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Title: Microchip device for liquid phase analysis

Technical Report ·
DOI:https://doi.org/10.2172/758295· OSTI ID:758295

The lab-on-a-chip concept has enabled miniature instruments to be developed that allow the rapid execution and automation of fluidic operations such as valving, separation, dilution, mixing, and flow splitting upon the proper application of a motive (driving) force. The integration of these simple operations to perform complete, multiple-step chemical assays is rapidly becoming a reality. Such compact, monolithic devices potentially enjoy advantages in speed, cost, automation, reagent consumption, and waste generation compared to existing laboratory-scale instruments. Initial reports of these microfluidic devices focused on combining various electrokinetically driven separation methods including microchip electrophoresis, gel electrophoresis, micellar electrokinetic chromatography (MEKC) and open channel electrochromatography (OCEC) with fluidic valving to introduce sample plugs into the separation channel. Other operations have quickly been integrated with the separations and fluidic valving on these microchips. For example, integrated devices with mixers/diluters for precolumn and postcolumn analyte derivatization, deoxyribonucleic acid (DNA) restriction digests, enzyme assays, and polymerase chain reaction (PCR) amplification have been added to the basic design. Integrated mixers that can perform solvent programming for both MEKC and OCEC have also been demonstrated. These examples are simple, yet powerful, demonstrations of the potential for lab-on-a-chip devices. In this report, three key areas for improved performance of these devices are described: on-chip calibration techniques, enhanced separative performance, and enhanced detection capabilities.

Research Organization:
Oak Ridge Y-12 Plant (Y-12), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Defense Programs (DP) (US)
DOE Contract Number:
AC05-84OR21400
OSTI ID:
758295
Report Number(s):
Y/NSP-305; TRN: AH200022%%84
Resource Relation:
Other Information: PBD: 1 May 2000
Country of Publication:
United States
Language:
English