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    • 1. 发明申请
    • APPARATUS AND METHOD FOR DYNAMIC CELLULAR PROBING AND DIAGNOSTICS USING HOLOGRAPHIC OPTICAL FORCING ARRAY
    • 使用全息光学强迫阵列进行动态细胞检测和诊断的装置和方法
    • WO2009134296A2
    • 2009-11-05
    • PCT/US2009/001490
    • 2009-03-09
    • ARRYX, INC.AKCAKIR, Osman
    • AKCAKIR, Osman
    • G01B9/021
    • G01B9/021G01N21/453G01N21/6456G01Q20/02G01Q30/04G01Q60/20G03H1/0443G03H2001/0033G03H2001/0077G03H2001/045G03H2001/0458G03H2223/23
    • The present invention utilizes a holographic optical forcing array for dynamic cellular probing and diagnostics. A holographic optical trapping system generates optical forces on objects so that deformations thereof may be quantified. In one embodiment, digital holography is used to generate an interference pattern, and an analysis thereof determines the phase profile which yields a measurement of the objects' shape deformation using only one image. In another embodiment, phase-stepped holography allows the phase profile of an object to be measured using only one image, by using a holographic optical element to make phase-shifted replicas of the beam in space. In another embodiment, the optical forcing array applies optical forces to beads placed on the objects' surface, deforming the objects. The beads' position is determined by applying Mie theory, and analysis thereof yields the three dimensional position of the beads, and a measurement of the deformation displacement on the objects' surface.
    • 本发明利用全息光学强制阵列进行动态细胞探测和诊断。 全息光学捕获系统在物体上产生光学力,从而可以量化其变形。 在一个实施例中,使用数字全息术来产生干涉图案,并且其分析确定相位轮廓,其仅使用一个图像来产生对象的形状变形的测量。 在另一个实施例中,相位阶全息术通过使用全息光学元件在空间中进行光束的相移复制,允许仅使用一个图像来测量物体的相位分布。 在另一个实施例中,光学强迫阵列将光学力施加到放置在物体表面上的珠子上,使物体变形。 通过应用米氏理论确定珠的位置,分析其产生珠的三维位置,并测量物体表面上的变形位移。
    • 2. 发明申请
    • BINDING METHOD AND APPARATUS FOR SORTING OBJECTS
    • 用于分类对象的绑定方法和装置
    • WO2009035623A1
    • 2009-03-19
    • PCT/US2008/010601
    • 2008-09-11
    • ARRYX, INC.CHAKRABARTY, Tania
    • CHAKRABARTY, Tania
    • B01D11/00
    • G01N33/5091G01N33/56966G01N2800/367
    • The present invention relates to a method and apparatus of sorting objects including, providing a sample having wanted and unwanted objects, coating a surface of a sample holder with an antibody, placing an eluted sample on the sample holder, binding an antigen in the wanted objects with the antibody on the surface of the sample holder to sort the objects into wanted and unwanted objects, separating the wanted objects, and performing PCR-based STR analysis on the wanted objects In one embodiment, holographic optical trapping is used to sort the wanted objects In other embodiments, the wanted objects are sperm and the antibody is a human sperm specific antibody, and the PCR is single cell PCR-based STR analysis
    • 本发明涉及一种分类物体的方法和装置,包括:提供具有想要和不想要的物体的样品,用抗体涂覆样品架的表面,将洗脱的样品放置在样品架上,将所需物体中的抗原结合 与样品架表面上的抗体一起将物体分类为有用和不需要的物体,分离所需物体,并对所需物体进行基于PCR的STR分析。在一个实施例中,全息光学捕获用于对所需物体进行分类 在其他实施方案中,所需物体是精子,抗体是人精子特异性抗体,并且PCR是基于单细胞PCR的STR分析
    • 4. 发明申请
    • APPARATUS AND METHOD FOR DETECTING DEFORMABILITY OF CELLS USING SPATIALLY MODULATED OPTICAL FORCE MICROSCOPY
    • 使用空间调制光学力学显微镜检测细胞的可变性的装置和方法
    • WO2007047761A1
    • 2007-04-26
    • PCT/US2006/040715
    • 2006-10-17
    • ARRYX, INC.AKCAKIR, Osman
    • AKCAKIR, Osman
    • G01B9/02
    • G01Q20/02G01N21/6456G01Q30/04G01Q60/20G03H2001/0077
    • The present invention utilizes spatially modulated optical force microscopy (SMOFM) with single beam optical force probing capability or with a holographic optical trapping system capable of multi-beam optical force probing coupled to a microscope objective, to generate a probe beam(s) as a force probe to perturb the object that is adhered or resting on a surface, so that deformations of the object may subsequently be quantified. This quantification is performed by imaging a sequence of four phase shifted replicas of the image using a computer-controlled spatial light modulator, and calculating the pixel by pixel optical path-length using existing algorithms. The change in optical path lengths, and consequently the viscoelastic or elastic response elicited, is an indication of damage or disease when the objects are cells. In another embodiment, the optical deformability of the cells may be measured and correlated with measurements of cytoskeletal/structural protein expression.
    • 本发明利用具有单光束光学力探测能力的空间调制光学力学显微镜(SMOFM)或利用能够与显微镜物镜耦合的多光束光学力探测的全息光学捕获系统,以产生探针光束 强力探测器扰乱粘附或搁置在表面上的物体,从而可以随后量化物体的变形。 该量化通过使用计算机控制的空间光调制器对图像的四个相移副本的序列进行成像,并使用现有算法计算逐像素光程长度来执行。 光路长度的变化以及因此引起的粘弹性或弹性响应是当物体是细胞时的损伤或疾病的指示。 在另一个实施方案中,可以测量细胞的光学可变形性并与细胞骨架/结构蛋白质表达的测量相关。
    • 7. 发明申请
    • METHODS AND DEVICES FOR IMMUNODIAGNOSTIC APPLICATIONS
    • 免疫组化应用的方法和装置
    • WO2014025895A1
    • 2014-02-13
    • PCT/US2013/053960
    • 2013-08-07
    • ARRYX, INC.
    • KNUTSON, Christopher, R.KURELLA, SrideviDOORNEWEERD, Derek, D.GRANT, Christopher, F.KLINE, Timothy, R.
    • G01N33/80G01N33/68
    • G01N33/80G01N33/6854
    • Methods and devices for evaluating a sample, e.g., a plasma sample, from a subject, for detecting a target red blood cell protein or antibody are disclosed. In one embodiment, optimized antibody screening methods and devices significantly reduce the level of non-specific binding to a surface (e.g., a test surface bound with a red blood cell (rbcm) preparation), thus allowing for more efficient detection and reduced test time. In one embodiment, the optimized antibody screening method includes an immunoglobulin G (IgG) binding moiety that binds selectively and specifically to the plasma IgG present relative to the binding to the lysed rbcm preparation. In another embodiment, an optimized antibody screening method is disclosed whereby non-specific binding caused by lysed red blood cell membrane preparations can be reduced by an agent that specifically cleaves a human IgG in the hinge region. In other embodiments, the invention provides methods and devices for target capturing that include a substantially planar surface, optionally having an optimized angle, for capture. Alternative solid phase geometries for capture are disclosed. Optimized methods for cell deposition are also disclosed. Thus, optimized methods, devices, kits, assays for evaluating a sample are disclosed.
    • 公开了用于评估来自受试者的用于检测靶红细胞蛋白或抗体的样品例如血浆样品的方法和装置。 在一个实施方案中,优化的抗体筛选方法和装置显着降低与表面的非特异性结合的水平(例如,与红细胞(rbcm)制剂结合的测试表面),从而允许更有效的检测和减少的测试时间 。 在一个实施方案中,优化的抗体筛选方法包括免疫球蛋白G(IgG)结合部分,所述免疫球蛋白G(IgG)结合部分相对于与裂解的rbcm制剂结合而选择性且特异性地结合存在的血浆IgG。 在另一个实施方案中,公开了优化的抗体筛选方法,其中由裂解的红细胞膜制剂引起的非特异性结合可以通过在铰链区中特异性切割人IgG的试剂降低。 在其他实施例中,本发明提供了用于目标捕获的方法和装置,其包括可选地具有优化角度的基本平坦的表面,用于捕获。 公开了用于捕获的替代固相几何形状。 还公开了细胞沉积的优化方法。 因此,公开了用于评估样品的优化方法,装置,试剂盒测定。