Collaborative Innovation Center of Advanced Drug Delivery System and Biotech Drugs, School of Pharmacy, Yantai University, Yantai, 264000, Shandong, People's Republic of China.
Department of Thoracic Surgery, Yantai Yuhuangding Hospital, Yantai, 264000, Shandong, People's Republic of China.
Drug Deliv Transl Res. 2024 Nov;14(11):3147-3162. doi: 10.1007/s13346-024-01536-7. Epub 2024 Feb 21.
Afatinib (AT), an FDA-approved aniline-quinazoline derivative, is a first-line treatment for metastatic non-small cell lung cancer (NSCLC). Combining it with cetuximab (CX), a chimeric human-murine derivative immunoglobulin-G1 monoclonal antibody (mAb) targeting the extracellular domain of epidermal growth factor receptor (EGFR), has shown significant improvements in median progression-free survival. Previously, we developed cetuximab-conjugated immunoliposomes loaded with afatinib (AT-MLP) and demonstrated their efficacy against NSCLC cells (A549 and H1975). In this study, we aimed to explore the potential of pulmonary delivery to mitigate adverse effects associated with oral administration and intravenous injection. We formulated AT-MLP dry powders (AT-MLP-DPI) via freeze drying using tert-butanol and mannitol as cryoprotectants in the hydration medium. The physicochemical and aerodynamic properties of dry powders were well analyzed firstly. In vitro cellular uptake and cytotoxicity study revealed concentration- and time-dependent cellular uptake behavior and antitumor efficacy of AT-MLP-DPI, while Transwell assay demonstrated the superior inhibitory effects on NSCLC cell invasion and migration. Furthermore, in vivo pharmacokinetic study showed that pulmonary delivery of AT-MLP-DPI significantly increased bioavailability, prolonged blood circulation time, and exhibited higher lung concentrations compared to alternative administration routes and formulations. The in vivo antitumor efficacy study carried on tumor-bearing nude mice indicated that inhaled AT-MLP-DPI effectively suppressed lung tumor growth.
阿法替尼(AT)是一种获得 FDA 批准的苯胺喹唑啉衍生物,是转移性非小细胞肺癌(NSCLC)的一线治疗药物。将其与西妥昔单抗(CX)联合使用,西妥昔单抗是一种针对表皮生长因子受体(EGFR)细胞外结构域的嵌合人鼠衍生免疫球蛋白 G1 单克隆抗体(mAb),已显示出在中位无进展生存期方面的显著改善。之前,我们开发了载有阿法替尼(AT-MLP)的西妥昔单抗偶联免疫脂质体,并证明了其对 NSCLC 细胞(A549 和 H1975)的疗效。在这项研究中,我们旨在探索通过肺部给药来减轻口服和静脉注射相关不良反应的潜力。我们通过使用叔丁醇和甘露醇作为水合介质中的冷冻保护剂,通过冷冻干燥来制备 AT-MLP 干粉(AT-MLP-DPI)。首先对干粉的物理化学和空气动力学性质进行了全面分析。体外细胞摄取和细胞毒性研究揭示了 AT-MLP-DPI 的浓度和时间依赖性细胞摄取行为和抗肿瘤功效,而 Transwell 测定表明其对 NSCLC 细胞侵袭和迁移具有优越的抑制作用。此外,体内药代动力学研究表明,与其他给药途径和制剂相比,肺部给予 AT-MLP-DPI 可显著提高生物利用度,延长血液循环时间,并在肺部表现出更高的浓度。在荷瘤裸鼠上进行的体内抗肿瘤功效研究表明,吸入 AT-MLP-DPI 可有效抑制肺部肿瘤生长。