Regulating the synthesis rate and yield of bio-assembled FeS nanoparticles for efficient cancer therapy.

Biosynthesis has gained growing interest due to its energy efficiency and environmentally benign nature. Recently, biogenic iron sulfide nanoparticles (FeS NPs) have exhibited excellent performance in environmental remediation and energy recovery applications. However, their biosynthesis regulation strategy and application prospects in the biomedical field remain to be explored. Herein, biogenic FeS NPs are controllably synthesized by Shewanella oneidensis MR-1 and applied for cancer therapy. Tuning the synthesis rate and yield of biogenic FeS NPs is realized by altering the initial iron precursor dosage. Notably, increasing the precursor concentration decreases and delays FeS NP biosynthesis. The biogenic FeS NPs (30 nm) are homogeneously anchored on the cell surface of S. oneidensis MR-1. Moreover, the good hydrophilic nature and outstanding Fenton properties of the as-prepared FeS NPs endow them with good cancer therapy performance. The intracellular location of the FeS NPs taken up is visualized with a soft X-ray microscope (SXM). Highly efficient cancer cell killing can be achieved at extremely low concentrations (<12 µg mL-1), lower than those in reported works. Such good performance is attributed to the Fe2+ release, elevated ROS, reduced glutathione (GSH) consumption, and lipid hydroperoxide (LPO) generation. The resulting FeS NPs show excellent in vivo therapeutic performance. This work provides a facile, eco-friendly, and scalable approach to produce nanomedicine, demonstrating the potential of biogenic nanoparticles for use in cancer therapy.

Directed Biofabrication of Nanoparticles through Regulating Extracellular Electron Transfer.

Biofabrication of nanomaterials is currently constrained by a low production efficiency and poor controllability on product quality compared to chemical synthetic routes. In this work, we show an attractive new biosynthesis system to break these limitations. A directed production of selenium-containing nanoparticles in Shewanella oneidensis MR-1 cells, with fine-tuned composition and subcellular synthetic location, was achieved by modifying the extracellular electron transfer chain. By taking advantage of its untapped intracellular detoxification and synthetic power, we obtained high-purity, uniform-sized cadmium selenide nanoparticles in the cytoplasm, with the production rates and fluorescent intensities far exceeding the state-of-the-art biosystems. These findings may fundamentally change our perception of nanomaterial biosynthesis process and lead to the development of fine-controllable nanoparticles biosynthesis technologies.

[Geometric distortion correction for hyperspectral image using a rotating scan reflector].

Offner imaging spectrometer is a kind of pushbroom imaging system. Hyperspectral images acquired by Offner imaging spectrometers require relative motion of sensor and scene that is translation or rotation. Via rotating scan with a reflector at the front of sensor's len, large objects can be entirely captured. But for the changes in object distances, geometric distortion occurs. A formula of space projection from an object point to an image point by one capture was derived. According to the projection relation and slit's motion curve, the object points' coordinates on a reference plan were obtained with rotation angle for a variable. A rotating scan device using a reflector was designed and installed on an Offner imaging spectrometer. Clear images were achieved from the processing of correction algorithm.

A nano-sized Au electrode fabricated using lithographic technology for electrochemical detection of dopamine.

One big challenge of fabricating nanosensors for spatially resolved electrochemical detection of neurochemicals, such as dopamine (DA), is the difficulty to assembly nanometer-scale patternable and integrated sensors. In this work we develop a novel approach to precisely manufacture nano-Au-electrode (NAE) using lithographic fabrication technique, and characterize the NAE for DA detection. A negative photoresist, SU-8, is used as a substrate and protection layer for the 127-nm Au active sensing layer. The cross surface morphology and thickness of the Au layer are imaged by scanning electron microscopy and an interference microscopy. This NAE could be precisely controlled, repeatedly fabricated and conveniently renewed for several times. The electrochemical sensitivity and selectivity of the NAE towards DA detection are significantly higher than those of a standard Au thin-film electrode. This work demonstrates that the NAE could be used as an attractive means for electrochemically sensing and recording DA.

Heterotrophs grown on the soluble microbial products (SMP) released by autotrophs are responsible for the nitrogen loss in nitrifying granular sludge.

In this work, nitrogen loss in the nitrite oxidation step of the nitrification process in an aerobic-granule-based reactor was characterized with both experimental and modeling approaches. Experimental results showed that soluble microbial products (SMP) were released from the nitrite-oxidizing granules and were utilized as a carbon source by the heterotrophs for denitrification. This was verified by the fluorescence in situ hybridization (FISH) analysis. Microelectrode tests showed that oxygen diffusion limitation did result in an anoxic micro-zone in the granules and allowed sequential utilization of nitrate as an electron acceptor for heterotrophic denitrification with SMP as a carbon source. To further elucidate the nitrogen loss mechanisms, a mathematic model was formulated to describe the growth of nitrite oxidizers, the formation and consumption of SMP, the anoxic heterotrophic growth on SMP and nitrate, as well as the oxygen transfer and the substrate diffusion in the granules. The results clearly indicate that the heterotrophs grown on the SMP released by the autotrophs are responsible for the nitrogen loss in the nitrifying granules, and give us a better understanding of the aerobic granules for nitrogen removal. Biotechnol. Bioeng. 2011;108: 2844-2852. © 2011 Wiley Periodicals, Inc.

An innovative miniature microbial fuel cell fabricated using photolithography.

Recently microbial fuel cells (MFCs) have attracted increasing interests in both environmental and energy fields. Among the various MFC configurations, miniature microbial fuel cell (mini-MFC) has a great potential for the application in medical, communication and other areas because of its miniature volume and high output power density. In this work, a 25-µL single-chamber mini-MFC was fabricated using the photolithography technique. The plate-shaped gold anodic electrode in the mini-MFC showed a higher electrochemical activity than the stripe-shaped one. A biofilm of Shewanella oneidensis MR-1 was formed on the surface of gold electrode in this micro-liter-scale MFCs. As a result, a maximum power density of 29 mW/m(2) and a maximum current density of 2148 mA/m(2) were achieved by this single-chamber mini-MFC.

A gold-sputtered carbon paper as an anode for improved electricity generation from a microbial fuel cell inoculated with Shewanella oneidensis MR-1.

Gold is among the highly conductive and stable materials, which are ideal anodes for microbial fuel cells (MFCs). However, previous studies have shown that bare gold surface is recalcitrant for the colonization of some exoelectrogens, e.g., Shewanella putrefacians. In this work, the problem regarding the poor bio-compatibility of gold as an anode material was sorted out through coupling it with carbon paper. A new composite anode material was fabricated through sputtering gold layer homogeneously on carbon paper matrix. Results of cyclic voltammetry and electrochemical impedance spectroscopy in Fe(CN)6(3-/4-) solution demonstrated better electrochemical performance of the carbon paper-gold (C-Au) composite than either carbon paper or bare gold, when they were used in MFCs. With Shewanella oneidensis MR-1 as the inoculum, the C-Au anode-based MFC produced total electric charges higher than the carbon-paper-anode-based MFC by 47%. The cyclic voltammetry analysis and the scanning electron microscopy observation showed that the MR-1 biofilm growth was accelerated when the carbon paper surface was sputtered with gold. Utilization of such a carbon paper-gold composite significantly enhanced the MFC performance.

Measurement of dissolved oxygen and its diffusivity in aerobic granules using a lithographically-fabricated microelectrode array.

A novel gold microelectrode array (MEA) was manufactured with microfabrication techniques and applied on the measurement of dissolved oxygen profile in an aerobic granule. The MEA contained five gold microelectrodes, which had a good linear response to dissolved oxygen and typically had a lifetime of more than 10 days. Dissolved oxygen microprofiles near the surface of an aerobic granule were monitored with this MEA. Based on the measurements, an oxygen effective diffusivity in the upper 100 microm layer of the aerobic granule was estimated to be 1.19 x 10(-9) m2/s. The experimental results demonstrate that the MEA was able to measure the DO levels in aerobic granules accurately and precisely and that the MEA could be used to determine constituents, profiles, and functions in situ in small spaces. Moreover, since the device shape and microelectrode arrangement were all defined by photolithography, the proposed fabrication procedure was flexible and appropriate for fabrication of various types of MEAs.

Simultaneous determination of nitrate and dissolved oxygen under neutral conditions using a novel silver-deposited gold microelectrode.

In this work a novel gold-based microelectrode was successfully fabricated using photolithographic techniques and electrochemical deposition for a simultaneous determination of nitrate and dissolved oxygen (DO) under neutral conditions. Three-dimensional tree-shaped silver nanorods were formed on the gold surface through electrochemical deposition and they had an electrochemical catalytic reductive activity for both nitrate and oxygen under neutral conditions. Thus, the silver nanorods served as the active center of the microelectrode. The microelectrode could be renewed over five times. Linear sweep voltammetry was employed to quantitatively analyze the nitrate and DO in solution. The microelectrode was used to measure the nitrate and DO microprofiles in a nitrifying aerobic granule from a sequencing batch reactor, which shows that denitrification did not occur in the tested granule. The measurement results demonstrate that the microelectrode was able to simultaneously determine the nitrate and DO levels in the granules under neutral conditions accurately and precisely.

Innovative solid-state microelectrode for nitrite determination in a nitrifying granule.

Nitrite is an intermediate of both nitrification and denitrification in biological removal of nitrogen from wastewater, and in situ measurement of nitrite concentration in a biofilm or microbial granules is highly desirable. However, a solid-state microelectrode for nitrite determination is not available yet In this work, a solid-state microelectrode was manufactured through electrochemical codeposition of Pt--Fe nanoparticles on a gold microelectrode fabricated using photolithography for in situ nitrite determination. This gold-based microelectrode could be used as a more cost-effective, efficient, and reliable alternative to the liquid membrane microelectrode. Nanoparticles with an average diameter of 50 nm were observed on the surface of the chemically modified electrode. A sigmoid peak at ca. 0.7 V (vs Ag/AgCl) was found on the linear sweep voltammogram in nitrite solutions by using the fabricated microelectrode. The peak height of the first-order derivative of the sigmoid peak was proportional to the nitrite concentration of 0.001--0.05 M and could be used for quantitative determination of nitrite. The detection limits (S/N = 3) were approximately 3 x 10(-5) M. The nitrite microprofiles of aerobic granules from a nitrifying reactor were measured with the microelectrode to demonstrate its potential applications with high spatial resolution.

An innovative microelectrode fabricated using photolithography for measuring dissolved oxygen distributions in aerobic granules.

In this work an innovative microelectrode was successfully fabricated using photolithography for determination of dissolved oxygen distributions in aerobic granules, which were sampled from a nitrifying sequencing batch reactor. A negative photoresist, SU-8, was used as a substrate for the microelectrode and a 70 microm wide needle was photopatterned on it. The microelectrode could be renewed several times. Cyclic voltammetry analysis and dissolved oxygen measurement demonstrated that the microelectrode was stable and reliable. Dissolved oxygen distribution in a nitrifying granule was successfully monitored with the microelectrode. The profiles indicated that the main active part of the nitrifying granule was the upper 150 microm layer. Using the procedures developed in this work, microelectrodes of the desired shape could be constructed with precise size control at micrometers-scale.