Khuram Shahzad, Muhammad Ali Abbasi, Muhammad Hassan Rafe, Anna Pestereva, Faheem Ullah, Muhammad Zaman, Muhammad Irfan, Muhammad Afzal, Anna Orlova
{"title":"用于提高抗癌活性的负载多柔比星的核@壳钴铁氧体-钛酸钡磁电纳米纤维。","authors":"Khuram Shahzad, Muhammad Ali Abbasi, Muhammad Hassan Rafe, Anna Pestereva, Faheem Ullah, Muhammad Zaman, Muhammad Irfan, Muhammad Afzal, Anna Orlova","doi":"10.1088/1748-605X/ad971e","DOIUrl":null,"url":null,"abstract":"<p><p>Conventional drug delivery systems often suffer from non-specific distribution and limited therapeutic efficacy, leading to significant side effects. To address these challenges, we developed magnetoelectric, cobalt ferrite@barium titanate (CFO@BTO) nanofibers (NFs), with a core-shell structure for targeted anticancer drug delivery. The electrospinning method was employed to synthesize polymeric NFs based on magnetoelectric core-shell nanostructures. The scanning electron microscopy, transmission electron microscopy, x-ray diffraction and Vibrating sample magnetometer analysis confirmed the successful loading of nanostructures on polymeric NF, the core-shell morphology and magnetoelectric phase of CFO@BTO, respectively. UV-Vis spectroscopy was applied to verify the drug attachment, the optimization of drug release in an applied external magnetic field (MF), and the time required for control drug release. The effectiveness of MF-assisted controlled drug release was demonstrated by achieving a 95 ± 1.03% drug release from magnetoelectric NFs (MENFs) within 30 min under a MF of 4 mT.<i>In vitro</i>cytotoxicity assay on human skin cancer (SK-MEL-28) cell lines exhibited a maximum 90 ± 2% cytotoxicity with 2 ± 0.03 cm of drug loaded MENFs. Furthermore, the Hemolysis assay was carried out to affirm the biocompatibility and non-toxicity of drug loaded MENFs, which is suitable for anticancer therapy.</p>","PeriodicalId":72389,"journal":{"name":"Biomedical materials (Bristol, England)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Doxorubicin-loaded core@shell cobalt ferrite-barium titanate magnetoelectric nanofibers for improved anticancer activity.\",\"authors\":\"Khuram Shahzad, Muhammad Ali Abbasi, Muhammad Hassan Rafe, Anna Pestereva, Faheem Ullah, Muhammad Zaman, Muhammad Irfan, Muhammad Afzal, Anna Orlova\",\"doi\":\"10.1088/1748-605X/ad971e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Conventional drug delivery systems often suffer from non-specific distribution and limited therapeutic efficacy, leading to significant side effects. To address these challenges, we developed magnetoelectric, cobalt ferrite@barium titanate (CFO@BTO) nanofibers (NFs), with a core-shell structure for targeted anticancer drug delivery. The electrospinning method was employed to synthesize polymeric NFs based on magnetoelectric core-shell nanostructures. The scanning electron microscopy, transmission electron microscopy, x-ray diffraction and Vibrating sample magnetometer analysis confirmed the successful loading of nanostructures on polymeric NF, the core-shell morphology and magnetoelectric phase of CFO@BTO, respectively. UV-Vis spectroscopy was applied to verify the drug attachment, the optimization of drug release in an applied external magnetic field (MF), and the time required for control drug release. The effectiveness of MF-assisted controlled drug release was demonstrated by achieving a 95 ± 1.03% drug release from magnetoelectric NFs (MENFs) within 30 min under a MF of 4 mT.<i>In vitro</i>cytotoxicity assay on human skin cancer (SK-MEL-28) cell lines exhibited a maximum 90 ± 2% cytotoxicity with 2 ± 0.03 cm of drug loaded MENFs. Furthermore, the Hemolysis assay was carried out to affirm the biocompatibility and non-toxicity of drug loaded MENFs, which is suitable for anticancer therapy.</p>\",\"PeriodicalId\":72389,\"journal\":{\"name\":\"Biomedical materials (Bristol, England)\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biomedical materials (Bristol, England)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1088/1748-605X/ad971e\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedical materials (Bristol, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1088/1748-605X/ad971e","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Conventional drug delivery systems often suffer from non-specific distribution and limited therapeutic efficacy, leading to significant side effects. To address these challenges, we developed magnetoelectric, cobalt ferrite@barium titanate (CFO@BTO) nanofibers (NFs), with a core-shell structure for targeted anticancer drug delivery. The electrospinning method was employed to synthesize polymeric NFs based on magnetoelectric core-shell nanostructures. The scanning electron microscopy, transmission electron microscopy, x-ray diffraction and Vibrating sample magnetometer analysis confirmed the successful loading of nanostructures on polymeric NF, the core-shell morphology and magnetoelectric phase of CFO@BTO, respectively. UV-Vis spectroscopy was applied to verify the drug attachment, the optimization of drug release in an applied external magnetic field (MF), and the time required for control drug release. The effectiveness of MF-assisted controlled drug release was demonstrated by achieving a 95 ± 1.03% drug release from magnetoelectric NFs (MENFs) within 30 min under a MF of 4 mT.In vitrocytotoxicity assay on human skin cancer (SK-MEL-28) cell lines exhibited a maximum 90 ± 2% cytotoxicity with 2 ± 0.03 cm of drug loaded MENFs. Furthermore, the Hemolysis assay was carried out to affirm the biocompatibility and non-toxicity of drug loaded MENFs, which is suitable for anticancer therapy.