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Polymeric carriers enhance targeted drug delivery by increasing efficacy while minimizing off-target effects. These carriers comprise a biodegradable polymeric backbone integrated with functional elements that enable targeting, improve physicochemical properties, and regulate drug release.Targeting MechanismsThe targeting ability of polymeric carriers is mediated by a homing device, which is a molecular recognition component designed to selectively bind to specific tissues or cells. Monoclonal...
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PBCA-based polymeric microbubbles for molecular imaging and drug delivery.

Patrick Koczera1, Lia Appold2, Yang Shi2

  • 1Department of Experimental Molecular Imaging (ExMI), Helmholtz Institute for Biomedical Engineering, University Hospital RWTH, Pauwelsstr. 30, 52074 Aachen, Germany; Department of Intensive Care, University Hospital RWTH Aachen, Pauwelsstr. 30, 52074 Aachen, Germany.

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Poly(n-butyl cyanoacrylate) microbubbles (MB) enable advanced ultrasound (US) imaging and drug delivery. These targeted MBs visualize disease and enhance drug penetration, improving diagnosis and therapy.

Keywords:
MicrobubblesNanomedicineSonoporationTumor targetingUltrasound

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Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Medical Imaging

Background:

  • Microbubbles (MB) are established ultrasound (US) contrast agents.
  • Targeted and drug-loaded MBs offer potential for advanced biomedical applications.
  • Poly(n-butyl cyanoacrylate) (PBCA) MBs are explored for molecular imaging and drug delivery.

Purpose of the Study:

  • To describe targeted and drug-loaded PBCA MBs.
  • To demonstrate their utility in molecular US imaging and US-mediated drug delivery.
  • To highlight their potential in improving disease diagnosis and therapy.

Main Methods:

  • Surface modification of PBCA MBs with peptides/antibodies for molecular imaging (targeting E-selectin, VCAM-1).
  • Utilizing stable and inertial cavitation of PBCA MBs for sonoporation and vessel permeabilization.
  • Investigating direct (US-induced release) and indirect (enhanced extravasation) drug delivery mechanisms.

Main Results:

  • PBCA MBs successfully visualized angiogenic tumor vessels and inflamed atherosclerotic endothelium.
  • Sonoporation and vessel permeabilization were achieved in tumors and the brain.
  • Both direct and indirect drug delivery strategies were demonstrated as effective.

Conclusions:

  • Targeted and drug-loaded PBCA MBs are suitable for molecular US imaging and US-mediated drug delivery.
  • Combining MBs with US shows broad applicability for improved disease diagnosis and therapy.
  • These findings align with recent advancements in patient-applicable MB technology.