Core-Shell Beads Made by Composite Liquid Marble Technology as A Versatile Microreactor for Polymerase Chain Reaction.

Over the last three decades, the protocols and procedures of the DNA amplification technique, polymerase chain reaction (PCR), have been optimized and well developed. However, there have been no significant innovations in processes for sample dispersion for PCR that have reduced the amount of single-use or unrecyclable plastic waste produced. To address the issue of plastic waste, this paper reports the synthesis and successful use of a core-shell bead microreactor using photopolymerization of a composite liquid marble as a dispersion process. This platform uses the core-shell bead as a simple and effective sample dispersion medium that significantly reduces plastic waste generated compared to conventional PCR processes. Other improvements over conventional PCR processes of the novel dispersion platform include increasing the throughput capability, enhancing the performance and portability of the thermal cycler, and allowing for the contamination-free storage of samples after thermal cycling.

CNC-Milled Superhydrophobic Macroporous Monoliths for 3D Cell Culture.

High-strength macroporous monoliths can be obtained by the simple mixing of boehmite nanofiber aqueous acetate dispersions with methyltrimethoxysilane. On the boehmite nanofiber-polymethylsilsesquioxane monoliths, we can fabricate structures smaller than a millimeter in size by computer numerical control (CNC) milling, resulting in a machined surface that is superhydrophobic and biocompatible. Using this strategy, we fabricated a superhydrophobic multiwell plate that holds water droplets to produce 3D cell culture environments for various cell types. We expect these superhydrophobic monoliths to have future applications in 3D tissue construction.

Millimeter-sized capsules prepared using liquid marbles: Encapsulation of ingredients with high efficiency and preparation of spherical core-shell capsules with highly uniform shell thickness using centrifugal force.

HYPOTHESIS: In our previous study, we prepared millimeter-sized spherical hard capsules by solidifying droplets of liquid monomer or polymer solution placed on superamphiphobic surface. Application of liquid marbles in place of the naked droplets for capsule preparation has a great potential to increase encapsulation efficiency of high volatile ingredients. Further, interfacial thermodynamic prediction of internal configuration of capsules from spreading coefficients may be effective to prepare core/shell capsule. EXPERIMENTS: Droplets of liquid monomer containing a volatile ingredient were rolled on superamphiphobic powders to prepare liquid marbles and solidified by photopolymerization. For preparation of core/shell capsules, the liquid marbles injected with an immiscible water droplet were also solidified. FINDINGS: A volatile ingredient could be encapsulated with higher efficiency than our previous method. Interfacial thermodynamic prediction of internal configuration of capsules from spreading coefficients indicated successful formation of core/shell capsules. However, photopolymerization of the liquid marbles in a static condition resulted in formation of not only core/shell capsules but also acorn-type capsules. Furthermore, the core/shell capsules were distorted and the shell thickness was not uniform. Rolling of the liquid marbles, which generated centrifugal force inside of the liquid marbles, was effective to prepare spherical capsules with highly uniform shell thickness.

Large-Scale Preparation of Giant Vesicles by Squeezing a Lipid-Coated Marshmallow-like Silicone Gel in a Buffer.

Giant vesicles were efficiently produced by squeezing a lipid (l-α-phosphatidylcholine from egg yolk)-coated marshmallow-like flexible macroporous silicone monolith in a buffer. The mean diameter of the obtained vesicles was 2 µm, showing a wide distribution, up to tens of micrometers, which was similar to that of vesicles formed by a natural swelling method. It was possible to prepare vesicle dispersions on a scale from several microliters to several hundred milliliters. A protein synthesis system (PURE system) contained in vesicles prepared using this method functioned effectively. Our absorbing-squeezing method is expected to help in studies that use giant vesicles such as artificial cells and drug delivery systems.

Polymethylsilsesquioxane-cellulose nanofiber biocomposite aerogels with high thermal insulation, bendability, and superhydrophobicity.

Polymethylsilsesquioxane-cellulose nanofiber (PMSQ-CNF) composite aerogels have been prepared through sol-gel in a solvent containing a small amount of CNFs as suspension. Since these composite aerogels do not show excessive aggregation of PMSQ and CNF, the original PMSQ networks are not disturbed. Composite aerogels with low density (0.020 g cm(-3) at lowest), low thermal conductivity (15 mW m(-1) K(-1)), visible light translucency, bending flexibility, and superhydrophobicity thus have been successfully obtained. In particular, the lowest density and bending flexibility have been achieved with the aid of the physical supporting effect of CNFs, and the lowest thermal conductivity is comparable with the original PMSQ aerogels and standard silica aerogels. The PMSQ-CNF composite aerogels would be a candidate to practical high-performance thermal insulating materials.

Transition from transparent aerogels to hierarchically porous monoliths in polymethylsilsesquioxane sol-gel system.

A transition from hierarchical pore structures (macro- and meso-pores) to uniform mesopores in monolithic polymethylsilsesquioxane (PMSQ, CH(3)SiO(1.5)) gels has been investigated using a sol-gel system containing surfactant Pluronic F127. The precursor methyltrimethoxysilane (MTMS) undergoes an acid/base two-step reaction, in which hydrolysis and polycondensation proceed in acidic and basic aqueous media, respectively, as a one-pot reaction. Porous morphology is controlled by changing the concentration of F127. Sufficient concentrations of F127 inhibit the occurrence of micrometer-scale phase separation (spinodal decomposition) of hydrophobic PMSQ condensates and lead to well-defined mesoporous transparent aerogels with high specific pore volume as a result of the colloidal network formation in a large amount of solvent. Phase separation regulates well-defined macropores in the micrometer range on decreasing concentrations of F127. In the PMSQ-rich gelling domain formed by phase separation, the PMSQ colloidal network formation forms mesopores, leading to monolithic PMSQ gels with hierarchical macro- and meso-pore structures. Mesopores in these gels do not collapse on evaporative drying owing to the flexible networks and repulsive interactions of methyl groups in PMSQ.