Luke P. Lee (Advisor)

LPL36: Behavior of water and ice in nanocavities

J. Tanner Nevill
2005

Nanogap sensors have been developed to study various biochemical reactions such as DNA hybridization, protein conformation, and polymer formation. Recently, the nanogap sensors have been used to study the dielectric properties of water and ice. It is well known that water plays a vital role in many processes on the molecular level. Without water, there would be no cell membranes, no ion transport, no protein ligand interaction, and the list can go on ad nauseum. Although we recognize how important water is to these functions, the precise role of water is still not completely...

LPL40: Digitized Microfluidic Device for Single Cell Analysis

Junyu Mai
Poorya Sabounchi
2005

Most of current clinical diagnosis is based on observation and analysis on a large number of cells, which provides averaged or integrated information about the disease state. However, many diseases start from a small number of mutated or unhealthy cells while most other cells remain normal. In order to detect these precursors as early as possible, a high throughput single cell based detection method is required for the analysis of large number of cells from tissue samples. Here we report a microfluidic device where individual cells are encapsulated in nano-liter aqueous compartments...

LPL34: Single-Cell Electroporation Microchip

Michelle Khine
Adrian Lau
Cristian Ionescu-Zanetti
2005

We previously demonstrated the feasibility of electroporating single cells using an elastomeric device with small (3x4 ìm) lateral trapping/electroporation channels. Single cell electroporation increases the cell membrane's permeability, allowing polar substances otherwise impermeant to the plasma membrane (such as dyes, drugs, DNA, proteins, peptides, and amino acids) to be thus introduced into the cell. Single cell electroporation techniques, pioneered by Lundqvist et al using carbon fiber electrodes, include: electrolyte-filled capillaries, micropipettes and microfabricated chips...

LPL32: Disposable Multi Patch Clamps Using Planar Fludic Channels

Jeonggi Seo
2005

Patch clamp technique has had a profound impact on electrophysiology, playing a crucial role in the characterization of cellular ion channels. Traditionally, the technique was accomplished with a glass pipette positioned by a micromanipulator under a microscope. Even though patch clamp technique has been improved, it is still laborious and requires precise micromanipulation of glass pipettes and skillful handling of the electrical sealing. In addition, the irreversible sealing between cell membranes and pipettes need a new pipette for every new experiment. Because of these...

LPL41: Raised Lateral Patch Clamp Array

Adrian Y. Lau
Paul J. Hung
2006

We are developing a prototype capable of reproducing both the geometry and the function of the traditional glass micropipette tip on chip in a high density configuration. Our technology provides a novel high throughput platform for ion channel studies and is highly compatible with existing multiple-well plate format, allowing simple integration with robotic sample handling system. The device is fabricated on transparent polymer substrate PDMS, and thus allows easy integration with immunofluorescent assay platform to provides electrical and optical measurement concurrently....

LPL35: Microfluidic Cell Culture Array

Philip Lee
2005

The investigation of biological processes on the cellular level is becoming increasingly important for medical and bioengineering purposes. We have learned from genomics and proteomics that a vast amount of molecular information is integrated on the cell level. However, current technology is limited in the ability to assay cellular responses to stimuli in high throughput format. Specifically, a standardized platform to perform array experiments on the laboratory scale is needed to help scientists unravel the complexities of eukaryotic cellular behavior. To this end, we are developing...

LPL39: Integrated Microfluidic SERS Devices

Beomseok Kim
Jeoggi Seo
2005

Raman is a label-free analytical method, which offers tremendous advantages for biomolecular detection. Surface-enhanced Raman scattering (SERS) technique can overcome the low cross-sectional problems inherent in Raman spectroscopy. SERS has been observed for a very large number of molecules adsorbed on the surface of Au or Ag in a variety of morphologies and physical environments. With these environments, its detection limit can reach up to 6-10 orders of magnitude over conventional Raman spectroscopy. We know nanoparticle sizes (15-200 nm) and interparticle spaces (0-10 nm) are...

LPL38: Electrophysiology Using a High-Density Microfluidic Array

Ionescu-Zanetti
Jeonggi Seo
2005

The fact that cellular ion channels are effective drug targets, coupled with the laboriousness of traditional patch clamp techniques, has created a need for hi-throughput electrophysiology platforms. Patch clamp based drug screening technology has been recently implemented by using microfabricated patch clamp designs that replace the traditional patch pipette with a pore in a silicon substrate. While successful at high-throughput measurements of channel activity, current devices have yet to achieve high densities of patched cells per unit volume and rely on robotically operated...

BPN314: Biomimetic Infrared sensor based on the nanogap junction array

Jeonggi Seo
2005

The research that will be conducted in this project is to study the phenomenon of IR detection in pyrophilous jewel beetles and then to implement a MEMS design in order to reach or exceed the thermal sensitivity of 20 mK, standardized detectivity (D*) of 10^8 and field-of-view of 180º for an uncooled photomechanic infrared sensor.

Project end date: 02/07/06

LPL5: Microfluidic Cellular Manipulation - Single cell trapping arrays for quantitiative cell biology

Dino Di Carlo
2006

Previously, microfluidic traps and dams have been used to trap multiple single cells without the control over the number of cells trapped, or precise cell position necessary for quantitative analysis of large numbers of cells. Single cell analysis is required to capture the response of cells and their signaling pathways to stimuli. Bulk averages may distort the actual chemical response by smoothing sharp fluctuations that occur within single cells.

Project end date: 08/01/06