omation mbers - Society for Laboratory Automation and Screening

omation mbers - Society for Laboratory Automation and Screening omation mbers - Society for Laboratory Automation and Screening

13.01.2013 Views

12:00 pm Wednesday, February 4 Microfluidics Room A4 Helene Andersson Silex Microsystems Electrum 222 Kista, 16440 Sweden helene.andersson@silex.se BIOMEMS Solutions at Silex Microsystems At Silex Microsystems we are applying micro-electro-mechanical-systems (MEMS) technology and manufacturing techniques to design and make components, such as sensors, actuators, and precision structures, for integration with customers’ end products. Miniaturization makes it possible to create life-saving applications that were impossible before. Lab-on-a-chip devices that conduct standard techniques such as electrophoresis, PCR and DNA sequencing have advanced significantly in the past few years. We’ve designed and manufactured a number of standard applications that can be used separately or together as a lab-on-a-chip. We have also created a number of devices for medical applications. For example, spiked electrodes for measuring bio-signals for Datex- Ohmeda. The individual spikes are designed to penetrate the human skin and are typically 40 µm wide and 150 µm high. The spike array is fabricated using deep reactive ion etching and is a promising alternative to standard electrodes in biomedical applications. For drug delivery applications we develop and manufacture a micropump for the company Debiotech in Switzerland. The pump chips are 6x10 mm and the pump demonstrates linear and accurate (±5%) pumping characteristics for flows up to 2 ml/h. We also develop chip-based solutions for high throughput ion-channel characterizations for Sophion Bioscience in Denmark. Silex is also manufacturing a pressure sensor that is used for measuring the blood pressure inside coronary arteries. The chip size is 0.1x0.1x1.3 mm and is developed for a Swedish company called Radi Medical. In addition, we design and manufacture a variety of microfluidic devices for biotech applications. 3:30 pm Wednesday, February 4 Microfluidics – Detection Room A4 David Cliffel Vanderbilt University VU Station B Box 1822 Nashville, Tennessee 37235-1822 d.cliffel@vanderbilt.edu Automating a Multichamber, Multianalyte Microphysiometer for Metabolic Responses Using Labview 74 Co-Author(s) Sven Eklund Eduardo Lima John Wikswo Commercial microphysiometers have been limited to the analytical detection of acidification rate using a photoelectrochemical pH sensor. We have built a multianalyte microphysiometer by modification of a commercial Cytosensor instrument that detects multiple analytes involved in the metabolic physiology simultaneously. Monitoring the uptake of glucose and oxygen, and the production of lactate and acid gives a more complete picture of the metabolic processes within the cell than just acidification alone. Metabolic processes such as glycolysis, mitochondrial ATP generation, and glycogenesis are all directly related to the flux of these analytes. The metabolic response of sub-lethal concentrations of toxins has been measured. We have recently modified 2 Cytosensor microphysiometers with independent multipotentiostat control for each chamber using Labview. This allows us to record 4 analytes simultaneously per chamber for all 4 or 8 chambers. Metabolic response analysis is performed in real-time as the raw electrochemical data is recorded. This talk will outline the modifications necessary, the calibration of the various sensors, biofouling problems of cells undergoing chemical stress, and the metabolic rate responses of Fibroblast and CHO cell lines to low concentrations of toxins and other agents including cyanide, fluoride, dinitrophenol, deoxyglucose, paraoxon, and antimycin. Temporal resolution of metabolic responses is much faster than conventional well-plate studies, leading to dynamic metabolic data. The generation of toxin dose response curves for multianalyte responses offers a big advantage to the detection and identification of toxins using cellular metabolic activity as the initial analytical sensing tool.

4:00 pm Wednesday, February 4 Microfluidics – Detection Room A4 Cengiz S. Ozkan University of California, Riverside Bourns Hall, A305 Riverside, California 92521 cozkan@engr.ucr.edu Heterostructures of Nanomaterials and Organic-Inorganic Nanoassemblies Conventional nanofabrication strategies must be augmented by new techniques including self assembly methods in order to truly take advantage of the quantum nature of novel nanoscale devices and systems and permit the use of these properties for “real” applications in a larger system (> 10 nm and < 1 micron). In this talk, I will describe a novel technique for the fabrication of nano-assemblies of carbon nanotubes (CNT) and quantum dots (QD) – formation of CNT-QD conjugates. CNT’s are primarily functionalized with carboxylic end groups by oxidation in concentrated sulfuric acid. Thiol stabilized QD’s in aqueous solution with amino end groups were conjugated to carbon nanotubes using the ethylene carbodiimide coupling reaction. Next, I will discuss the possibilities of using carbon nanotubes for encapsulation and mass transport and present our first observations in this area. Fourier transform infrared spectroscopy data for the chemical modification of carbon nanotubes and scanning and transmission electron microscopy images of the nanobuilding blocks and the nanotube filling process will be presented. Potential applications of our studies include the fabrication of novel electronic and biophotonic devices, crystal displays and biosensors. 4:30 pm Wednesday, February 4 Microfluidics – Detection Room A4 Wayne Weimer US Detection Technologies 2611 Internet Boulevard, Suite 109 Frisco, Texas 75034 wweimer@usdetect.com Surface Enhanced Raman Spectroscopy for Real World Samples Precise control of thermal evaporation deposition parameters allows the reproducible production of silver and gold island films on glass substrates with tunable surface plasmon resonance wavelengths. Specific combinations of substrate temperature, deposition rate, and film thickness produce films exhibiting surface plasmon resonance wavelengths that can be adjusted from throughout the visible and into the near infrared regions of the electromagnetic spectrum. The effects of deposition parameters on surface plasmon resonance wavelengths are quantified using a so-called “design of experiment” analysis. The analysis produces reliable predictive models for producing gold films with predetermined surface plasmon resonance wavelengths. Nonresonant enhancement factors in excess of eleven orders of magnitude for surface enhanced Raman spectroscopy were recorded for rhodamine 6G dye on optimally tuned gold films. Spectra were obtained from submonolayer samples, corresponding to the detection of at most 180 attograms of the dye. Techniques for the adaptation of these surface plasmon resonance tunable gold films for detection of biological and explosive compounds will be discussed. 75 PODIUM ABSTRACTS

12:00 pm Wednesday, February 4 Microfluidics Room A4<br />

Helene Andersson<br />

Silex Microsystems<br />

Electrum 222<br />

Kista, 16440 Sweden<br />

helene.<strong>and</strong>ersson@silex.se<br />

BIOMEMS Solutions at Silex Microsystems<br />

At Silex Microsystems we are applying micro-electro-mechanical-systems (MEMS) technology <strong>and</strong> manufacturing<br />

techniques to design <strong>and</strong> make components, such as sensors, actuators, <strong>and</strong> precision structures, <strong>for</strong> integration<br />

with customers’ end products. Miniaturization makes it possible to create life-saving applications that were<br />

impossible be<strong>for</strong>e. Lab-on-a-chip devices that conduct st<strong>and</strong>ard techniques such as electrophoresis, PCR <strong>and</strong><br />

DNA sequencing have advanced significantly in the past few years. We’ve designed <strong>and</strong> manufactured a number<br />

of st<strong>and</strong>ard applications that can be used separately or together as a lab-on-a-chip. We have also created a<br />

number of devices <strong>for</strong> medical applications. For example, spiked electrodes <strong>for</strong> measuring bio-signals <strong>for</strong> Datex-<br />

Ohmeda. The individual spikes are designed to penetrate the human skin <strong>and</strong> are typically 40 µm wide <strong>and</strong> 150 µm<br />

high. The spike array is fabricated using deep reactive ion etching <strong>and</strong> is a promising alternative to st<strong>and</strong>ard<br />

electrodes in biomedical applications. For drug delivery applications we develop <strong>and</strong> manufacture a micropump<br />

<strong>for</strong> the company Debiotech in Switzerl<strong>and</strong>. The pump chips are 6x10 mm <strong>and</strong> the pump demonstrates linear<br />

<strong>and</strong> accurate (±5%) pumping characteristics <strong>for</strong> flows up to 2 ml/h. We also develop chip-based solutions <strong>for</strong><br />

high throughput ion-channel characterizations <strong>for</strong> Sophion Bioscience in Denmark. Silex is also manufacturing<br />

a pressure sensor that is used <strong>for</strong> measuring the blood pressure inside coronary arteries. The chip size is<br />

0.1x0.1x1.3 mm <strong>and</strong> is developed <strong>for</strong> a Swedish company called Radi Medical. In addition, we design <strong>and</strong><br />

manufacture a variety of microfluidic devices <strong>for</strong> biotech applications.<br />

3:30 pm Wednesday, February 4 Microfluidics – Detection Room A4<br />

David Cliffel<br />

V<strong>and</strong>erbilt University<br />

VU Station B Box 1822<br />

Nashville, Tennessee 37235-1822<br />

d.cliffel@v<strong>and</strong>erbilt.edu<br />

Automating a Multichamber, Multianalyte Microphysiometer <strong>for</strong> Metabolic Responses<br />

Using Labview<br />

74<br />

Co-Author(s)<br />

Sven Eklund<br />

Eduardo Lima<br />

John Wikswo<br />

Commercial microphysiometers have been limited to the analytical detection of acidification rate using a<br />

photoelectrochemical pH sensor. We have built a multianalyte microphysiometer by modification of a commercial<br />

Cytosensor instrument that detects multiple analytes involved in the metabolic physiology simultaneously.<br />

Monitoring the uptake of glucose <strong>and</strong> oxygen, <strong>and</strong> the production of lactate <strong>and</strong> acid gives a more complete<br />

picture of the metabolic processes within the cell than just acidification alone. Metabolic processes such as<br />

glycolysis, mitochondrial ATP generation, <strong>and</strong> glycogenesis are all directly related to the flux of these analytes.<br />

The metabolic response of sub-lethal concentrations of toxins has been measured. We have recently modified 2<br />

Cytosensor microphysiometers with independent multipotentiostat control <strong>for</strong> each chamber using Labview. This<br />

allows us to record 4 analytes simultaneously per chamber <strong>for</strong> all 4 or 8 cha<strong>mbers</strong>. Metabolic response analysis<br />

is per<strong>for</strong>med in real-time as the raw electrochemical data is recorded. This talk will outline the modifications<br />

necessary, the calibration of the various sensors, biofouling problems of cells undergoing chemical stress, <strong>and</strong><br />

the metabolic rate responses of Fibroblast <strong>and</strong> CHO cell lines to low concentrations of toxins <strong>and</strong> other agents<br />

including cyanide, fluoride, dinitrophenol, deoxyglucose, paraoxon, <strong>and</strong> antimycin. Temporal resolution of<br />

metabolic responses is much faster than conventional well-plate studies, leading to dynamic metabolic data. The<br />

generation of toxin dose response curves <strong>for</strong> multianalyte responses offers a big advantage to the detection <strong>and</strong><br />

identification of toxins using cellular metabolic activity as the initial analytical sensing tool.

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