Further improvement of orally disintegrating tablets using micronized ethylcellulose

被引:18
|
作者
Okuda, Yutaka [1 ]
Irisawa, Yosuke [2 ]
Okimoto, Kazuto [1 ]
Osawa, Takashi [1 ]
Yamashita, Shinji [3 ]
机构
[1] Towa Pharmaceut Co Ltd, Kadoma, Osaka 5710033, Japan
[2] Towa Pharmaceut Co Ltd, Shoo, Okayama 7094321, Japan
[3] Setsunan Univ, Fac Pharmaceut Sci, Hirakata, Osaka 5730101, Japan
关键词
Orally disintegrating tablet; Micronized ethylcellulose; Physical strength; Capillary channels; Wicking action; Suspension spray-coating method; DIRECT COMPRESSION METHOD; CRYSTALLINE TRANSITION; AMORPHOUS SUCROSE; CELLULOSE; RELEASE; MOUTH; DISPERSIONS; ABSORPTION; MECHANISM;
D O I
10.1016/j.ijpharm.2011.10.050
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this study is to design a new orally disintegrating tablet (ODT) containing micronized ethylcellulose (MEC). The new ODT was prepared by physical mixing of rapidly disintegrating granules (RDGs) with MEC. To obtain RDGs, mannitol was spray-coated with a suspension of corn starch and crospovidone (9:1, w/w ratio) using a fluidized-bed granulator (suspension spray-coating method). The new ODTs were evaluated for their hardness, friability, thickness, internal structure (X-ray-CT scanning), in vivo disintegration time, and water absorption rate. Since MEC increases tablet hardness by increasing the contact frequency between the granules, the new ODTs could obtain high hardness (>50 N) and low friability (<0.5%) with relatively low compression force. In addition, fine capillary channels formed in ODTs facilitated the wicking action and enabled rapid disintegration in vivo (<30 s). On the other hand, since MEC has low hygroscopicity, the tablet hardness of ODTs containing MEC remained high for 1 month in high-humidity conditions. In conclusion, the new ODTs containing MEC developed in this study possessed superior properties for clinical use and are expected to be applied for a wide range of functionally released drugs for bitter taste masking, sustained release, and controlled release (pH-dependent film coating, matrix, and microcapsule). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:351 / 359
页数:9
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