DEVELOPMENT AND VALIDATION OF A GAS CHROMATOGRAPHY HEADSPACE METHOD FOR THE SIMULTANEOUS QUANTIFICATION OF SIX ORGANIC VOLATILE IMPURITIES IN SUMATRIPTAN SUCCINATEAPI AND ITS PHARMACEUTICAL DOSAGE FORMS

KRISHNA KISHORE J; PRASADA RAO K

doi:10.22159/ajpcr.2020.v13i5.37260

Authors

KRISHNA KISHORE J Department of Chemistry, ANU Research Centre, Bapatla Engineering College, Guntur, Andhra Pradesh, India.
PRASADA RAO K Department of Chemistry, ANU Research Centre, Bapatla Engineering College, Guntur, Andhra Pradesh, India.

DOI:

https://doi.org/10.22159/ajpcr.2020.v13i5.37260

Keywords:

Methanol, Acetone, Isopropyl alcohol, Dichloromethane, Benzene, Toluene, Sumatriptan Succinate active pharmaceutical ingredients, Method development and Validation

Abstract

Objective: The main aim of this study, to develop a validated analytical method for simultaneous quantification of six organic volatile impurities (OVI) in sumatriptan succinate active pharmaceutical ingredients (API) and its pharmaceutical dosage forms by headspace (HS)-gas chromatography (GC).

Methods: The method development and its validation were performed on a Shimadzu GC-2010 GC system equipped with a flame ionization detector and Teledynetekmar HT3TM HS analyzer. The method involved a thermal gradient elution of six OVI present in sumatriptan succinate API. DB-624, 30 m×0.53 mm, 3.0 μ column is used as a stationary phase and nitrogen gas is used as a carrier gas. The flow rate was 2.8 mL/min and the flame ionization detector temperature is 260°C.

Results: The correlation coefficient (r2) was not <0.99 at the limit of quantification (LOQ) to 150%. The limit of detection obtained for methanol, acetone, isopropyl alcohol, dichloromethane, benzene, and toluene was found 18.4, 8.8, 5.5, 4.3, 0.04, and 4.2 ppm. The LOQ obtained was 55.8, 26.8, 16.6, 13.0, 0.1, and 12.6 ppm. Accuracy results were obtained from 85 to 115% for six OVI’s. Furthermore, verified precision, ruggedness, robustness, solution stability, and pharmaceutical analysis. All the results are found within the acceptable limits.

Conclusion: The method presents a simple and reliable solution for the routine quantitative analysis of organic volatile impurities present in sumatriptan succinate API.

Downloads

Download data is not yet available.

References

Sagar DS, Paresh UP, Bhanubhai NS. Development and validation of reversed-phase high performance liquid chromatographic method for estimation of sumatriptan succinate in pharmaceutical dosage form. Int J Drug Dev Res 2011;3 Suppl 4:266-9.

First-Time Generic Approvals: Seasonale, Imodium Advanced, and Topamax. Available from: https://www.Medscape.com. [Last accessed on 2006 Sep 22; Last accessed on 2013 Jul 11].

Singh A, Singh SB. Simultaneous estimation of sumatriptan succinate, metoclopramide hydrochloride and paracetamol by RP-HPLC method. J Pharm Sci Res 2012;4 Suppl 6:1848-51.

International Council for Harmonisation. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. ICH Harmonized Tripartite Guidelines Q3C Impurities: Residual Solvents. Switzerland: International Council for Harmonisation; 1997.