Francis Lin

Dr. Francis Lin

Department of Physics and Astronomy & Immunology, University of Manitoba, Winnipeg, MB, Canada
orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2004 in Experimental Cell Research
Verified
Journal Article
Closed access
SWShur-Jen Wang
Shur-Jen Wang
WSWajeeh Saadi
Wajeeh Saadi
FLFrancis Lin
Francis Lin
CNConnie Minh-Canh Nguyen
Connie Minh-Canh Nguyen
NJNoo Li Jeon
Noo Li Jeon

24 March 2011 in Lab on a Chip
Verified
Journal Article
Closed access
PDF file
Suresh NeethirajanSuresh Neethirajan
Suresh Neethirajan
IKIsao Kobayashi
Isao Kobayashi
MNMitsutoshi Nakajima
Mitsutoshi Nakajima
DWDan Wu
Dan Wu
SNSaravanan Nandagopal
Saravanan Nandagopal
FLFrancis Lin
Francis Lin
Microfluidics, a rapidly emerging enabling technology has the potential to revolutionize food, agriculture and biosystems industries. Examples of potential applications of microfluidics in food industry include nano-particle encapsulation of fish oil, monitoring pathogens and toxins in food and water supplies, micro-nano-filtration for improving food quality, detection of antibiotics in dairy food products, and generation of novel food structures. In addition, microfluidics enables applications in agriculture and animal sciences such as nutrients monitoring and plant cells sorting for improving crop quality and production, effective delivery of biopesticides, simplified in vitrofertilization for animal breeding, animal health monitoring, vaccination and therapeutics. Lastly, microfluidics provides new approaches for bioenergy research. This paper synthesizes information of selected microfluidics-based applications for food, agriculture and biosystems industries.

1 June 2006 in Biomedical Microdevices
Verified
Journal Article
Closed access
PDF file
WSWajeeh Saadi
Wajeeh Saadi
SWShur-Jen Wang
Shur-Jen Wang
FLFrancis Lin
Francis Lin
NJNoo Li Jeon
Noo Li Jeon

22 February 2016 in Lab on a Chip
Verified
Journal Article
Closed access
PDF file
KYKe Yang
Ke Yang
HPHagit Peretz-Soroka
Hagit Peretz-Soroka
YLYong Liu
Yong Liu
FLFrancis Lin
Francis Lin
We review novel mobile sensing applications based on the integration of microfluidic devices and smartphones (MS2).

24 March 2004 in Lab on a Chip
Verified
Journal Article
Closed access
PDF file
FLFrancis Lin
Francis Lin
WSWajeeh Saadi
Wajeeh Saadi
SRSeog Woo Rhee
Seog Woo Rhee
SWShur-Jen Wang
Shur-Jen Wang
SMSukant Mittal
Sukant Mittal
NJNoo Li Jeon
Noo Li Jeon
This paper describes a microfluidic approach to generate dynamic temporal and spatial concentration gradients using a single microfluidic device. Compared to a previously described method that produced a single fixed gradient shape for each device, this approach combines a simple “mixer module” with gradient generating network to control and manipulate a number of different gradient shapes. The gradient profile is determined by the configuration of fluidic inputs as well as the design of microchannel network. By controlling the relative flow rates of the fluidic inputs using separate syringe pumps, the resulting composition of the inlets that feed the gradient generator can be dynamically controlled to generate temporal and spatial gradients. To demonstrate the concept and illustrate this approach, examples of devices that generate (1) temporal gradients of homogeneous concentrations, (2) linear gradients with dynamically controlled slope, baseline, and direction, and (3) nonlinear gradients with controlled nonlinearity are shown and their limitations are described.

4 September 2006 in Lab on a Chip
Verified
Journal Article
Closed access
PDF file
FLFrancis Lin
Francis Lin
EBEugene C. Butcher
Eugene C. Butcher
This paper describes the use of a simple microfluidic device for studying T cell chemotaxis. The microfluidic device is fabricated in poly(dimethylsiloxane) (PDMS) using soft-lithography and consists of a “Y” type fluidic channel. Solutions are infused into the device by syringe pumps and generate a concentration gradient in the channel by diffusion. We show that the experimentally measured gradient profiles agree nicely with theoretical predictions and the gradient is stable in the observation region for cell migration. Using this device, we demonstrate robust chemotaxis of human T cells in response to single and competing gradients of chemokine CCL19 and CXCL12. Because of the simplicity of the device, it can flexibly control gradient generation in space and time, and would allow generation of multiple gradient conditions in a single chip for highly parallel chemotaxis experimentation. Visualization of T cell chemotaxis has previously been limited to studies in 3D matrices or under agarose assays, which do not allow precise control or variation in conditions. Acknowledging the importance of lymphocyte homing in the adaptive immune response, the ability to study T cell chemotaxis in microfluidic devices offers a new approach for investigating lymphocyte migration and chemotaxis in vitro.