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Image-Guided Local Delivery Strategies Enhance Therapeutic Nanoparticle Uptake in Solid Tumors

机译:图像引导的局部递送策略增强了实体瘤中治疗性纳米颗粒的摄取。

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摘要

Nanoparticles (NP) have emerged as a novel class of therapeutic agents that overcome many of the limitations of current cancer chemotherapeutics. However, a major challenge to many current NP platforms is unfavorable biodistribution, and limited tumor uptake, upon systemic delivery. Delivery, therefore, remains a critical barrier to widespread clinical adoption of NP therapeutics. To overcome these limitations, we have adapted the techniques of image-guided local drug delivery to develop nano-ablation and nano-embolization. Nano-ablation is a tumor ablative strategy that employs image-guided placement of electrodes into tumor tissue to electroporate tumor cells, resulting in rapid influx of NPs that is not dependent on cellular uptake machinery or stage of the cell cycle. Nano-embolization involves the image-guided delivery of NPs and embolic agents directly into the blood supply of tumors. We describe the design and testing of our innovative local delivery strategies using doxorubicin functionalized superparamagnetic iron oxide nanoparticles (DOX-SPIOs) in cell culture, and the N1S1 hepatoma and VX2 tumor models, imaged by high resolution 7T MRI. We demonstrate that local delivery techniques result in significantly increased intra-tumoral DOX-SPIO uptake, with limited off-target delivery in tumor bearing animal models. The techniques described are versatile enough to be extended to any NP platform, targeting any solid organ malignancy that can be accessed via imaging guidance.
机译:纳米颗粒(NP)已经成为一类新型的治疗剂,可以克服当前癌症化学疗法的许多局限性。然而,对许多当前NP平台的主要挑战是在全身递送时不利的生物分布和有限的肿瘤吸收。因此,递送仍然是NP疗法在临床上广泛采用的关键障碍。为了克服这些限制,我们采用了图像引导的局部药物输送技术来发展纳米消融和纳米栓塞。纳米消融是一种肿瘤消融策略,该策略采用将图像引导下的电极置于肿瘤组织中以电穿孔肿瘤细胞,从而导致NP的快速流入,而这不依赖于细胞摄取机制或细胞周期的阶段。纳米栓塞涉及将图像引导的NP和栓塞剂直接递送到肿瘤的血液供应中。我们描述了在细胞培养中使用阿霉素功能化的超顺磁性氧化铁纳米颗粒(DOX-SPIOs)以及由高分辨率7T MRI成像的N1S1肝癌和VX2肿瘤模型的创新局部递送策略的设计和测试。我们证明,局部传递技术导致肿瘤内DOX-SPIO摄取显着增加,在荷瘤动物模型中有限的脱靶传递。所描述的技术具有足够的通用性,可以扩展到任何NP平台,针对可通过成像指导访问的任何实体器官恶性肿瘤。

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