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      Detection and Spatial Mapping of Mercury Contamination in Water Samples Using a Smart-Phone

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          Abstract

          Detection of environmental contamination such as trace-level toxic heavy metal ions mostly relies on bulky and costly analytical instruments. However, a considerable global need exists for portable, rapid, specific, sensitive, and cost-effective detection techniques that can be used in resource-limited and field settings. Here we introduce a smart-phone-based hand-held platform that allows the quantification of mercury(II) ions in water samples with parts per billion (ppb) level of sensitivity. For this task, we created an integrated opto-mechanical attachment to the built-in camera module of a smart-phone to digitally quantify mercury concentration using a plasmonic gold nanoparticle (Au NP) and aptamer based colorimetric transmission assay that is implemented in disposable test tubes. With this smart-phone attachment that weighs <40 g, we quantified mercury(II) ion concentration in water samples by using a two-color ratiometric method employing light-emitting diodes (LEDs) at 523 and 625 nm, where a custom-developed smart application was utilized to process each acquired transmission image on the same phone to achieve a limit of detection of ∼3.5 ppb. Using this smart-phone-based detection platform, we generated a mercury contamination map by measuring water samples at over 50 locations in California (USA), taken from city tap water sources, rivers, lakes, and beaches. With its cost-effective design, field-portability, and wireless data connectivity, this sensitive and specific heavy metal detection platform running on cellphones could be rather useful for distributed sensing, tracking, and sharing of water contamination information as a function of both space and time.

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          Most cited references32

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          Ecological effects, transport, and fate of mercury: a general review

          Chemosphere, 40(12), 1335-1351
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            MercuryII-mediated formation of thymine-HgII-thymine base pairs in DNA duplexes.

            The very specific binding of the HgII ion unexpectedly and significantly stabilizes naturally occurring thymine-thymine base mispairing in DNA duplexes. Following this finding, we prepared DNA duplexes containing metal-mediated base pairs at the desired sites, as well as novel double helical architectures consisting only of thymine-HgII-thymine pairs.
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              Point-of-care colorimetric detection with a smartphone.

              Paper-based immunoassays are becoming powerful and low-cost diagnostic tools, especially in resource-limited settings. Inexpensive methods for quantifying these assays have been shown using desktop scanners, which lack portability, and cameras, which suffer from the ever changing ambient light conditions. In this work, we introduce a novel approach of quantifying colors of colorimetric diagnostic assays with a smartphone that allows high accuracy measurements in a wide range of ambient conditions, making it a truly portable system. Instead of directly using the red, green, and blue (RGB) intensities of the color images taken by a smartphone camera, we use chromaticity values to construct calibration curves of analyte concentrations. We demonstrate the high accuracy of this approach in pH measurements with linear response ranges of 1-12. These results are comparable to those reported using a desktop scanner or silicon photodetectors. To make the approach adoptable under different lighting conditions, we developed a calibration technique to compensate for measurement errors due to variability in ambient light. This technique is applicable to a number of common light sources, such as sun light, fluorescent light, or smartphone LED light. Ultimately, the entire approach can be integrated in an "app" to enable one-click reading, making our smartphone based approach operable without any professional training or complex instrumentation.
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                Author and article information

                Journal
                ACS Nano
                ACS Nano
                nn
                ancac3
                ACS Nano
                American Chemical Society
                1936-0851
                1936-086X
                20 January 2014
                25 February 2014
                : 8
                : 2
                : 1121-1129
                Affiliations
                [1] Electrical Engineering Department, Bioengineering Department, §California NanoSystems Institute (CNSI), Department of Physics & Astronomy, and Department of Chemistry and Biochemistry, University of California, Los Angeles (UCLA) , Los Angeles, California 90095, United States
                Author notes
                [* ]Address correspondence to ozcan@ 123456ucla.edu .
                Article
                10.1021/nn406571t
                3949663
                24437470
                7fa7d3f1-eb5c-4b63-a111-623bbaa26bb2
                Copyright © 2014 American Chemical Society

                Terms of Use

                History
                : 24 December 2013
                : 19 January 2014
                Funding
                National Institutes of Health, United States
                Categories
                Article
                Custom metadata
                nn406571t
                nn-2013-06571t

                Nanotechnology
                smart-phone sensor,mercury detection,colorimetric sensor,gold nanoparticles,aptamers

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