Development of an innovative, ecological and stability-indicating analytical method for semiquantitative analysis of ampicillin sodium for injection by thin layer chromatography (TLC)

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.creatorTótoli, Eliane Gandolpho [UNESP]
dc.creatorSalgado, Hérida Regina Nunes [UNESP]
dc.date2016-01-28T16:56:36Z
dc.date2016-01-28T16:56:36Z
dc.date2014
dc.date.accessioned2023-09-12T08:16:32Z
dc.date.available2023-09-12T08:16:32Z
dc.identifierhttp://www.wjpps.com/wjpps_controller/abstract_id/1518
dc.identifierWorld Journal of Pharmacy and Pharmaceutical Sciences, v. 3, n. 6, p. 1944-1957, 2014.
dc.identifier2278-4357
dc.identifierhttp://hdl.handle.net/11449/133783
dc.identifier4663515659758888
dc.identifier9881720291571774
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8783035
dc.descriptionAmpicillin sodium is a β-lactam antimicrobial agent for parenteral use, widely used in many parts of the world and recommended by the World Health Organization. There are some methods described in the literature to identify ampicillin sodium employing Thin-Layer Chromatography (TLC). However, these methods are complex and require the use of solvents potentially toxic to the operators and environment. This paper describes the validation of an innovative semiquantitative method for the analysis of ampicillin sodium in powder for injectable solution, using TLC. This technique does not use toxic or expensive solvents, which is one great advantage over the described TLC analytical methods. This fact contributes to minimize the generation of toxic organic solvent waste by the industry and thereby reduces the impact of its activities on the environment. The method involved the use of a mobile phase comprised by a mixture of ethanol and water (90:10, v/v) and the stationary phase was silica gel impregnated in aluminum. Stress degradation studies of the pharmaceutical product were conducted under conditions of hydrolysis (acid, basic, and aqueous), oxidation and photolysis. The spots were detected by exposing the dry plate to UV chamber (254 nm) and/or iodine vapor and analyzed semiquantitatively by HPLC-UV. The method was successfully validated according to the ICH guidelines and Brazilian legislation, showing to be able to semiquantify ampicillin sodium in powder for injection preparation and it can be used as an environmentally friendly alternative for the routine analysis in quality control.
dc.descriptionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.descriptionConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.descriptionUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Fármacos e Médicamentos, Faculdade de Ciências Farmacêuticas de Araraquara, Araraquara, Rodovia Araraquara-Jaú, km1, Campus, CEP 14801-902, SP, Brasil
dc.descriptionUniversidade Estadual Paulista Júlio de Mesquita Filho, Departamento de Fármacos e Médicamentos, Faculdade de Ciências Farmacêuticas de Araraquara, Araraquara, Rodovia Araraquara-Jaú, km1, Campus, CEP 14801-902, SP, Brasil
dc.format1944-1957
dc.languageeng
dc.relationWorld Journal of Pharmacy and Pharmaceutical Sciences
dc.rightsAcesso restrito
dc.sourceCurrículo Lattes
dc.subjectAmpicillin sodium
dc.subjectAnalytical methods
dc.subjectQuality control
dc.subjectTLC
dc.subjectStability
dc.titleDevelopment of an innovative, ecological and stability-indicating analytical method for semiquantitative analysis of ampicillin sodium for injection by thin layer chromatography (TLC)
dc.typeArtigo


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