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    • 1. 发明授权
    • Method for detecting and controlling flow rates of the droplet forming
stream of an electrostatic particle sorting apparatus
    • 用于检测和控制静电颗粒分选装置的液滴形成流的流速的方法
    • US4325483A
    • 1982-04-20
    • US68231
    • 1979-08-20
    • Igino LombardoDonald E. BarryW. Peter Hansen
    • Igino LombardoDonald E. BarryW. Peter Hansen
    • G01N15/14B07C5/342
    • G01N15/1404G01N2015/1406G01N2015/149Y10S209/906
    • A novel method is disclosed for detecting and controlling the flow rate of a perturbed, droplet-forming stream in an electrostatic particle sorting apparatus. Detection apparatus is located at two points along the stream, at a first particle sensing point for sensing the presence of particles within a core portion of the stream, and at a second downstream point, preferably the stream breakpoint, for sensing light scatter and extinction characteristics which are proportional to the surface characteristics of the sheath portion of the stream. Changes in phase shift, pulse width, duty cycle, pulse area, or breakpoint location are detected by analyzing these sheath surface-related characteristics. An error signal is produced in response to such changes which drives an electromechanical fluid flow regulator to increase or decrease the fluid flow rate in a direction which tends to minimize the error signal. The flow rate is thus maintained at a reference flow rate setting.
    • 公开了一种用于检测和控制静电颗粒分选装置中扰动的液滴形成流的流速的新方法。 检测装置位于沿着流的两个点处,在用于感测流的核心部分内的颗粒的存在的第一颗粒感测点处,以及在第二下游点,优选地,流断点处,用于感测光散射和消光特性 其与流的护套部分的表面特性成比例。 通过分析这些鞘表面相关特征来检测相移,脉冲宽度,占空比,脉冲区域或断点位置的变化。 响应于这样的变化而产生误差信号,这些变化驱动机电流体流量调节器以使倾向于最小化误差信号的方向增加或减小流体流速。 因此,流速保持在参考流量设置。
    • 2. 发明授权
    • Method and apparatus for positioning the point of droplet formation in
the jetting fluid of an electrostatic sorting device
    • 用于在静电分选装置的喷射流体中定位液滴形成点的方法和装置
    • US4318480A
    • 1982-03-09
    • US068113
    • 1979-08-20
    • Igino LombardoW. Peter Hansen
    • Igino LombardoW. Peter Hansen
    • B03C5/00G01N15/14G01N33/49B07C5/342
    • G01N15/1404G01N2015/1406G01N2015/149Y10S209/906
    • A novel method for positioning the point of droplet formation in the jetting fluid of an electrostatic sorting device is disclosed. The formation of the uniform droplets is carried out via the application of vibrational energy inparted by a transducer to a jetting laminar flow stream. Previously sensed particles contained within the core portion of the laminar stream are subsequently sorted from the stream as part of a subsequently formed droplet. The disclosed method uses the dependency of the droplet formation point on the amplitude of the wave form applied to the transducer and the modulation of this amplitude to control the droplet formation point distance. The position of the droplet formation point is detected via the use of a light source and photodetector focused on the jetting stream at the position at which the droplet formation point is to be located, and a method for automatically maintaining the breakpoint at that position is described.
    • 公开了一种用于将静电分选装置的喷射流体中的液滴形成点定位的新颖方法。 均匀液滴的形成是通过将由换能器携带的振动能施加到喷射层流来进行的。 包含在层流芯的核心部分内的先前感测的颗粒随后从流中分离,作为随后形成的液滴的一部分。 所公开的方法使用液滴形成点对施加到换能器的波形的幅度的依赖性以及该幅度的调制以控制液滴形成点距离。 液滴形成点的位置通过使用聚焦在液滴形成点所在的位置处的喷射流的光源和光电检测器来检测,并且描述用于自动保持该位置处的断点的方法 。
    • 5. 发明授权
    • Light scatter-based immunoassay
    • 基于光散射的免疫测定
    • US06200820B1
    • 2001-03-13
    • US08473187
    • 1995-06-07
    • W. Peter HansenMichael CennerazzoCarl Theodore EdensManish Kochar
    • W. Peter HansenMichael CennerazzoCarl Theodore EdensManish Kochar
    • G01N33543
    • G01N33/54346G01N15/0205G01N15/14G01N33/553
    • Disclosed are an optical flow particle apparatus and method for conducting a particle light scatter-based immunoassay for simultaneously measuring the presence or amount of one or more analytes in a fluid sample which involves the use of a reagent set for each analyte including first binding molecule-coated monodisperse microspheres and second binding molecule-coated colloidal particles in which at least one of the first or second binding molecules specifically binds a respective one of the analytes. In the case where more than one analytes are detected, each monodisperse microperse microsphere of a particular reagent set has a light scatter signal resolvable from that of microspheres of any other reagent set. Changes determined in the distributions of the measured light scatter signals for individual microspheres of each of the particular reagent sets are indicative of the presence or amount of the respective analyte(s) in the sample.
    • 公开了一种用于同时测量流体样品中一种或多种分析物的存在或量的用于进行基于粒子光散射的免疫测定的光学流动颗粒装置和方法,其涉及使用每种分析物的试剂组,包括第一结合分子 - 涂覆的单分散微球和第二结合分子涂覆的胶体颗粒,其中第一或第二结合分子中的至少一个特异性结合相应的一种分析物。 在检测到多于一种分析物的情况下,特定试剂组的每个单分散微粉末微球具有可从任何其它试剂组的微球分解的光散射信号。 每个特定试剂组的单个微球的测量的光散射信号的分布中确定的变化指示样品中相应分析物的存在或量。
    • 8. 发明授权
    • Binding assays using optical resonance of colloidal particles
    • 使用胶体颗粒的光学共振的结合测定
    • US06413786B1
    • 2002-07-02
    • US09372444
    • 1999-08-11
    • W. Peter HansenPetra Krauledat
    • W. Peter HansenPetra Krauledat
    • G01N33553
    • G01N33/54346C12Q1/6816G01N33/54313G01N33/553G01N33/585G01N33/587Y10S435/975Y10S436/805Y10S436/808C12Q2565/632C12Q2563/149C12Q2537/101C12Q2545/114
    • A device and a method enable the rapid, quantitative evaluation of a large collection of ligands for binding affinity with a certain immobilized receptor, the improvements being that binding pan be detected without the need for a label and that binding is carried out in solution phase at a high rate. The instrument has at least two embodiments, one is based on a sensitive absorption photometer and the other on a sensitive light scatter photometer operating at a specific resonance wavelength, &lgr;R, of small, metallic, colloidal particles. The resonance is present in small particles having a complex refractive index with real part n(&lgr;) approaching 0 and imaginary part k(&lgr;) approaching 2 simultaneously at a specific wavelength &lgr;R. The particles are substantially spherical and substantially smaller than &lgr;R. The receptor is immobilized on a suspension of such particles and ligand binding is detected by a change in optical absorption or light scatter at the resonance wavelength.
    • 一种装置和方法使得能够快速,定量地评估大量的配体与一定固定化受体结合亲和力的配体,改进之处在于检测结合盘而不需要标记,并且在溶液相中进行结合 高利率。 仪器具有至少两个实施例,一个是基于敏感的吸收光度计,另一个基于在小的金属,胶体颗粒的特定共振波长(lambdR)下操作的敏感光散射光度计上。 共振存在于具有复数折射率的小颗粒中,实际部分n(lambd)接近0,虚部k(lambd)在特定波长lambdR下同时接近2。 颗粒基本上是球形的并且基本上小于lambdR。 受体被固定在这样的颗粒的悬浮液上,通过在共振波长处的光吸收或光散射的变化来检测配体结合。
    • 9. 发明授权
    • Light scatter-based immunoassay without particle self aggregation
    • 基于光散射的免疫测定,无颗粒自聚集
    • US5589401A
    • 1996-12-31
    • US286778
    • 1994-08-05
    • W. Peter HansenMichael Cennerazzo
    • W. Peter HansenMichael Cennerazzo
    • G01N15/02G01N15/14G01N33/543G01N33/553G01N33/538G01N33/544
    • G01N15/14G01N33/54313G01N33/553G01N15/0205
    • A homogeneous immunoassay method for the simultaneous determination of one or more antibody, antigen or hapten analytes in a fluid sample, that comprises the quantification of the effect of said analytes on the statistical changes in a dimension of a light scatter pulse height distribution histogram of relatively large diameter monodisperse binding molecule-coated polymeric microspheres induced by the binding to said microspheres of polydisperse binding molecule-coated colloid metal particles of relatively small diameter. For simultaneous assays of multiple analytes, different diameter or refractive index microspheres are assigned to each analyte. The assay may be used in forward binding, displacement, inhibition, and competition type systems, with the direction of the change in histogram dimension depending on the system. A convenient dimension to measure is the normalized peak width of a graphical representation of the histogram. For simultaneous assays for multiple analytes, a monodisperse polymeric microsphere of unique diameter or refractive index is dedicated to each analyte, so as to generate multiple histograms, one for each analyte. Polydisperse binding molecule-coated colloid metal particles, when used in effective concentrations, will also serve as a scavenger means to reduce the interfering effects of non-specific substances in the analyte-containing fluid samples, particularly when said samples are of biological origin.
    • 用于同时测定流体样品中一种或多种抗体,抗原或半抗原分析物的均匀免疫测定方法,其包括对所述分析物对相对较轻的光散射脉冲高度分布直方图的维度的统计变化的量化的量化 通过与所述微球体结合相对小直径的多分散结合分子包被的胶体金属颗粒诱导的大直径单分散结合分子包被的聚合物微球。 对于多个分析物的同时测定,将不同直径或折射率微球分配给每个分析物。 该测定可用于正向结合,置换,抑制和竞争类型系统,其中取决于系统的直方图尺寸的变化方向。 一个方便的测量尺寸是直方图的图形表示的归一化峰宽。 对于多个分析物的同时测定,独特直径或折射率的单分散聚合物微球专用于每个分析物,以便产生多个直方图,每个分析物一个。 当以有效浓度使用时,多分散结合分子涂覆的胶体金属颗粒也将用作清除剂手段,以减少非特异性物质在含分析物的流体样品中的干扰作用,特别是当所述样品是生物来源时。