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Particle size reduction to the nanometer range: a promising approach to improve buccal absorption of poorly water-soluble drugs

机译:将粒径减小至纳米范围:改善水溶性差的药物的口腔吸收的一种有前途的方法

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摘要

Poorly water-soluble drugs, such as phenylephrine, offer challenging problems for buccal drug delivery. In order to overcome these problems, particle size reduction (to the nanometer range) and cyclodextrin complexation were investigated for permeability enhancement. The apparent solubility in water and the buccal permeation of the original phenylephrine coarse powder, a phenylephrine–cyclodextrin complex and phenylephrine nanosuspensions were characterized. The particle size and particle surface properties of phenylephrine nanosuspensions were used to optimize the size reduction process. The optimized phenylephrine nanosuspension was then freeze dried and incorporated into a multi-layered buccal patch, consisting of a small tablet adhered to a mucoadhesive film, yielding a phenylephrine buccal product with good dosage accuracy and improved mucosal permeability. The design of the buccal patch allows for drug incorporation without the need to change the mucoadhesive component, and is potentially suited to a range of poorly water-soluble compounds.
机译:水溶性差的药物,例如去氧肾上腺素,对颊部药物的递送提出了具有挑战性的问题。为了克服这些问题,研究了减小粒度(至纳米范围)和环糊精络合以提高渗透性。表征了最初的去氧肾上腺素粗粉,去氧肾上腺素-环糊精复合物和去氧肾上腺素纳米悬浮液在水中的表观溶解度和颊渗透性。苯肾上腺素纳米悬浮液的粒径和颗粒表面性质用于优化粒径减小过程。然后将优化的去氧肾上腺素纳米悬浮液冷冻干燥,并掺入多层颊贴剂,该贴剂由粘附在粘膜粘附膜上的小片剂组成,制得的苯肾上腺素颊剂具有良好的剂量准确性和改善的粘膜通透性。口腔贴剂的设计无需改变粘膜粘附性成分即可掺入药物,并且可能适用于一系列水溶性差的化合物。

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