Archive for 2011

HOT: Gold compact disks in improved detection for cancer biomarkers

Microfluidic devices in bioanalysis offer advantages in terms of high-throuphput and reduced costs per analysis. In this paper James Rusling and colleagues at the University of Connecticut use gold compact disks in the construction of inexpensive immunomicroarrays. They then used their devices for the electrochemical detection of the cancer biomarker, interleukin-6 in diluted serum.

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Fabrication of immunosensor microwell arrays from gold compact discs for detection of cancer biomarker proteins
Chi K. Tang, Abhay Vaze and James F. Rusling
Lab Chip, 2012, Advance Article
DOI: 10.1039/C1LC20833K, Paper

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Top ten most accessed articles in October

This month sees the following articles in Lab on a Chip that are in the top ten most accessed:

Rapid prototyping polymers for microfluidic devices and high pressure injections
Elodie Sollier, Coleman Murray, Pietro Maoddi and Dino Di Carlo
Lab Chip, 2011, 11, 3752-3765
DOI: 10.1039/C1LC20514E

Droplet microfluidics—a tool for protein engineering and analysis
Haakan N. Joensson and Helene Andersson-Svahn
Lab Chip, 2011, 11, 4144-4147
DOI: 10.1039/C1LC90102H

Surfactants in droplet-based microfluidics
Jean-Christophe Baret
Lab Chip, 2012, Advance Article
DOI: 10.1039/C1LC20582J

Bubbles navigating through networks of microchannels
Wonjae Choi, Michinao Hashimoto, Audrey K. Ellerbee, Xin Chen, Kyle J. M. Bishop, Piotr Garstecki, Howard A. Stone and George M. Whitesides
Lab Chip, 2011, 11, 3970-3978
DOI: 10.1039/C1LC20444K

Integration of intra- and extravasation in one cell-based microfluidic chip for the study of cancer metastasis
Min Kyeong Shin, Sung Kyu Kim and Hyungil Jung
Lab Chip, 2011, 11, 3880-3887
DOI: 10.1039/C1LC20671K

Microfluidic static droplet arrays with tuneable gradients in material composition
Meng Sun, Swastika S. Bithi and Siva A. Vanapalli
Lab Chip, 2011, 11, 3949-3952
DOI: 10.1039/C1LC20709A

Controlled viable release of selectively captured label-free cells in microchannels
Umut Atakan Gurkan, Tarini Anand, Huseyin Tas, David Elkan, Altug Akay, Hasan Onur Keles and Utkan Demirci
Lab Chip, 2011, 11, 3979-3989
DOI: 10.1039/C1LC20487D

Droplet formation via flow-through microdevices in Raman and surface enhanced Raman spectroscopy—concepts and applications
Anne März, Thomas Henkel, Dana Cialla, Michael Schmitt and Jürgen Popp
Lab Chip, 2011, 11, 3584-3592
DOI: 10.1039/C1LC20638A

1-Million droplet array with wide-field fluorescence imaging for digital PCR
Andrew C. Hatch, Jeffrey S. Fisher, Armando R. Tovar, Albert T. Hsieh, Robert Lin, Stephen L. Pentoney, David L. Yang and Abraham P. Lee
Lab Chip, 2011, 11, 3838-3845
DOI: 10.1039/C1LC20561G

Large-scale plasmonic microarrays for label-free high-throughput screening
Tsung-Yao Chang, Min Huang, Ahmet Ali Yanik, Hsin-Yu Tsai, Peng Shi, Serap Aksu, Mehmet Fatih Yanik and Hatice Altug
Lab Chip, 2011, 11, 3596-3602
DOI: 10.1039/C1LC20475K

Why not take a look at the articles today and blog your thoughts and comments below.

Fancy submitting an article to Lab on a Chip? Then why not submit to us today or alternatively email us your suggestions.

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Automated micro particle image velocimetry and a heart on a chip on the cover of Issue 24

Welcome to the final issue of 2011!

On the front cover of Issue 24 we have an article from Per Augustsson et al., who have developed a platform for micro particle image velocimetry (μPIV) for analyzing two-dimensional acoustophoresis.  The device is automated, temperature-stable and has uncertainties below 5% and is therefore able to conduct high-precision measurement of the acoustophoretic velocity field in microchannels.

Automated and temperature-controlled micro-PIV measurements enabling long-term-stable microchannel acoustophoresis characterization
Per Augustsson, Rune Barnkob, Steven T. Wereley, Henrik Bruus and Thomas Laurell
DOI: 10.1039/C1LC20637K


The inside front cover highlights the article from Kevin Kit Parker and colleagues that recently featured in Chemistry World.  The article describes a ‘heart on a chip’, exploiting muscular thin film technology to measure contractility and the effect of cell architecture on tissue contraction.

Ensembles of engineered cardiac tissues for physiological and pharmacological study: Heart on a chip
Anna Grosberg, Patrick W. Alford, Megan L. McCain and Kevin Kit Parker
DOI: 10.1039/C1LC20557A

Also in this issue is the latest Research Highlights article from Ali Khademhosseini, and a Focus article on droplet microfluidics for protein engineering and analysis from Helene Andersson Svahn and Haakan Joensson.

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Lab on a Chip in the New Scientist: weighing single cells for cancer treatment

A Lab on a Chip article from Scott Manalis, MIT, and colleagues has been featured in the New Scientist! The article describes methods for trapping single cells and monitoring their response to drugs within a suspended microchannel resonator.

By measuring changes in cell size and growth when drugs are introduced to the micromechanical system Manalis hopes that we will eventually be able to predict whether cancer treatments will be effective for individual patients, ‘we plan to determine if the growth response of tumour cells can be predictive of how a patient will respond to a therapy’.

To learn more read the article in the New Scientist – ‘Microscopic scales weigh up cancer therapies‘ – or go straight to the research article:

Mass sensors with mechanical traps for weighing single cells in different fluids
Yaochung Weng, Francisco Feijó Delgado, Sungmin Son, Thomas P. Burg, Steven C. Wasserman and Scott R. Manalis
DOI: 10.1039/C1LC20736A

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New YouTube videos

View the new videos on the Lab on a Chip YouTube site below:

Single- and two-phase flow in microfluidic porous media analogs based on Voronoi tessellation

Quantitatively controlled in situ formation of hydrogel membranes in microchannels for generation of stable chemical gradients

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New YouTube videos

View the new videos on the Lab on a Chip YouTube site below:

Planar silicon microrings as wavelength-multiplexed optical traps for storing and sensing particles

Two-dimensional paper networks: programmable fluidic disconnects for multi-step processes in shaped paper

Converting steady laminar flow to oscillatory flow through a hydroelasticity approach at microscales

Lateral cavity acoustic transducer as an on-chip cell/particle microfluidic switch

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A lab you can wear?

Malaysian scientists have created a flexible and environmentally friendly microfluidic device using a cloth decorating technique for printing wax onto cotton.

Dedy Wicaksono at the University of Technology Malaysia was inspired by his batik-patterned clothes to create the device. ‘Batik processing is wax patterning to create regions of differing hydrophilicity and hydrophobicity on cloth,’ says Dedy. The technique is traditionally used to prevent dye spreading from one area of cloth to another, creating coloured patterns. Using wax printing methods for paper and silk based microfluidic devices is known, but these have required specialist equipment or expensive materials.

Wicaksono’s method needs neither of these things. First, his team prepared the cotton by scouring it with sodium hydroxide and anhydrous sodium carbonate solutions. The treatment removes the outer layer, exposing underlying cellulose fibres. Both the chemical composition (increased oxygen content) and physical structure (increased surface roughness) of the fibre surface were altered, increasing the wettability and wicking rate.

Microfluidic device in different stages

(a)-(f) are photographs showing two hydrophilic channels with different dye solutions that cross each other vertically and horizontally in three layers without mixing. (b)-(e) are front views of the device before, 5 seconds, 2 minutes and 5 minutes after dropping the dyes into different channels. (f) is the bottom layer 5 minutes after adding the dyes.

Then, they printed the pattern for the microfluidic device onto paper. The paper was dipped into hot batik wax, then dried, before the pattern was cut from the sheet and attached to the scoured cloth using a few pins. Heat treatment melted the wax again, and it spread onto the surface and into the cloth, filling the gaps in the weave and within the fibres. The fatty acids in the wax increase the hydrophobicity of the fibres where they are applied, creating barriers to liquid flow.

Dedy’s group made both 2D and 3D devices; the latter was made by folding layers of the patterned cloth. A test using ink solutions revealed the ink moving along the cloth’s hydrophilic channels, filling a device in minutes. In a further test, the team was able to detect the protein bovine serum albumin colorimetrically using the devices, with the result visible to the naked eye.

‘A key innovation here is the batik-inspired method of transferring patterned wax on paper to cotton cloth,’ comments Shashi Murthy, an expert in microfluidic devices at Northeastern University, US. He adds that the technology ‘has the potential to provide a rapid and low cost readout for analytes characterised by relatively simple colorimetric assays’.

Dedy is now investigating ways to exert more control over the liquid flow so that more complex microfluidic devices can be developed. ‘By making the channels inside a flexible cloth, we are envisioning an embeddable wearable lab in the very near future,’ he says.

Flexible microfluidic cloth-based analytical devices using a low-cost wax patterning technique
Azadeh Nilghaz, Dedy H. B. Wicaksono, Dwi Gustiono, Fadzilah Adibah Abdul Majid, Eko Supriyanto and Mohammed Rafiq Abdul Kadir
Lab Chip, 2012, Advance Article
DOI: 10.1039/C1LC20764D

Original article published at Chemistry World

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New YouTube Videos

View the new videos on the Lab on a Chip YouTube site below:

 

On-chip CO2 control for microfluidic cell culture

On-chip measurements of cell compressibility via acoustic radiation

A microfluidic device for self-synchronised production of droplets

A scalable microfluidic chip for bacterial suspension culture

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On the cover: train tracks for synchronising droplets, tunable gradients and cheap droplet emulsion manufacture

The front cover of Issue 23 shows work from Meng Sun et al. who have produced a static droplet array with the capability for tunable concentration gradients.   Their technique involves the controlled exchange of materials between moving plugs and stationary drops, and the concentration of soluble reagents can be varied from drop to drop  at well-defined time points.

Microfluidic static droplet arrays with tuneable gradients in material composition
Meng Sun, Swastika S. Bithi and Siva A. Vanapalli
DOI: 10.1039/C1LC20709A


On the inside front cover we have an image from Kwang Oh and coworkers describing their method for droplet combination in microfluidic devices that allows passive parallel synchronisation.  They describe the layout as being analogous to a train track, as the network consists of a top channel, a bottom channel, and ladder-like connections between the two main channels.

Parallel synchronization of two trains of droplets using a railroad-like channel network
Byungwook Ahn, Kangsun Lee, Hun Lee, Rajagopal Panchapakesan and Kwang W. Oh
DOI: 10.1039/C1LC20690G


The back cover highlights work from Nan-Nan Deng et al on the economical production of microfluidic devices for monodisperse droplet formation.  The simple device fabrication, using inexpensive tools and supplies, is flexible, offering easy spatial patterning of surface wettability, and good chemical compatibility and optical properties.

Simple and cheap microfluidic devices for the preparation of monodisperse emulsions
Nan-Nan Deng, Zhi-Jun Meng, Rui Xie, Xiao-Jie Ju, Chuan-Lin Mou, Wei Wang and Liang-Ying Chu
DOI: 10.1039/C1LC20629J

View the rest of the issue online here, which including all our latest hot articles on a micro-hydrocyclone for particle separation, sustainable microinjection moulding, broadband for droplets, clinical-scale bubble production and streaming potential for energy

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Heart-on-a-chip

A heart-on-a-chip device could help detect drugs that limit heart tissue contraction, say US scientists.

The device was created using small thin strips of tissue made from heart muscle cells that are connected to electrodes to stimulate contraction. Observing the contraction response of the tissue allows scientists to study the effect of physiological factors or test drugs for cardiotoxicity. Replicating segments of heart tissue makes it possible to rapidly measure contraction data at the tissue level, rather than just studying individual cells.

Heart on a chip

The researchers, led by Kevin Parker from Harvard University, Cambridge, created up to eight separate strips of tissue on one chip by growing a sheet of heart muscle cells in a flat film and then cutting away sections to leave isolated strips that were only connected to the film by one edge. Creating several strips on one chip allowed the team to conduct multiple experiments at once. The contraction experiments were observed by looking vertically down onto the chip and monitoring the change in length as the strips contracted and bent up. ‘The heart-on-a-chip allows us to capture in 2D what a healthy or diseased heart might look like and look at how much force the tissue will generate,’ says Anna Grosberg, a member of the research team.

The team then used the heart-on-a-chip to investigate the effects of different environments on contraction response. Experiments with epinephrine (adrenaline) showed the device can be used to measure the dose-dependent effect of drugs on contraction response. The team also showed that the heart-on-a-chip can be used as a platform to investigate the effect of cell architecture on tissue contraction.

‘The heart-on-a-chip technology is the first scalable technique that recapitulates in vitro the anisotropic cell organisation of native cardiac muscle, while simultaneously allowing coupled electrical and mechanical function to be quantitatively assayed,’ says Andrew McCulloch, an expert in cardiac bioengineering at the University of California, San Diego, US. ‘Once this technology can be deployed using human stem cell-derived cardiomyocytes, we will have a powerful new platform for screening new drugs for heart diseases like arrhythmia and heart failure.’

Ensembles of engineered cardiac tissues for physiological and pharmacological study: Heart on a chip
Anna Grosberg, Patrick W. Alford, Megan L. McCain and Kevin Kit Parker
DOI: 10.1039/C1LC20557A

Original article published at Chemistry World

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