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    • 2. 发明申请
    • DISEASE SPECIFIC DIAGNOSTIC AID
    • 疾病特异性诊断
    • WO2010011460A1
    • 2010-01-28
    • PCT/US2009/048463
    • 2009-06-24
    • SIEMENS HEALTHCARE DIAGNOSTIC INC.PUGIA, Michael, J.
    • PUGIA, Michael, J.
    • G01N33/50
    • G01N33/54386G01N2800/042G01N2800/347
    • A disease specific panel having at least one primary test for different analytes that are relevant for either early detection of a primary disease or management of patients already diagnosed with said primary disease. The panel also includes at least one secondary test which is relevant for detection of a co-morbid condition or complications of the primary disease. Generally, the primary and secondary tests are disposed on a support surface. The disease specific panel is different from the prior art screening tests in that there are no tests included in the panel whose results are not relevant or do not relate to either primary disease or a co-morbid condition or complications of the primary disease. The disease specific panel may also include systems and methods utilizing algorithms for creating and outputting diagnostic aids, as well as warnings about the presence of possible sample interferants, especially those commonly associated with the subject disease of the panel.
    • 一种疾病特异性小组,其具有与早期检测原发性疾病或管理已经诊断为所述原发性疾病的患者相关的不同分析物的至少一种初级测试。 该小组还包括至少一个与检测并发病症或原发性疾病并发症有关的二次检查。 通常,初级和次级试验设置在支撑表面上。 疾病特异性小组与现有技术的筛选试验不同,因为组合中没有包括结果不相关或与原发性疾病或并发病症或并发症无关的原发性疾病无关的检查。 疾病特异性面板还可以包括利用用于创建和输出诊断帮助的算法的系统和方法,以及关于可能的样品干扰物(特别是通常与面板的主题疾病相关的那些)的存在的警告。
    • 3. 发明申请
    • SYNTHESIS OF SINGLE-STRANDED DNA
    • 单链DNA的合成
    • WO2009097673A1
    • 2009-08-13
    • PCT/CA2008/000224
    • 2008-02-07
    • BIO-ID DIAGNOSTIC INC.VINAYAGAMOORTHY, Thuraiayah
    • VINAYAGAMOORTHY, Thuraiayah
    • C12P19/34C07H21/00C07H21/04C12N15/10C12Q1/68
    • C12P19/34
    • A method of producing single-stranded DNA. In one form, the method involves providing a uracil-containing oligonucleotide template molecule having a sequence that is complementary to a part of a target single-stranded DNA molecule of length greater than the template molecule; providing one or more parts of the target molecule including a base sequence complementary to a part of the template molecule; annealing the part(s) of the target molecule to the template molecule and forming the complete target molecule by ligating together at least two adjacent parts of the target molecule while annealed to the template molecule, andlor extending at least one part of the target molecule to form a sequence complementary to a remainder of the template molecule by nucleotide polymerization, and then separating the template molecule from the target molecule. In another form, an intermediate molecule is annealed to the template and then enzymatically cut, and one part is then extended by DNA polymerization using monomers of increased molecular weight or ionic charge compared to the monomers used to form the intermediate molecule.
    • 一种单链DNA的制备方法。 在一种形式中,该方法包括提供含有尿嘧啶的寡核苷酸模板分子,其具有与长度大于模板分子的目标单链DNA分子部分互补的序列; 提供靶分子的一个或多个部分,包括与模板分子的一部分互补的碱基序列; 将靶分子的部分退火至模板分子,并通过将靶分子的至少两个相邻部分与模板分子退火而形成完整的靶分子,同时将至少一部分目标分子延伸至 通过核苷酸聚合形成与模板分子的其余部分互补的序列,然后将模板分子与靶分子分离。 在另一种形式中,将中间体分子与模板退火,然后进行酶切,然后通过与用于形成中间分子的单体相比增加分子量或离子电荷的单体通过DNA聚合延伸一部分。
    • 8. 发明申请
    • AN AUTOMATED NON- INVASIVE REAL-TIME ACUTE RENAL FAILURE DETECTION SYSTEM
    • 自动化非实时急性真核失效检测系统
    • WO2005104702A3
    • 2006-02-09
    • PCT/US2005013852
    • 2005-04-22
    • RENAL DIAGNOSTIC INCTOWNSEND SETHKOMANSKI CHRISTOPHERBOYER RICHARDTEDFORD NATHANFINE DEREKSTAR ROBERT
    • TOWNSEND SETHKOMANSKI CHRISTOPHERBOYER RICHARDTEDFORD NATHANFINE DEREKSTAR ROBERT
    • G01N35/08G01N21/00
    • A61B5/201A61B5/14507A61B5/208A61B5/412
    • [0111] A real-time, non-invasive system and method for determining the level of an analyze of interest in the urine of a patient is disclosed. The system and method uses the measured level of an analyze of interest to detect the onset of acute renal failure (ARF) as early as possible to prevent that patient from developing the disease or mitigating the effects of the disease. The system and method may be used to monitor the recovery of a patient after an ARF diagnosis. Preferably, the analyze of interest is creatinine or urea. The system may be placed in the urine drain line of a patient between a Foley catheter or other urinary drain and a urine collection bag. The system makes substantially continuous measurements of the urine flow rate and the concentration of the analyze of interest to determine the mass excretion rate of the analyze so it may be monitored to detect if the patient experiences a delta change in the mass excretion rate of an analyze that is indicative of the onset of ARF or a change in renal function.
    • 公开了一种用于确定患者尿中感兴趣的分析水平的实时非侵入性系统和方法。 该系统和方法使用测量的感兴趣的分析水平尽可能早地检测急性肾衰竭(ARF)的发作,以防止该患者发展该疾病或减轻该疾病的影响。 该系统和方法可以用于在ARF诊断之后监视患者的恢复。 优选地,感兴趣的分析是肌酐或尿素。 该系统可以放置在患有Foley导尿管或其它排尿管和尿液收集袋之间的尿液排泄管线中。 该系统基本上连续测量尿流速和感兴趣分析的浓度,以确定分析物的质量排泄率,以便可以监测其可以监测以检测患者是否经历分析的质量排泄速率的δ变化 这表明ARF的发生或肾功能的变化。