JP2009519053A5 - - Google Patents
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- Publication number
- JP2009519053A5 JP2009519053A5 JP2008544536A JP2008544536A JP2009519053A5 JP 2009519053 A5 JP2009519053 A5 JP 2009519053A5 JP 2008544536 A JP2008544536 A JP 2008544536A JP 2008544536 A JP2008544536 A JP 2008544536A JP 2009519053 A5 JP2009519053 A5 JP 2009519053A5
- Authority
- JP
- Japan
- Prior art keywords
- analyte
- light
- fluorophore
- quencher
- boronic acid
- 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.)
- Pending
Links
- 239000012491 analyte Substances 0.000 claims 20
- 229920000642 polymer Polymers 0.000 claims 7
- 239000000178 monomer Substances 0.000 claims 6
- 239000000126 substance Substances 0.000 claims 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 4
- 125000005620 boronic acid group Chemical group 0.000 claims 4
- 239000011159 matrix material Substances 0.000 claims 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical group CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 3
- 239000000975 dye Substances 0.000 claims 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 claims 3
- -1 pyranine sulfonic acid derivative Chemical class 0.000 claims 3
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 2
- 239000002202 Polyethylene glycol Substances 0.000 claims 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 239000002168 alkylating agent Substances 0.000 claims 2
- 229940100198 alkylating agent Drugs 0.000 claims 2
- 235000019270 ammonium chloride Nutrition 0.000 claims 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N antipyrene Natural products C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims 2
- HBWDWGMBZIFBQE-UHFFFAOYSA-N benzylboronic acid Chemical compound OB(O)CC1=CC=CC=C1 HBWDWGMBZIFBQE-UHFFFAOYSA-N 0.000 claims 2
- 125000001246 bromo group Chemical group Br* 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 2
- 230000002596 correlated effect Effects 0.000 claims 2
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 claims 2
- 239000000017 hydrogel Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- WFKDPJRCBCBQNT-UHFFFAOYSA-N n,2-dimethylprop-2-enamide Chemical compound CNC(=O)C(C)=C WFKDPJRCBCBQNT-UHFFFAOYSA-N 0.000 claims 2
- 229920001223 polyethylene glycol Polymers 0.000 claims 2
- 150000003220 pyrenes Chemical class 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 229940096522 trimethylolpropane triacrylate Drugs 0.000 claims 2
- 229940044192 2-hydroxyethyl methacrylate Drugs 0.000 claims 1
- KFNGWPXYNSJXOP-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propane-1-sulfonic acid Chemical compound CC(=C)C(=O)OCCCS(O)(=O)=O KFNGWPXYNSJXOP-UHFFFAOYSA-N 0.000 claims 1
- MSQCQZMTRWHMFQ-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propane-1-sulfonic acid;sodium Chemical compound [Na].CC(=C)C(=O)OCCCS(O)(=O)=O MSQCQZMTRWHMFQ-UHFFFAOYSA-N 0.000 claims 1
- IHKHBKOJBAXLDY-UHFFFAOYSA-M 3-aminopropyl-dimethyl-(3-methyl-2-oxobut-3-enyl)azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)C[N+](C)(C)CCCN IHKHBKOJBAXLDY-UHFFFAOYSA-M 0.000 claims 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 102100026735 Coagulation factor VIII Human genes 0.000 claims 1
- 239000004971 Cross linker Substances 0.000 claims 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims 1
- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 claims 1
- 150000001543 aryl boronic acids Chemical class 0.000 claims 1
- 230000005540 biological transmission Effects 0.000 claims 1
- 210000004204 blood vessel Anatomy 0.000 claims 1
- 210000001124 body fluid Anatomy 0.000 claims 1
- 239000010839 body fluid Substances 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 239000000460 chlorine Chemical group 0.000 claims 1
- 229910052801 chlorine Chemical group 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 239000004020 conductor Substances 0.000 claims 1
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- 230000005284 excitation Effects 0.000 claims 1
- 239000008103 glucose Substances 0.000 claims 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- 239000012528 membrane Substances 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- KXXXUIKPSVVSAW-UHFFFAOYSA-K pyranine Chemical compound [Na+].[Na+].[Na+].C1=C2C(O)=CC(S([O-])(=O)=O)=C(C=C3)C2=C2C3=C(S([O-])(=O)=O)C=C(S([O-])(=O)=O)C2=C1 KXXXUIKPSVVSAW-UHFFFAOYSA-K 0.000 claims 1
- 239000002096 quantum dot Substances 0.000 claims 1
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 claims 1
- 229910052724 xenon Inorganic materials 0.000 claims 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/296,898 US7470420B2 (en) | 2000-12-05 | 2005-12-07 | Optical determination of glucose utilizing boronic acid adducts |
| PCT/US2006/046895 WO2007067743A2 (en) | 2005-12-07 | 2006-12-07 | Optical determination of glucose utilizing boronic acid adducts-ii |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012180379A Division JP5476638B2 (ja) | 2005-12-07 | 2012-08-16 | ボロン酸付加体‐II(BronicAcidAdducts−II)を使用したグルコースの光学的決定 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009519053A JP2009519053A (ja) | 2009-05-14 |
| JP2009519053A5 true JP2009519053A5 (https=) | 2010-01-28 |
Family
ID=38123527
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008544536A Pending JP2009519053A (ja) | 2005-12-07 | 2006-12-07 | ボロン酸付加体‐II(BronicAcidAdducts−II)を使用したグルコースの光学的決定 |
| JP2012180379A Expired - Fee Related JP5476638B2 (ja) | 2005-12-07 | 2012-08-16 | ボロン酸付加体‐II(BronicAcidAdducts−II)を使用したグルコースの光学的決定 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012180379A Expired - Fee Related JP5476638B2 (ja) | 2005-12-07 | 2012-08-16 | ボロン酸付加体‐II(BronicAcidAdducts−II)を使用したグルコースの光学的決定 |
Country Status (8)
| Country | Link |
|---|---|
| US (6) | US7470420B2 (https=) |
| EP (2) | EP1960779B1 (https=) |
| JP (2) | JP2009519053A (https=) |
| AT (1) | ATE479094T1 (https=) |
| AU (1) | AU2006321854A1 (https=) |
| CA (1) | CA2630790A1 (https=) |
| DE (1) | DE602006016478D1 (https=) |
| WO (1) | WO2007067743A2 (https=) |
Families Citing this family (103)
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| JP5159778B2 (ja) * | 2006-07-25 | 2013-03-13 | グルメトリックス,インコーポレイテッド | グルコース検知における使用のための蛍光色素 |
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| US20080044879A1 (en) * | 2006-08-17 | 2008-02-21 | The Charles Stark Draper Laboratory, Inc. | Systems and methods of voltage-gated ion channel assays |
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| US8738107B2 (en) * | 2007-05-10 | 2014-05-27 | Medtronic Minimed, Inc. | Equilibrium non-consuming fluorescence sensor for real time intravascular glucose measurement |
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