Article(id=1320388903002030462, tenantId=1146029695717560320, journalId=1319373289681944729, issueId=1320388874665316750, articleNumber=null, orderNo=null, doi=10.11876/mimt202503004, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1792734846115, onlineDateStr=2026-10-23, pubDate=1749484800000, pubDateStr=2025-06-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1792734846115, onlineIssueDateStr=2026-10-23, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1792734846115, creator=13701087609, updateTime=1792734846115, updator=13701087609, issue=Issue{id=1320388874665316750, tenantId=1146029695717560320, journalId=1319373289681944729, year='2025', volume='31', issue='3', pageStart='1', pageEnd='96', issueExtLink='null', onlineDate='null', pubDate='1749484800000', pubDateStr='2025-06-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792734839359, creator='13701087609', updateTime=1792746430009, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1320437489425305846, tenantId=1146029695717560320, journalId=1319373289681944729, issueId=1320388874665316750, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1320437489429500151, tenantId=1146029695717560320, journalId=1319373289681944729, issueId=1320388874665316750, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=24, endPage=29, ext={EN=ArticleExt(id=1320388903169802623, articleId=1320388903002030462, tenantId=1146029695717560320, journalId=1319373289681944729, language=EN, title=Porous hollow iron oxide nanosensitizers for enhanced radiofrequency ablation, columnId=null, journalTitle=Modern Instruments & Medical Treatment, columnName=null, runingTitle=null, highlight=null, articleAbstract=
Objective

To investigate the mechanism and effect of porous hollow iron oxide nanoparticles (HION) nanosensitizers (HION/VER) loaded with VER-155008 prepared to enhance the radiofrequency ablation on hepatocellular carcinoma tumors.

Methods

The construction of porous hollow iron oxide nanosensitizers and drug loading were investigated by transmission electron microscopy and zeta potential experiments. The in vitro anti-tumor ability of the sensitizers was examined by cell viability and cell live/dead staining experiments. The in vitro anti-tumor mechanism of the sensitizers was investigated by measuring the intracellular levels of reactive oxygen species (ROS), glutathione (GSH) and heat shock protein 70 (HSP70).

Results

Through material characterization analysis, porous hollow iron oxide nanosensitizers have been successfully constructed with a particle size of about 100 nm. HION/VER reduced tumor cell survival to 50% at 56.89 μg/mL and 45℃. Live/dead staining assay further confirmed that a large number of tumor cells died, indicating that HION/VER has good anti-tumor ability in vitro. Analysis by reactive oxygen fluorescence probe and glutathione level showed that reactive oxygen fluorescence was significantly enhanced and GSH levels decreased, indicating that HION/VER nano-sensitizer could promote iron death through the mechanism of disrupting redox balance. Analyzed by HSP70 immunofluorescence assay, the cellular HSP70 expression was significantly reduced after HION/VER treatment, indicating that the nano-sensitizer increased the sensitivity of tumor cells to mild radiofrequency ablation by inhibiting HSP70.

Conclusion

After HION/VER was endocytosed by the tumor cells, the drug uptake in the cells was increased, and the inhibition of HSP70 increased the sensitivity of the tumor cells to mild radiofrequency ablation by disrupting the redox balance to enhance the iron death, and the effect of radiofrequency ablation was achieved by effectively increasing the sensitivity of the tumor cells to mild radiofrequency ablation.

, authors=Zelong Jiang, Chang Zhao*, authorsList=Zelong Jiang, Chang Zhao, authorCompany=null, correspAuthors=Chang Zhao, authorNote=null, correspAuthorsNote=null, copyrightStatement=All copyrights in 2025 belong to the sponsor of the journal.Not content published by the journal may be reproduced or abridged without authorization., copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1320388903572455808, articleId=1320388903002030462, tenantId=1146029695717560320, journalId=1319373289681944729, language=CN, title=多孔空心氧化铁纳米增敏剂增强射频消融的研究, columnId=1320381056239387017, journalTitle=现代仪器与医疗, columnName=医学工程, runingTitle=null, highlight=null, articleAbstract=
目的

通过在多孔空心氧化铁纳米颗粒(hollow iron oxide nanoparticles,HION)上负载VER-155008制备纳米增敏剂(HION/VER),研究HION/VER增强射频消融对肝癌肿瘤的作用机制与效果。

方法

通过透射电镜及表面电位实验,考察多孔空心氧化铁纳米增敏剂的构建及药物负载。通过细胞生存率以及细胞活/死染色实验,考察增敏剂的体外抗肿瘤能力。通过检测细胞内活性氧(reactive oxygen species,ROS)、谷胱甘肽(glutathione,GSH)以及热休克蛋白70(heat shock protein 70,HSP70)水平,考察纳米增敏剂体外抗肿瘤机制。

结果

通过材料表征分析,多孔空心氧化铁纳米增敏剂已成功构建,粒径约为100 nm。在56.89 μg/mL和45℃条件下,HION/VER将肿瘤细胞生存率降低至50%。细胞活/死染色实验进一步证实,大量肿瘤细胞死亡,表明HION/VER具有良好的体外抗肿瘤能力。通过ROS荧光探针及GSH水平分析,ROS荧光明显增强,GSH水平下降,表明HION/VER可以通过破坏氧化还原平衡的机制来促进肿瘤铁死亡。通过HSP70免疫荧光实验分析,经过HION/VER处理后,细胞HSP70表达量明显减少,表明HION-VER通过抑制HSP70增加了肿瘤细胞对轻度射频消融的敏感性。

结论

HION/VER被肿瘤细胞内吞后,细胞摄取药物量增加,通过破坏氧化还原平衡增强铁死亡,抑制HSP70增加了肿瘤细胞对轻度射频消融的敏感性,有效提高了射频消融的效果。

, authors=江泽龙, 赵昌*, authorsList=江泽龙, 赵昌, authorCompany=null, correspAuthors=赵昌, authorNote=

江泽龙,男,硕士研究生,住院医师,研究方向:肿瘤仿生药物

, correspAuthorsNote=
赵昌,男,博士研究生,主任医师,研究方向:肿瘤仿生药物
, copyrightStatement=2025年版权归本刊主办单位所有未经本刊书面许可, 不得转载、摘编本刊所有文章内容。, copyrightOwner=中国科学器材公司, extLink=null, articleAbsUrl=null, sourceXml=A3QYUpwa/qQR6vrkfMHPQQ==, magXml=g2LTDF9yklVmBJ88Ufe9IQ==, pdfUrl=null, pdf=/cnc2OuDZPalcPGbMfAn5w==, pdfFileSize=2318188, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=rOk9qnzkbkvFrz8wHKxgIg==, mapNumber=null, fund=null)}, authors=[Author(id=1320388903962526085, tenantId=1146029695717560320, journalId=1319373289681944729, articleId=1320388903002030462, orderNo=0, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=0, email=null, emailSecond=null, emailThird=null, correspondingAuthor=0, authorType=1, ext={EN=AuthorExt(id=1320388904033829255, tenantId=1146029695717560320, journalId=1319373289681944729, articleId=1320388903002030462, authorId=1320388903962526085, language=EN, stringName=Zelong Jiang, firstName=Zelong, middleName=null, lastName=Jiang, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=Department of Interventional Therapy, Guangxi Medical University Cancer Hospital, Nanning 530000, China, bio=null, bioImg=null, bioContent=null, aboutCorrespAuthor=null), CN=AuthorExt(id=1320388905677996424, tenantId=1146029695717560320, journalId=1319373289681944729, articleId=1320388903002030462, authorId=1320388903962526085, language=CN, stringName=江泽龙, firstName=null, middleName=null, lastName=null, prefix=null, suffix=null, authorComment=null, nameInitials=null, affiliation=null, department=null, xref=null, address=广西医科大学附属肿瘤医院介入治疗科,南宁 530000, bio={"content":"

江泽龙,男,硕士研究生,住院医师,研究方向:肿瘤仿生药物

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多孔空心氧化铁纳米增敏剂增强射频消融的研究
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江泽龙 , 赵昌 *
现代仪器与医疗 | 医学工程 2025,31(3): 24-29
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现代仪器与医疗 |医学工程 2025 , 31 (3) : 24 -29
多孔空心氧化铁纳米增敏剂增强射频消融的研究
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江泽龙,男,硕士研究生,住院医师,研究方向:肿瘤仿生药物

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江泽龙,男,硕士研究生,住院医师,研究方向:肿瘤仿生药物

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江泽龙, 赵昌*
作者信息
  • 广西医科大学附属肿瘤医院介入治疗科,南宁 530000
通讯作者:
赵昌,男,博士研究生,主任医师,研究方向:肿瘤仿生药物
作者简介:

江泽龙,男,硕士研究生,住院医师,研究方向:肿瘤仿生药物

Porous hollow iron oxide nanosensitizers for enhanced radiofrequency ablation
Zelong Jiang, Chang Zhao*
Affiliations
  • Department of Interventional Therapy, Guangxi Medical University Cancer Hospital, Nanning 530000, China
出版时间: 2025-06-10 doi: 10.11876/mimt202503004
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目的

通过在多孔空心氧化铁纳米颗粒(hollow iron oxide nanoparticles,HION)上负载VER-155008制备纳米增敏剂(HION/VER),研究HION/VER增强射频消融对肝癌肿瘤的作用机制与效果。

方法

通过透射电镜及表面电位实验,考察多孔空心氧化铁纳米增敏剂的构建及药物负载。通过细胞生存率以及细胞活/死染色实验,考察增敏剂的体外抗肿瘤能力。通过检测细胞内活性氧(reactive oxygen species,ROS)、谷胱甘肽(glutathione,GSH)以及热休克蛋白70(heat shock protein 70,HSP70)水平,考察纳米增敏剂体外抗肿瘤机制。

结果

通过材料表征分析,多孔空心氧化铁纳米增敏剂已成功构建,粒径约为100 nm。在56.89 μg/mL和45℃条件下,HION/VER将肿瘤细胞生存率降低至50%。细胞活/死染色实验进一步证实,大量肿瘤细胞死亡,表明HION/VER具有良好的体外抗肿瘤能力。通过ROS荧光探针及GSH水平分析,ROS荧光明显增强,GSH水平下降,表明HION/VER可以通过破坏氧化还原平衡的机制来促进肿瘤铁死亡。通过HSP70免疫荧光实验分析,经过HION/VER处理后,细胞HSP70表达量明显减少,表明HION-VER通过抑制HSP70增加了肿瘤细胞对轻度射频消融的敏感性。

结论

HION/VER被肿瘤细胞内吞后,细胞摄取药物量增加,通过破坏氧化还原平衡增强铁死亡,抑制HSP70增加了肿瘤细胞对轻度射频消融的敏感性,有效提高了射频消融的效果。

射频消融  /  热休克蛋白  /  肝细胞癌  /  靶向  /  肿瘤治疗
Objective

To investigate the mechanism and effect of porous hollow iron oxide nanoparticles (HION) nanosensitizers (HION/VER) loaded with VER-155008 prepared to enhance the radiofrequency ablation on hepatocellular carcinoma tumors.

Methods

The construction of porous hollow iron oxide nanosensitizers and drug loading were investigated by transmission electron microscopy and zeta potential experiments. The in vitro anti-tumor ability of the sensitizers was examined by cell viability and cell live/dead staining experiments. The in vitro anti-tumor mechanism of the sensitizers was investigated by measuring the intracellular levels of reactive oxygen species (ROS), glutathione (GSH) and heat shock protein 70 (HSP70).

Results

Through material characterization analysis, porous hollow iron oxide nanosensitizers have been successfully constructed with a particle size of about 100 nm. HION/VER reduced tumor cell survival to 50% at 56.89 μg/mL and 45℃. Live/dead staining assay further confirmed that a large number of tumor cells died, indicating that HION/VER has good anti-tumor ability in vitro. Analysis by reactive oxygen fluorescence probe and glutathione level showed that reactive oxygen fluorescence was significantly enhanced and GSH levels decreased, indicating that HION/VER nano-sensitizer could promote iron death through the mechanism of disrupting redox balance. Analyzed by HSP70 immunofluorescence assay, the cellular HSP70 expression was significantly reduced after HION/VER treatment, indicating that the nano-sensitizer increased the sensitivity of tumor cells to mild radiofrequency ablation by inhibiting HSP70.

Conclusion

After HION/VER was endocytosed by the tumor cells, the drug uptake in the cells was increased, and the inhibition of HSP70 increased the sensitivity of the tumor cells to mild radiofrequency ablation by disrupting the redox balance to enhance the iron death, and the effect of radiofrequency ablation was achieved by effectively increasing the sensitivity of the tumor cells to mild radiofrequency ablation.

Radiofrequency ablation  /  Heat shock proteins  /  Hepatocellular carcinoma  /  Targeting  /  Tumor therapy
江泽龙, 赵昌. 多孔空心氧化铁纳米增敏剂增强射频消融的研究. 现代仪器与医疗, 2025 , 31 (3) : 24 -29 . DOI: 10.11876/mimt202503004
Zelong Jiang, Chang Zhao. Porous hollow iron oxide nanosensitizers for enhanced radiofrequency ablation[J]. Modern Instruments & Medical Treatment, 2025 , 31 (3) : 24 -29 . DOI: 10.11876/mimt202503004
  • 柳州市科技计划项目(2022SB017)
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2025年第31卷第3期
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doi: 10.11876/mimt202503004
  • 首发时间:2026-10-23
  • 出版时间:2025-06-10
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柳州市科技计划项目(2022SB017)
作者信息
    广西医科大学附属肿瘤医院介入治疗科,南宁 530000

通讯作者:

赵昌,男,博士研究生,主任医师,研究方向:肿瘤仿生药物
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鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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