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Silver Nanoparticles Accumulate in Food Chain. Nate Vetter Chem 4101- Professor Edgar Arriaga December 7, 2011. Problem Statement and Hypothesis . Problem Statement Silver nanoparticles are being used in wound dressings, catheters, and various household products.
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Silver Nanoparticles Accumulate in Food Chain Nate Vetter Chem 4101- Professor Edgar Arriaga December 7, 2011
Problem Statement and Hypothesis Problem Statement • Silver nanoparticles are being used in wound dressings, catheters, and various household products. • Little research has been conducted to evaluate the impact of nanoparticles on terrestrial ecosystems Hypothesis • My hypothesis is silver nanoparticles can end up in the drainage, sewage, and waste water we expel which can make its way to the terrestrial ecosystems. • Insects can uptake these nanoparticles and the nanoparticles can translate up the food chain as predators eat the prey.
Overview • Main Analyte: Ag0 Nanoparticles 5-20 nm • Limit of Detection: 2.0 to 7.0 μg kg−1 • Matrixes: Waste Water, Soil, Plant Material, Worm Tissues Figure 1. Retrieved from Judy J. D. ; Unrine J. M. ; Bertsch P. M. Environ. Sci. Technol.2011,45,776-78
Requirements for Successful Analysis • Must be able to detect small amounts of analyte • Low Limit of Detection • Must be able to detect small changes in analyte Concentration • High Sensitivity • Results must be reproducible and timely • High Precision • High Accuracy • Fast (minutes, not hours)
Studies Needed to Test Hypothesis • Identify Waste streams with nanoparticles present. Determine greatest area of concentration of silver nanoparticles. • Measure concentration of silver nanoparticles in soils near waste streams of interest. • Based on concentrations of silver nanoparticles found in soils, construct a study similar in the lab using concentrations below, at, and above to determine the effect on accumulation in worms.
Best Separation Technique: Ion-exchange Chromatography • Speed: Very fast (minutes) • It is a non-denaturing technique that can be used at all stages and scales of purification. • Selectivity: Can resolve molecules with small differences in charge. • Simplified Exchange Equilibrium: Figure 2. Retrieve from Skoog, D.A.; Holler, F. J.; Crouch, S. R. Principles of Instrumental Analysis, 6th ed.; Cengage Learning: California, 2007.
Best Detector: AAS Reproducibility: 5-10% High Sensitivity Easy to use Can buy commercially • Multi-element analysis • Limit of Detection: 0.1 – 100 pg Figure 3. Retrieved From Skoog, D.A.; Holler, F. J.; Crouch, S. R. Principles of Instrumental Analysis, 6th ed.; Cengage Learning: California, 2007.
Experimental Sample Preparation • Digestion/microcentrifuge - Using hydrochloric acid and hydrogen peroxide, digest the tissues of the worms or food source. Centrifuge the sample to extract the silver from the matix. • Vacuum Filter – Pores on filter should remove debris in sample but not impede nanoparticles. • Dry/Store – Rotovap to remove solvents and store at room temperature until needed
Possible Outcomes • Predicted Results: • Worms cannot shed the silver nanoparticles efficiently, resulting in concentration in tissues far exceeding that of their food source. • The results of this study should demonstrate trophic transfer and biomagnification of silver nanoparticles from a primary producer to a primary consumer. • The observation that nanoparticles can biomagnify highlights the importance of considering dietary uptake as a pathway for nanoparticle exposure. This raises questions about potential human exposure to nanoparticles from long-term land application of biosolids containing nanoparticles.
References • 1. AshaRani, P. V.; KahMun G. L.; Hande M. P.; Valiyaveettil, S. Cytotoxicity and Genotoxicity of Silver Nanoparticles in Human Cells. ACS Nano,2009,3 (2), 279-290 • 2. Jensen, T.; Schatz, G.C.; Van Duyne, R. P. Nanosphere Lithography: Surface Plasmon Resonance Spectrum of a Periodic Array of Silver Nanoparticles by Ultraviolet−Visible Extinction Spectroscopy and Electrodynamic Modeling. J. Phys. Chem. B.1999,103, 2394-2401 • 3. Judy J. D. ; Unrine J. M. ; Bertsch P. M. Evidence for Biomagnification of Gold Nanoparticles within a Terrestrial Food Chain. Environ. Sci. Technol.2011,45, 776-78 • 4. Lim, S. F.; Riehn R.; Ryu W. S. ; Khanarian N. ; Tung C. ; Tank D. ; Austin R. H. In Vivo and Scanning Electron Microscopy Imaging of UpconvertingNanophosphors in Caenorhabditiselegans. Am. Chem. Soc.2006, 6, 169-174 • 5. Link, S.; Wang, Z.L.; El-Sayed, M.A. Alloy Formation of Gold-Silver Nanoparticles and the Dependence of the Plasmon Absorption on Their Composition. J. Phys. Chem. B.1999,103, 3529-3533 • 6. Journal of Nanobiotechnology. Silver nanoparticles. http://www.jnanobiotechnology.com/content/3/1/6/figure/F1?highres=y(accessed Oct 26, 2011) • 7. Nanocs. Silver nanoparticles. http://www.nanocs.com/Silver_nanoparticles.htm (accessed Oct 26, 2011) • 8. Wei, G. T.; Liu, F.K.; Wang C. Shape Separation of Nanometer Gold Particles bySize-Exclusion Chromatography. Anal. Chem.1999,71, 2085-2091 • 9.Skoog, D.A.; Holler, F. J.; Crouch, S. R. Principles of Instrumental Analysis, 6th ed.; Cengage Learning: California, 2007.