free, it is desirable to incorporate in the contrast media a viscosity enhancing agent which attains its full viscosity enhancing effect only after administration of the contrast medium.
- the contrast medium is thus able to be ingested in a relatively tolerable form while yet developing the desired viscosity at or during passage towards the site which is to be imaged. Examples of suitable viscosity enhancers are described in WO-A- 91/01147 and WO-A-91/01148.
- One of the problems encountered in imaging of the g.i. tract is that the MR signal intensity has a tendency to vary due to physical movements in the region being imaged. This problem can to some extent be overcome by the use of fast imaging procedures.
- Techniques capable of generating images with time intervals of less than 20 seconds are preferred for use in accordance with the method of the invention.
- the gradient echo sequence should preferably be spoiled .
- contrast agent compositions for use in the invention are particularly suited to use, if required after dispersion in aqueous media, for imaging of the stomach, intestine, bile duct and gall bladder.
- the contrast media may be administered into the gastrointestinal tract orally, rectally or via a tube inserted orally or rectally.
- the method of imaging in accordance with the invention also provides enhanced imaging of the abdomen as a whole, in particular the liver.
- the invention thus provides a method of generating a magnetic resonance image of a human or non-human, preferably mammalian, animal body, which method comprises administering into the gastrointestinal tract of a said body an effective amount of a composition comprising (a) a first contrast agent comprising a physiologically tolerable manganese compound or a salt thereof, together with (b) a second contrast agent, preferably one capable with said first agent of achieving negative contrast in the gastrointestinal tract, and generating a functional image of the gastrointestinal tract of said body.
- the imaging technique used in preferably a spiral MR technique, equivalent to spiral CT techniques, which permits generation of an image corresponding to an internal (or external) transit along the gut.
- differences in manganese uptake by the gut wall due to localised malfunctions of the gut wall are readily visualised.
- differences in signal intensity from different regions of the gut wall can provide an indication of functioning and non-functioning areas of the gut .
- the method of the invention thus may conveniently be used to generate a series of images through the g.i. tract, resulting in the production of high quality 3D images. This effectively allows the radiologist to obtain a view through the inside of the intestinal tract .
- contrast medium compositions for use in accordance with the invention may include other components, for example conventional pharmaceutical formulation aids such as wetting agents, buffers, disintegrants, binders, fillers, flavouring agents and liquid carrier media such as sterile water, water/ethanol etc.
- conventional pharmaceutical formulation aids such as wetting agents, buffers, disintegrants, binders, fillers, flavouring agents and liquid carrier media such as sterile water, water/ethanol etc.
- the pH of the composition is preferably in the acid range, eg. 2 to 7 and while any uptake promoter present may itself serve to yield a composition with this pH, buffers or pH adjusting agents may be used.
- the contrast media may be formulated in conventional pharmaceutical administration forms, such as tablets, capsules, powders, solutions, dispersions, syrups, suppositories etc.
- the preferred dosage of the contrast media will vary according to a number of factors, such as the administration route, the age, weight and species of the subject and, if present, the particular uptake promoter used.
- the dosage of manganese may be in the range of from 2-400 times the normal recommended daily dose of manganese, e.g. from 5 to 500 ⁇ mol/kg bodyweight, preferably from 5 to 150 ⁇ mol/kg bodyweight, more preferably from 10 to 100 ⁇ mol/kg bodyweight, while the dosage of the uptake promoter, if present, may be in the range of from 5 ⁇ mol to 1 mmol/kg bodyweight, preferably from 25 ⁇ mol to 0.5 mmol/kg bodyweight.
- Lumirem ® was administered three times, at 0, 30 and 60 min after administration of MnCl 2 .
- the strong enhancement of the signal intensity of the liver and the intestinal wall is to be noted.
- Abdoscan ® was administered three times, at 0, 30 and 60 min after administration of MnCl 2 .
- the strong enhancement of the signal intensity of the liver and the intestinal wall is to be noted.
- BaSO ⁇ was administered three times, at 0, 30 and 60 min after administration of MnCl 2 .
- the strong enhancement of the signal intensity of the liver and the intestinal wall is to be noted.
- TR/TE 120/12 ms
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Nanotechnology (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Radiology & Medical Imaging (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)
- Magnetic Resonance Imaging Apparatus (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP97933806A EP0941127A2 (en) | 1996-09-23 | 1997-07-30 | Method |
AU37042/97A AU3704297A (en) | 1996-09-23 | 1997-07-30 | Method |
JP10514366A JP2001500871A (en) | 1996-09-23 | 1997-07-30 | Method |
US09/078,720 US6136292A (en) | 1996-09-23 | 1998-05-14 | Determination of non-functioning areas of the g.i. tract using MRI of manganese composition |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/602,289 US5863519A (en) | 1994-08-18 | 1996-02-16 | Composition and method of MRI using both a positive and a negative contrast agent |
GB9619758.7 | 1996-09-23 | ||
GBGB9619758.7A GB9619758D0 (en) | 1996-09-23 | 1996-09-23 | Method |
US77684697A | 1997-02-14 | 1997-02-14 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/078,720 Continuation US6136292A (en) | 1996-09-23 | 1998-05-14 | Determination of non-functioning areas of the g.i. tract using MRI of manganese composition |
Publications (2)
Publication Number | Publication Date |
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WO1998011922A2 true WO1998011922A2 (en) | 1998-03-26 |
WO1998011922A3 WO1998011922A3 (en) | 1998-08-27 |
Family
ID=27268489
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB1997/002073 WO1998011922A2 (en) | 1996-02-16 | 1997-07-30 | Method |
Country Status (1)
Country | Link |
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WO (1) | WO1998011922A2 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999061070A1 (en) * | 1998-05-26 | 1999-12-02 | Klaus Potthoff | Diagnostic method and diagnostic means used in carrying out said method |
WO2000009170A1 (en) * | 1998-08-10 | 2000-02-24 | Bracco Research S.A. | Combination of a positive mri contrast agent with a negative mri contrast agent |
WO2005058375A1 (en) * | 2003-12-19 | 2005-06-30 | Cmc Contrast Ab | Mri contrast medium composition for oral administration |
WO2011003818A2 (en) | 2009-07-06 | 2011-01-13 | Cmc Contrast Ab | Diagnostic method |
US10912847B2 (en) | 2019-06-07 | 2021-02-09 | Ascelia Pharma AB | Compressed solid composition for MRI |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5314681A (en) * | 1988-12-23 | 1994-05-24 | Nycomed Innovation Ab | Composition of positive and negative contrast agents for electron spin resonance enhanced magnetic resonance imaging |
WO1995002831A1 (en) * | 1993-07-12 | 1995-01-26 | Nycomed Imaging As | Methods and compositions for image contrast enhancing |
WO1996005867A2 (en) * | 1994-08-18 | 1996-02-29 | Nycomed Imaging A/S | Compositions |
WO1997002842A1 (en) * | 1995-07-11 | 1997-01-30 | Thomsen Henrik S | Mr contrast agent |
-
1997
- 1997-07-30 WO PCT/GB1997/002073 patent/WO1998011922A2/en not_active Application Discontinuation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5314681A (en) * | 1988-12-23 | 1994-05-24 | Nycomed Innovation Ab | Composition of positive and negative contrast agents for electron spin resonance enhanced magnetic resonance imaging |
WO1995002831A1 (en) * | 1993-07-12 | 1995-01-26 | Nycomed Imaging As | Methods and compositions for image contrast enhancing |
WO1996005867A2 (en) * | 1994-08-18 | 1996-02-29 | Nycomed Imaging A/S | Compositions |
WO1997002842A1 (en) * | 1995-07-11 | 1997-01-30 | Thomsen Henrik S | Mr contrast agent |
Non-Patent Citations (1)
Title |
---|
D'AGINCOURT L: "MRI AGENTS FOR ABDOMEN OFFER HIGH SENSITIVITY" DIAGNOSTIC IMAGING INTERNATIONAL, vol. 8, no. 6, 1 September 1992, pages 42-43, 45, 47 - 50, XP000321789 * |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999061070A1 (en) * | 1998-05-26 | 1999-12-02 | Klaus Potthoff | Diagnostic method and diagnostic means used in carrying out said method |
US6553249B1 (en) | 1998-05-26 | 2003-04-22 | Klaus Potthoff | Diagnostic method and diagnostic means used in delivering a medicament to a patient |
WO2000009170A1 (en) * | 1998-08-10 | 2000-02-24 | Bracco Research S.A. | Combination of a positive mri contrast agent with a negative mri contrast agent |
WO2005058375A1 (en) * | 2003-12-19 | 2005-06-30 | Cmc Contrast Ab | Mri contrast medium composition for oral administration |
EP2060273A3 (en) * | 2003-12-19 | 2009-09-30 | CMC Contrast AB | MRI contrast medium composition for oral administration |
AU2004298396B2 (en) * | 2003-12-19 | 2010-06-17 | Cmc Contrast Ab | MRI contrast medium composition for oral administration |
KR101131362B1 (en) * | 2003-12-19 | 2012-04-04 | 씨엠씨 콘트라스트 에이비 | Mri contrast medium composition for oral administration |
WO2011003818A2 (en) | 2009-07-06 | 2011-01-13 | Cmc Contrast Ab | Diagnostic method |
US10912847B2 (en) | 2019-06-07 | 2021-02-09 | Ascelia Pharma AB | Compressed solid composition for MRI |
Also Published As
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