Grant: Research Tools and Instruments - Category 1 (<$150,000)
University of Waterloo
$113,963.00
A droplet visualization system for lab-on-a-chip applications
EF 2010-11
Résumé
The proposed research aims to develop droplet-based microfluidic technology for high-throughput combinatorial studies which are critical to drug discovery and disease diagnosis applications. The majority of microfluidic chips are based on single phase systems consisting of various miscible aqueous streams, which has several limitations, particularly for large-scale combinatorial studies in chemistry, proteomics, genomics, drug screening and biology because it is plagued with cross-contamination between streams. Such a system also scales up poorly as it requires an approximately linear increase in active components and device footprint for each additional reactor. Two-phase droplet-based microfluidics is a viable alternative where discrete droplets are formed from immiscible fluids like water and oil. Each droplet is essentially an ideal microreactor with a specified volume that compartmentalizes reagents preventing them from diffusing away. Microfluidic droplets can scale up performance effectively as they can be generated at rates between 1-20 kHz over a range of picolitres to nanolitres with a standard deviation of only 1-3 %.
To develop such promising technology and devices, characterizing the flow field and droplet motion is essential. Flow field data can be obtained with Micro Particle Image Velocimetry (µ-PIV). A standard µ-PIV is available in the applicant's lab; however, it cannot be used to visualize droplet transport in microfluidic devices because the temporal nature of two phase flow usually limits the number of sequential images that can be obtained for averaging the flow field. Therefore, the current system must be upgraded by adding: i) a programmable motorized stage together with a high-speed, high-resolution camera (>2000 frames per second) for capturing the time dependent flow field at a high frequency; and ii) a phase contrast function for the visualization involving two phases and cells. The high-speed camera allows the droplet volume, speed, frequency of generation, spacing, and number to be analyzed using image analysis algorithms. Without these key parameters, it is extremely difficult, if not possible, to develop droplet-based microfluidic technology.
Programme
Research Tools and Instruments - Category 1 (<$150,000)
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
406855-2011
Name nom
Ren, Carolyn
Department département
Mechanical Engineering and Mechatronics
Organization id
33
Institution établissement
University of Waterloo
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2010
Competition year année de concours
2011
Award amount
113963
Program id
EQPEQ
Program name en
Research Tools and Instruments - Category 1 (<$150,000)
Program name fr
Outils et instruments de recherche - catégorie 1 (<150 000$)
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1512
Committee name en
Mechanical Engineering
Committee name fr
Génie mécanique
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
2109
Research subject group en
Mechanical engineering
Research subject group fr
Génie mécanique
Research subject en
Mechanical systems and instrumentation
Research subject fr
Instrumentation et systèmes mécaniques
Partie
1
Nb partie
1
Application title
A droplet visualization system for lab-on-a-chip applications
Keyword
NSERC
Application summary
The proposed research aims to develop droplet-based microfluidic technology for high-throughput combinatorial studies which are critical to drug discovery and disease diagnosis applications. The majority of microfluidic chips are based on single phase systems consisting of various miscible aqueous streams, which has several limitations, particularly for large-scale combinatorial studies in chemistry, proteomics, genomics, drug screening and biology because it is plagued with cross-contamination between streams. Such a system also scales up poorly as it requires an approximately linear increase in active components and device footprint for each additional reactor. Two-phase droplet-based microfluidics is a viable alternative where discrete droplets are formed from immiscible fluids like water and oil. Each droplet is essentially an ideal microreactor with a specified volume that compartmentalizes reagents preventing them from diffusing away. Microfluidic droplets can scale up performance effectively as they can be generated at rates between 1-20 kHz over a range of picolitres to nanolitres with a standard deviation of only 1-3 %.
To develop such promising technology and devices, characterizing the flow field and droplet motion is essential. Flow field data can be obtained with Micro Particle Image Velocimetry (µ-PIV). A standard µ-PIV is available in the applicant's lab; however, it cannot be used to visualize droplet transport in microfluidic devices because the temporal nature of two phase flow usually limits the number of sequential images that can be obtained for averaging the flow field. Therefore, the current system must be upgraded by adding: i) a programmable motorized stage together with a high-speed, high-resolution camera (>2000 frames per second) for capturing the time dependent flow field at a high frequency; and ii) a phase contrast function for the visualization involving two phases and cells. The high-speed camera allows the droplet volume, speed, frequency of generation, spacing, and number to be analyzed using image analysis algorithms. Without these key parameters, it is extremely difficult, if not possible, to develop droplet-based microfluidic technology.