CA2106474A1 - Polyoxypropylene/polyoxyethylene copolymers with improved biological activity - Google Patents

Polyoxypropylene/polyoxyethylene copolymers with improved biological activity

Info

Publication number
CA2106474A1
CA2106474A1 CA002106474A CA2106474A CA2106474A1 CA 2106474 A1 CA2106474 A1 CA 2106474A1 CA 002106474 A CA002106474 A CA 002106474A CA 2106474 A CA2106474 A CA 2106474A CA 2106474 A1 CA2106474 A1 CA 2106474A1
Authority
CA
Canada
Prior art keywords
polyoxypropylene
preparations
copolymers
polyoxyethylene
biological activity
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.)
Granted
Application number
CA002106474A
Other languages
French (fr)
Other versions
CA2106474C (en
Inventor
R. Martin Emanuele
Robert L. Hunter
Paula H. Culbreth
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.)
LadRx Corp
Original Assignee
Individual
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27100911&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CA2106474(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Individual filed Critical Individual
Publication of CA2106474A1 publication Critical patent/CA2106474A1/en
Application granted granted Critical
Publication of CA2106474C publication Critical patent/CA2106474C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/74Synthetic polymeric materials
    • A61K31/765Polymers containing oxygen
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/74Synthetic polymeric materials
    • A61K31/765Polymers containing oxygen
    • A61K31/77Polymers containing oxygen of oxiranes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/56Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/56Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
    • A61K47/59Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
    • A61K47/60Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/04Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
    • C08G65/06Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
    • C08G65/08Saturated oxiranes
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • C08G65/2603Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
    • C08G65/2606Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
    • C08G65/2609Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • C08G65/2618Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen
    • C08G65/2621Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups
    • C08G65/2624Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing nitrogen containing amine groups containing aliphatic amine groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/30Post-polymerisation treatment, e.g. recovery, purification, drying

Abstract

The present invention comprises novel preparations of polyoxypropylene/polyoxyethylene copolymers which retain the therapeutic activity of the commercial preparations, but are substantially free from the undesirable effects which are inherent in the prior art preparations. The preparation entails first condensing propylene oxide to produce a polyoxypropylene polymer and then condensing ethylene oxide with the polyoxypropylene polymer to produce a polyoxypropylene/polyoxyethylene block copolymer of the general formula:
HO(C2H4O)b(C3H6O)a(C2H4O)b H
wherein a and b are integers. Because the preparations of polyoxypropylene/polyoxyethylene copolymers which comprise the present invention are a less polydisperse population of molecules than the prior art polyoxypropylene/polyoxyethylene copolymers, the biological activity of the copolymers is better defined and more predictable. The polydispersity of the copolymer is very low, average less than 1.07.
CA002106474A 1991-03-19 1992-03-18 Polyoxypropylene/polyoxyethylene copolymers with improved biological activity Expired - Fee Related CA2106474C (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US67328991A 1991-03-19 1991-03-19
US673,289 1991-03-19
US84787492A 1992-03-13 1992-03-13
US847,874 1992-03-13
PCT/US1992/002254 WO1992016484A1 (en) 1991-03-19 1992-03-18 Polyoxypropylene/polyoxyethylene copolymers with improved biological activity

Publications (2)

Publication Number Publication Date
CA2106474A1 true CA2106474A1 (en) 1992-09-20
CA2106474C CA2106474C (en) 2004-02-10

Family

ID=27100911

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002106474A Expired - Fee Related CA2106474C (en) 1991-03-19 1992-03-18 Polyoxypropylene/polyoxyethylene copolymers with improved biological activity

Country Status (19)

Country Link
US (7) US5523492A (en)
EP (1) EP0576612B1 (en)
JP (1) JP2647556B2 (en)
KR (1) KR100224539B1 (en)
CN (1) CN1069741A (en)
AT (1) ATE187154T1 (en)
AU (1) AU662146B2 (en)
CA (1) CA2106474C (en)
CZ (1) CZ194693A3 (en)
DE (1) DE69230372T2 (en)
DK (1) DK0576612T3 (en)
ES (1) ES2140408T3 (en)
GR (1) GR3032726T3 (en)
HU (1) HUT67762A (en)
IE (1) IE920860A1 (en)
IL (1) IL101305A (en)
NO (1) NO307890B1 (en)
SK (1) SK100893A3 (en)
WO (1) WO1992016484A1 (en)

Families Citing this family (76)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5674911A (en) * 1987-02-20 1997-10-07 Cytrx Corporation Antiinfective polyoxypropylene/polyoxyethylene copolymers and methods of use
JP2647556B2 (en) * 1991-03-19 1997-08-27 サイトアーレクス・コーポレーシヨン Polyoxypropylene / polyoxyethylene copolymers with improved biological activity
USRE38558E1 (en) 1991-03-19 2004-07-20 Cytrx Corporation Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
US6933286B2 (en) 1991-03-19 2005-08-23 R. Martin Emanuele Therapeutic delivery compositions and methods of use thereof
US7202225B1 (en) 1993-10-15 2007-04-10 Emanuele R Martin Therapeutic delivery compositions and methods of use thereof
ZA933926B (en) * 1992-06-17 1994-01-03 Amgen Inc Polyoxymethylene-oxyethylene copolymers in conjuction with blomolecules
US6277410B1 (en) * 1992-10-08 2001-08-21 Supratek Pharma Inc. Copolymer compositions for oral delivery
US6093391A (en) * 1992-10-08 2000-07-25 Supratek Pharma, Inc. Peptide copolymer compositions
US6153193A (en) * 1993-04-28 2000-11-28 Supratek Pharma Inc. Compositions for targeting biological agents
DE69428521T2 (en) * 1993-02-02 2002-05-23 Xoma Technology Ltd MEDICINAL COMPOSITIONS CONTAINING A BACTERICIDAL PERMEABILITY-INCREASING PROTEIN AND A SURFACTANT
KR100361933B1 (en) 1993-09-08 2003-02-14 라 졸라 파마슈티칼 컴파니 Chemically defined nonpolymeric bonds form the platform molecule and its conjugate
EP0723440B1 (en) * 1993-10-15 2003-01-02 Cytrx Corporation Therapeutic delivery compositions and methods of use thereof
US5932544A (en) * 1994-05-31 1999-08-03 Xoma Corporation Bactericidal/permeability-increasing protein (BPI) compositions
EP1181937A3 (en) 1994-08-09 2004-02-04 Cytrx Corporation Novel vaccine adjuvant and vaccine
US6353055B1 (en) 1994-11-18 2002-03-05 Supratek Pharma Inc. Polynucleotide compositions
US6221959B1 (en) 1994-11-18 2001-04-24 Supratek Pharma, Inc. Polynucleotide compositions
WO1998013069A2 (en) * 1996-09-09 1998-04-02 Supratek Pharma, Inc. Fluorinated copolymeric pharmaceutical adjuncts
US6942859B2 (en) 1998-03-13 2005-09-13 University Of Southern California Red blood cells covalently bound with polymers
US6312685B1 (en) 1998-03-13 2001-11-06 Timothy C. Fisher Red blood cells covalently bound with two different polyethylene glycol derivatives
WO2000021543A1 (en) * 1998-10-09 2000-04-20 Cytrx Corporation Method and composition for treating ischemia and sickle cell anemia
CA2376057A1 (en) * 1999-06-08 2000-12-14 La Jolla Pharmaceutical Company Valency platform molecules comprising aminooxy groups
US6951939B2 (en) 2000-06-08 2005-10-04 La Jolla Pharmaceutical Company Multivalent platform molecules comprising high molecular weight polyethylene oxide
US20070092526A1 (en) * 2000-06-23 2007-04-26 Evans Robert K Polynucleotide vaccine adjuvants and formulations containing cationic surfactants, and methods of use
US6761824B2 (en) 2000-08-17 2004-07-13 Reeve Lorraine E Process for the fractionation of polymers
US20040266983A1 (en) * 2000-08-17 2004-12-30 Reeve Lorraine E Purified polyoxyalkylene block copolymers
WO2003079972A2 (en) 2002-02-22 2003-10-02 New River Parmaceuticals Inc. Active agent delivery systems and methods for protecting and administering active agents
CA2426582A1 (en) * 2000-10-20 2002-08-08 Valentis, Inc. Gene delivery formulations and methods for treatment of ischemic conditions
US20040009940A1 (en) * 2000-10-20 2004-01-15 Coleman Michael E. Gene delivery formulations and methods for treatment of ischemic conditions
US6492881B2 (en) * 2001-01-31 2002-12-10 Compaq Information Technologies Group, L.P. Single to differential logic level interface for computer systems
NZ529526A (en) * 2001-04-24 2006-06-30 Purdue Research Foundation Method and compositions for treating mammalian nerve tissue injuries
WO2004010941A2 (en) * 2002-07-29 2004-02-05 Transform Pharmaceuticals, Inc. Aqueous 2,6-diisopropylphenol pharmaceutical compositions
US6966990B2 (en) 2002-10-11 2005-11-22 Ferro Corporation Composite particles and method for preparing
JP4917263B2 (en) * 2002-12-23 2012-04-18 バイカル インコーポレイテッド Method for lyophilizing nucleic acid / block copolymer / cationic surfactant complex
EP1581201A4 (en) * 2002-12-23 2011-03-30 Vical Inc Method for producing sterile polynucleotide based medicaments
US7083748B2 (en) * 2003-02-07 2006-08-01 Ferro Corporation Method and apparatus for continuous particle production using supercritical fluid
JP4909071B2 (en) * 2003-03-24 2012-04-04 プルーローメッド, インコーポレイテッド Temporary embolization using reverse thermosensitive polymers
US20060008531A1 (en) * 2003-05-08 2006-01-12 Ferro Corporation Method for producing solid-lipid composite drug particles
EP1663261A2 (en) * 2003-09-05 2006-06-07 Mannarsamy Balasubramanian Purified polyoxypropylene/polyoxyethylene copolymers and method of preparing the same
JP4898447B2 (en) 2003-10-14 2012-03-14 プルーロームド インコーポレイテッド Confinement of kidney stone fragments during lithotripsy
WO2005046438A2 (en) 2003-11-06 2005-05-26 Pluromed, Inc. Internal clamp for surgical procedures
JP4521547B2 (en) * 2004-04-15 2010-08-11 株式会社サンメディカル技術研究所 Blood pump flow estimation device
US20060134221A1 (en) * 2004-12-03 2006-06-22 Vical Incorporated Methods for producing block copolymer/amphiphilic particles
AU2006216420B2 (en) * 2005-02-25 2010-07-15 The Regents Of The University Of Michigan Compositions and methods for treating and preventing cardiomyopathy and heart disease
EP1868652A2 (en) 2005-04-05 2007-12-26 Istituto di Richerche di Biologia Molecolare P. Angeletti S.p.A. Method for shielding functional sites or epitopes on proteins
EP2857041B9 (en) 2005-05-02 2018-02-14 Genzyme Corporation Non-lithotripsic kidney-stone therapy
US8815557B2 (en) * 2005-07-08 2014-08-26 University Of Chicago Compositions and methods for refolding of denatured proteins
WO2008018892A2 (en) * 2005-12-22 2008-02-14 Pluromed, Inc. Methods and kits for treating lacerations and puncture wounds using inverse thermosensitive polymers
WO2008016640A2 (en) * 2006-08-01 2008-02-07 Phrixus Pharmaceuticals, Incorporated Use of poloxamer for the prevention and/or treatment of heart failure
WO2008033728A2 (en) 2006-09-11 2008-03-20 Pluromed, Inc. Atraumatic occlusion balloons and skirts, and methods of use thereof
US20080181952A1 (en) * 2006-12-11 2008-07-31 Pluromed, Inc. Perfusive Organ Hemostasis
BRPI0807558A2 (en) * 2007-02-22 2014-07-01 Pluromed Inc Use of Reverse Thermosensitive Polymers to Control the Flow of Biological Fluid Subsequent to a Medical Procedure
MX2009010778A (en) * 2007-04-05 2010-01-29 Phrixus Pharmaceuticals Inc Compositions and methods for the treatment of heart failure.
EP2185162A4 (en) * 2007-08-10 2012-04-25 Synthrx Inc Polymer therapy for the treatment of chronic microvascular diseases
DK2222697T3 (en) 2007-11-01 2013-03-11 Perseid Therapeutics Llc Immunosuppressive polypeptides and nucleic acids
EP2219546B1 (en) 2007-11-29 2017-02-01 Genzyme Corporation Endoscopic mucosal resectioning using purified inverse thermosensitive polymers
ES2594302T3 (en) 2007-12-17 2016-12-19 The Regents Of The University Of Michigan Compositions and procedures for treatment and prevention of skeletal muscle deficiencies
EP2350274B1 (en) 2008-10-21 2019-01-23 The General Hospital Corporation Cell transplantation
DE102008043343A1 (en) * 2008-10-31 2010-05-06 Evonik Goldschmidt Gmbh Silicone polyether block copolymers with defined polydispersity in the polyoxyalkylene part and their use as stabilizers for the production of polyurethane foams
WO2010072769A1 (en) 2008-12-23 2010-07-01 Basf Se Method for producing polyether block copolymers
EP3508197A1 (en) 2009-10-21 2019-07-10 Otonomy, Inc. Modulation of gel temperature of poloxamer-containing formulations
GB201008902D0 (en) * 2010-05-27 2010-07-14 Imp Innovations Ltd Membrane enhanced polymer sythesis
EP2601299B1 (en) 2010-08-06 2019-04-24 The General Hospital Corporation D/B/A Massachusetts General Hospital System and apparatus for cell treatment
AU2011329088B2 (en) 2010-11-15 2016-02-25 Liferaft Biosciences, Inc. Methods for enhancing oxygenation of jeopardized tissue
CN103732233B (en) 2011-03-18 2016-08-10 贝克斯特国际公司 Comprise the peritoneal dialysis solution of glucose polymer
FR2977495B1 (en) * 2011-07-07 2014-03-07 Sanofi Sa PHARMACEUTICAL COMPOSITION AND SOLID GALENIC FORM WITH HIGH DRONEDARONE CONTENT AND PROCESS FOR PREPARING THE SAME
US9662345B2 (en) 2013-06-14 2017-05-30 Professional Compounding Centers Of America Antibiotic composition for inhalation and irrigation
CA2927361A1 (en) 2013-10-16 2015-04-23 Mast Therapeutics, Inc. Diuretic induced alterations of plasma volume
JP6202471B2 (en) 2013-10-31 2017-09-27 日油株式会社 Method for producing medical polyoxypropylene polymer and method for producing medical polyoxypropylene / polyoxyethylene block copolymer
US20160000823A1 (en) * 2014-07-07 2016-01-07 Mast Therapeutics, Inc. Methods and compositions for improving hemostasis
US9757411B2 (en) 2014-07-07 2017-09-12 Aires Pharmaceuticals, Inc. Poloxamer therapy for heart failure
WO2016007542A1 (en) 2014-07-07 2016-01-14 Mast Therapeutics, Inc. Poloxamer therapy for heart failure
US9403941B2 (en) 2014-07-07 2016-08-02 Mast Therapeutics, Inc. Poloxamer composition free of long circulating material and methods for production and uses thereof
JP6900378B2 (en) * 2015-12-22 2021-07-07 ビーエイエスエフ・ソシエタス・エウロパエアBasf Se Method for Purifying Polyether Block Copolymers
EP3580261A1 (en) 2017-02-09 2019-12-18 Basf Se A process for purification of polyether block copolymers
KR102544922B1 (en) * 2017-12-21 2023-06-16 시그마-알드리치 컴퍼니., 엘엘씨 Poloxamer compositions and methods of making and using the same
AU2019250128A1 (en) 2018-10-15 2020-04-30 Avent Inc. Compositions, systems, kits, and methods for neural ablation

Family Cites Families (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2979528A (en) * 1953-10-19 1961-04-11 Wyandotte Chemicals Corp Nitrogen-containing polyoxyalkylene detergent compositions
US2674619A (en) * 1953-10-19 1954-04-06 Wyandotte Chemicals Corp Polyoxyalkylene compounds
US3022335A (en) * 1955-03-30 1962-02-20 Wyandotte Chemicals Corp Surface active polyoxyalkylene compounds having a plurality of heteric polyoxypropylene-polyoxyethylene chains
US2854378A (en) * 1955-12-08 1958-09-30 Bristol Lab Inc Tetracycline suppository
US3036118A (en) * 1957-09-11 1962-05-22 Wyandotte Chemicals Corp Mixtures of novel conjugated polyoxyethylene-polyoxypropylene compounds
US3089818A (en) * 1960-06-02 1963-05-14 Baxter Laboratories Inc Water dispersible antibiotics
US3228834A (en) * 1962-06-08 1966-01-11 Hoffmann La Roche Pharmaceutical diluent compositions
US3140232A (en) * 1962-12-19 1964-07-07 Pfizer & Co C Color stabilization of tetracycline compositions with polypropylene glycols
US3391196A (en) * 1965-08-16 1968-07-02 Wyandotte Chemicals Corp High equivalent weight hydroxy-terminated ethylene oxide-butylene oxide polyether polyols
US3740421A (en) * 1966-09-19 1973-06-19 Basf Wyandotte Corp Polyoxyethylene-polyoxypropylene aqueous gels
US3450502A (en) * 1967-09-25 1969-06-17 Wyandotte Chemicals Corp Method of operating heart-lung apparatus
US3641240A (en) * 1968-09-27 1972-02-08 Wyandotte Chemicals Corp Method for the treatment of an embolus or thrombus
US3867533A (en) * 1968-12-20 1975-02-18 Basf Wyandotte Corp Preparation of aqueous gel compositions containing a water-insoluble organic ingredient
US3577522A (en) * 1969-10-10 1971-05-04 Wyandotte Chemicals Corp Methods for the treatment of shock with ethylene oxide-polypropylene glycol condensates as blood plasma substitutes
US3590125A (en) * 1969-10-10 1971-06-29 Wyandotte Chemicals Corp Physiological salt solutions of ethylene oxide-polypropylene glycol condensation products as blood plasma substitutes
US3980772A (en) * 1969-12-02 1976-09-14 Baxter Laboratories, Inc. Methods of dissolving blood clots and the like with streptokinase chemically bonded to a carbohydrate matrix
CA959759A (en) * 1970-01-15 1974-12-24 John J. Miskel Method for absorption of drugs
US3867521A (en) * 1970-08-26 1975-02-18 Scherer Corp R P Method for absorption of drugs
US4073886A (en) * 1973-01-30 1978-02-14 Baxter Travenol Laboratories, Inc. Blood fractionation process using block copolymers of ethylene oxide and polyoxypropylene
US3956259A (en) * 1973-01-30 1976-05-11 Baxter Laboratories, Inc. Fractionation of blood using block copolymer of ethylene oxide and polyoxypropylene polymer to recover fraction suitable for organ perfusate
US4179337A (en) * 1973-07-20 1979-12-18 Davis Frank F Non-immunogenic polypeptides
US3997458A (en) * 1974-04-12 1976-12-14 Deknatel, Incorporated Method of cleansing contaminated wounds and surgical scrub solutions for same
US4104455A (en) * 1975-03-25 1978-08-01 Toyo Soda Manufacturing Co., Ltd. Polymerization of monomer
US4100271A (en) * 1976-02-26 1978-07-11 Cooper Laboratories, Inc. Clear, water-miscible, liquid pharmaceutical vehicles and compositions which gel at body temperature for drug delivery to mucous membranes
US4195167A (en) 1976-05-28 1980-03-25 Union Carbide Corporation Gradient polymers of two or more cyclic, organic, ring-opening, addition polymerizable monomers and methods for making same
JPS545094A (en) 1977-06-09 1979-01-16 Tokyo Tanabe Co Production of pharmaceutical urokinase from contamination free human urine
DE2732929A1 (en) * 1977-07-21 1979-02-01 Bayer Ag POLYAETHER, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A LIPID ABSORPTION INHIBITOR
DE2961374D1 (en) * 1978-01-27 1982-01-28 Bp Chem Int Ltd A method for increasing the selectivity to acetic acid in the production of a mixture of c1 to c3 monocarboxylic acids by oxidation of paraffinic hydrocarbons
DE2808865A1 (en) * 1978-03-02 1979-09-13 Hoechst Ag MICROBIOCIDES BASED ON ALKYL DI GUANIDINIUM SALT
US4275244A (en) * 1978-05-11 1981-06-23 Basf Wyandotte Corporation Linear polyalkylene ether glycols of high molecular weight
JPS5533194A (en) 1978-08-07 1980-03-08 Scholz D Thomas Stringgfastener device including tremolant
US4305922A (en) * 1978-10-04 1981-12-15 University Patents, Inc. Labeling proteins with 99m-Tc by ligand exchange
US4186253A (en) * 1978-10-10 1980-01-29 The Green Cross Corporation Perfusate for preserving organ to be transplanted and preserving method
DE2850058A1 (en) * 1978-11-18 1980-05-29 Bayer Ag POLYAETHER DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS MEDICINAL PRODUCTS
FR2454409A1 (en) * 1979-04-18 1980-11-14 Sovam TRACTOR VEHICLE IN PARTICULAR FOR LARGE CARRIER AIRCRAFT
FI803077A (en) * 1979-10-12 1981-04-13 Ciba Geigy Ag FOERFARANDE FOER FRAMSTAELLNING AV MYRAMYLPEPTIDER
US4409209A (en) * 1979-10-12 1983-10-11 Ciba-Geigy Corporation Novel phosphorylmuramyl peptides and processes for the manufacture thereof
US4575484A (en) * 1980-05-05 1986-03-11 Montefiore Medical Center, Inc. Binding assay for the detection of mycobacteria
US4410660A (en) * 1980-05-05 1983-10-18 Montefiore Medical Center Binding assay for the detection of mycobacteria
US4489158A (en) * 1980-05-05 1984-12-18 Montefiore Hospital And Medical Center, Inc. Binding assay for the detection of mycobacteria
JPS578223A (en) * 1980-06-19 1982-01-16 Mitsui Petrochem Ind Ltd Production of alkylene oxide block copolymer
US4378347A (en) * 1980-06-30 1983-03-29 Franco Wayne P Composition for treating the heart for myocardial infarction
US4376118A (en) * 1980-10-06 1983-03-08 Miles Laboratories, Inc. Stable nonaqueous solution of tetracycline salt
GR78246B (en) * 1981-01-23 1984-09-26 Ciba Geigy Ag
US4395393A (en) * 1981-08-10 1983-07-26 Basf Wyandotte Corporation Artificial blood emulsifiers
US4407790A (en) * 1981-09-25 1983-10-04 Economics Laboratory, Inc. Method of controlling bloat using nonionic surfactants
US4609546A (en) * 1982-06-24 1986-09-02 Japan Chemical Research Co., Ltd. Long-acting composition
DE3234084A1 (en) * 1982-09-14 1984-03-15 B. Braun Melsungen Ag, 3508 Melsungen PHARMACEUTICAL PREPARATIONS FOR TREATING UNWANTED GROWTHS AND THEIR USE
SU1183112A1 (en) * 1983-08-04 1985-10-07 Научно-Исследовательский Институт Экспериментальной И Клинической Терапии Министерства Здравоохранения Гсср Method of treatment of acute myocardial ischemia
US4606918A (en) * 1983-08-22 1986-08-19 Syntex (U.S.A.) Inc. Polyoxypropylene-polyoxyethylene block polymer based adjuvants
US4600652A (en) * 1985-04-01 1986-07-15 Warner-Lambert Company Permanently bonded antithrombogenic polyurethane surface
US5183687A (en) * 1985-06-18 1993-02-02 Emory University Method of treating poultry for coccidiosis
US5114708A (en) * 1985-06-18 1992-05-19 Emory University Method for stimulating growth in animals
US4806352A (en) * 1986-04-15 1989-02-21 Ribi Immunochem Research Inc. Immunological lipid emulsion adjuvant
US4803070A (en) * 1986-04-15 1989-02-07 Ribi Immunochem Research Inc. Immunological emulsion adjuvants for polysaccharide vaccines
US5017370A (en) * 1986-05-15 1991-05-21 Emory University Improved method of performing angioplasty procedures
US5047236A (en) * 1986-05-15 1991-09-10 Emory University Method of treating stroke
JPH0610139B2 (en) * 1986-05-15 1994-02-09 エモリ ユニバーシティ Mixtures of fibrinolytic compounds and agents for dissolving blood clots in blood vessels
US4897263A (en) * 1986-05-15 1990-01-30 Emory University Methods and compositions for treatment of pathological hydrophobic interactions in biological fluids
US5089260A (en) * 1986-05-15 1992-02-18 Emory University Method of treating ischemic tissue
US4879109A (en) * 1986-05-15 1989-11-07 Emory University Method for treating burns
US5080894A (en) * 1986-05-15 1992-01-14 Emory University Method and composition for reducing tissue damage
US5028599A (en) * 1986-05-15 1991-07-02 Emory University Method of treating mycardial damage
US4837014A (en) * 1986-05-15 1989-06-06 Emory University An improved method of treating sickle cell anemia
US5064643A (en) * 1986-05-15 1991-11-12 Emory University Method for treating sickle cell disease
US5030448A (en) * 1986-05-15 1991-07-09 Emory University Method of delivering drugs to damaged or diseased tissue
US5032394A (en) * 1986-05-15 1991-07-16 Emory University Method of treating burns
US5198211A (en) * 1986-05-15 1993-03-30 Emory University Method of treating myocardial damage
US4937070A (en) * 1986-05-15 1990-06-26 Emory University Methods and compositions for treatment of pathological hydrophobic interactions in biological fluids
WO1987006831A1 (en) * 1986-05-15 1987-11-19 Emory University Composition and method for treating a thrombus and embolus
US4801452A (en) * 1986-05-15 1989-01-31 Hunter Robert L Fibrinolytic composition
US5250294A (en) * 1986-05-15 1993-10-05 Emory University Improved perfusion medium for transplantation of organs
US5041288A (en) * 1986-05-15 1991-08-20 Emory University Method of treating tissue damaged by reperfusion injury
US5071649A (en) * 1986-05-15 1991-12-10 Emory University Method of preventing blockage in catheters
US4997644A (en) * 1986-05-15 1991-03-05 Emory University Method of treating adult respiratory distress syndrome
US5039520A (en) * 1986-05-15 1991-08-13 Emory University Plasma extender
US5078995A (en) * 1986-05-15 1992-01-07 Emory University Fibrionolytic composition
US4873083A (en) * 1986-05-15 1989-10-10 Emory University Fibrinolytic composition
JP2527942B2 (en) * 1986-09-18 1996-08-28 ティーディーケイ株式会社 Magnetic recording media
US5554372A (en) 1986-09-22 1996-09-10 Emory University Methods and vaccines comprising surface-active copolymers
US4764567A (en) 1986-11-20 1988-08-16 Basf Corporation Process for the preparation of polyoxyalkylene block polyethers having enhanced properties
AU1396588A (en) * 1987-02-20 1988-09-14 Emory University Antiinfective compounds and method of use
US5811088A (en) 1987-02-20 1998-09-22 Emory University Antiinfective compounds and methods of use
JPH07109520B2 (en) 1987-02-24 1995-11-22 株式会社リコー Electrophotographic photoconductor
US5057540A (en) * 1987-05-29 1991-10-15 Cambridge Biotech Corporation Saponin adjuvant
DE4014923A1 (en) * 1990-05-10 1991-11-14 Basf Ag PROCESS FOR PRODUCING HARD FOAM MATERIALS CONTAINING URETHANE OR URETHANE AND ISOCYANURATE GROUPS BY THE POLYISOCYANATE POLYADDITIONAL PROCESS AND THE POLYOXYALKYLENE POLYOLS SUITABLE FOR THEM
JP2647556B2 (en) * 1991-03-19 1997-08-27 サイトアーレクス・コーポレーシヨン Polyoxypropylene / polyoxyethylene copolymers with improved biological activity
US5294365A (en) * 1991-12-12 1994-03-15 Basf Corporation Hydroxypolyethers as low-foam surfactants
US5371253A (en) * 1993-12-14 1994-12-06 Arco Chemical Technology, L.P. Process for producing esterified alkoxylated monoglycerides and diglycerides

Also Published As

Publication number Publication date
JP2647556B2 (en) 1997-08-27
DE69230372D1 (en) 2000-01-05
NO307890B1 (en) 2000-06-13
US20020183398A1 (en) 2002-12-05
NO933337D0 (en) 1993-09-17
CN1069741A (en) 1993-03-10
ES2140408T3 (en) 2000-03-01
AU662146B2 (en) 1995-08-24
US5523492A (en) 1996-06-04
IL101305A (en) 1995-11-27
DK0576612T3 (en) 2000-05-22
US6359014B1 (en) 2002-03-19
DE69230372T2 (en) 2000-06-15
IL101305A0 (en) 1992-11-15
USRE36665E (en) 2000-04-18
SK100893A3 (en) 1994-04-06
US5990241A (en) 1999-11-23
KR100224539B1 (en) 1999-10-15
NO933337L (en) 1993-11-17
IE920860A1 (en) 1992-09-23
AU1773092A (en) 1992-10-21
US6747064B2 (en) 2004-06-08
EP0576612A4 (en) 1994-11-09
EP0576612A1 (en) 1994-01-05
USRE37285E1 (en) 2001-07-17
HU9302628D0 (en) 1993-12-28
EP0576612B1 (en) 1999-12-01
CZ194693A3 (en) 1994-03-16
GR3032726T3 (en) 2000-06-30
HUT67762A (en) 1995-04-28
ATE187154T1 (en) 1999-12-15
CA2106474C (en) 2004-02-10
JPH06506258A (en) 1994-07-14
US5691387A (en) 1997-11-25
WO1992016484A1 (en) 1992-10-01

Similar Documents

Publication Publication Date Title
CA2106474A1 (en) Polyoxypropylene/polyoxyethylene copolymers with improved biological activity
CA2006953A1 (en) Methods and compositions for treatment of pathological hydrophobic interactions in biological fluids.
GB1390876A (en) Shapoo composition
HUT43488A (en) Process for preparing polymers decomposing by biological process and utilizable for pharmaceutical purposes
EP0835888A3 (en) Non-crosslinked anion exchange resin and pharmaceutical composition containing same
JP3520674B2 (en) Hair cosmetics
NZ243034A (en) Aqueous hair styling composition comprising a polymer formed from hydrophobic monomers and a water-insoluble volatile diluent for the polymer
CA2395493A1 (en) Hyaluronic acid in the treatment of cancer
US5280092A (en) Lactam-containing emulsifier systems for water-in-oil emulsion polymers
IE45370L (en) Allyl-acrylic monomers and derived polymers
GB1414182A (en) Base for opthalmological medicinal preparations and an opthalmological medicinal film
ES8203391A1 (en) Copolymers having bactericidal activity, process for the preparation thereof and pharmaceutical compositions therefrom
US5416158A (en) Crosslinked carboxylic copolymers useful as rheological additives in personal care and pharmaceutical products
DK0517160T3 (en) Ophthalmic extended release preparations
DE3373417D1 (en) Use of a sulfonated homo- or copolymer of styrene for the manufacture of a contraceptive composition
FI925570A (en) The cationic copolymer, which disperses and alternates with the best crystallization of the paper
WO1993014024A1 (en) Hair care compositions
IT7825994A0 (en) COATING COMPOSITION PROCEDURE FOR THE PREPARATION OF A LIQUID HAVING A HIGH CONTENT OF AN ACRYLATE COPOLYMER OF LOW IN SOLID PRODUCTS BASED ON THE MOLECULAR WEIGHT, AND OF AN ACRYLATE COPOLYMER SO OBTAINED.
FR2403353A1 (en) NEW DERIVATIVES OF POLYASPARTIC ACID, THEIR PREPARATION AND THEIR USE IN COSMETIC COMPOSITIONS
MY103428A (en) Hairdressing composition
RU93056161A (en) BLOCK-COPOLYMER POLYOXYPROPYLENE AND POLYOXYETHYLENE, SURFACE-ACTIVE COPOLYMER, METHOD OF OBTAINING NONTOXIC SURFACE-ACTIVE COPOLYMER, MEDICINE
JPS54138129A (en) Gelatinous or creamy composition
JPS62281810A (en) Separation-type liquid hair-dressing composition
IE922400L (en) Composition comprising an oxygen radical scavenger and a¹surface-active copolymer
JP2000327522A (en) Cosmetics

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed