Droplet Evaporation Study Applied to DNA Chip Manufacturing

• Published in: Langmuir 2005-09, Vol.21 (20), p.9130-9136
• Main Authors: Dugas, Vincent, Broutin, Jérôme, Souteyrand, Eliane
• Format: Article
• Language: English
• Subjects: Atmospheric Pressure; Biological and medical sciences; Biosensing Techniques; Biotechnology; Chemistry; Exact sciences and technology; Fundamental and applied biological sciences. Psychology; General and physical chemistry; Glass; Hydrophobic and Hydrophilic Interactions; Image Processing, Computer-Assisted; Methods. Procedures. Technologies; Microscopy, Video; Oligonucleotide Array Sequence Analysis - instrumentation; Oligonucleotide Array Sequence Analysis - methods; Sensitivity and Specificity; Solutions - chemistry; Surface-Active Agents - chemistry; Time Factors; Volatilization; Water - chemistry; Wettability
• ISSN: 0743-7463; 1520-5827
• DOI: 10.1021/la050764y

DNA chips are potentially powerful technologies for genotyping and gene expression profiling that rely on comparative analyses of up to thousands of “spots of analysis” on a glass support. The spot quality throughout the support influences spot-to-spot variations within an array and the repeatability of data across experiments. For glass slide DNA microarrays, droplets of DNA solution are deposited on functionalized glass slides and left to react through complete evaporation of the droplet. On hydrophobic flat surfaces, different modes of droplet evaporation can be attained. Under atmospheric pressure, water droplets tend to evaporate under two main regimes. Initially, the droplet flattens with a constant contact area, and then the droplet shrinks at a constant contact angle. As a result, the diameter and morphology of thousands of spots on microarrays are not uniform. This leads to poor and unreliable data processing results. In this work, we report the evaporation of an aqueous solution under a constant contact area mode. Evaporation under reduced pressure and the effect of reagent additives to the solution have been investigated. Video microscopy and digital image analysis techniques were applied to monitor the evaporation of the droplets. A mixture of surfactants was developed to maintain a constant area regime during evaporation and to form homogeneous spots. The control of some physicochemical properties (wetting, evaporation rate) of the droplet allows the formation of well-controlled spots compatible with DNA grafting. The influence of surfactant molecules on the mechanisms of evaporation is also discussed.