Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, the Netherlands.
Department of Pharmaceutical Technology and Biopharmacy, University of Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, the Netherlands.
Eur J Pharm Biopharm. 2018 Dec;133:104-111. doi: 10.1016/j.ejpb.2018.09.016. Epub 2018 Sep 29.
During the last decades the number of therapeutic proteins increased tremendously on the pharmaceutical market. However, due to their often poor stability and limitations of the administration route, the application of therapeutic proteins is a major challenge. The oral mucosa has been suggested as a possible route for protein delivery. In this study, we prepared protein loaded orodispersible films (ODFs), based on blends of trehalose/pullulan by air- and freeze-drying. These two carbohydrates were selected based on the excellent protein stabilizing capacity of trehalose and film-forming ability of pullulan. ODFs were loaded with three model proteins. Ovalbumin was used to study the effect of protein incorporation on the mechanical properties, disintegration time, uniformity of weight and thickness of the ODFs. Lysozyme and β-galactosidase were used to evaluate protein stability. Ovalbumin loading did not significantly influence the mechanical properties of freeze-dried ODFs, while incorporation of ovalbumin in air-dried ODFs led to a substantial reduction in tensile strength. The trehalose/pullulan ratio had no impact on the stability of lysozyme, while the stability of β-galactosidase increased with increasing trehalose/pullulan ratios. Furthermore, freeze-drying appeared to be favorable over air-drying for process stability while the reverse was found for storage stability. In conclusion, trehalose/pullulan-based ODFs are from a technical point promising for possible protein delivery via the oral cavity.
在过去的几十年中,治疗性蛋白在药物市场上的数量大幅增加。然而,由于其稳定性差和给药途径的限制,治疗性蛋白的应用是一个主要挑战。口腔黏膜被认为是一种可能的蛋白质给药途径。在这项研究中,我们通过空气干燥和冷冻干燥制备了基于海藻糖/普鲁兰混合物的载蛋白口溶膜(ODF)。这两种碳水化合物是基于海藻糖对蛋白质的优异稳定能力和普鲁兰的成膜能力选择的。ODF 加载了三种模型蛋白。卵清蛋白用于研究蛋白掺入对 ODF 机械性能、崩解时间、重量和厚度均匀性的影响。溶菌酶和β-半乳糖苷酶用于评估蛋白质稳定性。卵清蛋白的加载并没有显著影响冷冻干燥 ODF 的机械性能,而卵清蛋白掺入空气干燥 ODF 会导致拉伸强度显著降低。海藻糖/普鲁兰的比例对溶菌酶的稳定性没有影响,而β-半乳糖苷酶的稳定性随着海藻糖/普鲁兰比例的增加而增加。此外,冷冻干燥似乎比空气干燥更有利于工艺稳定性,而相反的情况则存在于储存稳定性方面。总之,从技术角度来看,基于海藻糖/普鲁兰的 ODF 是通过口腔递送来治疗蛋白的有前途的候选物。