AU667051B2 - Water-soluble, polymer-based reagents and conjugates comprising moieties derived from divinyl sulfone - Google Patents
Water-soluble, polymer-based reagents and conjugates comprising moieties derived from divinyl sulfone Download PDFInfo
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- AU667051B2 AU667051B2 AU23489/92A AU2348992A AU667051B2 AU 667051 B2 AU667051 B2 AU 667051B2 AU 23489/92 A AU23489/92 A AU 23489/92A AU 2348992 A AU2348992 A AU 2348992A AU 667051 B2 AU667051 B2 AU 667051B2
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- dextran
- soluble
- water
- molecular species
- conjugate
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- NMHMNPHRMNGLLB-UHFFFAOYSA-N phloretic acid Chemical compound OC(=O)CCC1=CC=C(O)C=C1 NMHMNPHRMNGLLB-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 238000002264 polyacrylamide gel electrophoresis Methods 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002704 polyhistidine Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002714 polyornithine Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000186 progesterone Substances 0.000 description 1
- 229960003387 progesterone Drugs 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000012205 qualitative assay Methods 0.000 description 1
- 238000012207 quantitative assay Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 239000003270 steroid hormone Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- 229910052713 technetium Inorganic materials 0.000 description 1
- GKLVYJBZJHMRIY-UHFFFAOYSA-N technetium atom Chemical compound [Tc] GKLVYJBZJHMRIY-UHFFFAOYSA-N 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 125000000341 threoninyl group Chemical group [H]OC([H])(C([H])([H])[H])C([H])(N([H])[H])C(*)=O 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- 239000012581 transferrin Substances 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
- 229960003726 vasopressin Drugs 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54353—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals with ligand attached to the carrier via a chemical coupling agent
Landscapes
- Health & Medical Sciences (AREA)
- Immunology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Physics & Mathematics (AREA)
- Microbiology (AREA)
- Cell Biology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Biotechnology (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Peptides Or Proteins (AREA)
- Cephalosporin Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Graft Or Block Polymers (AREA)
- Saccharide Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DK911309A DK130991D0 (da) | 1991-07-04 | 1991-07-04 | Polymere konjugater |
| DK1309/91 | 1991-07-04 | ||
| US789757 | 1991-11-08 | ||
| US07/789,757 US5543332A (en) | 1991-07-04 | 1991-11-08 | Water-soluble, polymer-based reagents and conjugates comprising moieties derived from divinyl sulfone |
| PCT/DK1992/000206 WO1993001498A1 (en) | 1991-07-04 | 1992-06-29 | Water-soluble, polymer-based reagents and conjugates comprising moieties derived from divinyl sulfone |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2348992A AU2348992A (en) | 1993-02-11 |
| AU667051B2 true AU667051B2 (en) | 1996-03-07 |
Family
ID=26065568
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU23489/92A Expired AU667051B2 (en) | 1991-07-04 | 1992-06-29 | Water-soluble, polymer-based reagents and conjugates comprising moieties derived from divinyl sulfone |
Country Status (12)
| Country | Link |
|---|---|
| EP (1) | EP0594772B1 (https=) |
| JP (1) | JP3340434B2 (https=) |
| AT (1) | ATE142021T1 (https=) |
| AU (1) | AU667051B2 (https=) |
| CA (1) | CA2112992C (https=) |
| DE (1) | DE69213240T2 (https=) |
| DK (1) | DK0594772T3 (https=) |
| ES (1) | ES2094920T3 (https=) |
| FI (1) | FI115413B (https=) |
| GR (1) | GR3021806T3 (https=) |
| NO (1) | NO315443B1 (https=) |
| WO (1) | WO1993001498A1 (https=) |
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- 1992-06-29 CA CA002112992A patent/CA2112992C/en not_active Expired - Lifetime
- 1992-06-29 AT AT92916161T patent/ATE142021T1/de active
- 1992-06-29 DE DE69213240T patent/DE69213240T2/de not_active Expired - Lifetime
- 1992-06-29 EP EP92916161A patent/EP0594772B1/en not_active Expired - Lifetime
- 1992-06-29 JP JP50189993A patent/JP3340434B2/ja not_active Expired - Lifetime
- 1992-06-29 AU AU23489/92A patent/AU667051B2/en not_active Expired
- 1992-06-29 ES ES92916161T patent/ES2094920T3/es not_active Expired - Lifetime
-
1994
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- 1994-01-04 NO NO19940030A patent/NO315443B1/no not_active IP Right Cessation
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- 1996-11-28 GR GR960403197T patent/GR3021806T3/el unknown
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4752339A (en) * | 1983-10-31 | 1988-06-21 | Hi-Tek Polymers, Inc. | Thixotropic aqueous solutions containing a divinylsulfone-crosslinked polygalactomannan gum |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3340434B2 (ja) | 2002-11-05 |
| FI940023A7 (fi) | 1994-02-25 |
| NO940030D0 (no) | 1994-01-04 |
| GR3021806T3 (en) | 1997-02-28 |
| CA2112992C (en) | 2002-06-11 |
| ES2094920T3 (es) | 1997-02-01 |
| EP0594772A1 (en) | 1994-05-04 |
| FI115413B (fi) | 2005-04-29 |
| DE69213240T2 (de) | 1997-04-24 |
| DE69213240D1 (de) | 1996-10-02 |
| NO940030L (no) | 1994-03-03 |
| EP0594772B1 (en) | 1996-08-28 |
| ATE142021T1 (de) | 1996-09-15 |
| AU2348992A (en) | 1993-02-11 |
| DK0594772T3 (https=) | 1997-02-24 |
| FI940023A0 (fi) | 1994-01-04 |
| NO315443B1 (no) | 2003-09-01 |
| WO1993001498A1 (en) | 1993-01-21 |
| JPH06509167A (ja) | 1994-10-13 |
| CA2112992A1 (en) | 1993-01-21 |
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