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Ultrasonic gene and drug delivery using eLiposomes.

Marjan Javadi1, William G Pitt, Christopher M Tracy

  • 1Department of Chemical Engineering, Brigham Young University, Provo, UT 84602, USA.

Journal of Controlled Release : Official Journal of the Controlled Release Society
|January 29, 2013
PubMed
Summary

Ultrasound-triggered eLiposomes enhance drug and gene delivery. Folate-targeted eLiposomes with perfluoropentane emulsions effectively deliver therapeutics to the cytosol of HeLa cells.

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Area of Science:

  • Biotechnology
  • Nanomedicine
  • Drug Delivery Systems

Background:

  • eLiposomes are advanced liposomal formulations designed for targeted therapeutic delivery.
  • Ultrasound application triggers the phase transition of encapsulated emulsions, leading to eLiposome rupture and payload release.

Purpose of the Study:

  • To investigate the efficacy of folate-targeted eLiposomes containing perfluoropentane (PFC5) emulsions for drug and gene delivery.
  • To evaluate the influence of folate ligands, PFC5 emulsions, and ultrasonic parameters on delivery into HeLa cells.

Main Methods:

  • Encapsulation of model drug (calcein) or GFP plasmid within folated eLiposomes containing PFC5 emulsions.
  • Utilizing confocal microscopy to quantify drug delivery and gene transfection efficiency in HeLa cells.

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  • Applying controlled ultrasonic acoustic parameters to trigger payload release.
  • Main Results:

    • Folate ligands and internal PFC5 emulsions were crucial for effective drug and gene delivery.
    • Ultrasound application significantly enhanced both drug delivery and plasmid transfection rates.
    • Therapeutics were delivered to the cytosol, suggesting disruption of both eLiposomes and endosomes.

    Conclusions:

    • Folate-targeted eLiposomes with PFC5 emulsions offer a promising ultrasound-triggered platform for enhanced drug and gene delivery.
    • The mechanism involves ultrasound-induced expansion and rupture of emulsion droplets, facilitating cytosolic delivery.
    • This technology holds potential for targeted intracellular delivery of therapeutics.