Fast and simple gas chromatographic method for simultaneous estimation of camphor, menthol and methyl salicylate in analgesic ointment: application in stability study

A simple, rapid and sensitive gas chromatographic (GC) method with flame ionization detector (FID) has been developed and validated for simultaneous estimation of camphor, menthol and methyl salicylate (MS). Camphor, menthol and MS were separated at about 2.753, 3.206 and 3.995 min respectively...

Full description

Bibliographic Details
Main Authors: Md Adib, Noor Adibah, Mandal, Uttam Kumar, Mohamed, Farahidah, Chatterjee, Bappaditya
Format: Article
Language:English
English
English
Published: SpringerLink 2017
Subjects:
Online Access:http://irep.iium.edu.my/56687/
http://irep.iium.edu.my/56687/
http://irep.iium.edu.my/56687/
http://irep.iium.edu.my/56687/1/GC%20JPI.pdf
http://irep.iium.edu.my/56687/7/56687_Fast%20and%20simple%20gas%20chromatographic.pdf
http://irep.iium.edu.my/56687/13/56687_Fast%20and%20simple%20gas%20chromatographic%20method_article.pdf
Description
Summary:A simple, rapid and sensitive gas chromatographic (GC) method with flame ionization detector (FID) has been developed and validated for simultaneous estimation of camphor, menthol and methyl salicylate (MS). Camphor, menthol and MS were separated at about 2.753, 3.206 and 3.995 min respectively on a capillary column with helium (3.3 ml/min) as carrier gas within 11 min run time. Noninterference of any peak with the peaks of interest confirms the selectivity of method. Derived quantitation limits (QL) were 0.847, 0.684 and 6.507 μg/ml for camphor, menthol and MS respectively. The linear relationship ( R2 > 0.999) between analyte concentration vs detector response was established within a range of QL to 150% of label claim concentration for each analyte. Recovery of each analyte at 50, 100 and 150% of label claim concentration levels were obtained within 99.67–101.53% establishing high accuracy of the method. The method showed acceptable precision with low relative standard deviation or RSD (0.24–1.03%) between percent recoveries for each analyte. RSD for intermediate precision (inter day analysis, analyst variation) was less than 1%. The validated method was successfully applied for quantitative determination of camphor, menthol and MS in stability samples of an analgesic ointment produced by IKOP Sdn. Bhd., Malaysia.