Microfluidics

Research that includes: 

  • Microvalves and fluidic flow control
  • Micropumps
  • Modeling of microfluidics
  • Particulate air monitoring
  • Flow Sensors
  • Capillary Pump Loop
  • Optoelectronic Transport & Tweezers

BPN409: Long-term Cytotoxic Drug Assay via Single-Cell Microfluidic Array

Liz Wu
2007

Understanding cellular dynamics of xenobiotic and ion transport are important for in-vitro drug assay since it is a critical step to estimate the performance, toxin and side effect of new drug candidates. Most current drug assays are based on the average cellular response of large cell populations. In conventional cell culture platforms the mass transport of cell cluster is affected by transport at neighboring cells. In order to study systematically xenobiotic and ion transport, isolated single cells on optofluidic multisensing platform are required. To observe cancer cells under...

BPN384: Single-cell Analysis via Raman Spectroscopy

Adrian Lau
2007

There has been significant interest in applying Raman Spectroscopy on cellular analysis in recent years. Advanced optics has allowed very high resolution Raman signal measurement at the sub-cellular level, fueling the emerging field of Single-cell Raman Spectroscopy. The fact that Raman Spectroscopy/Imaging is in few ways superior to conventional fluorescence techniques enables novel ways of monitoring cell processes. Recently, multiple studies have reported the use of Raman Spectroscopy methods in detecting specific cell behaviors. However, an extensive quantitative study has yet to...

BPN344: Microfluidic Platform for Quantitative Microcirculation Studies in Sickle Cell Disease

Sharon Hsu
2007

Soft Lithography has been pioneered in the past decade as a tool to manipulate cells under well controlled physical and chemical conditions. Despite the vast number of studies applied in various lines of cells, there have been few focusing on the membrane properties of erythrocytes. Here we present a novel and convenient alternative to traditional methods used to obtain physical properties of erythrocytes, and our objective is to establish a standard model for healthy red blood cells and derive clear model for quantification of severity in erythrocyte membrane disorders, with...

BPN401: Microjets for Single Cell Injections

Peter F.White
2007

The goal of this project is to develop a microfluidic system that uses a high speed micron sized jet to inject biological material into single cells in a highly controlled fashion.

Project end date: 01/29/08

BPN400: PZT-Actuated Flexure-Mode Membranes for Nanoscale Droplet Generation

Nathan Emley
2007

We report on the current status of device fabrication of a monolithic, micro-machined device able to generate sub-micron diameter (femtoliter) fluidic droplets. Such droplet-on-demand (DoD) devices are important for a wide range of maskless lithography and rapid prototyping technologies, including direct-write patterning on non-standard, highly topographical, or extremely temperature sensitive substrates. Printable circuitry from DoD devices can be generated in non-clean room, extreme, or dynamic conditions. The basic design of these DoD devices places a pressure source at the bottom...

BPN391: MEMS Power: Thermo-Fluidic Nanoparticle Reactor

Nicola M. Fung
2008

The long-term objective of this project, along with BPN406, is to produce monodisperse nanocrystals through a microfluidic reactor. The microfluidic reactor will utilize the unique physical properties of colloidal suspension of liquid droplets in a surrounding immiscible inert liquid. This project intends to develop and produce the design from BPN406; specifically the coin structure to control the temperature profile and flow geometry to allow for flow focusing and the formation of uniform droplets. This will allow flow and temperature control, which would correlate to control over...

BPN398: Single Cell Electroporation Array with OET/PDMS Integration

Hsan-Yin (Tony) Hsu
Yir-Shyuan Liz Wu
2008

Single cell analysis is an important technology for biological and medical research. The precision of manipulating the location of the single cell (relative to the assay sites or other neighboring cells) is a necessary factor. We have previously demonstrated cell manipulation and separation with optoelectronic tweezers (OET), the goal of this project is to integrate this powerful tool with the micrifluidic devices to provide a complete solution for single cell electroporation.

Project end date: 07/30/08

BPN406: Microfluidic reactor for production of semiconductor nanocrystals

Jeffrey D. Winterton
2008

Nearly all proposed applications of semiconductor nanocrystals (quantum dots) will require significant quantities of high quality nanocrystals with tightly controlled properties. Microfluidic nanocrystal synthesis techniques have recently been explored as an alternative to conventional production methods because they could potentially increase production rates, if used in parallel, while maintaining superior product quality. However, conventional microfluidic reactor designs suffer from two principal limitations: an inability to maintain a uniform reaction environment and an...

BPN301: Passive Microfluidic Mixers for Protein Folding Studies

Avinash Kane
2008

The purpose of this study is to design, fabricate and optimize microfluidic mixers to investigate the kinetics of protein secondary structure formation with Synchrotron Radiation Circular Dichroism (SRCD) spectroscopy. SRCD allows us to use wavelengths below 220 nm where differences between the CD spectra of random coil and the various secondary structure types are most pronounced. Microfluidic mixing allows a fast initiation of the protein folding reaction. By combining this with SRCD, we can clarify an intense debate in the protein folding community as to when, in the process of...

MCW2: Direct Image-Actuated Optoelectronic Tweezers

Aaron T. Ohta
2008

Optical manipulation provides a non-invasive, dynamic, and reconfigurable method of trapping, transporting, and sorting cells and other bioparticles. Optoelectronic tweezers (OET) enables optically-controlled cellular manipulation at much lower optical power densities than conventional optical tweezers. This enables the use of direct imaging and incoherent light to create a large (1.3 mm x 1.3 mm) manipulation area for the parallel processing of cells, microparticles, and nanoparticles. The use of direct image-actuated OET allows single-particle control for biological research and...