Improved Efficiency of Ibuprofen by Cationic Carbosilane Dendritic Conjugates

Mol Pharm. 2016 Oct 3;13(10):3427-3438. doi: 10.1021/acs.molpharmaceut.6b00420. Epub 2016 Sep 2.

Abstract

In order to improve the efficiency of the anti-inflammatory drug ibuprofen, cationic carbosilane dendrimers and dendrons with ibuprofen at their periphery or at their focal point, respectively, have been synthesized, and the release of the drug was studied using HPLC. Macrophages were used to evaluate the anti-inflammatory effect of the ibuprofen-conjugated dendritic systems and compared with mixtures of non-ibuprofen dendritic systems in the presence of the drug. The cationic ibuprofen-conjugated dendron was the compound that showed higher anti-inflammatory properties. It reduces the LPS-induced COX-2 expression and decreases the release of several inflammatory cytokines such as TNFα, IL-1β, IL-6, and CCL3. These results open new perspectives in the use of these compounds as drug carriers.

Keywords: anti-inflammatory; carbosilane dendrimers; dendrons; drug release; ibuprofen; macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents / chemistry*
  • Anti-Inflammatory Agents / pharmacology*
  • Cations / chemistry*
  • Cell Differentiation
  • Cells, Cultured
  • Chemokine CCL3 / metabolism
  • Dendrimers / chemistry*
  • Humans
  • Ibuprofen / chemistry*
  • Ibuprofen / pharmacology*
  • Interleukin-1beta / metabolism
  • Interleukin-6 / metabolism
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Receptors, Tumor Necrosis Factor / metabolism
  • Silanes / chemistry*

Substances

  • Anti-Inflammatory Agents
  • Cations
  • Chemokine CCL3
  • Dendrimers
  • Interleukin-1beta
  • Interleukin-6
  • Receptors, Tumor Necrosis Factor
  • Silanes
  • carbosilane
  • Ibuprofen