Analytical Progress in Olanzapine Characterization: A Comprehensive Review of RP-HPLC Method Development and Validation for Impurity Analysis
RP-HPLC Advancements for Olanzapine Impurity Analysis: A Comprehensive Review
DOI:
https://doi.org/10.61920/jddb.v1i01.22Keywords:
RP-HPLC, Olanzapine, Analytical Validation, Impurity Analysis, Method Development and ValidationAbstract
Olanzapine is an atypical antipsychotic drug, and chromatography is the backbone of separation science. It is utilized in all research laboratories and pharmaceutical industries throughout the world. The current review article focuses on the development and validation of an RP-HPLC method for olanzapine. Method development and validation are important in new drug discovery, development, and manufacturing, as well as a variety of other human and animal investigations. An analytical technique is developed to compare a defined characteristic of a drug substance or drug product to established acceptance criteria. Accuracy, precision, specificity, linearity, range and limit of detection, limit of quantification, robustness, and system suitability testing are all covered by validation of HPLC methods according to ICH Guidelines.Downloads
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Published
2024-04-25
How to Cite
Desai, R., & Dhumal, P. (2024). Analytical Progress in Olanzapine Characterization: A Comprehensive Review of RP-HPLC Method Development and Validation for Impurity Analysis: RP-HPLC Advancements for Olanzapine Impurity Analysis: A Comprehensive Review. Journal of Drug Delivery and Biotherapeutics, 1(01), 33–46. https://doi.org/10.61920/jddb.v1i01.22
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