The Effective Solubilization of Hydrophobic Drugs Using Epigallocatechin Gallate or Tannic Acid-Based Formulations.

J Pharm Sci

Faculty of Pharmaceutical Sciences, UBC, V6T1Z3 Vancouver, BC, Canada.

Published: October 2016

AI Article Synopsis

  • Researchers explored the potential of using epigallocatechin gallate (EGCG) and tannic acid as safer, millimolar solubilizing agents for hydrophobic drugs, contrasting with the toxic supramolar amounts of traditional hydrotropes.
  • Both EGCG and tannic acid significantly enhanced the aqueous solubility of drugs like paclitaxel and curcumin, shifting solubility from micrograms to milligrams per milliliter.
  • Notably, EGCG-based solutions allowed for better drug absorption in cells compared to traditional micellar formulations, indicating promising applications in various drug delivery methods.

Article Abstract

Hydrotropic solubilization of hydrophobic drugs requires supramolar amounts of hydrotropes with potential toxicity issues. We investigated the use of epigallocatechin gallate (EGCG) and tannic acid at millimolar concentrations, as hydrotrope-like solubilizing agents. Paclitaxel, docetaxel, amphotherecin B, curcumin, or rapamycin were dried down with EGCG or tannic acid from ethanol and then redissolved in aqueous media. Following centrifugation and filtration, the drug solubility was measured using HPLC. The uptake of docetaxel into cells from EGCG-based solutions was measured using radiolabeled drugs. Both EGCG and tannic acid effectively increased the aqueous solubility of all drugs from low levels (μg/mL) to high levels (mg/mL) in a concentration-dependent fashion at millimolar concentrations. Solutions were generally stable at room temperature over 24 h. Compared with micellar formulations, EGCG-based solutions of docetaxel demonstrated markedly improved drug uptake or transport levels in all cell lines. The use of these additives may provide improved formulation of various hydrophobic drugs using oral, parenteral, localized, or device-associated delivery systems.

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Source
http://dx.doi.org/10.1016/j.xphs.2016.06.027DOI Listing

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