Green and white-assessed validated chromatographic methods for Ondansetron purity testing in its pharmaceutical formulations; in silico toxicity profiling of impurities
[Display omitted] •Eco-friendly chromatographic methods for determination of ondansetron in the presence of five impurities in different pharmaceutical dosage forms.•Validation of the developed methods as per ICH guidelines.•Application of the developed methods to oral films; a newly developed dosag...
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Published in | Microchemical journal Vol. 199; p. 110104 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.04.2024
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Abstract | [Display omitted]
•Eco-friendly chromatographic methods for determination of ondansetron in the presence of five impurities in different pharmaceutical dosage forms.•Validation of the developed methods as per ICH guidelines.•Application of the developed methods to oral films; a newly developed dosage form.•Verification of developed methods’ greenness and whiteness using advanced assessment metrics.•Insilico toxicity profiling of impurities using pkcsm and preADMET softwares.
Drug impurities are seen as a crucial threat to drug safety, specifically when dealing with mutagenic/ toxic impurities. Here, we present LC-MS/MS and HPTLC-densitometric methods for simultaneous quantification of Ondansetron and its four official impurities. For the LC-MS/MS, the isocratic elution was applied using methanol and water containing 0.1 % formic acid in a ratio (70:30 v/v) at a flow rate of 1 mL/min, a stationary phase C18 column (4.6 × 50 mm, 5 µm) and mass detection using the MRM mode. For the HPTLC-densitometric method, the mobile phase consists of ethyl acetate: methanol in a ratio (6:4 v/v), and the UV detection was at 216 nm. The developed methods have been validated per ICH recommendations and then evaluated using five tools for whiteness and greenness assessment, offering promising results in comparison to reported chromatographic methods. Additionally, the toxicity profile of the impurities was expected by the online software; PreADMET and pkCSM. The developed methods are recommendedfor quality control due to their high analytical performance as well as their sustainability, simplicity, and cost-effectiveness, which improves the surveillance capability. |
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AbstractList | [Display omitted]
•Eco-friendly chromatographic methods for determination of ondansetron in the presence of five impurities in different pharmaceutical dosage forms.•Validation of the developed methods as per ICH guidelines.•Application of the developed methods to oral films; a newly developed dosage form.•Verification of developed methods’ greenness and whiteness using advanced assessment metrics.•Insilico toxicity profiling of impurities using pkcsm and preADMET softwares.
Drug impurities are seen as a crucial threat to drug safety, specifically when dealing with mutagenic/ toxic impurities. Here, we present LC-MS/MS and HPTLC-densitometric methods for simultaneous quantification of Ondansetron and its four official impurities. For the LC-MS/MS, the isocratic elution was applied using methanol and water containing 0.1 % formic acid in a ratio (70:30 v/v) at a flow rate of 1 mL/min, a stationary phase C18 column (4.6 × 50 mm, 5 µm) and mass detection using the MRM mode. For the HPTLC-densitometric method, the mobile phase consists of ethyl acetate: methanol in a ratio (6:4 v/v), and the UV detection was at 216 nm. The developed methods have been validated per ICH recommendations and then evaluated using five tools for whiteness and greenness assessment, offering promising results in comparison to reported chromatographic methods. Additionally, the toxicity profile of the impurities was expected by the online software; PreADMET and pkCSM. The developed methods are recommendedfor quality control due to their high analytical performance as well as their sustainability, simplicity, and cost-effectiveness, which improves the surveillance capability. |
ArticleNumber | 110104 |
Author | ELbalkiny, Heba T. El-Maraghy, Christine M. Nour, Mai S. |
Author_xml | – sequence: 1 givenname: Christine M. surname: El-Maraghy fullname: El-Maraghy, Christine M. organization: Analytical Chemistry Department, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), 11787 6th October City, Egypt – sequence: 2 givenname: Mai S. surname: Nour fullname: Nour, Mai S. organization: Pharmaceutical Chemistry Department, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), 11787 6th October City, Egypt – sequence: 3 givenname: Heba T. surname: ELbalkiny fullname: ELbalkiny, Heba T. email: htarek@msa.edu.eg organization: Analytical Chemistry Department, Faculty of Pharmacy, October University for Modern Sciences and Arts (MSA), 11787 6th October City, Egypt |
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Keywords | AGREE, GAPI LC-MS/MS Toxicity profiling Impurities White assessment HPTLC-densitometry Ondansetron |
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SubjectTerms | AGREE, GAPI HPTLC-densitometry Impurities LC-MS/MS Ondansetron Toxicity profiling White assessment |
Title | Green and white-assessed validated chromatographic methods for Ondansetron purity testing in its pharmaceutical formulations; in silico toxicity profiling of impurities |
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