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Updated: Jun 17, 2026

Real-time Monitoring of Ligand-receptor Interactions with Fluorescence Resonance Energy Transfer
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Biosensor-based evaluation of liposomal binding behavior.

Gerd Bendas1

  • 1Department of Pharmacy, Rheinische Friedrich Wilhelms University Bonn, Germany.

Methods in Molecular Biology (Clifton, N.J.)
|December 17, 2009
PubMed
Summary
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Biosensors using acoustic wave sensors quantify liposomal binding and appearance on surfaces. This technology aids in predicting and controlling liposome behavior for potential therapeutic applications.

Area of Science:

  • Biomedical Engineering
  • Materials Science
  • Analytical Chemistry

Background:

  • Biosensors offer label-free detection of biological interactions.
  • Liposomal behavior at binding sites impacts therapeutic efficacy.
  • Acoustic wave sensors provide mass-sensitive detection.

Purpose of the Study:

  • To investigate liposomal binding behavior on simulated biological surfaces using acoustic wave sensors.
  • To quantify liposomal binding intensity and analyze liposome appearance (deformation, fusion).
  • To explore the potential of biosensors for predicting and modulating liposomal behavior.

Main Methods:

  • Utilized quartz crystal microbalance (QCM) as an acoustic wave sensor.
  • Bio-functionalized quartz sensors with avidin.

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Real-time Monitoring of Ligand-receptor Interactions with Fluorescence Resonance Energy Transfer
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10:41

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  • Performed liposomal binding experiments using biotin-containing liposomes as model ligands.
  • Main Results:

    • Quantified liposomal binding intensity to avidin-modified sensors.
    • Gained insights into liposome deformation and fusion upon binding.
    • Demonstrated the influence of binding strength and lipid composition on liposomal behavior.

    Conclusions:

    • Acoustic wave biosensors are effective tools for studying liposomal-surface interactions.
    • Liposome appearance and binding behavior can be analyzed and potentially modulated.
    • This approach holds promise for optimizing liposome-based drug delivery systems.