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Abstract Stability issues in membrane-free coacervates have been addressed with coating strategies, but these approaches often compromise the permeability of the coacervate. Here we report a facile approach to maintain both stability and permeability using tannic acid and then demonstrate the value of this approach in enzyme-triggered drug release. First, we develop size-tunable coacervates via self-assembly of heparin glycosaminoglycan with tyrosine and arginine-based peptides. A thrombin-recognition site within the peptide building block results in heparin release upon thrombin proteolysis. Notably, polyphenols are integrated within the nano-coacervates to improve stability in biofluids. Phenolic crosslinking at the liquid-liquid interface enables nano-coacervates to maintain exceptional structural integrity across various environments. We discover a pivotal polyphenol threshold for preserving enzymatic activity alongside enhanced stability. The disassembly rate of the nano-coacervates increases as a function of thrombin activity, thus preventing a coagulation cascade. This polyphenol-based approach not only improves stability but also opens the way for applications in biomedicine, protease sensing, and bio-responsive drug delivery. 

A SV3CP-responsive peptide has various performance towards the aggregation of AuNPs with different charge valence. 

The development of synthetic methods for micro/nano materials with precisely controlled structures, morphologies, and local compositions is of great importance for the advancement of modern nanotechnology. The electrospray method is a “platform” approach for the preparation of a broad range of micro-/nanostructures; electrospray is simple and scalable. This review summarizes recent research on the micro-/nanostructures prepared via the electrospray route. These include spherical structures ( e.g. simple, porous, Janus, and core–shell particles), non-spherical structures ( e.g. red blood cell-like and spindle-like particles, multi-compartment microrods, 2D holey nanosheets, and nanopyramids), and assembled structures. The experimental details, underlying physical/chemical principles, and key benefits of these structures are comprehensively discussed. The effects and importance of nozzle design, properties of feeding solutions ( e.g. concentration of solute, polymer additives, solvent/nonsolvent combinations), working environment ( e.g. temperature and humidity), and types of collection media are highlighted.