Laser induced fluorescence spectroscopy of various carbon nanostructures (GO, G and nanodiamond) in Rd6G solution

Biomedical Optics Express

Volumn 6, Issue 5, 2015, Pages 1679-1693

  Bavali, A ^a   Parvin, P ^a   Mortazavi, S Z ^b   Nourazar, S S ^a  

^a AMIRKABIR UNIVERSITY OF TECHNOLOGY   (Iran)

^b IMAM KHOMEINI INTERNATIONAL UNIVERSITY   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

ENERGY TRANSFER; FLUORESCENCE; FLUORESCENCE MICROSCOPY; FLUORESCENCE SPECTROSCOPY; GRAPHENE; LASER OPTICS; LASER PRODUCED PLASMAS; NANOSTRUCTURES; OPTICAL PROPERTIES; QUENCHING; SCATTERING PARAMETERS;

CARBON NANOSTRUCTURES; FLUORESCENCE QUENCHING; FLUORESCENT SPECIES; LASER INDUCED FLUORESCENCE; LASER INDUCED FLUORESCENCE SPECTROSCOPY; RESONANCE ENERGY TRANSFER; SPECTRAL PROPERTIES; SURFACE FUNCTIONALITIES;

NANODIAMONDS;

GRAPHENE; GRAPHENE OXIDE; NANODIAMOND; NANOMATERIAL; RHODAMINE 6G;

ARTICLE; BLUE SHIFT; CONCENTRATION RESPONSE; CUVETTE; EXCITATION; FLUORESCENCE RESONANCE ENERGY TRANSFER; FLUORESCENCE SPECTROSCOPY; LASER INDUCED FLUORESCENCE SPECTROSCOPY; LIGHT EXPOSURE; LIGHT RELATED PHENOMENA; MATHEMATICAL PHENOMENA; NONLINEAR REGRESSION ANALYSIS; PHOTOCHEMICAL QUENCHING; PLOTS AND CURVES; RED SHIFT; SPECTRAL SENSITIVITY; ULTRAVIOLET SPECTROPHOTOMETRY;

EID: 84948765627     PISSN: None     EISSN: 21567085     Source Type: Journal    
DOI: 10.1364/BOE.6.001679     Document Type: Article

References (56)

1. A. S. Thakor and S. S. Gambhir, “Nanooncology: The future of cancer diagnosis and therapy,” CA Cancer J. Clin. 63(6), 395–418 (2013).
2. X. Wang, L. Yang, Z. G. Chen, and D. M. Shin, “Application of nanotechnology in cancer therapy and imaging,” CA Cancer J. Clin. 58(2), 97–110 (2008).
3. K. Y. Win and S. S. Feng, “In vitro and in vivo studies on vitamin E TPGS-emulsified poly(D,L-lactic-coglycolic acid) nanoparticles for paclitaxel formulation,” Biomaterials 27(10), 2285–2291 (2006).
4. M. Ferrari, “Cancer nanotechnology: opportunities and challenges,” Nat. Rev. Cancer 5(3), 161–171 (2005).
5. K. C. Li, S. D. Pandit, S. Guccione, and M. D. Bednarski, “Molecular imaging applications in nanomedicine,” Biomed. Microdevices 6(2), 113–116 (2004).
6. H. C. Huang, S. Barua, G. Sharma, S. K. Dey, and K. Rege, “Inorganic nanoparticles for cancer imaging and therapy,” J. Control. Release 155(3), 344–357 (2011).
7. X. Y. Yang, X. Y. Zhang, Z. F. Liu, Y. F. Ma, Y. Huang, and Y. S. Chen, “High efficiency loading and controlled release of doxorubicin hydrochloride on graphene oxide,” J. Phys. Chem. C 112(45), 17554–17558 (2008).
8. D. Konios, M. M. Stylianakis, E. Stratakis, and E. Kymakis, “Dispersion behaviour of graphene oxide and reduced graphene oxide,” J. Colloid Interface Sci. 430, 108–112 (2014).
9. S. Z. Mortazavi, P. Parvin, and A. Reyhani, “Fabrication of graphene based on Q-switched Nd:YAG laser ablation of graphite target in liquid nitrogen,” Laser Phys. Lett. 9(7), 547–552 (2012).
10. F. Schedin, A. K. Geim, S. V. Morozov, E. W. Hill, P. Blake, M. I. Katsnelson, and K. S. Novoselov, “Detection of individual gas molecules adsorbed on graphene,” Nat. Mater. 6(9), 652–655 (2007).
11. C. Stampfer, E. Schurtenberger, F. Molitor, J. Güttinger, T. Ihn, and K. Ensslin, “Tunable graphene single electron transistor,” Nano Lett. 8(8), 2378–2383 (2008).
12. D. A. Dikin, S. Stankovich, E. J. Zimney, R. D. Piner, G. H. B. Dommett, G. Evmenenko, S. T. Nguyen, and R. S. Ruoff, “Preparation and characterization of graphene oxide paper,” Nature 448(7152), 457–460 (2007).
13. Z. Liu, J. T. Robinson, X. Sun, and H. Dai, “PEGylated nanographene oxide for delivery of water-insoluble cancer drugs,” J. Am. Chem. Soc. 130(33), 10876–10877 (2008).
14. X. Yang, Y. Wang, X. Huang, Y. Ma, Y. Huang, R. Yang, H. Duan, and Y. Chen, “Multi-functionalized graphene oxide based anticancer drug-carrier with dual-targeting function and pH-sensitivity,” J. Mater. Chem. 21(10), 3448–3454 (2011).
15. K. Yang, S. Zhang, G. Zhang, X. Sun, S. T. Lee, and Z. Liu, “Graphene in mice: ultrahigh in vivo tumor uptake and efficient photothermal therapy,” Nano Lett. 10(9), 3318–3323 (2010).
16. L. Feng and Z. Liu, “Graphene in biomedicine: opportunities and challenges,” Nanomedicine (Lond) 6(2), 317–324 (2011).
17. L. Zhang, J. Xia, Q. Zhao, L. Liu, and Z. Zhang, “Functional graphene oxide as a nanocarrier for controlled loading and targeted delivery of mixed anticancer drugs,” Small 6(4), 537–544 (2010).
18. Y. Yang, Y. M. Zhang, Y. Chen, D. Zhao, J. T. Chen, and Y. Liu, “Construction of a graphene oxide based noncovalent multiple nanosupramolecular assembly as a scaffold for drug delivery,” Chemistry 18(14), 4208–4215 (2012).
19. A. J. Shen, D. L. Li, X. J. Cai, C. Y. Dong, H. Q. Dong, H. Y. Wen, G. H. Dai, P. J. Wang, and Y. Y. Li, “Multifunctional nanocomposite based on graphene oxide for in vitro hepatocarcinoma diagnosis and treatment,” J. Biomed. Mater. Res. A 100(9), 2499–2506 (2012).
20. S. He, B. Song, D. Li, C. Zhu, W. Qi, Y. Wen, L. Wang, S. Song, H. Fang, and C. Fan, “A Graphene Nanoprobe for Rapid, Sensitive, and Multicolor Fluorescent DNA Analysis,” Adv. Funct. Mater. 20(3), 453–459 (2010).
21. A. M. Schrand, S. A. C. Hens, and O. A. Shenderova, “Nanodiamond particles: Properties and perspectives for bioapplications,” Crit. Rev. Solid State Mater. Sci. 34(1), 18–74 (2009).
22. A. D. Salaam, P. Hwang, R. McIntosh, H. N. Green, H.-W. Jun, and D. Dean, “Nanodiamond-DGEA peptide conjugates for enhanced delivery of doxorubicin to prostate cancer,” Beilstein J Nanotechnol 5, 937–945 (2014).
23. Y. R. Chang, H. Y. Lee, K. Chen, C. C. Chang, D. S. Tsai, C. C. Fu, T. S. Lim, Y. K. Tzeng, C. Y. Fang, C. C. Han, H. C. Chang, and W. Fann, “Mass production and dynamic imaging of fluorescent nanodiamonds,” Nat. Nanotechnol. 3(5), 284–288 (2008).
24. M. Keraji, F. H. Mirzaee, A. Bavali, H. Mehravaran, and P. Parvin, “Laser induced fluorescence and breakdown spectroscopy and acoustic response, to discriminate malignant and normal tissues,” in Clinical and Biomedical Spectroscopy and Imaging III, V. Deckert and N. Ramanujam, eds., Vol. 8798 of SPIE Proceedings (Optical Society of America, 2013), paper 87980A.
25. M. Goutayer, S. Dufort, V. Josserand, A. Royère, E. Heinrich, F. Vinet, J. Bibette, J. L. Coll, and I. Texier, “Tumor targeting of functionalized lipid nanoparticles: Assessment by in vivo fluorescence imaging,” Eur. J. Pharm. Biopharm. 75(2), 137–147 (2010).
26. W. J. Akers, C. Kim, M. Berezin, K. Guo, R. Fuhrhop, G. M. Lanza, G. M. Fischer, E. Daltrozzo, A. Zumbusch, X. Cai, L. V. Wang, and S. Achilefu, “Non-invasive photoacoustic and fluorescence sentinel lymph node identification using dye-loaded per fluorocarbon nanoparticles,” ACS Nano 5(1), 173–182 (2011).
27. A. Paganin-Gioanni, E. Bellard, L. Paquereau, V. Ecochard, M. Golzio, and J. Teissié, “Fluorescence imaging agents in cancerology,” Radiol. Oncol. 44(3), 142–148 (2010).
28. X. F. Zhang and Q. Xi, “A graphene sheet as an efficient electron acceptor and conductor for photoinduced charge separation,” Carbon 49(12), 3842–3850 (2011).
29. A. Wojcik and P. V. Kamat, “Reduced Graphene Oxide and Porphyrin. An Interactive Affair in 2-D,” ACS Nano 4(11), 6697–6706 (2010).
30. Y. Liu, C.-Y. Liu, and Y. Liu, “Investigation on fluorescence quenching of dyes by graphite oxide and graphene,” Appl. Surf. Sci. 257(13), 5513–5518 (2011).
31. S. T. Huang, Y. Shi, N. B. Li, and H. Q. Luo, “Fast and sensitive dye-sensor based on fluorescein/reduced graphene oxide complex,” Analyst (Lond.) 137(11), 2593–2599 (2012).
32. X.-F. Zhang and F. Li, “Interaction of graphene with excited and ground state rhodamine revealed by steady state and time resolved fluorescence,” J. Photochem. Photobiol. Chem. 246(15), 8–15 (2012).
33. R. Zhang, M. Hummelga, G. Lv, and H. Olin, “Real time monitoring of the drug release of rhodamine B on graphene oxide,” Carbon 49(4), 1126–1132 (2011).
34. R. S. Swathi and K. L. Sebastian, “Resonance energy transfer from a dye molecule to graphene,” J. Chem. Phys. 129(5), 054703 (2008).
35. R. S. Swathi and K. L. Sebastian, “Long range resonance energy transfer from a dye molecule to graphene has (distance)-4 dependence,” J. Chem. Phys. 130(8), 086101 (2009).
36. S. A. Ahmed, Z. W. Zang, K. M. Yoo, M. A. Ali, and R. R. Alfano, “Effect of multiple light scattering and selfabsorption on the fluorescence and excitation spectra of dyes in random media,” Appl. Opt. 33(13), 2746–2750 (1994).
37. S. Fan, X. Zhang, Q. Wang, C. Zhang, Z. Wang, and R. Lan, “Inflection point of the spectral shifts of the random lasing in dye solution with TiO2 nano scatterers,” J. Phys. D Appl. Phys. 42(1), 015105 (2009).
38. A. Bavali, P. Parvin, S. Z. Mortazavi, M. Mohammadian, and M. R. Mousavi Pour, “Red/Blue Spectral Shifts of Laser-Induced Fluorescence Emission Due to Different Nanoparticle Suspensions in Various Dye Solutions,” Appl. Opt. 53(24), 5398–5409 (2014).
39. K. Huang and A. Rhys, “Theory of light absorption and non-radiative transitions in F-centres,” Proc. R. Soc. Lond. A. 204(1078), 406–423 (1950).
40. J. R. Lakowicz, Principles of Fluorescence Spectroscopy (Springer, 2006).
41. K. Busch, C. M. Soukoulis, and E. N. Economou, “Transport and scattering mean free paths of classical waves,” Phys. Rev. B Condens. Matter 50(1), 93–98 (1994).
42. F. Scheffold, R. Lenke, R. Tweer, and G. Maret, “Localization or classical diffusion of light,” Nature 398(6724), 206–207 (1999).
43. C. F. Bohren and D. R. Huffmann, Absorption and scattering of light by small particles (Wiley-Interscience, 1983).
44. F. L. Arbeloa, P. R. Ojeda, and I. L. Arbeloa, “Fluorescence Self-Quenching of the Molecular forms of Rhodamine B in Aqueous and Ethanolic Solution,” J. Lumin. 44(1–2), 105–112 (1989).
45. J. Yi, G. Feng, L. Yang, K. Yao, C. Yang, Y. Song, and S. Zhou, “Behaviors of the Rh6G random laser comprising solvents and scatterers with different refractive indices,” Opt. Commun. 285(24), 5276–5282 (2012).
46. K. Fan, Z. Guo, Z. Geng, J. Ge, S. Jiang, J. Hu, and Q. Zhang, “How graphene oxide quenches fluorescence of rhodamine,” Chin. J. Chem. Phys. 26(3), 252–258 (2013).
47. M. A. Ali, J. Moghaddasi, and S. A. Ahmed, “Optical properties of cooled rhodamine B in ethanol,” J. Opt. Soc. Am. B. 8(9), 1807–1810 (1991).
48. R. Vogel, P. Meredith, M. D. Harvey, and H. Rubinsztein-Dunlop, “Absorption and Fluorescence Spectroscopy of Rhodamine 6G in Titanium Dioxide Nanocomposites,” Spectrochim. Acta A Mol. Biomol. Spectrosc. 60(1- 2), 245–249 (2004).
49. A. Penzkofer and W. Leupacher, “Fluorescence behavior of highly concentrated Rhodamine 6G solutions,” J. Lumin. 37(2), 61–72 (1987).
50. D. Wu, F. Zhang, H. Liang, and X. Feng, “Nanocomposites and macroscopic materials: Assembly of chemically modified graphene sheets,” Chem. Soc. Rev. 41(18), 6160–6177 (2012).
51. H. Ren, D. D. Kulkarni, R. Kodiyath, W. Xu, I. Choi, and V. V. Tsukruk, “Competitive adsorption of dopamine and rhodamine 6G on the surface of graphene oxide,” ACS Appl. Mater. Interfaces 6(4), 2459–2470 (2014).
52. K. P. Loh, Q. Bao, G. Eda, and M. Chhowalla, “Graphene oxide as a chemically tunable platform for optical applications,” Nat. Chem. 2(12), 1015–1024 (2010).
53. A. De Vita, G. Galli, A. Canning, and R. Car, “A microscopic model for surface-induced diamond-to-graphite transitions,” Nature 379(6565), 523–526 (1996).
54. J. T. Paci, H. B. Man, B. Saha, D. Ho, and G. C. Schatz, “Understanding the surfaces of nanodiamonds,” J. Phys. Chem. C 117(33), 17256–17267 (2013).
55. S. Z. Mortazavi, P. Parvin, A. Reyhani, S. Mirershadi, and R. Sadighi-Bonabi, “Generation of various carbon nanostructures in water using IR/UV laser ablation,” J. Phys. D Appl. Phys. 46(16), 165303 (2013).
56. G. Gomez-Santos and T. Stauber, “Fluorescence quenching in graphene: A fundamental ruler and evidence for transverse plasmons,” Phys. Rev. B 84(16), 165438 (2011).