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    • 4. 发明授权
    • Conservative whole blood sample preparation technique
    • 保守的全血样品制备技术
    • US5437985A
    • 1995-08-01
    • US726467
    • 1991-07-08
    • Jorge A. QuintanaThomas R. RussellRonald D. PaulTimothy J. Fischer
    • Jorge A. QuintanaThomas R. RussellRonald D. PaulTimothy J. Fischer
    • A01N1/02G01N1/30G01N33/48G01N33/50G01N33/53G01N33/543G01N33/569G01N33/58
    • G01N33/56972G01N1/30G01N33/5094Y10S435/962Y10T436/25125Y10T436/2525
    • The method of this invention is directed to the rapid preparation of a whole blood sample for photooptical analysis. In the preferred embodiments of this method, a whole blood sample, lytic reagent system and immunological stain (optional) are contacted with the sample in a common reaction vessel (i.e. cuvette or test tube), with gentle asymmetric vortex mixing, so as to maintain the particulate matter of the sample at an essentially homogeneous concentration throughout the sample. An aliquot of the contents of the reaction vessel can, thereafter, be analyzed for identification and/or quantification of the analyte of interest. This process is conservative of the various endogenous constituents of the sample since virtually all of the manipulative steps involved in the preparation of the sample occur within a common vessel and any excess (unconsumed or unreacted) reagents and stain need not be separated from the sample during such preparation, thus, avoiding the multiple wash steps traditionally associated with this process. This process is uniquely applicable to the conservative preparation of aged whole blood samples (samples in which the endogenous nutrients have been essentially completely consumed) and whole blood samples from diseased state patients wherein the disease is manifest by changes in the morphology, total number and/or relative concentration of one or more of the lymphocyte sub-populations (i.e. B and/or T-cells).
    • 本发明的方法涉及用于光学光学分析的全血样品的快速制备。 在该方法的优选实施方案中,将全血样品,溶解试剂系统和免疫染色剂(任选的)在常规反应容器(即比色杯或试管)中与样品接触,并进行温和的不对称涡旋混合,以保持 在整个样品中样品的颗粒物质基本上均匀。 然后分析反应容器的内容物的等分试样,以便鉴定和/或定量所关注的分析物。 该过程对于样品的各种内生成分是保守的,因为实际上所有的样品制备中所涉及的所有操作步骤都发生在共同的容器内,任何过量的(未消耗的或未反应的)试剂和污渍都不需要从样品中分离出来 因此,避免了与该过程相关的多次洗涤步骤。 该方法独特地适用于老年全血样品(其中内源性营养素基本上完全消耗的样品)的保守制剂和来自患病状态患者的全血样品,其中疾病由形态学,总数和/ 或一个或多个淋巴细胞亚群(即B和/或T细胞)的相对浓度。
    • 5. 发明授权
    • Conservative whole blood sample preparation technique
    • 保守的全血样品制备技术
    • US5030554A
    • 1991-07-09
    • US128668
    • 1987-12-04
    • Jorge A. QuintanaThomas R. RussellRonald D. PaulTimothy J. Fischer
    • Jorge A. QuintanaThomas R. RussellRonald D. PaulTimothy J. Fischer
    • A01N1/02G01N1/30G01N33/48G01N33/50G01N33/53G01N33/543G01N33/569G01N33/58
    • G01N33/56972G01N1/30G01N33/5094Y10S435/962Y10T436/25125Y10T436/2525
    • The method of this invention is directed to the rapid preparation of a whole blood sample for photooptical analysis. In the preferred embodiments of this method, a whole blood sample, lytic reagent system and immunological stain (optional) are contacted with the sample in a common reaction vessel (i.e. cuvette or test tube), with gentle asymmetric vortex mixing, so as to maintain the particulate matter of the sample at an essentially homogeneous concentration throughout the sample. An aliquot of the contents of the reaction vessel can, thereafter, be analyzed for identification and/or quantification of the analyte of interest. This process is conservative of the various endogenous constituents of the sample since virtually all of the manipulative steps involved in the preparation of the sample occur within a common vessel and any excess (unconsumed or unreacted) reagents and stain need not be separated from the sample during such preparation, thus, avoiding the multiple wash steps traditionally associated with this process. This process is uniquely applicable to the conservative preparation of aged whole blood samples (samples in which the endogenous nutrients have been essentially completely consumed) and whole blood samples from diseased state patients wherein the disease is manifest by changes in the morphology, total number and/or relative concentration of one or more of the lymphocyte subpopulations (i.e. B and/or T-cells).
    • 本发明的方法涉及用于光学光学分析的全血样品的快速制备。 在该方法的优选实施方案中,将全血样品,溶解试剂系统和免疫染色剂(任选的)在常规反应容器(即比色杯或试管)中与样品接触,并进行温和的不对称涡旋混合,以保持 在整个样品中样品的颗粒物质基本上均匀。 然后分析反应容器的内容物的等分试样,以便鉴定和/或定量所关注的分析物。 该过程对于样品的各种内生成分是保守的,因为实际上所有的样品制备中所涉及的所有操作步骤都发生在共同的容器内,任何过量的(未消耗的或未反应的)试剂和污渍都不需要从样品中分离出来 因此,避免了与该过程相关的多次洗涤步骤。 该方法独特地适用于老年全血样品(其中内源性营养素基本上完全消耗的样品)的保守制剂和来自患病状态患者的全血样品,其中疾病由形态学,总数和/ 或相对浓度的一个或多个淋巴细胞亚群(即B和/或T细胞)。
    • 6. 发明授权
    • Methods and reagents for improved selection of biological materials
    • 改善生物材料选择的方法和试剂
    • US09435799B2
    • 2016-09-06
    • US10208939
    • 2002-07-31
    • Thomas R RussellPauline McGannMike MusickMichael Ciocci
    • Thomas R RussellPauline McGannMike MusickMichael Ciocci
    • G01N33/543
    • G01N33/5434G01N33/54326G01N33/54346G01N33/54353G01N33/553G01N33/577G01N2440/32
    • Methods, apparatus and compositions for separating a desired or undesired population or subpopulation from a biological sample are disclosed herein. The selection procedure is based on ferromagnetic, dense particles in a preferred size range from about 0.8 to about 1.2 microns. Specific binding agents are bound to the particles that recognize and bind to specific molecules on the targeted population or subpopulation, and the particles are mixed with the sample in such a way as to promote movement of the particles relative to the sample, promoting binding to the targeted population or subpopulation without non-specifically binding to non-targeted populations in the sample. Because of the large particle density, the bound population is separated from the fluid sample by gravity. Alternatively, the sample, including the bound, targeted population, is placed in a magnetic field such that the particles separate from the sample by evenly distributing over the vessel wall thus limiting non-specific trapping of the non-targeted population.
    • 本文公开了用于从生物样品中分离所需或不需要的群体或亚群体的方法,装置和组合物。 选择程序基于约0.8至约1.2微米的优选尺寸范围内的铁磁致密颗粒。 特异性结合剂与识别并结合目标群体或亚群体上的特定分子的颗粒结合,并且颗粒与样品混合以促进颗粒相对于样品的移动,促进与 目标群体或亚群,而不特异性地结合样本中的非目标群体。 由于粒子密度较大,结合的群体通过重力与流体样本分离。 或者,将包括结合的目标群体的样品置于磁场中,使得颗粒通过均匀分布在血管壁上而与样品分离,从而限制非目标群体的非特异性捕获。
    • 9. 发明授权
    • Non-corrosive security railing
    • 无腐蚀性安全栏杆
    • US4892292A
    • 1990-01-09
    • US862252
    • 1986-05-12
    • Thomas R. Russell
    • Thomas R. Russell
    • E04H17/14E04F11/18
    • E04F11/181
    • A security railing formed from plastics material pipe which is lightweight, low cost, and non-corrosive. The top railing and preferably the posts of the security railing are formed of double pipe construction comprising a first pipe and a second pipe inside the first pipe, the second pipe having an outside diameter related to the inside diameter of the first pipe. The first pipe is of plastics material and the second pipe preferably also is of plastics material. A lower railing utilizes a plastic pipe having the same outside diameter as the laminated top railing. T connectors and cross connectors are used at the joints between the upper and lower railings and the posts, and these T connectors and cross connectors are of the same outer dimension as the first pipe to give the railing a smooth contour. A plurality of holes in the lower surface of the upper railing and the upper surface of the lower railing permit the insertion of smaller diameter plastics pipe sections at closely spaced intervals to provide vertical railing elements. The security railing meets requirements of national building codes and will not permanently deform under test loads. The plastics material used is preferably polyvinyl chloride.