A "turn-on" fluorescence assay for lead(II) based on the suppression of the surface energy transfer between acridine orange and gold nanoparticles

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• 作者：Xiao-Feng Wang ; Li-Ping Xiang ; Yong-Sheng Wang ; Jin-Hua Xue…
• 关键词：Fluorescence enhancement ; Competitive binding ; Fluorescent probe ; Environmental analysis ; Fluorescence lifetime ; Zeta ; potential
• 刊名：Microchimica Acta
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：183
• 期：4
• 页码：1333-1339
• 全文大小：480 KB
• 参考文献：1.Lu L, Cheng H, Liu X, Xie J, Li Q, Zhou T (2015) Assessment of regional human health risks from lead contamination in Yunnan province, southwestern China. PLoS One 10:e0119562CrossRef
  2.Monnot AD, Christian WV, Abramson MM, Follansbee MH (2015) An exposure and health risk assessment of lead (Pb) in lipstick. Food Chem Toxicol 80:253–260CrossRef
  3.Cao S, Duan X, Zhao X, Wang B, Ma J, Fan D, Sun C, He B, Wei F, Jiang G (2015) Health risk assessment of various metal(loid)s via multiple exposure pathways on children living near a typical lead-acid battery plant, China. Environ Pollut 200:16–23CrossRef
  4.Zhang D, Yin L, Meng Z, Yu A, Guo L, Wang H (2014) A sensitive fluorescence anisotropy method for detection of lead (II) ion by a G-quadruplex-inducible DNA aptamer. Anal Chim Acta 812:161–167CrossRef
  5.Tang S, Tong P, Li H, Tang J, Zhang L (2013) Ultrasensitive electrochemical detection of Pb2+ based on rolling circle amplification and quantum dots tagging. Biosens Bioelectron 42:608–611CrossRef
  6.Shokri M, Beiraghi A, Seidi S (2015) In situ emulsification microextraction using a dicationic ionic liquid followed by magnetic assisted physisorption for determination of lead prior to micro-sampling flame atomic absorption spectrometry. Anal Chim Acta 889:123–129CrossRef
  7.Wang Y, Chen H, Tang J, Ye G, Ge H, Hu X (2015) Preparation of magnetic metal organic frameworks adsorbent modified with mercapto groups for the extraction and analysis of lead in food samples by flame atomic absorption spectrometry. Food Chem 181:191–197CrossRef
  8.Sharafi K, Fattahi N, Pirsaheb M, Yarmohamadi H, Fazlzadeh Davil M (2015) Trace determination of lead in lipsticks and hair dyes using microwave-assisted dispersive liquid-liquid microextraction and graphite furnace atomic absorption spectrometry. Int J Cosmet Sci 37:489–495CrossRef
  9.Rello L, Aramendia M, Belarra MA, Resano M (2015) Lead screening in DBS by solid sampling high-resolution continuum source graphite furnace atomic absorption spectrometry: application to newborns and pregnant women. Bioanalysis 7:2057–2070CrossRef
  10.Giakisikli G, Ayala Quezada A, Tanaka J, Anthemidis AN, Murakami H, Teshima N, Sakai T (2015) Automatic on-line solid-phase extraction-electrothermal atomic absorption spectrometry exploiting sequential injection analysis for trace vanadium, cadmium and lead determination in human urine samples. Anal Sci 31:383–389CrossRef
  11.Demirtas I, Bakirdere S, Ataman OY (2015) Lead determination at ng/mL level by flame atomic absorption spectrometry using a tantalum coated slotted quartz tube atom trap. Talanta 138:218–224CrossRef
  12.Aghamohammadi M, Faraji M, Shahdousti P, Kalhor H, Saleh A (2015) Trace determination of lead, chromium and cadmium in herbal medicines using ultrasound-assisted emulsification microextraction combined with graphite furnace atomic absorption spectrometry. Phytochem Anal 26:209–214CrossRef
  13.Lopez-Garcia I, Vicente-Martinez Y, Hernandez-Cordoba M (2014) Determination of cadmium and lead in edible oils by electrothermal atomic absorption spectrometry after reverse dispersive liquid-liquid microextraction. Talanta 124:106–110CrossRef
  14.Soares AR, Nascentes CC (2013) Development of a simple method for the determination of lead in lipstick using alkaline solubilization and graphite furnace atomic absorption spectrometry. Talanta 105:272–277CrossRef
  15.Uemoto M, Nagaoka M, Fujinuma H (2009) Interlaboratory testing for the determination of trace amounts of tin and lead in magnesium and magnesium alloys by inductively coupled plasma atomic emission spectrometry. Anal Sci 25:717–721CrossRef
  16.Xu Y, Zhou J, Wang G, Zhou J, Tao G (2007) Determination of trace amounts of lead, arsenic, nickel and cobalt in high-purity iron oxide pigment by inductively coupled plasma atomic emission spectrometry after iron matrix removal with extractant-contained resin. Anal Chim Acta 584:204–209CrossRef
  17.Ganjali MR, Babaei LH, Badiei A, Ziarani GM, Tarlani A (2004) Novel method for the fast preconcentration and monitoring of a ppt level of lead and copper with a modified hexagonal mesoporous silica compound and inductively coupled plasma atomic emission spectrometry. Anal Sci 20:725–729CrossRef
  18.Vaisanen A, Suontamo R, Silvonen J, Rintala J (2002) Ultrasound-assisted extraction in the determination of arsenic, cadmium, copper, lead, and silver in contaminated soil samples by inductively coupled plasma atomic emission spectrometry. Anal Bioanal Chem 373:93–97CrossRef
  19.Hepp NM (2015) Determination of arsenic, chromium, lead, manganese, and mercury in certifiable color additives by inductively coupled plasma/mass spectrometry. J AOAC Int 98:160–164CrossRef
  20.Chen Y, Huang L, Wu W, Ruan Y, Wu Z, Xue Z, Fu F (2014) Speciation analysis of lead in marine animals by using capillary electrophoresis couple online with inductively coupled plasma mass spectrometry. Electrophoresis 35:1346–1352CrossRef
  21.Yilmaz V, Arslan Z, Rose L (2013) Determination of lead by hydride generation inductively coupled plasma mass spectrometry (HG-ICP-MS): on-line generation of plumbane using potassium hexacyanomanganate(III). Anal Chim Acta 761:18–26CrossRef
  22.Amarasiriwardena CJ, Jayawardene I, Lupoli N, Barnes RM, Hernandez-Avila M, Hu H, Ettinger AS (2013) Comparison of digestion procedures and methods for quantification of trace lead in breast milk by isotope dilution inductively coupled plasma mass spectrometry. Anal Methods 5:1676–1681CrossRef
  23.Vassileva E, Hoenig M (2011) Determination of the total and extractable mass fractions of cadmium and lead in mineral feed by using isotope dilution inductively coupled plasma mass spectrometry. Anal Chim Acta 701:37–44CrossRef
  24.Sun Y, Lu X, Su F, Wang L, Liu C, Duan X, Li Z (2015) Real-time fluorescence ligase chain reaction for sensitive detection of single nucleotide polymorphism based on fluorescence resonance energy transfer. Biosens Bioelectron 74:705–710CrossRef
  25.Demchenko AP (2013) Nanoparticles and nanocomposites for fluorescence sensing and imaging. Methods Appl Fluoresc 1:022001(28pp)CrossRef
  26.Miller JN (2005) Fluorescence energy transfer methods in bioanalysis. Analyst 130:265–270CrossRef
  27.Wang C, Cheng H, Sun Y, Xu Z, Lin H, Lin Q, Zhang C (2015) Nanoclusters prepared from a silver/gold alloy as a fluorescent probe for selective and sensitive determination of lead(II). Microchim Acta 182:695–701CrossRef
  28.Xu J, Li Y, Guo J, Shen F, Luo Y, Sun C (2014) Fluorescent detection of clenbuterol using fluorophore functionalized gold nanoparticles. Food Control 46:67–74CrossRef
  29.Cao X, Shen F, Zhang M, Guo J, Luo Y, Xu J, Li Y, Sun C (2014) Highly sensitive detection of melamine based on fluorescence resonance energy transfer between rhodamine B and gold nanoparticles. Dyes Pigments 111:99–107CrossRef
  30.Darbha GK, Ray A, Ray PC (2007) Gold nanoparticle-based miniaturized nanomaterial surface energy transfer probe for rapid and ultrasensitive detection of mercury in soil, water, and fish. ACS Nano 1:208–214CrossRef
  31.Farzampour L, Amjadi M (2014) Sensitive turn-on fluorescence assay of methimazole based on the fluorescence resonance energy transfer between acridine orange and silver nanoparticles. J Lumin 155:226–230CrossRef
  32.Zheng AF, Chen JL, Wu GN, Wei HCY, Kai XM, Wu GH, Chen Y (2009) Optimization of a sensitive method for the “switch-on” determination of mercury(II) in waters using rhodamine B capped gold nanoparticles as a fluorescence sensor. Microchim Acta 164:17–27CrossRef
  33.Yan YQ, Tang X, Wang YS, Li MH, Cao JX, Chen SH, Zhu YF, Wang XF, Huang YQ (2015) A sensitive and selective fluorescence assay for metallothioneins by exploiting the surface energy transfer between rhodamine 6G and gold nanoparticles. Microchim Acta 182:1353–1360CrossRef
  34.Zhou B, Wang YS, Yang HX, Xue JH, Wang JC, Liu SD, Liu H, Zhao H (2014) A sensitive resonance light scattering assay for uranyl ion based on the conformational change of a nuclease-resistant aptamer and gold nanoparticles acting as signal reporters. Microchim Acta 181:1353–1360CrossRef
  35.Guan Y, Zhou W, Yao X, Zhao M, Li Y (2006) Determination of nucleic acids based on the fluorescence quenching of hoechst 33258 at pH 4.5. Anal Chim Acta 570:21–28CrossRef
  36.Wang CI, Huang CC, Lin YW, Chen WT, Chang HT (2012) Catalytic gold nanoparticles for fluorescent detection of mercury(II) and lead(II) ions. Anal Chim Acta 745:124–130CrossRef
  37.Sitko R, Turek E, Zawisza B, Malicka E, Talik E, Heimann J, Gagor A, Feist B, Wrzalik R (2013) Adsorption of divalent metal ions from aqueous solutions using graphene oxide. Dalton Trans 42:5682–5689CrossRef
  
• 作者单位：Xiao-Feng Wang (1)
  Li-Ping Xiang (1)
  Yong-Sheng Wang (1)
  Jin-Hua Xue (1)
  Yu-Feng Zhu (1)
  Yan-Qin Huang (1)
  Si-Han Chen (1)
  Xian Tang (1)
  
  1. College of Public Health, University of South China, Hengyang, 421001, People’s Republic of China
  
• 刊物类别：Chemistry and Materials Science
• 刊物主题：Chemistry
  Analytical Chemistry
  Inorganic Chemistry
  Physical Chemistry
  Characterization and Evaluation Materials
  Monitoring, Environmental Analysis and Environmental Ecotoxicology
  
• 出版者：Springer Wien
• ISSN：1436-5073

文摘

The authors describe a strategy for fluorometric determination of lead(II) that is based on the suppression of the surface energy transfer that occurs between acridine orange and gold nanoparticles (AuNPs). As a result, the fluorescence of the system is recovered. Under optimized conditions, the enhancement of fluorescence intensity is related to the concentration of lead(II) in the 44 nM to 4.8 μM range, with a detection limit of 13 nM. The relative standard deviations for 11 determinations at concentrations of 0.386 μM, 1.93 μM and 2.89 μM are 1.02 %, 1.06 % and 1.75 %, respectively. This result suggests that the method can potentially be used to monitor the level of lead(II) in environmental samples.