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Analytical Validation of Quantitative High-Performance Liquid Chromatographic Methods in Pharmaceutical Analysis: A Practical Approach
(Taylor & Francis Inc, 2012-01-01)
Analytical validation is an essential component in allowing a laboratory to ensure routine acceptable performance of analytical methods. Despite the considerable amount of important published work on this subject, diversity ...
Pharmaceutical impurities and degradation products: Uses and applications of NMR techniques
(Elsevier Science, 2014-04)
Current standards and regulations demand the pharmaceutical industry not only to produce highly pure drug substances, butto achieve a thorough understanding ofthe impurities accompanying their manufactured drug substances ...
Pharmaceutical impurities and degradation products: Uses and applications of NMR techniques
(Elsevier, 2014-04)
Current standards and regulations demand the pharmaceutical industry not only to produce highly pure drug substances, but to achieve a thorough understanding of the impurities accompanying their manufactured drug substances ...
Analysis of low molecular weight compounds using MALDI- and LDI-TOF-MS: Direct detection of active pharmaceutical ingredients in different formulations
(2017-11-01)
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is a high throughput, easy to use analytical technique. The simple sample preparation of this technique and its tolerance to the presence of contaminants ...
A simple and portable instrument for determination of captopril in pharmaceutical formulations
(2014-01-01)
Objective: This article describes the application and the performance of a cheap, simple and portable device that can be used for colorimetric quantitative determination of captopril (CPT) in pharmaceutical preparations. ...
Validation of analytical methodology for quantification of cefazolin sodium pharmaceutical dosage form by high performance liquid chromatography to be applied for quality control in pharmaceutical industry
(Universidade de São Paulo (USP), Conjunto Quimicas, 2014-01-01)
A reversed-phase high performance liquid chromatography method was validated for the determination of cefazolin sodium in lyophilized powder for solution for injection to be applied for quality control in pharmaceutical ...
Microbiological assay for gatifloxacin in pharmaceutical formulations
(Elsevier B.V., 2014)
Microbiological assay for gatifloxacin in pharmaceutical formulations
(Elsevier B.V., 2006-02-13)
A simple, sensitive and specific agar diffusion bioassay for the antibacterial gatifloxacin was developed using a strain of Bacillus subtilis ATCC 9372 as the test organism. Gatifloxacin could be measured in tablets and ...