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Imaging the Delivery of Drug-loaded Iron-stabilized Micelles

机译:成像载药的铁稳定胶束

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摘要

Nanoparticle drug carriers hold potential to improve current cancer therapy by delivering payload to the tumor environment and decreasing toxic side effects. Challenges in nanotechnology drug delivery include plasma instability, site-specific delivery, and relevant biomarkers. We have developed a triblock polymer comprising a hydroxamic acid functionalized center block that chelates iron to form a stabilized micelle that physically entraps chemotherapeutic drugs in the hydrophobic core. The iron-imparted stability significantly improves the integrity of the micelle and extends circulation pharmacokinetics in plasma over that of free drug. Furthermore, the paramagnetic properties of the iron-crosslinking exhibits contrast in the tumors for imaging by magnetic resonance. Three separate nanoparticle formulations demonstrate improved anti-tumor efficacy in xenograft models and decreased toxicity. We report a stabilized polymer micelle that improves the tolerability and efficacy of chemotherapeutic drugs, and holds potential for non-invasive MRI to image drug delivery and deposition in the tumor.
机译:纳米颗粒药物载体通过将有效载荷传递到肿瘤环境并减少毒性副作用,具有改善当前癌症治疗的潜力。纳米技术药物输送的挑战包括血浆不稳定,特定部位的输送和相关的生物标记物。我们已经开发了包含羟肟酸官能化的中心嵌段的三嵌段聚合物,其螯合铁以形成稳定的胶束,该胶束物理地将化学治疗药物截留在疏水核中。与游离药物相比,铁赋予的稳定性显着改善了胶束的完整性,并延长了血浆中的循环药代动力学。此外,铁交联的顺磁性在用于通过磁共振成像的肿瘤中表现出对比度。三种单独的纳米颗粒制剂在异种移植模型中显示出改善的抗肿瘤功效,并降低了毒性。我们报告了一种稳定的聚合物胶束,可改善化学治疗药物的耐受性和功效,并具有非侵入性MRI潜力,可在肿瘤中成像药物的输送和沉积。

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