HRP20151237T1 - Pripravci reagensa s niskom ukupnom soli i sustavi za biosenzore - Google Patents
Pripravci reagensa s niskom ukupnom soli i sustavi za biosenzore Download PDFInfo
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- HRP20151237T1 HRP20151237T1 HRP20151237TT HRP20151237T HRP20151237T1 HR P20151237 T1 HRP20151237 T1 HR P20151237T1 HR P20151237T T HRP20151237T T HR P20151237TT HR P20151237 T HRP20151237 T HR P20151237T HR P20151237 T1 HRP20151237 T1 HR P20151237T1
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/001—Enzyme electrodes
- C12Q1/004—Enzyme electrodes mediator-assisted
-
- 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
- G01N33/54366—Apparatus specially adapted for solid-phase testing
- G01N33/54373—Apparatus specially adapted for solid-phase testing involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
- G01N33/5438—Electrodes
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Medicinal Chemistry (AREA)
- Biophysics (AREA)
- Pathology (AREA)
- General Physics & Mathematics (AREA)
- Food Science & Technology (AREA)
- Cell Biology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Claims (15)
1. Ispitni senzor za određivanje koncentracije analita u uzorku, koji sadrži:
spremnik koji ima zapreminu spremnika;
barem dva vodiča u spremniku, gdje je jedan od vodiča radna elektroda koja ima površinu radne elektrode; te
pripravak reagensa smješten na radnoj elektrodi, a pripravak reagensa sadrži
vezivo, pufersku sol, posrednik, enzimski sustav i ne-ionski surfaktant,
te posrednik sadrži najviše 20% (w/w) neorganske soli, ne-prijelaznog metala;
gdje je puferska sol prisutna u koncentraciji od najviše 9.54 nmol po mm2 površine područja pripravka reagensa, ili najviše 67 nmol po µL volumena spremnika, ili najviše 167 nmol po mm2 površine radne elektrode; i
posrednik je prisutan u koncentraciji od najviše 4.76 nmol po mm2 površine područja pripravka reagensa, ili najviše 40 nmol po µL volumena spremnika, ili najviše 100 nmol po mm2 površine radne elektrode.
2. Senzor prema zahtjevu 1, naznačen time da pripravak reagensa sadrži
od oko 0.14 do oko 0.43 µg veziva po mm2 površine područja pripravka reagensa,
od oko 2.30 do 9.54 nmol, poželjno od oko 3.40 do oko 4.77 nmol, puferske soli po mm2 površine područja pripravka reagensa,
od oko 1.70 do 4.76 nmol, poželjno od oko 2.80 do oko 4.00 nmol, posrednika po mm2 površine područja pripravka reagensa,
od oko 0.07 do oko 0.3 Jedinica enzimskog sustava po mm2 površine područja pripravka reagensa, i
od oko 0.04 do oko 0.24 µg ne-ionskog surfaktanta po mm2 površine područja pripravka reagensa.
3. Senzor prema zahtjevu 1, naznačen time da pripravak reagensa sadrži
od oko 1 do oko 3 µg polimernog veziva po µL volumena spremnika,
od oko 16 do 67 nmol, poželjno od oko 24 do oko 34 nmol, puferske soli po µL volumena spremnika,
od oko 12 do 40 nmol, poželjno od oko 20 do oko 28 nmol, posrednika po µL volumena spremnika,
od oko 0.5 do oko 1.8 jedinica enzimskog sustava po µL volumena spremnika, i
od oko 0.3 do oko 1.7 µg ne-ionskog surfaktanta po µL volumena spremnika.
4. Senzor prema zahtjevu 1, naznačen time da pripravak reagensa sadrži
od oko 1 do oko 7.5 µg veziva po mm2 površine radne elektrode,
od oko 16 do 167 nmol, poželjno od oko 24 do oko 84 nmol, puferske soli po mm2 površine radne elektrode,
od oko 12 do 100 nmol, poželjno od oko 20 do oko 70 nmol, posrednika po mm2 površine radne elektrode,
od oko 0.5 do oko 5 jedinica enzimskog sustava po mm2 površine radne elektrode, te
od oko 0.3 do oko 4.3 µg ne-ionskog surfaktanta po mm2 površine radne elektrode.
5. Senzor prema bilo kojem od zahtjeva 1-4, naznačen time da dodatno sadrži ionski surfaktant.
6. Senzor prema zahtjevu 5, naznačen time da ionski surfaktant sadrži anionski surfaktant.
7. Senzor prema zahtjevu 6, naznačen time da sadrži od oko 3 do oko 16 ng anionskog surfaktanta po mm2 površine područja pripravka reagensa, ili od oko 20 do oko 140 ng anionskog surfaktanta po µL volumena spremnika, ili od oko 10 do oko 350 ng anionskog surfaktanta po mm2 površine radne elektrode.
8. Senzor prema bilo kojem od zahtjeva 1-7, naznačen time da puferska sol sadrži Na2HPO4.
9. Senzor prema bilo kojem od zahtjeva 1-8, naznačen time da posrednik sadrži najviše 15% (w/w), najviše 10% (w/w), najviše 5% (w/w) ili najviše 4% (w/w) soli neorganskog, ne-prijelaznog metala.
10. Senzor prema bilo kojem od zahtjeva 1-9, naznačen time da ne-ionski surfaktant sadrži surfaktant na bazi šećera.
11. Biosenzorski sustav, za određivanje koncentracije analita u uzorku, naznačen time da sadrži:
ispitni senzor koji ima spremnik, barem dva vodiča u spremniku gdje je jedan od vodiča radna elektroda, te pripravak reagensa smješten na ili blizu radne elektrode,
pripravak reagensa sadrži vezivo, pufersku sol, enzimski sustav, ne-ionski surfaktant, i posrednik koji sadrži najviše 20% (w/w) neorganske soli, ne-prijelaznog metala; i
uređaj za mjerenje u električnoj komunikaciji s ispitnim senzorom;
gdje uređaj za mjerenje mjeri vrijednost izlaznog signala iz ispitnog senzora kod maksimalnog kinetičkog djelovanja unutar najviše 7 sekundi od uvođenja uzorka u ispitni senzor, gdje vrijednost izlaznog signala reagira na koncentraciju analita u uzorku,
uređaj za mjerenje određuje barem jednu vrijednost ΔS koja reagira na barem jedan parametar greške, te
uređaj za mjerenje nadalje određuje koncentraciju analita u uzorku iz kompenzacijske jednadžbe koja uključuje barem jednu referentnu korelaciju i barem jednu vrijednost ΔS;
gdje kompenzacijska jednadžba ima vrijednost R2 od barem 0.5.
12. Sustav prema zahtjevu 11, naznačen time da pripravak reagensa ispitnog senzora sadrži:
pufersku sol u koncentraciji od najviše 9.54 nmol po mm2 površine područja pripravka reagensa,
posrednik u koncentraciji od najviše 4.76 nmol po mm2 površine područja pripravka reagensa.
13. Sustav prema zahtjevu 11, naznačen time da spremnik ispitnog senzora ima volumen spremnika, te pripravak reagensa sadrži:
pufersku sol u koncentraciji od najviše 67 nmol po µL volumena spremnika,
posrednik u koncentraciji od najviše 40 nmol po µL volumena spremnika.
14. Sustav prema zahtjevu 11, naznačen time da radna elektroda ispitnog senzora ima površinu radne elektrode, te pripravak reagensa sadrži:
pufersku sol u koncentraciji od najviše 167 nmol po mm2 površine radne elektrode,
posrednik u koncentraciji od najviše 100 nmol po mm2 površine radne elektrode.
15. Sustav prema bilo kojem od zahtjeva 11-14, naznačen time da mjerni uređaj mjeri vrijednost izlaznog signala iz ispitnog senzora kod maksimalnog kinetičkog djelovanja unutar najviše 5 sekundi od uvođenja uzorka u ispitni senzor, ili unutar najviše 3.5 sekundi od uvođenja uzorka u ispitni senzor.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20124208P | 2008-12-08 | 2008-12-08 | |
| EP09775437.8A EP2373805B1 (en) | 2008-12-08 | 2009-12-07 | Low total salt reagent compositions and systems for biosensors |
| PCT/US2009/066963 WO2010077598A1 (en) | 2008-12-08 | 2009-12-07 | Low total salt reagent compositions and systems for biosensors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20151237T1 true HRP20151237T1 (hr) | 2015-12-18 |
Family
ID=41800700
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRP20151237TT HRP20151237T1 (hr) | 2008-12-08 | 2009-12-07 | Pripravci reagensa s niskom ukupnom soli i sustavi za biosenzore |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US8871069B2 (hr) |
| EP (1) | EP2373805B1 (hr) |
| JP (2) | JP5773883B2 (hr) |
| CN (1) | CN102227505B (hr) |
| BR (1) | BRPI0923340A2 (hr) |
| CA (1) | CA2742377C (hr) |
| DK (1) | DK2373805T3 (hr) |
| ES (1) | ES2555215T3 (hr) |
| HR (1) | HRP20151237T1 (hr) |
| MX (1) | MX2011006046A (hr) |
| PL (1) | PL2373805T3 (hr) |
| PT (1) | PT2373805E (hr) |
| RU (1) | RU2546862C2 (hr) |
| WO (1) | WO2010077598A1 (hr) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9233788B2 (en) | 2010-01-22 | 2016-01-12 | Bayer Healthcare Llc | Biosensor desiccant system having enhanced measurement performance |
| TWI565943B (zh) * | 2011-07-22 | 2017-01-11 | 拜耳保健公司 | 具有增進測量性能之生物感測器乾燥劑系統 |
| EP3388823B1 (en) * | 2013-03-15 | 2024-07-10 | Roche Diabetes Care GmbH | Method of scaling data used to construct biosensor algorithms |
| EP3117006B1 (en) * | 2014-03-13 | 2018-07-18 | PAL Finland Oy | Test strip and apparatus for measuring the content of alcohol in blood, and a method for measuring the content of alcohol in blood |
| GB2531728A (en) * | 2014-10-27 | 2016-05-04 | Cilag Gmbh Int | Method for determining diffusion |
| WO2018147862A1 (en) * | 2017-02-10 | 2018-08-16 | Hewlett-Packard Development Company, L.P. | Determine viscosity of fluids using a capillary channel |
| US20210076991A1 (en) * | 2018-01-16 | 2021-03-18 | The Regents Of The University Of California | In-situ sweat rate monitoring for normalization of sweat analyte concentrations |
| RU197895U1 (ru) * | 2020-02-05 | 2020-06-04 | Общество с ограниченной ответственностью "МедТехПродукт" | Электрохимический биосенсор для определения концентрации глюкозы в крови |
| RU209089U1 (ru) * | 2021-10-22 | 2022-02-01 | Кирилл Владимирович Романенко | Электрохимический биосенсор для определения концентрации глюкозы в крови |
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| DE10243599A1 (de) * | 2002-09-19 | 2004-04-01 | MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. | Messvorrichtung und -verfahren für ein Screening bei auf Elektroden immobilisierten Zellen |
| TR201810169T4 (tr) | 2003-06-20 | 2018-08-27 | Hoffmann La Roche | Dar, homojen belirteç şeritlerinin üretilmesi için yöntem ve belirteç. |
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| EP3543348B1 (en) | 2006-09-22 | 2020-11-18 | Ascensia Diabetes Care Holdings AG | Biosensor system having enhanced stability and hematocrit performance |
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| EP3369825B1 (en) | 2007-12-10 | 2021-07-28 | Ascensia Diabetes Care Holdings AG | Porous particle reagent compositions and devices for biosensors |
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-
2009
- 2009-12-07 JP JP2011540801A patent/JP5773883B2/ja active Active
- 2009-12-07 EP EP09775437.8A patent/EP2373805B1/en active Active
- 2009-12-07 MX MX2011006046A patent/MX2011006046A/es active IP Right Grant
- 2009-12-07 BR BRPI0923340A patent/BRPI0923340A2/pt not_active Application Discontinuation
- 2009-12-07 CA CA2742377A patent/CA2742377C/en not_active Expired - Fee Related
- 2009-12-07 HR HRP20151237TT patent/HRP20151237T1/hr unknown
- 2009-12-07 CN CN200980147993.2A patent/CN102227505B/zh active Active
- 2009-12-07 ES ES09775437.8T patent/ES2555215T3/es active Active
- 2009-12-07 RU RU2011128002/10A patent/RU2546862C2/ru not_active IP Right Cessation
- 2009-12-07 WO PCT/US2009/066963 patent/WO2010077598A1/en not_active Ceased
- 2009-12-07 PL PL09775437T patent/PL2373805T3/pl unknown
- 2009-12-07 DK DK09775437.8T patent/DK2373805T3/en active
- 2009-12-07 PT PT97754378T patent/PT2373805E/pt unknown
-
2011
- 2011-06-06 US US13/154,088 patent/US8871069B2/en active Active
-
2014
- 2014-08-01 JP JP2014157974A patent/JP6081414B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| JP2012511159A (ja) | 2012-05-17 |
| US8871069B2 (en) | 2014-10-28 |
| RU2546862C2 (ru) | 2015-04-10 |
| EP2373805B1 (en) | 2015-11-04 |
| JP2014224828A (ja) | 2014-12-04 |
| EP2373805A1 (en) | 2011-10-12 |
| CN102227505B (zh) | 2016-05-11 |
| MX2011006046A (es) | 2011-07-20 |
| RU2011128002A (ru) | 2013-01-20 |
| PL2373805T3 (pl) | 2016-03-31 |
| WO2010077598A1 (en) | 2010-07-08 |
| US20110297540A1 (en) | 2011-12-08 |
| JP5773883B2 (ja) | 2015-09-02 |
| CN102227505A (zh) | 2011-10-26 |
| PT2373805E (pt) | 2015-12-30 |
| CA2742377A1 (en) | 2010-07-08 |
| JP6081414B2 (ja) | 2017-02-15 |
| CA2742377C (en) | 2018-05-22 |
| BRPI0923340A2 (pt) | 2018-05-29 |
| DK2373805T3 (en) | 2015-12-07 |
| ES2555215T3 (es) | 2015-12-29 |
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