WO1997014413A1 - Derives de chelate utilises comme protecteurs contre les lesions tissulaires - Google Patents
Derives de chelate utilises comme protecteurs contre les lesions tissulaires Download PDFInfo
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- WO1997014413A1 WO1997014413A1 PCT/US1996/016722 US9616722W WO9714413A1 WO 1997014413 A1 WO1997014413 A1 WO 1997014413A1 US 9616722 W US9616722 W US 9616722W WO 9714413 A1 WO9714413 A1 WO 9714413A1
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- WIPO (PCT)
- Prior art keywords
- compound
- doxorubicin
- mpedta
- mpeg
- edta
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- 0 C[C@]([*-])CN(CCN(C[*-])C[*-])CC(C*CCC(C)(*)OCCC(C)(C)OC)=O Chemical compound C[C@]([*-])CN(CCN(C[*-])C[*-])CC(C*CCC(C)(*)OCCC(C)(C)OC)=O 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- C07C237/08—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
- C07C229/10—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
- C07C229/16—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of hydrocarbon radicals substituted by amino or carboxyl groups, e.g. ethylenediamine-tetra-acetic acid, iminodiacetic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/06—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members
- C07D241/08—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having one or two double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
Definitions
- the present invention is directed to substances useful in the protection of living organisms against damage due to free radical reactions.
- Iron is involved in the pathogenesis of free radical tissue injury following inflammation. Activated leukocytes thus produce superoxide radicals which undergo dismutation to hydrogen peroxide and oxygen, and simultaneously reduce iron in ferritin. Fe , in turn, reacts with hydrogen peroxide, producing the destructive hydroxyl radical.
- the radical reactions may be summarized:
- Iron chelators including deferoxamine (DEF) have shown some effectiveness in reducing tissue injury, such as myocardial ischemia-reperfusion injury.
- DEF must be given parenterally, but its toxicity and rapid excretion limit its effectiveness.
- high molecular weight substances such as hydroxyethylstarch
- the circulation lifetime was increased and toxicity decreased (Hallaway, et al., Proc. Nat . Acad . Sci . USA, 86:10108, 1989).
- Other iron chelators have been explored in an effort to reduce tissue injury from free radicals (Voest, et al., Ann . Intern . Wed., 120:490-499, 1994).
- PEG Polyethylene glycol
- MPEG monomethyl ether
- H(0CH 2 CH 2 ) n 0H an amphiphilic polymer H(0CH 2 CH 2 ) n 0H that consists of a mixture of homologs with a range of similar molecular weights.
- the low molecular weight polymers PEG 200-600 are absorbed through the gastrointestinal tract when ingested orally and excreted unchanged in the urine. PEG is absorbed along with water directly through the intestinal mucosal cell membrane.
- PEG 200-600 being nontoxic and biologically inert, has often been used as a vehicle for administration of drugs insoluble in water.
- the PEG vehicle alone was empirically found to exhibit significant biological activity, leading to further studies of low molecular weight
- PEG 400 when given intraperitoneally (ip) either before or shortly after x-irradiation of mice, conferred significant protection against lethality and morbidity (Shaeffer and Schellenberg, Int . J . Radiat . Oncol . Biol . Phys. , 10:2329,
- PEG with a molecular weight around 400 is thus a uniquely nontoxic substance that exhibits a protective effect against injury to tissues.
- PEG with a molecular weight greater than 700 is not absorbed through the GI tract.
- the mechanism of the protective action of low molecular weight PEG has not been established, but probably involves interaction of PEG with the surface of lipid membranes or protein components. PEG aggregates near cell membranes, reduces water polarity at membrane surfaces, and increases hydrophobic interactions (Hoekstra, et al., J . Biol . Chem . , 264:6786, 1989)
- MPEG chelates can be effective iron chelators.
- MPEG can be linked with iminodiacetate terminus (MIDA) .
- MIAA iminodiacetate terminus
- n 3 to 8.
- MPEG 550- deferoxamine (ferrioxamine) , prepared by reacting MPEG molecular weight 550 with carbonyldiimidazole, followed by reaction of the resulting imidazolecarbonyl ester with deferoxa ine base, forming a urethane linkage.
- the material was produced as a chelate for gadolinium, to be used as a renal magnetic resonance contrast agent (Duewell, et al., Invest . Radiol . , 26:50, 1991).
- Deferoxamine is known to be an effective chelator for ferric iron.
- MIDA can be prepared by converting MPEG 350 to the chloride by reaction with thionyl chloride, and to the iminodiacetate by reaction of the chloride with sodium iminodiacetate ( uenschell et al., J. Chromatog. 543: 345-354, 1991) .
- the methyl ester can be prepared with methanolic HC1.
- the present invention is directed to methoxypolyethylene glycols (MPEG) , which are modified by chemically attaching chelating groups onto the nonmethyl end of the polymer.
- chelating groups include ethylene-diamine tetraacetic acid (EDTA) , diethylene triamine pentaacetic acid (DTPA) , and ethylene glycol aminoethyl ether tetraacetic acid (EGTA) .
- the present invention is directed to a derivative of methoxypolyethylene glycol having the formula :
- one embodiment of the present invention converts the terminal hydroxyl of MPEG to an amine, and then links the amine to ethylenediaminetetraacetate to produce methoxypolyethylene glycol amide of EDTA (MPEDTA) .
- MPEDTA methoxypolyethylene glycol amide of EDTA
- the present invention is also directed to a pharmaceutical composition
- a pharmaceutical composition comprising a compound as recited in claim 1, together with a pharmaceutically acceptable carrier.
- the present invention is further directed to a method of preventing tissue damage during radiation treatments. Further, the present invention is directed to a method of preventing renal toxicity during treatment of cancer.
- Figure 1 depicts the average scores of different treatment groups for radioprotection of compounds in mice.
- Figure 2 depicts the daily scores for different treatment groups for radioprotection of compounds in mice.
- Figure 3 depicts doxorubicin treatment results for different treatment groups.
- Figure 4 depicts the lack of effect of MPEDTA on tumor growth lag produced by doxorubicin.
- Figure 5 depicts the protection by MPEDTA against heart weight loss caused by doxorubicin.
- the compounds of the present invention are enhanced chelators in which the chelate is combined with low molecular weight PEG or other toxicity-lowering moiety.
- the present invention is directed to methoxypolyethylene glycols with an average weight of 200 to 600, and preferably 350 (MPEG 350) , which are modified by chemically attaching chelating groups onto the nonmethyl end of the polymer.
- the chelating groups that can be used to modify the methoxypolyethylene glycols include ethylene diamine tetraacetic acid (EDTA) , diethylene triamine pentaacetic acid (DTPA) , and ethylene glycol aminoethyl ether tetraacetic acid (EGTA) .
- EDTA ethylene diamine tetraacetic acid
- DTPA diethylene triamine pentaacetic acid
- EGTA ethylene glycol aminoethyl ether tetraacetic acid
- a particular embodiment of the present invention is the chelator obtained when methoxypolyethylene glycol amide is combined with EDTA (MPEDTA) .
- n 3 to 8.
- MPEDTA can be produced, for example, by first converting MPEG 350 to the chloride by reaction with thionyl chloride, then to an amine by reaction of the chloride with ammonia, and then coupling the amine with ethylenediamine tetraacetate monoanhydride (Takeshita et al., J . Am. Oil Chem . Soc , 59: 104, 1982) .
- MPEDTA can be produced by any standard method for amide formation, including the following: EDTA anhydride can be reacted with an amine in 0.3 M HEPES buffer at room temperature to form the amide (Lin et al., Biochemistry, 28:1054, 1989). EDTA in excess plus the amine in dimethylformamide at 120 degrees results in the amide (Hertzberg et al., J . Am . Chem . Soc , 104:313, 1982).
- EDTA triethyl ester plus the amine, in dimethylformamide at 120 degrees results in the amide, and EDTA triester plus carbonyl diimidazole in dimethylformamide at room temperature, followed by the addition of amine, result in the amide (Hertzberg et al., Biochemistry, 23:3934, 1984) .
- EDTA triester, an amine, and dicycloxexylcarbodiimide react to form the amide (Yanagisawa et al. , Prostaglandins , 31:1063, 1986).
- EDTA triester, an amine, ethyl-dimethylaminopropylcarbodiimide, and dimethylaminopyridine as a catalyst result in formation of the amide (Mazzarelli et al., Biochemistry, 32:2979, 1993).
- a novel method employed the cobaltic salt of EDTA which left one free carboxyl group to react with an amine in water catalyzed by ethyl-3-dimethylaminopropylcarbodiimide (Haner et al., Arch. Biochem . Biophys . , 231:477, 1984). The cobalt was later removed by extraction with dithizone in CCl_ j .
- MPEDTA is extremely effective in preventing damage from radiation or doxorubicin.
- the present invention provides a pharmaceutical formulation comprising MPEDTA or a pharmaceutically acceptable salt or solvate thereof, together with one or more pharmaceutically acceptable carriers thereof and optionally one or more other therapeutic ingredients.
- the carrier(s) must be "acceptable" in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
- the present invention may be administered by the following routes: intravenous; intraarterial; intraperitoneal; intrathecal; intramuscular; oral; sublingual; buccal; aerosol (inhalant or topical); subcutaneous; nasal drops; eye drops; ear drops; topical (both direct and as patches, for use on skin and on internal organs) ; intracranial; intracardiac; suppository; intravaginal; extracorporeal (for dialysis, dosing blood organs, and perfusion solutions) ; and electroporetic.
- routes may depend upon, for example, the condition and disorder of the recipient.
- the formulations may conveniently be presented in unit dosage form and may be prepared by any of the methods well known in the art of pharmacy. All methods include the step .of bringing into association MPEDTA or a pharmaceutically acceptable salt or solvate thereof ("active ingredient") with the carrier which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association the active ingredient with liquid carriers or finely divided solid carriers, or both, and then, if necessary, shaping the product into the desired formulation.
- Formulations of the present invention suitable for oral administration may be presented as discrete units, such as capsules, cachets or tablets, each containing a predetermined amount of the active ingredient; as a powder or granules; as a solution or a suspension in an aqueous liquid or a non-aqueous liquid; or as an oil-in-water liquid emulsion.
- the active ingredients may also be presented as a bolus, electuary or paste.
- a tablet may be made by compression or molding, optionally with one or more accessory ingredients.
- Compressed tablets may be prepared by compressing in a suitable machine the active ingredient in a free-flowing form, such as a powder or granules, optionally mixed with a binder, lubricant, inert diluent, lubricating, surface-active or dispersing agent.
- Molded tablets may be made by molding in a suitable machine a mixture of the powdered compound moistened with an inert liquid diluent.
- the tablets may optionally be coated or scored, and may be formulated so as to provide slow or controlled release of the active ingredient therein.
- Formulations for parenteral administration include aqueous and non-aqueous sterile injection solutions which may contain antioxidants, buffers, bacteriostats, and solutes which render the formulation isotonic with the blood of the intended recipient, and aqueous and non-aqueous sterile suspensions which may include suspending agents and thickening agents.
- the formulations may be presented in unit-dose or multi-dose containers, for example, sealed ampules and vials, and may be stored in a freeze-dried (lyophilized) condition requiring only the addition of the sterile liquid carrier, for example, saline or water-for-injection, immediately prior to use.
- Extemporaneous injection solutions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described.
- Formulations for rectal administration may be presented as a suppository with the usual carriers, such as cocoa butter or polyethylene glycol.
- Formulations for topical administration in the mouth include lozenges comprising the active ingredient in a flavored basis, such as sucrose and acacia or tragacanth, and pastilles comprising the active ingredient in a basis, such as gelatin and glycerin or sucrose and acacia.
- Preferred unit dosage formulations are those containing an effective dose, as hereinbelow recited, or an appropriate fraction thereof, of the active ingredient. It should be understood that, in addition to the ingredients particularly mentioned above, the formulations of this invention may include other agents conventional in the art having regard to the type of formulation in question, for example those suitable for oral administration may include flavoring agents.
- the present invention may be administered in the following doses: internal 1 pg/kg to 10 g/kg; topical 0.00001% to 100%, formulated as preparations for immediate or sustained release.
- the dosing regimens of the present invention include discrete doses of between 1 and 8 administrations per day, acute single dose, and chronic multiple dose, as drip (constant IV or other infusion), or as bolus.
- the invention may be formulated with solvent and other agents or compounds.
- the precise amount of MPEDTA compound administered to a patient will be the responsibility of the attendant physician. However, the dose employed will depend on a number of factors, including the age and gender of the patient, the precise disorder being treated, and its severity. Also, the route of administration may vary depending on the condition and its severity.
- the compounds of the present invention are useful in the treatment and prevention of tissue injury mediated by free radicals.
- Free radicals can be produced from ionizing radiation, cardiac toxicity from certain drugs (e . g. , doxorubicin, trauma, and ischemia-reperfusion of myocardial infarction and stroke.)
- drugs e . g. , doxorubicin, trauma, and ischemia-reperfusion of myocardial infarction and stroke.
- a free radical component may also be involved in auto-immune, chronic inflammatory, and viral diseases.
- the present invention is also directed to a method of preventing tissue damage during radiation treatments.
- a patient in need thereof is given an effective amount of MPEDTA by any of the effective routes of administration.
- the present invention is also directed to a method of preventing cardiac and renal toxicity of doxorubicin during treatment of cancer.
- a patient in need thereof is injected with an effective amount of MPEDTA.
- the MPEG-linked chelates were tested biologically for LD 50, radioprotection, and protection against doxorubicin toxicity. Attachment of MPEG to IDA, and EDTA results in derivatives that are of comparable toxicity to the parent compounds. Comparative Example _ Methoxypolyethylene ⁇ lycol iminod_acetate (MTDA) .
- MPEG 350 was converted to the chloride by reaction with thionyl chloride, and to the iminodiacetate by reaction of the chloride with sodium iminodiacetate (Wuenschell, et al., J. Chromatog . , 543:345-354, 1991).
- the product was purified by charcoal decolorization, gel filtration and ion exchange chromatography. Viscous oil, yield 35-48%.
- the methyl ester was prepared with methanolic HC1. TLC ( ethanol) MIDA Rf .39, MIDA methyl ester Rf .77.
- High resolution FAB MS, n 5, C 17 H 3 ⁇ 9 N, MH Calc. 396.2236. Found 396.2241.
- n 6, C 19 H 38 O 10 N, MH + Calc. 440.2495. Found 440.2513.
- Methoxypolyethylene ⁇ lycol amide with EDTA MPEDTA
- MPEG 350 was first converted to the chloride by reaction with thionyl chloride, then to the amine by reaction of the chloride with ammonia, and then the amine was coupled with ethylenediamine tetraacetate onoanhydride (Takeshita, et al.,
- TOXICITY STUDIES For all biological studies, the substances were dissolved in water and brought to pH 7. In the case of EDTA and MPEDTA, the calcium salts were used. Preliminary determination of the approximate toxicity level of the substances was by intraperitoneal (ip) injection of increasing doses into individual Swiss-Webster female mice until toxicity was evident. Then the LD 50 (ip) was determined by using at least three doses in 12 mice at each level, bracketing the approximate LD 50. The mice were followed for at least one week and examined for weight changes, general condition, and behavior. The LD 50 with lower and upper confidence limits was calculated from the data. The LD 50 (millimoles per kilogram) with lower and upper limits (LL and UL) for the substances and for parent compounds EDTA, iminodiacetate (IDA), and MPEG are shown in Table I.
- RADIOPROTECTION STUDIES The effect of PEG derivatives on tissue tolerance to radiation was tested. Groups of 12 female Swiss-Webster mice were given IP solutions of the derivatives at a dose of approximately one-half of the LD50. Ten minutes later, pentobarbital (PB) 0.262 mmole/kg was given IP, and twenty minutes after the first injection, the right hind leg only was irradiated with 30 Gy using the Philips RT-250 unit operated under the following conditions: 200 kVp, 20 mA, 0.2 mm Cu added filtration, HVL 0.57 mm Cu, dose rate of 1.834 Gy/min.
- PB pentobarbital
- mice were irradiated in groups of 12, and their legs were arranged within a 20 x 24 cm aperture cone at a 50 cm target-to-skin distance such that all their legs were within a 95% isodose.
- the output of the X-ray unit was calibrated using a Capintec PT- 06C Farmer chamber. Controls received only PB and 0.4 ml normal saline in place of the drug.
- the mice were examined daily by two independent observers for 24 days, and the limbs were scored for radiation damage graded on a scale of 0 to 3.5 according to criteria previously established (Fowler, et al., Int . J . Rad . Biol . , 9:241-252, 1964) .
- a score of 1 corresponds to definite reddening of the foot compared to normal, and a score of 2 is marked moist desquamation, loss of hair and skin, and sticking together of toes.
- the irradiated limbs began to show evidence of tissue damage at day 12, reaching a maximum average score on day 16-18, and gradually healing thereafter.
- the average scores in the different treatment groups for days 12-24 are shown in Table II and Figure 1, and the daily scores in Figure 2.
- the B16F1 malignant melanoma which grows in isologous C57B1/6 mice was used.
- the subcutaneous injection of one million cells (grown in cell culture from frozen stores) into the back of the mice resulted in formation of tumors that were palpable within 7-10 days post injection.
- the tumors reached an average of 6-8 mm diameter, they were placed in closely matched groups of 12 with similar average size tumors.
- Tumor volumes were assessed by daily caliper measurements in two orthogonal planes. Tumor length is defined as the diameter in the plane parallel to the body, while width is defined as the diameter perpendicular to the body. Diameter
- mice were killed by cervical dislocation.
- the results are summarized in Fig. 4.
- the solid circles indicate the groups receiving saline-saline or MPEDTA- saline
- the solid squares indicate the group receiving saline- doxorubicin
- the solid triangles indicate the group receiving MPEDTA-doxorubicin.
- the MPEDTA clearly did not interfere with the tumoricidal effect of doxorubidin.
- mice were used similarly to the tumor growth lag studies, except that nontumor-bearing C57BL/6 mice were used. Groups of 12 mice were injected with either saline- saline, saline-doxorubicin, MPEDTA-saline, or MPEDTA- doxorubicin, followed for 28 days, and tissues taken for study. A striking indication of cardiac toxicity was loss of heart weight in mice receiving doxorubicin. Results are summarized in Fig. 5. Doxorubicin alone caused a significant weight loss, which was partially prevented by the single dose of MPEDTA. MPEDTA alone was similar to the saline control. Thus, MPEDTA reduced the cardiac damage caused by doxorubicin.
- the new chelates described here have been shown to possess similar toxicity to parent compounds, and have been found to be potentially useful in reducing damage from radiation and doxorubicin, and, by implication, other disorders due to free radicals.
- the compounds may be useful in other clinical situations requiring chelation, such as iron-overload diseases, including thalassemia, sickle-cell disease, and hemochromatosis, and in the treatment of lead, mercury, or other heavy metal poisoning.
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Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU74547/96A AU7454796A (en) | 1995-10-20 | 1996-10-18 | Chelate derivatives as protectors against tissue injury |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US54656295A | 1995-10-20 | 1995-10-20 | |
US08/546,562 | 1995-10-20 |
Publications (2)
Publication Number | Publication Date |
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WO1997014413A1 true WO1997014413A1 (fr) | 1997-04-24 |
WO1997014413A9 WO1997014413A9 (fr) | 1997-07-24 |
Family
ID=24180979
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Application Number | Title | Priority Date | Filing Date |
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PCT/US1996/016722 WO1997014413A1 (fr) | 1995-10-20 | 1996-10-18 | Derives de chelate utilises comme protecteurs contre les lesions tissulaires |
Country Status (2)
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AU (1) | AU7454796A (fr) |
WO (1) | WO1997014413A1 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998047858A1 (fr) * | 1997-04-21 | 1998-10-29 | Eastern Virginia Medical School | Derives de chelates, utilises comme protecteurs contre les lesions tissulaires |
EP1986631A2 (fr) * | 2006-02-14 | 2008-11-05 | Eastern Virginia Medical School | Chélate de thioester de méthoxypolyéthylène glycol et utilisations correspondantes |
WO2009008802A1 (fr) * | 2007-07-09 | 2009-01-15 | Ge Healthcare Bio-Sciences Ab | Procédé pour la préparation d'un agent d'adsorption biomoléculaire |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991015467A1 (fr) * | 1990-04-09 | 1991-10-17 | Cockbain, Julian, Roderick, Michaelson | Agents chelateurs d'acide aminopolycarboxylique |
-
1996
- 1996-10-18 AU AU74547/96A patent/AU7454796A/en not_active Abandoned
- 1996-10-18 WO PCT/US1996/016722 patent/WO1997014413A1/fr active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991015467A1 (fr) * | 1990-04-09 | 1991-10-17 | Cockbain, Julian, Roderick, Michaelson | Agents chelateurs d'acide aminopolycarboxylique |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6020373A (en) * | 1995-10-20 | 2000-02-01 | Eastern Virginia Medical School | Chelate derivatives as protectors against tissue injury |
WO1998047858A1 (fr) * | 1997-04-21 | 1998-10-29 | Eastern Virginia Medical School | Derives de chelates, utilises comme protecteurs contre les lesions tissulaires |
EP1986631A2 (fr) * | 2006-02-14 | 2008-11-05 | Eastern Virginia Medical School | Chélate de thioester de méthoxypolyéthylène glycol et utilisations correspondantes |
EP1986631A4 (fr) * | 2006-02-14 | 2010-10-27 | Eastern Virginia Med School | Chélate de thioester de méthoxypolyéthylène glycol et utilisations correspondantes |
US8008347B2 (en) | 2006-02-14 | 2011-08-30 | Eastern Virginia Medical School | Methoxypolyethylene glycol thioester chelate and uses thereof |
WO2009008802A1 (fr) * | 2007-07-09 | 2009-01-15 | Ge Healthcare Bio-Sciences Ab | Procédé pour la préparation d'un agent d'adsorption biomoléculaire |
US8999157B2 (en) | 2007-07-09 | 2015-04-07 | Ge Healthcare Bio-Sciences Ab | Method for preparation of a biomolecule adsorbent |
Also Published As
Publication number | Publication date |
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AU7454796A (en) | 1997-05-07 |
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