ArticleElectrophoresis2026
Validated RP-HPLC-UV Method for the Quantitative Analysis and Stability Evaluation of Amoxicillin in Paediatric Gummy Tablets.
Article in Electrophoresis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Abstract
The development of products that encounter compliance from paediatric patients represents one of the challenges of pharmaceutical technology that aims to develop formulations able to overcome problems related to palatability and dosing flexibility and, in general, to patient acceptance. In this study, a fully validated reversed-phase high-performance liquid chromatography coupled with ultraviolet detection (RP-HPLC-UV) method was applied for the quantitative determination of amoxicillin (AMX) in an innovative gummy tablet formulation designed for paediatric use. The chromatographic method was optimized and validated largely (but not strictly) in accordance with ICH Q2(R1) guidelines, evaluating specificity, linearity, limit of quantification (LOQ), trueness, precision, robustness and ruggedness. A blank matrix derived from a blank formulation was employed to closely simulate the sample matrix during method validation and quantitative analysis. The method exhibited excellent linearity over the concentration range of 0.0039-0.25 mg/mL (R
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