CA2028094A1 - Copolymeres carbohydrateacryl- et methacryliques; procede de fabrication - Google Patents

Copolymeres carbohydrateacryl- et methacryliques; procede de fabrication

Info

Publication number
CA2028094A1
CA2028094A1 CA2028094A CA2028094A CA2028094A1 CA 2028094 A1 CA2028094 A1 CA 2028094A1 CA 2028094 A CA2028094 A CA 2028094A CA 2028094 A CA2028094 A CA 2028094A CA 2028094 A1 CA2028094 A1 CA 2028094A1
Authority
CA
Canada
Prior art keywords
methacrylcopolymers
carbohydrateacryl
manufacture
formula
kda
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
CA2028094A
Other languages
English (en)
Other versions
CA2028094C (fr
Inventor
Thomas Norberg
Elisabeth Kallin
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.)
Procur AB
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
Application filed by Individual filed Critical Individual
Publication of CA2028094A1 publication Critical patent/CA2028094A1/fr
Application granted granted Critical
Publication of CA2028094C publication Critical patent/CA2028094C/fr
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
    • C07H5/04—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to nitrogen
    • C07H5/06—Aminosugars
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H13/00—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids
    • C07H13/02—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids
    • C07H13/04—Compounds containing saccharide radicals esterified by carbonic acid or derivatives thereof, or by organic acids, e.g. phosphonic acids by carboxylic acids having the esterifying carboxyl radicals attached to acyclic carbon atoms
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/5308—Immunoassay; Biospecific binding assay; Materials therefor for analytes not provided for elsewhere, e.g. nucleic acids, uric acid, worms, mites
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/531—Production of immunochemical test materials

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Biotechnology (AREA)
  • Organic Chemistry (AREA)
  • Urology & Nephrology (AREA)
  • Biochemistry (AREA)
  • Biomedical Technology (AREA)
  • Genetics & Genomics (AREA)
  • Pathology (AREA)
  • Microbiology (AREA)
  • Cell Biology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Analytical Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Saccharide Compounds (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)

Abstract

L'invention concerne un copolymère de glycosylamine N-acylé ainsi qu'un amide ayant la formule générale (I), dans laquelle R2 représente un résidu de sucre de réduction; R3 représente H ou CH3; x représente un nombre entier compris entre 0 et environ 20; et m est tel que la masse moléculaire du copolymère est comprise entre environ 5 kDa et 2000 kDa; une glycosylamine N-acryloyle ou méthacryloyle ayant la formula (II), dans laquelle R2 représente un résidu de sucre de réduction; et R3 représente H ou CH3. L'invention concerne en outre des procédés de préparation du composé.
CA002028094A 1989-03-01 1990-02-16 Copolymeres carbohydrateacryl- et methacryliques; procede de fabrication Expired - Fee Related CA2028094C (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE8900605-0 1989-03-01
SE8900605A SE463314B (sv) 1989-03-01 1989-03-01 Sampolymerer av en n-acylerad glykosylamin och en amid, n-akryloyl-eller metakryloylglykosylaminer samt foerfarande foer framstaellning av dessa
PCT/SE1990/000107 WO1990010023A1 (fr) 1989-03-01 1990-02-16 Copolymeres a base d'acrylglucides et de methacrylglucides ainsi que leur fabrication

Publications (2)

Publication Number Publication Date
CA2028094A1 true CA2028094A1 (fr) 1990-09-02
CA2028094C CA2028094C (fr) 2000-11-21

Family

ID=20375126

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002028094A Expired - Fee Related CA2028094C (fr) 1989-03-01 1990-02-16 Copolymeres carbohydrateacryl- et methacryliques; procede de fabrication

Country Status (11)

Country Link
US (1) US5162471A (fr)
EP (1) EP0425601B1 (fr)
JP (1) JP2908558B2 (fr)
AT (1) ATE139239T1 (fr)
AU (1) AU5188490A (fr)
CA (1) CA2028094C (fr)
DE (1) DE69027397T2 (fr)
FI (1) FI905389A7 (fr)
NO (1) NO904720L (fr)
SE (1) SE463314B (fr)
WO (1) WO1990010023A1 (fr)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5718909A (en) * 1991-02-18 1998-02-17 Medscand Ab Sheet containing carbohydrate derivative for removal of E. coli
SE469256B (sv) * 1991-02-18 1993-06-14 Medscand Ab Rengoeringsprodukt
FR2695127B1 (fr) * 1992-08-28 1994-11-04 Beghin Say Eridania Procédé de préparation de glycosylamines à partir de sucres réducteurs.
JP2002503223A (ja) * 1997-04-11 2002-01-29 アドバンスト・メディシン・インコーポレイテッド 複数の活性分子を供与する分子
WO1999064563A1 (fr) * 1998-06-10 1999-12-16 Ústav Makromolekulární Chemie Akademie Věd České Republiky Support polymere pour la culture de keratinocytes
US6410668B1 (en) * 1999-08-21 2002-06-25 Marcella Chiari Robust polymer coating
FR2873123B1 (fr) * 2004-07-13 2006-09-15 Rhodia Chimie Sa Nouveaux glycopolymeres, leurs utilisations, et monomeres utiles pour leur preparation
CN102421787B (zh) * 2009-04-15 2015-11-25 巴斯夫欧洲公司 制备不饱和酰氨基烷基多羟基酰胺的方法
CN102395594A (zh) * 2009-04-15 2012-03-28 巴斯夫欧洲公司 单烯键式不饱和葡基胺的制备方法
FR2952642B1 (fr) * 2009-11-16 2012-01-06 Centre Nat Rech Scient Polymeres comprenant une majorite de monomeres amphiphiles destines au piegeage et a la manipulation de proteines membranaires
BR112012032218A2 (pt) 2010-06-17 2016-11-22 Basf Se "copolímero, uso de um copolímero, e, composição de detergente têxtil"
PL2582761T3 (pl) 2010-06-17 2015-08-31 Basf Se Wodne kompozycje środków wiążących
US8481639B2 (en) 2010-06-17 2013-07-09 Basf Se Polymers with saccharide side groups and their use

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE8301609D0 (sv) * 1983-03-23 1983-03-23 Svenska Sockerfabriks Ab Forening och komposition for terapeutisk eller diagnostisk anvendning jemte forfarande for terapeutisk behandling

Also Published As

Publication number Publication date
EP0425601B1 (fr) 1996-06-12
SE8900605D0 (sv) 1989-02-21
DE69027397D1 (de) 1996-07-18
NO904720L (no) 1990-12-28
AU5188490A (en) 1990-09-26
FI905389A0 (fi) 1990-10-31
WO1990010023A1 (fr) 1990-09-07
SE8900605L (sv) 1990-09-02
JP2908558B2 (ja) 1999-06-21
FI905389A7 (fi) 1990-10-31
EP0425601A1 (fr) 1991-05-08
US5162471A (en) 1992-11-10
SE463314B (sv) 1990-11-05
DE69027397T2 (de) 1997-01-23
ATE139239T1 (de) 1996-06-15
JPH04500092A (ja) 1992-01-09
CA2028094C (fr) 2000-11-21
NO904720D0 (no) 1990-10-31

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Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed