Formulation Research, Pharmaceutical Science and Technology Core Function Unit, Medicine Development Center, Eisai Co., Ltd., 1 Kawashimatakehaya-machi, Kakamigahara-shi, Gifu 501-6195, Japan; Department of Pharmaceutics and Drug Delivery, Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
Department of Pharmaceutics and Drug Delivery, Faculty of Pharmaceutical Sciences, Tokyo University of Science, 2641 Yamazaki, Noda, Chiba 278-8510, Japan.
Eur J Pharm Biopharm. 2018 Sep;130:83-95. doi: 10.1016/j.ejpb.2018.06.010. Epub 2018 Jun 18.
In the lyophilization process for injections, the shelf temperature (T) and chamber pressure (P) have mainly been investigated to optimize the primary drying process. The objective of this study was to show that lyophilization of protein formulations can be achieved by adopting a fast ramp rate of T in the beginning of the primary drying process. Bovine serum albumin was used as the model protein, and seven different lyophilized formulations obtained were stored at elevated temperature. We found that although acceptable cake appearance was confirmed by the fast ramp cycle, all formulations of lyophilized cakes obtained by the slow ramp cycle severely collapsed (macrocollapse). It is thought that the collapse in the slow ramp cycle occurred during the shelf ramp in the beginning of primary drying and that insufficient removal of water from the dried matrix caused viscous flow (product collapse). Regarding storage stability, moisture-induced degradation was confirmed in some of the formulations prepared by the slow ramp cycle, whereas all lyophilized BSA formulations prepared by the fast ramp cycle were stable. Thus, the results indicate that the ramp rate appears to be one of the critical operational parameters required to establish a successful lyophilization cycle.
在注射用冷冻干燥过程中,主要研究了搁板温度(T)和腔室压力(P),以优化初级干燥过程。本研究的目的是表明通过在初级干燥过程的开始采用快速升温速率,可以实现蛋白质制剂的冷冻干燥。牛血清白蛋白被用作模型蛋白,储存了七种不同的冷冻干燥制剂。我们发现,虽然快速升温循环可以确认可接受的块状外观,但通过慢速升温循环获得的所有冷冻干燥块状物都严重塌陷(大塌陷)。据认为,在慢速升温循环中,塌陷发生在初级干燥的搁板升温期间,并且从干燥基质中没有充分去除水分导致粘性流动(产品塌陷)。关于储存稳定性,在一些通过慢速升温循环制备的配方中确认了水分引起的降解,而通过快速升温循环制备的所有冷冻干燥 BSA 配方均稳定。因此,结果表明,升温速率似乎是建立成功的冷冻干燥循环所需的关键操作参数之一。