No abstract

Optically transparent antibacterial films capable of healing scratches and restoring transparency are fabricated by exponential layer‐by‐layer assembly of branched polyethylenimine (bPEI)/poly(acrylic acid) (PAA) films and post‐diffusion of cetyltrimethylammonium bromide micelles encapsulated with antibacterial agent triclosan. The triclosan‐loaded bPEI/PAA transparent films can effectively inhibit the growth of gram‐positive and gram‐negative bacteria by the sustained release of triclosan molecules. Healing of multiple scratches on the triclosan‐loaded bPEI/PAA films can be conveniently achieved by immersing the films in water or spraying water on the damaged films, which also fully restores their transparency. The self‐healing ability of these transparent antibacterial films originates from the ability of bPEI and PAA to flow and recombine in the presence of water. The triclosan‐loaded bPEI/PAA films have satisfactory mechanical stability under ambient conditions, and thus show potential for application as transparent protective films with antibacterial properties.

No abstract

Biomass-derived membrane used for uranium extraction of natural seawater from the East China Sea through the formation of metal–phenolic networks.

The targeted therapy of metastatic melanoma is an important yet challenging goal that has received only limited attention to date. Herein, green tea polyphenols, (–)‐epigallocatechin‐3‐gallate (EGCG), and lanthanide metal ions (Sm 3+ ) are used as building blocks to engineer self‐assembled Sm III ‐EGCG nanocomplexes with synergistically enhanced tumor inhibitory properties. These nanocomplexes have negligible systemic toxic effects on healthy cells but cause a significant reduction in the viability of melanoma cells by efficiently regulating their metabolic pathways. Moreover, the wound‐induced migration of melanoma cells can be efficiently inhibited by Sm III ‐EGCG, which is a key criterion for metastatic melanoma therapy. In a mouse melanoma tumor model, Sm III ‐EGCG is directly compared with a clinical anticancer drug, 5‐fluorouracil and shows remarkable tumor inhibition. Moreover, the targeted therapy of Sm III ‐EGCG is shown to prevent metastatic lung melanoma from spreading to main organs with no adverse side effects on the body weight or organs. These in vivo results demonstrate significant advantages of Sm III ‐EGCG over its clinical counterpart. The results suggest that these green tea‐based, self‐assembled nanocomplexes possess all of the key traits of a clinically promising candidate to address the challenges associated with the treatment of advanced stage metastatic melanoma.