Stability indicating assay method for the determination of medroxy progestrone aceate in bulk drug and formulation by HPTLC

Research output: Contribution to journalArticle

Abstract

A sensitive, accurate, precise and stability indicating high-performance thin layer chromatographic assay method for analysis of Medroxyprogestrone acetate (MPA) in both bulk drug and formulation was developed and validated. The method employed HTLC aluminium plates precoated with silica gel 60F-254 as the stationary phase. The solvent system consisted of Toluene: ethyl acetate: ammonia solution (80:20:0.1 %v/ v). This system was found to give compact spots for MPA (Rf value 0.32±0.02). MPA was subjected to acid, alkali and neutral hydrolysis, oxidation, sunlight and dry heat treatment. The degraded products were well separated from the pure drug with notably different Rf values. CAMAG HPTLC instrument was used for chromatographic separations. Densitometric analysis of MPA was carried out in the absorbance mode at 240 nm. The linear regression data for the calibration plots showed good linear relationship with correlation coefficient 0.9998 ±/0.001 in the concentration range of 50.0-1800.0ng spot-1. The value of slope and intercept were 11.68 and 73.414 respectively. The method was validated for precision, accuracy, robustness, and recovery. The limits of detection and quantitation were 16.5 and 50.0 ng spot-1 respectively.

Original languageEnglish
Pages (from-to)286-293
Number of pages8
JournalCurrent Trends in Biotechnology and Pharmacy
Volume11
Issue number3
Publication statusPublished - 01-07-2017

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Drug Compounding
Acetates
Sunlight
Silica Gel
Toluene
Alkalies
Aluminum
Ammonia
Calibration
Limit of Detection
Linear Models
Hydrolysis
Hot Temperature
Acids
Pharmaceutical Preparations

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Pharmaceutical Science
  • Drug Discovery

Cite this

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title = "Stability indicating assay method for the determination of medroxy progestrone aceate in bulk drug and formulation by HPTLC",
abstract = "A sensitive, accurate, precise and stability indicating high-performance thin layer chromatographic assay method for analysis of Medroxyprogestrone acetate (MPA) in both bulk drug and formulation was developed and validated. The method employed HTLC aluminium plates precoated with silica gel 60F-254 as the stationary phase. The solvent system consisted of Toluene: ethyl acetate: ammonia solution (80:20:0.1 {\%}v/ v). This system was found to give compact spots for MPA (Rf value 0.32±0.02). MPA was subjected to acid, alkali and neutral hydrolysis, oxidation, sunlight and dry heat treatment. The degraded products were well separated from the pure drug with notably different Rf values. CAMAG HPTLC instrument was used for chromatographic separations. Densitometric analysis of MPA was carried out in the absorbance mode at 240 nm. The linear regression data for the calibration plots showed good linear relationship with correlation coefficient 0.9998 ±/0.001 in the concentration range of 50.0-1800.0ng spot-1. The value of slope and intercept were 11.68 and 73.414 respectively. The method was validated for precision, accuracy, robustness, and recovery. The limits of detection and quantitation were 16.5 and 50.0 ng spot-1 respectively.",
author = "Kulyadi, {Girish Pai} and Vasanthraju and Prashanth Musmade and Sathyanarayana, {Muddukrishna Badamane}",
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AU - Kulyadi, Girish Pai

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AU - Sathyanarayana, Muddukrishna Badamane

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AB - A sensitive, accurate, precise and stability indicating high-performance thin layer chromatographic assay method for analysis of Medroxyprogestrone acetate (MPA) in both bulk drug and formulation was developed and validated. The method employed HTLC aluminium plates precoated with silica gel 60F-254 as the stationary phase. The solvent system consisted of Toluene: ethyl acetate: ammonia solution (80:20:0.1 %v/ v). This system was found to give compact spots for MPA (Rf value 0.32±0.02). MPA was subjected to acid, alkali and neutral hydrolysis, oxidation, sunlight and dry heat treatment. The degraded products were well separated from the pure drug with notably different Rf values. CAMAG HPTLC instrument was used for chromatographic separations. Densitometric analysis of MPA was carried out in the absorbance mode at 240 nm. The linear regression data for the calibration plots showed good linear relationship with correlation coefficient 0.9998 ±/0.001 in the concentration range of 50.0-1800.0ng spot-1. The value of slope and intercept were 11.68 and 73.414 respectively. The method was validated for precision, accuracy, robustness, and recovery. The limits of detection and quantitation were 16.5 and 50.0 ng spot-1 respectively.

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