Formula Optimization of 100 mg Chewable Ascorbic Acid Tablets
Uduma E. Osonwa , Eugene C. Uzuegbunam , Kenneth Ugoeze , Kingsley I. Chukwu and Onyinye J Uwaezuoke
1Department of Pharmaceutics and Pharmaceutical Technology, Faculty of
Pharmaceutical Sciences, Nnamdi Azikiwe University, Awka, Nigeria
2Department of Pharmacological and Pharmaceutical Sciences, University of Houston College of Pharmacy, Houston, Texas, United States
3Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, University of Port Harcourt, Port Harcourt, Nigeria
4.Department of Pharmaceutics, College of Pharmacy and Nutrition, University of Saskatchewan-Canada
5.Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, Olabisi Onabanjo University, Ago-Iwoye, Ogun state, Nigeria.
Corresponding author: Uduma Osonwa
Email: udumaosonwa@yahoo.com; Phone : +2348038733305
ABSTRACT
Background: Ascorbic acid is a water soluble nigh dose drug that usually degrades in the presence of moisture with the formation of not so biologically active substances.. Pharmaceutical excipients have long been used to impart functionalities that improve stability and enhance patient compliance while increasing cost. Optimization therefore aims at achieving a compromise between a given set of constraints that yields the best formulation.
Objectives: The aim of this work is to produce optimised formulation of 100 mg chewable ascorbic acid tablet.
Methods: The lubricant was stearic acid at 0.25 %, 0.5% or 0.75 %. The direct compression excipient (DCE) used was Avicel® PH 102 with sorbitol as sweetener in the ratios of sorbitol to Avicel of 1:0, 0:1, 1:1 1:2, 1:3, 1:4 respectively. The tablet weight was calculated such that the concentration of drug is 30-50% of the direct compression excipient (DCE). A step-wise optimization approach was employed. The best batch was selected as having the highest DCE dilution, hardness ≥4 kgf, minimal tablet defects, and acceptable weight variation, content and content variation.
Results: The optimal formula was obtained with the batch that has the following formula, 0.75 % stearic acid at a maximum DCE ratio of avicel: sorbitol of 4 :1 at dilution of 40 % w/w. The flow rate of the powder mix for this batch was 29.70 g/s, with Carrs compressibility index of 22%, and Hausner ratio of 1.28. The angle of repose determined by free flow from a height of 4 cm was 23 . Drug-excipient compatibility studies using DSC revealed no significant interaction between the tablet components except possible change in crystal structure.
Conclusion: The optimal formulation had the following formula: 0.75 % stearic acid, 4 Avicel: 1 sorbitol, and at a maximum DCE dilution of 40% w/w.
Keywords: Ascorbic acid; tablet; direct compression; sequential; optimal formula