Literature DB >> 10219525

Evaluation of rapidly disintegrating tablets prepared by a direct compression method.

Y X Bi1, H Sunada, Y Yonezawa, K Danjo.   

Abstract

To make rapidly disintegrating tablets with sufficient mechanical integrity as well as a pleasant taste, microcrystalline cellulose (MCC), Tablettose (TT), and crosslinked sodium carboxymethyl cellulose (Ac-di-sol) or erythritol (ET) were formulated. Tablets were made by a direct compression method (I). Tablet properties such as porosity, tensile strength, and disintegration time were determined. The tensile strength and disintegration time were selected as response variables, tablet porosity and parameters representing the characteristics of formulation were selected as controlling factors, and their relation was determined by the polynomial regression method. Response surface plots and contour plots of tablet tensile strength and disintegration time were also constructed. The optimum combination of tablet porosity and formulation was obtained by superimposing the contour diagrams of tablet tensile strength and disintegration time. Rapidly disintegrating tablets with durable structure and desirable taste could be prepared within the obtained optimum region.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10219525     DOI: 10.1081/ddc-100102211

Source DB:  PubMed          Journal:  Drug Dev Ind Pharm        ISSN: 0363-9045            Impact factor:   3.225


  41 in total

1.  Design of rapidly disintegrating oral tablets using acid-treated yeast cell wall: a technical note.

Authors:  Tetsuya Ozeki; Yuriko Yasuzawa; Hideyo Katsuyama; Yuuki Takashima; Takahide Kasai; Takahiro Eguchi; Hisaya Kakiuchi; Hiroshi Yuasa; Hiroaki Okada
Journal:  AAPS PharmSciTech       Date:  2003-12-31       Impact factor: 3.246

2.  Development and evaluation of cetirizine HCl taste-masked oral disintegrating tablets.

Authors:  Dionysios Dennis Douroumis; Andreas Gryczke; Silke Schminke
Journal:  AAPS PharmSciTech       Date:  2010-12-23       Impact factor: 3.246

3.  Functionality comparison of 3 classes of superdisintegrants in promoting aspirin tablet disintegration and dissolution.

Authors:  Na Zhao; Larry L Augsburger
Journal:  AAPS PharmSciTech       Date:  2005-12-12       Impact factor: 3.246

4.  Fast-disintegrating sublingual tablets: effect of epinephrine load on tablet characteristics.

Authors:  Mutasem M Rawas-Qalaji; F Estelle R Simons; Keith J Simons
Journal:  AAPS PharmSciTech       Date:  2006-04-28       Impact factor: 3.246

5.  Optimization studies on design and evaluation of orodispersible pediatric formulation of indomethacin.

Authors:  Jashanjit Singh; Anil K Philip; Kamla Pathak
Journal:  AAPS PharmSciTech       Date:  2008-01-09       Impact factor: 3.246

6.  Modified polysaccharides as fast disintegrating excipients for orodispersible tablets of roxithromycin.

Authors:  Vijay Sharma; Anil K Philip; Kamla Pathak
Journal:  AAPS PharmSciTech       Date:  2008-01-15       Impact factor: 3.246

7.  Preparation and evaluation of orodispersible tablets of pheniramine maleate by effervescent method.

Authors:  P V Swamy; S P Divate; S B Shirsand; P Rajendra
Journal:  Indian J Pharm Sci       Date:  2009-03       Impact factor: 0.975

8.  Formulation design and optimization of fast dissolving clonazepam tablets.

Authors:  S B Shirsand; Sarasija Suresh; P V Swamy
Journal:  Indian J Pharm Sci       Date:  2009-09       Impact factor: 0.975

9.  Plantago ovata Mucilage in the Design of Fast Disintegrating Tablets.

Authors:  S B Shirsand; Sarasija Suresh; M S Para; P V Swamy; D Nagendra Kumar
Journal:  Indian J Pharm Sci       Date:  2009-01       Impact factor: 0.975

10.  Formulation design of fast disintegrating tablets using disintegrant blends.

Authors:  S B Shirsand; Sarasija Suresh; P V Swamy; M S Para; D Nagendra Kumar
Journal:  Indian J Pharm Sci       Date:  2010-01       Impact factor: 0.975

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.