Significance Morpho butterflies are a brilliant spectacle of nature’s capability for photonic engineering. Their conspicuous appearance arises from the interference and diffraction of light within tree-like nanostructures on their scales. Scientific lessons learned from these butterflies have already inspired designs of new displays, fabrics, and cosmetics. This study reports a vertical surface polarity gradient in these tree-like structures. This biological pattern design may be applied to numerous technological applications ranging from security tags to self-cleaning surfaces, gas separators, protective clothing, and sensors. Here it has allowed us to unveil a general mechanism of selective vapor response in photonic Morpho nanostructures and to demonstrate attractive opportunities for chemically graded sensing units for high-performance sensing.

Background: The development of inexpensive small flow cytometers is recognized as an important goal for many applications ranging from medical uses in developing countries for disease diagnosis to use as an analytical platform in support of homeland defense. Although hydrodynamic focusing is highly effective at particle positioning, the use of sheath fluid increases assay cost and reduces instrument utility for field and autonomous remote operations. Methods: This work presents the creation of a novel flow cell that uses ultrasonic acoustic energy to focus small particles to the center of a flowing stream for analysis by flow cytometry. Experiments using this flow cell are described wherein its efficacy is evaluated under flow cytometric conditions with fluorescent microspheres. Results: Preliminary laboratory experiments demonstrate acoustic focusing of flowing 10‐μm latex particles into a tight sample stream that is ∼40 μm in diameter. Prototype flow cytometer measurements using an acoustic‐focusing flow chamber demonstrated focusing of a microsphere sample to a central stream ∼40 μm in diameter, yielding a definite fluorescence peak for the microspheres as compared with a broad distribution for unfocused microspheres. Conclusions: The flow cell developed here uses acoustic focusing, which inherently concentrates the sample particles to the center of the sample stream. This method could eliminate the need for sheath fluid, and will enable increased interrogation times for enhanced sensitivity, while maintaining high particle‐analysis rates. The concentration effect will also enable the analysis of extremely dilute samples on the order of several particles per liter, at analysis rates of a few particles per second. Such features offer the possibility of a truly versatile low‐cost portable flow cytometer for field applications. © 2005 Wiley‐Liss, Inc.

Creation of inexpensive small-flow cytometers is important for applications ranging from disease diagnosis in resource-poor areas to use in distributed sensor networks. In conventional-flow cytometers, hydrodynamics focus particles to the center of a flow stream for analysis, which requires sheath fluid that increases consumable use and waste while dramatically reducing instrument portability. Here we have evaluated, using quantitative measurements of fluorescent microspheres and cells, the performance of a flow cytometer that uses acoustic energy to focus particles to the center of a flow stream. This evaluation demonstrated measurement precision for fluorescence and side scatter CVs for alignment microspheres of 2.54% and 7.7%, respectively. Particles bearing 7 x 10(3) fluorophores were well resolved in a background of 50 nM free fluorophore. The lower limit of detection was determined to be about 650 fluorescein molecules. Analysis of Chinese hamster cells on the system demonstrated that acoustic focusing had no effect on cellular viability. These results indicate that the ultrasonic flow cytometer has the necessary performance for most flow cytometry applications. Furthermore, through robust engineering approaches and the combination of acoustic focusing with low-cost light sources, detectors, and data acquisition systems, it will be possible to achieve a low-cost, truly portable flow cytometer.

Acoustic particle manipulation has many potential uses in flow cytometry and microfluidic array applications. Currently, most ultrasonic particle positioning devices utilize a quasi-one-dimensional geometry to set up the positioning field. A transducer fit with a quarter-wave matching layer, locally drives a cavity of width one-half wavelength. Particles within the cavity experience a time-averaged drift force that transports them to a nodal position. Present research investigates an acoustic particle-positioning device where the acoustic excitation is generated by the entire structure, as opposed to a localized transducer. The lowest-order structural modes of a long cylindrical glass tube driven by a piezoceramic with a line contact are tuned, via material properties and aspect ratio, to match resonant modes of the fluid-filled cavity. The cylindrical geometry eliminates the need for accurate alignment of a transducer/reflector system, in contrast to the case of planar or confocal fields. Experiments show that the lower energy density in the cavity, brought about through excitation of the whole cylindrical tube, results in reduced cavitation, convection, and thermal gradients. The effects of excitation and material parameters on concentration quality are theoretically evaluated, using two-dimensional elastodynamic equations describing the fluid-filled cylindrical shell with a line excitation.

This is an open access article under the terms of the Creat ive Commo ns Attri butio n-NonCo mmerc ial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.