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NIST Debuts Simple Cell Assay on a Chip

By R&D Editors | February 9, 2012

The great artist and inventor Leonardo da Vinci once said that “simplicity is the ultimate sophistication.” National Institute of Standards and Technology (NIST) research engineer Javier Atencia certainly believes in the wisdom of what da Vinci preached; he has a reputation for creating novel microfluidic devices out of ordinary, inexpensive components. This time, he has combined a glass slide, plastic sheets and double-sided tape into a “diffusion-based gradient generator”—a tool to rapidly assess how changing concentrations of specific chemicals affect living cells.*

Atencia’s latest innovation offers a simple and inexpensive way to expose an array of cultured cells to a chemical gradient—a solution where the chemical concentration changes gradually and predictably across the array. Such gradients are a rapid, high-throughput way to evaluate the effect on cell growth or toxicity.

There are two distinct advantages to the new NIST system over traditional microfluidic cell assay devices. The first is that the gradient is created by diffusion—the gentle movement of matter from one point to another by random molecular motion. Conventional microfluidic systems usually mix fluids by pumping them in a circular motion or by twisting and folding them together. Diffusion greatly reduces the risk of cells being swept away or damaged by shearing forces in the test fluid.

The second big advantage is simplicity. The gradient generator is built in layers, with each section precisely positioned with an alignment tab. The base is a glass slide, upon which is attached a strip of double-sided tape cut to have a row of four micrometer-sized channels. Atop this goes a polystyrene strip cut to have two lines each of four tiny circular “wells” where each pair lines up with the ends of the channel below it. The next layer is another strip of double-sided tape, this time with a Y-shaped canal cut into it to serve as the flow path for the chemical gradient. Finally, a Mylar strip cut to have an identical Y-canal serves as the cover.

The hinged cover allows access to the wells for adding test cells. Once done, the cover is lowered and affixed, sealing the gradient generator. Fluid flow in and out of the system is accomplished using another Atencia innovation, magnetic connectors. Kept at constant pressure, this flow assures a steady-state stream through the device and creates a diffusion gradient in each buried channel. Cells in the channels are simultaneously exposed to a range of chemical concentrations from high to low.

To test the device, Atencia and his colleagues loaded it with cells genetically engineered to produce large amounts of green fluorescent protein (GFP) and then introduced cycloheximide (CHX), a chemical that shuts down ribosomes, the cell’s protein factories. Cells exposed to the toxin quickly stop synthesizing GFP, decreasing fluorescence by an amount directly related to the concentration of CHX.

This is exactly what the researchers observed in the gradient generator assays. The cells were exposed three times to CHX, and each time, the level of GFP fluorescence increased as the concentration of CHX in the gradient decreased, and vice versa.

In his previous microfluidics creations, Atencia turned a simple plastic dish into a “microfluidic palette” for exposing cells to multiple chemical concentrations in a single chamber and then merged donut-shaped magnets and plastic tubes to make a leak-free connector for getting fluids into and out of a microchannel.

Date: February 9, 2012
Source: National Institute of Standards and Technology 

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