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Cancer Chemotherapy and Pharmacology

, Volume 25, Issue 3, pp 195–201 | Cite as

Validated HPLC procedures for the analysis of BMY-28090 in human plasma and urine

  • Robert C. Gaver
  • George Deeb
  • Alice M. George
Article

Summary

The compound BMY-28090 (elsamicin A) is a new fermentation product with antitumor properties, which has the same aglycone as chartreusin but contains two novel sugars. To define the disposition of BMY-28090 during phase I trials, HPLC procedures were developed and validated for the quantitation of the drug in human plasma and urine. To 1.0 ml plasma were added 0.5 ml 0.2M phosphate buffer (pH 8.0), 125 ng 1-naphthol (internal standard) in 25 μl MeOH and 5 ml ethyl acetate. After mixing and centrifugation, 4 ml ethyl acetate layer was removed, evaporated to dryness, and the residue was dissolved in 250 μl mobile phase and injected (200 μl). To 1.0 ml urine were added 100 μl MeOH and 1.0 ml 0.5M succinate buffer (pH 4.0). After mixing (30 s) and sonication (1 min), the solution was filtered in an Amicon Centrifree micropartition unit and injected (30 μl). An IBM C-8 column 5-μm and fluorescence detection (excitation at 254 mm, 418 nm emission filter) were used for both analyses. The mobile phases for plasma (2 ml/min) and urine (1.3 ml/min) were H2O/CH3CN (7:3 v/v) and H2O/CH3CN/MeOH (6:3:1 (v/v), respectively, with 1.5 ml 85% H3PO4 and 1.5 ml triethylamine/1. BMY-28090 eluted at 8–10 min and 1-naphthol, at 10–11 min. The standard curves were linear from 1 to 50 ng/ml plasma and from 10 to 1000 ng/ml urine. The within- and between-day precision was <3% for plasma and <5% for urine. Accuracies were within 6% of the nominal value and recoveries were 75% and 90% for plasma and urine, respectively. At 37°C, BMY-28090 was stable in plasma for at least 8 h but had a half-life of 36 h in urine. The drug was stable in plasma and urine for 30 days at −20°C.

Keywords

Sugar Ethyl Phosphate Buffer Mobile Phase Ethyl Acetate 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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References

  1. 1.
    Catino JJ, Francher DM, Long BH, Casazza AM (1987) Cellular uptake of elsamicin and DNA breakage in P388 murine leukemia cells. Proc Am Assoc Cancer Res 28: 310Google Scholar
  2. 2.
    Konishi M, Sugawara K, Tsunakawa M, Nishiyama Y, Miyaki T, Kawaguchi H (1985) BMY-28090 (elsamicin), a new antitumor antibiotic related to chartreusin: isolation, chemistry and activity. In: Ishigami J (ed) Recent advances in chemotherapy. Proceedings of the International Congress on Chemotherapy., Anticancer section 1. Tokyo Press, Tokyo, pp 333–334Google Scholar
  3. 3.
    Konishi M, Sugawara K, Kofu F, Nishiyama Y, Tomita K, Miyaki T, Kawaguchi H (1986) Elsamicins, new antitumor antibiotics related to chartreusin: 1. Production, isolation, characterization and antitumor activity. J Antibiot 39(6): 784–791Google Scholar
  4. 4.
    Konishi M, Oki T (1987) Elsamicin A. Drugs Future 12 (12): 1104–1105Google Scholar
  5. 5.
    Schurig JE, Basler GA, Faulkner HC, Duncan GF, Rose WC, Bradner WT (1986) Experimental antitumor activity of elsamicin, a new antitumor antibiotic. Proc Am Assoc Cancer Res 27: 275Google Scholar
  6. 6.
    Schurig JE, Forenza S, Long BH, Rose WC, Catino JJ, Kamei H, Nishiyama Y, Bradner WH, Casazza AM, Stringfellow DA, Doyle TW (1988) Elsamicin and esperamicin: novel fermentation-derived cytotoxic antitumor agents with unique mechanisms of action. Proc Am Assoc Cancer Res 29: 538–539Google Scholar
  7. 7.
    Sugawara K, Tsunakawa M, Konishi M, Kawaguchi H, Krishnan B, Cunheng H, Clardy J (1987) Elsamicins A and B, new antitumor antibiotics related to chartreusin: 2. Structures of elsamicins A and B. J Org Chem 52: 996–1001Google Scholar

Copyright information

© Springer-Verlag 1989

Authors and Affiliations

  • Robert C. Gaver
    • 1
  • George Deeb
    • 1
  • Alice M. George
    • 1
  1. 1.Department of Metabolism and Pharmacokinetics, Pharmaceutical Research and Development DivisionBristol-Myers CompanySyracuseUSA

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