Literature DB >> 16408865

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

Na Zhao1, Larry L Augsburger.   

Abstract

The aims of this study are (1) to compare the disintegration efficiency, and (2) to develop a discriminating test model for the 3 classes of superdisintegrants represented by Ac-Di-Sol, Primojel, and Polyplasdone XL10. Using a digital video camera to examine the disintegration process of tablets containing the same wt/wt percentage concentration of the disintegrants, Ac-Di-Sol was found to disintegrate tablets rapidly into apparently primary particles; Primojel also apparently disintegrated tablets into primary particles but more slowly; Polyplasdone XL10 disintegrated tablets rapidly but into larger masses of aggregated particles. The differences in the size distribution generated in the disintegrated tablets likely contribute to the drug dissolution rate differences found for aspirin tablets with similar disintegration rates. The aspirin tablet matrix is proposed as a model formulation for disintegrant efficiency comparison and performance consistency testing for quality control purposes.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16408865      PMCID: PMC2750612          DOI: 10.1208/pt060479

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  10 in total

1.  Disintegration propensity of tablets evaluated by means of disintegrating force kinetics.

Authors:  G Massimo; P L Catellani; P Santi; R Bettini; G Vaona; A Bonfanti; L Maggi; P Colombo
Journal:  Pharm Dev Technol       Date:  2000       Impact factor: 3.133

2.  Evaluation of the functional equivalence of crospovidone NF from different sources. II. Standard performance test.

Authors:  U Shah; L Augsburge
Journal:  Pharm Dev Technol       Date:  2001-08       Impact factor: 3.133

3.  Effect of formulation solubility and hygroscopicity on disintegrant efficiency in tablets prepared by wet granulation, in terms of dissolution.

Authors:  J R Johnson; L H Wang; M S Gordon; Z T Chowhan
Journal:  J Pharm Sci       Date:  1991-05       Impact factor: 3.534

4.  Dissolution difference between acidic and neutral media of acetaminophen tablets containing a super disintegrant and a soluble excipient. II.

Authors:  C R Chen; S L Cho; C K Lin; Y H Lin; S T Chiang; H L Wu
Journal:  Chem Pharm Bull (Tokyo)       Date:  1998-03       Impact factor: 1.645

5.  Preparation and evaluation of a compressed tablet rapidly disintegrating in the oral cavity.

Authors:  Y Bi; H Sunada; Y Yonezawa; K Danjo; A Otsuka; K Iida
Journal:  Chem Pharm Bull (Tokyo)       Date:  1996-11       Impact factor: 1.645

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

Authors:  Y X Bi; H Sunada; Y Yonezawa; K Danjo
Journal:  Drug Dev Ind Pharm       Date:  1999-05       Impact factor: 3.225

7.  Effect of the mode of super disintegrant incorporation on dissolution in wet granulated tablets.

Authors:  M S Gordon; V S Rudraraju; K Dani; Z T Chowhan
Journal:  J Pharm Sci       Date:  1993-02       Impact factor: 3.534

8.  Disintegrating force as a new formulation parameter.

Authors:  P Colombo; U Conte; C Caramella; M Geddo; A La Manna
Journal:  J Pharm Sci       Date:  1984-05       Impact factor: 3.534

9.  The influence of swelling capacity of superdisintegrants in different pH media on the dissolution of hydrochlorothiazide from directly compressed tablets.

Authors:  Na Zhao; Larry L Augsburger
Journal:  AAPS PharmSciTech       Date:  2005-09-20       Impact factor: 3.246

10.  Evaluation of fast disintegrants in terfenadine tablets containing a gas-evolving disintegrant.

Authors:  E Sallam; H Ibrahim; R A Dahab; M Shubair; E Khalil
Journal:  Drug Dev Ind Pharm       Date:  1998-06       Impact factor: 3.225

  10 in total
  16 in total

1.  An investigation into the influence of experimental conditions on in vitro drug release from immediate-release tablets of levothyroxine sodium and its relation to oral bioavailability.

Authors:  Ivana Kocic; Irena Homsek; Mirjana Dacevic; Jelena Parojcic; Branislava Miljkovic
Journal:  AAPS PharmSciTech       Date:  2011-07-12       Impact factor: 3.246

2.  Functionality of disintegrants and their mixtures in enabling fast disintegration of tablets by a quality by design approach.

Authors:  Parind Mahendrakumar Desai; Patrick Xuan Hua Er; Celine Valeria Liew; Paul Wan Sia Heng
Journal:  AAPS PharmSciTech       Date:  2014-05-22       Impact factor: 3.246

3.  Comparison between the effect of strongly and weakly cationic exchange resins on matrix physical properties and the controlled release of diphenhydramine hydrochloride from matrices.

Authors:  Prasert Akkaramongkolporn; Kaewnapa Wongsermsin; Praneet Opanasopit; Tanasait Ngawhirunpat
Journal:  AAPS PharmSciTech       Date:  2010-07-09       Impact factor: 3.246

4.  Functional assessment of four types of disintegrants and their effect on the spironolactone release properties.

Authors:  John Rojas; Santiago Guisao; Vanesa Ruge
Journal:  AAPS PharmSciTech       Date:  2012-08-17       Impact factor: 3.246

5.  Improvement of Meloxicam Solubility Using a β-Cyclodextrin Complex Prepared via the Kneading Method and Incorporated into an Orally Disintegrating Tablet.

Authors:  Ahmad Ainurofiq; Syaiful Choiri; Muhamad Ali Azhari; Chaterin Romauli Siagian; Bambang Budi Suryadi; Fea Prihapsara; Sholichah Rohmani
Journal:  Adv Pharm Bull       Date:  2016-09-25

6.  The Impact of Disintegrant Type, Surfactant, and API Properties on the Processability and Performance of Roller Compacted Formulations of Acetaminophen and Aspirin.

Authors:  Junshu Zhao; Otilia Koo; Duohai Pan; Yongmei Wu; Dinesh Morkhade; Sandeep Rana; Partha Saha; Arturo Marin
Journal:  AAPS J       Date:  2017-06-12       Impact factor: 4.009

7.  Formulation and evaluation of bi-layer tablet of metoclopramide hydrochloride and ibuprofen.

Authors:  Bhavesh Shiyani; Surendra Gattani; Sanjay Surana
Journal:  AAPS PharmSciTech       Date:  2008-07-09       Impact factor: 3.246

8.  New direct compression excipient from tigernut starch: physicochemical and functional properties.

Authors:  Philip F Builders; Patricia A Anwunobi; Chukwuemeka C Mbah; Michael U Adikwu
Journal:  AAPS PharmSciTech       Date:  2013-05-07       Impact factor: 3.246

9.  Development of prednisone:polyethylene glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters.

Authors:  Darío Leonardi; María Gabriela Barrera; María Celina Lamas; Claudio Javier Salomón
Journal:  AAPS PharmSciTech       Date:  2007-12-14       Impact factor: 3.246

10.  Development of fast dispersible aceclofenac tablets: effect of functionality of superdisintegrants.

Authors:  C Mallikarjuna Setty; D V K Prasad; V R M Gupta; B Sa
Journal:  Indian J Pharm Sci       Date:  2008 Mar-Apr       Impact factor: 0.975

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.