Author(s): Shoeb Alahmad, Mhd. Amer Almardini, Mahzia yahia

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Address: Shoeb Alahmad*, Mhd. Amer Almardini, Mahzia yahia
Department of Pharmaceutical Chemistry and Quality Control, Faculty of Pharmacy, Damascus University, Damascus, Syria.
*Corresponding Author

Published In:   Volume - 7,      Issue - 2,     Year - 2014

This paper describes HS-GC-FID method for the determination of ethanol residue in solid dosage forms manufactured by alcoholic granulation. The first step in this study is the validation. A description of the procedure and simple calculation of validation parameters was presented. Specificity of the method was determined. Linearity was observed in the range from 2500 ppm to 6000 ppm of ethanol, Correlation Factor was 0.994. The relative standard deviation for repeatability and intermediate precision was 12.13 % and 6.6 % respectively. The limit of detection was calculated to be 0.887 ppm of ethanol per sample. The total run is 8 minutes.

Cite this article:
Shoeb Alahmad, Mhd. Amer Almardini, Mahzia yahia. Validated HS-GC-FID Method for Determination of Residual Ethanol in Solid Dosage Form. Research J. Pharm. and Tech. 7(2): Feb. 2014; Page 184-187.

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RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

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