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Biomedical subjects

Catherine R Cabrera

Publications and source records attributed to Catherine R Cabrera.

2 recordsLinked to original sources

Lab-on-a-chip for drug development.

Significant advances have been made in the development of micro-scale technologies for biomedical and drug discovery applications. The first generation of microfluidics-based analytical devices have been designed and are already functional. Microfluidic devices offer unique advantages in sample handling, reagent mixing, separation, and detection. We introduce and review microfluidic concepts, microconstruction techniques, and methods such as flow-injection analysis, electrokinesis, and cell manipulation. Advances in micro-device technology for proteomics, sample preconditioning, immunoassays, electrospray ionization mass spectrometry, and polymerase chain reaction are also reviewed.

Animals↗

Passive electrophoresis in microchannels using liquid junction potentials.

The formation of the liquid junction potential (LJP) is a well-studied phenomenon that occurs in the presence of ionic concentration gradients. Although the LJP has been well characterized, its impact has generally been overlooked in microfluidic applications. The characteristics of flow in microfluidic channels cause this phenomenon to be particularly important, both as a source of deviation from anticipated results and as a tool capable of being harnessed to perform useful tasks. It is demonstrated that LJPs formed in microchannels can induce appreciable electrophoretic transport of charged species without the use of electrodes or an external power supply. This process is demonstrated in an H-filter (an H-shaped microfluidic channel used to bring two fluids into contact allowing extraction of diffusing species from one stream to another) by generating junction potentials between two flowing streams containing different concentrations of strong electrolytes and observing the mass transport of the charged dye fluorescein between those streams. It is shown that the LJP can be controlled to either accelerate or decelerate mass transport across a fluid interface in the absence of an interposed membrane. A preliminary mathematical description of the phenomena is offered to support the hypothesis that the observed mass transport is a result of the LJP. Possible practical microfluidic applications of electrophoretic transport without electrodes are discussed.

Diffusion↗