A sheath flow device for an evaporation light scattering detector comprises an evaporation pipe fastener (110), an evaporation pipe heat insulating component (120), a sheath flow nozzle blocking plate (130), a sheath flow nozzle (140), a sheath flow sleeve (150), a sheath flow outlet piece (170) and a stainless steel spray needle (160). The evaporation pipe fastener, the evaporation pipe heat insulating component, the sheath flow nozzle blocking plate, the sheath flow nozzle, the sheath flow sleeve and the sheath flow outlet piece are concentrically connected orderly from front to back, and all provided with concentric inner holes. Said device is applicable to ELSD sheath flow devices ranging from nanoliter-scale to microliter-scale. On one hand, material particles entering a testing pool are enveloped and aggregated so that the formation of eddy and turbulence can be reduced, the chromatographic peak shape of a sample can be improved and the stability of sample detection can be enhanced; on the other hand, the testing pool can be cleaned so that baseline noise can be reduced and the signal to noise ratio can be increased.

A sheath flow device for an evaporation light scattering detector comprises an evaporation pipe fastener (110), an evaporation pipe heat insulating component (120), a sheath flow nozzle blocking plate (130), a sheath flow nozzle (140), a sheath flow sleeve (150), a sheath flow outlet piece (170) and a stainless steel spray needle (160). The evaporation pipe fastener, the evaporation pipe heat insulating component, the sheath flow nozzle blocking plate, the sheath flow nozzle, the sheath flow sleeve and the sheath flow outlet piece are concentrically connected orderly from front to back, and all provided with concentric inner holes. Said device is applicable to ELSD sheath flow devices ranging from nanoliter-scale to microliter-scale. On one hand, material particles entering a testing pool are enveloped and aggregated so that the formation of eddy and turbulence can be reduced, the chromatographic peak shape of a sample can be improved and the stability of sample detection can be enhanced; on the other hand, the testing pool can be cleaned so that baseline noise can be reduced and the signal to noise ratio can be increased.

In the present system and method, a conduit from a LC device continuously transports solvent, buffers, and analytes to the inlet of a solvent removal and analyte conversion device which evaporates the solvents, leaving non-volatile analytes for detection. The device comprises a rotating disk. The liquid chromatograph device can be any device using liquid chromatography to separate molecules. The solvents in the LC effluent can include, but are not limited to, water, methanol, acetonitrile, tetrahydrofuran, and acetone. After removal of the volatile components, the non-volatile analytes are converted with a concentrated energy source so that they may be detectable.

In an analyzing system including a commanding unit for sending a command and an executing unit for executing a processing upon receiving the command, a processing instruction may not be executed at the right time due to a heavy traffic of information and other factors. In order to solve this problem, in a preparative separation system 1 according to the present invention, a PC 20 provides the execution time for starting/finishing the fractionation processing to a controller 18. Therefore, even in the case where the time of the PC 20 and that of the controller 18 are not synchronized, the controller 18 can accurately set the execution time for starting/finishing the fractionation in a preparative separation unit 16. A piping 17 may be placed so that the traveling time of sample components is sufficiently larger than the delay time of signals due to the signal transfer lag and other reasons. This can absorb the delay time, allowing the units to cooperate with each other at a correct timing.

A pre-analysis treatment device usable for an amino acid, organic acid, and glucide includes an ion-exchange unit configured to load a test sample on a solid-phase cartridge S having a strong ion-exchange resin phase, to allow the strong ion-exchange resin phase to adsorb a predetermined organic compound, then supply a dehydration solvent to dehydrate the strong ion-exchange resin phase, and a derivatization unit configured to feed a predetermined amount of the derivatization reagent to the dehydrated strong ion-exchange resin phase to allow the derivatization reagent to retain for a predetermined time period, thereby trimethylsilylating the organic compound adsorbed on the strong ion-exchange resin phase, and simultaneously desorbing the trimethylsilylated organic compound from the strong ion-exchange resin phase, and then supply a push-out solvent to push the trimethylsilylated organic compound desorbed, out of the solid-phase cartridge S. The device enables at least one organic compound selected from amino acids, organic acids and glucides contained in a test sample to be derivatized and collected easily in a short period of time, and automation of the pre-analysis treatment.

A pre-analysis treatment device usable for an amino acid, organic acid, and glucide includes an ion-exchange unit configured to load a test sample on a solid-phase cartridge S having a strong ion-exchange resin phase, to allow the strong ion-exchange resin phase to adsorb a predetermined organic compound, then supply a dehydration solvent to dehydrate the strong ion-exchange resin phase, and a derivatization unit configured to feed a predetermined amount of the derivatization reagent to the dehydrated strong ion-exchange resin phase to allow the derivatization reagent to retain for a predetermined time period, thereby trimethylsilylating the organic compound adsorbed on the strong ion-exchange resin phase, and simultaneously desorbing the trimethylsilylated organic compound from the strong ion-exchange resin phase, and then supply a push-out solvent to push the trimethylsilylated organic compound desorbed, out of the solid-phase cartridge S. The device enables at least one organic compound selected from amino acids, organic acids and glucides contained in a test sample to be derivatized and collected easily in a short period of time, and automation of the pre-analysis treatment.

In the present system and method, a conduit from a LC device continuously transports solvent, buffers, and analytes to the inlet of a solvent removal and analyte conversion device which evaporates the solvents, leaving non-volatile analytes for detection. The device comprises a rotating disk. The liquid chromatograph device can be any device using liquid chromatography to separate molecules. The solvents in the LC effluent can include, but are not limited to, water, methanol, acetonitrile, tetrahydrofuran, and acetone. After removal of the volatile components, the non-volatile analytes are converted with a concentrated energy source so that they may be detectable.

A chromatography system for at least one of tangential flow chromatography and lateral flow chromatography comprising: an inlet; a functionalised adsorbent chromatography medium downstream of the inlet; an outlet downstream of the adsorbent chromatography medium; and a flow guide downstream of the inlet and upstream of the adsorbent chromatography medium and configured to distribute a flow of a liquid from the inlet across a width of the adsorbent chromatography medium; wherein the flow guide comprises a pattern of channels providing flow paths from the inlet to different parts of the adsorbent chromatography medium along the width of the adsorbent chromatography medium, wherein the pattern of channels is provided so as to reduce a difference in arrival time and/or flow velocity of liquid reaching the adsorbent chromatography medium across the width of the adsorbent chromatography medium.

A chromatography system for at least one of tangential flow chromatography and lateral flow chromatography comprising: an inlet; a functionalised adsorbent chromatography medium downstream of the inlet; an outlet downstream of the adsorbent chromatography medium; and a flow guide downstream of the inlet and upstream of the adsorbent chromatography medium and configured to distribute a flow of a liquid from the inlet across a width of the adsorbent chromatography medium; wherein the flow guide comprises a pattern of channels providing flow paths from the inlet to different parts of the adsorbent chromatography medium along the width of the adsorbent chromatography medium, wherein the pattern of channels is provided so as to reduce a difference in arrival time and/or flow velocity of liquid reaching the adsorbent chromatography medium across the width of the adsorbent chromatography medium.

Provided herein are new compositions and methods to target and deliver agents to pathological areas by utilizing multifunctional compounds. These compounds include three or more domains: (i) a vimentin-binding peptide, (ii) a linker, and (iii) a drug binding, a capturing reagent, or a detectable moiety. These compounds can be used to detect, isolate, and/or treat cancerous cells such as circulating tumor cells.