Characterization of the surface tension and viscosity effects on the formation of nano-liter droplet arrays by an instant protein micro stamper

Rapid and parallel protein micro/nano array formation provides a powerful tool for protein chip fabrication and protein preservation. This paper presents the characterization of the surface tension and viscosity effects on the formation of nano-liter droplet arrays by a novel instant micro stamper, which can simultaneously immobilize hundreds of proteins on a chip. Capillary force is the major driving mechanism of the micro stamper, flowing protein solutions through the chip channel for array-registration and droplet-size control. Three important properties have been characterized in this paper, including uniformity of the parallel printing process, surface wettability and solution viscosity effect on micro droplet size and the dynamic sequence of micro droplet formation. Experimental results demonstrated the uniformity of the parallel stamping process for protein micro arrays from area to area and chip to chip. The effects of surface wettability of bioassay chips and solution viscosity on droplet-size variation have been investigated in detail by experiments and simulations. Both simulation and experimental results demonstrate that the spot size increases with increasing surface wettability and decreasing solution viscosity, and they showed similar tends. The dynamic process of droplet formation has also been observed and analyzed by high-speed images, demonstrating that the footprint reduction rate, formation time and necking of the printed micro droplet are lower on the more hydrophobic surface. This is due to the rapid shrinkage of the droplet footprint area on a hydrophobic surface, resulting in smaller droplet formation. The droplet size can shrink up to 50% when the contact angle of the bioassay chip surface increases from 30° to 80°. On the other hand, the variation of solution viscosity from 1.02 to 10.08 cp makes the droplet size shrink to 70%.

[1]  G. Whitesides,et al.  Soft lithographic methods for nano-fabrication , 1997 .

[2]  Ronald W. Davis,et al.  Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray , 1995, Science.

[3]  R. Ekins,et al.  Ligand assays: from electrophoresis to miniaturized microarrays. , 1998, Clinical chemistry.

[4]  M. N. Yoder Microelectronics/nanoelectronics and the 21st century , 2001, Proceedings of the Fourteenth Biennial University/Government/Industry Microelectronics Symposium (Cat. No.01CH37197).

[5]  V. Morozov,et al.  Electrospray deposition as a method for mass fabrication of mono- and multicomponent microarrays of biological and biologically active substances. , 1999, Analytical chemistry.

[6]  J A Barron,et al.  Biological Laser Printing: A Novel Technique for Creating Heterogeneous 3-dimensional Cell Patterns , 2004, Biomedical microdevices.

[7]  W. Monty Reichert,et al.  Spreading Diagrams for the Optimization of Quill Pin Printed Microarray Density , 2002 .

[8]  Dieter Stoll,et al.  Protein microarray technology. , 2002, Frontiers in bioscience : a journal and virtual library.

[9]  Fan-Gang Tseng,et al.  Numerical simulation of the stamping process through microchannels , 2003 .

[10]  A. Roda,et al.  Protein microdeposition using a conventional ink-jet printer. , 2000, BioTechniques.

[11]  Brett D. Martin,et al.  Direct Protein Microarray Fabrication Using a Hydrogel “Stamper” , 1998 .

[12]  E. Delamarche,et al.  Fabricating microarrays of functional proteins using affinity contact printing. , 2002, Angewandte Chemie.

[13]  Eliot Marshall Companies Battle Over Technology That's Free on the Web , 1999, Science.

[14]  R. Christopherson,et al.  Antibody arrays: an embryonic but rapidly growing technology. , 2002, Drug discovery today.

[15]  G. Whitesides,et al.  Patterning proteins and cells using soft lithography. , 1999, Biomaterials.

[16]  P. Brown,et al.  Protein microarrays for highly parallel detection and quantitation of specific proteins and antibodies in complex solutions , 2001, Genome Biology.

[17]  L. G. Mendoza,et al.  High-throughput microarray-based enzyme-linked immunosorbent assay (ELISA). , 1999, BioTechniques.

[18]  Fan-Gang Tseng,et al.  Simultaneous immobilization of protein microarrays by a micro stamper with back-filling reservoir , 2004 .

[19]  Yong-Kweon Kim,et al.  Protein patterning by virtual mask photolithography using a micromirror array , 2003 .

[20]  N. V. Avseenko,et al.  Immunoassay with multicomponent protein microarrays fabricated by electrospray deposition. , 2002, Analytical chemistry.

[21]  J. Brackbill,et al.  A continuum method for modeling surface tension , 1992 .

[22]  Shih‐Chang Lin,et al.  Protein micro arrays immobilized by μ-stamps and -protein wells on PhastGel® pad , 2002 .

[23]  Fluorescence measurements of nanopillars fabricated by high-aspect-ratio nanoprint technology , 2004 .

[24]  R. Huang,et al.  Detection of multiple proteins in an antibody-based protein microarray system. , 2001, Journal of immunological methods.

[25]  R. Zengerle,et al.  Droplet release in a highly parallel, pressure driven nanoliter dispenser , 2003, TRANSDUCERS '03. 12th International Conference on Solid-State Sensors, Actuators and Microsystems. Digest of Technical Papers (Cat. No.03TH8664).