Updated 70/16/2020
In this article, they review the past applications of in vitro models in identifying human hepatotoxins and focus on the use of multiscale experimental models in drug development, including the use of zebrafish and human cell-based, 3-dimensional (3D), microfluidic systems of liver functions as key components in applying Quantitative Systems
Pharmacology (QSP). They have implemented QSP as a platform to improve the rate of success in the process of drug discovery and development of therapeutics.
The stakeholders involved in drug development from academia, industry, and government agencies know the need to improve drug candidate selection by optimizing efficacy while screening out potential toxins so as to concentrate efforts with favorable chances for market approval. A survey of the number of new drugs released between 2000 and 2009 demonstrated a 25-year low in drug approvals despite increases in research and development (R&D) investment.
SOURCE
Click to access nihms-1002432.pdf
Lab on a chip Enters a New Field
Reporter: Irina Robu, PhD
The basis of the lab-on-a-chip is to integrate thousands of biochemical operations onto a single chip that could be done by splitting a single drop of blood collected from the patient in order to get a precise diagnosis of potential diseases. Research on lab-on-a-chip primarily focuses on human diagnostics and DNA analysis. Miniaturization of biochemical operations normally handled in a laboratory has numerous advantages, such as cost efficiency, diagnostic speed and sensitivity. The emergence of the lab-on-a-chip field mainly relies on two core technologies: microfluidics and molecular biology.
The team led by Govind Kaigala at IBM Research-Zurich and the group of Moran Bercovici at Technion-Israel Institute of Technology designed a new device that can effectively control liquids and materials on the micro-scale and have demonstrated that the key to dynamic control of fluid mechanics may be electric. Their research is published on Proceedings of the National Academy of Sciences.
The research team turned to electric field to control the control the motion of fluid in a way that is adjustable. When liquid contacts a surface, it develops a layer of charge; applying an electric field to this layer moves the charges, dragging the liquid with them and creating a net flow.
Using this knowledge, the team calculated a device that uses disk-shaped electrodes implanted in the bottom of a fluidic chamber to produce dipole-like flow patterns in the liquid when an electric field is applied. Placing multiple electrodes together in an array generates “virtual channels” that guide the fluid stream. By altering the voltages on the electrodes, they could then reverse the pattern to create an inner region of flow bounded by an outer region of stagnation, which is useful for selective on-demand mixing. While more applications of these flow patterns have yet to be explored, the control and flexibility the team’s device offers recommend that the lab-on-a-chip dream may finally be within grasp.
SOURCE
https://physicsworld.com/a/microfluidics-enters-a-new-field/
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