Wittaya-Areekul S, Nail S L
School of Pharmacy, Purdue University, West Lafayette, Indiana 47907, USA.
J Pharm Sci. 1998 Apr;87(4):491-5. doi: 10.1021/js9702832.
The objective of this study was to identify significant formulation and processing variables affecting levels of tert-butyl alcohol (TBA) and isopropyl alcohol (IPA) in freeze-dried solids prepared from TBA/water cosolvent systems. The variables examined were the physical state of the solute (crystalline vs amorphous), initial TBA concentration, freezing rate, cake thickness, and the temperature and duration of secondary drying. Sucrose and glycine were used as models for noncrystallizing and crystallizing solutes, respectively. The TBA concentration above which eutectic crystallization takes place was determined by differential scanning calorimetry. Model formulations were subjected to extremes of freezing rate by either dipping in liquid nitrogen or by slowly freezing on the shelf of a freeze-dryer. Dynamics of solvent loss during secondary drying was determined by withdrawing samples as a function of time at different shelf temperatures using a thief system. On the basis of these studies, the most important determinant of residual TBA level is the physical state of the solute. Freeze-dried glycine contained very low levels of residual TBA (0.01-0.03%) regardless of freezing rate or initial TBA concentration. For freeze-dried sucrose, residual TBA levels were approximately 2 orders of magnitude higher and were significantly affected by initial TBA concentration and freezing rate. For the sucrose/TBA/water system, relatively low residual TBA levels were obtained when the initial TBA level was above the threshold concentration for eutectic crystallization of TBA, whereas samples freeze-dried from solutions containing TBA concentrations below this threshold contained significantly higher levels of TBA. Residual IPA levels increased continuously with initial concentration of TBA in the sucrose/TBA/water system. Formulations of sucrose/TBA/water which were frozen rapidly contained residual TBA levels which were approximately twice those measured in the same formulation after slow freezing and drying under the same conditions. For the sucrose/TBA/water system, the temperature and time of secondary drying had only minimal influence on residual TBA in the freeze-dried solid. At low initial TBA concentrations (2%), residual TBA increases with increased cake thickness, perhaps because of the influence of depth of fill on effective freezing rate.
本研究的目的是确定影响由叔丁醇(TBA)/水共溶剂体系制备的冻干固体中叔丁醇(TBA)和异丙醇(IPA)含量的重要制剂和工艺变量。所研究的变量包括溶质的物理状态(结晶态与非晶态)、初始TBA浓度、冷冻速率、饼层厚度以及二次干燥的温度和持续时间。分别使用蔗糖和甘氨酸作为非结晶溶质和结晶溶质的模型。通过差示扫描量热法确定发生共晶结晶的TBA浓度上限。模型制剂通过浸入液氮或在冷冻干燥机搁板上缓慢冷冻来经受极端的冷冻速率。使用取样系统在不同搁板温度下根据时间抽取样品,以确定二次干燥过程中溶剂损失的动态情况。基于这些研究,残留TBA水平的最重要决定因素是溶质的物理状态。无论冷冻速率或初始TBA浓度如何,冻干甘氨酸中的残留TBA水平都非常低(0.01 - 0.03%)。对于冻干蔗糖,残留TBA水平大约高2个数量级,并且受到初始TBA浓度和冷冻速率的显著影响。对于蔗糖/TBA/水体系,当初始TBA水平高于TBA共晶结晶的阈值浓度时,可获得相对较低的残留TBA水平,而从含有低于该阈值浓度TBA的溶液中冻干的样品含有显著更高水平的TBA。在蔗糖/TBA/水体系中,残留IPA水平随TBA的初始浓度持续增加。快速冷冻的蔗糖/TBA/水制剂中的残留TBA水平大约是在相同条件下缓慢冷冻和干燥后同一制剂中测量值的两倍。对于蔗糖/TBA/水体系,二次干燥的温度和时间对冻干固体中的残留TBA影响极小。在低初始TBA浓度(2%)下,残留TBA随饼层厚度增加而增加,这可能是由于填充深度对有效冷冻速率的影响。