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Article

Complexity in Estimation of Esomeprazole and its Related Impurities' Stability in Various Stress Conditions in Low-Dose Aspirin and Esomeprazole Magnesium Capsules

by
Palavai Sripal REDDY
1,2,*,
Kishore Kumar HOTHA
1 and
Shakil SAIT
1
1
Analytical Research and Development, IPDO, Dr. Reddy’s. Ltd. Hyderabad, 500072, India
2
JNT University, Kukatpally, Hyderabad, 500085, A.P, India
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2013, 81(2), 475-492; https://doi.org/10.3797/scipharm.1212-13
Submission received: 13 December 2012 / Accepted: 18 February 2013 / Published: 18 February 2013

Abstract

A complex, sensitive, and precise high-performance liquid chromatographic method for the profiling of impurities of esomeprazole in low-dose aspirin and esomeprazole capsules has been developed, validated, and used for the determination of impurities in pharmaceutical products. Esomeprazole and its related impurities’ development in the presence of aspirin was traditionally difficult due to aspirin’s sensitivity to basic conditions and esomeprazole’s sensitivity to acidic conditions. When aspirin is under basic, humid, and extreme temperature conditions, it produces salicylic acid and acetic acid moieties. These two byproducts create an acidic environment for the esomeprazole. Due to the volatility and migration phenomenon of the produced acetic acid and salicylic acid from aspirin in the capsule dosage form, esomeprazole’s purity, stability, and quantification are affected. The objective of the present research work was to develop a gradient reversed-phase liquid chromatographic method to separate all the degradation products and process-related impurities from the main peak. The impurities were well-separated on a RP8 column (150 mm x 4.6mm, X-terra, RP8, 3.5μm) by the gradient program using a glycine buffer (0.08 M, pH adjusted to 9.0 with 50% NaOH), acetonitrile, and methanol at a flow rate of 1.0 mL min−1 with detection wavelength at 305 nm and column temperature at 30°C. The developed method was found to be specific, precise, linear, accurate, rugged, and robust. LOQ values for all of the known impurities were below reporting thresholds. The drug was subjected to stress conditions of hydrolysis, oxidation, photolysis, and thermal degradation in the presence of aspirin. The developed RP-HPLC method was validated according to the present ICH guidelines for specificity, linearity, accuracy, precision, limit of detection, limit of quantification, ruggedness, and robustness.
Keywords: RP-HPLC; Forced degradation; Validation; Esomeprazole; Aspirin; Acetylsalicylic acid; Method development; Method validation; Degradants; Mmigration RP-HPLC; Forced degradation; Validation; Esomeprazole; Aspirin; Acetylsalicylic acid; Method development; Method validation; Degradants; Mmigration

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MDPI and ACS Style

REDDY, P.S.; HOTHA, K.K.; SAIT, S. Complexity in Estimation of Esomeprazole and its Related Impurities' Stability in Various Stress Conditions in Low-Dose Aspirin and Esomeprazole Magnesium Capsules. Sci. Pharm. 2013, 81, 475-492. https://doi.org/10.3797/scipharm.1212-13

AMA Style

REDDY PS, HOTHA KK, SAIT S. Complexity in Estimation of Esomeprazole and its Related Impurities' Stability in Various Stress Conditions in Low-Dose Aspirin and Esomeprazole Magnesium Capsules. Scientia Pharmaceutica. 2013; 81(2):475-492. https://doi.org/10.3797/scipharm.1212-13

Chicago/Turabian Style

REDDY, Palavai Sripal, Kishore Kumar HOTHA, and Shakil SAIT. 2013. "Complexity in Estimation of Esomeprazole and its Related Impurities' Stability in Various Stress Conditions in Low-Dose Aspirin and Esomeprazole Magnesium Capsules" Scientia Pharmaceutica 81, no. 2: 475-492. https://doi.org/10.3797/scipharm.1212-13

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