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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 ...
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 ...
Development and validation of the quantitative analysis of ampicillin sodium in powder for injection by Fourier-transform infrared spectroscopy (FT-IR)
(Scientific and Academic Publishing, 2012)
This paper describes the validation of an innovative analytical method for ampicillin sodium in powder for injection quantification, using Fourier-transform infrared (FT-IR) transmission spectroscopy. This technique does ...
Development and Validation of a Green Analytical Method of RP-HPLC for Quantification of Cefepime Hydrochloride in Pharmaceutical Dosage Form: Simple, Sensitive and Economic
(Bentham Science Publ Ltd, 2016-01-01)
Introduction: A green analytical method simple, rapid and economic was validated for the determination of cefepime hydrochloride and has been developed using reversed phase high performance liquid chromatography (RP-HPLC) ...
Validation of an HPLC analytical method for determination of pancuronium bromide in pharmaceutical injections
(TAYLOR & FRANCIS INC, 2008)
Pancuronium bromide is used with general anesthesia in surgery for muscle relaxation and as an aid to intubation. A high performance liquid chromatographic method was fully validated for the quantitative determination of ...
Validation of an analytical method for a comparative profiles of in vitro therapeutic equivalence of immediate release tablets of chlorpheniramine maleate 4 mg
(2019)
The present study was carried out with the purpose of validating an analytical method for the quantification of the
immediate release of tablets of chlorpheniramine maleate 4 mg and the determination or the dissolved ...
Standard addition calibration: Is it enough for an analytical result estimation?. Spectrophotometric experiments for analyte quantitation in real samples
(Research Trends, 2021-12)
Analytical method validation is the first step for quantitative analysis, and both validation and quantitation are usual and fundamental tasks in analytical work; hence it is extremely important to perform them in the most ...