Microfluidics

Research that includes: 

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

BPN381: SERS Signal Amplification by Optofluidic Photothermal Sample Preconcentration

Hansang Cho
2007

Integrated microfluidic devices. Preconcentration not only improves detection sensitivity of SERS signals but also improves the reliability of the analysis by significantly increasing signal-to-noise ratio. Another reason necessitating preconcentration is the discrepancy between volumes of sample available and those consumed for analysis. The general goal is to preconcentrate a molecule based on thermophoresis in a microfluidic platform to amplify the SERS signals. Our first specific goal is to preconcentrate target molecules using and the second goal is to amplify the SERS signal of...

DL5: DNA Transport in Microfluidic Systems

Shelly Gulati
2007

Fully integrated lab-on-a-chip systems for applications such as DNA sequencing and pathogen detection will incorporate significant microfluidic components. These systems will necessarily require the flow of large molecules such as DNA, which give the bulk fluid viscoelastic behavior. Additionally, the characteristic lengths of these molecules will approach those of the fluid channel, presenting a unique flow situation that is not well understood. The effects of microscale flow in canonical microfluidic structures on the conformation of DNA, and the reciprocal effects of DNA...

BPN360: Biomimetic Microfluidic Assembly of Spheroids and Dynamic Perfusion for Anti-Cancer Drug Discovery

Liz Wu
2007

Multicellular tumor spheroids may provide a better model than monolayer culture of in vivo tumors for drug assays. We present a novel microfluidic method for self-assembly of tumor spheroids for these studies. Our device traps cancer cells hydrodynamically and spheroid formation is enhanced by maintaining compact groups of the trapped cells due to continuous perfusion. It was found that spheroid formation speed and size uniformity increased with increased flow rate. A large amount of tumor spheroids (7,500 spheroids per square centimeter) with a narrow size distribution (10 ± 1...

BPN412: Signal Amplifications of SERS by Microfluidic CD-based Preconcentration Methods

Dukhyun Choi
2007

Signal amplifications of surface-enhanced Raman scattering (SERS) by microfluidic compact disk (CD)-based preconcentration method is accomplished for effective label-free bioassays and chemical detections. This is the first demonstration of the SERS-CD platform having capabilities of high-throughput microfluidic multifunctional on-chip biomedical devices. In order to achieve the preconcentration through the accumulation of biomolecules adsorbed on the SERS active site, we inject and dry biomolecular sample solution in the microfluidic channel prior to SERS detection and then repeat...

BPN323: MEMS Biopolymer: Bubble Time-of-Flight Flow Sensor

Julian Lippmann
2007

Liquid flow monitoring at nanoliter/min rates is important for many lab-on-a-chip and stand alone biomedical applications. Several technologies have been investigated to achieve this resolution. The majority require expensive detection systems and fabrication processes. To this end we have developed an injection molded fluidic flow sensor that requires no part-to-part micromachining of silicon, significantly reducing the cost. Further, many of these systems require extensive calibration and rely on phenomena impacted by diffusion (e.g. heat pulses) that quickly lose accuracy as flow...

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...