Department of Chemistry and Chemical Biology, Rutgers University, Piscataway, NJ 08854, United States.
Colloids Surf B Biointerfaces. 2011 Jun 1;84(2):591-6. doi: 10.1016/j.colsurfb.2011.01.014. Epub 2011 Jan 20.
Microscale plasma-initiated patterning (μPIP) is a novel micropatterning technique used to create biomolecular micropatterns on polymer surfaces. The patterning method uses a polydimethylsiloxane (PDMS) stamp to selectively protect regions of an underlying substrate from oxygen plasma treatment resulting in hydrophobic and hydrophilic regions. Preferential adsorption of the biomolecules onto either the plasma-exposed (hydrophilic) or plasma-protected (hydrophobic) regions leads to the biomolecular micropatterns. In the current work, laminin-1 was applied to an electrospun polyamide nanofibrillar matrix following plasma treatment. Radial glial clones (neural precursors) selectively adhered to these patterned matrices following the contours of proteins on the surface. This work demonstrates that textured surfaces, such as nanofibrillar scaffolds, can be micropatterned to provide external chemical cues for cellular organization.
微尺度等离子体引发图案化(μPIP)是一种新颖的微图案化技术,用于在聚合物表面上创建生物分子微图案。该图案化方法使用聚二甲基硅氧烷(PDMS)印章有选择地保护基底的区域免受氧气等离子体处理,从而产生疏水区和亲水区。生物分子优先吸附到等离子体暴露(亲水)或等离子体保护(疏水)区域上,从而导致生物分子微图案化。在当前的工作中,层粘连蛋白-1在等离子体处理后应用于电纺聚酰胺纳米纤维基质。径向神经胶质克隆(神经前体细胞)沿着表面上的蛋白质轮廓选择性地附着在这些图案化的基质上。这项工作表明,纹理表面(如纳米纤维支架)可以进行微图案化,以提供用于细胞组织的外部化学线索。