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...
Gespeichert in:
Veröffentlicht in: | Journal of controlled release 2024-03, Vol.367, p.135-147 |
---|---|
Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2919745070</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0168365924000403</els_id><sourcerecordid>2919745070</sourcerecordid><originalsourceid>FETCH-LOGICAL-c393t-abe5110d0d2fc52072352c7c5894636a56e8aef57ca7c02189ca905661ca13cc3</originalsourceid><addsrcrecordid>eNqFkbtuFDEUhi1ERJbAI4Bc0szgy3hsVwiFBJAipYHa8tge8GrGXnyJSMcbUPCGeZJ42U3aVJaOvnN--f8AeINRjxEe32_7rYkhuaUniAw9wj0i4hnYYMFpN0jJnoNN40RHRyZPwcuctwghRgf-ApxSQSgfBd-Avxfz7I13ocC6lKRzrMF2q7NeF2ehTfUHtG7xNy7dwhJhTOVnLHHnDfw_hKWuMWV49-cf_OSTMwWauO508jkGGGdo4--Y6tQyQrdEbdvRoEOc6jQtLkMdLFy9SQ-DV-Bk1kt2r4_vGfh-efHt_Et3df356_nHq85QSUunJ8cwRhZZMhtGECeUEcMNE3IY6ajZ6IR2M-NGc4MIFtJoidg4YqMxNYaegXeHu7sUf1WXi1p9Nm5ZdHCxZkUxo1xgJIYnUSKx5ANDHDWUHdD2oZyTm9Uu-VWnW4WR2mtTW3XUpvbaFMKqaWt7b48RdWrdP249eGrAhwPgWic33iWV99JM87TvXNnon4i4Bwu2r_M</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2919745070</pqid></control><display><type>article</type><title>Efficient ultrasound-mediated drug delivery to orthotopic liver tumors – Direct comparison of doxorubicin-loaded nanobubbles and microbubbles</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><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.</creator><creatorcontrib>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.</creatorcontrib><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.</description><identifier>ISSN: 0168-3659</identifier><identifier>ISSN: 1873-4995</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/j.jconrel.2024.01.028</identifier><identifier>PMID: 38237687</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>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</subject><ispartof>Journal of controlled release, 2024-03, Vol.367, p.135-147</ispartof><rights>2023</rights><rights>Copyright © 2023. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c393t-abe5110d0d2fc52072352c7c5894636a56e8aef57ca7c02189ca905661ca13cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jconrel.2024.01.028$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38237687$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nittayacharn, Pinunta</creatorcontrib><creatorcontrib>Abenojar, Eric</creatorcontrib><creatorcontrib>Cooley, Michaela B.</creatorcontrib><creatorcontrib>Berg, Felipe M.</creatorcontrib><creatorcontrib>Counil, Claire</creatorcontrib><creatorcontrib>Sojahrood, Amin Jafari</creatorcontrib><creatorcontrib>Khan, Muhammad Saad</creatorcontrib><creatorcontrib>Yang, Celina</creatorcontrib><creatorcontrib>Berndl, Elizabeth</creatorcontrib><creatorcontrib>Golczak, Marcin</creatorcontrib><creatorcontrib>Kolios, Michael C.</creatorcontrib><creatorcontrib>Exner, Agata A.</creatorcontrib><title>Efficient ultrasound-mediated drug delivery to orthotopic liver tumors – Direct comparison of doxorubicin-loaded nanobubbles and microbubbles</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><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.</description><subject>Animals</subject><subject>apoptosis</subject><subject>cancer therapy</subject><subject>Cavitation</subject><subject>Cell Line, Tumor</subject><subject>Doxorubicin</subject><subject>Doxorubicin - pharmacokinetics</subject><subject>Doxorubicin - therapeutic use</subject><subject>Drug delivery</subject><subject>Drug Delivery Systems - methods</subject><subject>drugs</subject><subject>Humans</subject><subject>liver</subject><subject>Liver metastasis</subject><subject>liver neoplasms</subject><subject>Liver Neoplasms - diagnostic imaging</subject><subject>Liver Neoplasms - drug therapy</subject><subject>metastasis</subject><subject>Microbubbles</subject><subject>Nanobubbles</subject><subject>Orthotopic tumor</subject><subject>patients</subject><subject>pharmacokinetics</subject><subject>Rats</subject><subject>Sonoporation</subject><subject>Tissue Distribution</subject><subject>ultrasonics</subject><subject>Ultrasound-mediated drug delivery</subject><issn>0168-3659</issn><issn>1873-4995</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkbtuFDEUhi1ERJbAI4Bc0szgy3hsVwiFBJAipYHa8tge8GrGXnyJSMcbUPCGeZJ42U3aVJaOvnN--f8AeINRjxEe32_7rYkhuaUniAw9wj0i4hnYYMFpN0jJnoNN40RHRyZPwcuctwghRgf-ApxSQSgfBd-Avxfz7I13ocC6lKRzrMF2q7NeF2ehTfUHtG7xNy7dwhJhTOVnLHHnDfw_hKWuMWV49-cf_OSTMwWauO508jkGGGdo4--Y6tQyQrdEbdvRoEOc6jQtLkMdLFy9SQ-DV-Bk1kt2r4_vGfh-efHt_Et3df356_nHq85QSUunJ8cwRhZZMhtGECeUEcMNE3IY6ajZ6IR2M-NGc4MIFtJoidg4YqMxNYaegXeHu7sUf1WXi1p9Nm5ZdHCxZkUxo1xgJIYnUSKx5ANDHDWUHdD2oZyTm9Uu-VWnW4WR2mtTW3XUpvbaFMKqaWt7b48RdWrdP249eGrAhwPgWic33iWV99JM87TvXNnon4i4Bwu2r_M</recordid><startdate>202403</startdate><enddate>202403</enddate><creator>Nittayacharn, Pinunta</creator><creator>Abenojar, Eric</creator><creator>Cooley, Michaela B.</creator><creator>Berg, Felipe M.</creator><creator>Counil, Claire</creator><creator>Sojahrood, Amin Jafari</creator><creator>Khan, Muhammad Saad</creator><creator>Yang, Celina</creator><creator>Berndl, Elizabeth</creator><creator>Golczak, Marcin</creator><creator>Kolios, Michael C.</creator><creator>Exner, Agata A.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>202403</creationdate><title>Efficient ultrasound-mediated drug delivery to orthotopic liver tumors – Direct comparison of doxorubicin-loaded nanobubbles and microbubbles</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-abe5110d0d2fc52072352c7c5894636a56e8aef57ca7c02189ca905661ca13cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>apoptosis</topic><topic>cancer therapy</topic><topic>Cavitation</topic><topic>Cell Line, Tumor</topic><topic>Doxorubicin</topic><topic>Doxorubicin - pharmacokinetics</topic><topic>Doxorubicin - therapeutic use</topic><topic>Drug delivery</topic><topic>Drug Delivery Systems - methods</topic><topic>drugs</topic><topic>Humans</topic><topic>liver</topic><topic>Liver metastasis</topic><topic>liver neoplasms</topic><topic>Liver Neoplasms - diagnostic imaging</topic><topic>Liver Neoplasms - drug therapy</topic><topic>metastasis</topic><topic>Microbubbles</topic><topic>Nanobubbles</topic><topic>Orthotopic tumor</topic><topic>patients</topic><topic>pharmacokinetics</topic><topic>Rats</topic><topic>Sonoporation</topic><topic>Tissue Distribution</topic><topic>ultrasonics</topic><topic>Ultrasound-mediated drug delivery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nittayacharn, Pinunta</creatorcontrib><creatorcontrib>Abenojar, Eric</creatorcontrib><creatorcontrib>Cooley, Michaela B.</creatorcontrib><creatorcontrib>Berg, Felipe M.</creatorcontrib><creatorcontrib>Counil, Claire</creatorcontrib><creatorcontrib>Sojahrood, Amin Jafari</creatorcontrib><creatorcontrib>Khan, Muhammad Saad</creatorcontrib><creatorcontrib>Yang, Celina</creatorcontrib><creatorcontrib>Berndl, Elizabeth</creatorcontrib><creatorcontrib>Golczak, Marcin</creatorcontrib><creatorcontrib>Kolios, Michael C.</creatorcontrib><creatorcontrib>Exner, Agata A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nittayacharn, Pinunta</au><au>Abenojar, Eric</au><au>Cooley, Michaela B.</au><au>Berg, Felipe M.</au><au>Counil, Claire</au><au>Sojahrood, Amin Jafari</au><au>Khan, Muhammad Saad</au><au>Yang, Celina</au><au>Berndl, Elizabeth</au><au>Golczak, Marcin</au><au>Kolios, Michael C.</au><au>Exner, Agata A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient ultrasound-mediated drug delivery to orthotopic liver tumors – Direct comparison of doxorubicin-loaded nanobubbles and microbubbles</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2024-03</date><risdate>2024</risdate><volume>367</volume><spage>135</spage><epage>147</epage><pages>135-147</pages><issn>0168-3659</issn><issn>1873-4995</issn><eissn>1873-4995</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 0168-3659 |
ispartof | Journal of controlled release, 2024-03, Vol.367, p.135-147 |
issn | 0168-3659 1873-4995 1873-4995 |
language | eng |
recordid | cdi_proquest_miscellaneous_2919745070 |
source | MEDLINE; Elsevier ScienceDirect Journals |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T09%3A26%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Efficient%20ultrasound-mediated%20drug%20delivery%20to%20orthotopic%20liver%20tumors%20%E2%80%93%20Direct%20comparison%20of%20doxorubicin-loaded%20nanobubbles%20and%20microbubbles&rft.jtitle=Journal%20of%20controlled%20release&rft.au=Nittayacharn,%20Pinunta&rft.date=2024-03&rft.volume=367&rft.spage=135&rft.epage=147&rft.pages=135-147&rft.issn=0168-3659&rft.eissn=1873-4995&rft_id=info:doi/10.1016/j.jconrel.2024.01.028&rft_dat=%3Cproquest_cross%3E2919745070%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2919745070&rft_id=info:pmid/38237687&rft_els_id=S0168365924000403&rfr_iscdi=true |