Nanoparticles containing magnetic materials, such as magnetite (Fe3O4), are particularly useful for imaging and separation techniques. As these nanoparticles are generally considered to be biologically and chemically inert, they are typically coated with metal catalysts, antibodies or enzymes to increase their functionality as separation agents. Here, we report that magnetite nanoparticles in fact possess an intrinsic enzyme mimetic activity similar to that found in natural peroxidases, which are widely used to oxidize organic substrates in the treatment of wastewater or as detection tools. Based on this finding, we have developed a novel immunoassay in which antibody-modified magnetite nanoparticles provide three functions: capture, separation and detection. The stability, ease of production and versatility of these nanoparticles makes them a powerful tool for a wide range of potential applications in medicine, biotechnology and environmental chemistry.

[1] We studied in situ colloid mobilization under transient flow conditions using columns repacked with Hanford sediments. Rainfall infiltration was experimentally simulated using different flow rates and initial moisture conditions. Five series of column experiments were performed with initial infiltration rates of 0.018, 0.036, 0.072, 0.144, and 0.288 cm/min, and the columns reached water saturations in the range of 53 to 81%. The infiltration of water into the columns provided unfavorable conditions for colloid attachment to the sediments. Colloids were eluted by the infiltrating water with the peak colloid concentrations in the outflow coinciding with the arrival of the infiltration front. A larger flow rate led to a greater amount of colloids released from the column. The cumulative amount of colloids released was proportional to the column water content established after steady state flow rates were achieved. We used the advection-dispersion equation with a first-order colloid release reaction to analyze the experimental data. The colloid release rate coefficient increased with the increase of water content. We calculated forces exerted on colloids, and found that electrostatic and van der Waals interactions, calculated based on the DLVO (Derjaguin-Landau-Verwey-Overbeek) theory, and hydrodynamic forces, were all less important than capillary forces in controlling colloid release. In one experiment, the ionic strength of the infiltration solution was increased, such that colloid attachment was favorable. Nonetheless, colloids were mobilized and eluted with the infiltration front, implying that non-DLVO forces, such as capillary forces, played a prominent role in colloid mobilization.Citation: Shang, J., M. Flury, G. Chen, and J. Zhuang (2008), Impact of flow rate, water content, and capillary forces on in situ colloid mobilization during infiltration in unsaturated sediments, Water Resour. Res., 44, W06411,

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Colloid transport may facilitate off-site transport of radioactive wastes at the Hanford site, Washington State. In this study, column experiments were conducted to examine the effect of irrigation schedule on releases of in situ colloids from two Hanford sediments during saturated and unsaturated transientflow and its dependence on solution ionic strength, irrigation rate, and sediment texture. Results show that transient flow mobilized more colloids than steady-state flow. The number of short-term hydrological pulses was more important than total irrigation volume for increasing the amount of mobilized colloids. This effect increased with decreasing ionic strength. At an irrigation rate equal to 5% of the saturated hydraulic conductivity, a transient multipulse flow in 100 mM NaNO3 was equivalent to a 50-fold reduction of ionic strength (from 100 mM to 2 mM) with a single-pulse flow in terms of their positive effects on colloid mobilization. Irrigation rate was more important for the initial release of colloids. In addition to water velocity, mechanical straining of colloids was partly responsible for the smaller colloid mobilization in the fine than in the coarse sands, although the fine sand contained much larger concentrations of colloids than the coarse sand.

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SUMMARY There is growing evidence that alterations in metabolism may contribute to tumorigenesis. Here, we report on members of families with the Li–Fraumeni syndrome who carry germline mutations in TP53, the gene encoding the tumor-suppressor protein p53. As compared with family members who are not carriers and with healthy volunteers, family members with these mutations have increased oxidative phosphorylation of skeletal muscle. Basic experimental studies of tissue samples from patients with the Li–Fraumeni syndrome and a mouse model of the syndrome support this in vivo finding of increased mitochondrial function. These results suggest that p53 regulates bioenergetic homeostasis in humans. (Funded by the National Heart, Lung, and Blood Institute and the National Institutes of Health; ClinicalTrials.gov number, NCT00406445.)

Development of enzyme mimics for the scavenging of excessive mitochondrial superoxide (O2•−) can serve as an effective strategy in the treatment of many diseases. Here, protein reconstruction technology and nanotechnology is taken advantage of to biomimetically create an artificial hybrid nanozyme. These nanozymes consist of ferritin‐heavy‐chain‐based protein as the enzyme scaffold and a metal nanoparticle core as the enzyme active center. This artificial cascade nanozyme possesses superoxide dismutase‐ and catalase‐like activities and also targets mitochondria by overcoming multiple biological barriers. Using cardiac ischemia‐reperfusion animal models, the protective advantages of the hybrid nanozymes are demonstrated in vivo during mitochondrial oxidative injury and in the recovery of heart functionality following infarction via systemic delivery and localized release from adhesive hydrogels (i.e., cardiac patch), respectively. This study illustrates a de novo design strategy in the development of enzyme mimics and provides a promising therapeutic option for alleviating oxidative damage in regenerative medicine.