Literature DB >> 15955365

Evaluation of rapidly disintegrating tablets manufactured by phase transition of sugar alcohols.

Yoshio Kuno1, Masazumi Kojima, Shuichi Ando, Hiroaki Nakagami.   

Abstract

The aim of the present study was to assess the properties of rapidly disintegrating (RD) tablets manufactured by the phase transition method. RD tablets were produced by compressing powder containing erythritol (melting point: 122 degrees C) and xylitol (melting point: 93 approximately 95 degrees C), and then heating at about 93 degrees C for 15 min. The hardness and oral disintegration time of the heated tablets increased with an increase of the xylitol content. These results suggested that the heating process and xylitol content might influence the properties of RD tablets. Then we evaluated the physicochemical properties of the RD tablets, including the median pore size, crystallinity, hardness, and oral disintegration time of tablets made with and without heating. After heating, the median pore size of the tablets was increased and tablet hardness was also increased. The increase of tablet hardness with heating and storage did not depend on the crystal state of the lower melting point sugar alcohol. It is concluded that a combination of low and high melting point sugar alcohols, as well as a phase transition in the manufacturing process, are important for making RD tablets without any special apparatus.

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Year:  2005        PMID: 15955365     DOI: 10.1016/j.jconrel.2005.01.018

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  9 in total

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2.  Maltodextrin: a novel excipient used in sugar-based orally disintegrating tablets and phase transition process.

Authors:  Yosra Shaaban R Elnaggar; Magda A El-Massik; Ossama Y Abdallah; Abd Elazim R Ebian
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3.  Formulation of Ebastine Fast-Disintegrating Tablet Using Coprocessed Superdisintegrants and Evaluation of Quality Control Parameters.

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4.  Fast Melt Cocoa Butter Tablet: Effect of Waxes, Starch, and PEG 6000 on Physical Properties of the Preparation.

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Journal:  Molecules       Date:  2022-05-13       Impact factor: 4.927

5.  Preparation and in vitro/in vivo characterization of porous sublingual tablets containing ternary kneaded solid system of vinpocetine with î-cyclodextrin and hydroxy Acid.

Authors:  Mona H Aburahma; Hanan M El-Laithy; Yassin El-Said Hamza
Journal:  Sci Pharm       Date:  2010-05-17

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Review 7.  Oral Dispersible System: A New Approach in Drug Delivery System.

Authors:  P A Hannan; J A Khan; A Khan; S Safiullah
Journal:  Indian J Pharm Sci       Date:  2016 Jan-Feb       Impact factor: 0.975

8.  Formulation and evaluation of carvedilol melt-in-mouth tablet using mucoadhesive polymer and PEG-6-stearate as hydrophilic waxy binder.

Authors:  Amish Ashvinkumar Dangi; Prakash Bhikhabhai Zalodiya
Journal:  Int J Pharm Investig       Date:  2012-10

9.  Development of Orodispersible Tablets of Candesartan Cilexetil- β -cyclodextrin Complex.

Authors:  Maddukuri Sravya; Rajamanickam Deveswaran; Srinivasan Bharath; Basappa Veerbadraiah Basavaraj; Varadharajan Madhavan
Journal:  J Pharm (Cairo)       Date:  2013-09-24
  9 in total

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