Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma

In recent years, carbon monoxide (CO) has garnered increased attention as a novel green therapy for hepatocellular carcinoma (HCC) treatment. However, the CO donor is still limited in clinical application due to its lack of targeted ability and unstable release rate. Here, self-assembled amphiphilic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular pharmaceutics 2024-10, Vol.21 (10), p.5015-5027
Hauptverfasser: Zhang, Congyi, Huang, Shizhuan, Ding, Kunhao, Wu, Haotian, Li, Minghui, Li, Tianwei, Shen, Zibo, Tai, Sheng, Li, Wenhua
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 5027
container_issue 10
container_start_page 5015
container_title Molecular pharmaceutics
container_volume 21
creator Zhang, Congyi
Huang, Shizhuan
Ding, Kunhao
Wu, Haotian
Li, Minghui
Li, Tianwei
Shen, Zibo
Tai, Sheng
Li, Wenhua
description In recent years, carbon monoxide (CO) has garnered increased attention as a novel green therapy for hepatocellular carcinoma (HCC) treatment. However, the CO donor is still limited in clinical application due to its lack of targeted ability and unstable release rate. Here, self-assembled amphiphilic nanomicelles glucose-polyethylene glycol (PEG)–lipoic acid (LA)–Fe2(CO)6 (Glu-Fe2(CO)6) are first designed as a CO donor and synthesized via a chemical method, combining glucose with Fe2(CO)6 through PEG–LA. Some advantages of this tumor-targeted Glu-Fe2(CO)6 delivery system include (I) good water-solubility, (II) the glutathione responsive CO slow release, (III) the active tumor-targeted ability of glucose as targeted ligands, and (IV) outstanding efficacy of antitumor and safety of CO therapy of HCC both in vitro and in vivo. These findings suggest that Glu-Fe2(CO)6 nanomicelles hold promise for enhancing antitumor therapeutic capabilities, presenting a novel tumor-targeted delivery strategy in gas therapy for HCC treatment.
doi_str_mv 10.1021/acs.molpharmaceut.4c00437
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3107505396</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3107505396</sourcerecordid><originalsourceid>FETCH-LOGICAL-a237t-e514bbbbb1b2b4c1a6e0751971d0c9669b9988b66f432ebee9f94ad0b9d58de43</originalsourceid><addsrcrecordid>eNqNkE1Pg0AQhjdGY2v1L5j15oW6yy4fezT4UZPGHqRnMsDQ0gCLu2DCvxfSauLNucwc3vedmYeQO86WnLn8ATK7rHXV7sHUkGHfLWXGmBTBGZlzTwonFMo9_51DOSNX1h4Yc6XniksyE0owN-TBnGzjvtbGicHssMOcRhv6Do3OsSq_0Az0Y7Ad1vQJbblrKDQ5jfdooB1ooQ1dYQudzrCq-goMjcBkZaNruCYXBVQWb059QbYvz3G0ctab17foce2AK4LOQY_LdCqeuqnMOPjIAo-rgOcsU76vUqXCMPX9QgoXU0RVKAk5S1XuhTlKsSD3x9zW6M8ebZfUpZ3OgQZ1bxPBxzzmCeWPUnWUZkZba7BIWlPWYIaEs2SimoxUkz9UkxPV0Xt7WtOnNea_zh-Mo8A7CqaMg-5NM379j-Bva52Mjw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3107505396</pqid></control><display><type>article</type><title>Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma</title><source>ACS Publications</source><creator>Zhang, Congyi ; Huang, Shizhuan ; Ding, Kunhao ; Wu, Haotian ; Li, Minghui ; Li, Tianwei ; Shen, Zibo ; Tai, Sheng ; Li, Wenhua</creator><creatorcontrib>Zhang, Congyi ; Huang, Shizhuan ; Ding, Kunhao ; Wu, Haotian ; Li, Minghui ; Li, Tianwei ; Shen, Zibo ; Tai, Sheng ; Li, Wenhua</creatorcontrib><description>In recent years, carbon monoxide (CO) has garnered increased attention as a novel green therapy for hepatocellular carcinoma (HCC) treatment. However, the CO donor is still limited in clinical application due to its lack of targeted ability and unstable release rate. Here, self-assembled amphiphilic nanomicelles glucose-polyethylene glycol (PEG)–lipoic acid (LA)–Fe2(CO)6 (Glu-Fe2(CO)6) are first designed as a CO donor and synthesized via a chemical method, combining glucose with Fe2(CO)6 through PEG–LA. Some advantages of this tumor-targeted Glu-Fe2(CO)6 delivery system include (I) good water-solubility, (II) the glutathione responsive CO slow release, (III) the active tumor-targeted ability of glucose as targeted ligands, and (IV) outstanding efficacy of antitumor and safety of CO therapy of HCC both in vitro and in vivo. These findings suggest that Glu-Fe2(CO)6 nanomicelles hold promise for enhancing antitumor therapeutic capabilities, presenting a novel tumor-targeted delivery strategy in gas therapy for HCC treatment.</description><identifier>ISSN: 1543-8384</identifier><identifier>ISSN: 1543-8392</identifier><identifier>EISSN: 1543-8392</identifier><identifier>DOI: 10.1021/acs.molpharmaceut.4c00437</identifier><identifier>PMID: 39302817</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Molecular pharmaceutics, 2024-10, Vol.21 (10), p.5015-5027</ispartof><rights>2024 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a237t-e514bbbbb1b2b4c1a6e0751971d0c9669b9988b66f432ebee9f94ad0b9d58de43</cites><orcidid>0009-0005-5459-3360</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.molpharmaceut.4c00437$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.molpharmaceut.4c00437$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39302817$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Congyi</creatorcontrib><creatorcontrib>Huang, Shizhuan</creatorcontrib><creatorcontrib>Ding, Kunhao</creatorcontrib><creatorcontrib>Wu, Haotian</creatorcontrib><creatorcontrib>Li, Minghui</creatorcontrib><creatorcontrib>Li, Tianwei</creatorcontrib><creatorcontrib>Shen, Zibo</creatorcontrib><creatorcontrib>Tai, Sheng</creatorcontrib><creatorcontrib>Li, Wenhua</creatorcontrib><title>Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma</title><title>Molecular pharmaceutics</title><addtitle>Mol. Pharmaceutics</addtitle><description>In recent years, carbon monoxide (CO) has garnered increased attention as a novel green therapy for hepatocellular carcinoma (HCC) treatment. However, the CO donor is still limited in clinical application due to its lack of targeted ability and unstable release rate. Here, self-assembled amphiphilic nanomicelles glucose-polyethylene glycol (PEG)–lipoic acid (LA)–Fe2(CO)6 (Glu-Fe2(CO)6) are first designed as a CO donor and synthesized via a chemical method, combining glucose with Fe2(CO)6 through PEG–LA. Some advantages of this tumor-targeted Glu-Fe2(CO)6 delivery system include (I) good water-solubility, (II) the glutathione responsive CO slow release, (III) the active tumor-targeted ability of glucose as targeted ligands, and (IV) outstanding efficacy of antitumor and safety of CO therapy of HCC both in vitro and in vivo. These findings suggest that Glu-Fe2(CO)6 nanomicelles hold promise for enhancing antitumor therapeutic capabilities, presenting a novel tumor-targeted delivery strategy in gas therapy for HCC treatment.</description><issn>1543-8384</issn><issn>1543-8392</issn><issn>1543-8392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqNkE1Pg0AQhjdGY2v1L5j15oW6yy4fezT4UZPGHqRnMsDQ0gCLu2DCvxfSauLNucwc3vedmYeQO86WnLn8ATK7rHXV7sHUkGHfLWXGmBTBGZlzTwonFMo9_51DOSNX1h4Yc6XniksyE0owN-TBnGzjvtbGicHssMOcRhv6Do3OsSq_0Az0Y7Ad1vQJbblrKDQ5jfdooB1ooQ1dYQudzrCq-goMjcBkZaNruCYXBVQWb059QbYvz3G0ctab17foce2AK4LOQY_LdCqeuqnMOPjIAo-rgOcsU76vUqXCMPX9QgoXU0RVKAk5S1XuhTlKsSD3x9zW6M8ebZfUpZ3OgQZ1bxPBxzzmCeWPUnWUZkZba7BIWlPWYIaEs2SimoxUkz9UkxPV0Xt7WtOnNea_zh-Mo8A7CqaMg-5NM379j-Bva52Mjw</recordid><startdate>20241007</startdate><enddate>20241007</enddate><creator>Zhang, Congyi</creator><creator>Huang, Shizhuan</creator><creator>Ding, Kunhao</creator><creator>Wu, Haotian</creator><creator>Li, Minghui</creator><creator>Li, Tianwei</creator><creator>Shen, Zibo</creator><creator>Tai, Sheng</creator><creator>Li, Wenhua</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0009-0005-5459-3360</orcidid></search><sort><creationdate>20241007</creationdate><title>Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma</title><author>Zhang, Congyi ; Huang, Shizhuan ; Ding, Kunhao ; Wu, Haotian ; Li, Minghui ; Li, Tianwei ; Shen, Zibo ; Tai, Sheng ; Li, Wenhua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a237t-e514bbbbb1b2b4c1a6e0751971d0c9669b9988b66f432ebee9f94ad0b9d58de43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Congyi</creatorcontrib><creatorcontrib>Huang, Shizhuan</creatorcontrib><creatorcontrib>Ding, Kunhao</creatorcontrib><creatorcontrib>Wu, Haotian</creatorcontrib><creatorcontrib>Li, Minghui</creatorcontrib><creatorcontrib>Li, Tianwei</creatorcontrib><creatorcontrib>Shen, Zibo</creatorcontrib><creatorcontrib>Tai, Sheng</creatorcontrib><creatorcontrib>Li, Wenhua</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Congyi</au><au>Huang, Shizhuan</au><au>Ding, Kunhao</au><au>Wu, Haotian</au><au>Li, Minghui</au><au>Li, Tianwei</au><au>Shen, Zibo</au><au>Tai, Sheng</au><au>Li, Wenhua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma</atitle><jtitle>Molecular pharmaceutics</jtitle><addtitle>Mol. Pharmaceutics</addtitle><date>2024-10-07</date><risdate>2024</risdate><volume>21</volume><issue>10</issue><spage>5015</spage><epage>5027</epage><pages>5015-5027</pages><issn>1543-8384</issn><issn>1543-8392</issn><eissn>1543-8392</eissn><abstract>In recent years, carbon monoxide (CO) has garnered increased attention as a novel green therapy for hepatocellular carcinoma (HCC) treatment. However, the CO donor is still limited in clinical application due to its lack of targeted ability and unstable release rate. Here, self-assembled amphiphilic nanomicelles glucose-polyethylene glycol (PEG)–lipoic acid (LA)–Fe2(CO)6 (Glu-Fe2(CO)6) are first designed as a CO donor and synthesized via a chemical method, combining glucose with Fe2(CO)6 through PEG–LA. Some advantages of this tumor-targeted Glu-Fe2(CO)6 delivery system include (I) good water-solubility, (II) the glutathione responsive CO slow release, (III) the active tumor-targeted ability of glucose as targeted ligands, and (IV) outstanding efficacy of antitumor and safety of CO therapy of HCC both in vitro and in vivo. These findings suggest that Glu-Fe2(CO)6 nanomicelles hold promise for enhancing antitumor therapeutic capabilities, presenting a novel tumor-targeted delivery strategy in gas therapy for HCC treatment.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>39302817</pmid><doi>10.1021/acs.molpharmaceut.4c00437</doi><tpages>13</tpages><orcidid>https://orcid.org/0009-0005-5459-3360</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 1543-8384
ispartof Molecular pharmaceutics, 2024-10, Vol.21 (10), p.5015-5027
issn 1543-8384
1543-8392
1543-8392
language eng
recordid cdi_proquest_miscellaneous_3107505396
source ACS Publications
title Tumor-Targeted CO Nanodelivery System Design and Therapy for Hepatocellular Carcinoma
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T05%3A36%3A31IST&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=Tumor-Targeted%20CO%20Nanodelivery%20System%20Design%20and%20Therapy%20for%20Hepatocellular%20Carcinoma&rft.jtitle=Molecular%20pharmaceutics&rft.au=Zhang,%20Congyi&rft.date=2024-10-07&rft.volume=21&rft.issue=10&rft.spage=5015&rft.epage=5027&rft.pages=5015-5027&rft.issn=1543-8384&rft.eissn=1543-8392&rft_id=info:doi/10.1021/acs.molpharmaceut.4c00437&rft_dat=%3Cproquest_cross%3E3107505396%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=3107505396&rft_id=info:pmid/39302817&rfr_iscdi=true