Literature DB >> 10071826

Matrix tablets of carrageenans. I. A compaction study.

K M Picker1.   

Abstract

Carrageenans can be used as excipients for controlled-release tablets. The aim of this study was to determine their compaction and consolidation behavior to prove their usefulness for tableting. The Carr indices of the three carrangeenans, two kappa-carrageenans(Gelcarin GP-812 NF and GP-911 NF) and one tau-carrageenan (Gelcarin GP-379 NF), indicate that the materials are free flowing. They are polymers in the rubbery state. Their glass transition-temperature is about 0 degree C analyzed by differential scanning calorimetry (DSC). The powders were analyzed regarding their compression behavior using an eccentric tableting machine. From data obtained during one compaction cycle, porosity-pressure and pressure-time plots were made. Compaction behavior is evaluated by fitting the pressure-time function to the pressure-time plot and by fitting the Heckel function to the porosity-pressure plot. The polymers show "viscoelastic" tableting behavior. Several additional tableting parameters were analyzed for strengthening the results obtained, namely, maximum work, maximum power, and the time between maximum upper punch force and maximum displacement of the upper punch. The crushing strength of the tablets is high; therefore, the carrageenans are able to form strong compacts. However, they remain in the rubbery state, as shown by thermomechanical analysis. In addition, elastic recovery is regarded at several times after ejection. Finally, after 10 days, it is about 30% as determined from the minimum of tablet height during the compression cycle. These results indicate that the carrageenans are suitable tableting excipients for controlled-release tablets. They show good compactibility and good consolidation behavior. Strong compacts with a high elastic recovery are formed; this means that the materials are able to embed drugs softly. Only a little stress and strain remains in the tablet. All three carrageenans show similar tableting behavior, and a flexible dosage form design is possible.

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Year:  1999        PMID: 10071826     DOI: 10.1081/ddc-100102178

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


  6 in total

1.  Effect of potassium chloride and cationic drug on swelling, erosion and release from kappa-carrageenan matrices.

Authors:  Syed Naim; Betty Samuel; Bhaskar Chauhan; Anant Paradkar
Journal:  AAPS PharmSciTech       Date:  2004-03-09       Impact factor: 3.246

2.  Direct compression behavior of low- and high-methoxylated pectins.

Authors:  Linda Salbu; Annette Bauer-Brandl; Ingunn Tho
Journal:  AAPS PharmSciTech       Date:  2009-12-15       Impact factor: 3.246

3.  The 3-D model: does time plasticity represent the influence of tableting speed?

Authors:  Katharina M Picker
Journal:  AAPS PharmSciTech       Date:  2003-12-16       Impact factor: 3.246

Review 4.  Marine Origin Polysaccharides in Drug Delivery Systems.

Authors:  Matias J Cardoso; Rui R Costa; João F Mano
Journal:  Mar Drugs       Date:  2016-02-05       Impact factor: 5.118

Review 5.  Carrageenan Based Bionanocomposites as Drug Delivery Tool with Special Emphasis on the Influence of Ferromagnetic Nanoparticles.

Authors:  Abida Kalsoom Khan; Ain Us Saba; Shamyla Nawazish; Fahad Akhtar; Rehana Rashid; Sadullah Mir; Bushra Nasir; Furqan Iqbal; Samina Afzal; Fahad Pervaiz; Ghulam Murtaza
Journal:  Oxid Med Cell Longev       Date:  2017-02-20       Impact factor: 6.543

Review 6.  Polymeric plant-derived excipients in drug delivery.

Authors:  Carien E Beneke; Alvaro M Viljoen; Josias H Hamman
Journal:  Molecules       Date:  2009-07-16       Impact factor: 4.411

  6 in total

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