DEVELOPMENT OF STABILITY INDICATING RP-HPLC METHOD FOR THE DETERMINATION OF RELATED SUBSTANCES IN ATORVASTATIN SOLID DOSAGE FORM AND BULK DRUGS

Authors

  • Manoj Kumar Vadlamudi School of Advanced Sciences, VIT University, Vellore-632 014, Tamil Nadu, India
  • Sangeetha Dhanaraj School of Advanced Sciences, VIT University, Vellore-632 014, Tamil Nadu, India
  • Sanjeeva Yarkala Analytical Research and Development, Ashland India Pvt Ltd, Hyderabad-500 078, Telangana, India
  • John Joseph Jayapal School of Advanced Sciences, VIT University, Vellore-632 014, Tamil Nadu, India
  • Pavan Kumar Kommavarapu Analytical Research and Development, Ashland India Pvt Ltd, Hyderabad-500 078, Telangana, India.

Keywords:

Atorvastatin calcium, Impurities, ICH guidelines, Method development, Analytical method validation, Degradation

Abstract

Objective: The present paper reports the development of simple, rapid, accurate and stability indicating reversed phase high-performance liquid chromatography method (RP-HPLC) for estimation of related substances in Atorvastatin calcium (ATV) bulk drug as well as in solid dosage form. The method was validated using Agela, Unisol C18 (250 mmX 4.6 mm; 5µ) column.

Methods: A method was developed to separate clearly the drug peak from the synthetic/process impurities and degradation products formed under stress conditions is attained on (T/%B) were set at 0/43, 18/43, 20/60, 33/60, 35/43, and 40/43 of 0.02 mM ammonium acetate buffer of pH4.9 was used as mobile phase A and 90:10 v/v, ratio of acetonitrile and tetrahydrofuran was used as mobile phase B. A flow rate of 1.4 ml/min and column temperature of 25 °C was used. The wavelength selected was 246 nm. The developed method was validated as per ICH guidelines for the specificity, precision, linearity, accuracy, limit of detection, limit of quantitation and robustness.

Results: Linearity of the impurities was accomplished in the range 0.3-6.0µg/ml for impurity A (Imp A), B (Imp B), C (Imp C), H (Imp H) and 0.4-6.0µg/ml for impurity D (Imp-D), correlation coefficient was found to be more than 0.999 for all impurities. Recovery of impurities was found to be in the range 93%-111%.

Conclusion: The developed method was simple, precise, accurate, robust and also cost effective as it has shorter run time for quantification of impurities in drug substance and drug product as well.

 

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Author Biography

Manoj Kumar Vadlamudi, School of Advanced Sciences, VIT University, Vellore-632 014, Tamil Nadu, India

Analytical science, Scientist II

References

Erturk S, Aktas ES, Ersoy L, Ficicioglu S. An HPLC method for the determination of atorvastatin and its impurities in bulk drug and tablets. J Pharm Biomed Anal 2003;33:1017-23.

United States Pharmacopeia. USP 38–NF 33; 2014.

International Conferences on Harmonization Q3A (R2). Draft Revised Guidance on Impurities in New Drug Substances; 2006.

Singh S, Junwal M, Modhe G, Tiwari H, Kurmi M, Parashar N, et al. Forced degradation studies to assess the stability of drugs and products. TrAC Trends Anal Chem 2013;49:71-88.

Kishore KH, Phani KRS, Kishore RV, Ravindranath LK. Forced degradation studies; practical approach-overview of regulatory guidance and literature for the drug products and drug substances. Int Res J Pharm 2013;4:78-85.

International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human use. Validation of Analytical Procedures: Text and Methodology ICH Q2 (R1); 2005.

Published

01-12-2015

How to Cite

Vadlamudi, M. K., S. Dhanaraj, S. Yarkala, J. J. Jayapal, and P. K. Kommavarapu. “DEVELOPMENT OF STABILITY INDICATING RP-HPLC METHOD FOR THE DETERMINATION OF RELATED SUBSTANCES IN ATORVASTATIN SOLID DOSAGE FORM AND BULK DRUGS”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 7, no. 12, Dec. 2015, pp. 184-9, https://mail.innovareacademics.in/journals/index.php/ijpps/article/view/8907.

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Original Article(s)