Phase‐shift Perfluoropentane Nanoemulsions Enhance Pulsed High‐intensity Focused Ultrasound Ablation in an Isolated Perfused Liver System and Their Potential Value for Cancer Therapy
Purpose To investigate whether phase‐shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high‐intensity focused ultrasound (HIFU) ablation. Methods PFP was encapsulated by poly(lactic‐co‐glycolic acid) (PLGA) to form a nanometer‐sized droplet (PLGA‐PFP), which was added to an isolated perfu...
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Published in | Journal of ultrasound in medicine Vol. 41; no. 1; pp. 107 - 121 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.01.2022
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Subjects | |
Online Access | Get full text |
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Abstract | Purpose
To investigate whether phase‐shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high‐intensity focused ultrasound (HIFU) ablation.
Methods
PFP was encapsulated by poly(lactic‐co‐glycolic acid) (PLGA) to form a nanometer‐sized droplet (PLGA‐PFP), which was added to an isolated perfused liver system. Meanwhile, phosphate‐buffered saline (PBS) was used as a control. The perfused liver was exposed to HIFU (150 W, t = 3/5/10 s) at various duty cycles (DCs). The ultrasound images, cavitation emissions, and temperature were recorded. Rabbits with subcutaneous VX2 tumors were exposed to HIFU (150 W) at various DCs with or without PLGA‐PFP. After ablation, necrosis volume and energy efficiency factor were calculated. Pathologic characteristics were observed.
Results
Compared to the PBS control, PLGA‐PFP nanoemulsions markedly enhanced HIFU‐induced necrosis volume in both perfused livers and subcutaneous VX2 tumor‐bearing rabbits (P <.05). Inertial cavitation was much stronger in the pulsed‐HIFU exposure at 10% than that in the continuous‐wave HIFU exposure (P <.01). Peak temperature at 100% DC was significantly higher than that at 10% (P <.05). Compared to 100% DC HIFU exposure, the mean necrosis volume induced by 10 s exposure at 50% DC was significantly larger (P <.005) but lower at 10% DC in the isolated perfused livers (P <.05). In addition, the mean necrosis volume in subcutaneous VX2 tumor‐bearing rabbits was significantly increased after HIFU exposure at 10% DC when compared to those at 100% DC (P <.05). Histopathologic analysis showed liquefaction necrosis in pulsed HIFU.
Conclusion
PLGA‐PFP nanoemulsions can enhance HIFU ablation in the isolated perfused livers and promote tumor ablation in the subcutaneous xenograft rabbit model. Appropriate pulsed HIFU exposure may increase the necrosis volume and reduce total ultrasound energy required for HIFU ablation. |
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AbstractList | Purpose
To investigate whether phase‐shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high‐intensity focused ultrasound (HIFU) ablation.
Methods
PFP was encapsulated by poly(lactic‐co‐glycolic acid) (PLGA) to form a nanometer‐sized droplet (PLGA‐PFP), which was added to an isolated perfused liver system. Meanwhile, phosphate‐buffered saline (PBS) was used as a control. The perfused liver was exposed to HIFU (150 W, t = 3/5/10 s) at various duty cycles (DCs). The ultrasound images, cavitation emissions, and temperature were recorded. Rabbits with subcutaneous VX2 tumors were exposed to HIFU (150 W) at various DCs with or without PLGA‐PFP. After ablation, necrosis volume and energy efficiency factor were calculated. Pathologic characteristics were observed.
Results
Compared to the PBS control, PLGA‐PFP nanoemulsions markedly enhanced HIFU‐induced necrosis volume in both perfused livers and subcutaneous VX2 tumor‐bearing rabbits (P <.05). Inertial cavitation was much stronger in the pulsed‐HIFU exposure at 10% than that in the continuous‐wave HIFU exposure (P <.01). Peak temperature at 100% DC was significantly higher than that at 10% (P <.05). Compared to 100% DC HIFU exposure, the mean necrosis volume induced by 10 s exposure at 50% DC was significantly larger (P <.005) but lower at 10% DC in the isolated perfused livers (P <.05). In addition, the mean necrosis volume in subcutaneous VX2 tumor‐bearing rabbits was significantly increased after HIFU exposure at 10% DC when compared to those at 100% DC (P <.05). Histopathologic analysis showed liquefaction necrosis in pulsed HIFU.
Conclusion
PLGA‐PFP nanoemulsions can enhance HIFU ablation in the isolated perfused livers and promote tumor ablation in the subcutaneous xenograft rabbit model. Appropriate pulsed HIFU exposure may increase the necrosis volume and reduce total ultrasound energy required for HIFU ablation. To investigate whether phase-shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high-intensity focused ultrasound (HIFU) ablation. PFP was encapsulated by poly(lactic-co-glycolic acid) (PLGA) to form a nanometer-sized droplet (PLGA-PFP), which was added to an isolated perfused liver system. Meanwhile, phosphate-buffered saline (PBS) was used as a control. The perfused liver was exposed to HIFU (150 W, t = 3/5/10 s) at various duty cycles (DCs). The ultrasound images, cavitation emissions, and temperature were recorded. Rabbits with subcutaneous VX2 tumors were exposed to HIFU (150 W) at various DCs with or without PLGA-PFP. After ablation, necrosis volume and energy efficiency factor were calculated. Pathologic characteristics were observed. Compared to the PBS control, PLGA-PFP nanoemulsions markedly enhanced HIFU-induced necrosis volume in both perfused livers and subcutaneous VX2 tumor-bearing rabbits (P <.05). Inertial cavitation was much stronger in the pulsed-HIFU exposure at 10% than that in the continuous-wave HIFU exposure (P <.01). Peak temperature at 100% DC was significantly higher than that at 10% (P <.05). Compared to 100% DC HIFU exposure, the mean necrosis volume induced by 10 s exposure at 50% DC was significantly larger (P <.005) but lower at 10% DC in the isolated perfused livers (P <.05). In addition, the mean necrosis volume in subcutaneous VX2 tumor-bearing rabbits was significantly increased after HIFU exposure at 10% DC when compared to those at 100% DC (P <.05). Histopathologic analysis showed liquefaction necrosis in pulsed HIFU. PLGA-PFP nanoemulsions can enhance HIFU ablation in the isolated perfused livers and promote tumor ablation in the subcutaneous xenograft rabbit model. Appropriate pulsed HIFU exposure may increase the necrosis volume and reduce total ultrasound energy required for HIFU ablation. To investigate whether phase-shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high-intensity focused ultrasound (HIFU) ablation.PURPOSETo investigate whether phase-shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high-intensity focused ultrasound (HIFU) ablation.PFP was encapsulated by poly(lactic-co-glycolic acid) (PLGA) to form a nanometer-sized droplet (PLGA-PFP), which was added to an isolated perfused liver system. Meanwhile, phosphate-buffered saline (PBS) was used as a control. The perfused liver was exposed to HIFU (150 W, t = 3/5/10 s) at various duty cycles (DCs). The ultrasound images, cavitation emissions, and temperature were recorded. Rabbits with subcutaneous VX2 tumors were exposed to HIFU (150 W) at various DCs with or without PLGA-PFP. After ablation, necrosis volume and energy efficiency factor were calculated. Pathologic characteristics were observed.METHODSPFP was encapsulated by poly(lactic-co-glycolic acid) (PLGA) to form a nanometer-sized droplet (PLGA-PFP), which was added to an isolated perfused liver system. Meanwhile, phosphate-buffered saline (PBS) was used as a control. The perfused liver was exposed to HIFU (150 W, t = 3/5/10 s) at various duty cycles (DCs). The ultrasound images, cavitation emissions, and temperature were recorded. Rabbits with subcutaneous VX2 tumors were exposed to HIFU (150 W) at various DCs with or without PLGA-PFP. After ablation, necrosis volume and energy efficiency factor were calculated. Pathologic characteristics were observed.Compared to the PBS control, PLGA-PFP nanoemulsions markedly enhanced HIFU-induced necrosis volume in both perfused livers and subcutaneous VX2 tumor-bearing rabbits (P <.05). Inertial cavitation was much stronger in the pulsed-HIFU exposure at 10% than that in the continuous-wave HIFU exposure (P <.01). Peak temperature at 100% DC was significantly higher than that at 10% (P <.05). Compared to 100% DC HIFU exposure, the mean necrosis volume induced by 10 s exposure at 50% DC was significantly larger (P <.005) but lower at 10% DC in the isolated perfused livers (P <.05). In addition, the mean necrosis volume in subcutaneous VX2 tumor-bearing rabbits was significantly increased after HIFU exposure at 10% DC when compared to those at 100% DC (P <.05). Histopathologic analysis showed liquefaction necrosis in pulsed HIFU.RESULTSCompared to the PBS control, PLGA-PFP nanoemulsions markedly enhanced HIFU-induced necrosis volume in both perfused livers and subcutaneous VX2 tumor-bearing rabbits (P <.05). Inertial cavitation was much stronger in the pulsed-HIFU exposure at 10% than that in the continuous-wave HIFU exposure (P <.01). Peak temperature at 100% DC was significantly higher than that at 10% (P <.05). Compared to 100% DC HIFU exposure, the mean necrosis volume induced by 10 s exposure at 50% DC was significantly larger (P <.005) but lower at 10% DC in the isolated perfused livers (P <.05). In addition, the mean necrosis volume in subcutaneous VX2 tumor-bearing rabbits was significantly increased after HIFU exposure at 10% DC when compared to those at 100% DC (P <.05). Histopathologic analysis showed liquefaction necrosis in pulsed HIFU.PLGA-PFP nanoemulsions can enhance HIFU ablation in the isolated perfused livers and promote tumor ablation in the subcutaneous xenograft rabbit model. Appropriate pulsed HIFU exposure may increase the necrosis volume and reduce total ultrasound energy required for HIFU ablation.CONCLUSIONPLGA-PFP nanoemulsions can enhance HIFU ablation in the isolated perfused livers and promote tumor ablation in the subcutaneous xenograft rabbit model. Appropriate pulsed HIFU exposure may increase the necrosis volume and reduce total ultrasound energy required for HIFU ablation. |
Author | Chao, Xu Zhao, Lu‐Yan Yang, Bing‐She Wu, Feng Zou, Jian‐Zhong Wang, Guo‐Guan |
Author_xml | – sequence: 1 givenname: Lu‐Yan orcidid: 0000-0002-9452-5937 surname: Zhao fullname: Zhao, Lu‐Yan email: drifty2008@163.com organization: Shaanxi University of Chinese Medicine – sequence: 2 givenname: Xu surname: Chao fullname: Chao, Xu organization: Shaanxi University of Chinese Medicine – sequence: 3 givenname: Bing‐She surname: Yang fullname: Yang, Bing‐She organization: The Second Affiliated Hospital of Shaanxi University of Chinese Medicine – sequence: 4 givenname: Guo‐Guan surname: Wang fullname: Wang, Guo‐Guan organization: Shaanxi University of Chinese Medicine – sequence: 5 givenname: Jian‐Zhong orcidid: 0000-0003-2500-0317 surname: Zou fullname: Zou, Jian‐Zhong organization: Chongqing Medical University – sequence: 6 givenname: Feng surname: Wu fullname: Wu, Feng organization: University of Oxford |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33724514$$D View this record in MEDLINE/PubMed |
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Keywords | cancer treatment thermal ablation poly(lactic-co-glycolic acid) nanoemulsions porcine liver perfusion high-intensity focused ultrasound cavitation perfusion flow rate |
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To investigate whether phase‐shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high‐intensity focused ultrasound (HIFU) ablation.
Methods... To investigate whether phase-shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high-intensity focused ultrasound (HIFU) ablation. PFP was... To investigate whether phase-shift perfluoropetane (PFP) nanoemulsions can enhance pulsed high-intensity focused ultrasound (HIFU) ablation.PURPOSETo... |
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SubjectTerms | Animals cancer treatment cavitation Fluorocarbons High-Intensity Focused Ultrasound Ablation high‐intensity focused ultrasound Liver - diagnostic imaging Liver - surgery Neoplasms perfusion flow rate poly(lactic‐co‐glycolic acid) nanoemulsions porcine liver perfusion Rabbits thermal ablation |
Title | Phase‐shift Perfluoropentane Nanoemulsions Enhance Pulsed High‐intensity Focused Ultrasound Ablation in an Isolated Perfused Liver System and Their Potential Value for Cancer Therapy |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjum.15686 https://www.ncbi.nlm.nih.gov/pubmed/33724514 https://www.proquest.com/docview/2501850898 |
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