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NIST Technicalendar
March 12 to March 16, 2007 The NIST Technicalendar is issued each Friday. All items MUST be submitted electronically from this web page by 12:00 NOON each Wednesday unless otherwise stated in the NIST Technicalendar. The address for online weekly editions of the NIST Technicalendar and NIST Administrative Calendar is: http://www.nist.gov/tcal/. |
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10:00 AM - Localized hot spot associated with nanoscale heat source - evidence and implications to nanoelectronicsTUESDAY - 3/13
10:30 AM - Small-Scale, Six-Axis Nanopositioners: New Concepts and Performance Limits for Nanomanufacturing Equipment/Instrumentation
10:30 AM - Underlying Technology Elements of the First Commercial MRAM
10:45 AM - Probing Hydration Phenomena in Sol-Gel and Glassy Matrices
2:00 PM - Probing Worm Mind and Prodding Cell Behavior with Microfluidics
10:30 AM - Microfluidic Cell SeparationWEDNESDAY - 3/14
11:00 AM - The Roles of Mechanical Damage and Remodeling in Intervertebral Disc Degeneration
2:00 PM - Matrices of single-photon avalanche diodes for biomolecular analysis
3:00 PM - Surface Wrinkling as a Metrology Tool
9:00 AM - NVLAP Assessor SeminarTHURSDAY - 3/15
10:30 AM - Ferroelasticity and Crack Tip Domain Switching in PZT
1:00 PM - Electrochemical Nanopatterning and Nanocharging using Precursor Polymers and Nanostructured Ultrathin Films
10:30 AM - Materials Design in the Nanometer Range at EMPA in SwitzerlandFRIDAY - 3/16
10:30 AM - Rapid Cell Growth On Biodegradable Polymer Scaffolds
1:00 PM - Annual Research Advisory Committee (RAC) All-Staff Briefing
Microfluidic devices can be engineered to address questions in neuroscience and cell biology that are difficult to approach with conventional techniques. Applied to the study of fundamental biological questions, these new techniques allow us to gather quantitative and often large-scale data about complex systems. Examples will be presented demonstrating the use of microfluidics to study the sensory neurobiology of C. elegans (a soil nematode), including oxygen sensation, pathogenic learning, and behavior neural circuitry. The use of microfluidic systems to study cell adhesion, migration, and chemotaxis in complex microenvironments will also be described. We hope to use these techniques to begin to understand the intricate signaling dynamics inside cells.
Hang Lu
, Professor of Chemical Engineering, Georgia Institute of Technology.
224 Bldg, Rm. A312.
(NIST Contact: Dean DeLongchamp, 301-975-5599, deand@nist.gov)
Microscale devices for the manipulation, culture and analysis of cells have seen significant development in recent years. One application in which microfluidics is particularly useful is the separation of selected cells from heterogeneous populations. Microfluidic cell separation has applications ranging from point-of-care diagnostics to tissue engineering. Microscale separation systems can be broadly classified based on how separation is achieved, for example, size, adhesion, magnetic affinity, or electrophoretic mobility.
This presentation will describe several applications of adhesion-based cell separation. These include the isolation of leukocyte subpopulations in the context of understanding the immune response to injury and trauma, understanding cell activation processes, and applications in cardiac tissue engineering. The fundamental principle behind this mode of separation is the adhesion of cells to specific ligands tethered within microfluidic devices. The effect of other parameters such as fluid shear and ligand density will also be discussed.
Adhesion-based separation is generally preferred when cell subpopulations of interest are of the same size and density as other cells in a heterogeneous suspension. However, when size differences exist, alternative separation strategies can be pursued. Size-based separation offers the advantage of not requiring a priori knowledge of cell surface markers and minimizing any cellular-level changes due to cell-ligand interactions. This presentation will describe two examples of size-based separation, namely red blood cell depletion from whole human blood and cardiac muscle cell enrichment for tissue engineering.
Shashi Murthy
, Professor of Chemical Engineering, Northeastern University.
224 Bldg, Rm. A312.
(NIST Contact: Dean DeLongchamp, 301-975-5599, deand@nist.gov)
Special Assistance Available
For more information please see < http://www-i.nist.gov/director/rac/reports.htm>
Craig Schlenoff
, 2006 RAC Chair.
Liz Donley
, 2007 RAC Chair.
Administration Bldg, Red Auditorium.
(NIST Contact: Craig Schlenoff, 301-975-3456, craig.schlenoff@nist.gov)