A passive sampling device is provided that is comprised of a member having a first surface and a second surface opposite the first surface and a hole through the member extending from the first surface to the second surface. An adsorbent material is positioned between two mesh members. The adsorbent material allows for efficient and selective removal of organic molecules, such as, for example, perfluoroalkyl substances.

A method of processing of a biological sample containing multiple metabolites is described The method comprising the steps of pre-treating the biological sample with a metabolite extraction solvent to provide a pre-treated sample, separating a first aliquot of the pretreated sample by reverse phase liquid chromatography (RPLC) to provide a first eluent containing resolved hydrophobic metabolites, and separating a second aliquot of the pre-treated sample by hydrophilic interaction liquid interaction chromatography (HILIC) to provide a second eluent containing resolved hydrophilic metabolites. The first and second eluents are assayed using targeted tandem mass spectroscopy operated in multiple reaction monitoring mode. Each liquid chromatography step (LC) is directly hyphenated with the tandem mass spectrometry (MS/MS) into a single LC-MS/MS analysis. The extraction solvent typically comprises methanol, isopropanol and an acetate buffer.

Methods, apparatuses, and systems associated with aerosol collection devices (such as, but not limited to, breath-aerosol collector devices, breathalyzers) are provided.

The present invention relates to a method and/or device for improving the separation behaviors and performance of aqueous two-phase system (ATPS) for the isolation and/or concentration of one or more target analytes from a sample. In one embodiment, the present method and device comprise ATPS components within a porous material and one or more phase separation behavior modifying agents that improve the separation behavior and performance characteristics of ATPS, including but not limited to the increasing the stability or reducing fluctuations of ATPS thought the adjustment of total volume of a sample solution that undergoes phase separation, volume ratio of the two phases of the ATPS, fluid flow rates, and concentrations of ATPS components.

A precipitate and/or an inclusion in a metal material are extracted by electrolysis using an electrolyte solution. The electrolyte solution contains an adsorbent physically adsorbed and/or chemically adsorbed to any metal other than a matrix metal of the metal material. The extracted precipitate and/or inclusion can be quantitatively analyzed with high accuracy.

A sensor system comprising a housing having an inlet aperture through which fluid enters the housing and a conditioning material in the housing, the conditioning material being adapted to control levels of a substance within the housing. The sensor system comprises a sensor for analysing the fluid in the housing. The sensor system comprises circulation means which is configured to alternate circulation of fluid within the housing between a sensing fluid path in which the fluid is analysed by the sensor and a second fluid path in which the fluid flow is conditioned. A method for analysing fluid in a housing using a sensor is also provided.

The present disclosure discusses a method of separating a sample (e.g., pharmaceutical drug, genotoxic impurity, biomarker, and/or biological metabolite) including coating a metallic flow path of a chromatographic system; injecting the sample into the chromatographic system; flowing the sample through the chromatographic system; separating the sample; and analyzing the separated sample using mass spectroscopy. In some examples, the coating applied to the surfaces defining the flow path is non-binding with respect to the sample—and the separated sample. Consequently, the sample does not bind to the low-binding surface of the coating of the flow path. The applied coating can increase the chromatographic peak area for the sample of the chromatographic system.

There is provided a multi-layered membrane for separating components in an aqueous sample. There is also provided a method of preparing said multi-layered membrane, a method of separating blood plasma from a whole blood sample and a diagnostic device for separation of blood plasma from a whole blood sample.

An in vitro intestinal drug disposition device (1) comprises a donor chamber (2) for a donor solution and having a bottom end (18) and a top end (19). The device (1) also comprises a receiver chamber (3) for an absorption solution and an absorption membrane (4) arranged in between and separating the chambers (2, 3). A first side (5) of the absorption membrane (4) is to be in contact with the donor solution and a second side (6) of the absorption membrane (4) is to be in contact with the absorption solution. A ratio of an internal volume of the donor chamber (2) to an area of the first membrane side (5) is equal to or smaller than 3 ml/cm.sup.2. A cross-sectional area of the donor chamber (2) at the bottom end (18) is larger than a cross-sectional area of the donor chamber (2) at the top end (19).

A cartridge sampler for collecting a target species from an environment for subsequent chemical analysis includes removable collection media having at least one molecule sensor thereon. The cartridge sampler includes a means for tagging a geospatial location and time that the fluid samples are provided to the collection media such that the location and time that the fluid samples are provided to the collection media can be later determined. Also disclosed are systems and methods for collecting species from various environments including a subsurface formation, a pipeline, and gaseous, soil or sub-slab, and aqueous environments. The cartridge sampler is fitted on or within a device designed for moving within each environment.