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    • 1. 发明申请
    • NONLINEAR MAGNETOPHORETIC SEPARATION OF BIOLOGICAL SUBSTANCES
    • 生物物质的非线性磁共振分离
    • US20100279887A1
    • 2010-11-04
    • US12452031
    • 2008-06-14
    • Gil U. LeeBenjamin YellenRandall Morgan Erb
    • Gil U. LeeBenjamin YellenRandall Morgan Erb
    • C40B30/04C40B40/18
    • G01N27/745
    • A method of separating a target biological analyte from a mixture of substances in a fluid sample employs nonlinear magnetophoresis. Magnetic particles having the capacity to bind to the target analyte are contacted with the fluid sample so that the analyte is immobilized on the surface of at least some of the particles. The magnetic particles are provided adjacent an array of micromagnets patterned on a substrate so that the particles are attracted the micromagnets. The magnetic particles are then subjected to a traveling magnetic field operating at or above a frequency effective to sweep those particles not bound to analyte to an adjacent micromagnet. Those magnetic particles bound to analyte have a larger size or smaller magnetic moment that prevents them from being moved to adjacent micromagnets, thereby affording separation of the analyte.
    • 从流体样品中的物质混合物中分离目标生物分析物的方法采用非线性磁电泳法。 具有结合目标分析物的能力的磁性颗粒与流体样品接触,使得分析物固定在至少一些颗粒的表面上。 磁性颗粒被设置在图案化在基板上的微阵列附近,使得颗粒被吸引到微型磁体。 然后磁性颗粒经受有效扫描未结合分析物的颗粒到相邻微型磁体上或高于频率的行进磁场。 与分析物结合的那些磁性颗粒具有更大的尺寸或更小的磁矩,从而防止它们被移动到相邻的微型磁体,从而提供分析物的分离。
    • 3. 发明授权
    • Chemical and biological sensor using an ultra-sensitive force transducer
    • 化学和生物传感器使用超灵敏力传感器
    • US5807758A
    • 1998-09-15
    • US505547
    • 1995-07-21
    • Gil U. LeeDavid A. KidwellRichard J. Colton
    • Gil U. LeeDavid A. KidwellRichard J. Colton
    • B81B3/00C12Q1/68C12Q1/70G01N33/543G01Q90/00G01N27/00G01N33/573C01N33/573
    • G01Q60/42B82Y35/00G01N27/745G01N33/54373
    • The present invention is a method and apparatus for detecting a target species. The target molecule may be in liquid phase (in solution) or (for some embodiments of the invention) in vapor phase. A sensor according to the present invention monitors whether a target species has selectively bound to groups on the cantilever surface by monitoring the displacement of the cantilever, and hence the force acting on the cantilever. This force acting on the cantilever arises from the force acting on a structure that moves in electric or magnetic field, and that may be selectively bound to the cantilever. In the case of target species having a sufficiently large net electric charge or dipole moment, the target species itself may serve as the structure that moves in an electric field. More typically however, separate modified structures, such as modified magnetic beads or modified beads having a net charge or a dipole moment, will, when selectively bound to the cantilever, exert a force on the cantilever that relates to the presence of the target species.
    • 本发明是用于检测目标物种的方法和装置。 靶分子在气相中可以是液相(溶液中)或(对于本发明的一些实施方案)。 根据本发明的传感器通过监测悬臂的位移以及因此作用在悬臂上的力来监视目标物种是否选择性地结合到悬臂表面上的组。 作用在悬臂上的力源自作用在电场或磁场中移动的结构上的力,并且可以选择性地结合到悬臂。 在具有足够大的净电荷或偶极矩的目标物种的情况下,目标物质本身可以用作在电场中移动的结构。 然而,更典型地,单独的改性结构,例如具有净电荷或偶极矩的改性磁珠或改性珠粒,当选择性地结合到悬臂时,将在悬臂上施加与靶物种的存在有关的力。
    • 4. 发明授权
    • Polymer coated microparticles
    • 聚合物涂层微粒
    • US08715739B2
    • 2014-05-06
    • US11552324
    • 2006-10-24
    • Gil U. LeeHao ShangWon-Suk Chang
    • Gil U. LeeHao ShangWon-Suk Chang
    • A61K9/50
    • B01J2/06A61K41/0028A61K41/0052A61K49/1887B01J13/12B01J13/14B82Y5/00B82Y25/00H01F1/0054
    • Methods for preparing uniformly sized micropanicles, with an optional polymeric coating generally include: 1) providing nanoparticles, preferably having a size of between 1 nm and 100 nm; 2) adding a hydrophobic surface layer to the nanoparticles; 3) making a suspension of the hydrophobic nanoparticles and a polymerization initiator in an hydrophobic solvent; 4) dissolving a monomer in the hydrophobic solvent; 5) making an emulsion by dispersing droplets of the hydrophobic solvent in a continuous aqueous phase with an emulsifier; 6) sizing the first emulsion to provide a second emulsion of the same components in which the droplets are substantially uniform and between 2 and 20 um in size; 7) evaporating at least a substantial portion of the dispersed hydrophobic droplets to assemble nanoparticles to form micropanicles suspended now in the aqueous phase; 8) replacing the first surfactant with a second surfactant, which is preferably a polymerizable surfactant; 9) adding a polymerizable monomer to the aqueous phase and allowing it to adsorb into the microparticle; 10) polymerizing the monomer(s) to provide a polymer layer on the micropanicles; and 11) functionalizing the polymer surface layer erf the micropanicles with one or more polymer, nanoparticle or biological macromolecular layers.
    • 用任选的聚合物涂层制备均匀尺寸的微粒子的方法通常包括:1)提供优选具有1nm至100nm尺寸的纳米颗粒; 2)向纳米颗粒中加入疏水表面层; 3)使疏水性纳米粒子和聚合引发剂在疏水性溶剂中的悬浮液; 4)将单体溶解在疏水溶剂中; 5)通过将疏水性溶剂的液滴与乳化剂分散在连续的水相中来制备乳液; 6)调整第一乳液的尺寸以提供相同组分的第二乳液,其中液滴基本上均匀且尺寸在2-20μm之间; 7)蒸发至少大部分分散的疏水液滴以组装纳米颗粒以形成现在悬浮于水相中的微球; 8)用优选可聚合表面活性剂的第二表面活性剂代替第一表面活性剂; 9)向水相中加入可聚合单体并使其吸附到微粒中; 10)聚合单体以在微粒上提供聚合物层; 和11)使用一种或多种聚合物,纳米颗粒或生物大分子层对聚合物表面层进行功能化。
    • 5. 发明授权
    • Force discrimination assay
    • 强制歧视测定
    • US06180418B2
    • 2001-01-30
    • US09008782
    • 1998-01-20
    • Gil U. Lee
    • Gil U. Lee
    • C12Q168
    • G01N27/745C12Q1/6816G01N33/54326G01N33/585C12Q2565/619C12Q2563/143
    • A sensor for a selected target species has (a) a substrate which has been chemically modified by attachment of substrate modifiers; (b) one or more magnetically active beads which have been chemically modified by attachment of bead modifiers, where these bead modifiers will have a binding affinity for the substrate modifiers in the presence of the target species, and a measurably different binding affinity for the substrate modifiers in the absence of the target species; (c) an adjustable source of a magnetic field for exerting a force on the beads; and (d) an imaging system, for observing and counting beads bound to the substrate. In a preferred embodiment, the invention further has a system for identifying clusters of beads, and for removing the effect of such clusters from measurements of the target analyte. As with other assays, the sensor relies on the ability of certain molecules to bind with specific target (analyte) molecules. By coating the beads and the substrate with appropriate molecules, the beads will (or will not) bind specifically to the substrate in the presence (or absence) of the target molecule. When a magnetic field is applied to the substrate, the magnetic beads will be pulled away from the substrate. If the beads are specifically bound to the substrate, however, the beads will be retained on the substrate, indicating the presence (or absence) of the target species.
    • 用于所选目标物种的传感器具有(a)通过附着底物改性剂化学改性的基底; (b)已经通过附着珠改性剂化学改性的一种或多种磁性活性珠,其中这些珠改性剂将在靶物质存在下对底物改性剂具有结合亲和性,并且对底物具有可测量的不同结合亲和力 没有目标物种的改性剂; (c)用于在珠上施加力的可调节磁场源; 和(d)用于观察和计数与基底结合的珠子的成像系统。 在优选的实施方案中,本发明还具有用于鉴定珠簇的系统,并且用于从所述目标分析物的测量中除去这些簇的影响。 与其他测定一样,传感器依赖于某些分子与特定靶(分析物)分子结合的能力。 通过用合适的分子涂布珠粒和底物,珠子将(或不会)在靶分子的存在(或不存在)下特异性结合底物。 当将磁场施加到基板时,磁珠将被从基板拉出。 然而,如果珠粒特异性地结合到底物上,则珠粒将保留在底物上,表明目标物质的存在(或不存在)。
    • 9. 发明授权
    • Method for measuring intramolecular forces by atomic force
    • 用原子力测量分子内力的方法
    • US5958701A
    • 1999-09-28
    • US272733
    • 1999-01-27
    • John-Bruce De Vault GreenAlexey NovoradovskyGil U. Lee
    • John-Bruce De Vault GreenAlexey NovoradovskyGil U. Lee
    • C12Q1/68G01Q30/20G01Q60/24
    • G01Q60/42B82Y35/00Y10S977/853Y10S977/863Y10S977/873Y10S977/881Y10S977/924
    • A method is disclosed for measuring intramolecular forces within a sample compound by providing an atomic force microscope that includes a sample support member and a cantilever. The sample support member has a plurality of protrusions, and each protrusion has an apical substrate region that has been chemically modified to have a sample compound immobilized thereon. The cantilever has a fixed end and a free end, the free end having a surface region that has been chemically modified to have a grasping compound immobilized thereon. To measure intramolecular forces within the sample compound, the relative position and orientation of the cantilever and the sample support member are controlled to select a particular protrusion and to allow a molecule of the grasping compound to bind with a molecule of the sample compound. Then, the relative position and orientation of the cantilever and the sample support member are controlled to vary the distance between the cantilever and the sample support member so that the forces exerted on the cantilever as the distance between the cantilever and the sample support member is varied and as the molecule of the sample compound is stretched between the cantilever and the sample support member can be measured.
    • 公开了一种用于通过提供包括样品支撑构件和悬臂的原子力显微镜来测量样品化合物内的分子内力的方法。 样品支撑构件具有多个突起,并且每个突起具有经化学修饰以固定其上的样品化合物的顶端基底区域。 悬臂具有固定端和自由端,自由端具有经化学修饰以具有固定在其上的抓握化合物的表面区域。 为了测量样品化合物内的分子内力,控制悬臂和样品支撑构件的相对位置和取向以选择特定的突起并使得抓握化合物的分子与样品化合物的分子结合。 然后,控制悬臂和样品支撑构件的相对位置和取向以改变悬臂和样品支撑构件之间的距离,使得当悬臂与样品支撑构件之间的距离变化时施加在悬臂上的力 并且可以测量样品化合物的分子在悬臂和样品支撑构件之间的拉伸。