Picone Remigio, Baum Buzz, McKendry Rachel
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA; Department of Pediatric Oncology, Howard Hughes Medical Institute, Boston, Massachusetts, USA; Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA; London Centre for Nanotechnology and Department of Medicine, University College London, London, United Kingdom; Medical Research Council - Laboratory for Molecular Cell Biology, University College London, London, United Kingdom; CoMPLEX, University College London, London, United Kingdom.
Medical Research Council - Laboratory for Molecular Cell Biology, University College London, London, United Kingdom.
Methods Cell Biol. 2014;119:73-90. doi: 10.1016/B978-0-12-416742-1.00005-6.
Plasma microcontact patterning (PμCP) is a simple, efficient, and cost-effective method for the precise patterning of molecules on surfaces. It combines the use of low-pressure plasma with an elastomeric 3D mask to spatially control the removal of molecules, such as proteins, from a surface. The entire PμCP process is subdivided into three main steps: surface precoating, plasma micropatterning, and a surface postcoating step. Surfaces are first precoated with a molecular species and then placed in close contact with the 3D mask. This allows the formation of two distinct regions: an un-masked open-region which is accessible to the plasma, from which the surface layer is removed, and, a contact region which is physically protected from exposure to the plasma. In the final step, a second molecule is added to back-fill the pattern generated through plasma-treatment. The PμCP technique allows the patterning of virtually any organic molecules on different surface materials and geometries (e.g., flat, curved surfaces, and 3D microstructures). Moreover, it is a simple and robust procedure. The main advantages of this approach over traditional microcontact printing are twofold: The stability of molecule binding to plasma-treated surfaces, and the separation of the surface functionalization step from the actual micropatterning step, which enables the precise control of concentration and uniformity of patterned molecules. In conclusion, PμCP is a simple way to generate surface patterns that are highly reproducible, stable and uniform, making it a useful method for many applications.
等离子体微接触图案化(PμCP)是一种在表面精确图案化分子的简单、高效且经济高效的方法。它将低压等离子体与弹性体3D掩膜结合使用,以空间控制从表面去除蛋白质等分子。整个PμCP过程可细分为三个主要步骤:表面预涂覆、等离子体微图案化和表面后涂覆步骤。首先在表面预涂覆一种分子物种,然后将其与3D掩膜紧密接触。这允许形成两个不同的区域:一个未被掩膜的开放区域,等离子体可到达该区域并去除表面层;以及一个接触区域,该区域受到物理保护,免受等离子体暴露。在最后一步,添加第二种分子以回填通过等离子体处理产生的图案。PμCP技术允许在不同的表面材料和几何形状(如平面、曲面和3D微结构)上对几乎任何有机分子进行图案化。此外,它是一个简单且稳健的过程。这种方法相对于传统微接触印刷的主要优点有两个:分子与等离子体处理过的表面结合的稳定性,以及表面功能化步骤与实际微图案化步骤的分离,这使得能够精确控制图案化分子的浓度和均匀性。总之,PμCP是一种生成高度可重复、稳定且均匀的表面图案的简单方法,使其成为许多应用的有用方法。