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    • 1. 发明授权
    • Method for detecting analyte(s) using magnetic colloidal particles
    • 使用磁性胶体颗粒检测分析物的方法
    • US07332353B2
    • 2008-02-19
    • US10496114
    • 2002-11-20
    • Jean BaudryJérôme BibetteAlain Rousseau
    • Jean BaudryJérôme BibetteAlain Rousseau
    • G01N33/553
    • G01N33/5434
    • The invention concerns a method for detecting and/or quantifying at least an analyte in a liquid medium, characterized in that it consists in using magnetic colloidal particles functionalized at the surface with at least a ligand specific of the analyte to be detected and/or assayed and in that it comprises: contacting said particles with said medium to be analyzed; applying a magnetic field to said medium, at an intensity sufficient to cause said magnetic particles to be structured in the form of chains; maintaining said magnetic field for a sufficient time interval to enable coupling or combination of the analyte concerned with at least two specific ligands present respectively on two neighbouring particles of a chain; cancelling the magnetic field, and determining the presence and/or absence of said analyte and, as the case may be, its concentration via the presence and/or the absence of said permanent chains of magnetic particles.
    • 本发明涉及用于检测和/或定量液体介质中的至少一种分析物的方法,其特征在于它使用在表面官能化的至少一种被检测和/或分析的分析物的配体特异性的磁性胶体颗粒 并且其包括:使所述颗粒与待分析的介质接触; 以足以使所述磁性颗粒以链的形式构造的强度向所述介质施加磁场; 保持所述磁场足够的时间间隔,以使所述分析物与分别存在于链的两个相邻颗粒上的至少两种特异性配体相耦合或组合; 消除磁场,并且通过所述永久磁性颗粒的存在和/或不存在来确定所述分析物的存在和/或不存在以及视情况而定的浓度。
    • 2. 发明申请
    • Method for detecting analyte(s) using magnetic colloidal particles
    • 使用磁性胶体颗粒检测分析物的方法
    • US20050048673A1
    • 2005-03-03
    • US10496114
    • 2002-11-20
    • Jean BaudryJerome BibetteAlain Rousseau
    • Jean BaudryJerome BibetteAlain Rousseau
    • G01N33/553C12N15/09C12Q1/68G01N21/78G01N33/53G01N33/543G01N33/566G01N33/569
    • G01N33/5434
    • The invention concerns a method for detecting and/or quantifying at least an analyte in a liquid medium, characterized in that it consists in using magnetic colloidal particles functionalized at the surface with at least a ligand specific of the analyte to be detected and/or assayed and in that it comprises: contacting said particles with said medium to be analyzed; applying a magnetic field to said medium, at an intensity sufficient to cause said magnetic particles to be structured in the form of chains; maintaining said magnetic field for a sufficient time interval to enable coupling or combination of the analyte concerned with at least two specific ligands present respectively on two neighbouring particles of a chain; cancelling the magnetic field, and determining the presence and/or absence of said analyte and, as the case may be, its concentration via the presence and/or the absence of said permanent chains of magnetic particles.
    • 本发明涉及用于检测和/或定量液体介质中的至少一种分析物的方法,其特征在于它使用在表面官能化的至少一种被检测和/或分析的分析物的配体特异性的磁性胶体颗粒 并且其包括:使所述颗粒与待分析的介质接触; 以足以使所述磁性颗粒以链的形式构造的强度向所述介质施加磁场; 保持所述磁场足够的时间间隔,以使所述分析物与分别存在于链的两个相邻颗粒上的至少两种特异性配体相耦合或组合; 消除磁场,并且通过所述永久磁性颗粒的存在和/或不存在来确定所述分析物的存在和/或不存在以及视情况而定的浓度。
    • 3. 发明授权
    • Unit cuvette for analyzing a biological fluid, automatic device for in vitro analysis
    • 用于分析生物液体的单位比色皿,用于体外分析的自动装置
    • US07959878B2
    • 2011-06-14
    • US12087492
    • 2007-01-17
    • Alain Rousseau
    • Alain Rousseau
    • B01L3/00
    • B01L3/50855B01L2200/025G01N21/03G01N35/025G01N2035/041G01N2035/0465
    • The bottom of the cuvette comprises a curved raceway placed so as to guide the oscillating movement of a ball inserted into the cuvette. In addition, the cuvette comprises means of attachment, in two perpendicular directions, to adjacent unit cuvettes. The cuvettes can thus be stored as plates in a feed magazine of an analytical device. The analytical device comprises several stations placed around a rotary ring. Only where it is desired to determine the clotting time of the blood contained in the cuvette a ball is introduced into the latter, at a ball distribution post. The cuvette equipped in this way is then brought to a station where the test is carried out. The major advantage of the invention is the polyvalence of the cuvette and of the analytical device.
    • 比色皿的底部包括弯曲的滚道,以便引导插入比色杯中的球的摆动运动。 此外,试管包括在两个垂直方向上连接到相邻的单位比色皿的装置。 因此,反应杯可以作为板储存在分析装置的进料仓中。 分析装置包括围绕旋转环放置的若干台。 只有在需要确定包含在比色杯中的血液的凝血时间的情况下,在球分配柱处将球引入后者。 以这种方式装备的比色杯然后被带到进行测试的工位。 本发明的主要优点是比色皿和分析装置的多价性。
    • 10. 发明授权
    • Gelled system and method for detecting microorganisms by separation and
culture on gelled system
    • 凝胶体系和通过分离和培养在凝胶体系上检测微生物的方法
    • US6020150A
    • 2000-02-01
    • US913757
    • 1997-09-22
    • Genevieve Contant-PussardFran.cedilla.oise Boisard-BeaupereJean-Luc MartinoliAlain Rousseau
    • Genevieve Contant-PussardFran.cedilla.oise Boisard-BeaupereJean-Luc MartinoliAlain Rousseau
    • C12M1/00C12M1/34C12Q1/02C12Q1/04C12Q1/24C12N1/02C12Q1/06C12Q1/08
    • C12Q1/04C12Q1/24Y10S435/975
    • A method for detecting the presence or absence of microorganisms belonging to the group which consists of bacteria and yeasts in a liquid sample (5) of a biological material. The method comprises placing the liquid sample (5) in a centrifuge tube (6a, 6b) above a gelled system (10) comprising at least (a) a first so-called development phase (1), i.e. a gel comprising a microorganism culture medium and a reagent for inducing a detectable optical measurement change in the presence of microorganisms, said gel being an intimate mixture of water and water-absorbing polymeric particles that have swelled in such a way that, in said intimate mixture, said polymeric particles have (.alpha.) a dry weight concentration of 0.05-0.2 g/ml, and (.beta.) a swollen-state diameter of 90-320 .mu.m, the water in the intimate mixture being at least partially provided by said culture medium; centrifuging; and revealing the presence or absence of microorganisms in said liquid sample (5) at said first phase (1) of the gelled system (10) by means of said reagent inducing a detectable optical measurement change.
    • PCT No.PCT / FR96 / 00419 Sec。 371日期:1997年9月22日 102(e)日期1997年9月22日PCT提交1996年3月20日PCT公布。 公开号WO96 / 29427 日期1996年9月26日在生物材料的液体样品(5)中检测属于由细菌和酵母组成的组的微生物的存在或不存在的方法。 该方法包括将液体样品(5)放置在凝胶系统(10)上方的离心管(6a,6b)中,所述凝胶系统(10)至少包含(a)第一所谓的显影相(1),即包含微生物培养物 介质和用于在微生物存在下诱导可检测的光学测量变化的试剂,所述凝胶是水和吸水聚合物颗粒的紧密混合物,其以这样的方式溶胀,使得在所述紧密混合物中所述聚合物颗粒具有 α)0.05-0.2g / ml的干重浓度,和(β)90-320μm的膨胀状态直径,紧密混合物中的水至少部分地由所述培养基提供; 离心; 并且通过所述试剂在凝胶系统(10)的所述第一阶段(1)处揭示所述液体样品(5)中存在或不存在微生物,从而引起可检测的光学测量变化。