Optically Driven Encapsulation Using Novel Polymeric Hollow Shells Containing an Azobenzene Polymer

A novel method of macromolecule encapsulation using micron‐sized polymeric shells constructed with a photoactive azobenzene containing polyelectrolyte is discussed. Fluorescently labeled dextran molecules were encapsulated using light to remotely shrink and change the wall permeability of new polymeric hollow shells. We observed that the proportion of shells with dye encapsulated increased along with the duration of irradiation. Electron microscopy imaging illustrated significant changes in the surface roughness of shells after being exposed to light. Finally, this new system was shown to possess a high thermal stability.

     

原位聚合法制备鱼藤酮微胶囊

原位聚合法制备;鱼藤酮微胶囊;鱼藤酮;原位聚合法;微胶囊;三聚氰胺甲醛树脂     

Hydrogel-shelled biodegradable microspheres for sustained release of encapsulants

Biodegradable microparticles are promising for the sustained release of encapsulated lipophilic drugs. In particular, the microparticles with uniform size show excellent linearity of cumulated release over time with minimized initial burst. Here, we encapsulate the biodegradable microparticles with a hydrogel shell to improve the controllability over the sustained release and suspension stability. With a capillary microfluidic device, monodisperse oil-in-water-in-oil (O/W/O) double-emulsion droplets are produced to have a toluene solution of polylactic acid (PLA) in the core and sodium alginate and calcium-ethylenediaminetetraacetic acid (EDTA) complex in the shell, whereas the continuous oil phase contains acetic acid. As the toluene evaporates, PLA consolidates to form a microsphere in the core. At the same time, acetic acid diffuses from the continuous phase to the water layer, which causes the dissociation of the Ca-EDTA complex and the gelation of alginate. The hydrogel-shelled PLA microspheres are transferred from the oil to an aqueous solution of calcium chloride, which further tightens the gel shell. The resulting core-shell microspheres show sustained release of encapsulants for extended periods as the hydrogel shell serves as a diffusion barrier. Moreover, the hydrogel shells prevent interparticle agglomeration and adhesion to the solid walls, securing high suspension stability during the injection.     

Mechanical characterization of soft microparticles prepared by droplet microfluidics

Droplet microfluidics is one of the most promising approaches that allows preparation of microparticles with tailored structure and composition. Various functional microparticles have been developed using microfluidics, where their controlled structure shows high potential for a wide range of applications. Among these, soft polymeric microparticles which exhibit low elastic modulus compared to ceramics and metals are extensively investigated in biomedical applications due to their biocompatibility, high surface-to-volume ratio, as well as soft and deformable nature. As the mechanical properties of soft microparticles play important role in determining how they function in each application, it is essential to adequately characterize them for the optimal design of functional microparticles. In this review, we mainly discuss the mechanical characterization methods of soft microparticles and their elastic property. A brief overview of the droplet microfluidics-assisted fabrication of microparticles is also provided before discussing the mechanical characterization techniques. We then describe the general characterization methods and models employed to determine the elastic properties of microparticles. In addition, we discuss the relationship between the physical parameters (size, composition, and structure) and the elastic properties of the microparticles, followed by the role of elastic properties in various applications including microcarrier, bioink, and self-healing to name a few.     

Improving the interlaminar fracture toughness of carbon fiber/epoxy composites using clustered microcapsules

The composite laminates are susceptible to delamination between reinforcing plies during their long-term service. In this paper, we propose a modified carbon fiber/epoxy composite laminate with embedded clustered dual-component microcapsules in order to increase the interlaminar fracture toughness of the lamina. The details of microcapsules were illustrated using scanning electron microscope (SEM). The modified CF/EP composite laminates were fabricated using hot-compaction technique. Mode I interlaminar fracture tests were conducted using double cantilever beam specimens, then the values of opening fracture toughness G_IC were calculated to evaluate the toughening effect of modified laminates. The toughening mechanism was revealed and discussed through micrographs of the fracture surfaces obtained by ultra-depth microscope and SEM. The results show that clustered microcapsules after polymerization are equal to special Z-pinning, significantly enhancing the ability of crack arrest, and largely and roundly improved the G_IC values of resultant composite laminates. Meanwhile, the clustered microcapsules and matrix resin formed a second-phase material layer, which also absorbed the fracture energy and suppressed the expansion of cracks.     

Microcapsules with compact wall from hydrocarbon/fluorocarbon composite surfactants for electrophoretic display

The components and their concentration ratio of surfactant mixture in aqueous solution of gelatin and sodium carboxymethylcellulose (NaCMC) are very important during the preparation of stable microcapsules for electrophoretic display.In this work,hydrocarbon/fluorocarbon composite surfactant was introduced for the first time into the capsule wall to improve the chemical resistance and barrier property of the microcapsules.By investigating surface tension and zeta potential of NaCMC with the mixture of sodiu...     

Polyurea microcapsules: Surface modification and capsule size control

A postmodification method for polyurea microcapsule (PUMC) surfaces using functional polyelectrolytes is reported in this article. Fluorescein isothiocyanate (FITC) was used to probe the chemistry on PUMC surface and label nucleophilic groups on the surface, in particular amines. As well, a fluorescently labeled polyanion containing electrophilic acetoacetate groups was used to covalently react with these nucleophilic groups on the PUMC surfaces. This modification causes charge reversion of the originally cationic PUMC and enables subsequent layer‐by‐layer (LbL) coating using other polyelectrolytes, allowing for covalent or noncovalent modification of the capsule surface. All modification steps were monitored using either laser scanning confocal microscopy or fluorescence microscopy. Optical and fluorescence microscopy of PUMC wall cross‐sections embedded in resin confirmed that the modifications were restricted to the outer surface of PUMCs, offering minimum interference of this modification method with other capsule wall properties. In addition, a simple T‐junction type microfluidic device based on a commercially available MicroTEE was designed to produce narrowdisperse PUMCs. This device was easy to set up and operate and was proved to be an useful tool for making monodisperse emulsions and narrowdisperse MCs. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011