Selective detection of dopamine in the presence of ascorbic acid via fluorescence quenching of inp/zns quantum dots

International Journal of Nanomedicine

Volumn 10, Issue , 2015, Pages 113-119

  Ankireddy, Seshadri Reddy ^a   Kim, Jongsung ^a  

^a Gachon University College of Medicine   (South Korea)

Author keywords

Ascorbic acid; InP ZnS QDs; L dopamine; Neurotransmitter; Parkinson s disease; Photoluminescence

Indexed keywords

ASCORBIC ACID; DOPAMINE; FLUORESCENT DYE; INDIUM; INDIUM PHOSPHIDE; PHOSPHINE DERIVATIVE; QUANTUM DOT; SULFIDE; ZINC DERIVATIVE; ZINC SULFIDE;

CHEMISTRY; LIMIT OF DETECTION; PROCEDURES; SPECTROFLUOROMETRY;

ASCORBIC ACID; DOPAMINE; FLUORESCENT DYES; INDIUM; LIMIT OF DETECTION; PHOSPHINES; QUANTUM DOTS; SPECTROMETRY, FLUORESCENCE; SULFIDES; ZINC COMPOUNDS;

EID: 84947426231     PISSN: 11769114     EISSN: 11782013     Source Type: Journal    
DOI: 10.2147/IJN.S88388     Document Type: Article

References (26)

1. Wood V, Halpert JE, Panzer MJ, Bawendi MG, Bulović V. Alternating current driven electroluminescence from ZnSe/ZnS:Mn/ZnS nanocrystals. Nano Lett. 2009;9:2367–2371.
2. Klimov VI, Mikhailovsky AA, Xu S, et al. Optical gain and stimulated emission in nanocrystal quantum dots. Science. 2000;290:314–317.
3. 2+ ions. J Colloid Interface Sci. 2009;339:78–82.
4. Xu B, Cai B, Liu M, Fan H. Microwave synthesis of water-dispersed cdte/cds/zns core-shell-shell quantum dots with excellent photostabilityand biocompatibility. Adv Mater. 2008;20:3416–3421.
5. Durgadas CV, Sreenivasan K, Sharma CP. Bright blue emitting CuSe/ ZnS/silica core/shell/shell quantum dots and their biocompatibility. Biomaterials. 2012;33:6420–6429.
6. Lin L, Chen J, Yao H, Chen Y, Zheng Y, Lin X. Simultaneous determination of dopamine, ascorbic acid and uric acid at poly (Evans Blue) modified glassy carbon electrode. Bioelectrochemistry. 2008;73:11–17.
7. Kalimuthu P, John SA. Electropolymerized film of functionalized thiadiazole on glassy carbon electrode for the simultaneous determination of ascorbic acid, dopamine and uric acid. Bioelectrochemistry. 2009;77: 13–18.
8. Giros B, Caron MG. Molecular characterization of the dopamine transporter. Trends Pharmacol Sci. 1993;14:43–43.
9. Usiello A, Baik JH, Rougé-Pont F, et al. Distinct functions of the two isoforms of dopamine D2 receptors. Nature. 2000;408:199–203.
10. Darvas M, Palmiter RD. Restricting dopaminergic signaling to either dorsolateral or medial striatum facilitates cognition. J Neurosci. 2010; 30:1158–1165.
11. Robinson DL, Hermans A, Seipel AT, Wightman RM. Monitoring rapid chemical communication in the brain. Chem Rev. 2008;108: 2554–2584.
12. Nikolaus S, Antke C, Müller H-W. In vivo imaging of synaptic function in the central nervous system: I. Movement disorders and dementia. Behav Brain Res. 2009;204:1–31.
13. Yi S-Y, Chang H-Y, Cho H-H, Park YC, Lee SH, Bae ZU. Resolution of dopamine and ascorbic acid using nickel(II) complex polymer-modified electrodes. J Electroanal Chem. 2007;602:217–225.
14. George O, Moal ML, Koob GF. Allostasis and addiction: role of the dopamine and corticotropin-releasing factor systems. Physiol Behav. 2012;106:58–64.
15. O’Neill RD. Microvoltammetric techniques and sensors for monitoring neurochemical dynamics in vivo. A review. Analyst. 1994;119: 767–779.
16. Capella P, Ghasemzadeh MB, Mitchell K, Adams RN. Nafion-coated carbon fiber electrodes for neurochemical studies in brain tissue. Electroanalysis. 1990;2:175–182.
17. Li L, Liu H, Shen Y, Zhang J, Zhu JJ. Electrogenerated chemiluminescence of Au nanoclusters for the detection of dopamine. Anal Chem. 2011;83:661–665.
18. Liu Q, Zhu X, Huo Z, He X, Liang Y, Xu M. Electrochemical detection of dopamine in the presence of ascorbic acid using PVP/graphene modified electrodes. Talanta. 2012;97:557–562.
19. Zhao Y, Zhao S, Huang J, Ye F. Quantum dot-enhanced chemiluminescence detection for simultaneous determination of dopamine and epinephrine by capillary electrophoresis. Talanta. 2012;85:2650–2654.
20. Liu L, Li S, Liu L, Deng D, Xia N. Simple, sensitive and selective detection of dopamine using dithiobis (succinimidyl propionate)modified gold nanoparticles as colorimetric probes. Analyst. 2012; 137:3794–3799.
21. Nikolajsen RPH, Hansen ÅM. Analytical methods for determining urinary catecholamines in healthy subjects. Anal Chim Acta. 2001;449: 1–15.
22. Zhang L, Teshima N, Hasebe T, Kurihara M, Kawashima T. Flowinjection determination of trace amounts of dopamine by chemiluminescence detection. Talanta. 1999;50:677–683.
23. Zhou Z, Wang Q. An efficient optical-electrochemical dual probe for highly sensitive recognition of dopamine based on terbium complex functionalized reduced graphene oxide. Nanoscale. 2014;6: 4583–4586.
24. Li Z, Li W, Cheng Y, Hao L. Chemiluminescent detection of DNA hybridization and single-nucleotide polymorphisms on a solid surface using target-primed rolling circle amplification. Analyst. 2008;133: 1164–1168.
25. Zhao D, Song H, Hao L, Liu X, Zhang L, Lv Y. Luminescent ZnO quantum dots for sensitive and selective detection of dopamine. Talanta. 2013;107:133–139.
26. Ariffin N, Yusof NA, Abdullah J, et al. Synthesis and surface modification of biocompatible water soluble core-shell quantum dots. Adv Mater Res. 2014;879:184–190.