Influence of PluronicF68 on Size Stability and AcousticBehavior of Monodisperse Phospholipid-Coated Microbubbles Producedat Room Temperature

Ultrasound contrast agents, comprised of phospholipid-coated microbubbles, can be produced as monodisperse populations using a microfluidic flow-focusing device. However, microbubble coalescence remains a significant challenge. High production temperatures (e.g., 55 °C) can be used to suppress coalescence, but it complicates the microfluidic device design and is incompatible with targeting agents and drug conjugates. This study investigates the production of monodisperse microbubbles at room temperature with the addition of the amphiphilic surfactant Pluronic F68. Two 1,2-distearoyl-<i>sn</i>-glycero-3-phosphocholine (DSPC)-based phospholipid formulations were investigated: F1, containing 1,2-dipalmitoyl-<i>sn</i>-glycero-3-phosphoethanolamine-<i>N</i>-[carbonyl-methoxypolyethylene glycol] (DPPE-PEG5000), and F2, which included both DPPE-PEG5000 and polyoxyethylene(40) stearate (PEG40-stearate). We characterized the size stability and acoustic behavior of monodisperse microbubbles produced with various Pluronic F68 concentrations. Adding 5–10 mol % Pluronic F68 was found to effectively suppress coalescence and facilitated the production of monodisperse microbubbles that remained shelf stable for at least 7 days. Acoustic attenuation measurements revealed a shell stiffness ranging from 0.78 to 0.93 N/m for these microbubbles. The 10 mol % Pluronic F68 addition (10PF) demonstrated superior monodispersity and was selected for further experiments. Upon dilution, the size and resonance frequencies of both F1–10PF and F2–10PF decreased over time, though F2–10PF showed better stability compared to F1–10PF for both metrics. Both F1–10PF and F2–10PF exhibited a stronger subharmonic scattering intensity than SonoVue (clinical approved microbubbles), which offers potential for blood pressure sensing. Our study shows that incorporating Pluronic F68 facilitates the production of monodisperse microbubbles at room temperature that are stable long-term and have excellent acoustical properties, with the F2–10PF formulation demonstrating better stability than the F1–10PF.

Publication Details

Journal
Figshare
Published
2025-02-03
DOI
https://doi.org/10.1021/acsami.4c18844.s001
Primary Topic
Ultrasound and Hyperthermia Applications
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article
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article

Influence of PluronicF68 on Size Stability and AcousticBehavior of Monodisperse Phospholipid-Coated Microbubbles Producedat Room Temperature

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Ultrasound and Hyperthermia Applications
article

Influence of PluronicF68 on Size Stability and AcousticBehavior of Monodisperse Phospholipid-Coated Microbubbles Producedat Room Temperature

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Abstract

Ultrasound contrast agents, comprised of phospholipid-coated microbubbles, can be produced as monodisperse populations using a microfluidic flow-focusing device. However, microbubble coalescence remains a significant challenge. High production temperatures (e.g., 55 °C) can be used to suppress coalescence, but it complicates the microfluidic device design and is incompatible with targeting agents and drug conjugates. This study investigates the production of monodisperse microbubbles at room temperature with the addition of the amphiphilic surfactant Pluronic F68. Two 1,2-distearoyl-<i>sn</i>-glycero-3-phosphocholine (DSPC)-based phospholipid formulations were investigated: F1, containing 1,2-dipalmitoyl-<i>sn</i>-glycero-3-phosphoethanolamine-<i>N</i>-[carbonyl-methoxypolyethylene glycol] (DPPE-PEG5000), and F2, which included both DPPE-PEG5000 and polyoxyethylene(40) stearate (PEG40-stearate). We characterized the size stability and acoustic behavior of monodisperse microbubbles produced with various Pluronic F68 concentrations. Adding 5–10 mol % Pluronic F68 was found to effectively suppress coalescence and facilitated the production of monodisperse microbubbles that remained shelf stable for at least 7 days. Acoustic attenuation measurements revealed a shell stiffness ranging from 0.78 to 0.93 N/m for these microbubbles. The 10 mol % Pluronic F68 addition (10PF) demonstrated superior monodispersity and was selected for further experiments. Upon dilution, the size and resonance frequencies of both F1–10PF and F2–10PF decreased over time, though F2–10PF showed better stability compared to F1–10PF for both metrics. Both F1–10PF and F2–10PF exhibited a stronger subharmonic scattering intensity than SonoVue (clinical approved microbubbles), which offers potential for blood pressure sensing. Our study shows that incorporating Pluronic F68 facilitates the production of monodisperse microbubbles at room temperature that are stable long-term and have excellent acoustical properties, with the F2–10PF formulation demonstrating better stability than the F1–10PF.

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Ultrasound and Hyperthermia Applications
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Influence of PluronicF68 on Size Stability and AcousticBehavior of Monodisperse Phospholipid-Coated Microbubbles Producedat Room Temperature · Figshare (2025) | TGRS Research Map | TGRS