Abstract: Apparatus for cooling a bundle of capillary tubes to prevent overheating of the tubes during a parallel capillary electrophoresis procedure. The apparatus includes a jacket of thermally conductive solid material comprising mating jacket members movable between an open position in which the jacket members are separated to allow placement of the bundle in the jacket and a closed position in which the jacket members are mated together and the bundle is disposed inside the jacket in thermally conductive relation with the jacket. Window openings in the mating jacket members define a window to permit the passage of light through the window and the capillary tubes of the bundle at the location of the window.

Abstract: A hydrodynamic injector for substantially concurrently loading fluid samples to be analyzed into multiple capillary tubes of a capillary electrophoresis system. The injector includes an enclosure defining a pressure chamber for holding multiple receptacles, each containing a fluid sample, and apertures in the enclosure for passing capillary tubes into a position inside the pressure chamber and in fluid communication with the samples in respective receptacles. Electrodes on the enclosure extend into the pressure chamber for reception in the receptacles. The pressure chamber is pressurized with gas to substantially concurrently force the fluid samples from respective receptacles into the capillary tubes in preparation for a capillary electrophoresis operation.

Abstract: A multiplexed capillary electrophoresis system with cooling sufficient to prevent overheating during chiral separation. The system includes a thermally insulated enclosure enclosing a bundle of capillary tubes, a light source and photodetector. A heat transfer system is provided for cooling closely spaced portions and spread apart portions of the capillary tubes to an extent sufficient to prevent overheating of the tubes and contents thereof due to the heat generated during chiral separation.

Abstract: The invention provides methods, apparatus, and systems for performing high-throughput preparation and screening of salts and polymorphs of drug candidates. The invention is directed towards enhancing the pre-formulation discovery process used for drug development. In particular, processes that determine suitable salts and processes that discover substantially every polymorph that can form from a particular drug candidate are provided. The processes are performed using several apparatuses that are specifically configured to carry-out various steps in a high-throughput characterization process. One such apparatus is configured for synthesizing a plurality of library members based on, for example, a library model generated by a computer system. Another apparatus may filter the synthesized solution to provide a substantially pure mixture that can be subjected to salt or polymorph testing.

Abstract: The invention provides methods, apparatus, and systems for performing high-throughput preparation and screening of salts and polymorphs of drug candidates. The invention is directed towards enhancing the pre-formulation discovery process used for drug development. In particular, processes that determine suitable salts and processes that discover substantially every polymorph that can form from a particular drug candidate are provided. The processes are performed using several apparatuses that are specifically configured to carry-out various steps in a high-throughput characterization process. One such apparatus is configured for synthesizing a plurality of library members based on, for example, a library model generated by a computer system. Another apparatus may filter the synthesized solution to provide a substantially pure mixture that can be subjected to salt or polymorph testing.

Abstract: A hydrodynamic injector for substantially concurrently loading fluid samples to be analyzed into multiple capillary tubes of a capillary electrophoresis system. The injector includes an enclosure defining a pressure chamber for holding multiple receptacles, each containing a fluid sample, and apertures in the enclosure for passing capillary tubes into a position inside the pressure chamber and in fluid communication with the samples in respective receptacles. Electrodes on the enclosure extend into the pressure chamber for reception in the receptacles. The pressure chamber is pressurized with gas to substantially concurrently force the fluid samples from respective receptacles into the capillary tubes in preparation for a capillary electrophoresis operation.

Abstract: A multiplexed capillary electrophoresis system with cooling sufficient to prevent overheating during chiral separation. The system includes a thermally insulated enclosure enclosing a bundle of capillary tubes, a light source and photodetector. A heat transfer system is provided for cooling closely spaced portions and spread apart portions of the capillary tubes to an extent sufficient to prevent overheating of the tubes and contents thereof due to the heat generated during chiral separation.

Abstract: A parallel capillary electrophoresis system for separating and analyzing the components of multiple chemical samples. The system comprises a bundle of capillary tubes arrayed to have at least portions of the tubes extending generally parallel to one another, a light source for emitting light to pass through the capillary tubes, and a photodetector comprising a linear array of photodetector elements for receiving light passing through the capillary tubes. The improvement involves mounting the photodetector for rotation whereby the angular position of the linear array of photodetector elements can be adjusted to an optimal position for analyzing the light passing through the capillary tubes.

Abstract: A multiplexed capillary electrophoresis system and process including a bundle of capillary tubes, a power source, a light source, a processor and an array of photodetector elements. Each element of the array generates a pixel signal corresponding to the light passing through the bundle of capillary tubes during the multiplexed capillary electrophoresis process. An A/D converter converts each of the pixel elements signals into a digital value corresponding to the light received by one of the photodetector elements. For each peak digital value, the processor selects five digital values corresponding to the light received by five contiguous photodetector elements and generates output signals. Each output signal corresponds to the light passing through the bundle of capillary tubes and is a function of the selected digital values. As a result, noise and drifts of the pixel signals are minimized.