Chemometric Assisted Development and Validation of a Stability-indicating LC Method for Determination of Related Substances in Haloperidol Decanoate Injection
Sudheer Kolla Babu1,2★, Madhusudhan Vallabhaneni Rao1, Srinivasa Puttagunta Babu3, Murthy Veera Venkata Satyanarayana Chakka2★ Corresponding author
- 1Vignan’s Foundation for Science, Technology and Research University, Vadlamudi, Guntur, Andhra Pradesh, INDIA.
- 2Department of Analytical Research and Development, Formulations, GVK Bio Sciences Pvt. Ltd., Mallapur, Hyderabad, Telanagana, INDIA.
- 3Department of Pharmaceutics, Vignan Pharmacy College, JNTU-Kakinada, Vadlamudi, Guntur, Andhra Pradesh, INDIA.
CORRESPONDENCE
Sudheer Kolla Babu
Mr. Sudheer Babu Kolla,Vignan’s Foundation for Science, Technology and Research University, Vadlamudi, Guntur-522213, Andhra Pradesh, INDIA.
Received: 27-02-2021; Revised: 10-04-2021; Accepted: 18-06-2021.
Volume 55, Issue 3 · pp. 904–915 · PUBLISHED 2021 · DOI: 10.5530/ijper.55.3.165
ABSTRACT
Aim: Haloperidol decanoate injection is a phenyl butyl piperadine derivative with antipsychotic, neuroleptic, antiemetic effects and has multiple related substances as process and degradant impurities. Objectives: This study focuses on chemometric assisted liquid chromatographic approach to develop a stability indicating impurity profile of Haloperidol decanoate injection. Methodology: Dual experimental designs (combined mixture I-optimal design and response surface historical data design) were employed to resolve all thirteen known impurities of Haloperidol decanoate. Chromatographic separation was achieved on a Hypersil BDS C18 (100 x 4.0 mm) 3-µm column to attain separation of related compounds. Results: The optimum conditions for the chromatographic system resulted in a mobile phase consisting of tetra butyl ammonium hydrogen sulphate/ 1-decane Sulphonate sodium buffer solution and acetonitrile with linear gradient elution at a flow rate of 1.4 mL/min. Selectivity, forced degradation, linearity, accuracy and precision were demonstrated in a range of 0.75-30.0 µg/mL. Conclusion: The optimized method was able to resolve the ghost peak observed because of gradient change of mobile phase and is able to separate both polar and non-polar impurities within 60 min, in single method, with resolution of more than 2.0 between adjacent impurities. The inter-day precision for all impurities and haloperidol decanoate were evaluated and found to have a % RSD of less than 10.
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Babu, S. K., Rao, M. V., Babu, S. P., & Chakka, M. V. V. S. (2021). Chemometric Assisted Development and Validation of a Stability-indicating LC Method for Determination of Related Substances in Haloperidol Decanoate Injection. Indian Journal of Pharmaceutical Education and Research, 55(3), 904–915. https://doi.org/10.5530/ijper.55.3.165
