Pharmacokinetic evaluation and In Vitro-In Vivo Correlation (IVIVC) of novel methylene-substituted 3,3′ diindolylmethane (DIM)

Apurva R. Patel, Shawn D. Spencer, Mahavir B. Chougule, Stephen Safe, Mandip Singh

Research output: Contribution to journalArticle

15 Scopus citations

Abstract

Purpose: 3,3′-Diindolylmethane (DIM) is the major in vivo product of the acid-catalyzed oligomerization of indole-3-carbinol present in cruciferous vegetables. 1, 1-bis (3′-indolyl)-1-(p-substituted phenyl) methanes [C-substituted diindolylmethanes (C-DIMs)] are a new class of anticancer compounds derived from indole 3-carbinol. Despite rapidly increasing knowledge regarding mechanisms responsible for the chemopreventive properties of DIM-C-pPhC 6H 5, there have been relatively few studies determining the absorption and pharmacokinetic properties of DIM-C-pPhC 6H 5 to explore its clinical utility. Methods: In this study, we assessed the solubility, lipophilicity and Caco-2 cell permeability of methylene-substituted DIM. Pharmacokinetic properties in rats were determined following i.v. and oral administration of a novel analog of DIM. Pharmacokinetic parameters were determined using non-compartmental and compartmental techniques with WinNonlin® 5.0 software. To explore potential In Vitro-In Vivo Correlation (IVIVC) between the in vitro permeability values, and the oral absorption pharmacokinetics, we employed deconvolution of i.v. and oral data using a three compartment Exact Loo-Riegelman method. Results: The oral absorption and disposition were described by a three compartment model with combined zero-order/Michaelis-Menten limited systemic uptake using differential equations, at physiologically relevant doses. The saturation model obtained accounts for a nonlinear change in C max/Dose, and the absolute bioavailability (0.13 ± 0.06) was also dose dependent. The absorption rate profile of DIM-C-pPhC 6H 5 across Caco-2 cells was significantly different than in vivo. Conclusions: The pharmacokinetic absorption model presented represents a useful basis for obtaining plasma level predictability for poorly bioavailable, highly lipophilic drugs, such as the DIM analog DIM-C-pPhC 6H 5.

Original languageEnglish (US)
Pages (from-to)8-16
Number of pages9
JournalEuropean Journal of Pharmaceutical Sciences
Volume46
Issue number1-2
DOIs
StatePublished - May 12 2012
Externally publishedYes

Keywords

  • Anticancer
  • Anticarcinogen
  • Chemoprevention
  • DIM
  • Pharmacokinetic model

ASJC Scopus subject areas

  • Pharmaceutical Science

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