Abstract

At the present, a high potential of 3,3’-diindolylmethane (DIM) as a new preventive and therapeutic agent in oncology is well established, due to its ability to target multiple components of cancer cell cycle regulation, survival and progression. However, a very low bioavailability of DIM remains the major challenge for its efficient development as novel medicine. In this work, we have developed a polymer based nano-formulation comprising a non-ionic block copolymer, Pluronic F127 that increases oral bioavailability of DIM by almost one order of magnitude, as compared to the presently marketed products such as crystalline DIM and BioResponse DIM. The pharmacokinetic parameters established in the present study revealed that AUC and Cmax of the new formulation dosed at 60 mg/kg were 7.06 ± 0.93 μg ∙ h/mL, and 3.08 ± 0.17 μg/mL, while in the case of crystalline DIM dosed at the same dose AUC and Cmax were 0.97 ± 0.08 μg ∙ h/mL, and 0.18 ± 0.02 μg/mL. BioResponce DIM showed AUC and Cmax of 1.05 ± 0.05 μg ∙ h/mL, and 0.22 ± 0.02 μg/mL, respectively.

Highlights

  • Epidemiology studies demonstrate that dietary consumption of cruciferous vegetables, including broccoli, cauliflower and Brussel’s sprouts may provide protection from some chronic diseases, including several types of cancer [1]

  • Phytochemicals derived from cruciferous vegetables include indole-3-carbinol (I3C) and its condensation product, 3,3’-diindolylmethane (DIM)

  • We have recently reported that DIM is a selective and potent inhibitor of cancer stem cells (CSCs) [5]

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Summary

Introduction

Epidemiology studies demonstrate that dietary consumption of cruciferous vegetables, including broccoli, cauliflower and Brussel’s sprouts may provide protection from some chronic diseases, including several types of cancer [1]. The concentrations of DIM required to suppress CSCs formation are in the close range to those achievable in human plasma, after oral dosing of the BR-DIM composition. A more efficient formulation with increased oral bioavailability of the compound could help fully explore potential of DIM as pharmaceutical agent.

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