Formulation and Characterization of Two Nystatin Lozenge Formulations as a New Pharmaceutical Dosage form in The Syrian Market

Author:

H. Alghanem Suhail1,N. Ibraheem Dimah1,M. Mansour Basem1,N. Shraiba Aktham1

Affiliation:

1. Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, Al-Andalus University, Tartous, Syria.

Abstract

The aim of this study was to prepare Nystatin lozenges (suitable for many age categories, easy to administrate and preferable in many medical cases) using a variety of excipients, then evaluate these formulations In vitro to select the best one for later use to treat Candida Albicans ( the cause of oral candidiasis). Two formulations were prepared, in F1 (only Arabic gum was used) while in F2 (Arabic gum with propylene glycol were used). A comparison was performed to evaluate the two formulations. The results of our comparison indicated that the F2 formula was the best (disintegrating time: 21.37±0.88 min, Td = 40.59 min is the time required to release 63.2% of the Nystatin content). Nystatin is released from the F2 formulation according to zero order kinetics (linearity between the amount of drug released with time).

Publisher

A and V Publications

Subject

Pharmacology (medical),Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

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