Abstract: Systems for quantifying one or more target analyte concentrations in a process solution are provided and can be used, for example, in methods for quantifying a target analyte concentration. These systems and methods include continuous and batchwise automated titration methods that use titration chemistries to measure the target analyte concentration in the process solution using a multiwavelength detector. The methods provide for efficient and robust automated titration methods for a variety of target analytes and can include methods that analyze more than one analyte and that provide for a dynamic range for measurement of more than one target analyte concentration.

Abstract: When an operation receiver receives an operation for starting automatic start-up processing, a display controller causes a display to display a first direction image indicating a working order of a plurality of objects to be controlled, sequentially changes a display mode of a status image corresponding to an object that has worked to a first mode, and changes a display state of each of a plurality of operation images to an operable first state or an inoperable second state. When the operation receiver receives an operation for starting automatic stop processing, the display controller causes the display to display a second direction image indicating a stopping order of the plurality of objects in a reversed manner of the first direction image, sequentially changes a display mode of a status image corresponding to an object that has stopped to a second mode.

Abstract: A separation container for extracting a portion of a sample for use or testing and method for preparing samples for downstream use or testing are provided. The separation container may include a body defining an internal chamber. The body may define an opening, and the body may be configured to receive the sample within the internal chamber. The separation container may further include a seal disposed across the opening, such that the seal may be configured to seal the opening of the body, and a plunger movably disposed at least partially inside the internal chamber. The plunger may be configured to be actuated to open the seal and express the portion of the sample.

Abstract: The present invention belongs to the technical field of analysis and detection and provides a method for detecting a selenoamino acid in a selenoprotein. The detection method includes: (1): mixing 10-30 mg of a selenoprotein sample with hydrochloric acid, and hydrolyzing with microwaves at 140-170° C. for 10-40 min to obtain a hydrolysate; (2): adjusting pH of the hydrolysate to 6-8 to obtain a pretreated solution; and, (3): detecting a selenoamino acid in the pretreated solution with high performance liquid chromatography-hydride generation-atomic fluorescence spectrometry (HPLC-HG-AFS) to obtain a content of the selenoamino acid. The method is simple in operation and provides an accurate and reliable result, and also reduces time and cost.

Abstract: The present disclosure relates to a combustion tube for a device for elemental analysis of a sample, comprising an outer tube including an outlet and an inner tube including an inlet, the inner tube detachably insertable into the outer tube, wherein the outer and inner tubes are arranged such that the sample passes through the inlet, through the inner tube into the outer tube, and out of the combustion tube through the outlet, wherein the inner and outer tubes are configured such that, at least in a region in which the inner tube is surrounded by the outer tube, the sample is essentially inside the inner tube. The outer tube is made of a quartz glass, and the inner tube is made of a ceramic. The present invention further relates to a device for elemental analysis of a sample comprising a combustion tube according to the present disclosure.

Abstract: An automatic analyzer cartridge, spinnable about a rotational axis, has fluid and aliquoting chambers, a metering chamber connected to a vent that is nearer to the rotational axis than the metering chamber, first and second ducts connecting the fluid and aliquoting chambers, and the metering and aliquoting chambers, respectively. Metering chamber side walls taper away from a central region, wherein capillary action next to the walls is greater than in the central region. Fluid flows to the metering chamber using capillary action via the second duct that has an entrance and exit in the aliquoting and metering chambers, respectively; the exit being closer to the rotational axis than the entrance. A downstream fluidic element connects to the metering chamber via a valve. A fluidic structure receives and processes a biological sample into the processed biological sample and has a measurement structure that enables measurement of the processed biological sample.

Abstract: The invention is directed to a method for chemiluminescent sulphur detection wherein the method comprises the following steps. (a) oxidation of a gaseous starting mixture comprising one or more sulphur compounds to obtain an oxidized gas mixture. (b) reduction of the oxidized gas mixture as obtained in step (a) to obtain a gaseous mixture of reduced sulphur compounds in the presence of a ceramic surface. (c) reacting the mixture of reduced sulphur compounds obtained in step (b) with ozone to obtain a sulphur compound in excited state and measuring a chemiluminescent emission of the sulphur compound in excited state to obtain a measure for the amount of sulphur compounds in the gaseous starting mixture. The ceramic surface in step (b) is a magnesium aluminium silicate comprising surface.

Abstract: The present invention relates to a method for purifying pure thioflavin T having a step of preparing a thioflavin T solution in which crude thioflavin T is dissolved in a polar solvent and a step of carrying out liquid-liquid extraction of the thioflavin T solution with a non-polar solvent.

Abstract: Systems for quantifying a target analyte concentration in a process solution are provided and can be used, for example, in methods for quantifying a target analyte concentration. These systems and methods include continuous automated titration methods that use titration chemistries to measure the target analyte concentration in the process solution. The method steps provide for efficient and robust automated titration methods for a variety of target analytes and can include methods that provide for methods that provide a dynamic range for measurement of target analyte concentrations.

Abstract: Systems for quantifying a target analyte concentration in a process solution are provided and can be used, for example, in methods for quantifying a target analyte concentration. These systems and methods include continuous automated titration methods that use titration chemistries to measure the target analyte concentration in the process solution. The method steps provide for efficient and robust automated titration methods for a variety of target analytes and can include methods that provide for methods that provide a dynamic range for measurement of target analyte concentrations.

Abstract: Embodiments are directed to a transfer arm with a probe and a crash detection mechanism for use in a clinical analyzer in an in vitro diagnostics environment. The mechanism requires no user-intervention after a collision event, unless the automated inspection mechanism determines that damage to the probe requires probe replacement. Moreover, the mechanism is capable of protecting the probe, in some instances, from damage during a collision. The mechanism provides for automatic resetting after a collision, self-checking, and alignment correction. The mechanism includes a crash detection printed circuit assembly with a switch, and a spring-loaded contact sensor assembly configured to secure a probe within the transfer arm and allow for electrical connection between the switch and the probe during normal operation and electrical disconnection between the switch and the probe upon contact of the probe with an obstruction.

Abstract: Oxy-pyrohydrolysis articles, systems and methods for total halogen, in particular fluorine analysis are provided. A sample containing halogen elements is provided into a pyrotube for combustion. A combustion-enhancing bed including ceramic fibers or fabrics is disposed inside the pyrotube to enhance the combustion and protect the pyrotube from damage by corrosive gases.

Abstract: Techniques are disclosed for calibration systems and methods for analyte detectors. In one example, a system may include a calibration device configured to operate with an analyte detector. The calibration device may include a chamber configured to receive a sample and pass at least a portion of the sample including analytes to the analyte detector for examination. The calibration device may further include a reservoir including a calibrant and configured to be selectively positioned in the chamber as the sample to provide the portion of the sample including the analytes to calibrate the analyte detector. Additional systems and related methods are provided.

Abstract: The invention relates to an integrated process for assessing one or more properties of a catalyst. In the method, a standard chemical reactor or reactors is/are provided, and a bypass means is also provided, to transport a sample of whatever is added to the industrial reactor, to the test reactor. Both gases and liquids are transferred to the test reactor.

Abstract: The present disclosure provides methods for detection and quantification of trimethylamine (TMA) or trimethylamine oxide (TMAO) comprising passing a sample over a sensor comprising a substrate having a plurality of chemically responsive dyes selected from the following classes of chemically responsive dyes: metal-containing dyes, pH indicators, or solvatochromic/vapochromic dyes. The disclosure also provides devices and sensors for the detection and quantification of TMA, and methods of diagnosing a subject having trimethylaminuria (TMAU).

Abstract: A simplified reagent system for the analysis of arsenic in an acidic aqueous environment is disclosed. In accordance with the inventive technology, a two reagent system is provided. The first reagent includes a combination of an acidifying agent and an oxidizing agent, and is in particulate form. The second reagent is zinc in particulate form, and is beneficially used in the analysis in the presence of an effective amount of an agent for increasing the rate of arsine gas production.

Abstract: Presented are improved and more sensitive methods for measuring levels of phytoestrogens in a biological sample, and specifically in a human urine sample, employing a High Pressure Liquid Chromatography method, coupled with a photodiode array analysis detection system. Calibration curve preparation for each of a panel of phytoestrogen analytes, including daidzein, equol and genistein, are provided employing techniques that demonstrate greater accuracy and sensitivity of sample level measurement. Clinically applicable techniques suitable for large population scale screening, diet and gut microflora characterization and disease analysis and correlation in human populations, such as in at risk breast cancer populations, through monitoring of phytoestrogen levels, is disclosed.

Abstract: The present invention relates to a quality control method for a Chinese patent drug, and specifically relates to an identification method and a content measurement method for the pediatric compound Endothelium Corneum Gigeriae Galli chewable tablet. Identification is carried out by using specific thin-layer chromatographic identification conditions, and the content is measured by using specific high-performance liquid chromatographic conditions. Accordingly, the specificity and the accuracy are high, chemical components of the product can be fully reflected, the sensitivity is high, the reproducibility is high, the operations are simple, and the change condition of the product quality can be reflected more objectively, comprehensively and sensitively, so that the product quality is controlled on the whole, and comprehensive monitoring of the quality of the Chinese Drug is implemented.

Abstract: This specimen treatment chip includes: a first fluid module having a first flow channel for performing a first treatment step on an object component in a specimen; a second fluid module having a second flow channel for performing a second treatment step on the object component subjected to the first treatment step; a substrate; and a connection flow channel for connecting the first fluid module and the second fluid module disposed on the substrate.

Abstract: The present invention relates to a process for the preparation of angiotensin receptor blockers or its pharmaceutically acceptable salts thereof containing less than 10 ppm of the azido impurities.