Electrically Induced Underwater Superaerophilicity/Superaerophobicity Switching on Polypyrrole-Coated Mesh Films for Selective Bubble Permeation.

Recently, materials with controllable superwettability have attracted much attention. However, almost all studies focused on controlling wetting of water and oil; research on underwater gas bubble wetting control is still rare. Herein, we report a mesh film prepared by coating polypyrrole (PPy) film on Ti mesh. Briefly, the film mesh is underwater superaerophilic when PPy is doped with perfluorooctanesulfonate ions (PFOS- ), and becomes underwater superaerophobic as the PFOS- are removed. The transition of the wettability can be triggered by electrical stimuli, which is attributed to the cooperative effect between the rough structure and chemical components variation. The controllable wettability allows adjustable bubble permeation. It can be envisioned that the film will provide potential applications in the future, such as underwater bubble capture/release and microfluidic devices.

Superlyophilic Shape Memory Porous Sponge for Smart Liquid Permeation.

Recently, smart liquid permeation has aroused much attention. However, existing strategies to achieve such a goal are often based on reversibly controlling hydrophobicity/hydrophilicity on static porous structures, which are unsuitable for oils with low surface tension, and meanwhile they cannot realize tunable permeation flux since the pore sizes are constant. Herein, we report a superlyophilic shape memory porous sponge (SSMS) that can demonstrate tunable pore size from about 28 nm to 900 µm as the material's shape is changed. Based on the controllability in pore size, not only ON/OFF penetration but also precisely tunable permeation flux can be obtained for both water and oil. Furthermore, by using the SSMS, an application in accurate release of small-molecule rhodamine B was also demonstrated. This work reports a material with tunable pore size for controllable liquid permeation, which provides some ideas for designing smart superwetting permeation materials.

Janus Copper Mesh Film with Unidirectional Water Transportation Ability toward High Efficiency Oil/Water Separation.

Inspired by the special asymmetric wettability and controllable permeation function of cell membranes, we report a Janus nanostructured copper mesh film with unidirectional water transportation ability. Water can permeate from the hydrophobic side to the hydrophilic side, but is retained in the opposite direction. Notably, based on this special unidirectional water permeation property, both heavy oil/water mixtures (ρoil >ρwater ) and light oil/water mixtures (ρoil <ρwater ) can be separated. Additionally, the film demonstrates high separation efficiency and good recyclability. This paper reports a new Janus film that achieved highly efficient oil/water separation based on smart control of the wettability of the film. It is believed to have the potential to be used in many practical applications, such as wastewater treatment and oil-spill cleanup.

Controllable Drug Release System in Living Cells Triggered by Enzyme-Substrate Recognition.

Vehicles can deliver the drug molecules into cells, yet immunoreaction of the commonly used capping agents and release triggers limit their biomedical use. This shortcoming might be circumvented through replacing these chemicals with certain biomolecules. Here, we show a new and facile way to encapsulate the drug delivery vehicles and release the cargos in a highly controllable manner via modulating supramolecular interactions between enzyme, substrate, and vehicle. The cargo release from the vehicles within cells can be achieved upon substrate treatment. Yeast cells were used, allowing for a fast and cost-effective way for imaging and morphological analysis. We believe this new platform can be readily extended to various carrier systems for different purposes based on shifting the recognition pattern of enzyme-substrate pairs.

DNA-carbon dots function as fluorescent vehicles for drug delivery.

Carbon dots (CDs) are a new representative in the carbon-based material family, attracting tremendous interest in a large variety of fields, including biomedicine. In this report, we described a facile and green system for synthesizing DNA-CDs using genomic DNA isolated from Escherichia coli. DNA-CDs can be purified using a simple column centrifugation-based system. During DNA-CD synthesis, ribose was collapsed, accompanied by the release of nitrogen, and several new bonds (C-OH, N-O, and N-P) were formed, while the other covalent bonds of DNA were largely maintained. The presence of abundant chemical groups, such as amino or hydroxyl groups on DNA-CDs, may facilitate their future functionalization. These highly biocompatible DNA-CDs can serve as a new type of fluorescent vehicle for cell imaging and drug delivery studies. Our research may hasten the development of CDs for prominent future biomedical applications.

Protein-gold hybrid nanocubes for cell imaging and drug delivery.

Multifunctional biocompatible nanomaterials containing both fluorescent and vehicle functions are highly favored in bioimaging, therapeutic, and drug delivery applications. Nevertheless, the rational design and synthesis of highly biocompatible multifunctional materials remain challenging. We present here the development of novel protein-gold hybrid nanocubes (PGHNs), which were assembled using gold nanoclusters, bovine serum albumin, and tryptophan as building blocks. The green-synthesized PGHNs in this study are blue-emitting under UV exposure and cube-shaped with a size of approximately 100 nm. These hybrid nanomaterials are highly biocompatible as shown by cytotoxicity experiments and can be readily internalized by different types of cells. Moreover, PGHNs can act as nanovehicles that successfully deliver dyes or drugs into the cells. The protein-metal hybrid nanocubes can serve as a new type of dual-purpose tool: a blue-emitting cell marker in bioimaging investigation and a nanocarrier in drug delivery studies.