Chemical modification of bioinspired superhydrophobic polystyrene surfaces to control cell attachment/proliferation

Soft Matter ◽  
2011 ◽  
Vol 7 (19) ◽  
pp. 8932 ◽  
Author(s):  
Sara M. Oliveira ◽  
Wenlong Song ◽  
Natália M. Alves ◽  
João F. Mano
2011 ◽  
Vol 361 (1) ◽  
pp. 71-78 ◽  
Author(s):  
Nan Cheng ◽  
Xudong Cao
Keyword(s):  

2015 ◽  
Vol 16 (5) ◽  
pp. 1556-1565 ◽  
Author(s):  
Nicholas P. Reynolds ◽  
Mirren Charnley ◽  
Marie N. Bongiovanni ◽  
Patrick G. Hartley ◽  
Sally L. Gras

2021 ◽  
Author(s):  
Hannah A Pearce ◽  
Yu Seon Kim ◽  
Emma Watson ◽  
Kiana Bahrami ◽  
Mollie M Smoak ◽  
...  

Abstract The field of biomaterials has advanced significantly in the past decade. With the growing need for high-throughput manufacturing and screening, the need for modular materials that enable streamlined fabrication and analysis of tissue engineering and drug delivery schema has emerged. Microparticles are a powerful platform that have demonstrated promise in enabling these technologies without the need to modify a bulk scaffold. This building block paradigm of using microparticles within larger scaffolds to control cell ratios, growth factors and drug release holds promise. Gelatin microparticles (GMPs) are a well-established platform for cell, drug and growth factor delivery. One of the challenges in using GMPs though is the limited ability to modify the gelatin post-fabrication. In the present work, we hypothesized that by thiolating gelatin before microparticle formation, a versatile platform would be created that preserves the cytocompatibility of gelatin, while enabling post-fabrication modification. The thiols were not found to significantly impact the physicochemical properties of the microparticles. Moreover, the thiolated GMPs were demonstrated to be a biocompatible and robust platform for mesenchymal stem cell attachment. Additionally, the thiolated particles were able to be covalently modified with a maleimide-bearing fluorescent dye and a peptide, demonstrating their promise as a modular platform for tissue engineering and drug delivery applications.


RSC Advances ◽  
2018 ◽  
Vol 8 (39) ◽  
pp. 21777-21785 ◽  
Author(s):  
Kai Zhang ◽  
Alexandra Arranja ◽  
Hongyu Chen ◽  
Serhii Mytnyk ◽  
Yiming Wang ◽  
...  

A method to transfer-print quenched, ultra-long copolymer cylindrical micelles to a flat surface and the use of these nano-structures to promote spontaneous cell alignment is proposed. Endless possibilities of corona end-group chemical modification provide a new tool to control cell response.


2006 ◽  
Vol 950 ◽  
Author(s):  
Sergiy Zankovych ◽  
Joerg Bossert ◽  
Ines Thiele ◽  
Klaus D. Jandt ◽  
Liga Berzina-Cimdina

ABSTRACTWe report preliminary results of using nanoparticles to control cell attachment and growth. We present the way to create titanium surfaces with different roughness in a rage between 2 nm and 117 nm by using nanoparticles as a superficial layer and varying the evaporation parameters. We examined cell proliferation on titanium substrates with increased surface roughness compared to smooth titanium surface. We used nanoparticles to create a micrometer-sized lateral layout onto substrates preliminary structured by microcontact printing. We demonstrate controlled cell growth on substrates laterally structured with nanoparticles.


Lab on a Chip ◽  
2010 ◽  
Vol 10 (15) ◽  
pp. 1937 ◽  
Author(s):  
Kihoon Jang ◽  
Kae Sato ◽  
Yo Tanaka ◽  
Yan Xu ◽  
Moritoshi Sato ◽  
...  

2013 ◽  
Vol 14 (7) ◽  
pp. 2305-2316 ◽  
Author(s):  
Nicholas P. Reynolds ◽  
Katie E. Styan ◽  
Christopher D. Easton ◽  
Yali Li ◽  
Lynne Waddington ◽  
...  

2017 ◽  
Vol 5 (25) ◽  
pp. 4926-4933 ◽  
Author(s):  
Xuan Xue ◽  
Lalitha Thiagarajan ◽  
Shwana Braim ◽  
Brian R Saunders ◽  
Kevin M Shakesheff ◽  
...  

We report the synthesis of thermo-responsive polymer brushes with Upper Critical Solution Temperature (UCST)-type behaviour on glass to provide a new means to control cell attachment.


2019 ◽  
Author(s):  
M. Cámara-Torres ◽  
R. Sinha ◽  
C. Mota ◽  
L. Moroni

AbstractIn order to ensure the long-term in vitro and in vivo functionality of cell-seeded 3D scaffolds, an effective and reliable method to control cell seeding efficiency and distribution is crucial. Static seeding on 3D additive manufactured scaffolds made of synthetic polymers still remains challenging, as it often results in poor cell attachment, high cell sedimentation and non-uniform cell distribution, due to gravity and to the intrinsic macroporosity and surface chemical properties of the scaffolds. In this study, the bio-inert macromolecules dextran and Ficoll were used for the first time as temporary supplements to alter the viscosity and density of the seeding media, respectively, and improve the static seeding output. The addition of these macromolecules drastically reduced the cell sedimentation velocities, allowing for homogeneous cell attachment to the scaffold filaments. Both dextran- and Ficoll-based seeding methods supported human mesenchymal stromal cells viability and osteogenic differentiation post-seeding. Interestingly, the improved cell distribution led to increased matrix production and mineralization compared to scaffolds seeded by conventional static method. These results suggest a simple and universal method for an efficient seeding of 3D additive manufactured scaffolds, independent of their material and geometrical properties, and applicable for bone and various other tissue regeneration.


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