Fluorescence properties of the anti-tumour alkaloid luotonin A and new synthetic analogues: PH modulation as an approach to their fluorimetric quantitation in biological samples

Journal of Luminescence

Volumn 132, Issue 9, 2012, Pages 2468-2475

  González Ruiz, Víctor ^a   González Cuevas, Yamisley ^a   Arunachalam, Sankaralingam ^a   Martín, M Antonia ^a   Olives, Ana I ^a   Ribelles, Pascual ^a   Ramos, M Teresa ^a   Menéndez, J Carlos ^a  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

Author keywords

1H and 13C NMR spectroscopy; Anti tumour agents; ESPT; Luotonin A; Steady state fluorescence; UV Vis spectrophotometry

Indexed keywords

ACID-BASE TITRATION; ACIDIC CONDITIONS; AQUEOUS MEDIA; BASIC NITROGEN; BIOLOGICAL SAMPLES; CAMPTOTHECIN (CPT); EMISSION SPECTRUMS; ESPT; FLUORESCENCE PROPERTIES; FLUORESCENCE QUANTUM YIELD; FLUORIMETRIC; GOOD CORRELATIONS; LUOTONIN A; NATIVE FLUORESCENCE; NEW EMISSION BAND; NITROGEN ATOM; ORGANIC MEDIA; PH VALUE; POLAR COMPOUNDS; SOLVENT POLARITY; STEADY-STATE FLUORESCENCE; SYNTHETIC ANALOGUES; TRANSFER EQUILIBRIUM; UV-VIS-SPECTROPHOTOMETRY; WEAK BASIS;

ACETONITRILE; ALKALINITY; EMISSION SPECTROSCOPY; ETHANOL; METABOLITES; NITROGEN COMPOUNDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; ORGANIC SOLVENTS; PROTONATION; QUANTUM YIELD; SOLUTIONS; SOLVENTS; TITRATION;

FLUORESCENCE;

EID: 84861011060     PISSN: 00222313     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jlumin.2012.03.056     Document Type: Article

References (49)

1. A.P. Demchenko Introduction to Fluorescence Sensing 2009 Springer Berlin
2. M. Hof, R. Hutterrer, V. Fidler (Eds.), Fluorescence Spectroscopy in Biology: Advanced Methods and Their Applications to Membranes, Proteins, DNA, and Cells, Springer, Berlin, 2005.
3. B. Valeur Molecular Fluorescence. Principles and Applications 2001 Wiley-VCH Weinheim
4. J.R. Lakowicz Principles of Fluorescence Spectroscopy 3rd Edn. 2006 Springer
5. R.H. Newman, M.D. Fosbrink, and J. Zhang Chem. Rev. 111 2011 3614 3666
6. X. Fang, and W. Tang Acc. Chem. Res. 43 2010 48 57
7. J. Guo, L. Yu, N.J. Turro, and J. Ju Acc. Chem. Res. 43 2010 551 563
8. Y. Sun, S. Bi, D. Song, C. Quiao, D. Mu, and H. Zhang Sens. Actuators B Chem. 129 2008 799 810
9. L. He, X. Wang, B. Liu, J. Wang, Y. Sun, E. Gao, and S. Xu J. Lumin. 131 2011 285 290
10. Y. Yue, Y. Zhang, Y. Li, J. Zhu, J. Qin, and X. Chen J. Lumin. 128 2008 513 520
11. G.-W. Song, Z.-X. Cai, Y. He, and Z.-W. Lou Sens. Actuators B Chem. 102 2004 320 324
12. P. Mussardo, E. Corda, V. González-Ruiz, J. Rajesh, S. Girotti, M.A. Martín, and A.I. Olives Anal. Bioanal. Chem. 400 2011 321 327
13. P. Zuck, G.T. ODonnell, J. Cassaday, P. Chase, P. Hodder, B. Strulovici, and M. Ferrer Anal. Biochem. 342 2005 254 259
14. R.A. Pufahl, T.P. Kasten, R. Hills, J.K. Gierse, B.A. Reitz, R.A. Weinberg, and J.L. Masferrer Anal. Biochem. 364 2007 204 212
15. E. Gravel, P. Bourget, L. Mercier, and A. Paci J. Pharm. Biomed. Anal. 39 2005 581 586
16. P.M. Loadman, and C.R. Calabrese J. Chromatogr. B 764 2001 193 206
17. M. Espinosa-Bosch, A.J. Ruiz-Sánchez, F. Sánchez-Rojas, and C. Bosch-Ojeda J. Pharm. Biomed. Anal. 48 2008 519 532
18. Z.-Z. Ma, Y. Hano, T. Nomura, and Y.-J. Chen Heterocycles 46 1997 541 546
19. K. Nacro, C. Zha, P.R. Guzzo, R.J. Herr, D. Peace, and T.D. Friedrich Bioorg. Med. Chem. 15 2007 4237 4246
20. C. Avendaño, and J.C. Menéndez Medicinal Chemistry of Anticancer Drugs 2008 Elsevier Amsterdam chapter 7
21. B.A. Teicher Biochem. Pharmacol. 75 2008 1262 1271
22. V.J. Venditto, and E.E. Simanek Mol. Pharmaceutics 7 2010 307 349
23. Y. Pommier, E. Leo, H.L. Zhang, and C. Marchand Chem. Biol. 17 2010 421 433
24. J.F. Pizzolato, and L.B. Saltz Lancet 361 2003 2235 2242
25. A. Cagir, S.H. Jones, R. Gao, B.M. Eisenhauer, and S.M. Hecht J. Am. Chem. Soc. 125 2003 13628 13629
26. C.J. Thomas, N.J. Rahier, and S.M. Hecht Bioorg. Med. Chem. 12 2004 1585 1604
27. Z. Ma, Y. Hano, and T. Nomura Heterocycles 65 2005 2203 2219
28. N. Malecki, P. Carato, B. Rigo, J.-F. Goossens, R. Houssin, C. Bailly, and J.-P. Hénicharta Bioorg. Med. Chem. 12 2004 641 647
29. V. Sridharan, P. Ribelles, M.T. Ramos, and J.C. Menéndez J. Org. Chem. 74 2009 5715 5718
30. J.L. Liang, H.C. Cha, and Y. Jahng Molecules 16 2011 4861 4883
31. J.-J. Aaron, and S. Trajkovska Curr. Drug Targets 7 2006 1067 1081
32. Z.P. Hu, X.X. Yang, X. Chen, E. Chan, and W. Duan J. Chromatogr. B 850 2007 575 580
33. X. Liu, Y. Wang, D. Vardeman, Z. Cao, and B. Giovanella J. Chromatogr. B 867 2008 84 89
34. T. Oguma J. Chromatogr. B 764 2001 49 58
35. V. González-Ruiz, P. Mussardo, E. Corda, S. Girotti, A.I. Olives, and M.A. Martín J. Sep. Sci. 33 2010 2086 2093
36. J.W. Eastman Photochem. Photobiol. 6 1967 55 72
37. W.S. Haynes (Ed.) CRC Handbook of Chemistry and Physics, 92nd Ed., CRC Press, Boca Raton, 2011.
38. British Pharmacopoeia Commission Office British Pharmacopoeia, Apendix VIII A vol.4 2009 Stationery Office (MHRA) London
39. J. Dey, and I.M. Warner J. Lumin. 71 1997 105 114
40. Y. Posokhov, H. Biner, and S. Icli J. Photochem. Photobiol. A: Chem. 158 2003 13 20
41. E.L. Wehry Effects of Molecular Environment on Fluorescence and Phosphorecence G.G. Guilbault, Practical Fluorescence 1990 Marcel Dekker Inc. New York
42. S.K. Droga J. Lumin. 114 2005 101 117
43. J. Dey, and I.M. Warner J. Photochem. Photobiol. A: Chem. 116 1998 27 37
44. A. Albert, and E.P. Serjeant The Determination of Ionization Constants A Laboratory Manual 1984 Chapman and Hall London
45. J. Dey, and I.M. Warner J. Photochem. Photobiol. A: Chem. 101 1996 21 27
46. B. Selvi, S. Patel, and M. Savva J. Pharm. Sci. 97 2008 4379 4390
47. M.R. di Nunzio, B. Cohen, and A. Douhal J. Phys. Chem. A 115 2011 5094 5104
48. G. Jahanbakhsh, A. Shahin, K. Mikael, and F. Amin J. Chem. Eng. Data 48 2003 1178 1182
49. R.F. Cookson Chem. Rev. 74 1974 5 28