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    • 52. 发明申请
    • MASS SPECTROMETRY ASSAY FOR ESTROGENIC COMPOUNDS
    • 雌激素化合物的质谱分析
    • US20160377636A1
    • 2016-12-29
    • US15251224
    • 2016-08-30
    • QUEST DIAGNOSTICS INVESTMENTS INCORPORATED
    • Midred GOLDMANNigel CLARKE
    • G01N33/74H01J49/00G01N30/72
    • G01N33/743G01N30/724G01N33/6848G01N33/6851G01N2458/15H01J49/00H01J49/0027
    • Methods are provided for detecting the amount of one or more HRT panel analytes (i.e., estrone (E1), estrone sulfate (E1s), 17α-estradiol (E2a), 17β-estradiol (E2b), estradiol sulfate (E2s), estriol (E3), equilin (EQ), 17α-dihydroequilin (EQa), 17β-dihydroequilin (EQb), Equilenin (EN), 17α-dihydroequilenin (ENa), 17β-dihydroequilenin (ENb), and Δ8,9-dehydroestrone (dE1)) in a sample by mass spectrometry. The methods generally involve ionizing one or more HRT panel analytes in a sample and quantifying the generated ions to determine the amount of one or more HRT panel analytes in the sample. In methods where amounts of multiple HRT panel analytes are detected, the amounts of multiple analytes are detected in the same sample injection.
    • 提供了用于检测一种或多种HRT面板分析物(即雌酮(E1),硫酸雌酮(E1s),17α-雌二醇(E2a),17β-雌二醇(E2b)),硫酸雌二醇(E2s),雌三醇 E3),平衡(EQ),17α-二氢等位基因(EQa),17β-二氢比例蛋白(EQb),平衡蛋白(EN),17α-二氢马来西林(ENa),17β-二氢马来西林(ENb)和Δ8,9-脱氢雌酮(dE1) )在样品中通过质谱法测定。 所述方法通常涉及将样品中的一种或多种HRT面板分析物离子化并量化产生的离子以确定样品中一种或多种HRT面板分析物的量。 在检测到多个HRT面板分析物的量的方法中,在相同的样品注入中检测到多种分析物的量。
    • 53. 发明授权
    • Versatile ambient ionization-based interface for LC/MS
    • 用于LC / MS的通用环境电离接口
    • US09400267B2
    • 2016-07-26
    • US14889625
    • 2013-10-02
    • Ohio University
    • Hao ChenYi Cai
    • G01N30/72
    • G01N30/724G01N30/7233G01N2030/8429H01J49/145
    • An apparatus (10) for coupling liquid chromatography with mass spectrometry and for splitting and analyzing a liquid sample includes a fluid conduit (16), which defines a flow passage (18) and is configured to supply the liquid sample. The fluid conduit (16) has an outer surface and a micro-hole (30) through the outer surface into the flow passage (18). The apparatus (10) also includes an ambient ionizer (40) configured to generate and direct a charged solvent (44) toward the micro-hole (30) at the outer surface for ionizing a portion of the liquid sample (32) that emerges out of the micro-hole (30). The apparatus (10) further includes a mass spectrometer (60) having a sample entrance (62) adjacent the micro-hole (30) configured to analyze an ionized portion of the liquid sample (54).
    • 用于将液相色谱与质谱耦合并用于分离和分析液体样品的装置(10)包括限定流路(18)并被配置为供应液体样品的流体导管(16)。 流体管道(16)具有外表面和穿过外表面进入流动通道(18)的微孔(30)。 设备(10)还包括环境离子发生器(40),其被配置为在外表面处向带电溶剂(44)产生并引导微孔(30),用于离开出现的液体样品(32)的一部分 的微孔(30)。 装置(10)还包括质谱仪(60),其具有邻近微孔(30)的样品入口(62),该样品入口构造成分析液体样品(54)的离子化部分。
    • 54. 发明申请
    • METHOD AND DEVICE FOR MASS SPECTROMETRY
    • 用于质谱分析的方法和装置
    • US20150371837A1
    • 2015-12-24
    • US14762916
    • 2014-01-27
    • HITACHI HIGH-TECHNOLOGIES CORPORATION
    • Hiroyuki YASUDAShinya ITOAkira FUJIIYasushi TERUI
    • H01J49/04G01N30/72
    • H01J49/0445G01N30/724H01J49/165
    • A mass spectrometry is equipped with a liquid specimen supply part which supplies a liquid specimen sandwiched between bubbles, an ion source part ionizes the specimen, and a mass spectrometry part which detects ions separated in accordance with mass. In particular the ion source part is configured so as to include a liquid supply tube for transporting a specimen from the liquid specimen supply part, a degassing/liquid retention part in which bubbles are removed, a spraying part which ionizes the specimen, and a high-voltage power supply part which applies a high voltage to the spraying part. The device is further characterized in that after removing the bubbles, a Taylor cone is formed from the resultant pre-solution, and the specimen is ionized thereafter. Thus, the ionization of an intended specimen is stabilized, and the measurement reproducibility is improved.
    • 质谱仪配备有液体试样供给部件,其供给夹在气泡之间的液体试样,离子源部件将样品离子化,以及检测根据质量分离的离子的质谱部分。 特别地,离子源部构成为包括用于从液体试样供给部输送试样的液体供给管,除去气泡的脱气/液体滞留部,使样本电离的喷射部, - 对喷涂部施加高电压的电压电源部。 该装置的特征还在于,在除去气泡之后,由所得预溶液形成泰勒锥体,然后将样品电离。 因此,期望的样品的电离稳定,并且测量再现性提高。
    • 58. 发明授权
    • Methods and apparatus for performing chromatography and mass spectroscopy with supercritical fluid samples
    • 用超临界流体样品进行色谱和质谱的方法和装置
    • US07897917B2
    • 2011-03-01
    • US12127313
    • 2008-05-27
    • Joseph A. Jarrell
    • Joseph A. Jarrell
    • H01J49/10
    • G01N30/724G01N30/7246H01J49/165B01D15/40
    • Embodiments of the present invention are directed to devices and methods for receiving NSC Fluids having at least one analyte from a chromatograph and directing analyte ions into the vacuum regions of a mass spectrometer. The device has a housing having at least one wall defining a chamber, sample inlet, an ionization media inlet and an outlet. The sample inlet has a position in communication with a chromatograph receiving a NSC Fluid. The sample inlet receives the NSC Fluid and directs the NSC Fluid into the chamber to form a sample jet of NSC Fluid. The ionization media inlet is placed in fluid communication with a source of ionization media and directs the ionization media into the chamber and the sample jet to create analyte ions. The analyte ions are received in the mass spectrometer vacuum region orifice.
    • 本发明的实施方案涉及用于接收具有来自色谱仪的至少一种分析物并将分析物离子导入质谱仪的真空区域的NSC流体的装置和方法。 该装置具有壳体,该壳体具有限定腔室,样品入口,离子化介质入口和出口的至少一个壁。 样品入口具有与接收NSC流体的色谱仪连通的位置。 样品入口接收NSC流体并将NSC流体引导到室中以形成NSC Fluid的样品射流。 离子化介质入口与离子化介质源流体连通,并将电离介质引导到室中,并将样品射流引导以产生分析物离子。 分析离子被接收在质谱仪真空区域孔中。
    • 59. 发明授权
    • Discrete drop dispensing device and method of use
    • 离散点滴装置及其使用方法
    • US07815798B2
    • 2010-10-19
    • US12170775
    • 2008-07-10
    • Arthur Schliefer
    • Arthur Schliefer
    • B01D15/08
    • G01N30/724B05B17/0646G01N30/32G01N30/34G01N30/7273
    • A discrete drop dispensing device comprises a substrate comprising an upper surface and a lower surface and orifices extending from the upper surface to the lower surface, adapted to receive a fluid at a flow rate. The discrete drop dispensing device also comprises an oscillator disposed adjacent to the substrate and configured to vibrate the substrate to expel drops having a substantially equal volume of the fluid. The flow rate is substantially identical to a drop dispensing rate. A method and a device for performing liquid chromatography are also described. The method comprises automatically adjusting the drop dispensing rate to a change in the flow rate or a change in a composition of a mobile phase of the fluid.
    • 离散液滴分配装置包括包括上表面和下表面的基底以及从上表面延伸到下表面的孔口,适于以流量接收流体。 离散液滴分配装置还包括与基底相邻设置的振荡器,并被配置为振动基底以排出具有基本相等体积流体的液滴。 流速基本上与滴液分配速率相同。 还描述了用于进行液相色谱的方法和装置。 该方法包括自动调节滴液分配速率以改变流速或流体流动相的组成变化。
    • 60. 发明授权
    • Mass spectrometry system and mass spectrometry method
    • 质谱系统和质谱法
    • US07626162B2
    • 2009-12-01
    • US12038829
    • 2008-02-28
    • Shuhei HashibaTakeshi Sakamoto
    • Shuhei HashibaTakeshi Sakamoto
    • B01D59/44H01J49/26H01J49/42
    • H01J49/0027G01N30/724Y10T436/13
    • When a liquid mixture of two samples such as biological samples labeled with stable isotopes is subjected to a relative quantitative analysis using a liquid chromatography-tandem mass spectrometry system, various constituents are simultaneously ionized. Accordingly, sufficient time required for second mass spectrometry is not ensured, whereby some ions remain unanalyzed after measurement. To address this problem, after second mass spectrometry, amino acid sequencing is performed using the analysis data of the second mass spectrometry, which enables determination on the presence/absence of a specific amino acid labeled with a stable isotope. When the specific amino acid is present, the m/z value of an isotopically-labeled-paired ion in an MS spectrum is calculated, and non-target information for use in second mass spectrometry is created using the calculated m/z information. This avoids redundant second mass spectrometry on sample components derived from the same peptide while allowing second mass spectrometry to be efficiently performed.
    • 当使用液相色谱 - 串联质谱系统进行相对定量分析,将诸如用稳定同位素标记的生物样品的两个样品的液体混合物进行相对定量分析时,同时电离各种成分。 因此,不能确保第二质谱所需的足够的时间,从而在测量之后一些离子保持未分析。 为了解决这个问题,在第二次质谱法之后,使用第二质谱分析数据进行氨基酸测序,其能够确定用稳定同位素标记的特定氨基酸的存在/不存在。 当存在特定氨基酸时,计算MS谱中同位素标记配对离子的m / z值,并使用所计算的m / z信息产生用于第二质谱的非目标信息。 这避免了来自相同肽的样品组分的冗余第二质谱,同时允许有效地进行第二质谱。