EP1080365A1 - Spr-sensor zur gleichzeitigen erfassung einer vielzahl von in fluider form vorliegenden proben - Google Patents
Spr-sensor zur gleichzeitigen erfassung einer vielzahl von in fluider form vorliegenden probenInfo
- Publication number
- EP1080365A1 EP1080365A1 EP99952120A EP99952120A EP1080365A1 EP 1080365 A1 EP1080365 A1 EP 1080365A1 EP 99952120 A EP99952120 A EP 99952120A EP 99952120 A EP99952120 A EP 99952120A EP 1080365 A1 EP1080365 A1 EP 1080365A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- spr sensor
- sensor according
- optical waveguide
- strip
- thin metal
- 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.)
- Withdrawn
Links
- 239000012530 fluid Substances 0.000 title claims abstract description 9
- 238000002198 surface plasmon resonance spectroscopy Methods 0.000 title abstract description 49
- 238000005259 measurement Methods 0.000 title abstract description 11
- 230000003287 optical effect Effects 0.000 claims abstract description 56
- 229910052751 metal Inorganic materials 0.000 claims abstract description 33
- 239000002184 metal Substances 0.000 claims abstract description 33
- 230000005284 excitation Effects 0.000 claims abstract description 15
- 239000013307 optical fiber Substances 0.000 claims description 14
- 238000001514 detection method Methods 0.000 claims description 13
- 238000000576 coating method Methods 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 claims description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 239000010703 silicon Substances 0.000 claims description 7
- 229910052710 silicon Inorganic materials 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 6
- 239000000969 carrier Substances 0.000 claims description 4
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 2
- 239000013078 crystal Substances 0.000 claims description 2
- 238000004382 potting Methods 0.000 claims description 2
- 230000000712 assembly Effects 0.000 claims 1
- 238000000429 assembly Methods 0.000 claims 1
- 238000005516 engineering process Methods 0.000 abstract description 9
- 239000010410 layer Substances 0.000 description 35
- 238000000034 method Methods 0.000 description 15
- 235000012431 wafers Nutrition 0.000 description 9
- 230000008569 process Effects 0.000 description 7
- 230000008878 coupling Effects 0.000 description 6
- 238000010168 coupling process Methods 0.000 description 6
- 238000005859 coupling reaction Methods 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- 210000004027 cell Anatomy 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000003491 array Methods 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CFAKWWQIUFSQFU-UHFFFAOYSA-N 2-hydroxy-3-methylcyclopent-2-en-1-one Chemical compound CC1=C(O)C(=O)CC1 CFAKWWQIUFSQFU-UHFFFAOYSA-N 0.000 description 2
- 239000012491 analyte Substances 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 230000010076 replication Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000012549 training Methods 0.000 description 2
- 239000001837 2-hydroxy-3-methylcyclopent-2-en-1-one Substances 0.000 description 1
- 201000009030 Carcinoma Diseases 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000000427 antigen Substances 0.000 description 1
- 102000036639 antigens Human genes 0.000 description 1
- 108091007433 antigens Proteins 0.000 description 1
- 238000012742 biochemical analysis Methods 0.000 description 1
- 210000002421 cell wall Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000007876 drug discovery Methods 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 238000005566 electron beam evaporation Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000002910 structure generation Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/251—Colorimeters; Construction thereof
- G01N21/253—Colorimeters; Construction thereof for batch operation, i.e. multisample apparatus
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/55—Specular reflectivity
- G01N21/552—Attenuated total reflection
- G01N21/553—Attenuated total reflection and using surface plasmons
Definitions
- the invention relates to an SPR sensor for the simultaneous detection of a large number of samples in fluid form, which enables rapid sample recognition in the context of a variety of applications.
- the proposed sensor is used for the parallel or serial detection of samples which have been placed in microtite slats.
- the background of the invention is the necessity to also provide the sensors used for the measurement in a parallel and miniaturized format, so that the measurements of a large number of samples can be carried out in a very short time and with a minimum sample volume and consumption, in order to increase the throughput characterizing substances to increase.
- a very sensitive method for characterizing interfaces is known in the literature as surface plasmon resonance spectroscopy, usually called SPR (surface plasmon resonance).
- SPR surface plasmon resonance
- the method is based on the optical excitation of surface plasmons in thin metal layers. This method is described in detail by Striebel, Ch .; Brecht, A .; Gauglitz, G. in Biosensors & Bioelectronics 9 (1994), 139-146.
- the resonance conditions for the excitation of the surface plasmons strongly depend on the optical properties of the dielectric surrounding the metal layer.
- the determination of refractive index and layer thickness of thin dielectric layers is fundamentally possible with a high degree of accuracy according to the known prior
- SPR spectroscopy is increasingly used e.g. in biochemical analysis, because with mr the direct investigation of the interaction between biomolecules is possible (e.g. antibodies / antigen reactions).
- one reaction partner ligand
- analyte is passed over the surface in solution.
- the interaction is directly detectable as an increase in layer thickness via the change in refractive index.
- Conventional SPR sensors see product description from Biacore AB, Rapsgatan 7, S-75450 Uppsala, Sweden 1996) use a prism that carries a thin metal layer.
- the sample to be measured is brought into contact with the metal or the modified metal surface, and the SPR reflection spectrum of the sample is measured by coupling light and measuring the intensity of the reflected light as a function of the angle of incidence or the wavelength.
- Newer methods and devices use fiber optic elements to build an SPR sensor.
- Commercial optical fibers with diameters between 1 ⁇ m and 2000 ⁇ m are used.
- the fibers are exposed at their ends or other defined areas, that is, the existing sheathing, consisting of waveguide sheath and buffer layer, is removed mechanically, chemically or thermally.
- the fibers are then provided with a metal layer radially or partially radially, and in the case of a fiber-optic sensor based on end reflection, the end face of the fiber is additionally mirrored.
- the radial coating is subject to very high requirements with regard to the layer thickness homogeneity, which can only be achieved technologically with great effort.
- a further disadvantage when using optical fibers is in particular the limited possibility of parallelization, since individual optical fibers must always be arranged manually in an array.
- the invention makes use of the task of planar waveguides, which are each provided with at least one SPR sensor area.
- SPR sensors according to the invention can be arranged in parallel and can simultaneously be brought into contact with a large number of samples (greater than 100).
- planar waveguides used lead the excitation light to the sensor area, which uses the measuring principle of surface plasmon resonance to characterize a solution that has been brought into contact with the sensor. Exactly one sample is brought into contact with each sensor area, so that n-different samples can be characterized with an SPR waveguide array consisting of n waveguides.
- An SPR waveguide array is to be manufactured using technologies from semiconductor production and integrated optics in order to provide a large number of sensors in parallel and to arrange them at a defined distance from one another.
- the invention further enables the SPR waveguide arrays in sample holders, e.g. B. integrate microtiter plates.
- the SPR waveguide arrays should be adaptable to existing formats of microtiter plates (96, 386, 1536, etc.) as well as to different or newly developed formats.
- Planar waveguides are receiving increasing attention in research and development in the field of integrated optics.
- a light-guiding layer is applied to a surface of a carrier material.
- the refractive index of the carrier material or a layer to be provided thereon for this purpose must be smaller than that of the waveguiding layer in order to guarantee an almost loss-free guidance of the light in the waveguide.
- Such flat waveguides are manufactured using known semiconductor technology and integrated optics, such as CVD processes, sputtering, electron beam evaporation, spin coating or various replication techniques.
- Known microtechnical processes also make it possible to produce finely structured waveguides and splitters. Waveguides with thicknesses in the range of a few micrometers to a few 100 ⁇ m and widths up to a few 1000 ⁇ m can be produced using a wide variety of structuring processes.
- the coating of defined waveguide sections with an SPR-capable layer can also be carried out in parallel in a few steps using known technologies.
- An SPR sensor according to the present invention consists of several planar strip-shaped optical waveguides, each of which has at least one two-dimensional measurement area between two end faces.
- These measuring areas are provided with an SPR-capable planar metal layer which is in direct contact with both the wave-guiding material and the sample to be characterized.
- the excitation light reaches the optical waveguide via known coupling mechanisms. There the light spreads along the waveguide and is guided to the sensor area. In the sensor area, the excitation of surface plasmons influences the light guided in the optical waveguide.
- the modified light is either decoupled from the optical waveguide directly after passing through the sensor region via the known coupling principles and passed on for further processing, or it is reflected in itself by a reflective coating on the end face in the optical waveguide and via the same coupling mechanism, through which the light enters the optical fiber reached, decoupled again and thus passed on for further processing.
- planar SPR waveguides based on the final reflection. If the coupled light emerges on the second side of the waveguide, one speaks of a waveguide sensor based on inline transmission.
- FIG. 1 shows a first possible embodiment of an emdimensional SPR sensor that can be expanded into an array
- FIG. 1 a shows a top view of the SPR sensor according to FIG
- FIG. 1b a section from FIG. 1,
- FIG. 2 shows a second embodiment of an SPR sensor which is essentially analogous to FIG. 1
- FIG. 3a shows a perspective view of an SPR sensor according to FIG. 1 or FIG. 2
- FIG. 3b shows an arrangement of several SPR sensors 3a to
- FIG. 4 shows a possibility of inserting a comb-like, sprinkled SPR sensor array consisting of planar SPR sensors according to FIGS. 1 or 2 into a microtitre plate in a sectional view
- FIG. 5 shows a possible arrangement of SPR sensors, whereby the mutual spacing of which is formed by cuvette walls
- FIG. 6a shows a possible arrangement of an SPR sensor, the individual sensor being additionally detected by cuvette walls
- FIG. 6b shows a further embodiment of an SPR sensor array according to FIG. 6a
- FIG. 6c shows a multiple arrangement a training according to Fig. 6a and Fig. 7 a further training possibility according to Fig. 6b.
- FIG. 1 shows a partial section of an SPR sensor in a first exemplary embodiment.
- a plurality of strip-shaped optical waveguides 2, which are arranged at a defined distance from one another, are provided on a planar carrier 1 in such a way that their end faces 21, 22 are flush with the sides 11, 12 of the planar carrier 1, each of the strip-shaped optical waveguides 2, in a section which is to be brought into contact with the fluid samples to be analyzed, which are not shown in FIG. 1, is provided with a thin metal layer 3 which enables the excitation of surface plasmons.
- a 4 "silicon wafer used in semiconductor technology has been assumed, in which the structures of a plurality of planar carriers 1 have first been transferred and structured. Long, narrow rectangular openings have been structured in the wafer 1.
- the geometry of a mask used for this purpose in the example is to be designed in such a way that the carcinoma structures that arise after it has been separated can be immersed in 1536-format microtiter plates (32-48 cavities). It can be seen that only a section of this is shown in Fig. 1.
- a silicon wafer with a crystal orientation (110) is selected, which makes it possible to have rectangular free spaces structure vertical edges on at least two edges structured wafers, in the example using the PE-CVD process, coated with S> 2 .
- This SiO 2 layer serves as an optical buffer between the optical fibers 2 provided and the Si substrate.
- the shaping of the optical waveguide 2 in the sense of the present invention is carried out by a customary dry etching process of the silicon oxynitride layer in such a way that parallel strips with widths between 10 ⁇ m to 2000 ⁇ m and distances between 10 ⁇ m and 5000 ⁇ m are formed. It is also possible within the scope of the invention to modify the aforementioned sequence of structure generation in such a way that all the coatings mentioned so far are initially on an unstructured Si wafer be carried out over the entire surface and then the known cam structure is produced in FIG. 1 by means of known selective structuring methods.
- the structures thus obtained are shown in plan view along a plane XX of FIG. 1.
- manufacture the optical waveguide 2 from a polymer that can be cured under the influence of UV light.
- a liquid polymer for example PMMA, polycarbonate, UV-curing adhesives or silicon-containing polymers (Cyclotene or ORMOCERE)
- the optical waveguides are structured by means of known photolithographic methods using an appropriately designed mask.
- the exposed areas are crosslinked and hardened by UV irradiation, the unexposed areas are detached again during development, so that the exposed areas remain as optical waveguides 2.
- the cross section of the optical waveguide 2 is to be made largely square, with manufacturing-related deviations being possible, and in the example according to FIG. 2 it is approximately 190 ⁇ m • 190 ⁇ m, the width b of the fingers f is approximately 550-600 ⁇ m, with the optical waveguide 2 should be arranged centrally on the fingers f.
- the optical refractive index of the material for the carrier 1 is lower than that of the polymer to be applied and that it is not absorbent, in the example according to FIG. 2 the additional previous application of an optical buffer layer 13, as shown in FIG . 1, to be dispensed with.
- the structures for the SPR sensors are advantageously produced on the wafer in such a way that the can structures oppose each other before mirroring.
- a subsequent sawing process for separating the comb structures it is necessary to passivate the optical waveguides 2 with the thin metal layers 3, which enable the excitation of surface plasmon, in order to prevent them from being damaged by splinters or the like. to preserve.
- a thick protective coating is applied.
- these recesses 14 can be produced before or after the application of the metal layer 3 mentioned.
- the application is then carried out at least to the areas of the optical waveguides 2 which are formed by the end face 22 in the area of the metal layer 3.
- the reflective coating 4 can be applied, for example, by a renewed coating process, for example sputtering an aluminum or silver layer.
- the entire surface of the wafer is provided with a protective layer prior to the separation process, which guarantees that the structures 2, 3 previously applied are not contaminated during the mirroring of the ends. After the mirror coating, this protective layer is removed.
- this protective layer is removed.
- the individual SPR sensor areas formed by the metal layers 3 are separated from one another by the comb-shaped recesses 14, so that each of the optical waveguides 2 can only be assigned to one sample, for example by immersing them in a complementarily distributed receptacle of a microtiter plate is.
- FIG. 3a shows a perspective view of an SPR sensor according to FIG. 1 or FIG. 2.
- several such strips are stacked one behind the other and, apart from the areas which are provided with the thin metal layer 3 which enables the excitation of surface plasmons, are grasped by a common holding means and are spaced apart from one another such that their spacing, e.g. corresponds to the recesses of an arbitrarily definable microtitre plate format.
- Arrays which can be adapted as desired, for example 8 • 12, as shown in FIG. 3b, can thus be produced by SPR sensors.
- Such an array is advantageously cast into a polymer after assembly in the area that does not carry the SPR-capable metal layer 3 in order to give the SPR waveguide array additional support, as is indicated schematically in FIG. 3 b by a polymer block encapsulation 6 .
- this SPR waveguide array is brought into contact with a microtitre plate which carries the samples to be characterized.
- the SPR waveguide array is introduced into the microtitre plate 7 until the SPR-capable metal regions 3 are completely wetted by a sample 8, as is shown schematically in FIG. 4.
- FIG. 5 Another possible arrangement of the SPR sensors is indicated in FIG. 5.
- the individual SPR sensors are spaced apart by cuvette walls 71, each one
- Optical fiber 9 shown which can be precisely positioned by means of an xy sliding table over the respective end faces of the optical waveguides 2.
- This optical fiber 9 couples light from a white light radiation source (not shown in more detail) into the respective optical waveguide 2, this light being guided to the excitation area of the surface plasmon and subsequently being reflected on the second, mirrored end face.
- the light is coupled out of the optical waveguide 2 via the end face and transferred into the common arm of a fiber splitter, not shown. From there it reaches, for example, a spectrometer (not shown) where it is spectrally evaluated.
- the spectrometer control and data acquisition is computer controlled via a PC.
- Another way of determining the spectrum is to measure the SPR array in transmission.
- a simple optical fiber 9 is used to couple the light into the optical waveguide 2.
- a second optical fiber is positioned at the output of the optical waveguide 2. This leads the light to a grating spectrometer.
- the mirroring of the end face of the optical waveguide 2 is dispensed with.
- the interaction length decreases, i.e. the effective sensor length by 50%. The signal is less pronounced by this factor.
- two coupling points have to be positioned, which increases the apperative and adjustment effort.
- FIGS. 6a and 6b it is provided that the means separating the detection areas of the individual thin metal layers 3 are formed by cuvette walls 15 connected to the planar carrier 1. Both of the above modes of operation are also possible here.
- An embodiment according to FIG. 6a is designed for an inline operating mode; one by Fig. 6b, by applying a mirror 4, for operation in reflection.
- FIG. 6c indicates how an SPR sensor array can be generated by a multiple arrangement, comparable to the stacking of individual cells of FIG. 6a carrying several SPR sensors, as described for FIG. 3b.
- planar carriers 1 are used, which are provided with essentially planar optical fibers, which each have at least one planar SPR-capable metal layer 3 in a sample detection area, each of which represents a sample detection area that is in contact with a sample is feasible. It is also within the scope of the invention to connect the created SPR-compatible areas with open bottoms of flow cells 16, FIG. 7, spaced apart from one another, which have a common inflow 17 and outflow 18. In such an embodiment in particular, one or more of the flow cells formed can be used as reference channels, for example for the compensation of temperature fluctuations.
- the invention speaks of at least one two-dimensional measurement area, this means that the metal layer 3 provided as the sensor area can also be subdivided into several partial areas 31, 32, 33, as indicated in FIG. 1b.
- the SPR sensor according to the invention can also be used in such a way that a single sample is first immobilized on the sensor areas 3. This immobilization serves to provide a chemically modified measuring surface with which another sample, preferably in solution, can interact.
- the immobilized sample one often speaks of ligands, the sample in solution often being referred to as a receptor or analyte.
- the interaction partners are thus, for example, ligand-receptor pairs.
- An SPR sensor according to the present invention then allows the simultaneous measurement of a large number of different samples (analytes). All of the features shown in the description, the subsequent claims and the drawing can be essential to the invention both individually and in a combination with one another. Reference list
Landscapes
- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
- Optical Measuring Cells (AREA)
Abstract
Description
Claims
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19822557 | 1998-05-20 | ||
DE19822557 | 1998-05-20 | ||
PCT/EP1999/003596 WO1999060382A1 (de) | 1998-05-20 | 1999-05-19 | Spr-sensor zur gleichzeitigen erfassung einer vielzahl von in fluider form vorliegenden proben |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1080365A1 true EP1080365A1 (de) | 2001-03-07 |
Family
ID=7868353
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP99952120A Withdrawn EP1080365A1 (de) | 1998-05-20 | 1999-05-19 | Spr-sensor zur gleichzeitigen erfassung einer vielzahl von in fluider form vorliegenden proben |
Country Status (7)
Country | Link |
---|---|
US (1) | US6373577B1 (de) |
EP (1) | EP1080365A1 (de) |
JP (1) | JP2002518663A (de) |
AU (1) | AU771043B2 (de) |
CA (1) | CA2319429A1 (de) |
DE (1) | DE19923820C2 (de) |
WO (1) | WO1999060382A1 (de) |
Families Citing this family (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002530668A (ja) * | 1998-11-20 | 2002-09-17 | グラフィニティー、ファーマスーティカル、デザイン、ゲゼルシャフト、ミット、ベシュレクテル、ハフツング | Sprセンサの並列読出しのための測定集成装置 |
US6728429B1 (en) * | 2000-02-16 | 2004-04-27 | Biotell, Inc. | Optical detection |
DE10008006C2 (de) | 2000-02-22 | 2003-10-16 | Graffinity Pharm Design Gmbh | SPR-Sensor und SPR-Sensoranordnung |
DE50112007D1 (de) | 2000-02-22 | 2007-03-22 | Santhera Pharmaceuticals Deuts | Spr-sensorsystem |
US20020127706A1 (en) | 2001-01-25 | 2002-09-12 | Fuji Photo Film Co., Ltd. | Surface plasmon resonance measuring chip and method of manufacture thereof |
WO2002103321A2 (en) * | 2001-06-14 | 2002-12-27 | Anadys Pharmaceuticals, Inc. | Methods of screening for ligands of target molecules |
GB2393246A (en) * | 2002-09-21 | 2004-03-24 | Sonoptix Ltd | Transducer sensor |
KR100480340B1 (ko) * | 2002-11-02 | 2005-03-31 | 한국전자통신연구원 | 정렬된 나노 크기의 금속 구조체들을 사용하는 국소 표면플라즈몬 센서 및 그 제조 방법 |
US7088449B1 (en) * | 2002-11-08 | 2006-08-08 | The Board Of Trustees Of The Leland Stanford Junior University | Dimension measurement approach for metal-material |
EP2368578A1 (de) | 2003-01-09 | 2011-09-28 | Macrogenics, Inc. | Identifizierung und Herstellung von Antikörpern mit abweichenden FC-Regionen und Anwendungsverfahren dafür |
JP2007525149A (ja) | 2003-01-13 | 2007-09-06 | マクロジェニクス,インコーポレーテッド | 可溶性FcγR融合タンパク質およびその使用法 |
WO2005048917A2 (en) * | 2003-06-06 | 2005-06-02 | Medimmune, Inc. | Use of epha4 and modulator or epha4 for diagnosis, treatment and prevention of cancer |
CN100520394C (zh) * | 2005-03-08 | 2009-07-29 | 中国科学院电子学研究所 | 一种单通道多参数表面等离子体谐振测试仪 |
EP1868650B1 (de) | 2005-04-15 | 2018-10-03 | MacroGenics, Inc. | Kovalente diabodies und ihre verwendung |
US9889197B2 (en) | 2005-04-15 | 2018-02-13 | Macrogenics, Inc. | Covalently-associated diabody complexes that possess charged coil domains and that are capable of enhanced binding to serum albumin |
DK2573114T3 (en) | 2005-08-10 | 2016-07-04 | Macrogenics Inc | The identification and production of antibodies with variant Fc regions, and methods of using same |
EP2027291A2 (de) | 2006-04-27 | 2009-02-25 | Pikamab, Inc. | Verfahren und zusammensetzungen für antikörpertherapie |
DK2029173T3 (en) | 2006-06-26 | 2016-11-07 | Macrogenics Inc | FC-RIIB-specific antibodies and methods of use thereof |
US20080129980A1 (en) * | 2006-11-30 | 2008-06-05 | North Carolina State University | In-line fiber optic sensor devices and methods of fabricating same |
CA2685213C (en) | 2007-05-04 | 2017-02-21 | Technophage, Investigacao E Desenvolvimento Em Biotecnologia, Sa | Engineered rabbit antibody variable domains and uses thereof |
CA2691434C (en) | 2007-06-21 | 2020-07-21 | Macrogenics, Inc. | Covalent diabodies and uses thereof |
HUE029925T2 (en) | 2008-04-02 | 2017-04-28 | Macrogenics Inc | HER2 / neu-specific antibodies and methods using them |
ES2589912T3 (es) | 2008-04-02 | 2016-11-17 | Macrogenics, Inc. | Anticuerpos específicos para el complejo BCR y procedimientos de uso de los mismos |
EP2282770B1 (de) | 2008-06-04 | 2018-03-07 | MacroGenics, Inc. | Antikörper mit veränderter bindung an fcrn und verwendungsverfahren dafür |
DE102008041825A1 (de) | 2008-09-05 | 2010-03-11 | Manroland Ag | Zerstörungsfreies Prüfverfahren des Aushärtungs- oder Trocknungsgrades von Farben und Lacken |
ES2732191T3 (es) | 2008-12-19 | 2019-11-21 | Macrogenics Inc | Diacuerpos covalentes y usos de los mismos |
NO2486141T3 (de) | 2009-10-07 | 2018-06-09 | ||
PL2635607T3 (pl) | 2010-11-05 | 2020-05-18 | Zymeworks Inc. | Projekt stabilnego przeciwciała heterodimerowego z mutacjami w domenie FC |
EP2714079B2 (de) | 2011-05-21 | 2019-08-28 | MacroGenics, Inc. | Entimmunisierte serumbindende domänen und ihre verwendung zur verlängerung der serumhalbwertzeit |
CA2849409A1 (en) | 2011-09-23 | 2013-03-28 | Technophage, Investigacao E Desenvolvimento Em Biotecnologia, Sa | Anti-tumor necrosis factor-alpha agents and uses thereof |
CN103958542A (zh) | 2011-09-23 | 2014-07-30 | 抗菌技术,生物技术研究与发展股份有限公司 | 经修饰的白蛋白结合结构域及其用于改善药代动力学的用途 |
CN109897103B (zh) | 2011-11-04 | 2024-05-17 | 酵活英属哥伦比亚有限公司 | 在Fc结构域中具有突变的稳定异源二聚的抗体设计 |
EP2847230B1 (de) | 2012-05-10 | 2020-08-12 | Zymeworks Inc. | Heteromultimerkonstrukte aus schweren immunoglobulinketten mit mutationen in der fc-domäne |
MX2015006758A (es) | 2012-11-28 | 2016-06-10 | Zymeworks Inc | Pares de cadena pesada-cadena ligera de inmunoglobulina modificados geneticamente y usos de estos. |
US11306156B2 (en) | 2014-05-28 | 2022-04-19 | Zymeworks Inc. | Modified antigen binding polypeptide constructs and uses thereof |
CN107787332B (zh) | 2015-04-24 | 2022-09-09 | 豪夫迈·罗氏有限公司 | 多特异性抗原结合蛋白 |
RU2018116846A (ru) | 2015-10-08 | 2019-11-08 | Займворкс Инк. | Антигенсвязывающие полипептидные конструкции, содержащие легкие цепи каппа и лямбда, и их применения |
KR102611853B1 (ko) | 2017-06-30 | 2023-12-08 | 자임워크스 비씨 인코포레이티드 | 안정화된 키메라 fabs |
SG11202100979QA (en) | 2018-08-17 | 2021-03-30 | Univ Rochester | Optical biosensor comprising disposable diagnostic membrane and permanent photonic sensing device |
CN114813654B (zh) * | 2022-04-18 | 2024-07-02 | 北京英柏生物科技有限公司 | 自黏贴片式spr传感芯片 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL8700851A (nl) * | 1987-04-10 | 1988-11-01 | Tno | Werkwijze en inrichting voor het detecteren van zeer lage concentraties van een in een meetmedium aanwezige chemische component onder toepassing van oppervlakte-plasmonresonantie en elektrochemisch gestimuleerde adsorptie. |
GB8811919D0 (en) * | 1988-05-20 | 1988-06-22 | Amersham Int Plc | Biological sensors |
SE462408B (sv) * | 1988-11-10 | 1990-06-18 | Pharmacia Ab | Optiskt biosensorsystem utnyttjande ytplasmonresonans foer detektering av en specific biomolekyl, saett att kalibrera sensoranordningen samt saett att korrigera foer baslinjedrift i systemet |
US5359681A (en) * | 1993-01-11 | 1994-10-25 | University Of Washington | Fiber optic sensor and methods and apparatus relating thereto |
FI96800C (fi) | 1994-02-16 | 1996-08-26 | Valtion Teknillinen | Laite analyysin suorittamiseksi |
JP3256647B2 (ja) * | 1995-07-19 | 2002-02-12 | オルガノ株式会社 | 被処理水中の過酸化水素の除去方法及び水処理装置 |
AT403745B (de) | 1996-02-29 | 1998-05-25 | Avl Verbrennungskraft Messtech | Messanordnung mit einem für anregungs- und messstrahlung transparentem trägerelement |
JP3926409B2 (ja) | 1996-04-30 | 2007-06-06 | 富士フイルム株式会社 | 表面プラズモンセンサー |
US5917607A (en) * | 1996-04-25 | 1999-06-29 | Fuji Photo Film Co., Ltd. | Surface plasmon sensor for multiple channel analysis |
DE69830529T2 (de) * | 1997-02-07 | 2006-05-11 | Fuji Photo Film Co., Ltd., Minami-Ashigara | Oberflächen-Plasmonen-Sensor |
DE19806681B4 (de) * | 1998-02-18 | 2006-07-27 | Carl Zeiss Jena Gmbh | Mikrotiterplatte |
US6111652A (en) * | 1998-07-14 | 2000-08-29 | Texas Instruments Incorporated | High throughput surface plasmon resonance analysis system |
-
1999
- 1999-05-19 EP EP99952120A patent/EP1080365A1/de not_active Withdrawn
- 1999-05-19 DE DE19923820A patent/DE19923820C2/de not_active Expired - Fee Related
- 1999-05-19 US US09/600,670 patent/US6373577B1/en not_active Expired - Fee Related
- 1999-05-19 JP JP2000549943A patent/JP2002518663A/ja active Pending
- 1999-05-19 CA CA002319429A patent/CA2319429A1/en not_active Abandoned
- 1999-05-19 WO PCT/EP1999/003596 patent/WO1999060382A1/de not_active Application Discontinuation
- 1999-05-19 AU AU42664/99A patent/AU771043B2/en not_active Ceased
Non-Patent Citations (1)
Title |
---|
See references of WO9960382A1 * |
Also Published As
Publication number | Publication date |
---|---|
WO1999060382A1 (de) | 1999-11-25 |
DE19923820C2 (de) | 2001-05-10 |
US6373577B1 (en) | 2002-04-16 |
CA2319429A1 (en) | 1999-11-25 |
AU771043B2 (en) | 2004-03-11 |
AU4266499A (en) | 1999-12-06 |
DE19923820A1 (de) | 2000-01-20 |
JP2002518663A (ja) | 2002-06-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE19923820C2 (de) | SPR-Sensor zur gleichzeitigen Erfassung einer Vielzahl von in fluider Form vorliegenden Proben | |
EP1257809B1 (de) | Spr-sensor und spr-sensoranordnung | |
DE69902023T2 (de) | Nachweis einer substanz durch brechzahländerung | |
DE19725050C2 (de) | Anordnung zur Detektion biochemischer oder chemischer Substanzen mittels Fluoreszenzlichtanregung und Verfahren zu deren Herstellung | |
DE69405087T2 (de) | Optischer Detektor | |
DE19955556B4 (de) | Meßanordnung zum parallelen Auslesen von SPR-Sensoren | |
DE69119750T2 (de) | Messzelle für chemische oder biochemische proben | |
EP1068511B1 (de) | Anordnung für die oberflächenplasmonen-resonanz-spektroskopie | |
EP0938660B1 (de) | Mikromechanische transmissionsmesszelle | |
DE68929019T2 (de) | Optische schnittstelle | |
WO2001069256A2 (de) | Sensorelement zur optischen detektion von chemischen oder biochemischen analyten | |
EP1000342A1 (de) | Optische detektoreinrichtung | |
WO2001063256A1 (de) | Spr-sensorsystem | |
EP1805502B1 (de) | Verfahren zur untersuchung biochemischer wechselwirkungen | |
DE19647644C2 (de) | Mikromechanische Transmissionsmeßzelle | |
DE10324973B4 (de) | Anordnung und Verfahren zur optischen Detektion von in Proben enthaltenen chemischen, biochemischen Molekülen und/oder Partikeln | |
EP2718691B1 (de) | Verfahren und vorrichtung zum bestimmen der konzentration eines in einer flüssigen probe enthaltenen analyten | |
DE102004015906B4 (de) | Mikrofluidische Vorrichtung für die optische Analyse | |
DE4228534C2 (de) | Verfahren zur Analyse einer Fremdsubstanz | |
DE10052165A1 (de) | SPR-Sensorsystem | |
WO2004025282A1 (de) | Anordnung zur bestimmung von schichtdickenänderungen | |
AT5152U1 (de) | Spr-sensorsystem | |
DE19817470A1 (de) | Transducer-Anordnung für einen optischen Sensor basierend auf der Oberflächenplasmonenresonanz |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20000707 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: FRAUNHOFER-GESELLSCHAFT ZUR FOERDERUNG DERANGEWAND Owner name: GRAFFINITY PHARMACEUTICALS AKTIENGESELLSCHAFT |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: WALDHAEUSL, RALF Inventor name: VETTER, DIRK Inventor name: SCHMIDT, KRISTINA Inventor name: DANZ, NORBERT Inventor name: BRAEUER, ANDREAS |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: FRAUNHOFER-GESELLSCHAFT ZUR FOERDERUNG DERANGEWAND Owner name: GRAFFINITY PHARMACEUTICALS AKTIENGESELLSCHAFT |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: FRAUNHOFER-GESELLSCHAFT ZUR FOERDERUNG DER ANGEWAN Owner name: GRAFFINITY PHARMACEUTICALS AKTIENGESELLSCHAFT |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 20071201 |