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Related Experiment Video

Updated: Jul 30, 2025

Preparation of Binary and Ternary Deep Eutectic Systems
06:15

Preparation of Binary and Ternary Deep Eutectic Systems

Published on: October 31, 2019

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Polymer-embedded deep eutectic solvents (PEDES) as a novel bio-enabling formulation approach.

Shaida Panbachi1, Josef Beranek2, Martin Kuentz3

  • 1University of Applied Sciences and Arts Northwest. Switzerland, Institute of Pharma Technology Hofackerstr. 30, Muttenz CH-4132, Switzerland; Institute of Pharmaceutical Technology, University of Basel, Klingelbergstrasse 50, Basel 4056, Switzerland.

European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|May 11, 2023
PubMed
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This study introduces polymer-embedded deep eutectic systems (PEDES) to prevent drug precipitation. These novel formulations enhance oral delivery of poorly soluble drugs, achieving significant supersaturation.

Area of Science:

  • Pharmaceutical Sciences
  • Materials Science
  • Chemical Engineering

Background:

  • Deep eutectic solvents (DES) show promise for delivering poorly water-soluble drugs.
  • Drug precipitation after oral administration remains a challenge for DES formulations.
  • Novel formulation strategies are needed to improve oral bioavailability.

Purpose of the Study:

  • To develop a polymer-embedded deep eutectic system (PEDES) as a new bio-enabling formulation principle.
  • To investigate the potential of PEDES in preventing drug precipitation and achieving supersaturation.
  • To evaluate PEDES using a model poorly water-soluble drug.

Main Methods:

  • Formulation screening to identify optimal PEDES composition.
  • Preparation of PEDES using polyvinyl pyrrolidone K30 (PVP) in a L-carnitine:ethylene glycol DES.
Keywords:
Deep eutectic solventsEnabling formulation(s)Low transition-temperature mixturesMolecular dynamics simulation(s)Precipitation inhibitionSolubilizing carrier

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  • Characterization of drug solubility, supersaturation factor, and release kinetics.
  • Inclusion of molecular dynamics simulations for formulation analysis.
  • Main Results:

    • A stable PEDES formulation was successfully created using 15% PVP in L-carnitine:ethylene glycol DES.
    • High indomethacin solubility (175.6 mg/mL) was achieved within the DES.
    • A maximum supersaturation factor of 9.8 was recorded upon release, with a "parachute effect" observed in release kinetics.

    Conclusions:

    • PEDES represents a viable and novel formulation approach for supersaturating drug delivery systems.
    • This strategy effectively addresses drug precipitation issues associated with DES.
    • Further research is warranted to explore the full therapeutic potential of PEDES.