| Acceptance rate | 46% |
|---|---|
| Time to first decision | 6 months* |
| Time to decision with review | 50 days* |
*Approximate number of days
**The days mentioned above are averages and do not indicate exact durations. The process may vary for each article.
ACTA Pharmaceutica Sciencia
2021 , Vol 59 , Num 2
Formulation Design and Optimization of Sustained Released Matrix Tablets of Propranolol HCl Using Natural and Synthetic Polymers
1 Chitkara College of Pharmacy, Chitkara University, IndiaDOI : 10.23893/1307-2080.APS.05920 Viewed : 15848 - Downloaded : 3876 The proposed research work aimed to design, formulate and finally to evaluate sustained released matrix tablets of propranolol hydrochloride using the combination of hydrophilic and hydrophobic polymers. Formulation and optimization of Propranolol HCl was done by direct compression technique using 32 factorial design. The amount of polymer Mastic gum (X1) and HPMC (X2) were chosen as independent variables and their effect on amount of drug release at 2 hours (Y1) , 4 hours (Y2) and 8 hours (Y3) at three levels low (-1), medium(0) and high(+1) was taken as dependent variable. Drug-excipient compatibility studies were performed by FTIR and DSC analysis. A total of 9 combinations of sustained released tablets were formulated and evaluated for both pre and post compression parameters. Design expert software version 10 was used to evaluate the effect of independent variable over dependent variable and to generate polynomial equation to represent experimental results. The B7 formulation containing 5 % of mastic gum and 25% of HPMC K-15 combination showed 60.13% drug release in 8 hours and was chosen as optimized formulation. Release kinetic mechanism indicated that the optimized formulation fitted well into Kosmeyer Peppas model (R2= 0.9974). Stability studies indicated that selected formulation was stable for 90 days. Formulation containing 5% of mastic gum and 25% HPMC was found to be effective and can be explored further to develop sustained released formulations. Keywords : Sustained release, mastic gum, factorial design, propranolol HCl