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We believe bone implants can be fabricated using 3DP techniques and their mechanical and biological performance can be tailored by modifying the internal architectures.
As a result, the magnetic anisotropy, the coercivity, and the remanence can be tailored by modifying the antidot diameter, the separation, and order among them, as well as the film thickness [10 13].
In addition, their magnetic properties can be tailored by modifying the particle size and aspect ratio [ 29].
This work demonstrates that the cytotoxicity of ZnO nanoparticles can be tailored by modifying their surface structures, providing a new approach for safer ZnO nanoparticles.
In this work, we demonstrate that the cytotoxicity of ZnO NP can be tailored by modifying their surface-bound chemical groups, while maintaining the core ZnO structure and related properties.
We demonstrate that the cytotoxicity of ZnO NP can be tailored by modifying their surface chemical structure by comparing the cytotoxicity, physicochemical properties, and crystal structure of two 9.26 ± 0.11 nm-sized ZnO NP samples, both prepared from the same zinc acetate precursor using a forced hydrolysis process in two different reaction media.
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The results demonstrated that the layer structure of the modified surfaces can be tailored by adjusting the treatment conditions.
Various ZnO nanostructures, such as nanorods (NRs) and nanowires in particular, are most promising because their properties can be tailored by changing their morphology, structure and size, or modifying their surface with coatings of other materials [5, 6].
Furthermore, the HgCdTe band structure can be continuously tailored by modifying cadmium content or temperature.
As the electrochemical properties of the gradient electrodes can be carefully tailored by modifying the nanotube size gradient, this approach provides new possibilities for the manufacturing of hybrid electrodes with integrated energy and power density gradients.
The mass loss profiles and bulk properties of the resulting scaffolds are easily tailored by modifying the structure of the starting macromers.
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