Obara S, Maruyama N, Nishiyama Y, Kokubo H
Specialty Chemicals Research Center, Shin-Etsu Chemical Co., Ltd., Niigata, Japan.
Eur J Pharm Biopharm. 1999 Jan;47(1):51-9. doi: 10.1016/s0939-6411(98)00087-3.
A novel enteric coating method was developed. This method involves direct feeding of coating polymer powder and simultaneous spraying of plasticizing agent, without either organic solvent or water, using a centrifugal granulator, fluidized bed, or tablet-coating machine. For film formation, a curing step was then necessary; this involved spraying a small amount (3-8% of core weight) of water or hydroxypropyl methylcellulose solution, followed by heating. Hydroxypropyl methylcellulose acetate succinate was used as the enteric coating polymer, and a combination of triethyl citrate and acetylated monoglyceride was used for plasticization. The coated beads and tablets were evaluated for gastric resistance, intestinal disintegration, and stability, in comparison with beads and tablets from a conventional aqueous coating with the same enteric polymer. The new method required a higher coating amount for gastric resistance compared with the conventional coating, but the processing time was dramatically reduced. The results show that this dry coating method is applicable to the preparation of enteric-coated beads and tablets using commercially available lab-scale apparatus.
开发了一种新型肠溶包衣方法。该方法包括直接进料包衣聚合物粉末并同时喷雾增塑剂,不使用有机溶剂或水,采用离心制粒机、流化床或片剂包衣机。为形成薄膜,随后需要进行固化步骤;这包括喷雾少量(占芯重的3-8%)的水或羟丙基甲基纤维素溶液,然后加热。使用醋酸羟丙基甲基纤维素琥珀酸酯作为肠溶包衣聚合物,并使用柠檬酸三乙酯和乙酰化单甘油酯的组合进行增塑。与使用相同肠溶聚合物的传统水性包衣的微丸和片剂相比,对包衣微丸和片剂进行了胃耐受性、肠道崩解性和稳定性评估。与传统包衣相比,新方法需要更高的包衣量来实现胃耐受性,但加工时间显著缩短。结果表明,这种干法包衣方法适用于使用市售实验室规模设备制备肠溶包衣微丸和片剂。