Development, Quantification and Validation of a HPLC-UV Method for Analysis of N-Nitroso Aryl Piperazine Quetiapine Impurity in Quetiapine Crude to better control in Final Drug Substance

Viraj Kapadekar; Pratibha Daroi; Mukesh Patel; Narayan P Maharana; Vaidhun Bhaskar

doi:10.52711/0974-360X.2025.00583

Research Journal of Pharmacy and Technology

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0974-360X (Online)
0974-3618 (Print)

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Development, Quantification and Validation of a HPLC-UV Method for Analysis of N-Nitroso Aryl Piperazine Quetiapine Impurity in Quetiapine Crude to better control in Final Drug Substance

Author(s): Viraj Kapadekar, Pratibha Daroi, Mukesh Patel, Narayan P Maharana, Vaidhun Bhaskar

Email(s): virajkapadekar0202@gmail.com , pratibhadaroi@gmail.com , mpanem0588@gmail.com , nmaharana565@gmail.com , gip.pharmacy@gmail.com

DOI: 10.52711/0974-360X.2025.00583

Address: Viraj Kapadekar1, Pratibha Daroi1, Mukesh Patel2, Narayan P Maharana2, Vaidhun Bhaskar1
1Department of Quality Assurance, Gahlot Institute of Pharmacy, University of Mumbai, Sector 14, Koparkhairane, Navi Mumbai - 400709, Maharashtra, India.
2Department of Analytical Development and Testing, Enem Nostrum, Plot 59-62, Andheri, Mumbai, Maharashtra.
*Corresponding Author

Published In: Volume - 18, Issue - 9, Year - 2025

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Cite this article:
Viraj Kapadekar, Pratibha Daroi, Mukesh Patel, Narayan P Maharana, Vaidhun Bhaskar. Development, Quantification and Validation of a HPLC-UV Method for Analysis of N-Nitroso Aryl Piperazine Quetiapine Impurity in Quetiapine Crude to better control in Final Drug Substance. Research Journal of Pharmacy and Technology. 2025;18(9):4062-8. doi: 10.52711/0974-360X.2025.00583

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