Mesoporous bioactive glass nanoparticles (MBGNs) have demonstrated promising properties for the local delivery of therapeutically active ions with the aim to improve their osteogenic properties. Manganese (Mn), zinc (Zn), and copper (Cu) ions have already shown promising pro‐osteogenic properties. Therefore, the concentration‐dependent impact of MBGNs (composition in mol%: 70 SiO2, 30 CaO) and MBGNs containing 5 mol% of either Mn, Zn, or Cu (composition in mol%: 70 SiO2, 25 CaO, 5 MnO/ZnO/CuO) on the viability and osteogenic differentiation of human marrow‐derived mesenchymal stromal cells (BMSCs) was assessed in this study. Mn‐doped MBGNs (5Mn‐MBGNs) showed a small “therapeutic window” with a dose‐dependent negative impact on cell viability but increasing pro‐osteogenic features alongside increasing Mn concentrations. Due to a constant release of Zn, 5Zn‐MBGNs showed good cytocompatibility and upregulated the expression of genes encoding for relevant members of the osseous extracellular matrix during the later stages of cultivation. In contrast to all other groups, BMSC viability increased with increasing concentration of Cu‐doped MBGNs (5Cu‐MBGNs). Furthermore, 5Cu‐MBGNs induced an increase in alkaline phosphatase activity. In conclusion, doping with Mn, Zn, or Cu can enhance the biological properties of MBGNs in different ways for their potential use in bone regeneration approaches.

No abstract

No abstract

A new prototype of reversible self‐assembly between functionalized gold and titanium dioxide nanoparticles (NPs) utilizing hydrogen bonding interactions was developed and established. The gold nanoparticles were functionalized with a Hamilton‐receptor functionality bearing a thiol moiety as anchoring group. The titanium dioxide nanoparticles were modified with cyanurate derivatives which contained phosphonic acids as anchoring groups. The host–guest type interaction between two functionalized nanoparticles yielded a highly integrated nanoparticle system in chloroform. Moreover, by presenting a competing ligand in an exchange reaction, the product of self‐assembly can be segregated into the individual soluble components of functionalized nanoparticles. The self‐assembly and the exchange reaction were followed and monitored in detail by UV/Vis spectroscopy. The structure of the self‐assembly product was investigated using scanning electron microscopy (SEM) and small‐angle X‐ray scattering (SAXS).

No abstract