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    • 1. 发明申请
    • METHOD FOR DECISION SUPPORT IN ALLERGY DIAGNOSIS
    • 在过敏诊断中的决策支持方法
    • WO2011152779A1
    • 2011-12-08
    • PCT/SE2011/050664
    • 2011-05-27
    • PHADIA ABANDERSSON, KarlMATSSON, Per
    • ANDERSSON, KarlMATSSON, Per
    • G01N33/53G01N33/68
    • G06F19/34G01N33/68G01N2800/24
    • A method of providing a clinical decision support in allergy diagnosis comprises the steps of: a) providing a body fluid sample from a patient, b) selecting (1 10) a plurality of allergens to be tested for in the sample, c) determining (120) for each allergen the concentration in the sample of at least one immunoglobulin directed against the allergen, d) transforming (130) each determined immunoglobulin concentration to a clinical effect value on a normalized scale common to allergens in general, e) assigning to each allergen tested for, based on known cross-reactivity information for the allergen, an allergen specificity value, representing the degree of cross-reactivity for the allergen, and f) presenting (140) determined clinical effect and allergen specificity values for each allergen, or a group or groups of the allergens. A computer-implemented method, a computer program product, and a patient information carrier device containing a diagnosis result are also disclosed.
    • 在过敏诊断中提供临床决定支持的方法包括以下步骤:a)从患者提供体液样品,b)在样品中选择(110)待测试的多种变应原,c)确定( 120)对于每种变应原,至少一种针对变应原的免疫球蛋白的样品中的浓度,d)将所测定的每种免疫球蛋白浓度转化(130)至通常与变应原共有的归一化量值的临床效应值,e)分配给每个 基于已知的变应原交叉反应性信息测试过敏原,表达变应原特异性值,表示变应原的交叉反应性程度,以及f)呈现(140)确定的每种变应原的临床效果和变应原特异性值,或 一组或一组过敏原。 还公开了一种计算机实现的方法,计算机程序产品和包含诊断结果的患者信息载体装置。
    • 4. 发明申请
    • TWO STEP LATERAL FLOW ASSAY METHODS AND DEVICES
    • 两步法横向流动分析方法和装置
    • WO2007063423A1
    • 2007-06-07
    • PCT/IB2006/003976
    • 2006-05-23
    • PHADIA ABRUNDSTROM, GerdMATSSON, PerCHRISTOPHER, Paul
    • RUNDSTROM, GerdMATSSON, PerCHRISTOPHER, Paul
    • G01N33/68G01N33/543
    • G01N33/558G01N33/543G01N33/6854G01N2800/24Y10S435/805Y10S435/81Y10S435/97Y10S435/973Y10S435/975Y10S436/805Y10S436/807Y10S436/808Y10S436/81Y10S436/821Y10T436/25125Y10T436/255
    • Lateral flow assay devices and methods for detecting a first member of a specific binding pair in a sample which comprises a plurality of nonspecific binding pair members are adapted for two step determinations. In one embodiment, a two step lateral flow assay method for identifying IgE antibodies in a sample comprises applying a sample to a sample port of a device, wherein the device is adapted to deliver the sample to a lateral flow matrix having a plurality of IgE antigen species immobilized at respective positions at a first location The two step method further comprises allowing the sample to travel along the lateral flow matrix through the immobilized plurality of IgE antigen species to a second location downstream of the first location, applying liquid buffer to the lateral flow matrix to mobilize labeled reagent which is adapted to bind anti-IgE antibody and is dried on the lateral flow matrix at a location upstream of the delivery of the filtered sample to the lateral flow matrix, and allowing labeled reagent mobilized by the liquid buffer to travel along the lateral flow matrix through the immobilized plurality of IgE antigen species to a location downstream of the first location. Further embodiments comprise additional lateral flow immunoassay devices and methods for identifying IgE antibodies in a sample.
    • 用于检测包含多个非特异性结合对成员的样品中的特异性结合对的第一成员的侧流测定装置和方法适于两步测定。 在一个实施方案中,用于鉴定样品中的IgE抗体的两步横向流动测定方法包括将样品应用于装置的样品端口,其中所述装置适于将样品递送至具有多种IgE抗原的横向流动基质 固定在第一位置的相应位置处的物质。所述两步法还包括使样品沿横向流动基质通过固定化的多种IgE抗原物质行进到第一位置下游的第二位置,将液体缓冲液施加到侧流 基质以调动适于结合抗IgE抗体的标记试剂,并在侧向流动基质上在过滤样品递送至侧流基质的上游位置处干燥,并允许由液体缓冲剂移动的标记试剂行进 沿着横向流动基质通过固定化的多个IgE抗原物种到达第一位置下游的位置。 进一步的实施方式包括用于鉴定样品中的IgE抗体的附加横向流动免疫测定装置和方法。
    • 8. 发明公开
    • METHOD FOR DECISION SUPPORT IN ALLERGY DIAGNOSIS
    • 决策支持在过敏诊断中的方法
    • EP2577308A1
    • 2013-04-10
    • EP11790083.7
    • 2011-05-27
    • Phadia AB
    • ANDERSSON, KarlMATSSON, Per
    • G01N33/53G01N33/68
    • G06F19/34G01N33/68G01N2800/24
    • A method of providing a clinical decision support in allergy diagnosis comprises the steps of: a) providing a body fluid sample from a patient, b) selecting (1 10) a plurality of allergens to be tested for in the sample, c) determining (120) for each allergen the concentration in the sample of at least one immunoglobulin directed against the allergen, d) transforming (130) each determined immunoglobulin concentration to a clinical effect value on a normalized scale common to allergens in general, e) assigning to each allergen tested for, based on known cross-reactivity information for the allergen, an allergen specificity value, representing the degree of cross-reactivity for the allergen, and f) presenting (140) determined clinical effect and allergen specificity values for each allergen, or a group or groups of the allergens. A computer-implemented method, a computer program product, and a patient information carrier device containing a diagnosis result are also disclosed.
    • 在过敏诊断中提供临床决策支持的方法包括以下步骤:a)提供来自患者的体液样品,b)选择(110)样品中要测试的多种过敏原,c)确定( 120)针对每种过敏原的至少一种针对过敏原的免疫球蛋白的样品中的浓度,d)将每种测定的免疫球蛋白浓度转化(130)到一般归因于过敏原常用规格化等级的临床效应值,e) 基于过敏原的已知交叉反应性信息,过敏原特异性值,代表过敏原的交叉反应性程度,和f)呈现(140)确定的每种过敏原的临床效果和过敏原特异性值,或 一组或多组过敏原。 还公开了包含诊断结果的计算机实现的方法,计算机程序产品和患者信息载体设备。