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Sonoporación mecánica sin microburbujas para la administración de fármacos guiada por RM en tumores sólidos: un
Deyssy Patrucco1, Martina Capozza1, Francesca Garello1
1Molecular and Preclinical Imaging Centre, Department of Molecular Biotechnology and Health Sciences, University of Torino, Turin, Italy.
Este estudio presenta un método de ultrasonido sin microburbujas para la entrega intracelular eficiente de fármacos. Este enfoque mejora la captación de fármacos y permite la monitorización no invasiva mediante imágenes de resonancia magnética (RM), superando las limitaciones de las técnicas actuales.
Área de la Ciencia:
- Biomedical Engineering
- Nanotechnology
- Molecular Imaging
Sus antecedentes:
- Ultrasound (US)-mediated drug delivery, often using microbubbles, faces challenges like short half-life, cost, and cytotoxicity.
- Clinical translation of microbubble-assisted sonoporation is hindered by these limitations.
Objetivo del estudio:
- To develop and validate a microbubble-free sonoporation technique for efficient intracellular delivery of hydrophilic agents.
- To demonstrate non-invasive monitoring of drug delivery using magnetic resonance imaging (MRI).
- To compare the efficacy and safety of microbubble-free sonoporation with existing permeabilization methods.
Principales métodos:
- A low-intensity, non-focused ultrasound protocol (1 MHz, MI 0.25, 25% duty cycle, 1 Hz PRF) was employed.
- Intracellular delivery of Gadoteridol (MRI contrast agent) and propidium iodide (PI) was assessed in vitro.
- Cell viability, membrane resealing, and agent distribution were evaluated.
- In vivo studies in K562 tumor-bearing mice utilized intravenous co-administration followed by local sonoporation.
Principales resultados:
- Efficient intracellular uptake of Gadoteridol (~7 × 10⁹ Gd ions/cell) was achieved in vitro with >70% cell viability.
- Complete membrane resealing occurred within 30 minutes post-sonoporation.
- Co-delivery with PI confirmed cytosolic distribution via fluorescence microscopy and MRI, with minimal passive uptake in controls.
- Microbubble-free sonoporation showed higher uptake and lower oxidative stress compared to electroporation, pinocytosis, and hypotonic swelling.
- In vivo, sonoporation led to significantly enhanced and prolonged T1 MRI contrast and increased intratumoral accumulation of agents.
Conclusiones:
- Microbubble-free sonoporation is an effective and controllable method for intracellular delivery of hydrophilic agents.
- The technique offers non-invasive MRI-based monitoring, addressing key limitations of microbubble-based approaches.
- This strategy shows significant potential for image-guided therapeutic applications, particularly in solid tumors.
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