Finding a needle in a haystack: A new technology is demonstrated to enrich circulating tumor cells (CTCs) with high efficiency by integrating an antibody‐coated silicon nanopillar (SiNP, see picture; gray) substrate with an overlaid polydimethylsiloxane (PDMS) microfluidic chaotic mixer (turquoise). It shows significantly improved sensitivity in detecting rare CTCs from whole blood, thus providing an alternative for monitoring cancer progression.
A chaotic micro mixer with multiple side channels is designed and investigated, in which fluid can be stirred by pumps through the side channels. By stretching and folding fluid in the main and side channels, chaotic mixing can be achieved. A simple mathematic model is derived to understand the movement of particles in the microchannel. Spatial trajectories of fluid particles are projected to Poincaré sections by mapping. The route from the quasi-period to chaos is revealed to be destruction of KAM curves and shrinkage of the quasi-periodic areas. Lyapunov exponents (LE) are used as the mixing index and the criteria to evaluate the chaotic behavior of the system. We found that LE is closely related to the amplitude and frequency of stirring and can be used to optimize our design and operation. From the relationship of LE and striation thickness, the minimal mixing length required can be estimated, which is much shorter than that needed in passive mixer design.
The motion of a DNA molecule in a solvent flow reflects the deformation of a nano/microscale flexible mass-spring structure by the forces exerted by the fluid molecules. The dynamics of individual molecules can reveal both fundamental properties of the DNA and basic understanding of the complex rheological properties of long-chain molecules. In this study, we report the dynamics of isolated DNA molecules under homogeneous extensional flow. Hydrodynamic focusing generates homogeneous extensional flow with uniform velocity in the transverse direction. The deformation of individual DNA molecules in the flow was visualized with video fluorescence microscopy. A coil-stretch transition was observed when the Deborah number (De) is larger than 0.8. With a sudden stopping of the flow, the DNA molecule relaxes and recoils. The longest relaxation time of T2 DNA was determined to be 0.63 s when scaling viscosity to 0.9 cP.
A new technology approach for the design, fabrication and application of an integrated free-solution capillary electrophoresis microsystem is presented. Combining the advantages of projection, contact photolithography and deep-reactive-ion-etching, this approach allows fast and flexible formation of micron-sized channels integrated with extremely high aspect-ratio (>50:1) sub-micron pillar arrays on a silicon substrate. Utilizing fluorescence video microscopy, free-solution DNA separation has been demonstrated. Furthermore, the detailed DNA molecular interaction with the pillars inside the microsystem can be analysed. In comparison with the previously reported fabrication technologies, such as electron beam lithography, the newly presented technology approach offers a significant improvement in fabrication time and design flexibility; both are highly desirable not only for potential commercialization of the free-solution electrophoresis microsystem in applications such as lab-on-a-chip but also for systematic studies of micro-scale DNA kinetics.
Abstract-This paper presents an integrated vibration power generator system. The system consists of a mini electromagnetic vibration power generator and a highly efficient energy harvesting circuit
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