Literature DB >> 18182258

Effect of preparation method on properties of orally disintegrating tablets made by phase transition.

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

Abstract

In order to evaluate the effect of preparation method on the properties of orally disintegrating (OD) tablets, OD tablets were prepared by compressing a mixture of high melting point sugar alcohol (HMP-SA) and low melting point sugar alcohol (LMP-SA) and subsequent heating. In the direct compression method (DCM) where the LMP-SA was added as a powder, both hardness and disintegration time were increased by decreasing the particle size of the LMP-SA. In the wet granule compression method (WGCM), where the LMP-SA was added as an aqueous binder solution, the tablets became harder with less heating compared to tablets prepared by DCM. Using 1% xylitol as the LMP-SA provided tablets with sufficient hardness when prepared by WGCM, as opposed to DCM where 5% xylitol was necessary to prepare tablets with similar hardness. These results suggest that uniformly distributed LMP-SA on the surface of HMP-SA particles in WGCM might diffuse more easily during the heating process compared to mechanically mixed LMP-SA in DCM, resulting in an increase in tablet hardness even with a short heating time and low content of LMP-SA. In addition, disintegration and hardness stability of the tablets were affected by the LMP-SA content when prepared by WGCM, suggesting that the LMP-SA content should be regulated to assure the stability of OD tablet characteristics.

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Year:  2007        PMID: 18182258     DOI: 10.1016/j.ijpharm.2007.11.046

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  5 in total

1.  Characterization of oral disintegrating film containing donepezil for Alzheimer disease.

Authors:  Kai Bin Liew; Yvonne Tze Fung Tan; Kok Khiang Peh
Journal:  AAPS PharmSciTech       Date:  2011-12-14       Impact factor: 3.246

2.  A novel spray-dried nanoparticles-in-microparticles system for formulating scopolamine hydrobromide into orally disintegrating tablets.

Authors:  Feng-Qian Li; Cheng Yan; Juan Bi; Wei-Lin Lv; Rui-Rui Ji; Xu Chen; Jia-Can Su; Jin-Hong Hu
Journal:  Int J Nanomedicine       Date:  2011-04-28

Review 3.  Formulation and Quality Control of Orally Disintegrating Tablets (ODTs): Recent Advances and Perspectives.

Authors:  Mohammadali Poursharifi Ghourichay; Seyed Hossein Kiaie; Ali Nokhodchi; Yousef Javadzadeh
Journal:  Biomed Res Int       Date:  2021-12-24       Impact factor: 3.411

4.  Study of Orally Disintegrating Tablets Using Erythritol as an Excipient Produced by Moisture-Activated Dry Granulation (MADG).

Authors:  Mizuki Yamada; Agata Ishikawa; Shun Muramatsu; Takayuki Furuishi; Yoshinori Onuki; Kaori Fukuzawa; Etsuo Yonemochi
Journal:  Pharmaceuticals (Basel)       Date:  2022-08-15

5.  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
  5 in total

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