![]() Sensor membrane for reversible detection of analytes
专利摘要:
In a sensor membrane for reversible detection of analytes, comprising a poly mer carrier membrane, a covalent bound to the support membrane indicator dye, such as optionally a cover layer on the support membrane another one of the indi katorfarbstoff different color having dye covalently defined. 公开号:AT514611A1 申请号:T6132013 申请日:2013-07-31 公开日:2015-02-15 发明作者: 申请人:Joanneum Res Forschungsgmbh; IPC主号:
专利说明:
The present invention relates to a sensor membrane for the reversible uetex tion of analytes, comprising a polymeric support membrane, an indicator dye covalently bound to the support membrane and optionally a cover layer. Sensor membranes which have a covalently fixed indicator dye for detecting analytes on a support membrane have been known for some time and are used for a wide variety of purposes depending on the bound indicator dyes. Indicator dyes are substances that indicate changes in state in chemical systems through a color change. For example, known uses besides the conventional absorption indicators (for example pH indicators and redox indicators) are also fluorescent indicators. Particularly in the case of redox indicators and pH indicators, the measuring principle is based on a color change of the indicator dye, for example at a specific pH or a certain redox potential. At present, a variety of indicator dyes are known which either have a single color change or, such as methylene blue, also show a plurality of color changes depending on the pH. A disadvantage of these known indicators, however, is that the color change often takes place either between two poorly distinguishable colors, or that a relatively slow transition takes place from one color to another, such as Bromthymolblau, in which an envelope from yellow to green to takes place blue, so that it is not or very difficult to see, especially with the naked eye, when exactly the change between the two colors has taken place. However, especially in sensors such as oxygen sensors, CO 2 sensors, NH 3 sensors and the like, it is of the utmost importance that an accurate color change and, in particular, an accurate detection of the time when the color change takes place, be accurate to a chemical reaction or to be able to monitor precisely. To improve the distinctness of the two colors of the indicators or to increase the scope of the indicators, long ago mixed indicators were made consisting of two or more indicator dyes, which on the one hand can show a plurality of color changes and, on the other hand, the individual color changes within a narrower range pH range or range of redox potential, so that a wide range of applications has been created and a more accurate detection has been made possible. The disadvantage of all these indicators is that there is still a non-negligible range in which a color change happens and not an exact point, which can be defined as a transition point. It has also been known for a long time to provide test strips or sensor elements on which indicator dyes are physically fixed and which sensors are either immersed or introduced into the reaction medium for monitoring chemical reactions. A disadvantage of such sensor elements on which the indicator dyes are physically bound, however, is the fact that when in contact with fluids to be examined media there is a risk that the indicator dye is washed out, so that especially in a prolonged use or multiple use the risk is to lose excessively large amounts of indicator dye, so that a color change can not or only with difficulty be determined. The document M. Roses, Analytioca Chimica Acta, 204 (1988) 311 et seq. Describes a computer program which calculates chromaticity parameters from spectrophotometric data, since the visual evaluation of color changes can lead to doubtful results and is furthermore subjective. In addition, it is possible with such a program to quickly and reliably provide a comparison of the indicator color changes available. US 5,853,669 already discloses a pH indicator element in which the indicator dye is covalently bonded to a matrix. Covalent binding of the indicator dye to the matrix or sensor membrane in such indicators avoids leaching of the indicator in multiple uses, however, the problem of inaccurate or extended over a wider range color change can not be solved with such a pH sensor become. DE 1603454 A discloses a fiber material, which is dyed on the one hand with an indicator dye which is covalently fixed to the fiber material and which indicator should be moved to a color change with materials commonly used in the home, such as lemon juice. According to DE 1603454 A, such materials are to be used, for example, in the toy industry in order to make the game interesting for a long time by achieving a color change. In such an indicator provided with color material is therefore completely irrelevant whether and how far the color change takes place within a range or exactly at one point, as long as the color change is reversible. Finally, US Pat. No. 6,531,322 B1 discloses an optically evaluable blood glucose test strip in which an indicator dye or a mixture of indicator dyes is integrated on a test strip consisting of two membranes and an inert dye is incorporated in another layer in order to achieve a mixed color, of which anyhow a color shows a pH envelope, to allow a more accurate determination of the pH is fixed. A disadvantage of this patent, however, is the fact that both dyes are only physically integrated and thus can be easily washed out of the membrane, so that the reversibility or multiple use of such a sensor membrane appears only very limited possible. The present invention now aims to provide a sensor membrane which, even after a plurality of uses, exhibits consistent color changes and color intensities during the color change and, in particular, provides a sensor membrane which exhibits a precise color change, which only occurs over one extends very narrow range of values, in order to make an exact measurement possible in this way. In order to achieve this object, the sensor membrane according to the invention is essentially characterized in that a further dye having a different color from the indicator dye is covalently attached to the support membrane. By further covalently fixing a dye having a different color from the indicator dye to the support membrane, it is possible to provide a sensor membrane which is available for a plurality of measurements without either the indicator dye or the second sensor membrane Dye are washed out. Furthermore, by covalently fixing both the indicator dye and the second dye, it is possible to provide a sensor element which has a reversible optical property in order to be able to continuously monitor, for example, a reaction proceeding over a long period of time or a chemical compound. Of course, the optical property of the sensor element, to which the indicator dye and the second dye are covalently fixed, can also be formed irreversibly, with which, for example, exceeding a limit value of a component to be monitored can be reliably detected. According to one embodiment of the invention, the sensor element is substantially designed so that the further dye with the indicator dye results in a clear color contrast in a color change of the indicator dye having mixed color. The fact that the further dye with the indicator dye results in a mixed color which allows a clear color contrast in a color change of the indicator dye, it is possible to determine the envelope and thus the measured optical property of the monitored component or the substance to be monitored significantly more accurate than with an indicator dye alone. With an indicator dye alone, the turning point with the naked eye can often not be clearly recognized, since until the actual color change a slow or continuous color change takes place, which is often very poorly recognized or distinguished by the naked eye. For example, when applying a yellow-to-red indicator dye, before a definite transfer, the yellow color slowly becomes more intense and the red component in the yellow dye slowly becomes higher. For a viewer, it is often difficult to detect in such a dye whether the color change has already taken place or not, but if such a dye indicator, for example, a dye with a dark color, such as blue, is mixed, the Farbum shock from green to dark red or violet, which envelope can be perceived significantly better with the naked eye than, for example, a color change from yellow to red. According to one embodiment of the invention, in a manner known per se, the indicator dye is a pH indicator dye or a redox indicator dye or other selective indicator dye. Both pH indicator and redox indicator dyes can be used to track a variety of chemical reactions and thus for a variety of uses. With selective indicator dyes, for example, oxygen, reactive oxygen species, such as hydrogen peroxide, C02, amines, carboxylic acids, ketones, Na +, K +, Ca2 +, Mg2 +, ions, saccharides, alcohols, diols, thiols, nitrogen oxides, proteins, metabolites, organophosphorus compounds and formic acid examined or these compounds and ions are tracked. A particularly clearly visible and smooth color change can be characterized according to the invention in that the indicator dye is, for example, an indicator dye turning from yellow to red, in particular 2 - ((4- (2-hydroxyethylsulfonyl) phenyl) diazenyl) -4-methoxyphenol, 4 Fluro-2 - ((4- (2-hydroxyethylsulfonyl) phenyl) diazenyl) phenol or 4-bromo-2 - ((4- (2-hydroxyethylsulfonyl) cyclohexa-1,4-the-nyl) diazenyl) phenol , By using an indicator dye turning from, for example, yellow to red and adding an inert dye which has a darker base color, it is possible to create a clear color change, so that the optical property in the form of a color change of the indicator element can be reliably perceived and, in particular, the smallest changes are perceived can be. Particularly clearly visible and in particular only a very narrow range extending color envelopes can be achieved according to the invention characterized in that the indicator dye, for example, 1-hydroxy-4- [4- (2-hydroxyethylsulfonyl) phenylazo] naphthalene-2-sulfonic acid potassium salt (Chromo-ionophore XVII), dilithium (1+) -iono-10-amino-3- (vinylsulfonyl) -2,4-dioxo-3-azatricy-o-oo [7.3.1.0Λ {5,13}] ^ βθ3-1 ( 13), 5,7,9,11-pentaenes-7,11-disulfonates (Lucifer Yellow VS dilithium salt), 4-hydroxy-3 - ((4- (2-hydroxyethylsulfonyl) phenyl) diazenyl) benzonitrile, 4- (Trifluoroacetyl) -4 '- [N- (11-methacryloxyundecyl) -N-ethylamino] azobenzene, N-allyl-4- (N-methylpiperazinyl) -1,8-naphthalimide, or 4- [N, N-bis (11th-11th) -methacryloxyundecyl) -amino] -4 '- (trifluoroacetyl) -stilbene. By, as corresponds to a development of the invention, the further dye, for example, 2- (3- (4-amino-9,10-dihydro-3-sulfo-9,10-dioxoanthracen-4-yl) aminobenzene-sulfonyl ) vinyl) disodium sulfate, trade name Reactive Blue 19, trisodium 5-acetamido-4-hydroxy-3- (2- {2-hydroxy-5- [2- (sulfonatooxy) ethanesulfonyl] phenyl} diazen-1-yl) naphthalenes-2,7-disulfonate, trade name Remazol Brilliant Violet 5R or tetrasodium (3Z) -5-amino-4-oxo-6- [4- (2-sulfonato-oxyethylsulfonyl) -phenyl] -diazenyl-3- [[4- (2-sulfonatooxyethylsulfonyl) phenyl] -hydrazinyl-dienes] -naphthalenes-2,7-disulfonates, trade name Reactiv Black 5, it is possible to achieve color changes with a very clear contrast and thus an exact detection of, for example the pH, a certain redox potential or the like. To enable. Furthermore, it is possible with a combination of a specific indicator dye and another dye to produce test strips and sensors for a variety of measuring ranges and it can also be set as desired contrast at the transition point, as corresponds to a development of the invention. For this purpose, the sensor membrane is essentially characterized in that the further dye and the indicator dye are used in a ratio of 1:20 to 1: 1. By choosing the ratio of the further dye and the indicator dye, it is possible to adjust the color depth and thus adjust the greatest possible contrast of the two colors of the indicator dye before and after the turnover by adding another dye. In order to prevent further unintentional change in the color of the sensor membrane or of a sensor, the invention is preferably developed in such a way that the polymeric carrier membrane is formed from a colorless, transparent polymer. By forming the polymeric membrane from a colorless, transparent polymer, no additional color effect is introduced so that the desired colors before and after the turnover of the indicator dye are achieved only by the mixture of the indicator dye with the further dye. By, as corresponds to a development of the invention, as a polymeric support membrane, for example cellulose membranes, polyurethane hydrogels, poly (hydroxyethylmeth-acrylates), aminopolymers, polyacrylates, silicones, epoxies, sol-gel glasses or polyolefins are used, the parameter of the membrane and by selecting the porosity, the diffusion properties and the layer thickness of the membrane, in particular the response speed of the sensor membrane are controlled and thus a fine adjustment of the measuring range can be achieved. By, as corresponds to a development of the invention, the polymeric carrier membrane is formed multi-layered, any sensor membranes or sensor elements can be produced. Thus, a support membrane layer may constitute a rigid layer, which is provided to protect the sensitive sensor membrane and the actual sensor membrane then applied only on this sensor, or it may be arranged one above the other several layers of the support membrane, of which further dyes and the Indicator dye are arranged only in one layer. For a particularly simple production of a sensor membrane according to the invention, the sensor membrane is preferably developed such that the further dye and the indicator dye are fixed to mutually different layers of the polymeric support membrane. With such a construction of a sensor membrane, it is possible to fix both dyes, both the indicator dye and the further dye separately on a layer of the polymeric support membrane and only after fixing the dye molecules this To connect membrane layers together or first determine one of the dyes on a layer of the support membrane and deposit a second layer on this and only then fix the second indicator dye on this second layer covalently. In this way, the differences in the chemical reactivity of the various dyes can be taken into account and it is safe and reliable to provide a homogeneous and uniformly doped sensor membrane available. By, as corresponds to a development of the invention, the indicator dyes and other dyes to nano and microparticles consisting of cellulose, polyurethane hydrogel, poly (hydroxyethyl methacrylate), amino, polyacrylates, silicones, epoxies, sol-gel glasses or polyolefins covalently bonded or polymerized, any sensor membranes or sensor elements can be prepared, wherein the micro- and nanoparticles are physically or chemically coupled to the polymeric support membrane. Indicator dyes and further dyes can be covalently bound to the same or to different nano- and microparticles. In order to optimize or increase the recyclability and the lifetime of a sensor membrane according to the invention as far as possible, the invention is so developed that the polymeric support membrane is covered with a porous, transparent cover layer at least on one side having the covalently bound indicator dye. By a porous, transparent cover layer on the sensor membrane or support membrane, containing the indicator dye, is applied, on the one hand manages to prevent damage to the sensor membrane and on the other hand to ensure that, for example, in a re-dox indicator the redox potentials despite the presence a cover layer can be detected and detected safely and reliably. The invention will be explained in more detail with reference to embodiments and figures. In these show a covalent coupling to polymer membranes. Example 1 2- (3- (4-Amino-9,10-dihydro-3-sulfo-9,10-dioxoanthracen-4-yl) aminobenzenesulfonyl) vinyl) disodium sulfate in combination with 1-hydroxy-4- [4- (2-hydroxyethylsulfonyl) phenyl-azo] naphthalene-2-sulfonic acid potassium salt at a dye ratio of 1: 5, a color change from olive green to violet Example 2 and FIG. 1: Tetrasodium (3Z) -5-amino-4-oxo-6- [4- (2-sulfonato-oxyethylsulfonyl) -phenyl] diazenyl-3 - [[4- (2-sulfonatooxyethylsulfonyl) phenyl] -hydrazinylidenes] -naphthalenes-2,7-disulfonates in combination with 2 - ((4- (2-hydroxyethylsulfonyl) phenyl) diazenyl) -4-methoxyphenol at a dye ratio of 1:10 a color change from yellow-green to deep red, wherein Figure 1 shows both the indicator alone determined and the covalently bound in-dikato and the further dye fixed, and ^ Example 3: 2- (3- (4-Amino-9,10-dihydro-3-sulfo-9,10-dioxoanthracen-4-yl) aminobenzene-sulfonyl) vinyl disodium sulphate in combination with 4-fluoro-2-one ((4- (2-hydroxyethylsulfonyl) phenyl) - diazenyl) phenol at a dye ratio of 1:10 a color change from green to deep red. In all examples, the procedure was analogous, wherein the covalent coupling was carried out as follows: 100 mg of the indicator dye are thoroughly mixed with 1 g of concentrated sulfuric acid in a mortar and allowed to stand for 30 minutes in a desiccator. Thereby, the 2-hydroxyethylsulfonyl group of the indicator dye could be converted into a reactive sulfonate. This mixture is then emptied into 900 ml of water and neutralized with 1.6 ml of 32% sodium hydroxide solution. Thereafter, 25.0 g of sodium carbonate in 100 ml of water and subsequently 5.3 ml of a 32% sodium hydroxide solution are added. At the same time, a solution of 20 mg of the further dye in 100 ml of water is added. The polymer membranes are placed in this staining solution. Under the basic conditions of the dyeing solution, the dye sulfonate is converted to a chemically reactive vinyl sulfonyl derivative which covalently bonds to the reactive groups of the polymer (for example, hydroxyl groups of the cellulose or amino groups of the polyurethane). The additional dye thus binds to the reactive groups of the polymer. After 60 minutes, the dyed polymer membranes are removed from the dyebath and washed several times with water. Thereafter, the colored polymer membranes are dried in air. As Fig. 1 is an example of an indistinct color change of a pure covalent bound to a polymer membrane indicator dye compared to a significant color change in a mixture of indicator dye and further dye covalently bonded to a polymer membrane. Herein, in the upper series, the color change of the pure indicator dye is shown with a color change from orange to red and in the lower series the color change of an indicator covalently attached to the support and a further dye covalently bonded to the support, with a color change from green to red ,
权利要求:
Claims (15) [1] 1. Sensor membrane for the reversible detection of analytes, comprising a polymeric support membrane, an indicator dye covalently bonded to the support membrane and optionally a cover layer, characterized in that on the support membrane another one of the indicator dye having different color dye is covalently fixed. [2] 2. Sensor membrane according to claim 1, characterized in that the further dye with the indicator dye gives a clear color contrast in a color change in the indicator dye having mixed color. [3] 3. Sensor membrane according to claim 1 or 2, characterized in that the indicator dye in a conventional manner is a pH indicator or redox indicator dye or other selective indicator dyes. [4] 4. Sensor membrane according to one of claims 1, 2 or 3, characterized in that the indicator dye is, for example, a yellow to red umschlagender indicator dye, in particular 2 - ((4- (2-hydroxyethylsulfonyl) phenyl) diazenyl) -4-methoxyphenol, 4-fluoro-2 - ((4- (2-hydroxyethylsulfonyl) phenyl) diazenyl) phenol or 4-bromo-2 - ((4- (2-hydroxyethylsulfonyl) cyclohexa-1,4-dienyl) diazenyl) phenol. [5] 5. Sensor membrane according to one of claims 1, 2 or 3, characterized in that the indicator dye, for example, 1-hydroxy-4- [4- (2-hydroxyethylsulfonyl) phenylazo] naphthalene-2-sulfonic acid potassium salt (Chromoionophore XVII), Dilithium (1+) ion 10-amino-3- (vinylsulfonyl) -2,4-dioxo-3-azatricyclo [7.3.1.0A {5,13}] trideca-1 (13), 5,7,9,11 pentaene-7,11-disulfonate (Lucifer Yellow VS dilithium salt), 4-hydroxy-3 - ((4- (2-hydroxyethylsulfonyl) phenyl) diazenyl) benzonitrile, 4- (trifluoroacetyl) -4 '- [N- (11 -methacryloxy and-ecyl) -N-ethylamino] azobenzene, N-allyl-4- (N-methylpiperazinyl) -1,8-naphthalimide or 4- [N, N-bis (11-methacryloxyundecyl) -amino] -4'- (Trifluoroacetyl) -stilbene is selected. [6] 6. Sensor membranes according to one of claims 1 to 5, characterized in that the further dye with a plurality of indicator dyes (mixing indicators) is combined. [7] 7. Sensor membrane according to one of claims 1 to 5, characterized in that the further dye, for example, 2- (3- (4-amino-9,10-dihydro-3-sulfo-9,10-dioxoanthra-cene-4- yl) aminobenzene-suVo7Tyl) viriyi) disodium sulfate (Reactive Blue 19), trisodium 5-acetamido-4-hydroxy-3- (2- {2-hydroxy-5- [2- (sulfonatooxy) ethanesulfonyl] phenyl} diazene -1-yl) naphthalene-2,7-disulfonate (Remazol Brilliant Violet 5R) or tetrasodium (3Z) -5-amino-4-oxo-6- [4- (2-sulfo-nato-oxyethylsulfonyl) -phenyl] diazenyl 3 - [[4- (2-sulfonato-oxy-ethylsulfonyl) -phenyl] -hydrazinyl-ne] -naphthalenes-2,7-disulfonate (Reactive Black 5). [8] 8. Sensor membrane according to one of claims 1 to 7, characterized in that the further dye and the indicator dye in a ratio of 1:20 to 1: 1 are used. [9] 9. sensor membrane according to one of claims 1 to 8, characterized in that the polymeric support membrane is formed from a colorless, transparent polymer. [10] 10. Sensor membrane according to one of claims 1 to 9, characterized in that as a polymeric support membrane, for example cellulose membranes, polyurethane hydrogels, poly (hydroxyethyl methacrylates) or amino polymers, polymer acrylates, silicones, epoxies, sol-gel glasses or polyolefins are used. [11] 11. Sensor membrane according to one of the Ansprächen 1 to 10, characterized in that the polymeric support membrane is formed multi-layered. [12] 12. Sensor membrane according to claim 11, characterized in that the further dye and the indicator dye are fixed to mutually different layers of the polymeric support membrane. [13] 13. Sensor membranes according to any one of claims 1-12, characterized in that the further dye and the indicator dye to nano or microparticles consisting of cellulose, polyurethane hydrogel, poly (hydroxyethyl methacrylate), amino, polyacrylates, silicones, epoxies, sol-gel Covalently bonded glasses or polyolefins, and then embedded in a polymeric support membrane or physically or chemically coupled. [14] 14. sensor membranes according to any one of claims 1-13, characterized in that the further dye and the indicator dye on mutually different nano- or microparticles consisting of cellulose, polyurethane hydrogel, poly (hydroxyethyl methacrylate), amino, polyacrylates, silicones, epoxides, sol Gel glasses or polyolefins are covalently attached, and then embedded in a polymeric support membrane or physically or chemically coupled. [15] 15. Sensor membrane according to one of claims 1 to 14, characterized in that the polymeric support membrane is covered at least on one, the covalently bound indicator dye having, side with a porous, transparent cover layer. Vienna, 3 JULY 1, 2013 Joanneum ReseapetT " ^^ Forschungsgesellschaft mbH by: -------- Cunow Patentanwalts KG
类似技术:
公开号 | 公开日 | 专利标题 DE2851138C2|1990-07-05| DE69913103T2|2004-07-22|OPTICAL SENSOR AND FUNCTIONAL METHOD EP0175990B1|1991-06-19|Membrane for carrying reagents, method for its preparation and its use as an analytical means and in analytical methods EP2872876B1|2020-02-19|Opto-chemical sensor and its use DE2752352C3|1981-06-04|Test equipment for the detection and determination of a component in a sample EP0821233A2|1998-01-28|Volume independent diagnostic test element and method to assay analytes using it DE2717817A1|1977-11-03|ANALYTICAL ELEMENT DE2801476A1|1978-07-20|COLORIMETRIC PROCEDURE FOR DETERMINING BILIRUBIN EP3030886A1|2016-06-15|Optical sensor and measuring assembly for quantitatively detecting an analyte in a sample DE102014107837A1|2015-12-17|Optical sensor for the quantitative detection of an analyte in a sample and method for producing the sensor EP0995992A2|2000-04-26|Spreading layers, wetting agents for their preparation and their use in test strips AT514611B1|2016-08-15|Sensor membrane for reversible detection of analytes DE3823151A1|1990-01-11|METHOD FOR DETERMINING THE ION STRENGTH OR THE SPECIFIC WEIGHT OF LARGER LIQUIDS DE2944980C2|1986-10-09|Composition, apparatus and method for determining the ionic strength or specific gravity of a liquid sample DE2626367C2|1982-04-22|Analytical material for the analytical determination of a substance in a liquid sample WO2007014710A2|2007-02-08|Irreversible passive gas sensor DE3213183C2|1992-02-20| DE2948904A1|1981-06-11|Optode for metering particle concn. with preceding reaction cell - contg. reagent in membrane, allowing continuous operation EP3578991B1|2020-12-23|Test for determining phosphate concentration EP0358991B1|1994-02-23|Test device for an optical determination of cations, anions or electrically neutral ionogenic species, and test method using said device WO2010105850A2|2010-09-23|Test element for determining a body fluid and measurement method EP3214447A1|2017-09-06|Test for the determination of a base concentration DE112012001473B4|2016-08-25|A method for measuring a sample solution concentration and apparatus for measuring a sample solution concentration AT384891B|1988-01-25|MEASURING DEVICE FOR DETERMINING THE CONCENTRATION OF HALOGENIDES AND PSEUDOHALOGENIDES, AND METHOD FOR PRODUCING A SENSOR ELEMENT FOR SUCH A DEVICE EP0584721A1|1994-03-02|Analytical element for analysing a liquid specimen
同族专利:
公开号 | 公开日 AT514611B1|2016-08-15| WO2015013731A1|2015-02-05|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 EP0244929A2|1986-02-13|1987-11-11|Howmedica Inc.|Fluorescent polymeric indicator sensor| WO2003036293A1|2001-10-26|2003-05-01|Chromeon Gmbh|Method for simultaneous optical measurement of a ph-value and dissolved oxygen content| US20080286155A1|2007-05-15|2008-11-20|Polestar Technologies, Inc.|Multilayered optical sensing patch and retaining plug therefor| DE102007053664A1|2007-11-08|2009-05-14|Friedrich-Schiller-Universität Jena|Optical sensor for the detection of ions, gases and biomolecules, comprises a matrix with indicator dyes consisting of thin layer of ionic fluids, which is absorbed with the indicator dyes in inert or reactive thin carrier material|CN111443007A|2020-04-13|2020-07-24|厦门大学附属厦门眼科中心有限公司|Detection method for measuring concentration of hyaluronidase based on flow velocity of hydrogel composite membrane|GB1121938A|1965-11-24|1968-07-31|Mattel Inc|Fiber dyeing method and article| US5853669A|1991-09-30|1998-12-29|Merck Patent Gesellschaft Mit Beschrankter Haftung|Sensor membrane for indicating the PH of a sample, the fabrication and use thereof| US6162397A|1998-08-13|2000-12-19|Lifescan, Inc.|Visual blood glucose test strip| DE10054382A1|2000-10-27|2002-05-08|Attomol Gmbh Molekulare Diagno|Method and test kit for the detection of analytes in a sample|WO2019051205A1|2017-09-07|2019-03-14|Portland State University|Hydrogel sensors for detection of metal ions|
法律状态:
2020-03-15| MM01| Lapse because of not paying annual fees|Effective date: 20190731 |
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 ATA613/2013A|AT514611B1|2013-07-31|2013-07-31|Sensor membrane for reversible detection of analytes|ATA613/2013A| AT514611B1|2013-07-31|2013-07-31|Sensor membrane for reversible detection of analytes| PCT/AT2014/000144| WO2015013731A1|2013-07-31|2014-07-21|Sensor membrane for the reversible detection of analytes| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|