Relevant Degree Programs
Affiliations to Research Centres, Institutes & Clusters
Open Research Positions
Complete these steps before you reach out to a faculty member!
- Familiarize yourself with program requirements. You want to learn as much as possible from the information available to you before you reach out to a faculty member. Be sure to visit the graduate degree program listing and program-specific websites.
- Check whether the program requires you to seek commitment from a supervisor prior to submitting an application. For some programs this is an essential step while others match successful applicants with faculty members within the first year of study. This is either indicated in the program profile under "Admission Information & Requirements" - "Prepare Application" - "Supervision" or on the program website.
- Identify specific faculty members who are conducting research in your specific area of interest.
- Establish that your research interests align with the faculty member’s research interests.
- Read up on the faculty members in the program and the research being conducted in the department.
- Familiarize yourself with their work, read their recent publications and past theses/dissertations that they supervised. Be certain that their research is indeed what you are hoping to study.
- Compose an error-free and grammatically correct email addressed to your specifically targeted faculty member, and remember to use their correct titles.
- Do not send non-specific, mass emails to everyone in the department hoping for a match.
- Address the faculty members by name. Your contact should be genuine rather than generic.
- Include a brief outline of your academic background, why you are interested in working with the faculty member, and what experience you could bring to the department. The supervision enquiry form guides you with targeted questions. Ensure to craft compelling answers to these questions.
- Highlight your achievements and why you are a top student. Faculty members receive dozens of requests from prospective students and you may have less than 30 seconds to pique someone’s interest.
- Demonstrate that you are familiar with their research:
- Convey the specific ways you are a good fit for the program.
- Convey the specific ways the program/lab/faculty member is a good fit for the research you are interested in/already conducting.
- Be enthusiastic, but don’t overdo it.
G+PS regularly provides virtual sessions that focus on admission requirements and procedures and tips how to improve your application.
Graduate Student Supervision
Doctoral Student Supervision (Jan 2008 - Nov 2019)
Silicon photonic biosensors have the potential to transform medical diagnostics and healthcare delivery. Hundreds of these nano-scale sensors can be integrated onto a single millimeter-sized silicon substrate. They are fabricated in established CMOS foundries leveraging similar economies-of-scale achieved by electronic integrated circuits. This also enables their potential integration with electronic read out circuitry on a single chip. As near-infrared light propagates through nanoscale silicon wires, a portion of the light resides outside the waveguide interacting with biomolecules on the waveguide’s surface. While silicon photonic biosensors have demonstrated performances approaching today’s gold-standard diagnostic, the enzyme-linked immunosorbent assay (ELISA), improving their performance expands the potential use for applications requiring higher sensitivities and detection limits. To this end, this thesis describes efforts to optimize established biosensor configurations and develop novel structures with performance that exceeds commercially available silicon photonic biosensor platforms. This involves improving the bulk and surface sensitivity, detection limit, and quality factor of transverse electric (TE) and magnetic (TM) mode resonators in various waveguide topologies. Specifically, TM mode microring resonators, microdisk resonators, thin waveguide resonators, and the first of its kind sub-wavelength grating microring resonator with a 10X sensitivity improvement over today’s commercially available ring resonators are presented. Furthermore the use novel TE mode slot-waveguide and TM mode strip waveguide Bragg gratings which facilitate higher sensitivities (8X) and lower detection limits for biosensing applications are described. Finally, suspended Bragg grating structures are investigated to further improve sensitivity. To support the design and characterization efforts required to efficiently investigate many different sensors, a testing platform and process design kit (PDK) was developed. The test platform automatically tests hundreds of devices and orchestrates complex, multi-hour assays. The PDK reduces first-time design risk and expedites chip testing. Both have been open-sourced and are in use by more than a dozen academic and commercial research groups in various countries.
Cell-based screening of cancer treatments is used early in the drug development process to test the efficacy and toxicity of treatment candidates prior to animal and human testing. Current cell-based screening methods offer limited predictive capacity, contributing to the high percentage of drugs that fail during the clinical trial stage (80-95% for cancer treatments). One shortcoming of traditional cell-based screening platforms is their inability to recreate many aspects of the natural environment of tumour cells, which can affect treatment response. One important aspect of the microenvironment that can affect cell behaviour and treatment response is oxygenation. Irregular blood vessel formation can cause tumour oxygenation to be much lower than that of surrounding tissue, and spatial and temporal variations in oxygen can be present. Temporal variations can occur at timescales up to several cycles/hour: changes that are too fast to recreate using standard technologies like well plates due to their long diffusion distances. This thesis presents a novel microfluidic platform to expose cells to both chronic and time-varying oxygen profiles and study their response. Microfluidics technology is combined with 3-D cell culture in tumour spheroids, which can better recreate other aspects of the tumour microenvironment (such as cell-cell and cell-matrix interactions) than traditional 2-D culture. The functionality of the oxygen control device is verified using both finite-element modelling and integrated optical oxygen sensors. Two novel methods for oxygen sensor microfabrication are presented, and the functionality of sensors during long-term experiments is studied. Precise oxygen control is demonstrated using the microfluidic system, with oxygen switching times of
Diffusive molecular communication (MC) is a promising strategy for the transfer of information in synthetic networks at the nanoscale. If such devices could communicate, then it would expand their cumulative capacity and potentially enable applications such as cooperative diagnostics in medicine, bottom-up fabrication in manufacturing, and sensitive environmental monitoring. Diffusion-based MC relies on the random motion of information molecules due to collisions with other molecules. This dissertation presents a novel system model for three-dimensional diffusive MC where molecules can also be carried by steady uniform flow or participate in chemical reactions. The expected channel impulse response due to a point source of molecules is derived and its statistics are studied. The mutual information between consecutive observations at the receiver is also derived. A simulation framework that accommodates the details of the system model is introduced. A joint estimation problem is formulated for the underlying system model parameters. The Cramer-Rao lower bound on the variance of estimation error is derived. Maximum likelihood estimation is considered and shown to be better than the Cramer-Rao lower bound when it is biased. Peak-based estimators are proposed for the low-complexity estimation of any single channel parameter. Optimal and suboptimal receiver design is considered for detecting the transmission of ON/OFF keying impulses. Optimal joint detection provides a bound on detector performance. The weighted sum detector is proposed as a suboptimal alternative that is more physically realizable. The performance of a weighted sum detector can become comparable to that of the optimal detector when the environment has a mechanism to reduce intersymbol interference.A model for noise sources that continuously release molecules is studied. The time-varying and asymptotic impact of such sources is derived. The model for asymptotic noise is used to approximate the impact of multiuser interference and also the impact of older bits of intersymbol interference.
Master's Student Supervision (2010 - 2018)
Biosensors have seen an increased use in recent years as an in situ testing device for various industries such as agriculture, environmental sustainability, food, health, etc. On-site testing devices have an advantage over traditional testing system because they can be used for real-time monitoring and improving the accuracy of time-sensitive detection results. Out of all the industries, the health industry benefits most from in situ devices as point-of-care diagnostic devices. Point-of-care devices are useful tools to quickly diagnose diseases and direct patients’ course of treatment in low-income countries with few resources. In 2014 there were approximately 9.6 million global cases of tuberculosis (TB) and 1.5 million deaths due to TB (caused by the infection of Mycobacterium Tuberculosis [MTB]). Globally, this made TB the second most common cause of death by an infection disease in 2014. With a rising incidence of multi drug-resistant and extensive drug-resistant TB, TB is again becoming a global issue that wealthy countries will likely be unable to ignore. Since transmission is commonly through airborne particulates, early diagnosis and correct treatment of TB are fundamental to not only preventing the spread of the disease, but also eradicating it. Currently, the screening and detection tools that lower resource countries have are limited. Although the MTB genome has been sequenced since 1998, cost-effective, point-of-care, gene-based detection technology has had limited development. Since the integration of MEMS technology to biologically relevant needs in the late 90s there has been much development in creating small, portable detection systems for point-of-care use. Furthermore, this work details the development of a novel heterogeneous 3-material 3-electrode electrochemical sensor in a PDMS based bonded device. This sensor was developed with the intention of integration into a biosensor system. The final 3-electrode system was composed of 3 different materials: Au counter electrode, carbon working electrode, and Ag/AgCl reference electrode. The 3 material 3-electrode system was tested as an electrochemical system by detection of aqueous 5 μM carminic acid in room temperature and post 65◦C heating conditions. Parallel work was done to develop a robust, leak-free bonding method that survived 65◦C heating conditions and preserved electrochemical functionality.
In vitro tumor spheroid models have been developed using microfluidic systems to generate 3-D hydrogel beads containing components of alginate and ECM protein, such as collagen, with high uniformity and throughput. During bead gelation, alginate acts as a fast gelling component helping to maintain the spherical shape of beads and to prevent adjacent or underlying beads from coalescing when working with the slower gelling temperature and pH-sensitivity of collagen components. There are also well-known limitations in using microfluidic systems when working with temperature-sensitive components of collagen type I, and it is determined that to produce uniform hydrogel droplets through a microfluidic system, the mixtures must be homogeneous. However, the issue of collagen’s sensitivity to temperature causes concern for chunks of collagen gel inside of the mixture before bead encapsulation; therefore causing the mixture to become non-uniform and risking chip clogging. In order to overcome this limitation, previous approaches have used a cooling system during bead encapsulation while tumor cells were also present in the mixture, but this procedure assisted in postponing collagen gelation prior to bead production and potentially contributing to a delay in cell proliferation.Here a novel yet simple method is developed to prepare homogeneous pre-bead-encapsulation-mixtures containing collagen through ultrasonication, while extending cell viability and proliferation. This method allows the cultivation of homogenous TS cultures with high uniformity and compact structure, and not only maintains cell viability but also stimulates the proliferation of cells in alginate/collagen hydrogel bead cultures. Depending on the sonication parameters, time and temperature, gelation of collagen is controlled by small sized fibrils to thick fibers. Human-source-Michigan-Cancer-Foundation-7 (MCF-7) cells isolated from a breast cancer cell line are successfully incorporated into alginate/collagen mixtures, followed by sonication, and then bead production. After bead gelation, the encapsulated MCF-7 cells remained viable and proliferated to form uniform TSs when the beads contained alginate and collagen. Results indicate that ultrasound treatment provides a powerful technique to change the structure of collagen from fiber to fibril, and to disperse collagen fibers in the mixture homogeneously for an application to generate uniform hydrogel beads and spheroids while not disturbing cell proliferation.
Inkjet bioprinting technology aims to accurately and precisely dispense biological materials in a spatially predefined pattern within a three-dimensional space. The technology has a multitude of applications in the biomedical field such as in drug discovery and tissue or organ engineering. However, there are known limitations in an inkjet nozzle's capabilities in dispensing cells as the cell ejection rate does not follow any predictable distributions. In this work, the cell behaviors within a piezoelectric nozzle due to droplet ejection were classified through high speed brightfield imaging. With each ejected droplet, one of three cell behaviors was observed to occur: cell travel, cell ejection, or cell reflection. Cell reflection is an undesirable phenomenon which may adversely affect an inkjet's capability to reliably dispense cells. To further study how the hydrodynamics within a nozzle can influence the cell's behavior, µPIV was performed to identify the flow field evolution during droplet ejection. Through the study of cell motion, it was observed that the viscosity of the media in the cell suspension plays an important role in influencing the cell behavior. This was experimentally studied with the tracking of cells within the inkjet nozzle in a higher viscosity 10% w/v Ficoll PM400 cell suspension. As hypothesized, the addition of Ficoll PM400 was effective in preventing the occurrence of cell reflection which promises to increase the reliability in inkjet bioprinting systems.
Three-dimensional analysis of particles in flows within microfluidic devices is a necessary technique in the majority of current microfluidics research. One method that allows for accurate determination of particle positions in channels is defocusing-based optical detection. This thesis investigates the use of the defocusing method for particles ranging in size from 2-18 μm without the use of a three-hole aperture. Using a calibration-based analysis motivated by previous work, we were able to relate the particle position in space to its apparent size in an image. This defocusing method was then employed in several studies in order to validate its effectiveness in a wide range of particle/flow profiles. An initial study of gravitational effects on particles in low Reynolds number flows was conducted, showing that the method is accurate for particles with sizes equal to or greater than approximately 2 μm. We also found that the resolution of particle position accuracy was within 1 μm of expected theoretical results. Further studies were conducted in inertial focusing conditions, where viscous drag and inertial lift forces balance to create unique particle focusing positions in straight channels. Steady-state inertial studies in both rectangular and cylindrical channel geometries showed focusing of particles to positions similar to previous work, further verifying the defocusing method. A new regime of inertial focusing, coined transient flow, was also investigated with the use of the 3D defocusing method. This study established new regimes of particle focusing due to the effects of a transient flow on inertial forces. Within the transient study, the effects of fluid and particle density on particle focusing positions were also investigated. Finally, we provide recommendations for future work on the defocusing method and transient flows, including potential applications.
Microfluidics provides an opportunity to create low cost devices that can potentially contain many elements of a diagnostics lab on a single chip. While the cost of the finished product may be low, a common method of fabricating microfluidic devices such as soft lithography can be expensive to prototype due to the use of photolithography equipment meant for the semiconductor industry. In addition, the majority of microfluidic research has been done using rectangular channels but in some cases the ability to make circular cross-section channel microfluidic devices would be very useful. For areas such as modelling cardiovascular flows, investigating micro flow cytometry and inertial particle focusing, the ability to create circular channels could provide improvement over the use of rectangular channels. To address these issues, an ultra low cost method of making silicon molds patterned with SU-8 has been developed as well as a method to create circular microfluidic channels via hot embossing and double casting techniques in both thermoplastic materials and PDMS. This hot embossing based method to create round channels allows for the rapid creation of straight and curving round channels in PMMA and other plastics as well as a method to create PDMS round channels using soft lithography.
With great strides in neuroscience that have been made in the past decade, further understandings of complex neural systems require extensive neural information from chronic implantation of biocompatible neural devices. Polyimide-based flexible microelectrode arrays were one of the earlier biocompatible neural devices due to its mechanical impedance matching with brain tissue. In this work, we propose to incorporate non-conventional laser ablation method for fabrication of flexible biocompatible microelectrodes. We also present a novel approach to modifying flexible microelectrodes with macroporous platinum film using latex polystyrene sphere template. Maskless laser ablation was used to pattern the electrode, and probe definition as well creating the contact openings of flexible polyimide electrodes. Laser ablation is a non-photolithographic method which does not require conventional cleanroom environment and is ideal for rapid prototyping of devices. An ordered polystyrene bead template was deposited by simple pipetting of bead solution over gold contact openings and evaporating in ambient room setting. Pulsed-potentiostatic mode electrochemical deposition of platinum through the polystyrene bead template resulted in increase in effective surface area of electrodes. The impedance of the platinum modified electrodes increased by two orders of magnitude compared to unmodified electrodes. Synergetic modification of microelectrodes with macroporous platinum film and polymer-brush coating can lead to fabrication of highly biocompatible microelectrode with low impedance characteristics.