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Microcontact printing (μCP) is a versatile and low-cost technique for surface patterning, allowing for the fabrication of intricate designs with relative ease. However, despite these clear advantages, the application of μCP has predominantly focused on smooth, uniform surfaces, while rough, capillary-active, or hydrogel surfaces have largely been neglected in existing literature. This article aims to review the latest advances in μCP, tracing the evolution of patterning techniques and highlighting recent applications across various fields. Our discussion will encompass both fundamental developments in technology and practical implementations that illustrate its potential. In the last section, we will address the question why non-smooth surfaces have gathered less interest and aim to propose strategies for overcoming the inherent challenges they pose. With this contribution, we will also provide a perspective by shifting our focus to the specific challenges posed by capillary-active surfaces. We will introduce the innovative concept of polymer brush-supported μCP (PolyBrushMiC), which could serve as a promising strategy to address these challenges. By incorporating polymer brushes, we can enhance the compatibility of μCP with rough surfaces, enabling more effective pattern transfer and improved stability of printed features.
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http://dx.doi.org/10.1039/d5sm00355e | DOI Listing |
Small Sci
September 2025
Fischell Department of Bioengineering University of Maryland, College Park Maryland 20742 USA.
Human induced pluripotent stem cells (hiPSCs) show great promise for personalized cell-based medicine, as they can be derived from easily accessible somatic cells and differentiated into all three germ layers without ethical concerns. This requires mass production of hiPSCs in 3D. However, contemporary methods for 3D culture result in hiPSC spheroids with significant size heterogeneity that is undesired for controlled differentiation and require the use of a high concentration of Rho-associated kinase inhibitor (RI) to improve the cell viability.
View Article and Find Full Text PDFACS Meas Sci Au
August 2025
Institute of Chemical Technologies and Analytics, TU Wien, 1060 Vienna, Austria.
Extracellular vesicles (EVs) are nanosized particles that are associated with various physiological and pathological functions. They play a key role in intercell communication and are used as transport vehicles for various cell components. In human milk, EVs are believed to be important for the development of acquired immunity.
View Article and Find Full Text PDFSmall
August 2025
Department of Materials Process Engineering, Graduate School of Engineering, Nagoya University, Nagoya, Aichi, 464-8603, Japan.
Here, a novel electroless deposition approach is proposed that utilizes the spontaneous assembly of micelles and metal ions on non-conductive substrate surfaces, induced by reducing agents, to fabricate mesoporous Pt (mPt) films. By utilizing the effective interaction between deposited initial nuclei and 3-aminopropyltriethoxysilane (APTES), the electroless deposition of mPt is achieved on APTES-modified glass surfaces during chemical reduction. Using this approach, mPt film on 4-inch glass wafers is successfully prepared.
View Article and Find Full Text PDFFront Dement
July 2025
Laboratory of Psychiatry and Experimental Alzheimer's Research, Medical University of Innsbruck, Innsbruck, Austria.
Alzheimer's disease (AD) is a severe neurodegenerative brain disorder molecularly characterized by extracellular β-amyloid plaques, intraneuronal tau neurofibrillary tangles, cholinergic neuron death, neuroinflammation, vascular damage, and astroglial and microglial activation. AD is a complex disorder, with >99% of all cases being sporadic and typically occuring around the age of 65. Due to this intricate nature of the disorder, experiments have limitations; however, three-dimensional organotypic brain slices may offer the best alternative for studying the mechanisms involved in the progression of AD.
View Article and Find Full Text PDFNat Commun
July 2025
Eidgenössische Technische Hochschule (ETH) Zurich, Department of Biosystems Science and Engineering, Klingelbergstrasse 48, Basel, Switzerland.
Mammalian cells adjust integrin-mediated adhesion based on the composition and structure of the extracellular matrix (ECM). However, how spatially confined ECM ligands regulate cell adhesion initiation remains unclear. Here, we investigate how cells adapt early adhesion to different ECM protein areas.
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