Skip to main content

Advertisement

Log in

Plasma and tissue disposition of non-liposomal DB-67 and liposomal DB-67 in C.B-17 SCID mice

  • PHASE II STUDIES
  • Published:
Investigational New Drugs Aims and scope Submit manuscript

Summary

Purpose: DB-67 is a silatecan, 7-silyl-modified camptothecin, with enhanced lipophilicity and increased blood stability of the active-lactone ring. The generation of a liposomal formulation of DB-67 may be an attractive method of intravenous (IV) administration and may maintain DB-67 in the active-lactone form. We evaluated the tissue and plasma disposition of DB-67 lactone and hydroxy acid after administration of non-liposomal (NL) and liposomal (L) DB-67 in severe combined immunodeficient (SCID) mice. Methods: NL-DB-67 and L-DB-67 10 mg/kg IV × 1 were administered via a tail vein in SCID mice. After dosing, mice (n = 3 per time point) were euthanized and blood (∼1 ml) and tissue were collected from 5 min to 48 h after administration. DB-67 lactone and hydroxy acid concentrations in plasma and DB-67 total (sum of lactone and hydroxyl acid) concentrations in tissues were determined by high-performance liquid chromatography (HPLC) with fluorescence detection. Results: Clearance of DB-67 lactone after administration of NL-DB-67 and L-DB-67 were 1.6 and 3.5 l/h/m2, respectively; DB-67 lactone half-lives after administration of NL-DB-67 and L-DB-67 were 1.4 and 0.9 h, respectively. The percentages of DB-67 lactone in plasma after administration of NL-DB-67 and L-DB-67 were 92% and 89%, respectively. Liver, kidney, spleen, and lung tissues had longer exposure times to DB-67 after administration of L-DB-67 compared with NL-DB-67. Conclusion: In plasma, the majority of DB-67 remained in the lactone form after administration of NL-DB-67 and L-DB-67. The plasma disposition of DB-67 was similar after administration of NL-DB-67 and L-DB-67, suggesting that most of the DB-67 is immediately released from the L-DB-67 formulation. Following administration of L-DB-67, the higher and longer exposure of DB-67 in the spleen, as compared with NL-DB-67, is consistent with splenic clearance of liposomes by the reticuloendothelial system.

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
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  1. Burke TG, Mi Z (1993) Preferential binding of the carboxylate form of camptothecin by human serum albumin. Anal Biochem 212:285–287

    Article  PubMed  CAS  Google Scholar 

  2. Mi Z, Burke TG (1994) Differential interactions of camptothecin lactone and carboxylate forms with human blood components. Biochemistry 33:10325–10336

    Article  PubMed  CAS  Google Scholar 

  3. Mi Z, Burke TG (1994) Marked interspecies variations concerning the interactions of camptothecin with serum albumins: a frequency-domain fluorescence spectroscopic study. Biochemistry 33:12540–12545

    Article  PubMed  CAS  Google Scholar 

  4. Pollack IF, Erff M, Bom D et al (2001) Potent topoisomerase I inhibition by novel silatecans eliminates glioma proliferation in vitro and in vivo. Can Res 59:4898–4905

    Google Scholar 

  5. Curran DP, Liu H (1991) 4 + 1 Radical annulations with isonitriles—a simple route to cyclopenta-fused quinolines. J Am Chem Soc 113:2127–2132

    Article  CAS  Google Scholar 

  6. Curran DP, Ko SB (1994) Synthesis of optically active alpha-hydroxy lactones by sharpless asymmetric dihydroxylations of ketene acetals, enol ethers, and ene lactones. J Org Chem 59:6139–6141

    Article  CAS  Google Scholar 

  7. Josien H, Bom D, Curran DP, Zheng YH, Chou T (1997) 7-Silylcamptothecins (Silatecans): a new family of camptothecin antitumor agents. Bioorg Med Chem Lett 7:3189–3295

    Article  CAS  Google Scholar 

  8. Burke TG, Mi Z, Jiang Y, Munshi CB (1995) The important role of albumin in determining the relative human blood stabilities of the camptothecin anticancer drugs. J Pharm Sci 84:518–519

    Article  PubMed  CAS  Google Scholar 

  9. Burke TG, Mi Z (1994) The structural basis of camptothecin interactions with human serum albumin: impact on drug stability. J Med Chem 37:40–46

    Article  PubMed  CAS  Google Scholar 

  10. Pollack IF, Erff M, Bom D et al (1999) Potent topoisomerase I inhibition by novel silatecans eliminates glioma proliferation in vitro and in vivo. Cancer Res 59:4898–905

    PubMed  CAS  Google Scholar 

  11. Newman MS, Colbern GT, Working PK et al (1999) Comparative pharmacokinetics, tissue distribution, and therapeutic effectiveness of cisplatin encapsulated in long-circulating, pegylated liposomes (SPI-077) in tumor bearing mice. Cancer Chemother Pharmacol 43:1–7

    Article  PubMed  CAS  Google Scholar 

  12. Forssen EA, Coulter DM, Proffitt RT (1992) Selective in vivo localization of daunorubicin small unilamellar vesicles in solid tumors. Cancer Res 52:3255–3261

    PubMed  CAS  Google Scholar 

  13. Forssen EA (1997) The design and development of DaunoXome for solid tumor targeting in vivo. Adv Drug Deliv Rev 24:133–150

    Article  CAS  Google Scholar 

  14. Zamboni WC (2005) Liposomal, nanoparticle, conjugated formulations of anticancer agents. Clin Cancer Res 11:8230–8234

    Article  PubMed  CAS  Google Scholar 

  15. Zamboni WC, Stewart CF, Thompson J et al (1998) Relationship between topotecan systemic exposure and tumor response in human neuroblastoma xenografts. J Natl Cancer Inst 90:505–511

    Article  PubMed  CAS  Google Scholar 

  16. Zamboni WC, Gervais AC, Egorin MJ, Schellens JH, Zuhowski EG, Pluim D, Joseph E, Hamburger DR, Working PK, Colbern G, Tonda ME, Potter DM, Eiseman JL (2004) Systemic and tumor disposition of platinum after administration of cisplatin or STEALTH liposomal-cisplatin formulations (SPI-077 and SPI-077 B103) in a preclinical tumor model of melanoma. Cancer Chemother Pharmacol 53:329–336

    Article  PubMed  CAS  Google Scholar 

  17. D’Argenio DZ, Schmuitzky A (1990) ADAPT II User’s Guide: Biomedical Simulations Resource

  18. Rowland M, Tozer T (1999) Clinical pharmacokinetics: concepts and applications. Lea and Febiger, Philadelphia

    Google Scholar 

  19. Mi Z, Malak H, Burke TG (1995) Reduced albumin binding promotes the stability and activity of topotecan in human blood. Biochem 34:13722–13728

    Article  CAS  Google Scholar 

  20. Smith JA, Newman RA, Hausheer FH, Madden T (2003) Evaluation of in vitro drug interactions with karenitecin, a novel, highly lipophilic camptothecin derivative in phase II clinical development. J Clin Pharmacol 43:1008–1014

    Article  PubMed  CAS  Google Scholar 

  21. Punt CJ, de Jonge MJ, Monfardini S, Daugaard G, Fiedler W, Baron B, Lacombe D, Fumoleau P, EORTC New Drug Development Group (2004) RFS2000 (9-nitrocamptothecin) in advanced small cell lung cancer, a phase II study of the EORTC New Drug Development Group. Eur J Cancer 40:1332–1334

    Article  PubMed  CAS  Google Scholar 

  22. Papahadjopoulos D, Allen TM, Gabizon A et al (1991) Sterically stabilized liposomes: improvements in pharmacokinetics and antitumor therapeutic efficacy. Proc Natl Acad Sci USA 88:11460–11464

    Article  PubMed  CAS  Google Scholar 

  23. Maeda H, Wu J, Sawa T, Matsumura Y, Hori K (2000) Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. J Control Release 65:271–284

    Article  PubMed  CAS  Google Scholar 

  24. Zamboni WC, Strychor S, Joseph E, Walsh DR, Parise RA, Tonda ME, Yu NY, Engber C, Eiseman JE (2005) Plasma and tumor disposition of STEALTH Liposomal CKD-602 (S-CKD602) and non-liposomal CKD-602, a camptothecin analogue, in mice bearing A375 human melanoma xenograft. Proc Am Acad Clin Res-NCI-EORTC: #B173

  25. Zamboni WC, Eiseman JE, Strychor S, Rice PM, Joseph E, Potter DM, Shurer J, Walsh DR, Parise RA, Tonda ME, Yu NY, Engber C, Basse PH (2006) Relationship between the plasma and tumor disposition of STEALTH liposomal CKD-602 and macrophages/dendritic cells (MDC) in mice bearing human tumor xenografts. Proc Am Acad Clin Res 47:1280 (abstract #5449)

    Google Scholar 

  26. Strychor S, Eiseman JE, Joseph E, Parise RA, Tonda ME, Yu NY, Engber C, Zamboni WC (2006) Plasma, tissue, and tumor disposition of STEALTH liposomal CKD-602 (S-CKD602) and non-liposomal CKD-602, a camptothecin analogue, in mice bearing A375 human melanoma xenografts. Proc Am Acad Clin Res 47:721 (abstract #3064)

    Google Scholar 

  27. Zamboni WC, Friedland DM, Ramalingam S, Edwards RP, Stoller RG, Belani CP, Strychor S, Ou YC, Tonda ME, Ramanathan RK (2006) Final results of a phase I and pharmacokinetic study of STEALTH liposomal CKD-602 (S-CKD602) in patients with advanced solid tumors. Proc Am Soc Clin Oncol 24:82s (abstract #2013)

    Google Scholar 

  28. National Research Council (1996) Guide for the care and use of laboratory animals. National Academy Press, Washington DC

Download references

Acknowledgements

The study was funded by STTR Grant R41 CA91700. We gratefully acknowledge Jeremy Hedges for his assistance in the submission of the manuscript.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to William C. Zamboni.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zamboni, W.C., Jung, L.L., Strychor, S. et al. Plasma and tissue disposition of non-liposomal DB-67 and liposomal DB-67 in C.B-17 SCID mice. Invest New Drugs 26, 399–406 (2008). https://doi.org/10.1007/s10637-007-9109-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10637-007-9109-9

Keywords

Navigation