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For the first time, mesoporous Fe3O4@ZnO sphere decorated graphene (GN-pFe3O4@ZnO) composites with uniform size, considerable porosity, high magnetization and extraordinary electromagnetic (EM) wave absorption properties were synthesized by a simple and efficient three-step method. Structure and morphology details were characterized by X-ray diffraction, transmission electron microscopy, high-resolution electron microscopy and field-emission scanning electron microscopy. Electron microscopy images reveal that pFe3O4@ZnO spheres with obvious porous and core-shell structures are uniformly coated on both sides of the GN sheets without significant numbers of vacancies or apparent aggregation. EM wave absorption properties of epoxy containing 30 wt% GN-pFe3O4@ZnO were investigated at room temperature in the frequency region of 0.2-18 GHz. The absorption bandwidth with reflection loss (RL) values less than -10 dB is up to 11.4 GHz, and the minimal RL is almost -40 dB. The intrinsic physical and chemical properties of the materials, the synergy of Fe3O4 and ZnO, and particularly the unique multi-interfaces are fundamental to the enhancement of EM absorption properties. The as-prepared GN-pFe3O4@ZnO composites are shown to be lightweight, have strong absorption, and broad frequency bandwidth EM absorbers.

Osteoporosis is a common metabolic bone disease, influenced by genetic and environmental factors, that increases bone fragility and fracture risk and, therefore, has a serious adverse effect on the quality of life of patients. However, epigenetic mechanisms involved in the development of osteoporosis remain unclear. There is accumulating evidence that epigenetic modifications may represent mechanisms underlying the links of genetic and environmental factors with increased risk of osteoporosis and bone fracture. Some RNAs, such as microRNAs (miRNAs), long non-coding RNAs (lncRNAs), and circular RNAs (circRNAs), have been shown to be epigenetic regulators with significant involvement in the control of gene expression, affecting multiple biological processes, including bone metabolism. This review summarizes the results of recent studies on the mechanisms of miRNA-, lncRNA-, and circRNA-mediated osteoporosis associated with osteoblasts and osteoclasts. Deeper insights into the roles of these three classes of RNA in osteoporosis could provide unique opportunities for developing novel diagnostic and therapeutic approaches to this disease.

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