Analytical Method Development And Validation For Determination Of Nitrosamine Impurities N-Nitrosodibutylamine (Ndba) & Nitroso Of N-Dimethyl Erythromycin In Sertraline Hcl Drug Substance By Lc-Ms/Ms

This work provides a thorough assessment of a method for measuring N-nitrosodibutylamine and N-nitroso of N-dimethyl erythromycin A, two substances with substantial regulatory interest because of their health hazards. The performance characteristics of the method were thoroughly investigated through a series of experiments, including standard solution analysis, quantitation and detection limit determination, linearity assessment, precision testing at various levels, and accuracy evaluation via recovery studies. The findings demonstrate that the technique performs exceptionally well in terms of linearity, accuracy, and precision over a broad range of concentrations. The results indicate that the suggested approach has the potential to accurately quantify these chemicals in a range of sample matrices, making it a useful tool for regulatory compliance and quality assurance in associated industries.

Publication Details

Journal
Nanotechnology Perceptions
Published
2024-11-04
DOI
https://doi.org/10.62441/nano-ntp.v20is14.18
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
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article

Analytical Method Development And Validation For Determination Of Nitrosamine Impurities N-Nitrosodibutylamine (Ndba) & Nitroso Of N-Dimethyl Erythromycin In Sertraline Hcl Drug Substance By Lc-Ms/Ms

Nanotechnology Perceptions
Analytical Methods in Pharmaceuticals
article

Analytical Method Development And Validation For Determination Of Nitrosamine Impurities N-Nitrosodibutylamine (Ndba) & Nitroso Of N-Dimethyl Erythromycin In Sertraline Hcl Drug Substance By Lc-Ms/Ms

article en

Abstract

This work provides a thorough assessment of a method for measuring N-nitrosodibutylamine and N-nitroso of N-dimethyl erythromycin A, two substances with substantial regulatory interest because of their health hazards. The performance characteristics of the method were thoroughly investigated through a series of experiments, including standard solution analysis, quantitation and detection limit determination, linearity assessment, precision testing at various levels, and accuracy evaluation via recovery studies. The findings demonstrate that the technique performs exceptionally well in terms of linearity, accuracy, and precision over a broad range of concentrations. The results indicate that the suggested approach has the potential to accurately quantify these chemicals in a range of sample matrices, making it a useful tool for regulatory compliance and quality assurance in associated industries.

Nanotechnology PerceptionsVol. 20(S14)
Industry, innovation and infrastructure
Openalex Percentile: Top 82%
Analytical Methods in Pharmaceuticals
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