scholarly journals Wettability patterning in microfluidic devices using thermally-enhanced hydrophobic recovery of PDMS

Soft Matter ◽  
2019 ◽  
Vol 15 (45) ◽  
pp. 9253-9260 ◽  
Author(s):  
Marc Pascual ◽  
Margaux Kerdraon ◽  
Quentin Rezard ◽  
Marie-Caroline Jullien ◽  
Lorène Champougny

In situ wettability patterning of PDMS microchannels is achieved through localized hydrophobic recovery enhancement using heating microresistors.

The Analyst ◽  
2015 ◽  
Vol 140 (23) ◽  
pp. 7896-7901 ◽  
Author(s):  
Yanlong Xing ◽  
Andreas Wyss ◽  
Norbert Esser ◽  
Petra S. Dittrich

Label-free biosensors based on in situ formed and functionalized TTF–Au wires were developed using an integrated microfluidic system.


TECHNOLOGY ◽  
2017 ◽  
Vol 05 (01) ◽  
pp. 1-12 ◽  
Author(s):  
Aslihan Gokaltun ◽  
Martin L. Yarmush ◽  
Ayse Asatekin ◽  
O. Berk Usta

In the last decade microfabrication processes including rapid prototyping techniques have advanced rapidly and achieved a fairly mature stage. These advances have encouraged and enabled the use of microfluidic devices by a wider range of users with applications in biological separations and cell and organoid cultures. Accordingly, a significant current challenge in the field is controlling biomolecular interactions at interfaces and the development of novel biomaterials to satisfy the unique needs of the biomedical applications. Poly(dimethylsiloxane) (PDMS) is one of the most widely used materials in the fabrication of microfluidic devices. The popularity of this material is the result of its low cost, simple fabrication allowing rapid prototyping, high optical transparency, and gas permeability. However, a major drawback of PDMS is its hydrophobicity and fast hydrophobic recovery after surface hydrophilization. This results in significant nonspecific adsorption of proteins as well as small hydrophobic molecules such as therapeutic drugs limiting the utility of PDMS in biomedical microfluidic circuitry. Accordingly, here, we focus on recent advances in surface molecular treatments to prevent fouling of PDMS surfaces towards improving its utility and expanding its use cases in biomedical applications.


Lab on a Chip ◽  
2005 ◽  
Vol 5 (2) ◽  
pp. 151 ◽  
Author(s):  
Helen M. Simms ◽  
Christopher M. Brotherton ◽  
Brian T. Good ◽  
Robert H. Davis ◽  
Kristi S. Anseth ◽  
...  

2011 ◽  
Vol 45 (1) ◽  
pp. 53-60 ◽  
Author(s):  
Yong Yu ◽  
Xuan Wang ◽  
Dominik Oberthür ◽  
Arne Meyer ◽  
Markus Perbandt ◽  
...  

A new crystallization system is described, which makes it possible to use an evaporation-based microfluidic crystallization technique for protein crystallization. The gas and water permeability of the used polydimethylsiloxane (PDMS) material enables evaporation of the protein solution in the microfluidic device. The rates of evaporation are controlled by the relative humidity conditions, which are adjusted in a precise and stable way by using saturated solutions of different reagents. The protein crystals could nucleate and grow under different relative humidity conditions. Using this method, crystal growth could be improved so that approximately 1 mm-sized lysozyme crystals were obtained more successfully than using standard methods. The largest lysozyme crystal obtained reached 1.57 mm in size. The disadvantage of the good gas permeability in PDMS microfluidic devices becomes an advantage for protein crystallization. The radius distributions of aggregrates in the solutions inside the described microfluidic devices were derived fromin situdynamic light scattering measurements. The experiments showed that the environment inside of the microfluidic device is more stable than that of conventional crystallization techniques. However, the morphological results showed that the protein crystals grown in the microfluidic device could lose their morphological stability. Air bubbles in microfluidic devices play an important role in the evaporation progress. A model was constructed to analyze the relationship of the rates of evaporation and the growth of air bubbles to the relative humidity.


Lab on a Chip ◽  
2015 ◽  
Vol 15 (4) ◽  
pp. 1072-1083 ◽  
Author(s):  
Huaying Chen ◽  
Jane Sun ◽  
Ernst Wolvetang ◽  
Justin Cooper-White

In this paper, the design, development and validation of a novel high throughput microfluidic device enabling both the robust and rapid trapping of 100's to 1000's of single cells and their in situ clonal growth is described.


Lab on a Chip ◽  
2019 ◽  
Vol 19 (23) ◽  
pp. 3954-3961 ◽  
Author(s):  
Jang Han Choi ◽  
Tae Soup Shim

Real-time, in situ internal pressure monitoring in a microchannel is realized by a deformable colloidal crystal membrane.


2005 ◽  
Vol 58 (6) ◽  
pp. 433 ◽  
Author(s):  
Michael J. Owen

There is considerable current interest in plasma and corona treatment of silicones. It is well established that a thin, silica-like layer is created on the surface by such treatments. Much fresh insight has emerged concerning the role of low-molecular-weight materials in the hydrophobic recovery of treated elastomers. Even if these diffusible species are removed before treatment, hydrophobic recovery still occurs above a threshold energy implying that they are produced in situ by the treatment. A particularly significant new direction in the plasma treatment field is plasma polymerization of organosilicon monomers using atmospheric pressure glow discharge (APGD).


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