Fakes M G, Dali M V, Haby T A, Morris K R, Varia S A, Serajuddin A T
Pharmaceutics R & D Department, Bristol-Myers Squibb Pharmaceutical Research Institute, New Brunswick, New Jersey, USA.
PDA J Pharm Sci Technol. 2000 Mar-Apr;54(2):144-9.
To develop a rational approach for the formulation of lyophilized products, six bulking agents commonly used in freeze-dried formulations were lyophilized under identical conditions, and their moisture sorption behavior, before and after lyophilization, were determined as a function of relative humidity at 25 degrees C. The bulking agents evaluated were mannitol, anhydrous lactose, sucrose, D(+)-trehalose, dextran 40 and povidone (PVP K24). The materials were also characterized for their crystal and thermal properties by powder X-ray diffraction, DSC and TG after exposure to various relative humidity conditions. Mannitol was crystalline and non-hygroscopic both before and after lyophilization with total moisture contents of 0.1 to 0.3% w/w between 10 and 60% RH. Anhydrous lactose, sucrose and trehalose were crystalline prior to lyophilization with moisture contents of 0.86, 0.15 and 9.2%, respectively, and the crystalline materials were relatively non-hygroscopic. Upon lyophilization, they converted to the amorphous form and had moisture contents of 1.6, 2.5 and 1.2%, respectively. The amorphous materials sorbed moisture rapidly upon exposure to increasing relative humidity conditions. The amorphous lactose converted to its crystalline hydrate form at 55% RH after sorption of an additional 10% moisture. This conversion to the crystalline hydrate form was accompanied by desorption of practically all the moisture sorbed by the amorphous form. Similarly, lyophilized sucrose converted to its crystalline form after the sorption of additional 4.5% moisture at 50% RH, and the lyophilized trehalose sorbed additional 10% moisture prior to its conversion to a crystalline hydrate form at 50% RH. Dextran and povidone were amorphous and hygroscopic both before and after lyophilization and they sorbed as much as 10-20% moisture at 50% RH. It is well established that different drugs, especially proteins, need different levels of moisture for optimal stability. The results of the present study show that moisture contents of lyophilized cakes may be varied and optimized by the selection of suitable excipients.
为制定冻干产品的合理配方,将冻干制剂中常用的六种填充剂在相同条件下进行冻干,并测定其冻干前后在25℃下作为相对湿度函数的吸湿行为。所评估的填充剂有甘露醇、无水乳糖、蔗糖、D(+)-海藻糖、右旋糖酐40和聚维酮(PVP K24)。在暴露于各种相对湿度条件后,还通过粉末X射线衍射、差示扫描量热法和热重分析法对这些材料的晶体和热性能进行了表征。甘露醇在冻干前后均为晶体且不吸湿,在10%至60%相对湿度下总水分含量为0.1%至0.3%(w/w)。无水乳糖、蔗糖和海藻糖在冻干前为晶体,水分含量分别为0.86%、0.15%和9.2%,且这些晶体材料相对不吸湿。冻干后,它们转变为无定形形式,水分含量分别为1.6%、2.5%和1.2%。无定形材料在暴露于相对湿度增加的条件下会迅速吸湿。无定形乳糖在额外吸附10%水分后,在55%相对湿度下转变为其结晶水合物形式。这种向结晶水合物形式的转变伴随着无定形形式吸附的几乎所有水分的解吸。同样,冻干蔗糖在50%相对湿度下额外吸附4.5%水分后转变为其结晶形式,冻干海藻糖在50%相对湿度下转变为结晶水合物形式之前额外吸附了10%水分。右旋糖酐和聚维酮在冻干前后均为无定形且吸湿,在50%相对湿度下它们可吸附多达10%至20%的水分。众所周知,不同药物,尤其是蛋白质,需要不同水平的水分以实现最佳稳定性。本研究结果表明,通过选择合适的辅料,可以改变和优化冻干饼的水分含量。