Provided is a preparative separation liquid chromatograph system and preparative separation condition searching method which allows for an easy setting of the preparative separation condition. A sample temporally separated into components by a separation column is introduced into a detector and a fraction collector, with each component fractionated and collected by the fraction collector based on the result of a detection by the detector. A controlling and processing unit holds the following data for each sample or compound in the form of a database: chromatogram data obtained when a liquid chromatograph analysis in a preparative separation condition searching mode is performed for various standard samples under a search condition; and chromatogram data obtained when a liquid chromatograph analysis in a preparative separation mode is performed under one or more sets of preparative separation conditions for the various standard samples, along with the preparative separation condition used in this analysis.

A method and system are disclosed for isolating intact acellular particles using size exclusion and for obtaining size and concentration of such isolated particles. In one embodiment, the disclosure is directed to use of Particle Purification Liquid Chromatography (PPLC), a high-resolution chromatographic size-guided turbidimetry-enabled system for dye-free isolation, on-line characterization, and retrieval of intact acellular particles, including extracellular vesicles (EVs) and membraneless condensate particles (MCs) from various biofluids.

A method and system are disclosed for isolating intact acellular particles using size exclusion and for obtaining size and concentration of such isolated particles. In one embodiment, the disclosure is directed to use of Particle Purification Liquid Chromatography (PPLC), a high-resolution chromatographic size-guided turbidimetry-enabled system for dye-free isolation, on-line characterization, and retrieval of intact acellular particles, including extracellular vesicles (EVs) and membraneless condensate particles (MCs) from various biofluids.

A supercritical fluid chromatography system comprises a first pump for pumping a first flow stream comprising a compressible fluid and a second pump for pumping a second flow stream comprising a modifier fluid. The second pump is in parallel with the first pump. A column is located in a combined flow stream. The column is located downstream of the first and second pumps. The combined flow stream comprises the first flow stream, the second flow stream, and a sample. A detector is located downstream of the column. A gas-liquid separator is located downstream of the detector. The gas-liquid separator is configured to vent a majority of the compressible fluid while maintaining a majority of the sample, thus preventing aerosolization of the flow stream and minimizing sample loss as well as cross contamination. An open bed collector is located after the gas-liquid separator.

The disclosure relates to a gradient twin column recycling chromatography method that is used to separate a mixture containing closely eluting compounds. In one embodiment, a sample includes a primary organic compound and one or more impurities that closely elute with the primary organic compound. A gradient mobile phase is initially used to remove unwanted early eluting and late eluting impurities from the sample. After the gradient removal of some of the impurities is complete, the remaining mixture of the primary organic compound and the closely eluting impurities are separated using recycle chromatography methodology with an isocratic mobile phase.

The disclosure relates to a gradient twin column recycling chromatography method that is used to separate a mixture containing closely eluting compounds. In one embodiment, a sample includes a primary organic compound and one or more impurities that closely elute with the primary organic compound. A gradient mobile phase is initially used to remove unwanted early eluting and late eluting impurities from the sample. After the gradient removal of some of the impurities is complete, the remaining mixture of the primary organic compound and the closely eluting impurities are separated using recycle chromatography methodology with an isocratic mobile phase.

In a method for processing successive fluidic sample portions provided by a sample source, sample reception volumes are filled successively temporarily with at least a respective one of the sample sections, and the sample sections are emptied successively out of the sample reception volumes in such a way, that, while emptying, it is avoided to bring two respective ones of the sample sections, which have not left the sample source directly adjacent to one another, in contact with one another.

In a preparative liquid chromatograph apparatus where a sample containing compounds temporally separated from each other by LC is introduced into a detector and a fraction collector to collect fractions of the sample each containing one or more compounds. A result storage section stores analysis results obtained for a plurality of samples by performing, for each identical sample, LC analyses under different separation conditions. A display-target selection receiver displays an analysis result display screen having a plurality of result display areas for individually displaying results of different LC analyses and a selection indication area for allowing a user operation for selecting one sample from a plurality of samples, and receives the user operation in the selection indication area. An analysis result display processor retrieves, from the result storage section, a plurality of analysis results corresponding to the selected sample, and displays the analysis results in the result display areas.

A main controller 201 of a main substrate 20 performs serial communications with a sub controller 214 of each flowrate control substrate 21. The flowrate of the carrier gas is controlled with the flowrate control circuit 213 under the control performed by each sub controller 214. Thus, the main controller 201 only needs to execute the processing of performing the serial communications with each sub controller 214. As a result, the processing executed by the main controller 201 can be reduced, and the processing executed by the main controller 201 is less likely to overwhelm its processing capability even when the number of flowrate control substrates 21 is increased. In addition, a signal line 40 between the main controller 201 and each sub controller 214 can be made long. Thus, the distance between the main substrate 20 and each of the flowrate control substrates 21 can be made long.

A main controller 201 of a main substrate 20 performs serial communications with a sub controller 214 of each flowrate control substrate 21. The flowrate of the carrier gas is controlled with the flowrate control circuit 213 under the control performed by each sub controller 214. Thus, the main controller 201 only needs to execute the processing of performing the serial communications with each sub controller 214. As a result, the processing executed by the main controller 201 can be reduced, and the processing executed by the main controller 201 is less likely to overwhelm its processing capability even when the number of flowrate control substrates 21 is increased. In addition, a signal line 40 between the main controller 201 and each sub controller 214 can be made long. Thus, the distance between the main substrate 20 and each of the flowrate control substrates 21 can be made long.