Trenkel Marie, Scherließ Regina
Department of Pharmaceutics and Biopharmaceutics, Kiel University, 24118 Kiel, Germany.
Pharmaceutics. 2021 Mar 13;13(3):385. doi: 10.3390/pharmaceutics13030385.
Nasal drug delivery is still primarily associated with locally-effective drugs, but next-generation products utilising the benefits of nasal administration-such as easy access to a relatively permeable mucosa, the presence of immunocompetent cells, and a direct route to the brain-are under investigation. Nasal powders offer the potential to improve the drugs' effects by providing higher resistance against the mucociliary clearance, and thus prolonging the contact time of the drug with its target site. However, suitable and easy-to-use in-vitro setups tailored to the characterisation of this effect are missing. In this study, a selection of excipients for powder formulations were used to evaluate the applicability of different methods which investigate the influence on the contact time. The combination of the assessment of rheological properties, dynamic vapour sorption, and adhesiveness on agar-mucin plates was found to be a valuable predictive tool. For the additional assessment of the sensations associated with the close contact of powders and the mucosa, a slug mucosal irritation assay was conducted and adapted to powders. These methods are regarded as being especially useful for comparative screenings in early formulation development.
鼻腔给药仍然主要与局部起效药物相关,但利用鼻腔给药优势(如易于接触相对可渗透的黏膜、存在免疫活性细胞以及通向大脑的直接途径)的下一代产品正在研究中。鼻用粉剂有可能通过对黏液纤毛清除提供更高抗性来改善药物效果,从而延长药物与其靶部位的接触时间。然而,缺少适合且易于使用的针对这种效果表征的体外装置。在本研究中,选用了一系列用于粉剂制剂的辅料来评估不同方法对接触时间影响的适用性。流变学性质评估、动态蒸汽吸附以及在琼脂 - 黏蛋白平板上的黏附性相结合被发现是一种有价值的预测工具。为了额外评估与粉剂和黏膜紧密接触相关的感觉,进行了并针对粉剂调整了弹丸黏膜刺激性试验。这些方法被认为对早期制剂开发中的比较筛选特别有用。