Determination of the in vitro disintegration profile of rapidly disintegrating tablets and correlation with oral disintegration

被引:123
作者
Abdelbary, G [1 ]
Eouani, C [1 ]
Prinderre, P [1 ]
Joachim, J [1 ]
Reynier, J [1 ]
Piccerelle, P [1 ]
机构
[1] Fac Pharm Marseille, Lab Pharm Galen Ind & Cosmetol, F-13385 Marseille, France
关键词
rapidly disintegrating tablets; in vitro disintegration profile; texture analyser; oral disintegration;
D O I
10.1016/j.ijpharm.2004.08.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The assessment of the in vitro disintegration profile of rapidly disintegrating tablets (RDT) is very important in the evaluation and the development of new formulations of this type. So far neither the US Pharmacopoeia nor the European Pharmacopoeia has defined a specific disintegration test for RDT; currently, it is only possible to refer to the tests on dispersible or effervescent tablets for the evaluation of RDT's disintegration capacity. In the present study, we have evaluated the disintegration profile of RDT manufactured by main commercialised technologies, using the texture analyser (TA). In order to simulate as much as possible the oral disintegration of these dosage forms, a new operating structure was developed. This structure mimics the situation in the patient's mouth and provides a gradual elimination of the detached particles during the disintegration process. The obtained time-distance profiles or disintegration profiles enabled the calculation of certain quantitative values as the disintegration onset (t(1)) and the total disintegration time (t(2)). These values were used in the characterisation of the effect of test variables as the disintegration medium and temperature on the disintegration time of RDT. Moreover, the oral disintegration time of the same products was evaluated by 14 healthy volunteers. Results obtained when artificial saliva at 37 degrees C was employed as disintegration medium were used to correlate the in vitro (t(2)) and oral disintegration times. Excellent correlation was found and in addition, we were able to achieve a qualitative measure of the mouthfeel by comparing the thickness of the tablets and the penetration distance obtained from the disintegration profile. This method also permitted the discrimination between different RDT, where differences in the disintegration mechanism were reflected on the disintegration profile achieved for each tablet. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:29 / 41
页数:13
相关论文
共 24 条
[1]   The preparation of orally disintegrating tablets using a hydrophilic waxy binder [J].
Abdelbary, G ;
Prinderre, P ;
Eouani, C ;
Joachim, J ;
Reynier, JP ;
Piccerelle, P .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 278 (02) :423-433
[2]  
ABUIZZA K, 2000, AAPS PHARMSCI, V2
[3]  
BARBERO MW, 1998, Patent No. 0027357
[4]  
Bi YX, 1996, CHEM PHARM BULL, V44, P2121
[5]  
Cousin G, 1995, US Patent, Patent No. 5464632
[6]  
CREMER K, 2001, ORALLY DISINTEGRATIN
[7]  
DEMICHELIS AG, 1997, Patent No. 6106861
[8]  
Dobetti L., 2001, PHARM TECHNOL, P44
[9]   In vitro determination of disintegration time of quick-dissolve tablets using a new method [J].
Dor, PJM ;
Fix, JA .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2000, 5 (04) :575-577
[10]  
DOR PJM, 1999, P INT S CONTR REL BI, V26, P939