可吸入的全氟碳纳米胶囊用于基于rna的肺转移免疫治疗。

Kasturi Siddhanta, Atefehsadat Monirvaghefi, Aditya Sundar, Braeden R Pinkerton, Neha Kumari, Ling Ding, C J Woslager, Marjina Akter Kalpana, Chinmay M Jogdeo, Ashley R Ravnholdt, Jill A Poole, Joshua L Santarpia, James E Talmadge, David Oupický
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引用次数: 0

摘要

虽然化疗和肺转移切除术是肺转移的主要临床治疗方法,但其有效性受到高复发率和全身副作用的限制。临床前治疗表明,基于吸入的RNA治疗是一种可行的方法,可以绕过首过代谢并减少全身暴露。在这里,我们开发了一种可吸入的全氟碳纳米胶囊,用于靶向递送RNA干扰治疗肺转移。雾化纳米胶囊可被肺上皮细胞和肿瘤细胞吸收,延长滞留时间超过48小时,炎症反应最小,肺免疫细胞的清除可忽略不计,在其他器官的积累最小。与标准化疗相比,我们的治疗不仅大大减少了转移性肿瘤的负担,而且在肿瘤微环境中显示出增强的抗肿瘤免疫,在两周内仅服用三次剂量后,寿命几乎翻了一番。最后,研究团聚倾向的分子动力学模拟表明,硬脂酸盐和维生素E等赋形剂与纳米胶囊结合强烈,可能抑制团聚,从而提高这些配方的保质期。总之,这项研究表明,可吸入的全氟碳基给药系统作为一种非侵入性、生物相容性和有效的肺肿瘤靶向平台,可以克服当前治疗的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhalable Perfluorocarbon RNA Nanocapsules Bypass Immune Clearance While Targeting Lung Epithelial and Lung Tumor Cells.

Inhalation RNA therapy offers to transform treatment of pulmonary diseases, yet mucus trapping, immune clearance, and navigation of heterogeneous lung tissue architecture still prevents RNA from reaching its target cells. Here, we develop perfluorocarbon (PFC) RNA nanocapsules that show negligible immune clearance, minimal inflammatory response, and efficient mucus transport, while passively homing to lung epithelial and tumor cells. After a single aerosolized dose in orthotopic lung metastasis model, more than 60% of tumor cells and most type II alveolar and bronchial epithelial cells internalized the nanocapsules, with observed pulmonary retention exceeding 48 h. The nanocapsule provoke negligible cytokine release, enabling repeated dosing. Treatment with therapeutic miR34-a suppresses metastatic outgrowth, potentiates anti-tumor immunity, and almost doubles median survival relative to control paclitaxel chemotherapy. By combining unique PFC disposition with RNA versatility, the delivery platform overcomes the main biological barriers for inhalable RNA medicines and opens a translatable path for treating diverse pulmonary diseases.

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