The preparation of rapidly disintegrating tablets in the mouth

被引:41
作者
Sugimoto, M [1 ]
Matsubara, K [1 ]
Koida, Y [1 ]
Kobayashi, M [1 ]
机构
[1] Tanabe Seiyaku Co Ltd, Dept Pharmaceut, Prod Technol Dev Lab, Yodogawa Ku, Osaka 5328505, Japan
关键词
amorphous sucrose; crystallization; porosity; rapidly disintegrating tablet; tensile strength;
D O I
10.1081/PDT-120000287
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Elderly people, children and patients sometimes have difficulties swallowing tablets. To solve this problem, a novel method of preparing tablets that disintegrate rapidly in the mouth was developed. A tablet with high porosity is required for rapid disintegration, but such a tablet is generally fragile. To make a tablet having both high porosity and practical strength, amorphous sucrose, which has good compactability, was used. Mannitol powder with freeze-dried amorphous sucrose was tabletted at low compression and stored under certain conditions. The tablet disintegrated rapidly in the mouth, because of its high porosity. The tensile strength of the tablet increased remarkably during storage, while the porosity of the tablet seemed almost unchanged. The results of thermal analysis and powder x-ray diffraction measurement showed that the amorphous sucrose in tablet crystallized during storage. The increase in the tensile strength of the tablet was due to crystallization of the amorphous sucrose and formation of new internal contact points in the tablet. It was concluded that this crystalline transition method is a very useful method to prepare a rapidly disintegrating tablet.
引用
收藏
页码:487 / 493
页数:7
相关论文
共 16 条
[2]
Bi YX, 1996, CHEM PHARM BULL, V44, P2121
[3]
Formulation and production of rapidly disintegrating tablets by lyophilisation using hydrochlorothiazide as a model drug [J].
Corveleyn, S ;
Remon, JP .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 152 (02) :215-225
[4]
ASPARTAME-MANNITOL RESOLIDIFIED FUSED MIXTURE - CHARACTERIZATION STUDIES BY DIFFERENTIAL SCANNING CALORIMETRY, THERMOMICROSCOPY, PHOTOMICROGRAPHY AND X-RAY-DIFFRACTOMETRY [J].
ELSHATTAWY, HH ;
KILDSIG, DO ;
PECK, GE .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1984, 10 (01) :1-17
[5]
HANAWA T, 1995, CHEM PHARM BULL, V43, P284
[6]
Ito A, 1996, CHEM PHARM BULL, V44, P2132
[7]
PROPERTIES OF FUSED MANNITOL IN COMPRESSED TABLETS [J].
KANIG, JL .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1964, 53 (02) :188-&
[8]
New method of preparing high-porosity rapidly saliva soluble compressed tablets using mannitol with camphor, a subliming material [J].
Koizumi, K ;
Watanabe, Y ;
Morita, K ;
Utoguchi, N ;
Matsumoto, M .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 152 (01) :127-131
[9]
DRUG DELIVERY SYSTEMS FOR THE ELDERLY - PROBLEMS AND RESPONSES [J].
KOTTKE, MK ;
RHODES, CT ;
GRADY, LT .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 1989, 15 (10) :1635-1692
[10]
Drug-delivery products and the Zydis fast-dissolving dosage form [J].
Seager, H .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1998, 50 (04) :375-382