LeClair Daniel A, Cranston Emily D, Xing Zhou, Thompson Michael R
Department of Chemical Engineering, McMaster University, Hamilton, Ontario L8S 4L7, Canada.
McMaster Immunology Research Centre & Department of Pathology and Molecular Medicine, McMaster University, Canada.
Int J Pharm. 2016 Jun 15;506(1-2):289-301. doi: 10.1016/j.ijpharm.2016.04.067. Epub 2016 Apr 26.
We have produced a thermally stable recombinant human type 5 adenoviral vector (AdHu5) through spray drying with three excipient formulations (l-leucine, lactose/trehalose and mannitol/dextran). Spray drying leads to immobilization of the viral vector which is believed to prevent viral protein unfolding, aggregation and inactivation. The spray dried powders were characterized by scanning electron microscopy, differential scanning calorimetry, Karl Fischer titrations, and X-ray diffraction to identify the effects of temperature and atmospheric moisture on the immobilizing matrix. Thermal stability of the viral vector was confirmed in vitro by infection of A549 lung epithelial cells. Mannitol/dextran powders showed the greatest improvement in thermal stability with almost no viral activity loss after storage at 20°C for 90days (0.7±0.3 log TCID50) which is a significant improvement over the current -80°C storage protocol. Furthermore, viral activity was retained over short term exposure (72h) to temperatures as high as 55°C. Conversely, all powders exhibited activity loss when subjected to moisture due to amplified molecular motion of the matrix. Overall, a straightforward method ideal for the production of thermally stable vaccines has been demonstrated through spray drying AdHu5 with a blend of mannitol and dextran and storing the powder under low humidity conditions.
我们通过喷雾干燥,使用三种辅料配方(L-亮氨酸、乳糖/海藻糖和甘露醇/右旋糖酐)制备了一种热稳定的重组人5型腺病毒载体(AdHu5)。喷雾干燥导致病毒载体固定化,据信这可防止病毒蛋白展开、聚集和失活。通过扫描电子显微镜、差示扫描量热法、卡尔费休滴定法和X射线衍射对喷雾干燥粉末进行表征,以确定温度和大气湿度对固定化基质的影响。通过感染A549肺上皮细胞在体外证实了病毒载体的热稳定性。甘露醇/右旋糖酐粉末在热稳定性方面表现出最大的改善,在20°C储存90天后几乎没有病毒活性损失(0.7±0.3 log TCID50),这比当前-80°C储存方案有显著改善。此外,在短期暴露(72小时)于高达55°C的温度下,病毒活性得以保留。相反,由于基质分子运动加剧,所有粉末在受潮时均表现出活性损失。总体而言,通过将AdHu5与甘露醇和右旋糖酐混合进行喷雾干燥,并在低湿度条件下储存粉末,已证明了一种适用于生产热稳定疫苗的直接方法。