CA2283597C - Reduced cortisol conjugates - Google Patents
Reduced cortisol conjugates Download PDFInfo
- Publication number
- CA2283597C CA2283597C CA002283597A CA2283597A CA2283597C CA 2283597 C CA2283597 C CA 2283597C CA 002283597 A CA002283597 A CA 002283597A CA 2283597 A CA2283597 A CA 2283597A CA 2283597 C CA2283597 C CA 2283597C
- Authority
- CA
- Canada
- Prior art keywords
- cortisol
- conjugate
- labeled
- reduced
- bound
- 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.)
- Expired - Lifetime
Links
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- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- AJFXNBUVIBKWBT-UHFFFAOYSA-N disodium;boric acid;hydrogen borate Chemical compound [Na+].[Na+].OB(O)O.OB(O)O.OB(O)O.OB([O-])[O-] AJFXNBUVIBKWBT-UHFFFAOYSA-N 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940116332 glucose oxidase Drugs 0.000 description 1
- 235000019420 glucose oxidase Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 125000004404 heteroalkyl group Chemical group 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000008105 immune reaction Effects 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 125000000842 isoxazolyl group Chemical group 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- 230000037356 lipid metabolism Effects 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- CSJDCSCTVDEHRN-UHFFFAOYSA-N methane;molecular oxygen Chemical group C.O=O CSJDCSCTVDEHRN-UHFFFAOYSA-N 0.000 description 1
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 description 1
- 229960004465 metyrapone Drugs 0.000 description 1
- FJLBFSROUSIWMA-UHFFFAOYSA-N metyrapone Chemical compound C=1C=CN=CC=1C(C)(C)C(=O)C1=CC=CN=C1 FJLBFSROUSIWMA-UHFFFAOYSA-N 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- JULKJDRBSRRBHT-UHFFFAOYSA-N n-(3-chloro-4-hydroxyphenyl)acetamide Chemical compound CC(=O)NC1=CC=C(O)C(Cl)=C1 JULKJDRBSRRBHT-UHFFFAOYSA-N 0.000 description 1
- 239000004081 narcotic agent Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000036963 noncompetitive effect Effects 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 230000022558 protein metabolic process Effects 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000026313 regulation of carbohydrate metabolic process Effects 0.000 description 1
- 230000003248 secreting effect Effects 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- BBMHARZCALWXSL-UHFFFAOYSA-M sodium dihydrogenphosphate monohydrate Chemical compound O.[Na+].OP(O)([O-])=O BBMHARZCALWXSL-UHFFFAOYSA-M 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229940126585 therapeutic drug Drugs 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 125000004001 thioalkyl group Chemical group 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 210000001235 zona fasciculata Anatomy 0.000 description 1
- 210000002327 zona reticularis Anatomy 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/815—Test for named compound or class of compounds
- Y10S436/817—Steroids or hormones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Enzymes And Modification Thereof (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10283698P | 1998-10-02 | 1998-10-02 | |
| US60/102,836 | 1998-10-02 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2283597A1 CA2283597A1 (en) | 2000-04-02 |
| CA2283597C true CA2283597C (en) | 2008-02-05 |
Family
ID=22291927
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002283597A Expired - Lifetime CA2283597C (en) | 1998-10-02 | 1999-09-24 | Reduced cortisol conjugates |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6383766B1 (enExample) |
| EP (1) | EP0992512B1 (enExample) |
| JP (2) | JP2000143691A (enExample) |
| AT (1) | ATE312842T1 (enExample) |
| CA (1) | CA2283597C (enExample) |
| DE (1) | DE69928888T2 (enExample) |
| DK (1) | DK0992512T3 (enExample) |
| ES (1) | ES2253866T3 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100361933B1 (ko) * | 1993-09-08 | 2003-02-14 | 라 졸라 파마슈티칼 컴파니 | 화학적으로정의된비중합성결합가플랫폼분자및그것의콘주게이트 |
| CA2376057A1 (en) * | 1999-06-08 | 2000-12-14 | La Jolla Pharmaceutical Company | Valency platform molecules comprising aminooxy groups |
| NZ511705A (en) * | 2001-05-14 | 2004-03-26 | Horticulture & Food Res Inst | Methods and rapid immunoassay device for detecting progesterone and other steroids |
| JP2004063363A (ja) * | 2002-07-31 | 2004-02-26 | Semiconductor Energy Lab Co Ltd | 電界発光素子用材料、およびそれを用いた電界発光素子 |
| DE102004034008A1 (de) * | 2004-07-14 | 2006-02-09 | Rösner Research GmbH & Co.KG | Verfahren zur Herstellung von Albumin-Corticoid-Konjugaten |
| GB2418665B8 (en) * | 2004-10-04 | 2008-03-25 | Biotrin Intellectual Pty Ltd | Stabilising diluent for a protein-horseradish peroxidase conjugate |
| CN104251903A (zh) * | 2007-11-22 | 2014-12-31 | 特拉斯医药有限公司 | 血液试样的品质评估方法 |
| JP2017150815A (ja) * | 2014-05-29 | 2017-08-31 | 株式会社日立製作所 | 臨床検査キット及び化学物質検出方法 |
| JP7579190B2 (ja) * | 2020-03-30 | 2024-11-07 | ミナリスメディカル株式会社 | 競合法による検体中のステロイドホルモンの測定用キットの安定化方法 |
| CN119306830B (zh) * | 2023-07-11 | 2025-06-20 | 东莞市朋志生物科技有限公司 | 抗皮质醇抗体、检测皮质醇的试剂和试剂盒 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3992158A (en) | 1973-08-16 | 1976-11-16 | Eastman Kodak Company | Integral analytical element |
| US3867258A (en) | 1973-11-08 | 1975-02-18 | American Cyanamid Co | Lactate dehydrogenase test material |
| CA1054034A (en) | 1975-06-20 | 1979-05-08 | Barbara J. Bruschi | Multilayer analytical element |
| US4042435A (en) | 1976-01-05 | 1977-08-16 | The Goodyear Tire & Rubber Company | Closed torus wound carcass for a closed torus tire |
| US4050898A (en) | 1976-04-26 | 1977-09-27 | Eastman Kodak Company | Integral analytical element |
| US4081525A (en) * | 1976-08-16 | 1978-03-28 | Beckman Instruments, Inc. | Radioimmunoassay of plasma steroids |
| US4128629A (en) * | 1977-07-05 | 1978-12-05 | Corning Glass Works | Extraction-free cortisol assay |
| US4153668A (en) | 1978-01-03 | 1979-05-08 | Eastman Kodak Company | Multi-zone analytical element and method using same |
| IL56467A (en) * | 1978-02-10 | 1982-04-30 | Sin Hang Lee | Cytochemical agents and methods for the detection of steroid hormone receptors in human tissues |
| US4258001A (en) | 1978-12-27 | 1981-03-24 | Eastman Kodak Company | Element, structure and method for the analysis or transport of liquids |
| JPS55164356A (en) | 1979-06-08 | 1980-12-22 | Fuji Photo Film Co Ltd | Multi-layer analysis sheet for liquid sample analysis |
| JPS5634700A (en) * | 1979-08-29 | 1981-04-06 | Teikoku Hormone Mfg Co Ltd | Novel tetrahydrocorticosteroid derivative and antiserum |
| US4372745A (en) | 1979-12-19 | 1983-02-08 | Electro-Nucleonics, Inc. | Chemical luminescence amplification substrate system for immunochemistry involving microencapsulated fluorescer |
| US4879219A (en) | 1980-09-19 | 1989-11-07 | General Hospital Corporation | Immunoassay utilizing monoclonal high affinity IgM antibodies |
| JPS57101761A (en) | 1980-12-17 | 1982-06-24 | Konishiroku Photo Ind Co Ltd | Analyzing element |
| US4483921A (en) | 1981-01-12 | 1984-11-20 | Collaborative Research, Inc. | Immunoassay with antigen or antibody labeled liposomes sequestering enzyme |
| US4517288A (en) | 1981-01-23 | 1985-05-14 | American Hospital Supply Corp. | Solid phase system for ligand assay |
| DE3380125D1 (en) | 1982-03-22 | 1989-08-03 | Amersham Int Plc | Assay for the free portion of substances in biological fluids |
| US5599720A (en) * | 1982-08-27 | 1997-02-04 | Multilyte Limited | Measurement of analyte concentration |
| US4510251A (en) * | 1982-11-08 | 1985-04-09 | Abbott Laboratories | Fluorescent polarization assay for ligands using aminomethylfluorescein derivatives as tracers |
| JPS6020149A (ja) * | 1983-07-15 | 1985-02-01 | Teikoku Hormone Mfg Co Ltd | 免疫化学的測定方法及びその試薬 |
| US4847080A (en) | 1984-03-07 | 1989-07-11 | New York Blood Center, Inc. | Pre-S gene coded peptide hepatitis B immunogens, vaccines, diagnostics, and synthetic lipide vesicle carriers |
| DE3662730D1 (en) | 1985-01-24 | 1989-05-11 | Inst Int Pathologie Cellulaire | Immunoassay method for antibodies of different classes in a liquid sample |
| JPS61272661A (ja) | 1985-05-29 | 1986-12-02 | Hitachi Ltd | イムノアツセイ法 |
| EP0204523B1 (en) | 1985-05-31 | 1992-02-26 | Syntex (U.S.A.) Inc. | Glucose-6-phosphate dehydrogenase conjugates, their preparation and use |
| US4859610A (en) | 1985-06-05 | 1989-08-22 | Synbiotics Corporation | Immunoassay incubation device |
| US4855226A (en) | 1985-06-07 | 1989-08-08 | Beckman Instruments, Inc. | Novel competitive assay for theophylline and reagent for use therein |
| US4670381A (en) | 1985-07-19 | 1987-06-02 | Eastman Kodak Company | Heterogeneous immunoassay utilizing horizontal separation in an analytical element |
| JP2591738B2 (ja) | 1985-08-21 | 1997-03-19 | ベーリンガー マンヘイム コーポレイション | 特異的結合アッセイにおける成分の分離，混合および検出のための方法および装置 |
| US4868106A (en) | 1985-10-17 | 1989-09-19 | Konishiroku Photo Industry Co., Ltd. | Analytical element and method for determining a component in a test sample |
| JPS62119457A (ja) * | 1985-11-19 | 1987-05-30 | Sapporo Imuno Diagnostic Lab:Kk | 先天性副腎皮質過形成のマススクリ−ニング用診断薬キツト |
| US4822747A (en) | 1986-12-09 | 1989-04-18 | Miles Inc. | Polyacrylamide gel particles having hapten moieties bound thereto as immunoassay reagent |
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| US4853335A (en) | 1987-09-28 | 1989-08-01 | Olsen Duane A | Colloidal gold particle concentration immunoassay |
| AU3359493A (en) * | 1992-01-17 | 1993-08-03 | Selective Antibodies Limited | Determination of haptens |
| US5559256A (en) | 1992-07-20 | 1996-09-24 | E. R. Squibb & Sons, Inc. | Aminediol protease inhibitors |
| US5338671A (en) | 1992-10-07 | 1994-08-16 | Eastman Kodak Company | DNA amplification with thermostable DNA polymerase and polymerase inhibiting antibody |
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| US5663054A (en) | 1995-03-03 | 1997-09-02 | Abbott Laboratories | Determination of steroids by competitive immunoassay |
| US5912114A (en) * | 1997-09-12 | 1999-06-15 | Johnson & Johnson Medical, Inc. | Wound diagnosis by quantitating cortisol in wound fluids |
-
1999
- 1999-09-24 CA CA002283597A patent/CA2283597C/en not_active Expired - Lifetime
- 1999-09-30 US US09/408,931 patent/US6383766B1/en not_active Expired - Lifetime
- 1999-10-01 ES ES99307762T patent/ES2253866T3/es not_active Expired - Lifetime
- 1999-10-01 DK DK99307762T patent/DK0992512T3/da active
- 1999-10-01 AT AT99307762T patent/ATE312842T1/de active IP Right Revival
- 1999-10-01 EP EP99307762A patent/EP0992512B1/en not_active Expired - Lifetime
- 1999-10-01 DE DE69928888T patent/DE69928888T2/de not_active Expired - Lifetime
- 1999-10-04 JP JP11282460A patent/JP2000143691A/ja not_active Withdrawn
-
2011
- 2011-04-14 JP JP2011090267A patent/JP2011148821A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE69928888D1 (de) | 2006-01-19 |
| DK0992512T3 (da) | 2008-03-03 |
| JP2000143691A (ja) | 2000-05-26 |
| HK1027111A1 (en) | 2001-01-05 |
| EP0992512A2 (en) | 2000-04-12 |
| JP2011148821A (ja) | 2011-08-04 |
| CA2283597A1 (en) | 2000-04-02 |
| ES2253866T3 (es) | 2006-06-01 |
| US6383766B1 (en) | 2002-05-07 |
| EP0992512A3 (en) | 2002-04-17 |
| ATE312842T1 (de) | 2005-12-15 |
| DE69928888T2 (de) | 2006-08-24 |
| EP0992512B1 (en) | 2005-12-14 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKEX | Expiry |
Effective date: 20190924 |