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    • 1. 发明申请
    • METHODS FOR UNIFORM METAL IMPREGNATION INTO A NANOPOROUS MATERIAL
    • 将金属均匀地纳入纳米材料的方法
    • US20100171950A1
    • 2010-07-08
    • US12575369
    • 2009-10-07
    • Selena CHANSunghoon KwonNarayan Sundararajan
    • Selena CHANSunghoon KwonNarayan Sundararajan
    • G01J3/44
    • G01N21/658B01D67/0062B01D67/0086B01D67/0088B01D71/02B82Y15/00B82Y30/00C12Q1/6825G01J3/44G01N21/65G01N2021/6439G01N2021/655G01N2021/656C12Q2565/632C12Q2563/155
    • The methods, systems 400 and apparatus disclosed herein concern metal 150 impregnated porous substrates 110, 210. Certain embodiments of the invention concern methods for producing metal-coated porous silicon substrates 110, 210 that exhibit greatly improved uniformity and depth of penetration of metal 150 deposition. The increased uniformity and depth allow improved and more reproducible Raman detection of analytes. In exemplary embodiments of the invention, the methods may comprise oxidation of porous silicon 110, immersion in a metal salt solution 130, drying and thermal decomposition of the metal salt 140 to form a metal deposit 150. In other exemplary embodiments of the invention, the methods may comprise microfluidic impregnation of porous silicon substrates 210 with one or more metal salt solutions 130. Other embodiments of the invention concern apparatus and/or systems 400 for Raman detection of analytes, comprising metal-coated porous silicon substrates 110, 210 prepared by the disclosed methods.
    • 本文公开的方法,系统400和装置涉及金属150浸渍的多孔基材110,210。本发明的某些实施方案涉及用于制造金属涂覆的多孔硅基板110,210的方法,其显示出显着改善金属150沉积物的均匀性和深度的渗透 。 增加的均匀性和深度允许分析物的改进和更可重复的拉曼检测。 在本发明的示例性实施例中,所述方法可以包括多孔硅110的氧化,浸入金属盐溶液130中,干燥和热分解金属盐140以形成金属沉积物150.在本发明的其它示例性实施方案中, 方法可以包括多孔硅衬底210与一种或多种金属盐溶液130的微流体浸渍。本发明的其它实施方案涉及用于分析物的拉曼检测的装置和/或系统400,包括金属涂覆的多孔硅衬底110,210,由 公开的方法。
    • 2. 发明授权
    • Controlled alignment of nano-barcodes encoding specific information for scanning probe microscopy (SPM) reading
    • 用于扫描探针显微镜(SPM)读数的纳米条形码的控制对准编码特定信息
    • US07476786B2
    • 2009-01-13
    • US10667004
    • 2003-09-19
    • Selena ChanXing SuMineo Yamakawa
    • Selena ChanXing SuMineo Yamakawa
    • C12Q1/68G01N33/53C07H21/04A61K38/00C07K1/00
    • C12Q1/6816B82Y5/00B82Y10/00B82Y30/00Y10S977/702Y10S977/704Y10S977/705Y10S977/728Y10S977/729Y10S977/734Y10S977/742Y10S977/773Y10S977/774Y10S977/924C12Q2565/601C12Q2563/185
    • The methods, apparatus and compositions disclosed herein concern the detection, identification and/or sequencing of biomolecules, such as nucleic acids or proteins. In certain embodiments of the invention, coded probes comprising a probe molecule attached to one or more nano-barcodes may be allowed to bind to one or more target molecules. After binding and separation from unbound coded probes, the bound coded probes may be aligned on a surface and analyzed by scanning probe microscopy. The nano-barcodes may be any molecule or complex that is distinguishable by scanning probe microscopy (SPM), such as carbon nanotubes, fullerenes, submicrometer metallic barcodes, nanoparticles or quantum dots. Where the probes are oligonucleotides, adjacent coded probes hybridized to a target nucleic acid may be ligated together before alignment and scanning probe microscopy (SPM) analysis. Compositions comprising coded probes are also disclosed herein. Systems for biomolecule analysis may comprise a scanning probe microscopy (SPM) instrument and at least one coded probe attached to a surface.
    • 本文公开的方法,装置和组合物涉及生物分子如核酸或蛋白质的检测,鉴定和/或测序。 在本发明的某些实施方案中,包含与一个或多个纳米条形码连接的探针分子的编码探针可以被允许与一个或多个靶分子结合。 在结合和分离未结合的编码探针之后,结合编码的探针可以在表面上对准并通过扫描探针显微镜进行分析。 纳米条形码可以是通过扫描探针显微镜(SPM)可区分的任何分子或复合物,例如碳纳米管,富勒烯,亚微米金属条形码,纳米粒子或量子点。 当探针为寡核苷酸时,与靶核酸杂交的相邻编码探针可在对准和扫描探针显微镜(SPM)分析之前连接在一起。 包含编码探针的组合物也在本文中公开。 用于生物分子分析的系统可以包括扫描探针显微镜(SPM)仪器和连接到表面的至少一个编码探针。
    • 3. 发明授权
    • Methods and device for DNA sequencing using surface enhanced raman scattering (SERS)
    • 使用表面增强拉曼散射(SERS)进行DNA测序的方法和装置
    • US07476501B2
    • 2009-01-13
    • US10108128
    • 2002-03-26
    • Selena ChanXing SuTae-Woong Koo
    • Selena ChanXing SuTae-Woong Koo
    • C12Q1/68
    • C12Q1/6869B01L3/5027C12Q2565/60C12Q2565/631C12Q2565/632G01N21/658G01N33/587G01N2021/653G01N2021/656
    • The methods and apparatus disclosed herein concern nucleic acid sequencing by enhanced Raman spectroscopy. In certain embodiments of the invention, exonuclease treatment of the nucleic acids 109 results in the release of nucleotides 110. The nucleotides may pass from a reaction chamber 101 through a microfluidic channel 102 and enter a nanochannel or microchannel 103. The nanochannel or microchannel 103 may be packed with nanoparticle 111 aggregates containing hot spots for Raman detection. As the nucleotides 110 pass through the nanoparticle 111 hot spots, they may be detected by surface enhanced Raman spectroscopy (SERS), surface enhanced resonance Raman spectroscopy (SERRS) and/or coherent anti-Stokes Raman spectroscopy (CARS). Identification of the sequence of nucleotides 110 released from the nucleic acid 109 provides the nucleic acid sequence. Other embodiments of the invention concern apparatus 100 for nucleic acid sequencing.
    • 本文公开的方法和装置涉及通过增强拉曼光谱进行的核酸测序。 在本发明的某些实施方案中,核酸109的核酸外切酶处理导致核苷酸110的释放。核苷酸可以从反应室101通过微流体通道102并进入纳米通道或微通道103.纳米通道或微通道103可以 填充含有用于拉曼检测的热点的纳米颗粒111聚集体。 当核苷酸110通过纳米颗粒111热点时,它们可以通过表面增强拉曼光谱(SERS),表面增强共振拉曼光谱(SERRS)和/或相干抗斯托克斯拉曼光谱(CARS)来检测。 从核酸109释放的核苷酸序列110的鉴定提供了核酸序列。 本发明的其它实施方案涉及用于核酸测序的设备100。
    • 5. 发明授权
    • Methods for uniform metal impregnation into a nanoporous material
    • 均匀金属浸渍到纳米多孔材料中的方法
    • US07361313B2
    • 2008-04-22
    • US10368976
    • 2003-02-18
    • Selena ChanSunghoon KwonNarayan Sundararajan
    • Selena ChanSunghoon KwonNarayan Sundararajan
    • G01N21/65G01J3/44
    • G01N21/658B01D67/0062B01D67/0086B01D67/0088B01D71/02B82Y15/00B82Y30/00C12Q1/6825G01J3/44G01N21/65G01N2021/6439G01N2021/655G01N2021/656C12Q2565/632C12Q2563/155
    • The methods, systems 400 and apparatus disclosed herein concern metal 150 impregnated porous substrates 110, 210. Certain embodiments of the invention concern methods for producing metal-coated porous silicon substrates 110, 210 that exhibit greatly improved uniformity and depth of penetration of metal 150 deposition. The increased uniformity and depth allow improved and more reproducible Raman detection of analytes. In exemplary embodiments of the invention, the methods may comprise oxidation of porous silicon 110, immersion in a metal salt solution 130, drying and thermal decomposition of the metal salt 140 to form a metal deposit 150. In other exemplary embodiments of the invention, the methods may comprise microfluidic impregnation of porous silicon substrates 210 with one or more metal salt solutions 130. Other embodiments of the invention concern apparatus and/or systems 400 for Raman detection of analytes, comprising metal-coated porous silicon substrates 110, 210 prepared by the disclosed methods.
    • 本文公开的方法,系统400和装置涉及金属150浸渍的多孔基材110,210。本发明的某些实施方案涉及用于制造金属涂覆的多孔硅基板110,210的方法,其显示出显着改善金属150沉积物的均匀性和深度的渗透 。 增加的均匀性和深度允许分析物的改进和更可重复的拉曼检测。 在本发明的示例性实施例中,所述方法可以包括多孔硅110的氧化,浸入金属盐溶液130中,干燥和热分解金属盐140以形成金属沉积物150.在本发明的其它示例性实施方案中, 方法可以包括多孔硅衬底210与一种或多种金属盐溶液130的微流体浸渍。本发明的其它实施方案涉及用于分析物的拉曼检测的装置和/或系统400,包括金属涂覆的多孔硅衬底110,210,由 公开的方法。
    • 7. 发明申请
    • Methods for uniform metal impregnation into a nanoporous material
    • 均匀金属浸渍到纳米多孔材料中的方法
    • US20070116882A1
    • 2007-05-24
    • US11436489
    • 2006-05-18
    • Selena ChanSunghoon KwonNarayan Sundararajan
    • Selena ChanSunghoon KwonNarayan Sundararajan
    • B05D1/18
    • G01N21/658B01D67/0062B01D67/0086B01D67/0088B01D71/02B82Y15/00B82Y30/00C12Q1/6825G01J3/44G01N21/65G01N2021/6439G01N2021/655G01N2021/656C12Q2565/632C12Q2563/155
    • The methods, systems 400 and apparatus disclosed herein concern metal 150 impregnated porous substrates 110, 210. Certain embodiments of the invention concern methods for producing metal-coated porous silicon substrates 110, 210 that exhibit greatly improved uniformity and depth of penetration of metal 150 deposition. The increased uniformity and depth allow improved and more reproducible Raman detection of analytes. In exemplary embodiments of the invention, the methods may comprise oxidation of porous silicon 110, immersion in a metal salt solution 130, drying and thermal decomposition of the metal salt 140 to form a metal deposit 150. In other exemplary embodiments of the invention, the methods may comprise microfluidic impregnation of porous silicon substrates 210 with one or more metal salt solutions 130. Other embodiments of the invention concern apparatus and/or systems 400 for Raman detection of analytes, comprising metal-coated porous silicon substrates 110, 210 prepared by the disclosed methods.
    • 本文公开的方法,系统400和装置涉及金属150浸渍的多孔基材110,210。本发明的某些实施方案涉及用于制造金属涂覆的多孔硅基板110,210的方法,其显示出显着改善金属150沉积物的均匀性和深度的渗透 。 增加的均匀性和深度允许分析物的改进和更可重复的拉曼检测。 在本发明的示例性实施例中,所述方法可以包括多孔硅110的氧化,浸入金属盐溶液130中,干燥和热分解金属盐140以形成金属沉积物150.在本发明的其它示例性实施方案中, 方法可以包括多孔硅衬底210与一种或多种金属盐溶液130的微流体浸渍。本发明的其它实施方案涉及用于分析物的拉曼检测的装置和/或系统400,包括金属涂覆的多孔硅衬底110,210,由 公开的方法。
    • 8. 发明授权
    • Detecting molecular binding by monitoring feedback controlled cantilever deflections
    • 通过监测反馈控制的悬臂偏转来检测分子结合
    • US07105301B2
    • 2006-09-12
    • US10667776
    • 2003-09-22
    • Xing SuSelena ChanTae-Woong KooMineo YamakawaAndrew A. Berlin
    • Xing SuSelena ChanTae-Woong KooMineo YamakawaAndrew A. Berlin
    • C12Q1/68C12Q1/70G01N33/566G01N33/563
    • C12Q1/6825B82Y5/00G01N33/54373G01N2800/52Y10S977/924C12Q2565/501
    • The present methods and apparatus concern the detection and/or identification of target analytes using probe molecules. In various embodiments of the invention, the probes or analytes are attached to one or more cantilevers. Binding of a probe to an analyte results in deflection of the cantilever, detected by a detection unit. A counterbalancing force may be applied to restore the cantilever to its original position. The counterbalancing force may be magnetic, electrical or radiative. The detection unit and the mechanism generating the counterbalancing force may be operably coupled to an information processing and control unit, such as a computer. The computer may regulate a feedback loop that maintains the cantilever in a fixed position by balancing the deflecting force and the counterbalancing force. The concentration of analytes in a sample may be determined from the magnitude of the counterbalancing force required to maintain the cantilever in a fixed position.
    • 本方法和装置涉及使用探针分子检测和/或鉴定目标分析物。 在本发明的各种实施方案中,探针或分析物附着到一个或多个悬臂。 将探针与分析物结合导致由检测单元检测到的悬臂的偏转。 可以应用平衡力将悬臂恢复到其原始位置。 平衡力可以是磁性的,电的或辐射的。 生成平衡力的检测单元和机构可以可操作地耦合到诸如计算机的信息处理和控制单元。 计算机可以通过平衡偏转力和平衡力来调节将悬臂维持在固定位置的反馈回路。 样品中分析物的浓度可以从将悬臂维持在固定位置所需的平衡力的大小来确定。