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    • 1. 发明授权
    • Cardiomyocytes-containing device and method for manufacturing and using the same
    • 含有心肌细胞的装置及其制造和使用方法
    • US08506793B2
    • 2013-08-13
    • US13147607
    • 2010-02-02
    • Ronald DekkerAnja Van De Stolpe
    • Ronald DekkerAnja Van De Stolpe
    • G01N27/327
    • G01N1/30C12N5/0657C12N2503/02C12N2535/10G01N33/5061
    • Disclosed is a device for determining the cardiotoxicity of a chemical compound, comprising a substrate (10) carrying a deformable stack (34), said stack being partially detached from the substrate by a cavity (32) allowing an out-of-plane deformation of the stack, said stack comprising a first deformable layer (16), a second deformable layer (20) and a multi-electrode structure (18) sandwiched between the first and second deformable layers, the second deformable layer carrying a pattern of cardiomyocytes (28) adhered thereto; and a liquid container (26) mounted on the substrate for exposing the cardiomyocytes to the chemical compound. A method of manufacturing such a device is also disclosed. The present invention further relates to the use of the device for drug target discovery and/or drug development and a method for developing a disease model for a disease that is caused by or modified by stretching of cells, in particular a cardiac disease model.
    • 公开了一种用于确定化合物的心脏毒性的装置,包括承载可变形叠层(34)的基底(10),所述叠层通过空腔(32)部分地从基底分离, 所述堆叠包括夹在所述第一和第二可变形层之间的第一可变形层(16),第二可变形层(20)和多电极结构(18),所述第二可变形层承载心肌细胞图案(28 ) 和安装在基板上的用于将心肌细胞暴露于化合物的液体容器(26)。 还公开了制造这种装置的方法。 本发明还涉及该装置用于药物靶发现和/或药物开发的用途,以及用于开发由细胞拉伸,特别是心脏疾病模型引起或改变的疾病的疾病模型的方法。
    • 2. 发明申请
    • CARDIOMYOCYTES-CONTAINING DEVICE AND METHOD FOR MANUFACTURING AND USING THE SAME
    • 含有血小板活性的装置及其制造和使用方法
    • US20120094323A1
    • 2012-04-19
    • US13147607
    • 2010-02-02
    • Ronald DekkerAnja Van De Stolpe
    • Ronald DekkerAnja Van De Stolpe
    • C12Q1/18H01B13/00B05D5/00C12M1/34B05D1/36
    • G01N1/30C12N5/0657C12N2503/02C12N2535/10G01N33/5061
    • Disclosed is a device for determining the cardiotoxicity of a chemical compound, comprising a substrate (10) carrying a deformable stack (34), said stack being partially detached from the substrate by a cavity (32) allowing an out-of-plane deformation of the stack, said stack comprising a first deformable layer (16), a second deformable layer (20) and a multi-electrode structure (18) sandwiched between the first and second deformable layers, the second deformable layer carrying a pattern of cardiomyocytes (28) adhered thereto; and a liquid container (26) mounted on the substrate for exposing the cardiomyocytes to the chemical compound. A method of manufacturing such a device is also disclosed. The present invention further relates to the use of the device for drug target discovery and/or drug development and a method for developing a disease model for a disease that is caused by or modified by stretching of cells, in particular a cardiac disease model.
    • 公开了一种用于确定化合物的心脏毒性的装置,包括承载可变形叠层(34)的基底(10),所述叠层通过空腔(32)部分地与基底分离,允许外部变形 所述堆叠包括夹在所述第一和第二可变形层之间的第一可变形层(16),第二可变形层(20)和多电极结构(18),所述第二可变形层承载心肌细胞图案(28 ) 和安装在基板上的用于将心肌细胞暴露于化合物的液体容器(26)。 还公开了制造这种装置的方法。 本发明还涉及该装置用于药物靶发现和/或药物开发的用途,以及用于开发由细胞拉伸,特别是心脏疾病模型引起或改变的疾病的疾病模型的方法。
    • 6. 发明授权
    • Genomic selection and sequencing using encoded microcarriers
    • 使用编码的微载体的基因组选择和测序
    • US08932811B2
    • 2015-01-13
    • US13203637
    • 2010-02-26
    • Anja Van De StolpeJacob Marinus Jan Den ToonderPieter Jan Van Der Zaag
    • Anja Van De StolpeJacob Marinus Jan Den ToonderPieter Jan Van Der Zaag
    • C12Q1/68C12P19/34C12M1/00C12M1/34B32B5/16C07H21/02C07H21/04
    • C12Q1/6869Y10T428/2982C12Q2565/519C12Q2563/149C12Q2537/143
    • The present invention relates to a method for determining the sequence of a nucleic molecule. Herein a capture oligonucleotide probe is attached to an encoded microcarrier, wherein the code of said microcarrier identifies the sequence of said oligonucleotide probe. The capture oligonucleotide probe is hybridized with a sample comprising nucleic acids molecules, wherein said DNA fragment comprises a sequence which is complementary to the sequence of the capture oligonucleotide probe. The sequence of the DNA molecule is determined, wherein the capture oligonucleotide probe serves as a primer for a DNA polymerase, in the case of single molecule sequencing this is a sequencing primer. After the sequence determination, the nucleotide sequence of the capture oligonucleotide probe is identified by determining the code on the microcarrier, which corresponds with the capture oligonucleotide probe. This sequence information directly identifies the location of the sequenced DNA fragment on the genome, allowing direct comparison.
    • 本发明涉及确定核酸分子序列的方法。 本文中,捕获寡核苷酸探针连接到编码的微载体上,其中所述微载体的编码识别所述寡核苷酸探针的序列。 捕获寡核苷酸探针与包含核酸分子的样品杂交,其中所述DNA片段包含与捕获寡核苷酸探针的序列互补的序列。 确定DNA分子的序列,其中捕获寡核苷酸探针用作DNA聚合酶的引物,在单分子测序的情况下,这是测序引物。 序列测定后,通过测定与捕获寡核苷酸探针对应的微载体上的编码来鉴定捕获寡核苷酸探针的核苷酸序列。 该序列信息直接识别基因组上测序的DNA片段的位置,从而直接比较。
    • 7. 发明申请
    • GENOMIC SELECTION AND SEQUENCING USING ENCODED MICROCARRIERS
    • 使用编码微控制器的基因选择和序列
    • US20110311975A1
    • 2011-12-22
    • US13203637
    • 2010-02-26
    • Anja Van De StolpeJacob Marinus Jan Den ToonderPieter Jan Van Der Zaag
    • Anja Van De StolpeJacob Marinus Jan Den ToonderPieter Jan Van Der Zaag
    • C12Q1/68C12M1/34
    • C12Q1/6869Y10T428/2982C12Q2565/519C12Q2563/149C12Q2537/143
    • The present invention relates to a method for determining the sequence of a nucleic molecule. Herein a capture oligonucleotide probe is attached to an encoded microcarrier, wherein the code of said microcarrier identifies the sequence of said oligonucleotide probe. The capture oligonucleotide probe is hybridized with a sample comprising nucleic acids molecules, wherein said DNA fragment comprises a sequence which is complementary to the sequence of the capture oligonucleotide probe. The sequence of the DNA molecule is determined, wherein the capture oligonucleotide probe serves as a primer for a DNA polymerase, in the case of single molecule sequencing this is a sequencing primer. After the sequence determination, the nucleotide sequence of the capture oligonucleotide probe is identified by determining the code on the microcarrier, which corresponds with the capture oligonucleotide probe. This sequence information directly identifies the location of the sequenced DNA fragment on the genome, allowing direct comparison.
    • 本发明涉及确定核酸分子序列的方法。 本文中,捕获寡核苷酸探针连接到编码的微载体上,其中所述微载体的编码识别所述寡核苷酸探针的序列。 捕获寡核苷酸探针与包含核酸分子的样品杂交,其中所述DNA片段包含与捕获寡核苷酸探针的序列互补的序列。 确定DNA分子的序列,其中捕获寡核苷酸探针用作DNA聚合酶的引物,在单分子测序的情况下,这是测序引物。 序列测定后,通过测定与捕获寡核苷酸探针对应的微载体上的编码来鉴定捕获寡核苷酸探针的核苷酸序列。 该序列信息直接识别基因组上测序的DNA片段的位置,从而直接比较。
    • 10. 发明申请
    • IN VITRO DIAGNOSTIC TESTING INCLUDING AUTOMATED BROKERING OF ROYALTY PAYMENTS FOR PROPRIETARY TESTS
    • 在体外诊断测试中,包括自动检测专有费用的专有费用
    • US20130226621A1
    • 2013-08-29
    • US13881512
    • 2011-10-24
    • Pieter Jan Van Der ZaagNevenka DimitrovaAnja Van De StolpeHendrik Van Houten
    • Pieter Jan Van Der ZaagNevenka DimitrovaAnja Van De StolpeHendrik Van Houten
    • G06Q20/10G06Q50/22
    • G06Q20/10G06Q10/00G06Q50/22G16B20/00G16H40/20G16H40/63
    • A method comprises: recording an electronic record of diagnostic events including the performing of in-vitro diagnostic tests; during the recording, identifying the performing of a licensed in-vitro diagnostic test for which license information is stored in a licenses database; and computing license compensation due to a licensor for the performing of the licensed in-vitro diagnostic test based on royalty calculation information stored in the licenses database. The recording, identifying, and computing operations are performed by one or more computers. The method may further include remitting the computed license compensation to the licensor, the remitting also being performed by one or more computers. The licensed in-vitro diagnostic test may comprise a licensed biomarker test, for example one obtained by DNA or RNA sequencing, and the method may further comprise: performing the licensed biomarker test using a genome sequencer, wherein the performing of the licensed biomarker test and the computing of license compensation are both performed at a single medical facility.
    • 一种方法包括:记录诊断事件的电子记录,包括进行体外诊断测试; 在记录期间,识别许可证体验诊断测试的执行,许可信息被存储在许可证数据库中; 以及根据许可人根据存储在许可证数据库中的版税计算信息执行许可的体外诊断测试来计算许可证补偿。 记录,识别和计算操作由一个或多个计算机执行。 该方法还可以包括将所计算的许可证补偿递交给许可方,还由一个或多个计算机执行。 许可的体外诊断测试可以包括许可的生物标志物测试,例如通过DNA或RNA测序获得的测试,并且该方法还可以包括:使用基因组测序仪进行许可的生物标志物测试,其中执行许可的生物标志物测试和 许可证补偿的计算都在单一医疗机构进行。