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Life Sciences Seminar Series
Abstract
The past 25 years have seen considerable progress in the development of microfabricated systems for use in the chemical and biological sciences. At a basic level, microfluidic activities have been stimulated by the fact that physical processes can be more easily controlled when instrumental dimensions are reduced to the micron scale.1 The relevance of such technology is significant and characterized by a range of features that accompany system miniaturization. Such features include the ability to process small volumes of fluid, enhanced analytical performance, reduced instrumental footprints, low unit costs, facile integration of functional components within monolithic substrates and the capacity to exploit atypical fluid behaviour to control chemical and biological entities in both time and space.
My lecture will discuss how the spontaneous formation of droplets in microfluidic systems can be exploited to perform a chemical (and biological) experiments and why the marriage of such systems with optical spectroscopies provides a direct route to high-throughput and high-information content experimentation.
Droplet-based microfluidic systems allow the generation and manipulation of discrete droplets contained within an immiscible continuous phase.2 They leverage immiscibility to create discrete volumes that reside and move within a continuous flow. Significantly, such segmented-flows allow for the production of monodisperse droplets at rates in excess of tens of KHz and independent control of each droplet in terms of size, position and chemical makeup. Moreover, the use of droplets in complex chemical and biological processing relies on the ability to perform a range of integrated, unit operations in high- throughput. Such operations include droplet generation, droplet merging/fusion, droplet sorting, droplet splitting, droplet dilution, droplet storage and droplet sampling.3-4 I will provide examples of how droplet-based microfluidic systems can be used to perform a range of experiments including nanomaterial synthesis5 and DNA amplification.6 In addition, I will describe recent studies focused on the development of novel imaging flow cytometry platform that leverages the integration of inertial microfluidics with stroboscopic illumination7 to allow for high-resolution imaging of cells at throughputs approaching 105 cells/second.8
[1] A.J. deMello, Nature, 442 (2006) 394-402. [2] X. Casadevall-i-Solvas & A.J. deMello, Chemical Communications, 47 (2011) 1936–1942. [3] X. Niu, S. Gulati, J.B. Edel & A.J. deMello, Lab Chip, 8 (2008) 1837–1841. [4] X.Niu, F. Gielen, J.B. Edel & A.J. deMello, Nature Chemistry, 3 (2011) 437-442. [5] I. Lignos et al., Nano Letters, 16 (2016) 1869–1877. [6] Yolanda Schaerli et al., Analytical Chemistry, 81 (2009) 302-306. [7] Hess et al., Analytical Chemistry, 87 (2015) 4965-4972. [8] Rane et al., Chem, 3 588-602. (2017)