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Direct quantitative analysis of indicine-N-oxide in cancer patient samples by gas chromatography using the internal standard heliotrine-N-oxide including a mass spectral comparison of their trimethylsilyl derivatives.

Abstract
Indicine-N-oxide was analyzed quantitatively in biological samples using a direct partial purification method involving acetonitrite precipitation or methanol precipitation followed by ion exchange chromatography. Trimethylsilyl derivatization of the resultant provided either of two derivatives, depending on the reaction conditions used, both of which had good gas chromatographic qualities. Heliotrine-N-oxide was used as the internal standard for this work. Data are presented to show that this is a reliable and useful internal standard based on its behavior in the partial purification method and on the gas chromatographic characteristics of its two derivatives. In addition, both low and high resolution mass spectral data indicate that heliotrine-N-oxide produces two trimethylsilyl derivatives analogous to those produced by indicine-N-oxide under the same conditions. Application of this procedure to urine and blood samples from cancer patients in clinical trials indicates that over 95% of the drug is removed from the circulation and excreted in the urine over the course of 48 h.
AuthorsJ V Evans, S K Daley, G A McClusky, C J Nielsen
JournalBiomedical mass spectrometry (Biomed Mass Spectrom) Vol. 7 Issue 2 Pg. 65-73 (Feb 1980) ISSN: 0306-042X [Print] England
PMID7407334 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antineoplastic Agents, Phytogenic
  • Cyclic N-Oxides
  • Pyrrolizidine Alkaloids
  • Trimethylsilyl Compounds
  • indicine-N-oxide
  • heliotrine N-oxide
Topics
  • Antineoplastic Agents, Phytogenic (metabolism, therapeutic use)
  • Chemical Precipitation
  • Chromatography, Ion Exchange
  • Cyclic N-Oxides (analysis)
  • Gas Chromatography-Mass Spectrometry
  • Humans
  • Infusions, Parenteral
  • Neoplasms (metabolism)
  • Pyrrolizidine Alkaloids (analysis)
  • Time Factors
  • Trimethylsilyl Compounds (analysis)

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