Miniaturized spectometer using optical waveguide and integrated Raman system on-chip
    1.
    发明申请
    Miniaturized spectometer using optical waveguide and integrated Raman system on-chip 有权
    微型光谱仪采用光波导和集成拉曼系统片上

    公开(公告)号:US20070077595A1

    公开(公告)日:2007-04-05

    申请号:US11239100

    申请日:2005-09-30

    IPC分类号: G01N33/53 G01J3/45 G01B9/02

    摘要: One embodiment relates to an analyzer having an interferometer, a detector and a microprocessor, wherein the analyzer does not contain a spectrometer having a dispersive grating, the interferometer is to create a phase shift in an original spectrum of electromagnetic radiation emitted from a sample and Fourier transform the original spectrum to a Fourier transform spectrum, the detector is to detect a characteristic of the Fourier transform spectrum, and the microprocessor comprises software or a hardware to inverse transform the Fourier transform spectrum and reproduce the original spectrum. Another embodiment relates to a Raman analyzer having an interferometer, wherein the Raman analyzer contains no dispersive grating or moving parts and has an ability to analyze a Raman signal. The embodiments of the invention could be used for analyzing a sample by striking a laser to the sample and examining the spectrum of the emitted electromagnetic radiation from the sample.

    摘要翻译: 一个实施例涉及一种具有干涉仪,检测器和微处理器的分析仪,其中分析仪不包含具有分散光栅的光谱仪,干涉仪将在从样品和傅里叶发射的电磁辐射的原始光谱中产生相移 将原始频谱转换为傅里叶变换频谱,检测器检测傅里叶变换频谱的特性,微处理器包括软件或硬件,对傅立叶变换频谱进行逆变换,再现原始频谱。 另一个实施方案涉及具有干涉仪的拉曼分析仪,其中拉曼分析仪不含分散光栅或运动部件,并且具有分析拉曼信号的能力。 本发明的实施例可以用于通过将激光撞击到样品并检查来自样品的发射的电磁辐射的光谱来分析样品。

    Cellular analysis using Raman surface scanning
    2.
    发明授权
    Cellular analysis using Raman surface scanning 有权
    使用拉曼表面扫描的细胞分析

    公开(公告)号:US07776547B2

    公开(公告)日:2010-08-17

    申请号:US11027470

    申请日:2004-12-30

    IPC分类号: G01N33/53

    摘要: Methods and apparatus are provided for assaying cell samples, which may be living cells, using probes labeled with composite organic-inorganic nanoparticles (COINs) and microspheres with COINs embedded within a polymer matrix to which the probe moiety is attached. COINs intrinsically produce SERS signals upon laser irradiation, making COIN-labeled probes particularly suitable in a variety of methods for assaying cells, including biological molecules that may be contained on or within cells, most of which are not inherently Raman-active. The invention provides variations of the sandwich immunoassay employing both specific and degenerate binding, methods for reverse phase assay of tissue samples and cell microstructures, in solution displacement and competition assays, and the like. Systems and chips useful for practicing the invention assays are also provided.

    摘要翻译: 提供了用于使用用复合有机 - 无机纳米颗粒(COIN)标记的探针和嵌入探针部分所连接的聚合物基质内的COIN的微球来测定可能为活细胞的细胞样品的方法和装置。 COIN在激光照射下固有地产生SERS信号,使得COIN标记的探针特别适用于多种测定细胞的方法,包括可能包含在细胞内或细胞内的生物分子,其中大部分不是固有的拉曼活性的。 本发明提供使用特异性和简并结合的夹心免疫测定的变体,组织样品和细胞微结构的反相测定方法,溶液置换和竞争测定等。 还提供了用于实施本发明测定的系统和芯片。

    Programmable molecular barcodes
    4.
    发明申请
    Programmable molecular barcodes 审中-公开
    可编程分子条形码

    公开(公告)号:US20070054288A1

    公开(公告)日:2007-03-08

    申请号:US11430612

    申请日:2006-05-08

    IPC分类号: C12Q1/68 C12M1/34 G06K7/10

    摘要: The present disclosure concerns methods for producing and/or using molecular barcodes. In certain embodiments of the invention, the barcodes comprise polymer backbones that may contain one or more branch structures. Tags may be attached to the backbone and/or branch structures. The barcode may also comprise a probe that can bind to a target, such as proteins, nucleic acids and other biomolecules or aggregates. Different barcodes may be distinguished by the type and location of the tags. In other embodiments, barcodes may be produced by hybridization of one or more tagged oligonucleotides to a template, comprising a container section and a probe section. The tagged oligonucleotides may be designed as modular code sections, to form different barcodes specific for different targets. In alternative embodiments, barcodes may be prepared by polymerization of monomeric units. Bound barcodes may be detected by various imaging modalities, such as, surface plasmon resonance, fluorescent or Raman spectroscopy.

    摘要翻译: 本公开涉及用于生产和/或使用分子条形码的方法。 在本发明的某些实施方案中,条形码包含可包含一个或多个分支结构的聚合物主链。 标签可以附加到骨干和/或分支结构。 条形码还可以包含可以与靶标结合的探针,例如蛋白质,核酸和其他生物分子或聚集体。 可以通过标签的类型和位置区分不同的条形码。 在其它实施方案中,条形码可以通过将一个或多个标记的寡核苷酸与包含容器部分和探针部分的模板杂交来产生。 标记的寡核苷酸可以被设计为模块代码部分,以形成针对不同靶标的不同条形码。 在替代实施例中,条形码可以通过单体单元的聚合来制备。 可以通过各种成像方式,例如表面等离子体共振,荧光或拉曼光谱来检测结合条形码。

    Detecting molecular binding by monitoring feedback controlled cantilever deflections
    6.
    发明申请
    Detecting molecular binding by monitoring feedback controlled cantilever deflections 有权
    通过监测反馈控制的悬臂偏转来检测分子结合

    公开(公告)号:US20050244820A1

    公开(公告)日:2005-11-03

    申请号:US11111308

    申请日:2005-04-20

    摘要: The present methods and apparatus concern the detection and/or identification of target analytes using probe molecules. In various embodiments of the invention, the probes or analytes are attached to one or more cantilevers. Binding of a probe to an analyte results in deflection of the cantilever, detected by a detection unit. A counterbalancing force may be applied to restore the cantilever to its original position. The counterbalancing force may be magnetic, electrical or radiative. The detection unit and the mechanism generating the counterbalancing force may be operably coupled to an information processing and control unit, such as a computer. The computer may regulate a feedback loop that maintains the cantilever in a fixed position by balancing the deflecting force and the counterbalancing force. The concentration of analytes in a sample may be determined from the magnitude of the counterbalancing force required to maintain the cantilever in a fixed position.

    摘要翻译: 本方法和装置涉及使用探针分子检测和/或鉴定目标分析物。 在本发明的各种实施方案中,探针或分析物附着到一个或多个悬臂。 将探针与分析物结合导致由检测单元检测到的悬臂的偏转。 可以应用平衡力将悬臂恢复到其原始位置。 平衡力可以是磁性的,电的或辐射的。 生成平衡力的检测单元和机构可以可操作地耦合到诸如计算机的信息处理和控制单元。 计算机可以通过平衡偏转力和平衡力来调节将悬臂维持在固定位置的反馈回路。 样品中分析物的浓度可以从将悬臂维持在固定位置所需的平衡力的大小来确定。

    Method for sequencing nucleic acids by observing the uptake of nucleotides modified with bulky groups
    7.
    发明申请
    Method for sequencing nucleic acids by observing the uptake of nucleotides modified with bulky groups 审中-公开
    通过观察用大体积改性的核苷酸摄取来测序核酸的方法

    公开(公告)号:US20050026163A1

    公开(公告)日:2005-02-03

    申请号:US10705389

    申请日:2003-11-10

    摘要: The present methods and apparatus concern nucleic acid sequencing by incorporation of nucleotides into nucleic acid strands. The incorporation of nucleotides is detected by changes in the mass and/or surface stress of the structure. In some embodiments of the invention, the structure comprises one or more nanoscale or microscale cantilevers. In certain embodiments of the invention, each different type of nucleotide is distinguishably labeled with a bulky group and each incorporated nucleotide is identified by the changes in mass and/or surface stress of the structure upon incorporation of the nucleotide. In alternative embodiments of the invention only one type of nucleotide is exposed at a time to the nucleic acids. Changes in the properties of the structure may be detected by a variety of methods, such as piezoelectric detection, shifts in resonant frequency of the structure, and/or position sensitive photodetection.

    摘要翻译: 本发明的方法和装置涉及通过将核苷酸掺入核酸链而进行的核酸测序。 通过结构的质量和/或表面应力的变化来检测核苷酸的掺入。 在本发明的一些实施例中,该结构包括一个或多个纳米级或微尺寸悬臂。 在本发明的某些实施方案中,每种不同类型的核苷酸可以用大体积区分地标记,并且每个掺入的核苷酸通过结合核苷酸时结构的质量和/或表面应力的变化来鉴定。 在本发明的替代实施方案中,一次仅将一种类型的核苷酸暴露于核酸。 可以通过各种方法来检测结构的性质的变化,例如压电检测,结构的谐振频率偏移和/或位置敏感的光电检测。

    Method for sequencing nucleic acids by observing the uptake of nucleotides modified with bulky groups
    9.
    发明申请
    Method for sequencing nucleic acids by observing the uptake of nucleotides modified with bulky groups 审中-公开
    通过观察用大体积改性的核苷酸摄取来测序核酸的方法

    公开(公告)号:US20070059733A1

    公开(公告)日:2007-03-15

    申请号:US11445884

    申请日:2006-06-02

    IPC分类号: C12Q1/68 G06F19/00 C12M3/00

    摘要: The present methods and apparatus concern nucleic acid sequencing by incorporation of nucleotides into nucleic acid strands. The incorporation of nucleotides is detected by changes in the mass and/or surface stress of the structure. In some embodiments of the invention, the structure comprises one or more nanoscale or microscale cantilevers. In certain embodiments of the invention, each different type of nucleotide is distinguishably labeled with a bulky group and each incorporated nucleotide is identified by the changes in mass and/or surface stress of the structure upon incorporation of the nucleotide. In alternative embodiments of the invention only one type of nucleotide is exposed at a time to the nucleic acids. Changes in the properties of the structure may be detected by a variety of methods, such as piezoelectric detection, shifts in resonant frequency of the structure, and/or position sensitive photodetection.

    摘要翻译: 本发明的方法和装置涉及通过将核苷酸掺入核酸链而进行的核酸测序。 通过结构的质量和/或表面应力的变化来检测核苷酸的掺入。 在本发明的一些实施例中,该结构包括一个或多个纳米级或微尺寸悬臂。 在本发明的某些实施方案中,每种不同类型的核苷酸可以用大体积区分地标记,并且每个掺入的核苷酸通过结合核苷酸时结构的质量和/或表面应力的变化来鉴定。 在本发明的替代实施方案中,一次仅将一种类型的核苷酸暴露于核酸。 可以通过各种方法来检测结构的性质的变化,例如压电检测,结构的谐振频率偏移和/或位置敏感的光电检测。