Straller Georg, Lee Geoffrey
Division of Pharmaceutics, Cauerstrasse 4, Friedrich-Alexander University, Erlangen, Germany.
Division of Pharmaceutics, Cauerstrasse 4, Friedrich-Alexander University, Erlangen, Germany.
Int J Pharm. 2017 Oct 30;532(1):444-449. doi: 10.1016/j.ijpharm.2017.09.036. Epub 2017 Sep 18.
Spray-freeze-drying was used to produce shrivelled, partially-collapsed microparticles of pure proteins that may be suitable for use in a ballistic injector. Various modifications of the freeze drying cycle were examined for their effects on collapse of the pure protein microparticles. The use of annealing at a shelf temperature of up to +10°C resulted in no visible particle shrinkage. This was because of the high T of the pure protein. Inclusion of trehalose or sucrose led to particle shrinkage because of the plasticizing effects of the disaccharides on the protein. Only by extending the duration of primary drying from 240 to 2745min at shelf temperatures in the range -12 to -8°C were shrivelled, wrinkled particles of bSA and bCA of reduced porosity obtained. Manipulation of the freeze-drying cycle used for SFD can therefore be used to modify particle morphology and increase particle density.
喷雾冷冻干燥被用于制备可能适用于弹道注射器的皱缩、部分塌陷的纯蛋白质微粒。研究了冷冻干燥循环的各种变化对纯蛋白质微粒塌陷的影响。在搁板温度高达+10°C时进行退火处理,未观察到颗粒明显收缩。这是由于纯蛋白质的玻璃化转变温度较高。加入海藻糖或蔗糖会导致颗粒收缩,这是因为二糖对蛋白质有增塑作用。只有在搁板温度为-12至-8°C的范围内将一次干燥时间从240分钟延长至2745分钟,才能得到孔隙率降低的皱缩、有褶皱的牛血清白蛋白(bSA)和牛碳酸酐酶(bCA)颗粒。因此,用于喷雾冷冻干燥的冷冻干燥循环的操控可用于改变颗粒形态并提高颗粒密度。