EP0820348B1 - Analysis card - Google Patents
Analysis card Download PDFInfo
- Publication number
- EP0820348B1 EP0820348B1 EP97901736A EP97901736A EP0820348B1 EP 0820348 B1 EP0820348 B1 EP 0820348B1 EP 97901736 A EP97901736 A EP 97901736A EP 97901736 A EP97901736 A EP 97901736A EP 0820348 B1 EP0820348 B1 EP 0820348B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- chambers
- partition
- card
- card according
- cavities
- 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
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
- Y10T436/2575—Volumetric liquid transfer
Definitions
- the present invention relates to the treatment of a analysis card.
- analysis is meant any process or process allowing to identify, separate, isolate, determine, detect, or quantify, a material, a product, a substance, or compound, referred to as generic "analyte", from a sample or sample to be analyzed, previously diluted or not with any suitable medium, for example a solvent.
- the analyte sought may be chemical, biochemical, or still biological, for example in the latter case a antigen or antibody.
- analysis card any device, module, or system, internally arranged for carry out the different processes or reactions necessary for the identification, separation, detection or quantification of the analyte, different treatments, in particular within said card, or manipulation of the analysis card, for example automatically.
- Such an analysis card well known to those skilled in the art, constitutes a closed assembly vis-à-vis the outside or its immediate environment, with the exception of course of all passages or means equivalent, allowing in particular and initially introduce the sample or sample to be analyzed.
- a such analysis card contains the reagent (s), physico-chemical, chemical, biochemical, or organic, distributed and maintained in the card, according to the flow of the sample to be analyzed, and the reaction processes or reactions to perform for complete the analysis.
- An analysis card such that envisaged by the present invention, constituting in general a disposable device or assembly, i.e. thrown away or destroyed after use, understands or incorporates within it a plurality of chambers, arranged in series and / or in parallel, one of which, for example the last, is notably an optical measurement chamber.
- These analysis cards can be produced or produced according to all appropriate techniques, for example in one or several parts assembled (for example welding) together to others, made for example by molding one or several identical or different plastics.
- room is meant in the claims and the description of any enclosure, or passage, ensuring reception and / or circulation of any liquid, fluid, or gas present in the analysis card.
- the present invention relates to a card particular analysis, allowing a setting operation in communication of at least two rooms, arranged in an analysis card, and initially isolated one by compared to the other, this operation being carried out at distance and no action or mechanical contact with the card analysis.
- the present invention lies in cooperation of two essential means, namely, on the one hand a light beam, in particular coherent, having at least one predetermined wavelength ⁇ , and a power predetermined P, obtained from a light source, in particular laser, and on the other hand of a structure or arrangement of an analysis card, in which are provided at least two isolated rooms, one with respect to to the other, and to the outside; but this structure is specifically adapted to the implementation of this light beam, to establish at least one passage between at least two chambers of said card.
- the two rooms are separated from each other by a partition, perforable, arranged within the card, in absorbent material, in particular plastic, absorbing light energy from the light beam above, to transform it into thermal energy likely to eliminate at least locally said material ; and two cavities are formed on the side and on the other side of the bulkhead, and are in communication with or included in the two rooms respectively; and an window in transparent material at least for the wavelength ⁇ is arranged opposite said partition, and delimits with the latter one of said cavities, called the incidence of a light ray.
- the light beam used according to the invention can be convergent, parallel, or divergent, the essential condition being the density of power of the light beam striking the partition penetrable.
- suitable guiding means can be provided before and / or after the beam, to satisfy the essential condition mentioned above.
- the method of using the card according to the present invention allows therefore its manipulation, in particular by automatic track, driving, in relation to the beam luminous, in particular laser, at the perforation of any partition, arranged within said card, and this in preserving the rest or the integrity of the latter.
- a such a process therefore appears particularly suitable for analysis devices today, working for a large part, if not all, automatically.
- the analysis card 1 shown is intended for cooperate with or adapted to a laser light source 4, emitting a coherent light or light beam 5, having a predetermined wavelength ⁇ , and a power predetermined light P.
- the analysis card 1 has a general shape substantially flattened, and includes, so assembled, for example by gluing, a flat body 14, by example polystyrene or polycarbonate wafer, previously engraved or imprinted, as described below, between two external walls, or films 15 and 16, for example in transparent plastic vis-à-vis the beam luminous.
- films 15 and 16 can be in polypropylene, silicon or germanium.
- two chambers 2 and 3 are obtained and included in the analysis card 1, in being, on the one hand isolated each with respect to outside the map, and on the other hand isolated at the start one over the other.
- the two rooms 2 and 3 are separated from each other by a partition 7 that can be pierced by laser light from source 4, absorbent material, in particular plastic material, absorbing light energy of wavelength ⁇ from the laser source, to transform it into thermal energy or calorific likely to eliminate or make disappear at least locally or occasionally the material of the partition 7.
- Two cavities 8 and 9 are provided on either side and on the other side of the partition 7, and are respectively in communication with the two rooms 2 and 3.
- the incidence of the radius bright 12 illuminating the partition 7 is at the same time substantially perpendicular to the plane of the map 1 analysis, and corresponds to the reference direction 6 of the light beam 5 emitted by the source 4.
- the axis of the light ray 12 illuminating the partition 7 crosses the latter substantially at its center, in providing a border on either side of the hole perforating 7a, unaffected by the light energy of the laser ray.
- the light ray 12 illuminating the partition 7 is converging at a point focal 13 arranged in the center or within the partition 7.
- the light ray 12 can also be, or parallel, or divergent, for the purposes of the illumination of partition 7, according to the distribution of light energy, desired in the impact zone of the light ray 12.
- the embodiment shown in Figures 3 to 5 differs from that shown in Figures 1 to 2, by the fact that the analysis card 1 includes "n", in the occurrence 3 chambers 2, 3, 17, arranged in series, but can also be arranged in parallel, separated two to two by "n-1", in this case two partitions perforables 7 and 18, "n” being an integer, and one bedrooms 2, 3 and 17, which can in particular be a bedroom optical measurement. So as to allow a process automatic with a single laser light beam, the perforable partitions 7 and 18 are distributed in the card 1, so that two partitions cannot be aligned with a single light beam incident 12. As previously indicated, the card of analysis of Figures 3 to 5 contains a liquid filling chamber 3, which will travel towards the chamber 2, after perforation of the partition 7, as shown in Figure 4, then to room 17, after perforation of the partition 18, as partially shown in Figure 5.
- the generator 20 emits a light at 800 nm, with guide light at 670 nm.
- the power of the light source thus constituted is 700 mW, for a power actually used of the order 300 mW.
- the optical fiber 21 used is a fiber multimode with a core diameter of 200 ⁇ m.
- a lens 30 makes it possible to focus the light energy on the center 13, located on or in each partition 7 or 18.
- the present invention can be implemented according to different modes of execution; especially one rooms, connected according to this invention, can itself communicate with the atmosphere or the environment in which the analysis card is located.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Clinical Laboratory Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Sampling And Sample Adjustment (AREA)
- Optical Measuring Cells (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
- Multi-Process Working Machines And Systems (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Investigating Or Analyzing Materials Using Thermal Means (AREA)
- Credit Cards Or The Like (AREA)
Abstract
Description
La présente invention concerne le traitement d'une carte d'analyse.The present invention relates to the treatment of a analysis card.
Par "analyse", on entend tout procédé ou processus permettant d'identifier, séparer, isoler, déterminer, détecter, ou quantifier, une matière, un produit, une substance, ou un composé, désigné sous l'expression générique d'"analyte", à partir d'un échantillon ou prélèvement à analyser, préalablement dilué ou non avec tout milieu approprié, par exemple un solvant. L'analyte recherché peut être de nature chimique, biochimique, ou encore biologique, par exemple dans ce dernier cas un antigène ou un anticorps.By "analysis" is meant any process or process allowing to identify, separate, isolate, determine, detect, or quantify, a material, a product, a substance, or compound, referred to as generic "analyte", from a sample or sample to be analyzed, previously diluted or not with any suitable medium, for example a solvent. The analyte sought may be chemical, biochemical, or still biological, for example in the latter case a antigen or antibody.
Par "carte d'analyse", on entend tout dispositif, module, ou système, agencé de manière interne pour effectuer les différents processus ou réactions nécessaires à l'identification, la séparation, la détection ou la quantification de l'analyte, moyennant différents traitements, en particulier au sein de ladite carte, ou manipulations de la carte d'analyse, par exemple par voie automatique. Une telle carte d'analyse, bien connue de l'homme de métier, constitue un ensemble fermé vis-à-vis de l'extérieur ou de son environnement immédiat, à l'exception bien entendu de tous passages ou moyens équivalents, permettant notamment et initialement d'introduire l'échantillon ou prélèvement à analyser. Une telle carte d'analyse contient le ou les réactifs, physico-chimiques, chimiques, biochimiques, ou biologiques, distribués et maintenus dans la carte, selon le cheminement de l'échantillon à analyser, et les processus réactionnels ou réactions à effectuer pour accomplir l'analyse. Une carte d'analyse telle qu'envisagée par la présente invention, constituant en général un dispositif ou ensemble à usage unique, c'est-à-dire jeté ou détruit après son emploi, comprend ou intègre en son sein une pluralité de chambres, disposées en série et/ou en parallèle, dont l'une, par exemple la dernière, est notamment une chambre de mesure optique. Ces cartes d'analyse peuvent être réalisées ou produites selon toutes techniques appropriées, par exemple en une ou plusieurs pièces assemblées (par exemple soudage) les unes aux autres, réalisées par exemple par moulage d'une ou plusieurs matières plastiques identiques ou différentes.By "analysis card" is meant any device, module, or system, internally arranged for carry out the different processes or reactions necessary for the identification, separation, detection or quantification of the analyte, different treatments, in particular within said card, or manipulation of the analysis card, for example automatically. Such an analysis card, well known to those skilled in the art, constitutes a closed assembly vis-à-vis the outside or its immediate environment, with the exception of course of all passages or means equivalent, allowing in particular and initially introduce the sample or sample to be analyzed. A such analysis card contains the reagent (s), physico-chemical, chemical, biochemical, or organic, distributed and maintained in the card, according to the flow of the sample to be analyzed, and the reaction processes or reactions to perform for complete the analysis. An analysis card such that envisaged by the present invention, constituting in general a disposable device or assembly, i.e. thrown away or destroyed after use, understands or incorporates within it a plurality of chambers, arranged in series and / or in parallel, one of which, for example the last, is notably an optical measurement chamber. These analysis cards can be produced or produced according to all appropriate techniques, for example in one or several parts assembled (for example welding) together to others, made for example by molding one or several identical or different plastics.
Par "chambre", on désigne dans les revendications et la description toute enceinte, ou passage, assurant la réception et/ou la circulation de tout liquide, fluide, ou gaz présent dans la carte d'analyse.By "room" is meant in the claims and the description of any enclosure, or passage, ensuring reception and / or circulation of any liquid, fluid, or gas present in the analysis card.
La présente invention a pour objet une carte d'analyse particulière, permettant une opération de mise en communication d'au moins deux chambres, ménagées dans une carte d'analyse, et au départ isolées l'une par rapport à l'autre, cette opération étant effectuée à distance et sans action ou contact mécanique avec la carte d'analyse.The present invention relates to a card particular analysis, allowing a setting operation in communication of at least two rooms, arranged in an analysis card, and initially isolated one by compared to the other, this operation being carried out at distance and no action or mechanical contact with the card analysis.
La présente invention réside dans la coopération de deux moyens essentiels, à savoir, d'une part d'un faisceau lumineux, notamment cohérent, ayant au moins une longueur d'onde prédéterminée λ, et une puissance prédéterminée P, obtenu à partir d'une source lumineuse, notamment laser, et d'autre part d'une structure ou agencement d'une carte d'analyse, dans laquelle sont ménagées au moins deux chambres isolées l'une par rapport à l'autre, et par rapport à l'extérieur ; mais cette structure est spécifiquement adaptée à la mise en oeuvre de ce faisceau lumineux, pour établir au moins un passage entre deux chambres au moins de ladite carte.The present invention lies in cooperation of two essential means, namely, on the one hand a light beam, in particular coherent, having at least one predetermined wavelength λ, and a power predetermined P, obtained from a light source, in particular laser, and on the other hand of a structure or arrangement of an analysis card, in which are provided at least two isolated rooms, one with respect to to the other, and to the outside; but this structure is specifically adapted to the implementation of this light beam, to establish at least one passage between at least two chambers of said card.
Plus précisément, selon la présente invention, les deux chambres sont séparées l'une de l'autre par une cloison, perforable, disposée au sein de la carte, en matériau absorbant, notamment en matière plastique, absorbant l'énergie lumineuse du faisceau lumineux précité, pour la transformer en une énergie thermique susceptible d'éliminer au moins localement ledit matériau ; et deux cavités sont ménagées de part et d'autre de la cloison, et sont en communication avec ou comprises dans respectivement les deux chambres ; et une fenêtre en un matériau transparent au moins pour la longueur d'onde λ est disposée en vis-à-vis de ladite cloison, et délimite avec cette dernière l'une desdites cavités, dite d'incidence d'un rayon lumineux.More specifically, according to the present invention, the two rooms are separated from each other by a partition, perforable, arranged within the card, in absorbent material, in particular plastic, absorbing light energy from the light beam above, to transform it into thermal energy likely to eliminate at least locally said material ; and two cavities are formed on the side and on the other side of the bulkhead, and are in communication with or included in the two rooms respectively; and an window in transparent material at least for the wavelength λ is arranged opposite said partition, and delimits with the latter one of said cavities, called the incidence of a light ray.
Une carte d'analyse conforme à la présente
invention permet de mettre en oeuvre le procédé suivant,
et plus particulièrement les étapes suivantes, coopérant
les unes avec les autres :
Il est bien entendu que le faisceau lumineux utilisé selon l'invention peut être convergent, parallèle, ou divergent, la condition essentielle étant la densité de puissance du rayon lumineux frappant la cloison perforable. Quand le faisceau lumineux est parallèle ou divergent, des moyens de guidage appropriés peuvent être prévus avant et/ou après le faisceau, pour satisfaire la condition essentielle précitée. It is understood that the light beam used according to the invention can be convergent, parallel, or divergent, the essential condition being the density of power of the light beam striking the partition penetrable. When the light beam is parallel or diverging, suitable guiding means can be provided before and / or after the beam, to satisfy the essential condition mentioned above.
Comme décrit dans le document US-A-5 411 065, on a déjà proposé d'utiliser un faisceau lumineux laser pour perforer à distance une paroi. Cependant, jusqu'à présent, faute d'un agencement particulier conforme à la présente invention, il n'avait pas été possible d'utiliser le même moyen pour établir une communication contrôlée entre deux chambres au sein d'une même carte d'analyse.As described in document US-A-5 411 065, we have already proposed to use a laser light beam for perforate a wall from a distance. However, so far, in the absence of a particular arrangement in accordance with this invention it had not been possible to use the same means for establishing controlled communication between two rooms within the same analysis card.
Le procédé d'utilisation de la carte conforme à la présente invention permet donc sa manipulation, notamment par voie automatique, conduisant, en relation avec le faisceau lumineux, notamment laser, à la perforation de toute cloison, disposée au sein de ladite carte, et ceci en préservant le reste ou l'intégrité de cette dernière. Un tel procédé apparaít donc particulièrement adapté aux appareils d'analyse d'aujourd'hui, travaillant pour une large part, sinon en totalité, de manière automatique.The method of using the card according to the present invention allows therefore its manipulation, in particular by automatic track, driving, in relation to the beam luminous, in particular laser, at the perforation of any partition, arranged within said card, and this in preserving the rest or the integrity of the latter. A such a process therefore appears particularly suitable for analysis devices today, working for a large part, if not all, automatically.
La présente invention est maintenant décrite par référence au dessin annexé, dans lequel :
- la Figure 1 représente, de manière schématique, une étape du procédé de traitement d'une carte d'analyse, selon l'invention ;
- la Figure 2 représente cette même carte d'analyse, telle qu'obtenue après l'étape ou opération représentée schématiquement à la Figure 1 ;
- les Figures 3 à 5 représentent respectivement, toujours de manière schématique, trois étapes successives d'un procédé de traitement selon l'invention, mises en oeuvre avec une carte d'analyse réalisée selon un autre mode d'exécution de l'invention ;
- la Figure 6 représente, de manière schématique, un dispositif de traitement d'une carte d'analyse, selon l'invention.
- Figure 1 shows, schematically, a step in the method of processing an analysis card according to the invention;
- Figure 2 shows this same analysis card, as obtained after the step or operation shown schematically in Figure 1;
- Figures 3 to 5 show respectively, still schematically, three successive stages of a treatment method according to the invention, implemented with an analysis card produced according to another embodiment of the invention;
- Figure 6 shows, schematically, a device for processing an analysis card according to the invention.
Conformément aux représentations des Figures 1
et 2, la carte d'analyse 1 représentée est destinée à
coopérer avec ou adaptée à une source 4 lumineuse laser,
émettant une lumière ou faisceau lumineux 5 cohérent,
ayant une longueur d'onde prédéterminée λ, et une puissance
lumineuse prédéterminée P .In accordance with the representations of Figures 1
and 2, the analysis card 1 shown is intended for
cooperate with or adapted to a laser light source 4,
emitting a coherent light or
La carte d'analyse 1 a une forme générale
substantiellement aplatie, et comprend, de manière
assemblée, par exemple par collage, un corps plat 14, par
exemple galette en polystyrène ou polycarbonate,
préalablement gravé ou empreint, comme décrit ci-après,
entre deux parois externes, ou films 15 et 16, par exemple
en matière plastique transparente vis-à-vis du faisceau
lumineux. Notamment les films 15 et 16 peuvent être en
polypropylène, silicium ou germanium.The analysis card 1 has a general shape
substantially flattened, and includes, so
assembled, for example by gluing, a
Comme décrit ci-après, deux chambres 2 et 3 sont
obtenues et comprises au sein de la carte d'analyse 1, en
étant, d'une part isolées chacune par rapport à
l'extérieur de la carte, et d'autre part isolées au départ
l'une par rapport l'autre. A cette fin, les deux
chambres 2 et 3 sont séparées l'une de l'autre par une
cloison 7 perforable par la lumière laser de la source 4,
en matériau absorbant, notamment en matière plastique,
absorbant l'énergie lumineuse de longueur d'onde λ de la
source laser, pour la transformer en une énergie thermique
ou calorifique susceptible d'éliminer ou faire disparaítre
au moins localement ou ponctuellement le matériau de la
cloison 7. Deux cavités 8 et 9 sont ménagées de part et
d'autre de la cloison 7, et sont respectivement en
communication avec les deux chambres 2 et 3. Deux
fenêtres 10 et 11, obtenues en un matériau transparent
pour la longueur d'onde λ de la lumière laser de la
source 4, sont disposées de part et d'autre et en
vis-à-vis de la cloison 7, et délimitent avec cette
dernière les deux cavités 8 et 9, l'une 8 servant à
l'incidence d'un rayon lumineux identique ou issu du
faisceau lumineux 5 provenant de la source 4, et l'autre
servant à l'émergence du rayon lumineux, après perforation
de la cloison 7. As described below, two
En pratique, compte tenu du mode de construction retenu pour la carte d'analyse 1, les dispositions précédemment décrites sont obtenues de la manière suivante :
- dans le
corps 14, sont empreintes ou gravées les deuxchambres 2 et 3, ainsi que les deuxcavités 8 et 9 ; et les parois externes 15 et 16 ferment ces chambres et cavités vis-à-vis de l'extérieur ; - comme représenté aux figures 1 et 2, et dans la position
horizontale de la carte d'analyse, la
chambre 2 est située au-dessous de lacavité 8, et lachambre 3 est située au-dessus de lacavité 9 ; l'une 2 des chambres et lacavité 8 qui lui correspond sont fermées par l'une 15 des parois externes, et l'autrechambre 3 et l'autrecavité 9 qui lui correspond, sont fermées par l'autre paroi externe 16 ; - la cloison perforable 7 est formée dans le corps plat 14, et donc dans son matériau constitutif qui est absorbant de l'énergie lumineuse de longueur d'onde λ ;
- les deux
fenêtres 10 et 11 sont formées dans les parois externes 15 et 16 respectivement, dont le matériau constitutif est, comme dit précédemment, transparent pour la longueur d'onde λ.
- in the
body 14, the two 2 and 3 are imprinted or engraved, as well as the twochambers 8 and 9; and thecavities 15 and 16 close these chambers and cavities with respect to the outside;external walls - as shown in Figures 1 and 2, and in the horizontal position of the analysis card, the
chamber 2 is located below thecavity 8, and thechamber 3 is located above thecavity 9; one 2 of the chambers and thecavity 8 which corresponds to it are closed by one of the external walls, and theother chamber 3 and theother cavity 9 which corresponds to it, are closed by the otherexternal wall 16; - the perforable partition 7 is formed in the
flat body 14, and therefore in its constituent material which is absorbing light energy of wavelength λ; - the two
10 and 11 are formed in thewindows 15 and 16 respectively, the constituent material of which is, as said above, transparent for the wavelength λ.external walls
Le
procédé de traitement avec la carte d'analyse selon l'invention comporte les
étapes suivantes :
Comme montré à la Figure 1, l'incidence du rayon
lumineux 12 illuminant la cloison 7 est en même temps
sensiblement perpendiculaire au plan de la carte 1
d'analyse, et correspond à la direction de référence 6 du
faisceau lumineux 5 émis par la source 4.As shown in Figure 1, the incidence of the radius
bright 12 illuminating the partition 7 is at the same time
substantially perpendicular to the plane of the map 1
analysis, and corresponds to the reference direction 6 of the
L'axe du rayon lumineux 12 illuminant la cloison 7
traverse cette dernière sensiblement en son centre, en
ménageant une bordure de part et d'autre du trou
perforant 7a, non affectée par l'énergie lumineuse du
rayon laser.The axis of the
Préférentiellement, le rayon lumineux 12
illuminant la cloison 7 est convergent selon un point
focal 13 disposé au centre ou au sein de la cloison 7.
Mais le rayon lumineux 12 peut être aussi, ou parallèle,
ou divergent, aux fins de l'illumination de la cloison 7,
selon la répartition de l'énergie lumineuse, désirée dans
la zone d'impact du rayon lumineux 12.Preferably, the
Lorsque la chambre 3 au moins est remplie avec un
liquide, préférentiellement pendant les étapes (c) et (d),
on contrôle le déplacement du liquide présent dans la
chambre 3, par exemple par capillarité et/ou aspiration,
en sorte que la cavité 9, de l'autre côté de la cavité 8
d'incidence par rapport à la cloison perforable 7, demeure
pleine ou vide de tout liquide. Une cavité 9 demeurant
vide de tout liquide au moment de l'illumination avec le
faisceau lumineux 5 permet en particulier de préserver le
liquide ou les liquides circulant dans la carte d'analyse,
de tout échauffement intempestif ou excessif.When at least
Le mode de réalisation représenté aux Figures 3
à 5 diffère de celui représenté aux Figures 1 à 2, par le
fait que la carte d'analyse 1 comprend "n", en
l'occurrence 3 chambres 2, 3, 17, disposées en série, mais
pouvant être aussi disposées en parallèle, séparées deux à
deux par "n-1", en l'occurrence deux cloisons
perforables 7 et 18, "n" étant un nombre entier, et l'une
des chambres 2,3 et 17 pouvant être notamment une chambre
de mesure optique. De manière à permettre un processus
automatique avec un seul et même rayon lumineux laser, les
cloisons perforables 7 et 18 sont distribuées dans la
carte 1, de manière à ce que deux cloisons ne puissent pas
être alignées avec un seul et même rayon lumineux
incident 12. Comme indiqué précédemment, la carte
d'analyse des Figures 3 à 5 comporte un liquide
remplissant la chambre 3, lequel va cheminer vers la
chambre 2, après perforation de la cloison 7, comme
représenté à la Figure 4, puis vers la chambre 17, après
perforation de la cloison 18, comme partiellement
représenté à la Figure 5.The embodiment shown in Figures 3
to 5 differs from that shown in Figures 1 to 2, by the
fact that the analysis card 1 includes "n", in
the
Comme représenté à la Figure 6, un dispositif 19 de traitement d'une carte d'analyse 1 selon l'invention comprend :
un générateur 20 de lumière cohérente, ayant la longueur d'onde prédéterminée λ et la puissance lumineuse P, comprenant une source laser, et des moyens 25 de collimation et de mise en forme du faisceau lumineux émis par la source laser ; un faisceau de puissance limitée, par exemple de 2 mW, est émis par un pointeur en lumière visible et superposé au faisceau laser pour son guidage ;- des moyens optiques 29 de couplage du faisceau lumineux
quasi-parallèle, pour injecter ce dernier dans une
fibre optique 21, ou des moyens optiques de guidage tels que prisme ou lentille, avec un bon rendement ; - des moyens optiques 30 de collimation et/ou de mise en
forme du faisceau, permettant d'obtenir un "spot"
circulaire de diamètre et de densité de puissance,
déterminés sur le plan de travail où le perçage sera
effectué, situé sur ou dans chaque cloison 7
ou 18 ; - des moyens 51 de positionnement de la carte d'analyse 1,
dans un plan perpendiculaire par rapport à la direction
de référence 6, en sorte que l'incidence du rayon
lumineux 12 illuminant chaque cloison perforable 7
ou 18, soit sensiblement perpendiculaire à chaque dite cloison ; ces moyens de positionnement 51 assurent un déplacement de la carte d'analyse selon deux directions de référence 22 et 23 sensiblement perpendiculaires.
- a
coherent light generator 20, having the predetermined wavelength λ and the light power P, comprising a laser source, and means 25 for collimating and shaping the light beam emitted by the laser source; a beam of limited power, for example of 2 mW, is emitted by a pointer in visible light and superimposed on the laser beam for its guidance; - optical means 29 for coupling the quasi-parallel light beam, to inject the latter into an
optical fiber 21, or optical guide means such as a prism or lens, with good efficiency; - optical means 30 for collimating and / or shaping the beam, making it possible to obtain a circular "spot" of diameter and power density, determined on the work surface where the drilling will be carried out, located on or in each
partition 7 or 18; - means 51 for positioning the analysis card 1, in a plane perpendicular to the reference direction 6, so that the incidence of the
light ray 12 illuminating eachperforable partition 7 or 18 is substantially perpendicular to each said partition; these positioning means 51 ensure a displacement of the analysis card in tworeference directions 22 and 23 substantially perpendicular.
A titre d'exemple, le générateur 20 émet une
lumière à 800 nm, avec une lumière de guidage à 670 nm. La
puissance de la source lumineuse ainsi constituée est de
700 mW, pour une puissance réellement utilisée de l'ordre
de 300 mW. La fibre optique 21 utilisée est une fibre
multimode de diamètre de coeur de 200 µm. A la sortie de
la fibre optique 21, une lentille 30 permet de focaliser
l'énergie lumineuse sur le centre 13, situé sur ou dans
chaque cloison 7 ou 18.For example, the
Avec les conditions suivantes :
- cloison 7
ou 18 réalisée en polystyrène, ayant une épaisseur de 0,3 mm ; - parois externes 15
et 16, réalisées en polypropylène, silicium ou germanium, selon une épaisseur de 2 à 7/10è de mm pour un film en polypropylène ; un générateur 20 de lumière cohérente, tel que décrit précédemment ;- aucun liquide n'étant présent dans les chambres 2
et 3et cavités 8et 9 ;
-
partition 7 or 18 made of polystyrene, having a thickness of 0.3 mm; -
15 and 16, made of polypropylene, silicon or germanium, with a thickness of 2 to 7 / 10ths of a mm for a polypropylene film;external walls - a
coherent light generator 20, as described previously; - no liquid being present in
2 and 3 andchambers 8 and 9;cavities
La présente invention peut être mise en oeuvre selon différents modes d'exécution ; en particulier l'une des chambres, mise en communication selon la présente invention, peut elle-même communiquer avec l'atmosphère ou le milieu dans lequel se trouve la carte d'analyse.The present invention can be implemented according to different modes of execution; especially one rooms, connected according to this invention, can itself communicate with the atmosphere or the environment in which the analysis card is located.
Claims (9)
- Analysis card (1), in which two chambers (2, 3), which are isolated from one another, are formed, characterized in that the two chambers -are separated from one another by a perforable partition (7) which is arranged within the said card and is made of material, in particular plastic, absorbing light energy having at least a predetermined wavelength λ to convert it into heat energy which can at least locally remove the said material, two cavities (8, 9) are formed on either side of the partition (7) and are respectively in communication with or contained in the two chambers (2, 3) respectively, a window (10, 11) made of a material which is transparent at least to the wavelength λ is arranged facing the said partition (7) and defines therewith one (8) of the said cavities, referred to as the incident light ray (12) cavity.
- Card according to Claim 1, characterized in that another window (11), made of a material which is transparent at least to the wavelength λ, facing the said partition (7), defines therewith the other (9) of the said cavities, referred to as the emergent light ray cavity.
- Card according to Claim 1, characterized in that it comprises a body (14) in which the two chambers (2, 3) and the two cavities (8, 9) are embossed or etched and at least one external wall (15, 16) which closes off the said chambers and cavities from the outside.
- Card according to Claim 3, of substantially flattened shape, characterized in that it comprises a flat body (14) between two external walls (15, 16).
- Card according to Claim 3, characterized in that one (2) of the chambers and the cavity (8) which corresponds to it are closed off by one (15) of the external walls, and the other chamber (3) and the other cavity (9), which corresponds to it, are closed off by the other external wall (16).
- Card according to Claim 3, characterized in that the perforable partition (7) is formed in the flat body (14), the constituent material of which absorbs light energy of wavelength λ.
- Card according to Claim 3, characterized in that the window (10) is formed in the external wall (15), the constituent material of which is transparent to the wavelength λ.
- Card according to Claim 1, characterized in that it comprises n chambers (2, 3, 17) which are arranged in series and/or parallel and are separated in pairs by n-1 perforable partitions (7, 18), "n" being a whole number, and one of the chambers being, in particular, an optical measurement chamber, the said perforable partitions being distributed in the said card in such a way that no two partitions can be aligned with the same incident light beam (12).
- Ready-to-use analysis card according to Claim 1, in which at least one chamber (3) is filled with a liquid.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9601984A FR2744803B1 (en) | 1996-02-12 | 1996-02-12 | METHOD AND DEVICE FOR PROCESSING AN ANALYSIS CARD |
FR9601984 | 1996-02-12 | ||
PCT/IB1997/000112 WO1997028899A1 (en) | 1996-02-12 | 1997-02-12 | Analysis card |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0820348A1 EP0820348A1 (en) | 1998-01-28 |
EP0820348B1 true EP0820348B1 (en) | 2002-01-09 |
Family
ID=9489316
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97901736A Expired - Lifetime EP0820348B1 (en) | 1996-02-12 | 1997-02-12 | Analysis card |
Country Status (7)
Country | Link |
---|---|
US (1) | US5869002A (en) |
EP (1) | EP0820348B1 (en) |
AT (1) | ATE211657T1 (en) |
CA (1) | CA2218415C (en) |
DE (1) | DE69709499T2 (en) |
FR (1) | FR2744803B1 (en) |
WO (1) | WO1997028899A1 (en) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19716683C1 (en) * | 1997-04-21 | 1998-06-04 | Fraunhofer Ges Forschung | Miniature encapsulation device for sensitive materials |
DE19858443A1 (en) * | 1998-12-17 | 2000-07-06 | Inst Mikrotechnik Mainz Gmbh | Method for dispensing a fluid, fluidic component and device for handling such components |
US6720187B2 (en) * | 2000-06-28 | 2004-04-13 | 3M Innovative Properties Company | Multi-format sample processing devices |
US6734401B2 (en) | 2000-06-28 | 2004-05-11 | 3M Innovative Properties Company | Enhanced sample processing devices, systems and methods |
ES2449445T3 (en) * | 2000-06-28 | 2014-03-19 | 3M Innovative Properties Co. | Improved devices, systems and methods for the treatment of samples |
US7192560B2 (en) * | 2001-12-20 | 2007-03-20 | 3M Innovative Properties Company | Methods and devices for removal of organic molecules from biological mixtures using anion exchange |
US7347976B2 (en) * | 2001-12-20 | 2008-03-25 | 3M Innovative Properties Company | Methods and devices for removal of organic molecules from biological mixtures using a hydrophilic solid support in a hydrophobic matrix |
US6889468B2 (en) * | 2001-12-28 | 2005-05-10 | 3M Innovative Properties Company | Modular systems and methods for using sample processing devices |
DE10200541A1 (en) * | 2002-01-09 | 2003-07-24 | Zeiss Carl Jena Gmbh | Microtiter plate, for use in fluorescence analysis of cell samples, has cylindrical wells whose walls are at angle to its base |
WO2004050244A1 (en) * | 2002-11-29 | 2004-06-17 | The National Blood Authority | Opening sample containers using laser |
JP2006508790A (en) | 2002-12-04 | 2006-03-16 | スピンクス インコーポレイテッド | Apparatus and method for programmable microanalytical scale manipulation of fluids |
EP1930635A3 (en) * | 2002-12-04 | 2008-08-13 | Spinx, Inc. | Devices and methods for programmable microscale manipulation of fluids |
US7981600B2 (en) * | 2003-04-17 | 2011-07-19 | 3M Innovative Properties Company | Methods and devices for removal of organic molecules from biological mixtures using an anion exchange material that includes a polyoxyalkylene |
US20050130177A1 (en) | 2003-12-12 | 2005-06-16 | 3M Innovative Properties Company | Variable valve apparatus and methods |
US7939249B2 (en) * | 2003-12-24 | 2011-05-10 | 3M Innovative Properties Company | Methods for nucleic acid isolation and kits using a microfluidic device and concentration step |
US20070095393A1 (en) * | 2004-03-30 | 2007-05-03 | Piero Zucchelli | Devices and methods for programmable microscale manipulation of fluids |
JP4516346B2 (en) * | 2004-04-14 | 2010-08-04 | 積水化学工業株式会社 | Micro total analysis system |
EP1693471A1 (en) * | 2005-02-16 | 2006-08-23 | Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno | Method for refining a liquor, comprising an aqueous solution of a carbohydrate |
WO2007057788A2 (en) * | 2005-06-03 | 2007-05-24 | Spinx, Inc. | Dosimeter for programmable microscale manipulation of fluids |
US7754474B2 (en) | 2005-07-05 | 2010-07-13 | 3M Innovative Properties Company | Sample processing device compression systems and methods |
US7323660B2 (en) * | 2005-07-05 | 2008-01-29 | 3M Innovative Properties Company | Modular sample processing apparatus kits and modules |
US7763210B2 (en) * | 2005-07-05 | 2010-07-27 | 3M Innovative Properties Company | Compliant microfluidic sample processing disks |
US20070031282A1 (en) * | 2005-08-04 | 2007-02-08 | Piero Zucchelli | Devices and methods for interfacing microfluidic devices with fluid handling devices |
US8464760B2 (en) * | 2006-08-16 | 2013-06-18 | Samsung Electronic Co., Ltd. | Valve unit, reaction apparatus with the same, and method of forming valve in channel |
ES2753136T3 (en) | 2006-12-22 | 2020-04-07 | Diasorin S P A | Thermal transfer methods for microfluidic systems |
KR20090105934A (en) * | 2006-12-22 | 2009-10-07 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | Enhanced sample processing devices, systems and methods |
EP2140001A2 (en) * | 2007-04-25 | 2010-01-06 | 3M Innovative Properties Company | Methods for nucleic acid amplification |
WO2010084190A1 (en) * | 2009-01-23 | 2010-07-29 | Dublin City University | Fluidic single use valve and microfluidic systems incorporating said valve |
US8834792B2 (en) | 2009-11-13 | 2014-09-16 | 3M Innovative Properties Company | Systems for processing sample processing devices |
USD667561S1 (en) | 2009-11-13 | 2012-09-18 | 3M Innovative Properties Company | Sample processing disk cover |
USD638550S1 (en) | 2009-11-13 | 2011-05-24 | 3M Innovative Properties Company | Sample processing disk cover |
USD638951S1 (en) | 2009-11-13 | 2011-05-31 | 3M Innovative Properties Company | Sample processing disk cover |
US20110117607A1 (en) * | 2009-11-13 | 2011-05-19 | 3M Innovative Properties Company | Annular compression systems and methods for sample processing devices |
WO2012158988A1 (en) | 2011-05-18 | 2012-11-22 | 3M Innovative Properties Company | Systems and methods for valving on a sample processing device |
ES2755078T3 (en) | 2011-05-18 | 2020-04-21 | Diasorin S P A | Systems and methods for volumetric measurement in a sample processing device |
USD672467S1 (en) | 2011-05-18 | 2012-12-11 | 3M Innovative Properties Company | Rotatable sample processing disk |
ES2870874T3 (en) | 2011-05-18 | 2021-10-27 | Diasorin S P A | Systems and methods for detecting the presence of a selected volume of material in a sample processing device |
CN103394382A (en) * | 2013-08-07 | 2013-11-20 | 苏州扬清芯片科技有限公司 | Microfluidic chip with optical filtering characteristics |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5362654A (en) * | 1984-07-20 | 1994-11-08 | Sangstat Medical Corporation | Self-contained quantitative assay |
ATE77483T1 (en) * | 1986-04-23 | 1992-07-15 | Avl Medical Instr Ag | SENSOR ELEMENT FOR DETERMINING SUBSTANCE CONCENTRATIONS. |
US5137808A (en) * | 1987-04-07 | 1992-08-11 | Syntex (U.S.A.) Inc. | Immunoassay device |
US5472671A (en) * | 1989-04-26 | 1995-12-05 | Nilsson; Sven-Erik | Cuvette |
US5364591A (en) * | 1992-06-01 | 1994-11-15 | Eastman Kodak Company | Device for moving a target-bearing solid through a liquid for detection while being contained |
US5290518A (en) * | 1992-08-17 | 1994-03-01 | Eastman Kodak Company | Flexible extraction device with burstable sidewall |
EP0594259B1 (en) * | 1992-10-23 | 1996-09-25 | Johnson & Johnson Clinical Diagnostics, Inc. | Flow control in a containment device |
US5500187A (en) * | 1992-12-08 | 1996-03-19 | Westinghouse Electric Corporation | Disposable optical agglutination assay device and method for use |
US5411065A (en) * | 1994-01-10 | 1995-05-02 | Kvm Technologies, Inc. | Liquid specimen transfer apparatus and method |
-
1996
- 1996-02-12 FR FR9601984A patent/FR2744803B1/en not_active Expired - Fee Related
-
1997
- 1997-02-12 DE DE69709499T patent/DE69709499T2/en not_active Expired - Lifetime
- 1997-02-12 AT AT97901736T patent/ATE211657T1/en not_active IP Right Cessation
- 1997-02-12 US US08/913,726 patent/US5869002A/en not_active Expired - Lifetime
- 1997-02-12 WO PCT/IB1997/000112 patent/WO1997028899A1/en active IP Right Grant
- 1997-02-12 EP EP97901736A patent/EP0820348B1/en not_active Expired - Lifetime
- 1997-02-12 CA CA002218415A patent/CA2218415C/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
ATE211657T1 (en) | 2002-01-15 |
WO1997028899A1 (en) | 1997-08-14 |
US5869002A (en) | 1999-02-09 |
FR2744803B1 (en) | 1998-03-13 |
CA2218415C (en) | 2006-05-30 |
EP0820348A1 (en) | 1998-01-28 |
DE69709499D1 (en) | 2002-02-14 |
FR2744803A1 (en) | 1997-08-14 |
DE69709499T2 (en) | 2002-09-26 |
CA2218415A1 (en) | 1997-08-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0820348B1 (en) | Analysis card | |
US6710870B1 (en) | Method and device for measuring luminescence | |
EP0959343A1 (en) | Optical sensor utilizing an immunological reaction and a fluorescence marker | |
CA1103631A (en) | Conditioning device for a liquid sample before its analysis | |
US7968839B2 (en) | Miniaturized optical tweezers based on high-NA micro-mirrors | |
EP0519623A2 (en) | Multiple surface evanescent wave sensor system | |
EP2302366A1 (en) | Device for supporting chromophoric elements | |
EP3146312B1 (en) | Integrated semiconductor device for detecting fluorescent particles | |
JPH05505874A (en) | How to improve test sensitivity | |
WO2003012403A1 (en) | Device for analysing a sample in particular by flow cytometry | |
WO2018138223A1 (en) | Optical detector of particles | |
US20100253945A1 (en) | Particle characterization | |
EP2710351B1 (en) | Biochip device | |
FR2710755A1 (en) | Velocimetric and clinometric laser probe. | |
EP3317664B1 (en) | System for analysing a liquid sample | |
EP2565623B1 (en) | Device for optically measuring materials using light multiplexing | |
US20060228260A1 (en) | Optical analysis device | |
US7012692B2 (en) | Photothermal conversion spectroscopic analysis method, and photothermal conversion spectroscopic analysis apparatus for carrying out the method | |
FR3033407A1 (en) | DEVICE FOR COLLECTING A LIQUID SAMPLE BY CAPILLARITY. | |
JP4550323B2 (en) | Method for forming optical waveguide | |
EP0943946A1 (en) | Manufacturing method for a multiribbon of optical fibres separable in at least two ribbons of optical fibres | |
EP3099221B1 (en) | Device generating evanescent waves, and method for the implementation thereof | |
WO2003012504A2 (en) | Improvements to optical fibres provided with a lens by photopolymerization and related novel optical components | |
JP2000019091A (en) | Optical fiber probe and its manufacturing method | |
EP4111830A1 (en) | Composite optical fibre based plasma generation device |
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: 19970917 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
17Q | First examination report despatched |
Effective date: 20010702 |
|
GRAG | Despatch of communication of intention to grant |
Free format text: ORIGINAL CODE: EPIDOS AGRA |
|
GRAH | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOS IGRA |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020109 Ref country code: IE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020109 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020109 Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020109 Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020109 |
|
REF | Corresponds to: |
Ref document number: 211657 Country of ref document: AT Date of ref document: 20020115 Kind code of ref document: T |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D Free format text: FRENCH |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020212 |
|
REF | Corresponds to: |
Ref document number: 69709499 Country of ref document: DE Date of ref document: 20020214 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: NV Representative=s name: MICHELI & CIE INGENIEURS-CONSEILS |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020409 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020409 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020409 |
|
GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) |
Effective date: 20020326 |
|
NLV1 | Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act | ||
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20020730 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FD4D |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20020901 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
NLV1 | Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 20120321 Year of fee payment: 16 Ref country code: FR Payment date: 20120316 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20120224 Year of fee payment: 16 Ref country code: GB Payment date: 20120217 Year of fee payment: 16 Ref country code: IT Payment date: 20120223 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20120320 Year of fee payment: 16 |
|
BERE | Be: lapsed |
Owner name: *BIO MERIEUX Effective date: 20130228 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20130212 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130228 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130228 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20131031 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 69709499 Country of ref document: DE Effective date: 20130903 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130212 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130212 Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130228 Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130903 Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20130228 |