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1.
Sci Rep ; 8(1): 9147, 2018 Jun 14.
Article in English | MEDLINE | ID: mdl-29904111

ABSTRACT

Research in functional magnetic materials often employs thin films as model systems for finding new chemical compositions with promising properties. However, the scale-up of thin films towards bulk-like structures is challenging, since the material synthesis conditions are entirely different for thin films and e.g. rapid quenching methods. As one of the consequences, the type and degree of order in thin films and melt-spun ribbons are usually different, leading to different magnetic properties. In this work, using the example of magnetocaloric Ni-Co-Mn-Al melt-spun ribbons and thin films, we show that the excellent functional properties of the films can be reproduced also in ribbons, if an appropriate heat treatment is applied, that installs the right degree of order in the ribbons. We show that some chemical disorder is needed to get a pronounced and sharp martensitic transition. Increasing the order with annealing improves the magnetic properties only up to a point where selected types of disorder survive, which in turn compromise the magnetic properties. These findings allow us to understand the impact of the type and degree of disorder on the functional properties, paving the way for a faster transfer of combinatorial thin film research towards bulk-like materials for magnetic Heusler alloys.

2.
Eur Cell Mater ; 22: 403-19, 2011 Dec 17.
Article in English | MEDLINE | ID: mdl-22179938

ABSTRACT

Due to their broad differentiation potential and their persistence into adulthood, human neural crest-derived stem cells (NCSCs) harbour great potential for autologous cellular therapies, which include the treatment of neurodegenerative diseases and replacement of complex tissues containing various cell types, as in the case of musculoskeletal injuries. The use of serum-free approaches often results in insufficient proliferation of stem cells and foetal calf serum implicates the use of xenogenic medium components. Thus, there is much need for alternative cultivation strategies. In this study we describe for the first time a novel, human blood plasma based semi-solid medium for cultivation of human NCSCs. We cultivated human neural crest-derived inferior turbinate stem cells (ITSCs) within a blood plasma matrix, where they revealed higher proliferation rates compared to a standard serum-free approach. Three-dimensionality of the matrix was investigated using helium ion microscopy. ITSCs grew within the matrix as revealed by laser scanning microscopy. Genetic stability and maintenance of stemness characteristics were assured in 3D cultivated ITSCs, as demonstrated by unchanged expression profile and the capability for self-renewal. ITSCs pre-cultivated in the 3D matrix differentiated efficiently into ectodermal and mesodermal cell types, particularly including osteogenic cell types. Furthermore, ITSCs cultivated as described here could be easily infected with lentiviruses directly in substrate for potential tracing or gene therapeutic approaches. Taken together, the use of human blood plasma as an additive for a completely defined medium points towards a personalisable and autologous cultivation of human neural crest-derived stem cells under clinical grade conditions.


Subject(s)
Cell Culture Techniques , Neural Crest/cytology , Neural Stem Cells/cytology , Antigens, Differentiation/metabolism , Biomimetic Materials , Cell Differentiation , Cell Proliferation , Culture Media, Serum-Free , Fibrin/ultrastructure , Gene Expression Profiling , Humans , Nanofibers/ultrastructure , Nerve Regeneration , Neural Stem Cells/metabolism , Neural Stem Cells/physiology , Plasma , Porosity , Spheroids, Cellular/cytology
3.
Bioinspir Biomim ; 6(4): 046007, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21993204

ABSTRACT

Polymeric nanowires of polypyrrole have been implemented as artificial cilia on giant-magneto-resistive multilayer sensors for a biomimetic sensing approach. The arrays were tagged with a magnetic material, the stray field of which changes relative to the underlying sensor as a consequence of mechanical stimuli which are delivered by a piezoactuator. The principle resembles balance sensing in mammals. Measurements of the sensor output voltage suggest a proof of concept at frequencies of around 190 kHz and a tag thickness of ∼300 nm. Characterization was performed by scanning electron microscopy and magnetic force microscopy. Micromagnetic and finite-element simulations were conducted to assess basic sensing aspects.


Subject(s)
Biomimetic Materials , Cilia/physiology , Mechanoreceptors/physiology , Micro-Electrical-Mechanical Systems/instrumentation , Nanostructures/chemistry , Polymers/chemistry , Transducers , Animals , Computer-Aided Design , Equipment Design , Equipment Failure Analysis , Humans , Magnetics/instrumentation , Mechanotransduction, Cellular/physiology , Miniaturization , Nanotechnology/instrumentation , Stress, Mechanical
4.
Biosens Bioelectron ; 26(4): 1152-63, 2010 Dec 15.
Article in English | MEDLINE | ID: mdl-20638263

ABSTRACT

This article reviews recent developments on magnetoresistive detection of magnetic beads or nanoparticles by nanoscale sized sensors. Sensors are analyzed from an experimental and a numerical point of view in respect to their capability to either localize the position of a single magnetic particle or to detect the number of particles in a certain range. Guidelines are shown up on how to extend single sensors to sensor arrays with very high spatial resolution and how to modify the sensor shape in order to provide long distance measurements. Further, sensors in biological lab-on-a-chip environments are discussed. The magnetic ratchet and a gravitation based microfluidic component are reviewed as important tools to position and, therefore, detect biological components in continuous-flow devices.


Subject(s)
Biosensing Techniques/instrumentation , Equipment Design , Gravitation , Humans , Lab-On-A-Chip Devices , Magnetics , Microfluidic Analytical Techniques/instrumentation , Models, Theoretical , Nanoparticles
5.
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