A new method for creating substrates made out of ordered collagen fibers, on which cells in culture can align, is proposed. The substrates can be used for research in cell culture, and this research presents a significant advance in the technology to coat implants in order to improve cell adhesion. In the procedure presented here, a molecular solution of collagen is spread at the interface of a saline solution and air to induce fiber formation, compressed at a high speed to induce orientation and deposited on solid substrates via Langmuir-Blodgett transfer. Several interfacial techniques are employed to investigate the behavior of collagen, which is shown to be dependent on the salt concentration of the subphase as well as the temperature. After Langmuir-Blodgett transfer, primary human fibroblasts and adipose-derived stem cells are cultured on the collagen substrates. Both types of cells respond favorably to the collagen orientation and align with the deposited fibers. The technique presented here provides a simple method to produce well-controlled, oriented collagen substrates that can be used in tissue culture research or scaffolding applications without the use of additives and/or bioincompatible materials.
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http://dx.doi.org/10.1021/la9031317 | DOI Listing |
Langmuir
December 2024
Department of Chemistry and Biochemistry, Concordia University, 7141 Sherbrooke Street West, Montréal, Québec H4B 1R6, Canada.
Control over the orientation of polycyclic aromatic dyes in thin films is paramount to tailoring their optical, electronic, and mechanical properties. Their supramolecular assembly in films is tuned here by converting the macrocyclic dyes to large amphiphiles. Two octaalkythio-substituted tetraazaporphyrins (TAPs) with one 5-carboxypentyl and one pentyl or dodecyl chain per pyrrole ring were synthesized as statistical mixtures of four regioisomers.
View Article and Find Full Text PDFRSC Adv
November 2024
Thin Film Materials Research Group, Korea Research Institute of Chemical Technology Daejeon 34114 South Korea
In this study, we developed an HS gas sensor based on a MXene/MoS heterostructure, using the Langmuir-Blodgett (LB) technique and chemical vapor deposition (CVD). TiCT MXene nanosheets were uniformly transferred onto SiO/Si substrates the LB technique, achieving near-complete coverage. Subsequently, flower-like MoS was grown on the MXene-coated substrate through CVD, with vertical growth observed on the MXene layers.
View Article and Find Full Text PDFJ Colloid Interface Sci
February 2025
Leibniz Institute of Photonic Technology (IPHT), Albert-Einstein-Str. 9, 07745 Jena, Germany; Sciclus GmbH & Co. KG, Moritz-von-Rohr-Str. 1a, 07745 Jena, Germany; Center for Energy and Environmental Chemistry Jena (CEEC Jena), Friedrich Schiller University Jena, Philosophenweg 7a, 07743 Jena, Germany. Electronic address:
The construction of ultrathin membranes from linearly aligned π-electron systems is advantageous for targeted energy, charge, or mass transfer. The Langmuir-Blodgett (LB) technique enables the creation of such membranes, especially with amphiphilic π-electron systems. However, these systems often aggregate, forming rigid Langmuir monolayers with defects or holes.
View Article and Find Full Text PDFLangmuir
November 2024
Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai 200438, China.
Molecular structure, external stimuli, and environmental factors all have a strong effect on the internal molecular rotation and vibration of aggregate-induced emission (AIE) luminogens. Here, we report the AIE effect for several newly synthesized amphiphilic tetra(benzimidazole)phenylethene (TBiPE) derivatives and their binuclear N-heterocyclic carbene silver (NHC-Ag) metallacycles in solutions, aggregates, and Langmuir-Blodgett (LB) films. Monolayer behaviors and microscopic images indicate that introducing alkyl chains and binuclear NHC-Ag metallacycles can facilitate the formation of a well-defined insoluble monomolecular layer at the air-water interface.
View Article and Find Full Text PDFHeliyon
October 2024
Departamento de Química Física, Facultad de Ciencias, Universidad de Zaragoza, 50009, Zaragoza, Spain.
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