METHOD AND DEVICE FOR ABSOLUTE QUANTIFICATION OF ANALYTES

    公开(公告)号:US20240345099A1

    公开(公告)日:2024-10-17

    申请号:US18683332

    申请日:2022-08-11

    申请人: Cenios GmbH

    摘要: The invention relates to a method for the absolute quantification of at least one analyte by means of a rapid test, in particular by spectroscopic determination. In order to provide a method and a device for the absolute quantification of analytes and to enable the creation of a database for the improved individual dosing of therapeutics, whereby a particularly accurate quantification of at least one analyte is possible in a simple manner, particularly inexpensively, particularly quickly and at any location without the need for a laboratory, it is provided, that at least one nanomaterial is used as a luminescent substance for quantification, which interacts directly or indirectly with the analyte, wherein at least one signal generated by the nanomaterial is measured and wherein in addition an internal and/or external standard series, in particular by means of Raman-labeled targets and/or fluorescence-labeled targets, is measured and subsequently the generated signal is standardized or referenced on the basis of the internal and/or external standard series, so that an absolute quantification is achieved.

    DNA DETECTION METHOD AND DNA DETECTION SYSTEM

    公开(公告)号:US20240344120A1

    公开(公告)日:2024-10-17

    申请号:US18567061

    申请日:2021-06-07

    IPC分类号: C12Q1/686 G01N21/64 G01N33/58

    摘要: The present invention provides a DNA detection method comprising: a first step of dividing a specimen solution containing a fluorescent-labeled probe or a DNA intercalator and multiple types of DNA to be detected into a plurality of aliquots; a second step of performing PCR in microcompartments, each containing one of the aliquots; a third step of measuring fluorescence intensity from the fluorescent-labeled probe or the DNA intercalator in each of the microcompartments as temperature changes; a fourth step of calculating a melting temperature of the multiple type of DNA to be detected from each measured fluorescence intensity; a fifth step of identifying any microcompartment affected by one or more bubbles; and a sixth step of excluding data obtained for the microcompartment affected by one or more bubbles from all data obtained for the plurality of microcompartments.