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Giulia Magnabosco

Publications and source records attributed to Giulia Magnabosco.

4 recordsLinked to original sources

Effect of surface chemistry on incorporation of nanoparticles within calcite single crystals

Inclusion of additives into calcite crystals allows one to embed non-native proprieties into the inorganic matrix and obtain new functional materials. Up to now, few parameters have been taken into account to evaluate the efficiency of inclusion of an additive. Taking inspiration from Nature, we grew calcite crystals in the presence of fluorescent silica nanoparticles carrying different functional groups (PluS-X) to investigate the effect of surface chemistry on the inclusion of the additives. PluS-X allowed us to keep constant all the particle characteristics, including size, while changing exposed functional groups and thus Zeta-potential. The effect on crystal morphology, the loading and distribution of PluS-X within the crystals have been evaluated with different microscopy techniques. Our data indicate that hydroxyl functionalized particles are entrapped more efficiently inside calcite single crystals without distortion of the crystal structure and inhibition of the growth.

cond-mat.mtrl-sci

Synthesis of calcium carbonate in trace water environments

Calcium carbonate (CaCO3) was synthesized from diverse water-free alcohol solutions, resulting in the formation of vaterite and calcite precipitates, or stable particle supensions, with dimension and morphology depending upon the condition used. The obtained results shed light on the importance of water molecules during crystallization of CaCO3 and open a novel synthetic route for its precipitation in organic solvents.

physics.chem-ph

Calcite single crystals as hosts for atomic-scale entrapment and slow release of drugs

This study presents a complete structural and biological characterization of Doxorubicin CaCO3 single crystals as a pH responsive drug carrier. Using a biomimetic approach, it was demonstrated that calcite single crystals are able, during their growth in presence of doxorubicin, to entrap drug molecules inside their lattice, along specific crystallographic directions. High resolution synchrotron powder diffraction measurements allowed the determination of the lattice distortion and microstructural parameters. Confocal microscopy confirmed that doxorubicin is uniformly embedded in the crystal and that the drug is not only adsorbed on the crystal surface. A slow release of DOX is obtained that occurs preferentially in proximity of the crystals, targeting cancer cells.

cond-mat.mtrl-sci