Methods for achieving complete sequence coverage of monoclonal antibodies by trypsin digestion and dual-column LC-MS system are provided. The disclosed method improves upon current techniques for standard peptide mapping.

The disclosure describes embodiments of an apparatus including a first gas chromatograph including a fluid inlet, a fluid outlet, and a first temperature control. A controller is coupled to the first temperature control and includes logic to apply a first temperature profile to the first temperature control to heat, cool, or both heat and cool the first gas chromatograph. Other embodiments are disclosed and claimed.

This disclosure relates a device for a chromatographic system, comprising: a chamber defining an internal portion, a capillary disposed within the chamber, the capillary having an input, an output, and an elongate body extending between the input and the output, a cold finger having a first portion in thermal contact with a portion of the elongate body to define a capillary trapping zone, wherein the first portion of the cold finger extends to a second portion that is situated external to the chamber, a heater in thermal contact with the trapping zone of the capillary and configured to transfer heat to the trapping zone, a thermal buffer configured to buffer the heat from the heater into the cold finger and thereby retain the heat within the trapping zone of the capillary, a cooling device arranged external to the chamber and thermally connected to the second portion of the cold finger to define a primary conduction zone, wherein the cooling device is configured to generate a cooling temperature zone at the primary conduction zone, a controller configured to selectively alternate the trapping zone between a cooling temperature by turning off the heat and using the cooling device together with its engagement with the cold finger, and an injection temperature using the heater, wherein the heater alternates between an off state and an on state and a user defined frequency.

Lowering of a switching recovery rate is suppressed without degrading separating ability in a second analytical column. A multidimensional GC includes a sample injector for injecting a sample, a first analytical column for separating the sample injected from the sample injector into one or more components, the first analytical column communicating with the sample injector, a detector for detecting the components of the sample separated in the first analytical column, a second analytical column provided separately from the first analytical column, a switching device connected to an outlet side of the first analytical column and configured to lead the sample out of the first analytical column to the detector or to the second analytical column, and a temperature adjuster configured to adjust temperature of the switching device to a predetermined temperature independently of a temperature of the first analytical column and a temperature of the second analytical column.

A laminated microfluidic device is described that includes an internal microchannel formed from laminating individual layers of the laminated microfluidic device to each other. The laminated microfluidic device also includes a first port, a second port, a third port, and a fourth port each fluidically coupled to the internal microchannel. The laminated microfluidic device permits flow of sample into the laminated microfluidic device through the first port. The laminated microfluidic device fluidically couples to an external pressure source through the second port. The laminated microfluidic device permits the flow of the sample to a first component fluidically coupled to the third port and to a second component fluidically coupled to the fourth port depending on pressure within the internal microchannel of the laminated microfluidic device.

The disclosure describes embodiments of an apparatus including a first gas chromatograph including a fluid inlet, a fluid outlet, and a first temperature control. A controller is coupled to the first temperature control and includes logic to apply a first temperature profile to the first temperature control to heat, cool, or both heat and cool the first gas chromatograph. Other embodiments are disclosed and claimed.

The invention features compact systems and methods for vacuum liquid purification and extraction of a liquid sample.

A gas analysis device suited for e.g. medical analysis of exhaled breath from a subject. A gas inlet receives a gas sample to a flow path for guiding the gas sample to two or more gas separators, e.g. gas chromatography columns, with respective molecule selectivity properties which are different. One or more detectors, each with a sensor, are arranged to generate respective responses to outputs from the two or more gas separators. A communication module generate output data in response to the respective responses from the one or more detectors, e.g. data indicative of selected molecules in the gas sample, e.g. data indicative of one or more diseases identified as a result of identified biomarkers in the gas sample. The device is suitable as a compact device, e.g. a handheld breath analysis device, since the use of a plurality of gas separators allows use of very molecule specific gas separators which can be implemented with a small size. E.g. a flow path with several parallel paths each comprising one or more gas separator may be used.

Methods for achieving complete sequence coverage of monoclonal antibodies by trypsin digestion and dual-column LC-MS system are provided. The disclosed method improves upon current techniques for standard peptide mapping.

A method for modulating analytes in a gaseous stream passing through a capillary, wherein the analytes are retained in a trapping zone of the capillary, or allowed to pass therethrough, based on certain conditions. The method includes, during a first time period, heating the trapping zone of the capillary to a first temperature to desorb analytes therewithin and allow the analytes to pass therethrough, and during a second time period, cooling the capillary to a second temperature that is sufficient to trap and focus the analytes within the trapping zone. During the first time period, the method also includes retaining heat at the capillary during to minimize the load on a cooling device thermally connected thereto, and during the second time period, selectively allowing thermal transfer toward the cooling device.