{"title":"亥姆霍兹线圈和超顺磁性纳米载体在局部抑制癌细胞迁移和侵袭中的应用","authors":"Sheng-Jie Shiue , Ming-Shun Wu , Xiao-Zhu Tang , Hsin-Yi Lin","doi":"10.1016/j.surfin.2025.106942","DOIUrl":null,"url":null,"abstract":"<div><div>Patients with advanced hepatocellular carcinoma (HCC) have a high death rate, and sorafenib, which has low solubility, is a common drug for HCC treatment. A system was designed to increase the bioavailability of sorafenib: sorafenib was loaded into iron oxide nanoparticles and extremely low frequency electromagnetic field (EMF; 100 Hz, 5mT) was applied to enhance sorafenib release from the nanocarrier. FTIR spectrum of the nanocarrier confirmed the existence of alginate coating and sorafenib. The nanoparticles were seen internalized by liver cancer cells HepG2 under fluorescence microscopy. The amount of sorafenib released from 1 mg of nanocarrier increased from 0.102 μg to 0.454 μg (<em>p</em> < 0.001) in the presence of EMF generated by a pair of Helmholtz coils. Similar degrees of HepG2 cell apoptosis were observed between the group treated with free sorafenib (4μg/mL) and the group treated with sorafenib-loaded nanocarriers and EMF. The scratch migration test results showed that the group treated with sorafenib-loaded nanocarrier and EMF showed <5 % of recovery while the group treated with free sorafenib had <1 % recovery, both significantly lower than the untreated group (41.3 %, <em>p</em> < 0.001). Compared to the untreated group, sorafenib-loaded nanocarrier with EMF reduced cell invasion by 79.2 %, and free sorafenib by 69.5 % (<em>p</em> < 0.05). The combination of the SFB-loaded nanocarrier and EMF slowly released low levels of sorafenib and had similar inhibitory effects on cancer cells as did free sorafenib at therapeutic concentration. This indicates that less sorafenib may be used to treat HCC, possibly reducing side effects.</div></div>","PeriodicalId":22081,"journal":{"name":"Surfaces and Interfaces","volume":"72 ","pages":"Article 106942"},"PeriodicalIF":5.7000,"publicationDate":"2025-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Application of Helmholtz Coils and superparamagnetic nanocarrier in localized inhibition of cancer cell migration and invasion\",\"authors\":\"Sheng-Jie Shiue , Ming-Shun Wu , Xiao-Zhu Tang , Hsin-Yi Lin\",\"doi\":\"10.1016/j.surfin.2025.106942\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Patients with advanced hepatocellular carcinoma (HCC) have a high death rate, and sorafenib, which has low solubility, is a common drug for HCC treatment. A system was designed to increase the bioavailability of sorafenib: sorafenib was loaded into iron oxide nanoparticles and extremely low frequency electromagnetic field (EMF; 100 Hz, 5mT) was applied to enhance sorafenib release from the nanocarrier. FTIR spectrum of the nanocarrier confirmed the existence of alginate coating and sorafenib. The nanoparticles were seen internalized by liver cancer cells HepG2 under fluorescence microscopy. The amount of sorafenib released from 1 mg of nanocarrier increased from 0.102 μg to 0.454 μg (<em>p</em> < 0.001) in the presence of EMF generated by a pair of Helmholtz coils. Similar degrees of HepG2 cell apoptosis were observed between the group treated with free sorafenib (4μg/mL) and the group treated with sorafenib-loaded nanocarriers and EMF. The scratch migration test results showed that the group treated with sorafenib-loaded nanocarrier and EMF showed <5 % of recovery while the group treated with free sorafenib had <1 % recovery, both significantly lower than the untreated group (41.3 %, <em>p</em> < 0.001). Compared to the untreated group, sorafenib-loaded nanocarrier with EMF reduced cell invasion by 79.2 %, and free sorafenib by 69.5 % (<em>p</em> < 0.05). The combination of the SFB-loaded nanocarrier and EMF slowly released low levels of sorafenib and had similar inhibitory effects on cancer cells as did free sorafenib at therapeutic concentration. This indicates that less sorafenib may be used to treat HCC, possibly reducing side effects.</div></div>\",\"PeriodicalId\":22081,\"journal\":{\"name\":\"Surfaces and Interfaces\",\"volume\":\"72 \",\"pages\":\"Article 106942\"},\"PeriodicalIF\":5.7000,\"publicationDate\":\"2025-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Surfaces and Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468023025011988\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Surfaces and Interfaces","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468023025011988","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Application of Helmholtz Coils and superparamagnetic nanocarrier in localized inhibition of cancer cell migration and invasion
Patients with advanced hepatocellular carcinoma (HCC) have a high death rate, and sorafenib, which has low solubility, is a common drug for HCC treatment. A system was designed to increase the bioavailability of sorafenib: sorafenib was loaded into iron oxide nanoparticles and extremely low frequency electromagnetic field (EMF; 100 Hz, 5mT) was applied to enhance sorafenib release from the nanocarrier. FTIR spectrum of the nanocarrier confirmed the existence of alginate coating and sorafenib. The nanoparticles were seen internalized by liver cancer cells HepG2 under fluorescence microscopy. The amount of sorafenib released from 1 mg of nanocarrier increased from 0.102 μg to 0.454 μg (p < 0.001) in the presence of EMF generated by a pair of Helmholtz coils. Similar degrees of HepG2 cell apoptosis were observed between the group treated with free sorafenib (4μg/mL) and the group treated with sorafenib-loaded nanocarriers and EMF. The scratch migration test results showed that the group treated with sorafenib-loaded nanocarrier and EMF showed <5 % of recovery while the group treated with free sorafenib had <1 % recovery, both significantly lower than the untreated group (41.3 %, p < 0.001). Compared to the untreated group, sorafenib-loaded nanocarrier with EMF reduced cell invasion by 79.2 %, and free sorafenib by 69.5 % (p < 0.05). The combination of the SFB-loaded nanocarrier and EMF slowly released low levels of sorafenib and had similar inhibitory effects on cancer cells as did free sorafenib at therapeutic concentration. This indicates that less sorafenib may be used to treat HCC, possibly reducing side effects.
期刊介绍:
The aim of the journal is to provide a respectful outlet for ''sound science'' papers in all research areas on surfaces and interfaces. We define sound science papers as papers that describe new and well-executed research, but that do not necessarily provide brand new insights or are merely a description of research results.
Surfaces and Interfaces publishes research papers in all fields of surface science which may not always find the right home on first submission to our Elsevier sister journals (Applied Surface, Surface and Coatings Technology, Thin Solid Films)