Wirelessly powered dielectrophoresis of metal oxide particles using spark-gap Tesla coil

Wirelessly powered dielectrophoresis (DEP) of metal oxide particles was performed using a spark-gap Tesla coil (TC). The main contribution of this work is the simplification of the conventional DEP setup that requires attaching wires directly to the electrodes. Wireless power from the TC generates a high output frequency and voltage, which corresponds to that used for the DEP. Therefore, a spark-gap TC was built and utilized to conduct the DEP process. Metal oxides (ZnO and Fe₂O₃) were used as targets for the assembly. The results showed that the wirelessly powered DEP technique via a TC was successful in assembling the metal oxide particles. Positive and negative DEP phenomena were observed. Positive DEP occurred during ZnO assembly, making particles chain grow 0.92 mm toward the sparks within 60 s. Negative DEP was observed during Fe₂O₃ assembly, where the repulsion of particles formed a void around the sparks with a 1.45 mm radius. The mechanism of this wireless DEP system is discussed.     

Fabrication of a micro-direct methanol fuel cell using microfluidics

A direct-methanol fuel cell containing three parts: microchannels, electrodes, and a proton exchange membrane (PEM), was investigated. Nafion resin (NR) and polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (PS) were used as PEMs. Preparation of PEMs, including compositing with other polymers and their solubility, was performed and their proton conductivity was measured by a four point probe. The results showed that the 5 % Nafion resin has lower conductivity than the 5 % PS solution. The micro-fuel cell contained two acrylic channels, PEM, and two platinum catalyst electrodes on a silicon wafer. The assembled micro-fuel cells used 2 M methanol at the flow rate of 1.5 mL min^?1 in the anode channel and 5 × 10^?3 M KMnO₄ at the flow rate of 1.5 mL min^?1 in the cathode channel. The micro-fuel cell with the electrode distance of 300 ??m provided the power density of 59.16 ??W cm^?2 and the current density of 125.60 ??A cm^?2 at 0.47 V.     

Fabrication of gradient hydrogels using a microfluidics/photopolymerization process

A method of fabricating photo-cross-linked hydrogels with gradients of immobilized molecules and crosslinking densities is introduced. Two macromer/initiator solutions are injected into a unique poly(dimethylsiloxane) channel system that produces a prepolymer gradient that is subsequently polymerized into a water-swollen hydrogel with ultraviolet light exposure. The gradient is controlled by the injection flow rate (optimized to 0.3 microL/min per inlet to produce a linear gradient). The technique is investigated both through fabrication of adhesive ligand gradients that modulate spatial distribution of attached endothelial cells and gradients of cross-linking densities that led to unique hydrogel architectures and spatially dependent swelling.     

Capillary liquid chromatography fraction collection and postcolumn reaction using segmented flow microfluidics

A challenge for capillary LC (cLC) is fraction collection and the manipulation of fractions from microscale columns. An emerging approach is the use of segmented flow or droplet technology to perform such tasks. In this work, a fraction collection and postcolumn reaction system based on segmented flow was developed for the gradient cLC of proteins. In the system, column effluent and immiscible oil are pumped into separate arms of a tee resulting in regular fractions of effluent segmented by oil. Fractions were generated at 1 Hz corresponding to 5 nL volumes. The fraction collection rate was high enough to generate over 30 fractions per peak and preserve chromatographic resolution achieved for a five‐protein test mixture. The resulting fractions could be stored and subsequently derivatized for fluorescence detection by pumping them into a second tee where naphthalene dicarboxyaldehyde, a fluorogenic reagent, was pumped into a second arm and added to each fraction. Proteins were derivatized within the droplets enabling postcolumn fluorescence detection of the proteins. The experiments demonstrate that fraction collection from cLC by segmented flow can be extended to proteins. Further, they illustrate a potential workflow for protein analysis based on postcolumn derivatization for fluorescence detection.     

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.     

Electrochemical droplet-based microfluidics using chip-based carbon paste electrodes for high-throughput analysis in pharmaceutical applications

This paper presents the first example of a pharmaceutical application of droplet-based microfluidics coupled with chronoamperometric detection using chip-based carbon paste electrodes (CPEs) for determination of dopamine (DA) and ascorbic acid (AA). Droplets were generated using an oil flow rate of 1.80 μL min⁻¹, whereas a flow rate of 0.80 μL min⁻¹ was applied to the aqueous phase, which resulted in a water fraction of 0.31. The optimum applied potential for chronoamperometric measurements in droplets was found to be 150 mV. Highly reproducible analysis of DA and AA was achieved with relative standard deviations of less than 5% for both intra-day and inter-day measurements. The limit of detection (LOD) and limit of quantitation (LOQ) were found to be 20 and 70 μM for DA and 41 and 137 μM for AA, respectively. Linearity of this method was in the ranges of 0.02–3.0 mM for DA and 0.04–3.0 mM for AA. This system was successfully applied to determine the amounts of DA and AA in intravenous drugs. Calibration curves of DA and AA for quantitative analysis were obtained with good linearity with R² values of 0.9984 and 0.9988, respectively. Compared with the labeled amounts, the measured concentrations of DA and AA obtained from this system were insignificantly different, with error percentages of less than ±3.0%, indicating a high accuracy of the developed method.     

Fabrication of an ammonia gas sensor using inkjet-printed polyaniline nanoparticles

This work details the fabrication and performance of a sensor for ammonia gas analysis which has been constructed via the inkjet-printed deposition of polyaniline nanoparticle films. The conducting films were assembled on interdigitated electrode arrays and characterised with respect to their layer thickness and thermal properties. The sensor was further combined with heater foils for operation at a range of temperatures. When operated in a conductimetric mode, the sensor was shown to exhibit temperature-dependent analytical performance to ammonia detection. At room temperature, the sensor responded rapidly to ammonia (t₅₀ = 15 s). Sensor recovery time, response linearity and sensitivity were all significantly improved by operating the sensor at temperatures up to 80 °C. The sensor was found to have a stable logarithmic response to ammonia in the range of interest (1-100 ppm). The sensor was also insensitive to moisture in the range from 35 to 98% relative humidity. The response of the sensor to a range of common potential interferents was also studied.     

A dielectrophoresis-based platform of cancerous cell capture using aptamer-functionalized gold nanoparticles in a microfluidic channel

In this paper, a microfluidic chip for the manipulation and capture of cancer cells was introduced, in which the combination of dielectrophoresis (DEP) and a binding method based on chemical interactions by using cell-specific aptamers was performed to enhance the capture strength and specificity. The device has been simply constructed from a straight-channel PDMS placed on a glass substrate that has patterned electrode structures and a self-assembled monolayer of gold nanoparticles (AuNPs). The target cells were transported to the manipulation area by flow and attracted down to the region between the electrodes under the influence of positive DEP force. This approach facilitated subsequent selective capture by the modified aptamers on the AuNPs. The distribution of the electric field in the channel has also been simulated to clarify the DEP operation. As a result, the device has been shown to effectively capture target lung cancer cells with a concentration as low as $2\times {10}^4$cells/mL. The capture specificity in a sample of mixed cells is up to 80.4%. This technique has the potential to be applied to detection methods for many types of cancer.     

Fabrication of flexible light shutter using liquid crystals with polymer structure

We fabricated a light shutter using plastic substrates for high visibility of a flexible see-through display. To achieve a flexible light shutter using liquid crystals (LC), it is essential to maintain the cell gap when the light shutter is bent. We studied methods to fabricate flexible LC light shutters using plastic substrates. We demonstrated light shutters that are initially transparent and flexible with or without polymer walls. We have elucidated that polymer walls and networks provide mechanical stability against the bending of an LC light shutter without any degradation in the electro-optic characteristics. We predict that a flexible light shutter provides not only high visibility but also mechanical stability to a flexible see-through display by positioning it at the back of a flexible see-through display panel.     

Picomolar detection of carcinoembryonic antigen in whole blood using microfluidics and surface‐enhanced Raman spectroscopy

Carcinoembryonic antigen (CEA) is a wide‐spectrum biomarker. Clinically, we generally use serum sample to detect CEA, which needs to be centrifuged to pretreat the raw blood sample. In this study, we realized direct CEA detection in raw blood samples exploiting microfluidics. The LOD was as low as 10^?12 M.     

脂质体类药物载体的微流控制备

脂质体在药物输送、人造细胞等许多领域有着巨大的应用前景。作为药物载体,脂质体可以保护药物、提高药效、减小药物对机体的毒性、使药物具有靶向性,因此发展或改进脂质体制备方法有着重要的意义。然而,传统的脂质体制备存在耗时长、设备贵、制备条件易变、前后处理步骤多、粒径不均一以及难重复等问题,基于此,脂质体的微流控制备技术逐渐发展起来。研究表明微流控技术在脂质体制备方面有着独特的优势,包括精确地控制脂质体的大小和尺寸分布。本文综述了近年来基于微流控技术的几种脂质体制备方法的研究进展,并对比了几种方法制备的脂质体的性质;进一步分析和探讨了当前微流控技术制备脂质体存在的问题,并展望了其发展趋势和方向。     

Fabrication of hollow multifunctional spheres containing MCM-41 nanoparticles and magnetite nanoparticles using layer-by-layer method

Macroscopic mesoporous silica spheres have been fabricated by alternatively depositing preformed MCM-41 nanoparticles and polyelectrolytes onto polystyrene lattices. High surface area hollow mesoporous spheres were obtained by removal of the core by solvent or calcination. Further, the versatility of the layer-by-layer (LBL) method was extended to fabricate magnetite-mesoporous silica composites by depositing magnetite and MCM-41 nanoparticles onto polystyrene beads. Such high surface area composites are important since the mesopores can be used for encapsulation of varied materials like enzymes and drugs while the presence of magnetite ensures application in biocatalysis and separation under magnetic field.     

Fabrication of palladium nanoparticles as effective catalysts by using supramolecular gels

Two-component supramolecular gels were made through self-assembly of tetrazolyl derivatives and Pd(OAc)₂. The robust gels indicated high storage modulus(>10,000 Pa) and loss modulus, which were studied by rheological measurements. The formed Pd nanoparticles(~9 nm) obtained during the formation of the gel showed effective catalytic hydrogenation of nitrobenzene and could be recovered and reused without loss of activity.     

Fabrication of monodisperse luminescent nanoparticles with core/shell poly(styrene/thiophene) structure

Luminescent poly(styrene/thiophene) (PSt/PT) core/shell nanoparticles were prepared by oxidative polymerization in the presence of PSt seed particles. PSt seed particles with uniform size distribution were prepared with an anionic surfactant by an emulsion polymerization process, and were used as a template to prepare monodispersive PT‐coated nanoparticles. A luminescent Polythiophene (PT) layer was formed on the surface of PSt nanoparticles by oxidation polymerization with iron chloride (FeCl₃) and hydrogen peroxide (H₂O₂). The mechanism of core/shell formation was found to be the interface‐dominant polymerization induced by the electrostatic attraction between the sulfonate group of anionic surfactant and Fe³⁺ ions after the diffusion of thiophene monomer to the PSt nanoparticles. Field‐emission scanning electron microscopy and transmission electron microscopy (TEM) proved the core/shell structure, which provided key evidence that PT was incorporated onto the surface of PSt nanoparticles. In addition, the effect of the PT shell thickness on photoluminescent (PL) intensity was investigated by changing the shell thickness of PSt/PT nanoparticles. We observed that the PL intensity increased up to about 30 nm of PT shell thickness, and then decreased due to self‐absorption. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 5968–5975, 2008     

Preparation of magnetic glycoprotein‐imprinted nanoparticles with dendritic polyethyleneimine as a monomer for the specific recognition of ovalbumin from egg white

Glycoproteins are crucial in massive physiological events and clinical application. It is necessary to prepare new materials to isolate the specific glycoprotein. New and simple core–shell molecularly imprinted polymers were prepared by surface imprinting. The polymers are synthesized with magnetic nanoparticles as the core, water‐soluble dendritic polyethyleneimine as the monomer and the ovalbumin as the template. The prepared imprinted polymers showed thin imprinted shell, biocompatibility and superparamagnetic properties. The resultant materials exhibited fast kinetics, high adsorption capacity, perfect selectivity and reusability. More important, they can absorb the template glycoprotein from the neutral solution and successfully be applied to recognize the ovalbumin from egg white, which means that they can provide an alternate method to isolate glycoprotein from bodily fluids.