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Formulation and development of paediatric orally disintegrating carbamazepine tablets.
Canadell-Heredia, R; Suñé-Pou, M; Nardi-Ricart, A; Pérez-Lozano, P; Suñé-Negre, J M; García-Montoya, E.
Afiliación
  • Canadell-Heredia R; Department of Pharmacy and Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII, 27-31, 08028 Barcelona, Spain.
  • Suñé-Pou M; Department of Pharmacy and Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII, 27-31, 08028 Barcelona, Spain.
  • Nardi-Ricart A; Pharmacotherapy, Pharmacogenetics and Pharmaceutical Technology research group. Bellvitge Biomedical Research Institute (IDIBELL), Av. Granvia de l'Hospitalet, 199-203, 08090 L'Hospitalet de Llobregat, Spain.
  • Pérez-Lozano P; Department of Pharmacy and Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII, 27-31, 08028 Barcelona, Spain.
  • Suñé-Negre JM; Department of Pharmacy and Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII, 27-31, 08028 Barcelona, Spain.
  • García-Montoya E; Pharmacotherapy, Pharmacogenetics and Pharmaceutical Technology research group. Bellvitge Biomedical Research Institute (IDIBELL), Av. Granvia de l'Hospitalet, 199-203, 08090 L'Hospitalet de Llobregat, Spain.
Saudi Pharm J ; 30(11): 1612-1622, 2022 Nov.
Article en En | MEDLINE | ID: mdl-36465846
ABSTRACT
Carbamazepine is a medicine used to manage epilepsy and partial or tonic-clonic seizures. This study aimed at formulating and obtaining carbamazepine orodispersible tablets for paediatric use at a 50 mg dose, with a diameter not greater than 6 mm and a tablet weight of 80 mg, through a direct compression process. The SeDeM pre-formulation/formulation method was used to define the characteristics of both carbamazepine and the selected excipients for direct compression. This study succeeded in formulating and obtaining the proposed tablets. Following the application of the SeDeM method, the tablets met the mass uniformity test and showed appropriate hardness values for orodispersible tablets. The tablets also met the United States Pharmacopeia (USP) test specifications at t = 60 min. The orodispersible tablets obtained may improve compliance with paediatric treatment with carbamazepine, ensuring the safety and effectiveness of the medicine.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Saudi Pharm J Año: 2022 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Saudi Pharm J Año: 2022 Tipo del documento: Article País de afiliación: España