Article citationsMore>>
Müller, L., Mauthe, R.J., Riley, C.M., Andino, M.M., De Antonis, D., Beels, C., De George, J., De Knaep, A.G.M., Ellison, D., Fagerland, J.A., Frank, R., Fritschel, B., Galloway, S., Harpur, E., Humfrey, C.D.N., Jacks, A.S.J., Jagota, N., Mackinnon, J., Mohan, G., Ness, D.K., O’Donovan, M.R., Smith, M.D., Vudathala, G. and Yotti, L. (2006) A Rationale for Determining, Testing, and Controlling Specific Impurities in Pharmaceuticals That Possess Potential for Genotoxicity. Regulatory Toxicology and Pharmacology, 44, 198-211.
https://doi.org/10.1016/j.yrtph.2005.12.001
has been cited by the following article:
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TITLE:
Quantification of Structurally Alert Mutagenic Impurities in Meropenem Trihydrate Drug Substance by Liquid Chromatography with High Resolution Mass Spectrometer (LC-HRMS)
AUTHORS:
Anwar Sulaiman, K. Ramakrishna Reddy, Vundavilli Jagadeesh Kumar, Hemant Kumar Sharma
KEYWORDS:
Mutagenic Impurities, LC-HRMS, Meropenem Trihydrate, Method Validation
JOURNAL NAME:
American Journal of Analytical Chemistry,
Vol.15 No.3,
March
19,
2024
ABSTRACT: Potential mutagenic impurities in Active Pharmaceutical Ingredient, Meropenem Trihydrate were assessed and a novel analytical method for their quantification was developed and validated. This Liquid Chromatographic method using High Resolution Mass Spectrometer (LC-HRMS) technique is proved to be suitable for simultaneous quantification of all ten identified impurities with required specificity, sensitivity, resolution, precision, accuracy, and other method characteristics as per ICH Guidelines. The acceptable limit of less than 2.9 μg/g was considered for evaluations, based on drug substance dosage and duration of treatment. The method stands most sensitive with a Limit of Detection of 0.35 μg/g, considering the challenge full acceptance criteria as per current regulatory standards.
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