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Magnetically actuated cisplatin-loaded nanoparticle collectives enhance drug penetration for potentiated ovarian cancer chemotherapy
We propose a strategy utilizing magnetic nanoparticle collectives to enhance drug targeted delivery and penetration for potentiated ovarian cancer chemotherapy. The designed magnetic pH-responsive nanoparticle collectives could active deliver chemotherapeutics to the tumor site, and enhance drug pen...
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Published in: | Journal of colloid and interface science 2025-01, Vol.678 (Pt A), p.108-118 |
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container_end_page | 118 |
container_issue | Pt A |
container_start_page | 108 |
container_title | Journal of colloid and interface science |
container_volume | 678 |
creator | Chen, Ying Zhang, Qiang Shen, Jian Liu, Zhiran Cui, Xiaoyu Ma, Li Zheng, Yuanyi Wang, Longchen Ying, Tao |
description | We propose a strategy utilizing magnetic nanoparticle collectives to enhance drug targeted delivery and penetration for potentiated ovarian cancer chemotherapy. The designed magnetic pH-responsive nanoparticle collectives could active deliver chemotherapeutics to the tumor site, and enhance drug penetration into deep tumors by the torque-force hybrid magnetic field, offering potentially clinically feasible strategy for enhancing tumor chemotherapy.
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Chemotherapy is the main clinical treatment for ovarian cancer, but still faces challenges of low drug targeting efficiency and insufficient drug permeability. Drug-loaded nanoparticle collectives, which are actuated by magnetic field, could be targeted to a designated location and achieve targeted drug delivery. In this work, we report a strategy that utilizes magnetic mesoporous silica nanoparticles loaded with cis-diaminodichloroplatinum (Fe3O4@SiO2-CDDP) for targeted delivery of chemotherapeutic drugs and enhances penetration into deep tumors. The Fe3O4@SiO2-CDDP collectives actively moved to the target tumor site, and this movement was regulated by a magnetic actuation system. Under the action of a torque-force hybrid magnetic field (TFMF), Fe3O4@SiO2-CDDP could further penetrate into the interior of tumors and achieve pH-responsive drug release in the tumor environment. The feasibility of this strategy was verified in three-dimensional cell spheres in vitro and in a tumor-bearing mouse model in vivo. This magnetically actuated nanoparticle collectives enhanced drug penetration strategy provides a new paradigm for targeted drug delivery and potentiated tumor therapy. |
doi_str_mv | 10.1016/j.jcis.2024.08.160 |
format | article |
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[Display omitted]
Chemotherapy is the main clinical treatment for ovarian cancer, but still faces challenges of low drug targeting efficiency and insufficient drug permeability. Drug-loaded nanoparticle collectives, which are actuated by magnetic field, could be targeted to a designated location and achieve targeted drug delivery. In this work, we report a strategy that utilizes magnetic mesoporous silica nanoparticles loaded with cis-diaminodichloroplatinum (Fe3O4@SiO2-CDDP) for targeted delivery of chemotherapeutic drugs and enhances penetration into deep tumors. The Fe3O4@SiO2-CDDP collectives actively moved to the target tumor site, and this movement was regulated by a magnetic actuation system. Under the action of a torque-force hybrid magnetic field (TFMF), Fe3O4@SiO2-CDDP could further penetrate into the interior of tumors and achieve pH-responsive drug release in the tumor environment. The feasibility of this strategy was verified in three-dimensional cell spheres in vitro and in a tumor-bearing mouse model in vivo. This magnetically actuated nanoparticle collectives enhanced drug penetration strategy provides a new paradigm for targeted drug delivery and potentiated tumor therapy.</description><identifier>ISSN: 0021-9797</identifier><identifier>ISSN: 1095-7103</identifier><identifier>EISSN: 1095-7103</identifier><identifier>DOI: 10.1016/j.jcis.2024.08.160</identifier><identifier>PMID: 39182385</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Drug delivery ; Magnetic nanoparticles ; Ovarian cancer ; Tumor penetration</subject><ispartof>Journal of colloid and interface science, 2025-01, Vol.678 (Pt A), p.108-118</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c237t-2130decc87ef3378b17632bcee1f8d0db97780772e495bb013dab72937d4b3133</cites><orcidid>0000-0001-7468-2268</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39182385$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Ying</creatorcontrib><creatorcontrib>Zhang, Qiang</creatorcontrib><creatorcontrib>Shen, Jian</creatorcontrib><creatorcontrib>Liu, Zhiran</creatorcontrib><creatorcontrib>Cui, Xiaoyu</creatorcontrib><creatorcontrib>Ma, Li</creatorcontrib><creatorcontrib>Zheng, Yuanyi</creatorcontrib><creatorcontrib>Wang, Longchen</creatorcontrib><creatorcontrib>Ying, Tao</creatorcontrib><title>Magnetically actuated cisplatin-loaded nanoparticle collectives enhance drug penetration for potentiated ovarian cancer chemotherapy</title><title>Journal of colloid and interface science</title><addtitle>J Colloid Interface Sci</addtitle><description>We propose a strategy utilizing magnetic nanoparticle collectives to enhance drug targeted delivery and penetration for potentiated ovarian cancer chemotherapy. The designed magnetic pH-responsive nanoparticle collectives could active deliver chemotherapeutics to the tumor site, and enhance drug penetration into deep tumors by the torque-force hybrid magnetic field, offering potentially clinically feasible strategy for enhancing tumor chemotherapy.
[Display omitted]
Chemotherapy is the main clinical treatment for ovarian cancer, but still faces challenges of low drug targeting efficiency and insufficient drug permeability. Drug-loaded nanoparticle collectives, which are actuated by magnetic field, could be targeted to a designated location and achieve targeted drug delivery. In this work, we report a strategy that utilizes magnetic mesoporous silica nanoparticles loaded with cis-diaminodichloroplatinum (Fe3O4@SiO2-CDDP) for targeted delivery of chemotherapeutic drugs and enhances penetration into deep tumors. The Fe3O4@SiO2-CDDP collectives actively moved to the target tumor site, and this movement was regulated by a magnetic actuation system. Under the action of a torque-force hybrid magnetic field (TFMF), Fe3O4@SiO2-CDDP could further penetrate into the interior of tumors and achieve pH-responsive drug release in the tumor environment. The feasibility of this strategy was verified in three-dimensional cell spheres in vitro and in a tumor-bearing mouse model in vivo. 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The designed magnetic pH-responsive nanoparticle collectives could active deliver chemotherapeutics to the tumor site, and enhance drug penetration into deep tumors by the torque-force hybrid magnetic field, offering potentially clinically feasible strategy for enhancing tumor chemotherapy.
[Display omitted]
Chemotherapy is the main clinical treatment for ovarian cancer, but still faces challenges of low drug targeting efficiency and insufficient drug permeability. Drug-loaded nanoparticle collectives, which are actuated by magnetic field, could be targeted to a designated location and achieve targeted drug delivery. In this work, we report a strategy that utilizes magnetic mesoporous silica nanoparticles loaded with cis-diaminodichloroplatinum (Fe3O4@SiO2-CDDP) for targeted delivery of chemotherapeutic drugs and enhances penetration into deep tumors. The Fe3O4@SiO2-CDDP collectives actively moved to the target tumor site, and this movement was regulated by a magnetic actuation system. Under the action of a torque-force hybrid magnetic field (TFMF), Fe3O4@SiO2-CDDP could further penetrate into the interior of tumors and achieve pH-responsive drug release in the tumor environment. The feasibility of this strategy was verified in three-dimensional cell spheres in vitro and in a tumor-bearing mouse model in vivo. This magnetically actuated nanoparticle collectives enhanced drug penetration strategy provides a new paradigm for targeted drug delivery and potentiated tumor therapy.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39182385</pmid><doi>10.1016/j.jcis.2024.08.160</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-7468-2268</orcidid></addata></record> |
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subjects | Drug delivery Magnetic nanoparticles Ovarian cancer Tumor penetration |
title | Magnetically actuated cisplatin-loaded nanoparticle collectives enhance drug penetration for potentiated ovarian cancer chemotherapy |
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