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Droplet-Based Microfluidics Enabling Impact on Drug Discovery

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TLDR
The impact of microfluidics in the area of high-throughput screening and drug discovery is discussed and some of the most pertinent studies in the recent literature are highlighted.
Abstract
Over the past two decades, the application of microengineered systems in the chemical and biological sciences has transformed the way in which high-throughput experimentation is performed. The ability to fabricate complex microfluidic architectures has allowed scientists to create new experimental formats for processing ultra-small analytical volumes in short periods and with high efficiency. The development of such microfluidic systems has been driven by a range of fundamental features that accompany miniaturization. These include the ability to handle small sample volumes, ultra-low fabrication costs, reduced analysis times, enhanced operational flexibility, facile automation, and the ability to integrate functional components within complex analytical schemes. Herein we discuss the impact of microfluidics in the area of high-throughput screening and drug discovery and highlight some of the most pertinent studies in the recent literature.

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Citations
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Journal ArticleDOI

Automating drug discovery

TL;DR: This article aims to identify the approaches and technologies that could be implemented robustly by medicinal chemists in the near future and to critically analyse the opportunities and challenges for their more widespread application.
Journal ArticleDOI

The Poisson distribution and beyond: methods for microfluidic droplet production and single cell encapsulation

TL;DR: Both passive and active methods for droplet production are examined and how these can be used to deterministically and non-deterministically encapsulate cells are explored.
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Microfluidic Devices for Drug Delivery Systems and Drug Screening.

TL;DR: The emergence of fabricated microfluidic cell-free protein synthesis systems for potential use at point of care as well as cell-, organ-, and human-on-a-chip models as smart, sensitive, and reproducible platforms, allowing the investigation of the effects of drugs under conditions imitating the biological system.
Journal Article

Life at Low Reynolds Number

TL;DR: The demonstration involved a tall rectangular transparent vessel of corn syrup, projected by an overhead projector turned on its side, and the figures reproduce transparencies used in the talk.
Journal ArticleDOI

Microfluidics for cell-based high throughput screening platforms—A review

TL;DR: The screening methods mentioned in this paper include approaches using the perfusion flow mode, the droplet mode, and the microarray mode and the future development of microfluidic based high throughput screening platform for drug discovery is discussed.
References
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Journal ArticleDOI

Mass spectrometry-based proteomics

TL;DR: The ability of mass spectrometry to identify and, increasingly, to precisely quantify thousands of proteins from complex samples can be expected to impact broadly on biology and medicine.
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Rapid prototyping of microfluidic systems in poly(dimethylsiloxane)

TL;DR: A procedure that makes it possible to design and fabricate microfluidic systems in an elastomeric material poly(dimethylsiloxane) (PDMS) in less than 24 h by fabricating a miniaturized capillary electrophoresis system is described.
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Microfluidics: Fluid physics at the nanoliter scale

TL;DR: A review of the physics of small volumes (nanoliters) of fluids is presented, as parametrized by a series of dimensionless numbers expressing the relative importance of various physical phenomena as mentioned in this paper.
Journal ArticleDOI

Life at low Reynolds number

TL;DR: Weisskopf as mentioned in this paper presented a transparencies of a tall rectangular transparent vessel of corn syrup, projected by an overhead projector turned on its side, which was itself a slightly edited transcript of a tape.
Journal ArticleDOI

Specific Enzymatic Amplification of DNA In Vitro: The Polymerase Chain Reaction

TL;DR: An alternative method for the synthesis of specific DNA sequences is explored that involves the reciprocal interaction of two oligonucleotides and the DNA polymerase extension products whose synthesis they prime, when they are hybridized to different strands of a DNA template in a relative orientation such that their extension products overlap.
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