The present invention relates to a liquid chromatography system for the separation of bio-molecules in a fluid including at least two unit operations, wherein the first unit operation is a step of multi-column chromatography and the second unit operation is a step modifying said bio-molecules and/or the fluid, wherein the modification comprises feeding the fluid resulting from the last chromatography column of the first unit operation into a system comprising at least two containers, wherein each container has a volume and a moveable sidewall arranged to divide the volume into a first sub-volume and a second sub-volume, and each container comprises a first port connected to the first volume and a second port connected to the second sub-volume. The invention also relates to a virus inactivation device for a chromatography system according to the invention, which enables continuous or semi-continuous processing of biomolecules, as well as a method of using such a device.

Described is a dual mode sample manager for a liquid chromatography system. The dual mode sample manager includes a sample needle, a sample loop, a metering pump, a needle seat and first and second valves. Each valve is configurable in two valve states to enable two modes of operation. In one mode, sample acquired and stored in the sample needle is injected into a chromatography system flow and, in the other mode, sample acquired through the sample needle and stored in the sample loop is injected into the chromatography system flow. The automated switching of the sample manager between the two modes of operation avoids the need for maintaining two separate liquid chromatography systems or manual reconfiguration of a chromatography system for users desiring the capability of both modes of operation.

Disclosed is a sample dispatcher configured for individually introducing a plurality of portions of one or more sample fluids into a flow of a mobile phase of a separation system configured for separating compounds of the sample fluids. The separation system comprises a mobile phase drive configured for driving the mobile phase through a separation unit configured for separating compounds of the sample fluids in the mobile phase. The sample dispatcher comprises a plurality of sample reservoirs, each configured for receiving and temporarily storing a respective sample fluid portion or at least a part thereof. The sample dispatcher is configured for selectively coupling one of the plurality of sample reservoirs between the mobile phase drive and the separation unit, and further for coupling at least two of the plurality of sample reservoirs in parallel between the mobile phase drive and the separation unit.

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.

Certain embodiments described herein are directed to chromatography systems that include a microfluidic device. The microfluidic device can be fluidically coupled to a switching valve to provide for selective control of fluid flow in the chromatography system. In some examples, the microfluidic device may include a charging chamber, a bypass restrictor or other features that can provide for added control of the fluid flow in the system. Methods of using the devices and methods of calculating lengths and diameters to provide a desired flow rate are also described.

An autosampler for a chromatograph includes a first injection port through which a sample is injected into a first analysis flow path of the chromatograph, a second injection port through which a sample is injected into a second analysis flow path of the chromatograph, a needle that is movable to both of the first injection port and the second injection port, and injects a sample into the first injection port and the second injection port, a first sample loop that stores a sample to be injected into the first analysis flow path, a second sample loop that stores a sample to be injected into the second analysis flow path, and a metering pump that loads a sample in the first sample loop and the second sample loop.

Described is a multi-channel fluidic device that includes a diffusion-bonded body having a device surface and a plurality of fluid channels. Each fluid channel includes a channel segment defined in a plane that is parallel to the device surface and parallel to each of the planes of the other channel segments. The plane of each channel segment is at a depth below the device surface that is different from the depth below the device surface for the other planes. Each channel segment may have a volume equal to the volume of each of the other channel segments. One of the fluid channels may include a plurality of channel segments serially connected to each other and each defined in a plane that is different from the planes of the other channel segments.

Certain embodiments described herein are directed to chromatography systems that include a microfluidic device. The microfluidic device can be fluidically coupled to a switching valve to provide for selective control of fluid flow in the chromatography system. In some examples, the microfluidic device may include a charging chamber, a bypass restrictor or other features that can provide for added control of the fluid flow in the system. Methods of using the devices and methods of calculating lengths and diameters to provide a desired flow rate are also described.

A chromatography valve for use in fluid analysis and chromatography applications is provided. The valve includes a first body having passages extending therethrough and opening on a flat face of the first body at respective passage ports. The valve also includes a second body engaged with the first body in a sealed relationship, whereby one of the first and second bodies is movable relative to the other one between two or more positions for controlling fluid circulation through the passages. The second body includes at least one cartridge receiving cavity for receiving at least one cartridge removably provided therein. The cartridge has channel(s) for channeling fluid of pairs of the passage ports, depending on the position of the first body relative to the second body, thereby channeling fluid through selected ones of the passages via the at least one channel. A method of operating the valve is also provided.

A fluid chromatograph includes a flow path switching part configured to switch to one of states including a sampling state in which the measuring pump is connected to a proximal end side of the sampling flow path, a total volume introduction state in which the mobile phase sending part is connected to a proximal end side of the sampling flow path and the needle port and the analysis flow path are connected to each other, an injection state in which the measuring pump is connected to the proximal end side of the sampling flow path and the needle port and the second sample loop are connected to each other, and a loop introduction state in which the mobile phase sending part is connected to one end side of the sample loop and the analysis flow path is connected to the other end side of the sample loop.