Division of Pharmaceutics, Freeze Drying Focus Group, University of Erlangen , Erlangen , Germany .
Pharm Dev Technol. 2014 Mar;19(2):137-47. doi: 10.3109/10837450.2012.757784. Epub 2013 Jan 17.
The taste of oral dosage forms is an important argument regarding patient's compliance and acceptability. For this reason, it is often necessary to mask an undesirable and unpleasant taste of an active pharmaceutical ingredient. The purpose of this study was to mask the taste of naproxen sodium by a new fluid-bed coating approach. Different compositions of coating suspensions were used to coat naproxen sodium granules. It was found that products with the addition of a plasticizer were not stable at 40 °C and tended to agglomerate. Subsequently, formulations without plasticizer were used and the ratio between water and Eudragit® E was varied. Increasing the fraction of water in the suspension from 3% to 14% reduced the effective release of naproxen sodium. An optimum ratio between naproxen sodium granules and Eudragit® E was found to be 1:1.576, where less naproxen sodium was released than the threshold bitter value and an appropriate taste masking for more than 5 min was guaranteed. Investigation of the particle size distribution revealed a d(10) of 138.35 ± 21.52 µm, a d(50 )= 256.40 ± 11.27 µm and a d(90 )= 500.85 ± 69.08 µm, which guarantees an acceptable mouthfeel for patients.
口服剂型的口感是影响患者顺应性和可接受性的重要因素。因此,通常需要掩盖药物活性成分的不良和不愉快味道。本研究旨在通过新的流化床包衣方法来掩盖萘普生钠的味道。使用不同组成的包衣悬浮液来包衣萘普生钠颗粒。结果发现,添加增塑剂的产品在 40°C 下不稳定,容易团聚。随后,使用不含增塑剂的配方,并改变水和 Eudragit® E 的比例。将悬浮液中的水分比例从 3%增加到 14%,会降低萘普生钠的有效释放。发现萘普生钠颗粒和 Eudragit® E 的最佳比例为 1:1.576,在此比例下,释放的萘普生钠少于阈值苦味值,并能保证超过 5 分钟的适当口感掩盖。对粒径分布的研究表明,d(10)为 138.35±21.52μm,d(50)=256.40±11.27μm,d(90)=500.85±69.08μm,这保证了患者可接受的口感。