Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, 8000 Utopia Parkway, Queens, New York, 11439, USA.
Pharm Res. 2020 Mar 12;37(3):67. doi: 10.1007/s11095-020-02790-3.
This exploration is aimed at developing sorafenib (SF)-loaded cationically-modified polymeric nanoparticles (NPs) as inhalable carriers for improving the therapeutic efficacy of SF against non-small cell lung cancer (NSCLC).
The NPs were prepared using a solvent evaporation technique while incorporating cationic agents. The optimized NPs were characterized by various physicochemical parameters and evaluated for their aerosolization properties. Several in-vitro evaluation studies were performed to determine the efficacy of our delivery carriers against NSCLC cells.
Optimized nanoparticles exhibited an entrapment efficiency of 40%, <200 nm particle size and a narrow poly-dispersity index. Cationically-modified nanoparticles exhibited enhanced cellular internalization and cytotoxicity (5-fold IC reduction vs SF) in various lung cancer cell types. The inhalable nanoparticles displayed efficient aerodynamic properties (MMAD ~ 4 μM and FPF >80%). In-vitro evaluation also resulted in a superior ability to inhibit cancer metastasis. 3D-tumor simulation studies further established the anti-cancer efficacy of NPs as compared to just SF.
The localized delivery of SF-loaded nanoparticles resulted in improved anti-tumor activity as compared to SF alone. Therefore, this strategy displays great potential as a novel treatment approach against certain lung cancers.
本研究旨在开发索拉非尼(SF)负载的阳离子改性聚合物纳米颗粒(NPs)作为可吸入载体,以提高 SF 治疗非小细胞肺癌(NSCLC)的疗效。
采用溶剂蒸发技术制备 NPs,同时加入阳离子剂。通过各种物理化学参数对优化后的 NPs 进行表征,并对其气溶胶化特性进行评价。进行了多项体外评估研究,以确定我们的给药载体对 NSCLC 细胞的疗效。
优化后的纳米颗粒表现出约 40%的包封效率、<200nm 的粒径和较窄的多分散指数。阳离子改性纳米颗粒在各种肺癌细胞类型中表现出增强的细胞内化和细胞毒性(与 SF 相比,IC 降低约 5 倍)。可吸入纳米颗粒显示出高效的空气动力学特性(MMAD~4μm 和 FPF>80%)。体外评估还导致了抑制癌症转移的卓越能力。3D 肿瘤模拟研究进一步证实了 NPs 的抗癌功效优于 SF 单独治疗。
与 SF 单独治疗相比,SF 负载的纳米颗粒的局部给药导致抗肿瘤活性得到改善。因此,该策略显示出作为某些肺癌新型治疗方法的巨大潜力。