Literature DB >> 26827922

Application of general multilevel factorial design with formulation of fast disintegrating tablets containing croscaremellose sodium and Disintequick MCC-25.

Amanda Solaiman1, Ammar Said Suliman1, Swapnil Shinde1, Sidra Naz1, Amal Ali Elkordy2.   

Abstract

Despite the popularity of orally fast disintegrating tablets (FDTs), their formulation can sometimes be challenging, producing tablets with either poor mechanical properties or high disintegration times. The aim of this research was to enhance the properties of FDTs produced by direct compression to have both sufficient hardness to withstand manual handling, and rapid disintegration time. General multilevel factorial design was applied to optimise and evaluate main and interaction effects of independent variables (i) disintegrant concentration, (ii) % filler (Disintequick MCC-25) to mannitol on the responses hardness, tensile strength and disintegration time. In this experiment mannitol was used as a diluent, Disintequick MCC-25 (to best of our knowledge there is no publication available yet for its use with FDTs) was termed in this study as a filler and croscaremellose sodium was used as the superdisintegrant. Seven formulations were prepared following a progressive two-stage approach. Each stage involved the change in the ratio of excipients (Mannitol:Filler) (1:0), (1:0.25), (1:0.50), (1:1), (0.50:1), (0.25:1), (0:1) w/w and concentration of superdisintegrant (1%, 3%, 5%, 7%, 10% w/w). All FDTs were tested for different parameters such as diameter, hardness, tensile strength, thickness, friability and disintegration time. The results of multiple linear regression analysis show a good degree of correlation between experimental (R(2):0.84, 0.94, 0.91) and predicted response (R(2):0.83, 0.96, 0.95) for hardness, tensile strength and disintegration time respectively. The optimum formulations (regarding disintegration time with acceptable hardness and friability properties) consisted of: (i) 5% w/w disintegrant and 20% w/w filler to mannitol, showing a disintegration time of 30s, a hardness of 66.6N (6.8 kg/cm(2)) and friability of 2.2%; (ii) 7% or 10% w/w disintegrant with 33.33% w/w filler to mannitol, showing disintegration time of 84 s (for 7% disintegrant) and 107 s (for 10% disintegrant), hardness of 73.86N (for 7% disintegrant) and 72.68N (for 10% disintegrant) and friability of 1.44 (for 7% disintegrant) and 1.15% (for 10% disintegrant).
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Disintegration time; Fast disintegrating tablets; General multilevel factorial design; Tablet hardness; Tensile strength

Mesh:

Substances:

Year:  2016        PMID: 26827922     DOI: 10.1016/j.ijpharm.2016.01.065

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


  3 in total

1.  Enhancing the Low Oral Bioavailability of Sulpiride via Fast Orally Disintegrating Tablets: Formulation, Optimization and In Vivo Characterization.

Authors:  Hesham M Tawfeek; Yasser A Hassan; Mohammed F Aldawsari; Mohamed H Fayed
Journal:  Pharmaceuticals (Basel)       Date:  2020-12-05

2.  Design, Optimization, and Correlation of In Vitro/In Vivo Disintegration of Novel Fast Orally Disintegrating Tablet of High Dose Metformin Hydrochloride Using Moisture Activated Dry Granulation Process and Quality by Design Approach.

Authors:  Alhussain H Aodah; Mohamed H Fayed; Ahmed Alalaiwe; Bader B Alsulays; Mohammed F Aldawsari; El-Sayed Khafagy
Journal:  Pharmaceutics       Date:  2020-06-27       Impact factor: 6.321

3.  Exploitation of Design-of-Experiment Approach for Design and Optimization of Fast-Disintegrating Tablets for Sublingual Delivery of Sildenafil Citrate with Enhanced Bioavailability Using Fluid-Bed Granulation Technique.

Authors:  Amer S AlAli; Mohammed F Aldawsari; Ahmed Alalaiwe; Bjad K Almutairy; Ramadan Al-Shdefat; Ismail A Walbi; Mohamed H Fayed
Journal:  Pharmaceutics       Date:  2021-06-12       Impact factor: 6.321

  3 in total

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