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Synthesis and characterization of dextran coated magnetite nanoparticles for diagnostics and therapy

机译:葡聚糖包被的磁铁矿纳米颗粒的合成和表征,用于诊断和治疗

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Introduction Expansion of efficacious theranostic systems is of pivotal significance for medicine and human healthcare. Magnetic nanoparticles (MNPs) are known as drug delivery system and magnetic resonance imaging (MRI) contrast agent. MNPs as drug carriers have attracted significant attention because of the delivery of drugs loaded onto MNPs to solid tumors, maintaining them in the target site by an external electromagnetic field, and subsequently releasing drugs in a controlled manner. On the other hand, it is believed that MNPs possess high potential as MRI contrast agents. The aim of this work was to payload curcumin into dextran coated MNPs and investigate their potential as theranostic systems for controlled drug delivery and MRI imaging. Methods MNPs were synthesized as a core and coated with dextran as polymeric shell to provide steric stabilization. Curcumin as anticancer drug was selected to be loaded into NPs. To characterize the synthesized NPs, various techniques (e.g., DLS, FESEM, FT-IR, XRD, and VSM) were utilized. In vitro drug release of curcumin was evaluated at 37??C at the pH value of 5.4 and 7.4.The feasibility of employment of dextran coated MNPs as MRI contrast agents were also studied. Results Formulations prepared from dextran coated MNPs showed high loading (13%) and encapsulation efficiency (95%). In vitro release study performed in the phosphate-buffered saline (PBS, pH= 7.4, 5.4) revealed that the dextran coated MNPs possess sustained release behavior at least for 4 days with the high extent of drug release in acidic media. Vibrating sample magnetometer (VSM) analysis proved the superparamagnetic properties of the dextran coated MNPs with relatively high-magnetization value indicating that they were sufficiently sensitive to external magnetic fields as magnetic drug carriers. Furthermore, dextran coated MNPs exhibited high potential as T2 contrast agents for MRI. Conclusion Based on our findings, we propose the dextran coated MNPs as promising nanosystem for the delivery of various drugs such as curcumin and MRI contrast agent.
机译:简介有效的治疗学系统的扩展对于医学和人类医疗保健具有至关重要的意义。磁性纳米颗粒(MNP)被称为药物输送系统和磁共振成像(MRI)造影剂。由于将装载在MNP上的药物递送至实体瘤,通过外部电磁场将其保持在靶位点并随后以受控方式释放药物,MNP作为药物载体已引起了广泛的关注。另一方面,据信MNP具有作为MRI造影剂的高潜力。这项工作的目的是将姜黄素有效负载到葡聚糖包被的MNP中,并研究其作为治疗性药物输送和MRI成像治疗系统的潜力。方法以MNPs为核心,以葡聚糖为聚合物外壳包覆,以提供空间稳定作用。姜黄素作为抗癌药物被选入NP。为了表征合成的NP,使用了各种技术(例如,DLS,FESEM,FT-IR,XRD和VSM)。在37℃,pH分别为5.4和7.4的条件下评价姜黄素的体外药物释放。还研究了使用葡聚糖包被的MNP作为MRI造影剂的可行性。结果由葡聚糖包被的MNP制备的制剂显示出高载量(13%)和包封效率(95%)。在磷酸盐缓冲盐水(PBS,pH = 7.4,5.4)中进行的体外释放研究表明,葡聚糖包被的MNP具有持续释放行为至少4天,并且在酸性介质中具有高度的药物释放。振动样品磁力计(VSM)分析证明,葡聚糖包被的MNP的超顺磁性具有较高的磁化值,表明它们对作为磁性药物载体的外部磁场足够敏感。此外,葡聚糖包被的MNPs作为MRI的T2造影剂具有很高的潜力。结论基于我们的发现,我们建议使用葡聚糖包被的MNP作为有前景的纳米系统,用于递送各种药物,如姜黄素和MRI造影剂。

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