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into the UPLC–MS/MS system for analysis. Method Validation According to the guidelines for bioanalytical method development and validation issued by the Food and Drug Administration (FDA) [ 11 ] and European Medicines

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included in this article, our extensive previous experience in drug product analysis and exhaustive literature searches through SciFinder® (Chemical Abstracts), ISI Web of Science, and Google Scholar were employed to guide our method development and

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the analyte signal at the same retention time of an LOQ sample prepared from the same matrix. Results and discussion Method development and validation The development and validation of an analytical method for quantification of nicotine in e

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Acta Chromatographica
Authors: Mohammed Hamed Alqarnı, Mohamad Ayman Salkini, Prawez Alam, Mazen Talal Alanazı, Maged Saad Abdel-Kader, and Samah M. El Sohafy

.2.8 (Dionex, Thermo Fisher Scientific®) was used for data analysis and processing. Obtained data were statistically treated using least square linear regression analysis. Results and discussion Method development and validation The mobile phase used in the

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condition on bench top for 48 h at room temperature. The freshly prepared sample and standard were injected by using the stored mobile phase at a time interval of 24 h. Results and Discussion Method development

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development and validation. The output signal (254 nm) was monitored and processed using QuickStart Empower Waters 2002 software. A Phenomenex Luna C-18 (150 × 4.6 mm, 5 μ) column was used for the HPLC studies and method development, as well as the

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://doi.org/10.7439/ijbar . 30. Dhandapani , B. ; Anjaneyulu , N. ; Venkateshwarlu , Y. ; Rasheed , S. H. HPTLC method development and validation for the simultaneous estimation of amlodipine besylate and Nebivolol hydrochloride in tablet dosage form

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granted the permission of the Governmental Office of Pest County, Hungary (PE/EA/385-5/2018). Biological specimens The serum of untreated rats, allocated for disposal, was used for method development and validation. Stock solutions or the aqueous working

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development and validation of acetaminophen, caffeine, phenylephrine hydrochloride, dextromethorphan hydrobromide and chlorpheniramine Maleate in tablet dosage form by RP- HPLC . Int. J. Pharm. Res. 2017 , 1 , 10 – 13 . 17. Kumar , M. S

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, C. S. ; Panda , J. An overview of experimental designs in HPLC method development and validation . J. Pharm. Biomed. Anal. 2018 , 147 , 590 – 611 . 10.1016/j.jpba.2017.05.006 23. Unger , K. K. ; Skudas , R. ; Schulte , M. M. Particle

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