Efficient ultrasound-mediated drug delivery to orthotopic liver tumors – Direct comparison of doxorubicin-loaded nanobubbles and microbubbles

Liver metastasis is a major obstacle in treating aggressive cancers, and current therapeutic options often prove insufficient. To overcome these challenges, there has been growing interest in ultrasound-mediated drug delivery using lipid-shelled microbubbles (MBs) and nanobubbles (NBs) as promising...

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Veröffentlicht in:Journal of controlled release 2024-03, Vol.367, p.135-147
Hauptverfasser: Nittayacharn, Pinunta, Abenojar, Eric, Cooley, Michaela B., Berg, Felipe M., Counil, Claire, Sojahrood, Amin Jafari, Khan, Muhammad Saad, Yang, Celina, Berndl, Elizabeth, Golczak, Marcin, Kolios, Michael C., Exner, Agata A.
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container_end_page 147
container_issue
container_start_page 135
container_title Journal of controlled release
container_volume 367
creator Nittayacharn, Pinunta
Abenojar, Eric
Cooley, Michaela B.
Berg, Felipe M.
Counil, Claire
Sojahrood, Amin Jafari
Khan, Muhammad Saad
Yang, Celina
Berndl, Elizabeth
Golczak, Marcin
Kolios, Michael C.
Exner, Agata A.
description Liver metastasis is a major obstacle in treating aggressive cancers, and current therapeutic options often prove insufficient. To overcome these challenges, there has been growing interest in ultrasound-mediated drug delivery using lipid-shelled microbubbles (MBs) and nanobubbles (NBs) as promising strategies for enhancing drug delivery to tumors. Our previous work demonstrated the potential of Doxorubicin-loaded C3F8 NBs (hDox-NB, 280 ± 123 nm) in improving cancer treatment in vitro using low-frequency unfocused therapeutic ultrasound (TUS). In this study, we investigated the pharmacokinetics and biodistribution of sonicated hDox-NBs in orthotopic rat liver tumors. We compared their delivery and therapeutic efficiency with size-isolated MBs (hDox-MB, 1104 ± 373 nm) made from identical shell material and core gas. Results showed a similar accumulation of hDox in tumors treated with hDox-MBs and unfocused therapeutic ultrasound (hDox-MB + TUS) and hDox-NB + TUS. However, significantly increased apoptotic cell death in the tumor and fewer off-target apoptotic cells in the normal liver were found upon the treatment with hDox-NB + TUS. The tumor-to-liver apoptotic ratio was elevated 9.4-fold following treatment with hDox-NB + TUS compared to hDox-MB + TUS, suggesting that the therapeutic efficacy and specificity are significantly increased when using hDox-NB + TUS. These findings highlight the potential of this approach as a viable treatment modality for liver tumors. By elucidating the behavior of drug-loaded bubbles in vivo, we aim to contribute to developing more effective liver cancer treatments that could ultimately improve patient outcomes and decrease off-target side effects. [Display omitted] •Bubble size is a critical factor in ultrasound-mediated drug delivery to tumors.•Nanobubbles excited with ultrasound deliver more drugs to tumors than microbubbles.•Nanobubbles + ultrasound increase apoptotic cell death in tumors while sparing normal liver.
doi_str_mv 10.1016/j.jconrel.2024.01.028
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To overcome these challenges, there has been growing interest in ultrasound-mediated drug delivery using lipid-shelled microbubbles (MBs) and nanobubbles (NBs) as promising strategies for enhancing drug delivery to tumors. Our previous work demonstrated the potential of Doxorubicin-loaded C3F8 NBs (hDox-NB, 280 ± 123 nm) in improving cancer treatment in vitro using low-frequency unfocused therapeutic ultrasound (TUS). In this study, we investigated the pharmacokinetics and biodistribution of sonicated hDox-NBs in orthotopic rat liver tumors. We compared their delivery and therapeutic efficiency with size-isolated MBs (hDox-MB, 1104 ± 373 nm) made from identical shell material and core gas. Results showed a similar accumulation of hDox in tumors treated with hDox-MBs and unfocused therapeutic ultrasound (hDox-MB + TUS) and hDox-NB + TUS. However, significantly increased apoptotic cell death in the tumor and fewer off-target apoptotic cells in the normal liver were found upon the treatment with hDox-NB + TUS. The tumor-to-liver apoptotic ratio was elevated 9.4-fold following treatment with hDox-NB + TUS compared to hDox-MB + TUS, suggesting that the therapeutic efficacy and specificity are significantly increased when using hDox-NB + TUS. These findings highlight the potential of this approach as a viable treatment modality for liver tumors. By elucidating the behavior of drug-loaded bubbles in vivo, we aim to contribute to developing more effective liver cancer treatments that could ultimately improve patient outcomes and decrease off-target side effects. 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To overcome these challenges, there has been growing interest in ultrasound-mediated drug delivery using lipid-shelled microbubbles (MBs) and nanobubbles (NBs) as promising strategies for enhancing drug delivery to tumors. Our previous work demonstrated the potential of Doxorubicin-loaded C3F8 NBs (hDox-NB, 280 ± 123 nm) in improving cancer treatment in vitro using low-frequency unfocused therapeutic ultrasound (TUS). In this study, we investigated the pharmacokinetics and biodistribution of sonicated hDox-NBs in orthotopic rat liver tumors. We compared their delivery and therapeutic efficiency with size-isolated MBs (hDox-MB, 1104 ± 373 nm) made from identical shell material and core gas. Results showed a similar accumulation of hDox in tumors treated with hDox-MBs and unfocused therapeutic ultrasound (hDox-MB + TUS) and hDox-NB + TUS. However, significantly increased apoptotic cell death in the tumor and fewer off-target apoptotic cells in the normal liver were found upon the treatment with hDox-NB + TUS. The tumor-to-liver apoptotic ratio was elevated 9.4-fold following treatment with hDox-NB + TUS compared to hDox-MB + TUS, suggesting that the therapeutic efficacy and specificity are significantly increased when using hDox-NB + TUS. These findings highlight the potential of this approach as a viable treatment modality for liver tumors. By elucidating the behavior of drug-loaded bubbles in vivo, we aim to contribute to developing more effective liver cancer treatments that could ultimately improve patient outcomes and decrease off-target side effects. [Display omitted] •Bubble size is a critical factor in ultrasound-mediated drug delivery to tumors.•Nanobubbles excited with ultrasound deliver more drugs to tumors than microbubbles.•Nanobubbles + ultrasound increase apoptotic cell death in tumors while sparing normal liver.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38237687</pmid><doi>10.1016/j.jconrel.2024.01.028</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
apoptosis
cancer therapy
Cavitation
Cell Line, Tumor
Doxorubicin
Doxorubicin - pharmacokinetics
Doxorubicin - therapeutic use
Drug delivery
Drug Delivery Systems - methods
drugs
Humans
liver
Liver metastasis
liver neoplasms
Liver Neoplasms - diagnostic imaging
Liver Neoplasms - drug therapy
metastasis
Microbubbles
Nanobubbles
Orthotopic tumor
patients
pharmacokinetics
Rats
Sonoporation
Tissue Distribution
ultrasonics
Ultrasound-mediated drug delivery
title Efficient ultrasound-mediated drug delivery to orthotopic liver tumors – Direct comparison of doxorubicin-loaded nanobubbles and microbubbles
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