Department of Pharmacy, Pharmaceutical Technology and Biopharmaceutics, Ludwig-Maximilians-Universität München, 81337 Munich, Germany.
Department of Oncology, Wayne State University School of Medicine, 4100 John R St, Detroit, MI 48201, United States; Department of Pharmaceutical Sciences, Wayne State University, 259 Mack Ave, Detroit, MI 48201, United States.
Eur J Pharm Biopharm. 2019 Oct;143:61-69. doi: 10.1016/j.ejpb.2019.08.012. Epub 2019 Aug 21.
Localized aerosol delivery of gene therapies is a promising treatment of severe pulmonary diseases including lung cancer, cystic fibrosis, COPD and asthma. The administration of drugs by inhalation features multiple benefits including an enhanced patient acceptability and compliance. The application of a spray dried powder formulation has advantages over solutions due to their increased stability and shelf life. Furthermore, optimal sizes of the powder can be obtained by spray drying to allow a deep lung deposition. The present study optimized the parameters involved with spray drying polyplexes formed by polyethylenimine (PEI) and nucleic acids in inert excipients to generate a nano-embedded microparticle (NEM) powder with appropriate aerodynamic diameter. Furthermore, the effects of the excipient matrix used to generate the NEM powder on the biological activity of the nucleic acid and the ability to recover the embedded nanoparticles was investigated. The study showed that bioactivity and nucleic acid integrity was preserved after spray drying, and that polyplexes could be reconstituted from the dry powders made with trehalose but not mannitol as a stabilizer. Scanning electron microscopy (SEM) showed trehalose formulations that formed fused, lightly corrugated spherical particles in the range between 1 and 5 µm, while mannitol formulations had smooth surfaces and consisted of more defined particles. After redispersion of the microparticles in water, polyplex dispersions are obtained that are comparable to the initial formulations before spray drying. Cellular uptake and transfection studies conducted in lung adenocarcinoma cells show that redispersed trehalose particles performed similar to or better than polyplexes that were not spray dried. A method for quantifying polymer and nucleic acid loss following spray drying was developed in order to ensure that equal nucleic acid amounts were used in all in vitro experiments. The results confirm that spray dried NEM formulations containing nucleic acids can be prepared with characteristics known to be optimal for inhalation therapy.
局部气溶胶输送基因疗法是一种有前途的治疗严重肺部疾病的方法,包括肺癌、囊性纤维化、COPD 和哮喘。药物吸入给药具有多种益处,包括提高患者的接受度和依从性。与溶液相比,喷雾干燥粉末制剂由于其增加的稳定性和保质期而具有优势。此外,可以通过喷雾干燥获得最佳尺寸的粉末,以允许深肺沉积。本研究优化了在惰性赋形剂中形成聚乙二亚胺 (PEI) 和核酸的多聚物的喷雾干燥参数,以生成具有适当空气动力学直径的纳米嵌入微颗粒 (NEM) 粉末。此外,研究了用于生成 NEM 粉末的赋形剂基质对核酸的生物学活性和回收嵌入纳米颗粒的能力的影响。研究表明,喷雾干燥后生物活性和核酸完整性得以保留,并且可以从含有海藻糖但不含甘露醇作为稳定剂的干粉中重新构建多聚物。扫描电子显微镜 (SEM) 显示,海藻糖配方形成融合的、轻度波纹的球形颗粒,范围在 1 到 5 μm 之间,而甘露醇配方具有光滑的表面,由更明确的颗粒组成。在将微颗粒重新分散在水中后,获得的多聚物分散体与喷雾干燥之前的初始制剂相当。在肺腺癌细胞中进行的细胞摄取和转染研究表明,重新分散的海藻糖颗粒的性能与未喷雾干燥的多聚物相似或更好。为了确保所有体外实验中使用等量的核酸,开发了一种定量喷雾干燥后聚合物和核酸损失的方法。结果证实,可以用已知对吸入治疗最优化的特性来制备含有核酸的喷雾干燥 NEM 制剂。