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。

Khuram Shahzad, Muhammad Ali Abbasi, Muhammad Hassan Rafe, Anna Pestereva, Faheem Ullah, Muhammad Zaman, Muhammad Irfan, Muhammad Afzal, Anna O Orlova
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引用次数: 0

摘要

传统的给药系统往往存在非特异性分布和疗效有限的问题,从而导致严重的副作用。为了应对这些挑战,我们开发了具有核壳结构的磁电钴铁氧体@钛酸钡(CFO@BTO)纳米纤维,用于抗癌药物的靶向递送。采用电纺丝方法合成了基于磁电核壳纳米结构的聚合物纳米纤维。扫描电子显微镜(SEM)、透射电子显微镜(TEM)、X射线衍射(XRD)和振动样品磁力计(VSM)分析分别证实了纳米结构在聚合物纳米纤维上的成功负载、钴铁氧体@钛酸钡CFO@BTO的核壳形貌和磁电相。为了验证药物的附着情况、外加磁场中药物释放的优化情况以及控制药物释放所需的时间,使用了紫外可见光谱。在 4mT 的磁场下,磁电纳米纤维在 30 分钟内实现了 95 ± 1.03% 的药物释放,证明了磁场辅助药物控释的有效性。对人类皮肤癌(SK-MEL-28)细胞系进行的体外细胞毒性试验表明,2±0.03 cm 的磁电纳米纤维负载药物后,细胞毒性最高可达 90 ± 2%。此外,还进行了溶血试验,以确定载药 MENFs 的生物相容性和无毒性,适用于抗癌治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Doxorubicin-loaded core@shell cobalt ferrite-barium titanate magnetoelectric nanofibers for improved anticancer activity.

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, with a core-shell structure for targeted anticancer drug delivery. The electrospinning method was employed to synthesize polymeric nanofibers based on magnetoelectric core-shell nanostructures. The Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), X-ray diffraction (XRD) and Vibrating sample magnetometer (VSM) analysis confirmed the successful loading of nanostructures on polymeric nanofiber, the core-shell morphology and magnetoelectric phase of cobalt ferrite@barium titanate CFO@BTO, respectively. To verify the drug attachment, the optimization of drug release in an applied external magnetic field, and the time required for control drug release, UV-Vis spectroscopy was used. The effectiveness of magnetic field-assisted controlled drug release was demonstrated by achieving a 95 ± 1.03% drug release from magnetoelectric nanofibers (MENFs) within 30 minutes under a magnetic field of 4mT. In vitro 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.

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