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    • 61. 发明授权
    • Computer system and method for performing integrity detection on the same
    • 用于执行完整性检测的计算机系统和方法
    • US08468342B2
    • 2013-06-18
    • US12083894
    • 2006-03-15
    • Yi ZhangJian ZhouZhenxin XiHongping Tian
    • Yi ZhangJian ZhouZhenxin XiHongping Tian
    • G06F7/20G06F11/30
    • G06F21/577G06F11/2284
    • The present invention proposes a computer system and a method capable of performing integrity detection, comprising: a running mode unit which comprises an integrity detection boot variable to determine whether or not to initiate an integrity detection boot mode by judging said running mode unit; an EFI integrity detection unit (5), which is used for performing an integrity detection on EFI image codes in the integrity detection boot mode, and comprises an integrity metric value for being compared with an EFI integrity calculated value generated after the EFI integrity detection unit performs the integrity detection on the EFI image codes, to determine the integrity of the EFI image codes; an operating system integrity detection unit (6); and an integrity management unit. The present invention is based on the EFI BIOS to perform the integrity detection on the operating system during the pre-boot stage, having better reliability and security.
    • 本发明提出一种能够执行完整性检测的计算机系统和方法,包括:运行模式单元,其包括完整性检测引导变量,以通过判断所述运行模式单元来确定是否启动完整性检测引导模式; EFI完整性检测单元(5),其用于对完整性检测引导模式中的EFI图像代码执行完整性检测,并且包括与EFI完整性检测单元之后生成的EFI完整性计算值进行比较的完整性度量值 对EFI图像代码执行完整性检测,以确定EFI图像代码的完整性; 操作系统完整性检测单元(6); 和诚信管理单位。 本发明基于EFI BIOS,以在预引导阶段对操作系统执行完整性检测,具有更好的可靠性和安全性。
    • 62. 发明申请
    • COMPOSITIONS AND METHODS FOR LEUKOCYTE-TARGETING MULTI-VALENT IMAGING PROBES
    • 用于低成本定位多成像成像探针的组合物和方法
    • US20130144035A1
    • 2013-06-06
    • US13642670
    • 2011-04-21
    • Dongfeng PanStuart S. BerrYi Zhang
    • Dongfeng PanStuart S. BerrYi Zhang
    • A61K51/08
    • A61K51/088A61K49/0002A61K49/0034A61K51/06
    • The present application discloses a new multivalent peptide ligand specifically targeting polymorphonuclear leukocytes (PMNs) with favorable pharmacological parameters to monitor sites of inflammation for imaging. The detailed synthesis, characterization, and pharmacological evaluation of the ligands are reported here. Two separate peptide binding ligands for formyl peptide and tuftsin receptors were chosen to link together based on the high expression levels of the two receptors on activated PMNs The heterobivalency and pegylated links were incorporated in the structural design to improve the sensitivity of the detection and to improve the bioavailability along with blood clearance profile, respectively. Two chemical constructs: cFLFLF-(PEG)n-TKPPR-99mTc (n=4, 12) were evaluated in vitro with human PMNs for binding affinity and bioavailability. As a result, FLFLF-(PEG)12-TKPPR99mTc was found to have more favorable pharmacological properties and was therefore used for further in vivo studies. Preliminary in vivo assessment of the agent was performed using Single Gamma Emission Computed Tomography (SPECT) imaging of a mouse model of ear inflammation. The results of these studies indicate cFLFLF-(PEG)12-TKPPR-99mTc may be a desirable imaging agent for binding to PMNs to identify sites of inflammation by SPECT.
    • 本申请公开了一种特异靶向多形核白细胞(PMN)的新型多价肽配体,具有良好的药理学参数,用于监测成像的炎症部位。 这里报道了配体的详细合成,表征和药理学评估。 基于激活的PMN上的两种受体的高表达水平,选择两种单独的用于甲酰肽和簇状蛋白受体的肽结合配体连接在一起。将异源和聚乙二醇化的链接并入结构设计中,以提高检测的灵敏度和改善 分别具有生物利用度和血液清除曲线。 两种化学构建体:cFLFLF-(PEG)n-TKPPR-99mTc(n = 4,12)在体外用人PMNs进行了评估,用于结合亲和力和生物利用度。 结果发现FLFLF-(PEG)12-TKPPR99mTc具有更好的药理学特性,因此用于进一步的体内研究。 使用单发伽马发射计算机断层扫描(SPECT)成像小鼠耳炎的模型进行药物的初步体内评估。 这些研究的结果表明,cFLFLF-(PEG)12-TKPPR-99mTc可能是用于结合PMN的理想显像剂,以通过SPECT鉴定炎症部位。
    • 64. 发明申请
    • SELF-SUSTAINED FLUIDIC DROPLET CASSETTE AND SYSTEM FOR BIOCHEMICAL ASSAYS
    • 自主持续流体液体和生物化学测定系统
    • US20130096035A1
    • 2013-04-18
    • US13805625
    • 2011-07-26
    • Tza-Huei WangSeungkyung ParkSamuel YangYi Zhang
    • Tza-Huei WangSeungkyung ParkSamuel YangYi Zhang
    • C12Q1/68
    • C12Q1/686C12Q1/6844C12Q2565/629
    • A fluidic cartridge for biochemical assays includes a cartridge body defining a first droplet region and a second droplet region with a droplet restraining barrier therebetween. The droplet restraining barrier has a gap between the first and the second droplet regions. The fluidic cartridge also includes a first droplet dispensed in the first droplet region. The first droplet includes a plurality of magnetic particles dispersed therein. The fluidic cartridge also includes a second droplet disposed in the second droplet region. The plurality of magnetic particles are sufficiently small to be drawn through the gap between the first and second droplet regions when compelled by an applied magnetic field, and the first droplet is restrained by the restraining barrier while the plurality of magnetic particles are drawn through the gap. A biochemical assay system includes a stage adapted to receive a fluidic cartridge, and a magnetic control assembly that includes a magnet. The magnet of the magnetic control assembly is movable to direct motion of magnetic particles contained within the fluidic cartridge.
    • 用于生物化学测定的流体盒包括限定第一液滴区域的盒体和在其间具有液滴限制屏障的第二液滴区域。 液滴限制屏障在第一和第二液滴区域之间具有间隙。 流体盒还包括分配在第一液滴区域中的第一液滴。 第一液滴包括分散在其中的多个磁性颗粒。 流体盒还包括设置在第二液滴区域中的第二液滴。 当被施加的磁场强迫时,多个磁性颗粒足够小以便被吸入第一和第二液滴区域之间的间隙,并且第一液滴被约束屏障约束,同时多个磁性颗粒被吸引通过间隙 。 生物化学测定系统包括适于接收流体盒的阶段和包括磁体的磁性控制组件。 磁性控制组件的磁体可移动以引导包含在流体盒内的磁性颗粒的运动。
    • 69. 发明授权
    • Light source driving circuit with low operating output voltage
    • 光源驱动电路,工作输出电压低
    • US08334660B2
    • 2012-12-18
    • US12783484
    • 2010-05-19
    • Eric LiChun LuYi Zhang
    • Eric LiChun LuYi Zhang
    • G05F1/00H05B37/02H05B39/04H05B41/36H05B39/02H05B37/00H05B39/00H05B41/00
    • H05B33/0827
    • A driving circuit for regulating current in a light source using a tracking component. The tracking component detects the voltage difference between an input node in the input stage and an output node in the output stage. The input stage is connected to a current source and includes an input transistor. The output stage is connected to the light source and includes an output transistor. The tracking component generates an output that controls the input and output transistors based on the voltage difference between the input node and the output node so that the voltage at the input node tracks the voltage at the output node. By using the tracking component, the LED driver can achieve accurate current control through one output transistor instead of cascaded transistors, resulting in lower output operating voltage and reduced power dissipation of the LED driver. Further, the tracking component is intermittently operated or shared across different channels to reduce energy consumption of the LED driver.
    • 一种用于使用跟踪部件调节光源中的电流的驱动电路。 跟踪组件检测输入级中的输入节点与输出级中的输出节点之间的电压差。 输入级连接到电流源并包括输入晶体管。 输出级连接到光源并包括输出晶体管。 跟踪组件产生输出,其基于输入节点和输出节点之间的电压差来控制输入和输出晶体管,使得输入节点处的电压跟踪输出节点处的电压。 通过使用跟踪组件,LED驱动器可以通过一个输出晶体管而不是级联晶体管实现精确的电流控制,从而降低输出工作电压并降低LED驱动器的功耗。 此外,跟踪部件在不同的通道间歇地操作或共享以减少LED驱动器的能量消耗。