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    • 5. 发明公开
    • MICROSCALE DIFFUSION IMMUNOASSAY
    • DIFFUSIONSIMMUNOASSAY IM MIKROMASSSTAB
    • EP1179181A4
    • 2004-12-29
    • EP00932644
    • 2000-05-19
    • UNIV WASHINGTON
    • WEIGL BERNHARD HYAGER PAULKAMHOLZ ANDREWHATCH ANSON
    • G01N30/00G01N33/532G01N33/558B01D11/00B01D11/04G01N15/06G01N21/00G01N21/29G01N21/41G01N21/47G01N33/00G01N33/48G01N33/543G01N33/557
    • G01N33/558G01N30/0005
    • Methods and apparatuses are provided for determining presence and concentration of analytes by exploiting molecular binding reactions and differential diffusion rates. Analyte particles and binding particles are allowed to diffuse toward each other, and slowing of the diffusion front is detected when they meet. From the position of the diffusion front, presence and concentration of analyte particles can be determined. One embodiment provides a competitive immunoassay in a microfluidic format. This diffusion immunoassay (DIA) relies on measuring the concentration of labeled antigen along one dimension of a microchannel after allowing it to diffuse for a short time into a region containing specific antibodies. A simple microfluidic device, the T-Sensor, was used to implement a DIA to measure the concentration of phenytoin, a small drug molecule. Concentrations of analyte over the range of 50 to 1600 nM can be measured in less than a minute. The assay is homogenous, rapid, requires only microliter volumes of reagents and sample, and is applicable to a wide range of analytes, including therapeutic drugs, molecular biological markers, and environmental contaminants. Methods for separating particles of similar size in a diffusion separator are also provided.
    • 提供了通过利用分子结合反应和差异扩散速率来确定分析物的存在和浓度的方法和设备。 允许分析物颗粒和结合颗粒朝向彼此扩散,并且当它们相遇时检测到扩散前沿的减慢。 从扩散前沿的位置可以确定分析物颗粒的存在和浓度。 一个实施方案提供微流体形式的竞争性免疫测定。 该扩散免疫测定法(DIA)依赖于在允许其短时间扩散到含有特异性抗体的区域中后,沿着微通道的一维测量标记抗原的浓度。 使用简单的微流体装置T传感器来实施DIA以测量苯妥英(一种小分子药物)的浓度。 在不到一分钟的时间内可以测量50至1600 nM范围内的分析物浓度。 该检测方法均匀,快速,只需要微升体积的试剂和样品,适用于各种分析物,包括治疗药物,分子生物标志物和环境污染物。 还提供了用于在扩散分离器中分离相似尺寸的颗粒的方法。
    • 8. 发明申请
    • WAVELENGTH TUNABLE SURFACE PLASMON RESONANCE SENSOR
    • 波长能表面等离子体共振传感器
    • WO2004040717A2
    • 2004-05-13
    • PCT/US0334265
    • 2003-10-28
    • UNIV WASHINGTONYAGER PAULFU ELAIN S
    • YAGER PAULFU ELAIN S
    • G01N21/55H01S
    • G01N21/553G01N21/648
    • This invention provides methods, devices and device components for sensing, imaging and characterizing changes in the composition of a probe region. More particularly, the present invention provides methods and devices for detecting changes in the refractive index of a probe region positioned adjacent to a sensing surface, preferably a sensing surface comprising a thin conducting film supporting surface plasmon formation. In addition, the present invention provides methods and device for generating surface plasmons in a probe region and characterizing the composition of the probe region by generating one or more surface plasmon resonances curves and/or surface plasmon resonance images of the probe region.
    • 本发明提供用于感测,成像和表征探针区域的组成的变化的方法,装置和装置部件。 更具体地,本发明提供了用于检测位于邻近检测表面的探针区域的折射率变化的方法和装置,优选地包括支撑表面等离子体激元形成的薄导电膜的感测表面。 此外,本发明提供了用于在探针区域中产生表面等离子体激元的方法和装置,并且通过产生探针区域的一个或多个表面等离子体共振曲线和/或表面等离子体共振图像来表征探针区域的组成。
    • 10. 发明申请
    • MICROSCALE DIFFUSION IMMUNOASSAY
    • WO0072020A9
    • 2002-08-29
    • PCT/US0013864
    • 2000-05-19
    • UNIV WASHINGTON
    • WEIGL BERNHARD HYAGER PAULKAMHOLZ ANDREWHATCH ANSON
    • G01N30/00G01N33/532G01N33/558B01D11/00B01D11/04G01N15/06G01N21/00G01N21/29G01N21/41G01N21/47G01N33/00G01N33/48G01N33/543G01N33/557
    • G01N33/558G01N30/0005
    • Methods and apparatuses are provided for determining presence and concentration of analytes by exploiting molecular binding reactions and differential diffusion rates. Analyte particles and binding particles are allowed to diffuse toward each other, and slowing of the diffusion front is detected when they meet. From the position of the diffusion front, presence and concentration of analyte particles can be determined. One embodiment provides a competitive immunoassay in a microfluidic format. This diffusion immunoassay (DIA) relies on measuring the concentration of labeled antigen along one dimension of a microchannel after allowing it to diffuse for a short time into a region containing specific antibodies. A simple microfluidic device, the T-Sensor, was used to implement a DIA to measure the concentration of phenytoin, a small drug molecule. Concentrations of analyte over the range of 50 to 1600 nM can be measured in less than a minute. The assay is homogenous, rapid, requires only microliter volumes of reagents and sample, and is applicable to a wide range of analytes, including therapeutic drugs, molecular biological markers, and environmental contaminants. Methods for separating particles of similar size in a diffusion separator are also provided.
    • 提供了通过开发分子结合反应和差异扩散速率来确定分析物的存在和浓度的方法和装置。 允许分析物颗粒和结合颗粒彼此扩散,并且当它们相遇时检测到扩散前沿的减慢。 从扩散前沿的位置可以确定分析物颗粒的存在和浓度。 一个实施方案提供了以微流体形式的竞争性免疫测定。 这种扩散免疫测定(DIA)依赖于在允许其在短时间内扩散到含有特异性抗体的区域之后测量沿着微通道的一个维度的标记抗原的浓度。 使用简单的微流体装置T-Sensor来实施DIA来测量苯妥英(一种小药物分子)的浓度。 可以在不到一分钟的时间内测量分析物在50至1600nM范围内的浓度。 该测定法是均匀的,快速的,仅需要微量体积的试剂和样品,并且适用于广泛的分析物,包括治疗药物,分子生物标志物和环境污染物。 还提供了在扩散分离器中分离类似尺寸的颗粒的方法。