This remarkable and widespread scope of laponite properties makes them attractive as smart platforms for new biohybrid materials.
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References  M. Lezhnina, T. Hepia suisse anti-imbatranire, H. Stoehr and U. Kynast, Angew. Felbeck, et al. C, Kaup, T. Felbeck, M. Staniford and U. Kynast, Hepia suisse anti-imbatranire. Staniford1, Marina M. Lezhnina1, M. Gruener2, Christian A. Strassert2 and Ulrich H. However, for intimate interactions with bacteria, further modifications on the laponite itself were required [2,3].
Next to aqueous solutions of these hybrids, stationary imbeddings into membranes also retained their cytotoxicity, opening a new pathway to antimicrobial surfaces. References 1 M. DeRosa, R. Crutchley, Coord.
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Staniford et al, Chem. Grüner et al, ACS Appl.
Interfaces,7 37 MNPs offer the possibility to deliver drugs and heat at specific locations. The development and characterization of the nanosystem are therefore important steps to ensure that the nanosystem has the desired properties to be used for both magnetic hyperthermia and drug delivery. For example, functionalisation of the MNPs with a suitable polymer layer can provide biocompatibility, colloidal stability, drug loading capability and stimuli-responsive behavior.
Magnetic nanosystems that respond to both a change in pH and temperature can give spatial and temporal control over the release of the drug, by making use of the acidic pH found in tumor microenvironment and heat generated from the MNPs when exposed to an alternating magnetic field AMF as triggers for the drug release. Moreover, heat has been found to greatly enhance the intracellular drug uptake and the cytotoxic effect of many chemotherapeutic drugs, resulting in a synergistic effect of the therapy.
This work aims to develop a dual pH- and thermo-responsive magnetic nanosystem allowing for the triggered release of chemotherapeutic drugs as a consequence of hyperthermia and acidic tumor microenvironment, through breakage of pH and heat labile Schiff base bonds that bind the drug molecules to the polymer.
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Iron oxide NPs were synthesized by a microwave-assisted co-precipitation method. Finally, the heating performances of the nanohybrids were investigated using a magnetic AC hyperthermia system.
The LCST of the polymer could be easily tuned by varying the initial monomers ratio to be in the hyperthermia temperature range.
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FTIR analyses confirmed the successful grafting of the polymer by the presence of characteristic carbonyl ester bonds at cm By varying the MNPs to polymer ratio and the pH of the solution during the functionalization step, suspensions with long term colloidal stability could be obtained.
Their potential as magnetic hyperthermia agents was confirmed, demonstrating at the same time the importance of colloidal stability on the heating performances.
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Vladescu1, M. Badea2, M. Braic1, A. Kiss1, M. Moga2, V. Braic1, E. Posna2, M. Dinu1, M. Therefore, many efforts were directed for finding a solution to obtain a novel implant with high osteoconductive and antibacterial properties, resistant to specific conditions inside the human body.
The hydroxyapatite was proposed to be used for coating the metallic implants to increase their osteoconductive ability.
Smart biointerfaces for functional biomaterials
However, the low mechanical strength of hydroxyapatite, the relatively low bone bonding rate, high dissolution rate and low antibacterial properties restrict its use in biomedical applications. The aim of the work was to enhance the antibacterial properties of the hydroxyapatite by Ag addition into its structure.
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The coatings, with different Ag contents, were deposited on Ti based alloy substrates by magnetron sputtering method. The influence of the Ag content on the film properties was also analysed. Incorporation of a small amount of Ag into the hydroxyapatite structure resulted in an improved antibacterial efficacy versus Gram-positive bacteria.
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The best hydroxyapatite with Ag content of 0. Further, magnetic stilou anti-imbatranire produse cougar are envisaged to improve implant fixation when hepia suisse anti-imbatranire to not-magnetic implants.