Recently, there has been an increase in the use of algal physiology as a convenient and useful indicator for monitoring of water quality in aquatic ecosystems. However, current methods for monitoring algal physiology are high-cost, power intensive, and have limited sensitivity for practical samples in which algal concentration is low. In order to alleviate these problems, we developed a simple-to-fabricate acoustophoretic particle trapping device that can effectively enrich various types of microalgae such as chlorella and diatoms for real-time monitoring of water quality. This microalgae trap is fabricated by embedding a piezoelectric resonator in a single channel. In comparison to previously reported acoustophoretic particle traps, this device has a simple structure and does not require sheath flows, which makes the device low cost and simple to fabricate and operate. Using Chlorella kessleri and the marine diatom Thalassiosira pseudonana as model algae, the microalgae trap has demonstrated notable particle trapping efficiencies between 82 % to 74 % for Chlorella with a through-flow of 0.5 mu l/min to 2.7 mu l/min and 85 % to 79 % for diatoms with a 0.5 mu l/min to 4 mu l/min through-flow. The trap has also shown to simultaneously trap Chlorella and diatoms at different heights of the microchannel. This device has high promise for trapping, separating and manipulating microalgae.

Green algae have been studied as an important and effective biomarker to indicate water quality due to their sensitivity to toxic agents in freshwater sources. However, conventional methods to monitor algal physiology use a chlorophyll fluorometer whose use is hampered by high-cost, large footprint, and limited sensitivity for practical samples containing low algal concentration. To overcome these constraints, we developed a multi-level electrode platform for resettable trapping of algae via AC electro-osmosis (ACEO) and negative dielectrophoresis. Preliminary experiments were performed in freshwater with conductivity of 0.02 S/m. Algal trapping was demonstrated at a low voltage of 2 V. The concentration effect was experimentally verified by measuring the fluorescence intensity of algae and using hemocytometer counting chambers at the inlet and outlet of the multilevel microchannel lab-on-a-chip. An optimal frequency was found for trapping, which agrees with the frequency dependence of ACED flow velocity. Through-flow rate and electrode dimensions were optimized as well. Trapping efficiencies within the range of 26%-65% have been obtained. A maximum trapping rate of 182 cells/s was obtained with a flow rate of 20 l/min. This lab-on-a-chip shows high potential for improving the limit of detection in algal monitoring and enabling the development of a portable, integrated and automated system for monitoring the quality of source drinking waters.(C) 2016 Elsevier B.V. All rights reserved.

In oxygenic plants, photons are captured with high quantum efficiency by two specialized reaction centers (RC) called Photosystem I (PS I) and Photosystem II (PS II). The captured photon triggers rapid charge separation and the photon energy is converted into an electrostatic potential across the nanometer-scale ( ~ 6 nm) reaction centers. The exogenous photovoltages from a single PS I RC have been previously measured using the technique of Kelvin force probe microscopy (KFM). However, biomolecular photovoltaic applications require two-terminal devices. This paper presents for the first time, a micro-device for detection and characterization of isolated PS I RCs. The device is based on an AlGaN/GaN high electron mobility transistor (HEMT) structure. AlGaN/GaN HEMTs show high current throughputs and greater sensitivity to surface charges compared to other field-effect devices. PS I complexes immobilized on the floating gate of AlGaN/GaN HEMTs resulted in significant changes in the device characteristics under illumination. An analytical model has been developed to estimate the RCs of a major orientation on the functionalized gate surface of the HEMTs.

This chapter presents an overview of optical stimulation of neural cells by synthetic chromophores and their potential use in the field of artificial sight. The chromophores and techniques that are discussed include azo chromophores, photo release of caged neurotransmitters, pore blockers and photoisomerization, the channelrhodopsins, melanopsin, and the Photosystem I reaction center of green plants.

Purpose.: To study the feasibility of anterior vitreal oxygenation for the treatment of acute retinal ischemia. Methods.: Twenty rabbits were randomized into an oxygenation group, a sham treatment group, and a no treatment group. Baseline electroretinography (ERG) and preretinal oxygen (Po 2) measurements were obtained 3 to 5 days before surgery. Intraocular pressure was raised to 100 mm Hg for 90 minutes and then normalized. The oxygenation group underwent vitreal oxygenation for 30 minutes using intravitreal electrodes. The sham treatment group received inactive electrodes for 30 minutes while there was no intervention for the no treatment group. Preretinal Po 2 in the posterior vitreous was measured 30 minutes after intervention or 30 minutes after reperfusion (no treatment group) and on postoperative days (d) 3, 6, 9, and 12. On d14, rabbits underwent ERG and were euthanatized. Results.: Mean final (d12) Po 2 was 10.64 ± 0.77 mm Hg for the oxygenation group, 2.14 ± 0.61 mm Hg for the sham group, and 1.98 ± 0.63 mm Hg for the no treatment group. On ERG, scotopic b-wave amplitude was significantly preserved in the oxygenation group compared with the other two groups. Superoxide dismutase assay showed higher activity in the operated eyes than in the nonoperated control eyes in the sham treatment group and no treatment group only. Histopathology showed preservation of retinal architecture and choroidal vasculature in the oxygenation group, whereas the sham-treated and nontreated groups showed retinal thinning and choroidal atrophy. Conclusions.: In severe total ocular ischemia, anterior vitreal oxygenation supplies enough oxygen to penetrate the retinal thickness, resulting in rescue of the RPE/choriocapillaris that continues to perfuse, hence sparing the retinal tissue from damage.

The development of a retinal prosthesis for artificial sight includes a study of the factors affecting the structural and functional stability of chronically implanted microelectrode arrays. Although neuron depolarization and propagation of electrical signals have been studied for nearly a century, the use of multielectrode stimulation as a proposed therapy to treat blindness is a frontier area of modern ophthalmology research. Mapping and characterizing the topographic information contained in the electric field potentials and understanding how this information is transmitted and interpreted in the visual cortex is still very much a work in progress. In order to characterize the electrical field patterns generated by the device, all ill vitro prototype that mimics several of the physical and chemical parameters of the in vivo visual implant device was fabricated. We carried Out multiple electrical measurements in a model "eye," beginning with a single electrode, followed by a 9-electrode array structure, both idealized components based on the Argus II retinal implants. Correlating the information contained in the topographic features of the electric fields with psychophysical testing in patients may help reduce the time required for patients to convert the electrical patterns into graphic signals.

This presentation is a report on the in situ characterization of stimulating microelectrodes in the context of multielectrode retinal prosthetic implants. The experimental system approximately replicates the geometric and electrical parameters of Second Sight Medical Products' Argus II Retinal Implant. Topographic maps of electric potentials have been prepared for a 60 electrode structure in which selected electrodes were stimulated with biphasic repetitively pulsed charge densities at 100 microC·cm(-2). Surface contour maps were prepared using a 10 microm diameter recording electrode.