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Nasal Powder Formulations: In-Vitro Characterisation of the Impact of Powders on Nasal Residence Time and Sensory Effects

机译:鼻粉制剂:体外表征粉末对鼻腔停留时间和感觉效应的影响

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摘要

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.
机译:鼻药递送仍然主要与局部有效的药物相关,而是利用鼻给药的益处的下一代产品 - 例如易于进入相对渗透的粘膜,存在免疫活性细胞,以及直接途径到脑在调查中。鼻粉通过提供更高的粘膜间隙的耐受性,促进药物的效果,并因此延长药物与靶位点的接触时间来提高药物的效果。然而,缺少适用于对这种效果表征的体外设置进行了易于使用的体外设置。在该研究中,用于评估研究影响对接触时间的不同方法的适用性。发现流变性,动态蒸汽吸附和琼脂蛋白板上的粘合性评估的组合是有价值的预测工具。对于与粉末和粘膜紧密接触相关的感觉的额外评估,进行粘粘粘膜刺激测定并适合于粉末。这些方法被认为对早期配方发育中的比较筛查特别有用。

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