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In addition, hybrid matrices are prepared to tentatively address their effectiveness as scaffolds for bone tissue engineering.
The matrices are prepared by reducing CuCl2 with vitamin C (VC) in the existence of polyacrylamide (PAM) at 180 °C, accompanied by the partial carbonization of VC.
From this starting material, sequencing libraries and/or PCR matrices are prepared, for use in either NGS or conventional Sanger sequencing.
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Chitosan matrices were prepared by compression molding.
Type II collagen matrices were prepared using purified, pepsin-treated, type II collagen.
Nanomatrices and solid walled matrices were prepared using the extracted PHB.
After resin polymerization, photoelastic silicone matrices were prepared for each photoelastic ring, and the rings were placed inside the matrices.
A series of TiO2 nanotube (TNT /ionic liquid matrices were prepared, and their lithium ion conductive properties were studied.
Macroporous poly 3-hydroxybutyric acid-co-3-hydroxyvaleric acid) (poly 3-hydroxybutyricrepared after solvent evaporation and solute leaching.
The sorbent matrices were prepared in the form of beads and surface functionalized to enable enhanced sorption of fluoride ions.
Chitosan matrices were prepared by sodium tripolyphosphate crosslinking from a chitosan suspension containing the model BCS class II drug, indomethacin.
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