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    METHOD AND DEVICE FOR DETECTING LOW-CONTRAST AND HIGH-CONTRAST DEFECTS IN TRANSPARENT OR TRANSLUCENT OBJECTS
    191.
    发明申请
    METHOD AND DEVICE FOR DETECTING LOW-CONTRAST AND HIGH-CONTRAST DEFECTS IN TRANSPARENT OR TRANSLUCENT OBJECTS 审中-公开
    用于检测透明或透明物体中的低对比度和高对比度缺陷的方法和装置

    公开(公告)号：WO2008050066A2

    公开(公告)日：2008-05-02

    申请号：PCT/FR2007052238

    申请日：2007-10-24

    Applicant: TIAMA ,  LECONTE MARC

    Inventor： LECONTE MARC

    IPC: G01N21/90

    CPC classification number: G01N21/90 ,  G01N2021/8832 ,  G01N2201/0628

    Abstract: The invention relates to an in-line optical method of inspecting transparent or translucent objects (2) running at high speed between a light source (3) and means (4) for taking images of the objects and for analyzing the images taken, so as to detect defects in the objects. According to the invention the method consists: in controlling the single light source (3) so that said source produces in succession two types of illumination for each object running past said source, the first type being a homogenous illumination whereas the second type is formed from alternate dark zones and light zones with a discontinuous spatial variation; in taking images of each running object when each of them is illuminated in succession by the two types of illumination; and in analyzing the images taken with the illuminations of the first and second types for the purpose of detecting high-contrast defects and low-contrast defects respectively.

    Abstract translation: 本发明涉及一种在线光学方法，用于检查在光源（3）和装置（4）之间高速运行的透明或半透明物体（2），用于拍摄物体的图像并分析所拍摄的图像，以便 以检测物体中的缺陷。 根据本发明，该方法包括：在控制单个光源（3）中，使得所述光源相继产生用于运行经过所述光源的每个物体的两种类型的照明，第一类型是均匀照明，而第二类型由 交替的暗区和具有不连续空间变化的轻区; 在拍摄每个运行对象的图像时，通过两种类型的照明连续照亮每个对象; 并且分析用于分别检测高对比度缺陷和低对比度缺陷的第一和第二类型的照明拍摄的图像。

    VORRICHTUNG ZUM AUSWERTEN BIOCHEMISCHER PROBEN
    192.
    发明申请
    VORRICHTUNG ZUM AUSWERTEN BIOCHEMISCHER PROBEN 审中-公开
    评价装置生化样品

    公开(公告)号：WO2006026796A1

    公开(公告)日：2006-03-16

    申请号：PCT/AT2005/000338

    申请日：2005-08-24

    Applicant: NANOIDENT TECHNOLOGIES AG ,  PADINGER, Franz ,  SCHRÖTER, Klaus, G.

    Inventor： PADINGER, Franz ,  SCHRÖTER, Klaus, G.

    IPC: G01N21/75 ,  G01N21/78 ,  H01L51/46 ,  H01L27/146

    CPC classification number: G01N21/78 ,  G01N21/75 ,  G01N2201/0628 ,  H01L27/146

    Abstract: Es wird eine Vorrichtung zum Auswerten biochemischer Proben (1) mit einem Probenträger (2), mit einer Bilderfassungseinrichtung, die eine an eine Auswerteschaltung (10) angeschlossene lichtempfindliche Lage (3) aufweist, und mit einer Beleuchtungseinrichtung für die Proben (1) beschrieben. Um einfache Konstruktionsbedingungen zu schaffen, wird vorgeschlagen, daß die auf dem Probenträger (2) vorgesehene lichtempfindliche Lage (3) der Bilderfassungseinrichtung eine photoaktive Schicht (4) auf der Basis organischer Halbleiter zwischen zwei Elektrodenschichten (5, 6) umfaßt, von denen die Elektrodenschicht (6) zwischen der photoaktiven Schicht (4) und den Proben (1) zumindest bereichsweise lichtdurchlässig ausgebildet ist.

    Abstract translation: 提供了一种用于评估生化样品（1），包括一个样品（2）的载体，与已连接至评估电路（10）的图像捕获装置的光敏层（3），并具有用于样品（1）的照明装置提供了一种装置。 为了提供简单的设计条件，所以建议的样品载体（2）上的步骤包括的所述图像捕获装置包含光活性层基于两个电极层之间的有机半导体（5,6），（3）（4）设置的感光层，其在所述电极层的 （6）光敏层（4）和所述样本（1）之间的至少部分透明的光来形成。

    DETECTION SYSTEM
    195.
    发明申请
    DETECTION SYSTEM 审中-公开
    检测系统

    公开(公告)号：WO02042747A1

    公开(公告)日：2002-05-30

    申请号：PCT/GB2001/004521

    申请日：2001-10-10

    IPC: G01N21/03 ,  G01N21/05 ,  G01N21/25 ,  G01N21/27 ,  G01N21/31 ,  G01N21/64 ,  G01N33/483 ,  G01N37/00 ,  B01J19/00 ,  B81B1/00

    CPC classification number: G01N21/6454 ,  G01N21/05 ,  G01N21/253 ,  G01N21/31 ,  G01N2021/0346 ,  G01N2021/6482 ,  G01N2201/0628

    Abstract: A microfabricated detection system, comprising: a substrate chip; a chamber defined by the substrate chip to which a fluid sample is in use delivered; and at least one detector comprising at least one light-emitting diode including an organic semiconductor element for emitting light into the chamber and at least one photocell including an organic semiconductor element for receiving light from the chamber.

    Abstract translation: 一种微加工检测系统，包括：基板芯片; 由流体样品在其中使用的衬底芯片限定的室; 以及至少一个检测器，包括至少一个发光二极管，该发光二极管包括用于向室内发射光的有机半导体元件和至少一个包含用于从腔室接收光的有机半导体元件的光电池。

    Sensor having integrated photodetector and/or light source
    199.
    发明专利
    Sensor having integrated photodetector and/or light source 审中-公开
    具有一体化光电传感器和/或光源的传感器

    公开(公告)号：JP2007147578A

    公开(公告)日：2007-06-14

    申请号：JP2005357355

    申请日：2005-12-12

    Applicant: Agilent Technol Inc ,  アジレント・テクノロジーズ・インクAgilent Technologies, Inc.

    Inventor： HELBING RENE P

    IPC: G01N21/78 ,  G01N33/543

    CPC classification number: G01N21/77 ,  A61B5/14532 ,  A61B5/14546 ,  A61B5/1455 ,  A61B2562/0295 ,  G01N2201/0628

    Abstract: PROBLEM TO BE SOLVED: To provide a sensor of a remarkably reduced cost and size, requiring no secondary attachment and no positional alignment. SOLUTION: This sensor 30 is a sensor such as a lateral flow sensor including a chemical layer 32 and a detector 36 on a flexible substrate 40. An optical signal is generated in response to an analyte 34 arranged on the chemical layer. The presence or absence and a concentration of the analyte are detected by detecting the optical signal by the detector. The detector is mounted on the substrate. The chemical layer and the substrate are layered each other to form the integrated sensor. The sensor may include a light source 42. The light source may be arranged on the substrate, or on a side opposite to the detector in the chemical layer. COPYRIGHT: (C)2007,JPO&INPIT

    Abstract translation: 要解决的问题：为了提供显着降低的成本和尺寸的传感器，不需要二次附接和不进行位置对准。 解决方案：该传感器30是诸如横向流量传感器的传感器，其包括柔性基板40上的化学层32和检测器36.响应于布置在化学层上的分析物34产生光信号。 通过检测器检测光信号来检测分析物的存在或不存在和浓度。 检测器安装在基板上。 化学层和基板彼此层叠以形成集成的传感器。 传感器可以包括光源42.光源可以布置在基板上，或者在化学层中的与检测器相对的一侧上。 版权所有（C）2007，JPO＆INPIT

    Monitoring apparatus for dna polymerase chain reaction
    200.
    发明专利
    Monitoring apparatus for dna polymerase chain reaction 审中-公开
    监测DNA聚合酶链反应的装置

    公开(公告)号：JP2005274579A

    公开(公告)日：2005-10-06

    申请号：JP2005119102

    申请日：2005-04-15

    Applicant: Applera Corp ,  アプレラ コーポレイション

    Inventor： GAMBINI MICHAEL R ,  ATWOOD JOHN G ,  YOUNG EUGENE F ,  LAKATOS EDWARD J ,  CERRONE ANTHONY L

    IPC: B01L7/00 ,  C12M1/34 ,  C12N15/09 ,  C12Q1/68 ,  G01N21/03 ,  G01N21/25 ,  G01N21/64 ,  G01N21/78

    CPC classification number: G01N21/6428 ,  B01L3/5085 ,  B01L7/52 ,  B01L2200/10 ,  B01L2300/0654 ,  B01L2300/0663 ,  B01L2300/1811 ,  C12Q1/686 ,  C12Q2545/101 ,  G01N21/0303 ,  G01N21/274 ,  G01N21/645 ,  G01N21/6452 ,  G01N2021/6419 ,  G01N2021/6421 ,  G01N2021/6439 ,  G01N2021/6441 ,  G01N2021/6463 ,  G01N2021/6482 ,  G01N2201/0245 ,  G01N2201/06113 ,  G01N2201/0628 ,  G01N2201/0635 ,  G01N2201/0636 ,  G01N2201/068 ,  C12Q2563/107

    Abstract: PROBLEM TO BE SOLVED: To provide a PCR (polymerase chain reaction) equipment being an optical equipment for quantitative monitoring of replicative DNA which is improved in a dynamic range, capable of automatically selecting the exposure time for expanding a dynamic range, capable of automatic drift adjustment, easy to operate, relatively low price, and easy to change the optical system for storing a different fluorescence dye. SOLUTION: The equipment includes a light source, a light guide means for guiding a light beam, an optical detector, and a means for processing a data signal. The light source emits source beam containing at least one frequency of primary excitation frequency capable of making fluorescence emit with emission frequency. A 1st means is so arranged as to activate an excitation beam of excitation frequency while receiving the source beam. A 1st focus means is arranged to focus the excitation beam in each suspension to make the primary dye emit emission beams with intensity indicating the emission frequency and the DNA concentration of each suspension. A focus means receives an emission beam and makes it pass through. A 2nd means is arranged to receive the emission beam to pass through the emission beam of emission frequency to the other focus means which focuses the emission beam on the detector. The detector generates a primary data signal representing the emission beam and generates the concentration corresponding to the DNA of each small bottle. The processor displays the concentration of DNA by acquiring the primary data signal. COPYRIGHT: (C)2006,JPO&NCIPI

    Abstract translation: 要解决的问题：为了提供PCR（聚合酶链反应）设备，其是用于定量监测在动态范围内改进的复制DNA的光学设备，能够自动选择用于扩大动态范围的曝光时间，能够 的自动漂移调整，操作方便，价格相对较低，并且易于更换用于存储不同荧光染料的光学系统。 解决方案：设备包括光源，用于引导光束的光导装置，光学检测器和用于处理数据信号的装置。 光源发射含有能够使荧光发射具有发射频率的初级激发频率的至少一个频率的源束。 第一装置被布置为在接收源光束的同时激活激发频率的激发光束。 第一焦点装置被布置成将激发光束聚焦在每个悬浮液中，以使主染料发射具有指示每个悬浮液的发射频率和DNA浓度的强度的发射光束。 聚焦装置接收发射光束并使其通过。 第二装置被布置为接收发射光束以将发射频率的发射光束传递到将发射光束聚焦在检测器上的另一个聚焦装置。 检测器产生表示发射光束的主要数据信号，并产生与每个小瓶子的DNA相对应的浓度。 处理器通过获取主数据信号显示DNA的浓度。 版权所有（C）2006，JPO＆NCIPI

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