Detection of 6-Thioguanine by surface-enhanced Raman scattering spectroscopy using silver nanoparticles-coated silicon wafer

Colloids and Surfaces A: Physicochemical and Engineering Aspects

Volumn 493, Issue , 2016, Pages 52-58

  Li, Hongli ^a   Chong, Xiaoli ^b   Chen, Yufeng ^b   Yang, Lei ^a   Luo, Lan ^a   Zhao, Bing ^b   Tian, Yuan ^a  

^a JILIN UNIVERSITY   (China)

^b Jilin University   (China)

Author keywords

6 Thioguanine; Internal standard; Silver nanoparticles coated silicon wafer; Surface enhanced Raman scattering

Indexed keywords

METAL NANOPARTICLES; NANOPARTICLES; RAMAN SCATTERING; SILICON; SILICON WAFERS; SILVER; SUBSTRATES;

6-THIOGUANINE; BAND INTENSITY RATIO; CORRELATION COEFFICIENT; EXPERIMENTAL PARAMETERS; INTERNAL STANDARDS; SILVER NANOPARTICLES; SURFACE ENHANCED RAMAN SCATTERING (SERS); SURFACE-ENHANCED RAMAN SCATTERING SPECTROSCOPY;

SURFACE SCATTERING;

SILICON; SILVER NANOPARTICLE; TIOGUANINE;

ARTICLE; CONTROLLED STUDY; CORRELATION COEFFICIENT; DRUG DETERMINATION; LIMIT OF DETECTION; LIMIT OF QUANTITATION; PH; PRIORITY JOURNAL; PROCESS OPTIMIZATION; RAMAN SPECTROMETRY; SENSITIVITY AND SPECIFICITY; STANDARD; TIME;

EID: 84955566687     PISSN: 09277757     EISSN: 18734359     Source Type: Journal    
DOI: 10.1016/j.colsurfa.2016.01.032     Document Type: Article

References (38)

1. Huynh T.P., Wojnarowicz A., Sosnowska M., Srebnik S., Benincori T., Sannicolò F., D'Souza F., Kutner W. Cytosine derivatized bis(2,2'-bithienyl) methane molecularly imprinted polymer for selective recognition of 6-thioguanine, an antitumor drug. Biosens. Bioelectron. 2015, 70:153-160.
2. Civcir P.U. Tautomerism of 6-thioguanine in the gas and aqueous phases using AM1 and PM3 methods. J. Mol. Struct. 2001, 536:161-171.
3. Rubin Y.V. Physical properties of anticancer drug 6-thioguanine. Proc. SPIE 2004, 5507:346-357.
4. Li B.Z. Density functional theory calculations on 7-thioguanine tautomers. Acta Chim. Sin. 2004, 62:1963-1967.
5. Harms D.O., Janka-Schaub G.E. Co-operative study group for childhood acute lymphoblastic leukemia (COALL): long-term follow-up of trials 82, 85, 89 and 92. Leukemia 2000, 14:2234-2239.
6. Hindorf U., Lindqvist M., Peterson C., Söderkvist P., Ström M., Hjortswang H., Pousette A., Almer S. Pharmacogenetics during standardised initiation of thiopurine treatment in inflammatory bowel disease. Inflamm. Bowel Dis. 2006, 55:1423-1431.
7. Louis E., Belaiche J. Optimizing treatment with thioguanine derivatives in inflammatory bowel disease. Best Pract. Res. Clin. Gastroenterol. 2003, 17:37-46.
8. Zakrzewsk R. Application of the iodine-azide postcolumn reaction in RP-HPLC for the determination of thioguanine in urine. J. Sep. Sci. 2008, 31:2199-2205.
9. Cangemi G., Barabino A., Barco S., Parodi A., Arrigo S., Melioli G. A validated HPLC method for the monitoring of thiopurine metabolites in whole blood in paediatric patients with inflammatory bowel disease. Int. J. Immunopathol. Pharmacol. 2012, 25:435-444.
10. Wu J.H., Huang M., Tang L.F., Zhang J.P., Cai K.H. A simple and rapid HPLC method for determination of 6-thioguanine concentration in human leukemic cells. Chin. J. Pharm. Anal. 2002, 22:237-239.
11. Chen D.F., Deng Z.Y. Determination of thioguanine and its related substances by RP-HPLC. Chin. J. Mod. Appl. Pharm. 2009, 26:846-849.
12. Wang W., Wang S.F., Xie F. An electrochemical sensor of non-electroactive drug 6-thioguanine based on the dsDNA/AET/Au. Sens. Actuators B 2006, 120:238-244.
13. Liu C.S., Dong C., Feng K.C. Simultaneous determination of trace of 2,6-diaminopurine and thioguanine by synchronous derivative solid substrate room temperature phosphorimetry. Chin. J. Anal. Chem. 1992, 20:993-996.
14. Bi N., Hu M., Zhu H., Qi H., Tian Y., Zhang H. Determination of 6-thioguanine based on localized surface plasmon resonance of gold nanoparticle. Spectrochim. Acta A 2013, 107:24-30.
15. Deng X.Y., Tang Y., Wu L.H., Liu L.J., Wang X., Chen Y.H., Zhang H.Q., Tian Y. Determination of 6-thioguanine based on localized surface plasmon resonance of gold nanoparticle. Chin. J. Anal. Chem. 2009, 37:79.
16. Amjadi M., Farzampour L. Selective turn-on fluorescence assay of 6-thioguanine by using harmine-modified silver nanoparticles. Luminescence 2014, 29:689-694.
17. Jana B.N.R., Pal T. Anisotropic metal nanoparticles for use as surface-enhanced Raman substrates. Adv. Mater. 2007, 19:1761-1765.
18. Le Ru E.C., Etchegoin P.G., Meyer M. Enhancement factor distribution around a single surface-enhanced Raman scattering hot spot and its relation to single molecule detection. J. Chem. Phys. 2006, 125. 204701-1-204701-13.
19. Kneipp K., Kneipp H., Itzkan I., Dasari R.R., Feld M.S. Surface-enhanced non-linear Raman scattering at the single-molecule level. Chem. Phys. 1999, 247:155-162.
20. Doering W.E., Nie S. Single-molecule and single-nanoparticle SERS: examining the roles of surface active sites and chemical enhancement. J. Phys. Chem. B 2002, 2:311-317.
21. Schatz G.C., Young M.A., Van Duyne R.P. Electromagnetic mechanism of SERS. Top. Appl. Phys. 2006, 103:19-46.
22. Mao Z., Song W., Chen L., Ji W., Xue X.X., Ruan W.D., Li Z.S., Mao H.J., Ma S., Lombardi J.R., Zhao B. Metal-semiconductor contacts induce the charge-transfer mechanism of surface-enhanced Raman scattering. J. Chem. Phys. 2011, 115:18378-18383.
23. Fan M.K., Andrade Gustavo F.S., Alexandre G., Brolo A. A review on the fabrication of substrates for surface enhanced Raman spectroscopy and their applications in analytical chemistry. Anal. Chim. Acta 2011, 693:7-25.
24. Li W.Y., Camargo P.H.C., Au L., Zhang Q., Rycenga M., Xia Y.N. Etching and dimerization: a simple and versatile route to dimers of silver nanospheres with a range of sizes. Angew. Chem. Int. Ed. 2010, 49:164-168.
25. Zhang S., Shao Y.Y., Yin G.P., Lin Y.H. Carbon nanotubes decorated with Pt nanoparticles via electrostatic self-assembly: a highly active oxygen reduction electrocatalyst. J. Mater. Chem. 2010, 20:2826-2830.
26. Marcelo G., Tarazona M.P., Saiz E. Solution properties of poly(diallyldimethylammonium chloride) (PDDA). Polymer 2005, 46:2584-2594.
27. Jiang H., Chen Z.H., Cao H.Y., Huang Y.M. The peroxidase-like activity of chitosan stabilized silver nanoparticles for visual and colorimetric detection of glucose. Analyst 2012, 137:5560-5564.
28. Chen Z.P., Fevotte G., Caillet A., Littlejohn D., Morris J. Advanced calibration strategy for in situ quantitative monitoring of phase transition processes in suspensions using FT-Raman spectroscopy. Anal. Chem. 2008, 80:6658-6665.
29. Bell S.E., Sirimuthu N.M. Quantitative surface-enhanced Raman spectroscopy. Chem. Soc. Rev. 2008, 37:1012-1024.
30. Lee P.C., Meisel D. Adsorption and surface-enhanced Raman of dyes on silver and gold sols. J. Phys. Chem. 1982, 86:3391-3395.
31. Li X.L., Xu W.Q., Zhang J.H., Jia H.Y., Yang B., Zhao B., Li B.F., Ozaki Y. Self-assembled metal colloid films: two approaches for preparing new SERS active substrates. Langmuir 2004, 20:1298-1304.
32. Meng Y.J., Lai Y.C., Jiang X.H., Zhao Q.Q., Zhan J.H. Silver nanoparticles decorated filter paper via self-sacrificing reduction for membrane extraction surface-enhanced Raman spectroscopy detection. Analyst 2013, 138:2090-2095.
33. VI) by normal Raman spectroscopy and surface-enhanced Raman spectroscopy using poly(diallyldimethylammonium) chloride-capped gold nanoparticles. Laser Phys. 2012, 22:1481-1488.
34. Szeghalmi A.V., Leopold L., Pinzaru S., Chisc V., Silaghi-Dumitrescu I., Schmitt M., Popp J., Kiefer W. Adsorption of 6-mercaptopurine and 6-mercaptopurine riboside on silver colloid: a pH dependent surface enhanced Raman spectroscopy and density functional theory study. Part I. 6-mercaptopurine. J. Mol. Struct. 2005, 735-736:103-113.
35. Skadtchenko B.O., Aroca R. Surface-enhanced Raman scattering of p-nitrothiophenol: molecular vibrations of its silver salt and the surface complex formed on silver islands and colloids. Spectrochim. Acta A 2001, 57:1009-1016.
36. Giese B., McNaughton D. Interaction of anticancer drug cisplatin with guanine: density functional theory and surface-enhanced Raman spectroscopy study. Biopolymers 2003, 72:472-489.
37. Cordes M.M., Walter J.L. Infrared and Raman studies of heterocyclic compounds-II infrared spectra and normal vibrations of benzimidazole and bis-(benzimidazolato)-metal complexes. Spectrochim. Acta A 1968, 24:1421-1435.
38. Chu H., Yang H.F., Huan S.Y., Shen G.L., Yu R.Q. Orientation of 6-mercaptopurine SAMs at the silver electrode as studied by Raman mapping and in situ SERS. J. Phys. Chem. B 2006, 110:5490-5497.