Department of Pharmaceutics, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), Giza, Egypt.
Hematology section, Department of Clinical Pathology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
AAPS PharmSciTech. 2021 Jul 7;22(5):202. doi: 10.1208/s12249-021-02078-8.
Risedronate sodium (RS) is a potent nitrogen-containing bisphosphonate which is known to induce osteoclast apoptosis. As a drug repurposing approach, the current work explored the potential of nebulizable RS-chitosan (CS) microspheres to induce alveolar macrophage apoptosis. RS-CS microspheres were assessed for lung deposition, cytotoxicity, and cellular uptake percentage in Calu-3 cells. The potential of nebulizable microspheres for treating elastase-induced emphysema in rats was investigated, compared to RS marketed oral tablets®, with respect to histopathological, immunohistochemical, and flow cytometric studies. The in vitro lung deposition pattern suggested deep alveolar deposition of RS microspheres, with respect to high FPF% and suitable MMAD (66% and 1.506 μm, respectively, at a flow rate of 28.3 L min). No apparent cytotoxicity was observed, with a cell viability > 90%. The inhalation of RS-CS microspheres was suggested to inhibit airspace enlargement and lung rarefaction after elastase instillation and reduce the macrophage accumulation in alveolar parenchyma. Immunohistochemical and cytometric analyses revealed significant low expression levels of CD68 and CD11b surface markers, respectively, with significantly (P < 0.05) lower detected numbers of intact alveolar macrophages following inhalation of RS-CS microspheres. The nebulization of RS-CS microspheres could induce apoptosis in alveolar macrophages and be promisingly adopted for attenuation of pulmonary emphysema.
利塞膦酸钠(RS)是一种具有强大作用的含氮双膦酸盐,已知可诱导破骨细胞凋亡。作为一种药物再利用的方法,本研究探索了可雾化的 RS-壳聚糖(CS)微球诱导肺泡巨噬细胞凋亡的潜力。评估了 RS-CS 微球在 Calu-3 细胞中的肺部沉积、细胞毒性和细胞摄取百分比。与市售的 RS 口服片剂®相比,研究了可雾化微球治疗弹性蛋白酶诱导的大鼠肺气肿的潜力,分别从组织病理学、免疫组织化学和流式细胞术研究方面进行了比较。体外肺部沉积模式表明,RS 微球具有较深的肺泡沉积,高 FPF%和合适的 MMAD(分别为 66%和 1.506μm,流速为 28.3 L min)。未观察到明显的细胞毒性,细胞活力>90%。雾化 RS-CS 微球可抑制弹性蛋白酶注入后的气腔扩大和肺稀疏,并减少肺泡实质中巨噬细胞的积累。免疫组织化学和细胞术分析显示,CD68 和 CD11b 表面标志物的表达水平显著降低(P<0.05),吸入 RS-CS 微球后完整的肺泡巨噬细胞数量明显减少。雾化 RS-CS 微球可诱导肺泡巨噬细胞凋亡,并有望用于减轻肺气肿。