The metabolism and pharmacokinetics of phospho-sulindac (OXT-328) and the effect of difluoromethylornithine

G. Xie, T. Nie, Gerardo Mackenzie, Y. Sun, L. Huang, N. Ouyang, N. Alston, C. Zhu, O. T. Murray, P. P. Constantinides, L. Kopelovich, B. Rigas

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

BACKGROUND AND PURPOSE Phospho-sulindac (PS; OXT-328) prevents colon cancer in mice, especially when combined with difluoromethylornithine (DFMO). Here, we explored its metabolism and pharmacokinetics. EXPERIMENTAL APPROACH PS metabolism was studied in cultured cells, liver microsomes and cytosol, intestinal microsomes and in mice. Pharmacokinetics and biodistribution of PS were studied in mice. KEY RESULTS PS undergoes reduction and oxidation yielding PS sulphide and PS sulphone; is hydrolysed releasing sulindac, which generates sulindac sulphide (SSide) and sulindac sulphone (SSone), all of which are glucuronidated. Liver and intestinal microsomes metabolized PS extensively but cultured cells converted only 10% of it to PS sulphide and PS sulphone. In mice, oral PS is rapidly absorbed, metabolized and distributed to the blood and other tissues. PS survives only partially intact in blood; of its three major metabolites (sulindac, SSide and SSone), sulindac has the highest C max and SSone the highest t 1/2; their AUC 0-24h are similar. Compared with conventional sulindac, PS generated more SSone but less SSide, which may contribute to the safety of PS. In the gastroduodenal wall of mice, 71% of PS was intact; sulindac, SSide and SSone together accounted for <30% of the total. This finding may explain the lack of gastrointestinal toxicity by PS. DFMO had no effect on PS metabolism but significantly reduced drug level in mouse plasma and other tissues. CONCLUSIONS AND IMPLICATIONS Our findings establish the metabolism of PS define its pharmacokinetics and biodistribution, describe its interactions with DFMO and largely explain its gastrointestinal safety.

Original languageEnglish (US)
Pages (from-to)2152-2166
Number of pages15
JournalBritish Journal of Pharmacology
Volume165
Issue number7
DOIs
StatePublished - Apr 1 2012
Externally publishedYes

Keywords

  • difluoromethylornithine
  • gastrointestinal toxicity
  • liver microsomes
  • metabolism
  • pharmacokinetics
  • phospho-sulindac

ASJC Scopus subject areas

  • Pharmacology

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