Large-area dual-scaled porous nitrocellulose (p-NC) membranes are fabricated by a facile, inexpensive and scalable perforating approach. These p-NC membranes show stable superhydrophilicity in air and underwater superoleophobicity. The p-NC membranes with intrinsic nanopores and array of microscale perforated pores could selectively and efficiently separate water from various oil/water mixtures with high efficiency (>99%) rapidly.

Inspired by the swimming of natural microorganisms, synthetic micro-/nanomachines, which convert energy into movement, are able to mimic the function of these amazing natural systems and help humanity by completing environmental and biological tasks. While offering autonomous propulsion, conventional micro-/nanomachines usually rely on the decomposition of external chemical fuels (e.g., H O ), which greatly hinders their applications in biologically relevant media. Recent developments have resulted in various micro-/nanomotors that can be powered by biocompatible fuels. Fuel-free synthetic micro-/nanomotors, which can move without external chemical fuels, represent another attractive solution for practical applications owing to their biocompatibility and sustainability. Here, recent developments on fuel-free micro-/nanomotors (powered by various external stimuli such as light, magnetic, electric, or ultrasonic fields) are summarized, ranging from fabrication to propulsion mechanisms. The applications of these fuel-free micro-/nanomotors are also discussed, including nanopatterning, targeted drug/gene delivery, cell manipulation, and precision nanosurgery. With continuous innovation, future autonomous, intelligent and multifunctional fuel-free micro-/nanomachines are expected to have a profound impact upon diverse biomedical applications, providing unlimited opportunities beyond one's imagination.

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Because of the frequent oil spill accidents in marine environment, stable superoleophobic coatings under seawater are highly desired. Current underwater superoleophobic surfaces often suffer from mechanical damages and lose their superoleophobicity gradually. It remains a challenge to fabricate a stable and robust underwater superoleophobic film which can endure harsh conditions in practical application. Nacre is one of most extensively studied rigid biological materials. Inspired by the outstanding mechanical property of seashell nacre and those underwater superoleophobic surfaces from nature, we fabricated a polyelectrolyte/clay hybrid film via typical layer-by-layer (LBL) method based on building blocks with high surface energy. 'Bricks-and-mortar' structure of seashell nacre was conceptually replicated into the prepared film, which endows the obtained film with excellent mechanical property and great abrasion resistance. In addtion, the prepared film also exhibits stable underwater superoleophobicity, low oil adhesion, and outstanding environment durability in artificial seawater. We anticipate that this work will provide a new method to design underwater low-oil-adhesion film with excellent mechanical property and improved stability, which may advance the practical applications in marine antifouling and microfluidic devices.

The aggregation of Aβ peptides is a crucial factor leading to Alzheimer's disease (AD). Inhibiting the Aβ peptide aggregation has become one of the most essential strategies to treat AD. In this work, efficient and low-cytotoxicity inhibitors, graphene quantum dots (GQDs) are reported for their application in inhibiting the aggregation of Aβ peptides. Compared to other carbon materials, the low cytotoxicity and great biocompatibility of GQDs give an advantage to the clinical research for AD. In addition, the GQDs may cross the blood-brain barrier (BBB) because of the small size. It is believed that GQDs may be therapeutic agents against AD. This work provides a novel insight into the development of Alzheimer's drugs.

A simple, sensitive, and label-free method for microRNA (miRNA) biosensing was described using oligonucleotide encapsulated silver nanoclusters (Ag-NCs) as effective electrochemical probes. The functional oligonucleotide probe integrates both recognition sequence for hybridization and template sequence for in situ synthesis of Ag-NCs, which appears to possess exceptional metal mimic enzyme properties for catalyzing H(2)O(2) reduction. The miRNA assay employs gold electrodes to immobilize the molecular beacon (MB) probe. After the MB probe subsequently hybridizes with the target and functional probe, the oligonucleotide encapsulated Ag-NCs are brought to the electrode surface and produce a detection signal, in response to H(2)O(2) reduction. An electrochemical miRNA biosensor down to 67 fM with a linear range of 5 orders of magnitude was obtained. Meanwhile, the MB probe allows the biosensor to detect the target with high selectivity. The Ag-NCs-based approach provides a novel avenue to detect miRNA with high sensitivity and selectivity while avoiding laborious label and signal amplification. It is convinced that rational introduction of signal amplification strategy to the Ag-NCs-based bioanalysis can further improve the sensitivity. To our best knowledge, this is the first application of the electrocatalytic activity of Ag-NCs in bioanalysis, which would be attractive for genetic analysis and clinic biomedical application.

A sensitive nucleic acid detection platform based on superhydrophilic microwells spotted on a superhydrophobic substrate is fabricated. Due to the wettability differences, ultratrace DNA molecules are enriched and the fluorescent signals are amplified to allow more sensitive detection. The biosensing interface based on superwettable materials provides a simple and cost-effective way for ultratrace DNA sensing.

The measurement of sulfide, especially hydrogen sulfide, has held the attention of the analytical community due to its unique physiological and pathophysiological roles in biological systems. Electrochemical detection offers a rapid, highly sensitive, affordable, simple, and real-time technique to measure hydrogen sulfide concentration, which has been a well-documented and reliable method. This review details up-to-date research on the electrochemical detection of hydrogen sulfide (ion selective electrodes, polarographic hydrogen sulfide sensors, etc.) in biological samples for potential therapeutic use.