Control over vesicle size during nanoscale liposome synthesis is critical for defining the pharmaceutical properties of liposomal nanomedicines. Microfluidic technologies capable of size-tunable liposome generation have been widely explored, but scaling these microfluidic platforms for high production throughput without sacrificing size control has proven challenging. Here we describe a microfluidic-enabled process in which highly vortical flow is established around an axisymmetric stream of solvated lipids, simultaneously focusing the lipids while inducing rapid convective and diffusive mixing through application of the vortical flow field. By adjusting the individual buffer and lipid flow rates within the system, the microfluidic vortex focusing technique is capable of generating liposomes with precisely controlled size and low size variance, and may be operated up to the laminar flow limit for high throughput vesicle production. The reliable formation of liposomes as small as 27 nm and mass production rates over 20 g/h is demonstrated, offering a path toward production-scale liposome synthesis using a single continuous-flow vortex focusing device.

Over the past years, the layer-by-layer (LbL) assembly has been widely developed as one of the most powerful techniques to prepare multifunctional films with desired functions, structures and morphologies because of its versatility in the process steps in both material and substrate choices. Among various functional nanoscale objects, carbon-based nanomaterials, such as carbon nanotubes and graphene sheets, are promising candidates for emerging science and technology with their unique physical, chemical, and mechanical properties. In particular, carbon-based functional multilayer coatings based on the LbL assembly are currently being actively pursued as conducting electrodes, batteries, solar cells, supercapacitors, fuel cells and sensor applications. In this article, we give an overview on the use of carbon materials in nanostructured films and capsules prepared by the LbL assembly with the aim of unraveling the unique features and their applications of carbon multilayers prepared by the LbL assembly.

Injectable hydrogels are adaptable drug delivery systems capable of forming localized depots that align with the anatomical and physiological constraints of administration sites. Their performance depends on both the injection environment and the properties of the therapeutic cargo. Applications span ocular, intra-articular, subcutaneous, intramuscular, tumoral, central nervous system, and mucosal delivery, where hydrogels address challenges of clearance, retention, and compatibility. Beyond bulk depots, particulate hydrogel formats such as microgels and nanogels improve syringeability, modularity, and integration with nanoparticle carriers. Functional versatility arises from stimuli responsiveness, including pH, enzymatic, thermal, redox, and light triggers, and from hybrid designs that integrate multiple cues for precision control. Loading strategies range from passive encapsulation to affinity binding and covalent conjugation, with release governed by diffusion, degradation, and stimuli-modulated kinetics. Translational progress depends on reproducible fabrication, scalable manufacturing, and device integration, while site-dependent constraints and regulatory hurdles remain significant challenges.

Hydrogel is one of the most prominent biomaterials in therapeutic and biomedical engineering, benefiting from its biocompatibility, chemical/physical tunability, and wide versatility to various fabrication techniques. One remarkable advance in the latest hydrogel research is the micro/nanofabrication technologies, which utilize unique mechanical and chemical properties of hydrogel, various chemical reaction mechanisms, and multidisciplinary approaches to realize innovative systems at these size scales. This review reports a comprehensive overview on the latest advances in fabrication of hydrogel-based micro- and nano-systems with an emphasis on their biomedical and therapeutic applications. Challenges and prospects are discussed from the material, fabrication, and system design perspectives to develop effective, personalized, and versatile hydrogel-based therapies.

Rapid and efficient isolation of bacteria from complex biological matrices is necessary for effective pathogen identification in emerging single-cell diagnostics. Here, we demonstrate the isolation of intact and viable bacteria from whole blood through the selective lysis of blood cells during flow through a porous silica monolith. Efficient mechanical hemolysis is achieved while providing passage of intact and viable bacteria through the monoliths, allowing size-based isolation of bacteria to be performed following selective lysis. A process for synthesizing large quantities of discrete capillary-bound monolith elements and millimeter-scale monolith bricks is described, together with the seamless integration of individual monoliths into microfluidic chips. The impact of monolith morphology, geometry, and flow conditions on cell lysis is explored, and flow regimes are identified wherein robust selective blood cell lysis and intact bacteria passage are achieved for multiple gram-negative and gram-positive bacteria. The technique is shown to enable rapid sample preparation and bacteria analysis by single-cell Raman spectrometry. The selective lysis technique presents a unique sample preparation step supporting rapid and culture-free analysis of bacteria for the point of care.