Displaying publications 1 - 20 of 114 in total

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  1. Removal performance of elemental mercury by low-cost adsorbents prepared through facile methods of carbonisation and activation of coconut husk
    Johari K, Alias AS, Saman N, Song ST, Mat H
    Waste Manag Res, 2015 Jan;33(1):81-8.
    PMID: 25492720 DOI: 10.1177/0734242X14562660
    The preparation of chars and activated carbon as low-cost elemental mercury adsorbents was carried out through the carbonisation of coconut husk (pith and fibre) and the activation of chars with potassium hydroxide (KOH), respectively. The synthesised adsorbents were characterised by using scanning electron microscopy, Fourier transform infrared spectroscopy and nitrogen adsorption/desorption analysis. The elemental mercury removal performance was measured using a conventional flow type packed-bed adsorber. The physical and chemical properties of the adsorbents changed as a result of the carbonisation and activation process, hence affecting on the extent of elemental mercury adsorption. The highest elemental mercury (Hg°) adsorption capacity was obtained for the CP-CHAR (3142.57 µg g(-1)), which significantly outperformed the pristine and activated carbon adsorbents, as well as higher than some adsorbents reported in the literature.
    Matched MeSH terms: Mercury/chemistry*
  2. Fulltext The detrimental effects of lead on human and animal health
    Assi MA, Hezmee MN, Haron AW, Sabri MY, Rajion MA
    Vet World, 2016 Jun;9(6):660-71.
    PMID: 27397992 DOI: 10.14202/vetworld.2016.660-671
    Lead, a chemical element in the carbon group with symbol Pb (from Latin: Plumbum, meaning "the liquid silver") and has an atomic number 82 in the periodic table. It was the first element that was characterized by its kind of toxicity. In animal systems, lead (Pb) has been incriminated in a wide spectrum of toxic effects and it is considered one of the persistent ubiquitous heavy metals. Being exposed to this metal could lead to the change of testicular functions in human beings as well as in the wildlife. The lead poising is a real threat to the public health, especially in the developing countries. Accordingly, great efforts on the part of the occupational and public health have been taken to curb the dangers of this metal. Hematopoietic, renal, reproductive, and central nervous system are among the parts of the human body and systems that are vulnerable toward the dangers following exposure to high level of Pb. In this review, we discussed the massive harmful impact that leads acetate toxicity has on the animals and the worrying fact that this harmful toxicant can be found quite easily in the environment and abundance. Highlighting its (Pb) effects on various organs in the biological systems, its economic, as well as scientific importance, with the view to educate the public/professionals who work in this area. In this study, we focus on the current studies and research related to lead toxicity in animals and also to a certain extent toward human as well.
    Matched MeSH terms: Mercury
  3. Fulltext Isolation and Characterisation of a Molybdenum-reducing and Metanil Yellow Dye-decolourising Bacillus sp. strain Neni-10 in Soils from West Sumatera, Indonesia
    Mansur R, Gusmanizar N, Roslan MA, Ahmad SA, Shukor MY
    Trop Life Sci Res, 2017 Jan;28(1):69-90.
    PMID: 28228917 MyJurnal DOI: 10.21315/tlsr2017.28.1.5
    A molybdenum reducing bacterium with the novel ability to decolorise the azo dye Metanil Yellow is reported. Optimal conditions for molybdenum reduction were pH 6.3 and at 34°C. Glucose was the best electron donor. Another requirement includes a narrow phosphate concentration between 2.5 and 7.5 mM. A time profile of Mo-blue production shows a lag period of approximately 12 hours, a maximum amount of Mo-blue produced at a molybdate concentration of 20 mM, and a peak production at 52 h of incubation. The heavy metals mercury, silver, copper and chromium inhibited reduction by 91.9, 82.7, 45.5 and 17.4%, respectively. A complete decolourisation of the dye Metanil Yellow at 100 and 150 mg/L occurred at day three and day six of incubations, respectively. Higher concentrations show partial degradation, with an approximately 20% decolourisation observed at 400 mg/L. The bacterium is partially identified based on biochemical analysis as Bacillus sp. strain Neni-10. The absorption spectrum of the Mo-blue suggested the compound is a reduced phosphomolybdate. The isolation of this bacterium, which shows heavy metal reduction and dye-decolorising ability, is sought after, particularly for bioremediation.
    Matched MeSH terms: Mercury
  4. Fulltext An inhibitive enzyme assay to detect mercury and zinc using protease from Coriandrum sativum
    Baskaran G, Masdor NA, Syed MA, Shukor MY
    ScientificWorldJournal, 2013;2013:678356.
    PMID: 24194687 DOI: 10.1155/2013/678356
    Heavy metals pollution has become a great threat to the world. Since instrumental methods are expensive and need skilled technician, a simple and fast method is needed to determine the presence of heavy metals in the environment. In this study, an inhibitive enzyme assay for heavy metals has been developed using crude proteases from Coriandrum sativum. In this assay, casein was used as a substrate and Coomassie dye was used to denote the completion of casein hydrolysis. In the absence of inhibitors, casein was hydrolysed and the solution became brown, while in the presence of metal ions such as Hg²⁺ and Zn²⁺, the hydrolysis of casein was inhibited and the solution remained blue. Both Hg²⁺ and Zn²⁺ exhibited one-phase binding curve with IC₅₀ values of 3.217 mg/L and 0.727 mg/L, respectively. The limits of detection (LOD) and limits of quantitation (LOQ) for Hg were 0.241 and 0.802 mg/L, respectively, while the LOD and LOQ for Zn were 0.228 and 0.761 mg/L, respectively. The enzyme exhibited broad pH ranges for activity. The crude proteases extracted from Coriandrum sativum showed good potential for the development of a rapid, sensitive, and economic inhibitive assay for the biomonitoring of Hg²⁺ and Zn²⁺ in the aquatic environments.
    Matched MeSH terms: Mercury/analysis*
  5. An evaluation of direct measurement techniques for mercury dry deposition
    Lai SO, Huang J, Hopke PK, Holsen TM
    Sci Total Environ, 2011 Mar 1;409(7):1320-7.
    PMID: 21257194 DOI: 10.1016/j.scitotenv.2010.12.032
    In this project, several surrogate surfaces designed to directly measure Hg dry deposition were investigated. Static water surrogate surfaces (SWSS) containing deionized (DI), acidified water, or salt solutions, and a knife-edge surrogate surface (KSS) using quartz fiber filters (QFF), KCl-coated QFF and gold-coated QFF were evaluated as a means to directly measure mercury (Hg) dry deposition. The SWSS was hypothesized to collect deposited elemental mercury (Hg⁰), reactive gaseous/oxidized mercury (RGM), and mercury associated with particulate matter (Hg(p)) while the QFF, KCl-coated QFF, and gold-coated QFF on the KSS were hypothesized to collect Hg(p), RGM+Hg(p), and Hg⁰+RGM+Hg(p), respectively. The Hg flux measured by the DI water was significantly smaller than that captured by the acidified water, probably because Hg⁰ was oxidized to Hg²+ which stabilized the deposited Hg and decreased mass transfer resistance. Acidified BrCl, which efficiently oxidizes Hg⁰, captured significantly more Hg than other solutions. However, of all collection media, gold-coated QFFs captured 6 to 100 times greater Hg mass than the other surfaces, probably because there is no surface resistance for Hg⁰ deposition to gold surfaces. In addition, the Hg⁰ concentration is usually 100-1000 times higher than RGM and Hg(p). For all other media, co-located samples were not significantly different, and the combination of daytime plus nighttime results were comparable to 24-h samples, implying that Hg⁰, RGM and Hg(p) were not released after they deposited nor did the surfaces reach equilibrium with the atmosphere. Based on measured Hg ambient air concentrations and fluxes, dry deposition velocities of RGM and Hg⁰ to DI water and other surfaces were 5.6±5.4 and 0.005-0.68 cm s⁻¹ in this study, respectively. These results suggest surrogate surfaces can be used to measure Hg dry deposition; however, extrapolating the results to natural surface can be challenging.
    Matched MeSH terms: Mercury/analysis*
  6. Mercury in scalp hair of healthy Singapore residents
    Foo SC, Ngim CH, Phoon WO, Lee J
    Sci Total Environ, 1988 Jun 15;72:113-22.
    PMID: 3406725
    Two hundred and twenty-five hair samples (150 Chinese, 44 Malays and 31 Indians) from healthy residents not occupationally exposed to mercury were analyzed by cold vapour atomic absorption spectrophotometry to determine their total, inorganic and organic mercury levels. The arithmetic means of total mercury levels in hair were 6.1, 5.2 and 5.4 ppm for the Chinese, Malays and Indians, respectively. Factors contributing to the amount of mercury in hair, including consumption of fish and marine products, use of traditional ethnic medicines, artificial hair waving, age, sex and ethnicity were analyzed. Fish consumption, sex and ethnicity are factors found to contribute significantly (p less than 0.05) to mercury levels in hair.
    Matched MeSH terms: Mercury/analysis*; Organomercury Compounds/analysis
  7. Selective magnetic mercury(ii) ion capturing ligand-doped silica gel for water analysis
    Khor SW, Lee YK, Tay KS
    Analyst, 2019 Mar 21;144(6):1968-1974.
    PMID: 30694266 DOI: 10.1039/c8an02362j
    Preparation of selective magnetic adsorbents for dispersive micro-solid phase extraction often involves multi-step reactions which are time consuming. This study demonstrates a simplified method for the synthesis of a magnetic adsorbent, which is selective towards the adsorption of mercury(ii) ions (Hg2+). In this method, the incorporation of a metal capturing ligand (3-oxo-1,3-diphenylpropyl-2-(naphthalen-2-ylamino) ethylcarbamodithioate) and the coating of magnetic particles with silica gel was performed in a single step. This adsorbent was then used in solid-phase microextraction for the preconcentration of Hg2+ in water. In this study, a mercury analyzer was used to quantify the Hg2+. Under optimized conditions, the developed analytical method achieved a low detection limit (4.0 ng L-1), satisfactory enrichment factor (96.4) and wide linearity range (50.0-5000 ng L-1) with a good coefficient of determination (0.9985) and good repeatability (<7%). The preconcentration factor of this method was 100. This proposed method was also successfully utilized for the determination of Hg2+ in drinking water, tap water and surface water with good recovery (>91%) and high intra-day and inter-day precision.
    Matched MeSH terms: Mercury
  8. Development of an Hg(II) fibre-optic sensor for aqueous environmental monitoring
    Ahmad M, Hamzah H, Sufliza Marsom E
    Talanta, 1998 Oct;47(2):275-83.
    PMID: 18967326
    An optical sensor for Hg(II) monitoring using a complex of zinc dithizonate immobilised on XAD 7 which is based on reflectance spectrophotometry has been developed in this study. Measurements were made using a kinetic approach whereby the reflectance signal is measured at a fixed time of 5 min. The sensor could be regenerated using a saturated solution of KCl in 1 M sulphuric acid. The sensor was found to have an optimum response at pH 3.0 with respective measurement repeatability and probe-to-probe reproducibility of 1.53% and 5.26%. A linear response was observed in the Hg(II) concentration range of 0.0-180.0 ppm with a calculated limit of detection (LOD) of 0.05 ppm. The results obtained for aqueous Hg(II) determination using this probe were found to be comparable with the well-established method of atomic absorption spectrometry.
    Matched MeSH terms: Mercury
  9. A lead(II) ion selective electrode via a metal complex of poly(hydroxamic acid)
    Anuar K, Hamdan S
    Talanta, 1992 Dec;39(12):1653-6.
    PMID: 18965586
    A new lead(II) electrode has been constructed with poly(hydroxamic acid) (PHXA) as the active material and silicone rubber as the supporting material. The electrode gave near Nerstian response over the concentration range 4 x 10(-5)-1 x 10(-2)M lead(II). The detection limit of the electrode is approximately 4 x 10(-6)M and the electrode works well in the pH range 4.5-6.0. The response time was 50-120 sec over the whole concentration range and the electrode has a working life of at least 4 weeks. Iron(III) severely poisoned the electrode membrane. Nickel(II) and mercury(II) gave very strong interference compared to copper(II), silver(I), cobalt(II), sodium(I), potassium(I), zinc(II) and cadmium(II) which gave some or little interference. Values determined with atomic absorption (AAS) and a commercial lead(II) electrode were in good agreement with those measured with the lead(II) electrode reported here.
    Matched MeSH terms: Mercury
  10. Optical test strip for trace Hg(II) based on doped sol-gel film
    Yusof NA, Kadir WA
    Spectrochim Acta A Mol Biomol Spectrosc, 2009 Feb;72(1):32-5.
    PMID: 19010723 DOI: 10.1016/j.saa.2008.07.019
    Optical test strip based on the use of Br-PADAP as a sensitive reagent immobilised into sol-gel thin film for detection of Hg(II) in aqueous solution had been thoroughly carried out. It has a square-sensing zone (1.0 cm x 1.0 cm) containing the sensitive reagent necessary to produce response to trace level of mercury. This method offer sensitivity and simplicity in detecting Hg(II) as no prior treatment or extraction is required. A linear response was attained in the Hg(II) concentration in the range of 0.5-2.5 ppm with calculated limit of detection of 6.63 ppb. This method also showed a reproducible result with relative standard deviation (R.S.D.) of 2.15% and response time of approximately 5 min. Interference studies showed that Al(III), Co(II) and Ni(II) significantly interfered during the determination. The developed sensor has been validated against Atomic Absorption Spectroscopy method and proven comparable.
    Matched MeSH terms: Mercury/analysis*
  11. Fulltext A new electrochemical sensor based on task-specific ionic liquids-modified palm shell activated carbon for the determination of mercury in water samples
    Abu Ismaiel A, Aroua MK, Yusoff R
    Sensors (Basel), 2014 Jul 21;14(7):13102-13.
    PMID: 25051034 DOI: 10.3390/s140713102
    In this study, a potentiometric sensor composed of palm shell activated carbon modified with trioctylmethylammonium thiosalicylate (TOMATS) was used for the potentiometric determination of mercury ions in water samples. The proposed potentiometric sensor has good operating characteristics towards Hg (II), including a relatively high selectivity; a Nernstian response to Hg (II) ions in a concentration range of 1.0 × 10(-9) to 1.0 × 10(-2) M, with a detection limit of 1 × 10(-10) M and a slope of 44.08 ± 1.0 mV/decade; and a fast response time (~5 s). No significant changes in electrode potential were observed when the pH was varied over the range of 3-9. Additionally, the proposed electrode was characterized by good selectivity towards Hg (II) and no significant interferences from other cationic or anionic species.
    Matched MeSH terms: Mercury/chemistry*
  12. Fulltext An overview of mercury emission sources and application of activated carbon for mercury removal from flue gas
    Hidayu Abdul Rani, Nor Fadilah Mohamad, Sherif Abdulbari Ali, Matali, Sharmeela, Sharifah Aishah Sheikh Abdul kadir
    Scientific Research Journal, 2013;10(1):0-0.
    MyJurnal
    Mercury emission into the atmosphere is a global concern due to its detrimental effects on human health in general. The two main sources of mercury emission are natural sources and anthropogenic sources. Mercury emission from natural sources include volcanic activity, weathering of rocks, water movement and biological processes which are obviously inevitable. The anthropogenic sources of mercury emission are from coal combustion, cement production and waste incineration. Thus, in order to reduce mercury emission it is appropriate to investigate how mercury is released from the anthropogenic sources and consequently the mercury removal technology that can be implemented in order to reduce mercury emission into the atmosphere. Many alternatives have been developed to reduce mercury emission and the recent application of activated carbon showed high potential in the adsorption of elemental mercury. This paper discusses the ability of activated carbon and variable parameters that influence mercury removal efficiency in flue gas.
    Matched MeSH terms: Mercury
  13. Bioaccumulation and histopathological changes induced by toxicity of mercury (hgcl2) to tilapia fish oreochromis niloticus
    Mohammed A. Jasim, Mohd Sofian-azirun, Yusoff, Motior Rahman M
    Sains Malaysiana, 2016;45:119-127.
    In this paper we have studied the acute toxicity effect of Hg on hybrid tilapia (Oreochromis niloticus). For this, the tissues of tilapia have been digested by means of acids in microwave oven and was analyzed by flameless atomic absorption spectrophotometer (FAAS). We have identified that the levels of Hg varied significantly in different tissues and the metal concentration was in the following order: liver > gills > muscles; of which the maximum level recorded for Hg was 0.799 mg/kg. We have also observed the alterations towards histopathological aspects in the gills and liver of treated fishes were studied using light and electron microscopy, subjected to the exposure of Hg for 24 h and furthermore we have also noticed the extent of the increased alterations during the 96 h of exposure to median lethal concentration LC50 (0.3 mg/L) a severe disorganization of epithelial cells and modifications of the structure of the secondary lamellae. Moreover the severity has also found to increase to sub-lethal concentration (0.03 mgHg/L) in 21 days of exposure; Liver was slightly affected by the contamination of Hg. Ultimately, histopathology is considered as a sensitive technique of bioaccumulation and for the observing the potential damage from Hg exposure.
    Matched MeSH terms: Mercury
  14. Fulltext Spatial and temporal variation on distributions of dissolved and particulate arsenic and mercury in Sungai Kuantan, Pahang
    Fikriah Faudzi, Mohd Fuad Miskon, Kamaruzzaman Yunus, Mokhlesur Rahman
    Sains Malaysiana, 2017;46:393-399.
    It is important to monitor the concentration of toxic metals in the Sungai Kuantan as it serves many communities in terms of domestic, fisheries and agriculture purpose. In order to determine the distributions of dissolved and particulate As and Hg in Sungai Kuantan and evaluate its changes temporally and spatially, water samples were collected from the surface and bottom layers in a grid of 9 stations from estuary towards the upstream of Sungai Kuantan from May 2012 till October 2012. The dissolved metals were pre-concentrated using Chelex-100 while particulate metals were digested using Teflon bomb and subsequently were analyzed using ICP-MS. Dissolved As ranging from 4.650 to 36.894 µg L-1 while dissolved Hg ranging from BDL to 0.011 µg L-1. Particulate As and Hg varied from 0.650 to 86.087 mg L-1 and BDL to 5.873 mg L-1, respectively. Higher concentration of the dissolved elements were found mainly in October 2012 and particulate elements concentration mostly higher in May 2012. The source of the studied metals in the river may be the run-off from the effluent discharges and other natural sources. The toxic elements studied in Sungai Kuantan waters were still below the Interim Marine Water Quality Standard (INWQS) permissible limits.
    Matched MeSH terms: Mercury
  15. Neutron activation analysis and assessment of trace elements in fingernail from residents of Tokyo, Japan
    Wee B, Ebihara M
    Sains Malaysiana, 2017;46:605-613.
    We report herewith the study of fingernail clippings obtained from the residents of Tokyo, Japan. A total of 18 participants with no health problems and occupational exposure to metals were recruited to provide fingernails samples for this study. Through the use of instrumental neutron activation analysis (INAA), 18 elements (Ag, Al, As, Ca, Cl, Co, Cu, Fe, Hg, K, Mg, Mn, Na, S, Sb, Se, V, and Zn) were determined. The results showed that the toxic elements in the fingernails are in the lower range when compared to literature values. There were no chronic exposures to toxic elements such as As and Hg found. The level of Hg found is lower than that reported 20 years ago, possibly due to the strict regulation control in Japan on the release of Hg to the environment. The elements Se and Zn are found to be rather uniformly distributed among participants and are in agreement with results from other countries. There were no significant differences in elemental concentrations due to genders and smoking habits. The overall data from this study showed similar concentrations to those of healthy participants from other countries. Thus, the current data could represent the background level of elemental concentrations in fingernails of residents in Tokyo, which could serve as reference values for future study.
    Matched MeSH terms: Mercury
  16. Trace metals in Thais clavigera along coastal waters of the east coast of Peninsular Malaysia
    Miskon FM, Noor Azhar Mord Shazili, Faridah Mohammad, Kamaruzzaman Yunus
    Sains Malaysiana, 2014;43:529-534.
    The selected trace metals in the soft tissue of Thais clavigera from 11 sampling sites along the coastal waters of the east coast of Peninsular Malaysia were studied. Significant inter-spatial variations in trace metals were recorded. Sites with relatively high concentrations of the contaminant metals Hg, Cd, Pb and Zn are correlated to their close proximity to industrial and urban sites or to boating and aquaculture activities. This could possibly be contributed by the high growth of industrial activities like port and sewage release. Interspatial comparison with previous studies indicated lower measurement. Meanwhile, comparison with other studies around the world also designated lower values except for Zn. The metal accumulation patterns indicated an enrichment of essential metals over non-essential metals. Comparison of metal concentration with maximum permissible limits of toxic metals in food established in different countries, as well as Malaysian Food Act 1983 and Food Regulations 1985 Fourteen Schedule, indicated the values were well within safety levels.
    Matched MeSH terms: Mercury
  17. Experimental study on permeability stress sensitivity in tight sandstone oil reservoirs
    Xiaofeng Tian, Linsong Cheng, Wenqi Zhao, Yiqun Yan, Xiaohui He, Qiang Guo
    Sains Malaysiana, 2015;44:719-725.
    In this paper, seven permeability stress sensitivity experiments were conducted to show the features of permeability stress
    sensitivity. The cores in the experiments were taken from the tight sandstone oil reservoir in Ordos Basin. Then advanced
    technologies, such as casting thin section, scanning electron microscope and rate-controlled mercury penetration, were
    applied to explain the mechanism of permeability stress sensitivity in tight oil reservoirs. The results indicated that
    the permeability reduction and recovery in gas permeability stress sensitivity increases as the permeability decreases.
    This was resulted from the maximal throat radius. The permeability reduction in liquid permeability stress sensitivity
    increases at first and then decreases as the permeability decreases. The permeability recovery decreases to zero as the
    permeability decreases. Additionally, the differences between gas and liquid permeability stress sensitivity become greater
    as the permeability decreases. These were resulted from the effect of the critical throat radius. This paper corrects the
    mistakes about the stress sensitivity in tight oil reservoirs from gas permeability stress sensitivity experiments which is
    significant to the development of tight sandstone oil reservoirs.
    Matched MeSH terms: Mercury
  18. Mercury pollution in Malaysia
    Hajeb P, Jinap S, Ismail A, Mahyudin NA
    Rev Environ Contam Toxicol, 2012;220:45-66.
    PMID: 22610296 DOI: 10.1007/978-1-4614-3414-6_2
    Although several studies have been published on levels of mercury contamination of the environment, and of food and human tissues in Peninsular Malaysia, there is a serious dearth of research that has been performed in East Malaysia (Sabah and Sarawak). Industry is rapidly developing in East Malaysia, and, hence, there is a need for establishing baseline levels of mercury contamination in environmental media in that part of the country by performing monitoring studies. Residues of total mercury and inorganic in food samples have been determined in nearly all previous studies that have been conducted; however, few researchers have analyzed samples for the presence of methlymercury residues. Because methylmercury is the most toxic form of mercury, and because there is a growing public awareness of the risk posed by methylmercury exposure that is associated with fish and seafood consumption, further monitoring studies on methylmercury in food are also essential. From the results of previous studies, it is obvious that the economic development in Malaysia, in recent years, has affected the aquatic environment of the country. Primary areas of environmental concern are centered on the rivers of the west Peninsular Malaysian coast, and the coastal waters of the Straits of Malacca, wherein industrial activities are rapidly expanding. The sources of existing mercury input to both of these areas of Malaysia should be studied and identified. Considering the high levels of mercury that now exists in human tissues, efforts should be continued, and accelerated in the future, if possible, to monitor mercury contamination levels in the coastal states, and particularly along the west Peninsular Malaysian coast. Most studies that have been carried out on mercury residues in environmental samples are dated, having been conducted 20-30 years ago; therefore, the need to collect much more and more current data is urgent. Furthermore, establishing baseline levels of mercury exposure to humans in Malaysia will be useful in establishing the levels at which detrimental effects in both humans and marine life may occur, and therefore the levels at which warning should be raised or limits established. In particular, we believe that two or three monitoring centers should be established in Peninsular Malaysia, and one in East Malaysia for the specific purpose of monitoring for the presence of hazardous environmental chemicals, and particularly monitoring for heavy metals such as mercury that reach food that is subject to consistent human consumption.
    Matched MeSH terms: Mercury/toxicity*
  19. Mercury contamination in facial skin lightening creams and its health risks to user
    Ho YB, Abdullah NH, Hamsan H, Tan ESS
    Regul Toxicol Pharmacol, 2017 Aug;88:72-76.
    PMID: 28554823 DOI: 10.1016/j.yrtph.2017.05.018
    This study aims to determine concentrations of mercury in facial skin lightening cream according to different price categories (category I:
    Matched MeSH terms: Mercury/analysis*
  20. Smartphone Assisted Naked Eye Detection of Mercury (II) Ion using Horseradish Peroxidase Inhibitive Assays
    Jamadon NK, Busairi N, Syahir A
    Protein Pept Lett, 2018;25(1):90-95.
    PMID: 29237368 DOI: 10.2174/0929866525666171214111503
    BACKGROUND: Mercury (II) ion, Hg2+ is among the most common pollutants with the ability to affect the environment. The implications of their elevation in the environment are mainly due to the industrialization and urbanization process. Current methods of Hg2+ detection primarily depend on sophisticated and expensive instruments. Hence, an alternative and practical way of detecting Hg2+ ions is needed to go beyond these limitations. Here, we report a detection method that was developed using an inhibitive enzymatic reaction that can be monitored through a smartphone. Horseradish peroxidase (HRP) converted 4-aminoantipyrene (4-AAP) into a red colored product which visible with naked eye. A colorless product, on the other hand, was produced indicating the presence of Hg2+ that inhibit the reaction.

    OBJECTIVES: The aim of this study is to develop a colorimetric sensor to detect Hg2+ in water sources using HRP inhibitive assay. The system can be incorporated with a mobile app to make it practical for a prompt in-situ analysis.

    METHODS: HRP enzyme was pre-incubated with different concentration of Hg2+ at 37°C for 1 hour prior to the addition of chromogen. The mix of PBS buffer, 4-AAP and phenol which act as a chromogen was then added to the HRP enzyme and was incubated for 20 minutes. Alcohol was added to stop the enzymatic reaction, and the change of colour were observed and analyse using UV-Vis spectrophotometer at 520 nm wavelength. The results were then analysed using GraphPad PRISM 4 for a non-linear regression analysis, and using Mathematica (Wolfram) 10.0 software for a hierarchical cluster analysis. The samples from spectroscopy measurement were directly used for dynamic light scattering (DLS) evaluation to evaluate the changes in HRP size due to Hg2+ malfunctionation. Finally, molecular dynamic simulations comparing normal and malfunctioned HRP were carried out to investigate structural changes of the HRP using YASARA software.

    RESULTS: Naked eye detection and data from UV-Vis spectroscopy showed good selectivity of Hg2+ over other metal ions as a distinctive color of Hg2+ is observed at 0.5 ppm with the IC50 of 0.290 ppm. The mechanism of Hg2+ inhibition towards HRP was further validated using a dynamic light scattering (DLS) and molecular dynamics (MD) simulation to ensure that there is a conformational change in HRP size due to the presence of Hg2+ ions. The naked eye detection can be quantitatively determined using a smartphone app namely ColorAssist, suggesting that the detection signal does not require expensive instruments to be quantified.

    CONCLUSION: A naked-eye colorimetric sensor for mercury ions detection was developed. The colour change due to the presence of Hg2+ can be easily distinguished using an app via a smartphone. Thus, without resorting to any expensive instruments that are mostly laboratory bound, Hg2+ can be easily detected at IC50 value of 0.29 ppm. This is a promising alternative and practical method to detect Hg2+ in the environment.

    Matched MeSH terms: Mercury/analysis*
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