CONCENTRATION DECIDING SYSTEM FOR SUBSTANCE MIXED WITH FLUORESCENT MATERIAL AND ITS USING METHOD

    公开(公告)号:JP2000131236A

    公开(公告)日:2000-05-12

    申请号:JP30152499

    申请日:1999-10-22

    Abstract: PROBLEM TO BE SOLVED: To provide a decoder suitable for a chip having a small number of small-size contacts with sufficient intervals between the contact by determining the quantity of fluorescence of a contact to decide a density of substance mixed with the fluorescent material. SOLUTION: An image acquisition means 4 is focused on a matrix disposed and fixed below an optical axis of a microscope 1, and a reference contact aligned to the optical center of this system is automatically retrieved, while an image of one contact of the matrix is acquired. The system has a calculation part for calculating fluorescence of the contact and deducing the density of substance. An illuminating means has a ring-shaped light source 11 and a laser light source 13 for exciting a fluorescent material contained in a mixture constituting the substance. The system also has a means for recording the image of the contact and a processing means 7 for analyzing the image. Thereby, the system can determine a quantity of the fluorescence of the contact to decide the density of the substance mixed with the fluorescent material.

    POLARIZATION-FLUORESCENT IMAGING DEVICE
    2.
    发明专利

    公开(公告)号:JP2002072142A

    公开(公告)日:2002-03-12

    申请号:JP2001236615

    申请日:2001-08-03

    Abstract: PROBLEM TO BE SOLVED: To provide a fluorescent imaging device capable of easily discriminating molecules which are different in size. SOLUTION: This fluorescent imaging device comprises the first means in which a component to be analyzed is put, the second means which illuminates the component to be analyzed by polarization and the third means which measures fluorescence emitting from the component under the effect of the polarization. In this case, characteristically, the first means comprises a parallel micro channel structure (4), and the second means has at least one combining device (2, 5) which guides polarized light to the micro channel.

    DEVICE FOR FLUORESCENCE MICROSCOPY OF SAMPLES, IN PARTICULAR SEQUENTIALLY
    4.
    发明申请
    DEVICE FOR FLUORESCENCE MICROSCOPY OF SAMPLES, IN PARTICULAR SEQUENTIALLY 审中-公开
    荧光显微镜样品的设备,特别是序列

    公开(公告)号:WO02065160A3

    公开(公告)日:2002-12-12

    申请号:PCT/FR0200435

    申请日:2002-02-05

    CPC classification number: G02B21/04 G02B21/16

    Abstract: The invention concerns a device for microscopic observation of at least a sample (2) such as a biological sample, arranged on a support (6), said device comprising at least a light source (42) for illuminating the sample, means (48) for reflecting said light towards the sample, a catadioptric lens (38) for observing the sample, said lens forming an image of the sample, and means (52) for acquiring said image. The reflecting means are arranged between the lens and the support.

    Abstract translation: 本发明涉及用于显微观察至少一个布置在支撑体(6)上的生物样品(2)的样品(2)的装置,所述装置至少包括用于照射样品的光源(42),装置(48) 用于将所述光反射到样品,用于观察样品的反射折射透镜(38),所述透镜形成样品的图像,以及用于获取所述图像的装置(52)。 反射装置设置在透镜和支架之间。

    FLUORESCENCE IMAGING DEVICE WITH TWO WAVELENGTH REFLECTION
    5.
    发明申请
    FLUORESCENCE IMAGING DEVICE WITH TWO WAVELENGTH REFLECTION 审中-公开
    具有两次波长反射的荧光成像装置

    公开(公告)号:WO2006087437A3

    公开(公告)日:2007-04-26

    申请号:PCT/FR2006000131

    申请日:2006-01-20

    CPC classification number: G01N21/64 A61B1/00186 A61B1/043 A61B1/0638

    Abstract: The inventive device comprises a first light source and a first wavelength (?1) corresponding to an excitation wavelength (?Ex) of a fluorophore. The excitation wavelength (?Ex) and an emission wavelength (?Em) of the fluorophore delimit a predetermined interval (?Em). The device also comprises a second light source having a second wavelength (?2) offset with regard to the first wavelength (?1) in such a manner that it is outside said predetermined interval (?Em). The offset (?12) between the first (?1) and second (?2) wavelengths is between 30 nm and 100 nm. A camera is provided comprising a filter opaque to the first (?1) and second (?2) wavelengths and transparent to the emission wavelength (?Em) and to the wavelengths noticeably greater than the highest of the first (?1) and second (?2) wavelengths. The light sources and the camera are synchronized for alternately activating one of the light sources and enabling the camera to alternately acquire a fluorescence image and a background noise image.

    Abstract translation: 本发明的装置包括对应于荧光团的激发波长(λEx)的第一光源和第一波长(λ1)。 荧光团的激发波长(ΔEx)和发射波长(ΔEm)限定预定间隔(ΔEm)。 该装置还包括具有相对于第一波长(θ1)偏移的第二波长(λ2)的第二光源,使得其在所述预定间隔(ΔEm)之外。 第一(λ1)和第二(λ2)波长之间的偏移(θ12)在30nm和100nm之间。 提供一种照相机,包括对第一(λ1)和第二(λ2)波长不透明并且对于发射波长(θEm)透明的滤光器和明显大于第一(λ1)和第二 (λ2)波长。 光源和照相机被同步以交替地激活光源之一并且使相机能够交替地获取荧光图像和背景噪声图像。

    6.
    发明专利
    未知

    公开(公告)号:DE602007000275D1

    公开(公告)日:2009-01-08

    申请号:DE602007000275

    申请日:2007-04-03

    Abstract: The method involves introducing a fluorescent marker e.g. antibody/fluorophore conjugate, into a biological tissue e.g. organ. The marker is excited by incident light radiations, where the marker is sequentially excited at different incident excitation wavelengths. Bands of emission relating to fluorescence emitted by the marker are detected in response to the excitation. Intensities of fluorescence relative to the emission bands are analyzed. The marker is based on a group of fluorophores that are excited by the wavelengths and based on an up-converting semiconductor inorganic nanocrystal.

    SONDE OPTIQUE PER-OPERATOIRE BI-SPECTRALE.

    公开(公告)号:FR2916339A1

    公开(公告)日:2008-11-28

    申请号:FR0703738

    申请日:2007-05-25

    Abstract: Le domaine général de l'invention est celui des sondes optiques per-opératoires destinées à aider le chirurgien dans son geste médical.Les sondes optiques à fluorescence selon l'invention sont destinées à être utilisées sur des tissus vivants où les zones malades ont été marquées par un marqueur fluorescent. Elles possèdent un double éclairage. Le premier (1, 2) situé dans le rouge ou le proche infra-rouge est nécessaire pour réaliser la fluorescence des zones marquées (30) et obtenir une image exploitable par une caméra (7). Le second (9, 10) situé dans le visible est nécessaire pour éclairer en lumière visible les zones marquées, facilitant ainsi le travail du chirurgien. L'éclairage visible peur être soit ponctuel, soit être réalisé par un projecteur d'images. Dans ce dernier cas, l'image projetée éclaire uniquement les zones malades.

    8.
    发明专利
    未知

    公开(公告)号:FR2900043B1

    公开(公告)日:2008-07-04

    申请号:FR0603610

    申请日:2006-04-24

    Abstract: The method involves introducing a fluorescent marker e.g. antibody/fluorophore conjugate, into a biological tissue e.g. organ. The marker is excited by incident light radiations, where the marker is sequentially excited at different incident excitation wavelengths. Bands of emission relating to fluorescence emitted by the marker are detected in response to the excitation. Intensities of fluorescence relative to the emission bands are analyzed. The marker is based on a group of fluorophores that are excited by the wavelengths and based on an up-converting semiconductor inorganic nanocrystal.

    PROCEDE D'IMAGERIE OPTIQUE PAR FLUORESCENCE DE TISSUS BIOLOGIQUES, NOTAMMENT POUR DELIMITER DES REGIONS D'INTERET DES TISSUS A ANALYSER PAR TOMOGRAPHIE

    公开(公告)号:FR2900043A1

    公开(公告)日:2007-10-26

    申请号:FR0603610

    申请日:2006-04-24

    Abstract: La présente invention concerne un procédé d'imagerie optique par fluorescence d'au moins un tissu biologique, notamment pour délimiter des régions d'intérêt du ou des tissu(s) à analyser par tomographie.Le procédé selon l'invention comprend les étapes suivantes :a) l'introduction d'au moins un marqueur fluorescent dans le(s) tissu(s),b) l'excitation du ou de chaque marqueur par des rayonnements lumineux incidents et une détection de bandes d'émission relatives à des rayonnements fluorescents émis par le ou chaque marqueur en réponse à cette excitation, puisc) l'analyse de la fluorescence de ces bandes d'émission,et il est caractérisé en ce que l'étape b) comprend :- une excitation séquentielle, par n longueurs d'onde d'excitation lambdai incidentes différentes, du ou de chaque marqueur apte à être excité par au moins deux de ces lambdai et à émettre en réponse, pour chaque lambdai, une série Si de m bandes d'émission Bj simultanées de différentes longueurs d'onde lambda'j qui sont sensiblement les mêmes d'une série Si à une autre (où n et m >= 2, et où i et j varient de 1 à n et de 1 à m), et- une détection de ces séries, pour en déduire une estimation de la localisation tridimensionnelle du ou de chaque marqueur dans le(s) tissu(s) et/ou des coefficients d'absorption moyens de tissu(s) vis-à-vis des excitations lambdai.

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