Skip to main content
Log in

Kinetics and mechanism of the reduction of (ImH)[trans-RuCl4(dmso)(Im)] by ascorbic acid in acidic aqueous solution

  • Original Paper
  • Published:
JBIC Journal of Biological Inorganic Chemistry Aims and scope Submit manuscript

Abstract

A systematic study of the reduction of (ImH)[trans-RuCl4(dmso)(Im)] (NAMI-A; dmso is dimethyl sulfoxide, Im is imidazole), a promising antimetastasing agent entering phase II clinical trial, by l-ascorbic acid is reported. The rapid reduction of trans-[RuIIICl4(dmso)(Im)] results in formation of trans-[RuIICl4(dmso)(Im)]2− in acidic medium (pH = 5.0) and is followed by successive dissociation of the chloride ligands, which cannot be suppressed even in the presence of a large excess of chloride ions. The reduction of NAMI-A strongly depends on pH and is accelerated on increasing the pH. Over the small pH range 4.9−5.1, the reaction is quite pH-independent and the influence of temperature and pressure on the reaction could be studied. On the basis of the reported activation parameters and other experimental data, it is suggested that the redox process follows an outer-sphere electron transfer mechanism. A small contribution from a parallel reaction ascribed to inner-sphere reduction of aqua derivatives of NAMI-A, was found to be favored by lower concentrations of the NAMI-A complex and higher temperature. In the absence of an excess of chloride ions, the reduction process is catalyzed by the Ru(II) products being formed. The reduction of NAMI-A is also catalyzed by Cu(II) ions and the apparent catalytic rate constant was found to be 1.5 × 106 M−2 s−1 at 25 °C.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Scheme 1
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Scheme 2
Fig. 7
Fig. 8
Scheme 3

Similar content being viewed by others

References

  1. Clarke MJ (2003) Coord Chem Rev 236:209–233

    Article  CAS  Google Scholar 

  2. Dyson PA, Sava G (2006) Dalton Trans 1929–1933

  3. Kapitza S, Pongratz M, Jakupec MA, Heffeter P, Berger W, Lackinger L, Keppler BK, Marian B (2005) J Cancer Res Clin Oncol 131:101–110

    Article  PubMed  CAS  Google Scholar 

  4. Rademaker-Lakhai JM, van den Bongard D, Pluim D, Beijnen JH, Schellens JHM (2004) Clin Cancer Res 10:3717–3727

    Article  PubMed  CAS  Google Scholar 

  5. Sava G, Zorzet S, Turrin C, Vita F, Soranzo M, Zabucchi G, DiGiovani S, Pezzoni G, Sartor L, Garbisa S (2003) Clin Cancer Res 9:1898–1905

    PubMed  CAS  Google Scholar 

  6. Pacor S, Zorzet S, Cocchietto M, Bacac M, Vadori M, Turrin C, Gava B, Castellarin A, Sava G (2004) J Pharmacol Exp Ther 310:737–744

    Article  PubMed  CAS  Google Scholar 

  7. Gava B, Zorzet S, Spessotto P, Cocchietto M, Sava G (2006) J Pharmacol Exp Ther 317:284–291

    Article  PubMed  CAS  Google Scholar 

  8. Cocchietto M, Zorzet S, Sorc S, Sava G (2003) Invest New Drugs 21:55–62

    Article  PubMed  CAS  Google Scholar 

  9. Sava G, Bergamo A, Zorzet S, Gava B, Casarsa C, Cocchietto M, Furlani A, Scarcia V, Serli B, Iengo E, Alessio E, Mestroni G (2002) Eur J Cancer 38:427–435

    Article  PubMed  CAS  Google Scholar 

  10. Bergamo A, Gagliardi R, Scarcia V, Furlani A, Alessio E, Mestroni G, Sava G (1999) J Pharmacol Exp Ther 289:559–564

    PubMed  CAS  Google Scholar 

  11. Morbidelli L, Donnini S, Fillipi F, Messori L, Piccioli F, Orioli P, Sava G, Ziche M (2003) Br J Cancer 88:1484–1491

    Article  PubMed  CAS  Google Scholar 

  12. Sava G, Frausin F, Cocchietto M, Vita F, Podda E, Spessotto P, Furlani A, Scarcia V, Zabucchi G (2004) Eur J Cancer 40:1383–1396

    Article  PubMed  CAS  Google Scholar 

  13. Gallori E, Vettori C, Alessio E, Vilchez FG, Vilaplana R, Orioli P, Casini A, Messori L (2000) Arch Biochem Biophys 376:156–162

    Article  PubMed  CAS  Google Scholar 

  14. Barca A, Pani B, Tamaro M, Russo E (1999) Mutat Res 423:171–181

    PubMed  CAS  Google Scholar 

  15. Pastorea A, Federicia G, Bertinib E, Piemonte F (2003) Clin Chim Acta 333:19–39

    Article  Google Scholar 

  16. Sava G, Alessio E, Bergamo A, Mestroni G (1999) In: Clarke MJ, Sadler PJ (eds) Topic in biological inorganic chemistry. Springer, Berlin, pp 143–169

  17. Ravera M, Baracco S, Cassino C, Zanello P, Osella D (2004) Dalton Trans 2347–2351

  18. Schluga P, Hartinger CG, Egger A, Reisner E, Galanski M, Jakupec MA, Keppler B (2006) Dalton Trans 1796–1802

  19. Duffy JP, Eibl G, Reber HA, Hines OJ (2003) Mol Cancer 2

  20. Gerweck LE, Vijayappa S, Kozin S (2006) Mol Cancer Ther 5:1275–1279

    Article  PubMed  CAS  Google Scholar 

  21. Gerweck LE, Seetharaman K (1996) Cancer Res 56:1194–1198

    PubMed  CAS  Google Scholar 

  22. Clarke MJ, Zhu F, Frasca D (1999) Chem Rev 99:2511–2533

    Article  PubMed  CAS  Google Scholar 

  23. Mestroni G, Alessio E, Sava G (1998) Int Patent WO 98/00431

  24. van Eldik R, Palmer DA, Schmidt R, Kelm H (1981) Inorg Chim Acta 50:131–135

    Article  Google Scholar 

  25. van Eldik R, Gaede W, Wieland S, Kraft J, Spitzer M, Palmer DA (1993) Rev Sci Instrum 64:1355–1357

    Article  Google Scholar 

  26. Alessio E, Balducci E, Lutman A, Mestroni G, Calligaris M, Attia M (1993) Inorg Chim Acta 203:205–217

    Article  CAS  Google Scholar 

  27. Martinez P, Zuluaga J, Uribe D, van Eldik R (1987) Inorg Chim Acta 136:11–16

    Article  CAS  Google Scholar 

  28. Martinez P, Zuluaga J, Kraft J, van Eldik R (1988) Inorg Chim Acta 146:9–12

    Article  CAS  Google Scholar 

  29. Wanat A, van Eldik R, Stochel G (1998) J Chem Soc Dalton Trans 2497–2501

  30. Martinez P, Zuluaga J, Noheda P, van Eldik R (1992) Inorg Chim Acta 195:249–253

    Article  CAS  Google Scholar 

  31. Bänsch B, van Eldik R, Martinez P (1992) Inorg Chim Acta 201:75–82

    Article  Google Scholar 

  32. Bouma M, Nuijen B, Jansen MT, Sava G, Flaibani A, Bult A, Beijnen JH (2002) Int J Pharm 248:239–246

    Article  PubMed  CAS  Google Scholar 

  33. Bacac M, Hotze ACG, van der Schilden K, Haasnoot JG, Pacor S, Alessio E, Sava G, Reedijk J (2004) J Inorg Biochem 98:402–412

    Article  PubMed  CAS  Google Scholar 

  34. Espenson HE (1995) Chemical kinetics and reaction mechanism. McGraw-Hill, Singapore

    Google Scholar 

  35. Taqui Khan MM, Shukla RS (1991) Polyhedron 10:2711–2715

    Article  Google Scholar 

  36. Hoiland H (1974) J Chem Soc Faraday Trans I 70:1180–1185

    Article  Google Scholar 

  37. Sachinidis JI, Shalders RD, Tregloan PA (1994) Inorg Chem 33:6180–6186

    Article  CAS  Google Scholar 

  38. Macpherson BP, Alzoubi BM, Bernhardt PV, Martinez M, Tregloan PA, van Eldik R (2005) Dalton Trans 1459–1467

  39. Bänsch B, Martinez P, Zuluaga J, Uribe D, van Eldik R (1991) Z Phys Chem 170:59–71

    Google Scholar 

  40. Davies MB, Mortimer RJ, Vine TR (1988) Inorg Chim Acta 146:59–63

    Article  CAS  Google Scholar 

  41. Xu J, Jordan RB (1990) Inorg Chem 29:2933–2936

    Article  CAS  Google Scholar 

  42. Bouma M, Nuijen B, Sava G, Perbellini A, Flaibani A, van Steenbergen MJ, Talsma H, Kettenes van den Bosch JJ, Bult A, Beijnen JH (2002) Int J Pharm 248:247–259

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

The authors gratefully acknowledge financial support from the Deutsche Forschungsgemeinschaft (SFB 583), the European Commission for the AQUACHEM Research Training Network (contract no. MRTN-CT-2003-503864) and the Polish Ministry of Science and Higher Education (grant PB-1283/T09/2005/29). They kindly acknowledge the technical assistance of Anna Szumlanska in the early stage of this work.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Grażyna Stochel or Rudi van Eldik.

Electronic supplementary material

Below is the link to the electronic supplementary material.

ESM1 (DOC 455 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Brindell, M., Piotrowska, D., Shoukry, A.A. et al. Kinetics and mechanism of the reduction of (ImH)[trans-RuCl4(dmso)(Im)] by ascorbic acid in acidic aqueous solution. J Biol Inorg Chem 12, 809–818 (2007). https://doi.org/10.1007/s00775-007-0234-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00775-007-0234-x

Keywords

Navigation