Klinger Janosch, Daniels Rolf
Department of Pharmaceutical Technology, Eberhard Karls University, Auf der Morgenstelle 8, 72076 Tuebingen, Germany.
Pharmacy (Basel). 2021 Mar 8;9(1):56. doi: 10.3390/pharmacy9010056.
Despite the steadily improving medical care situation in pediatrics, some drugs are still not available in a suitable dose or dosage form and thus need to be prepared extemporaneously. Capsules can be easily compounded at the hospital and public pharmacies, offering an alternative to liquid formulations. This study aims at testing a mass-based approach for the extemporaneous preparation of low-dose pediatric capsules and investigating systematically the API loss during this procedure. A total of 54 capsule batches were prepared with baclofen and spironolactone as pediatric-relevant drugs. The hard capsules were prepared using three different bulking agents consisting of either mannitol, lactose-monohydrate and microcrystalline cellulose mixed with 0.5% colloidal silica. Capsules were tested according to Ph. Eur. method "2.9.40 Content Uniformity" as well as for occurring powder loss and mass uniformity. The results reveal that the mass-based approach, in general, allows the preparation of low-dose pediatric capsules of appropriate quality. However, absolute quality is highly dependent on the homogeneity of the powder mixture and the use of defined parameters for capsule preparation.
尽管儿科医疗状况在稳步改善,但仍有一些药物没有合适的剂量或剂型,因此需要临时配制。胶囊剂可以在医院和公共药房轻松配制,为液体制剂提供了一种替代选择。本研究旨在测试一种基于质量的方法用于临时制备低剂量儿科胶囊,并系统研究该过程中的活性成分损失。共制备了54批以巴氯芬和螺内酯作为儿科相关药物的胶囊。硬胶囊使用三种不同的填充剂制备,填充剂由甘露醇、一水乳糖和微晶纤维素与0.5%胶态二氧化硅混合而成。根据欧洲药典方法“2.9.40含量均匀度”对胶囊进行测试,并测试粉末损失和质量均匀度。结果表明,一般来说,基于质量的方法能够制备出质量合适的低剂量儿科胶囊。然而,绝对质量高度依赖于粉末混合物的均匀性以及胶囊制备所使用的特定参数。