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Ultra-permeable and robust membranes are prepared by creating a gradient nanoporous structure in low-cost phenolics, enabled by the spontaneous assembly of gradually enlarged phenolic nanoparticles., Membrane technology is playing a pivotal role in providing potable water to our thirsty planet. However, the strong demand for highly permeable and durable membranes with affordable costs remains. Such membranes are synthesized herein by designing gradient nanopores in low-cost phenolics. The gradient nanopores are achieved by spontaneous assembly of phenolic nanoparticles with gradually enlarged sizes. These particles nucleate and grow as a result of ZnCl2-accelerated thermopolymerization of resol in the progressive downward gelating polymer. Subsequent removal of the gelated polymer and ZnCl2 exposes the gradient nanopores. The gradient nanopores endow the phenolic structures with unprecedented permselectivity when used in membrane separation, totally rejecting fine particulates down to 5 nm dispersed in water or aggressive solvents while allowing water to permeate up to two orders of magnitude faster than other membranes with similar rejections. Our work opens up an avenue for the rational design and affordable synthesis of ultrafast membranes.

Mesenchymal stem cells (MSCs) are ubiquitously present in many tissues. Due to their unique advantages, MSCs have been widely employed in clinical studies. Emerging evidences indicate that MSCs can also migrate to the tumor surrounding stroma and exert complex effects on tumor growth and progression. However, the effect of MSCs on tumor growth is still a matter of debate. Several studies have shown that MSCs could favor tumor growth. On the contrary, other groups have demonstrated that MSCs suppressed tumor progression. Extracellular vesicles have emerged as a new mechanism of cell-to-cell communication in the development of tumor diseases. MSCs-derived extracellular vesicles (MSC-EVs) could mimic the effects of the mesenchymal stem cells from which they originate. Different studies have reported that MSC-EVs may exert various effects on the growth, metastasis, and drug response of different tumor cells by transferring proteins, messenger RNA, and microRNA to recipient cells. In the present review, we summarize the components of MSC-EVs and discuss the roles of MSC-EVs in different malignant diseases, including the related mechanisms that may account for their therapeutic potential. MSC-EVs open up a promising opportunity in the treatment of cancer with increased efficacy.