SciELO - Scientific Electronic Library Online

 
vol.14 número2Concordancia de antígenos de dengue en el ELISA de captura de IgM (MAC ELISA) en el IICS-UNASistema de vigilancia epidemiológica comunitaria "Bonis". Estado actual y proyecciones futuras índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Revista

Articulo

Indicadores

  • No hay articulos citadosCitado por SciELO

Links relacionados

  • No hay articulos similaresSimilares en SciELO

Compartir


Memorias del Instituto de Investigaciones en Ciencias de la Salud

versión On-line ISSN 1812-9528

Resumen

FRETES DE AQUINO, Sonia Lorena; VAZQUEZ MESA, Marta  y  LUGO RODRIGUEZ, Gladys Beatriz. Evaluation comparative between dissolution profiles of tablets 25mg Lamotrigine similar and innovative drug, traded in Paraguay. Mem. Inst. Investig. Cienc. Salud [online]. 2016, vol.14, n.2, pp.53-60. ISSN 1812-9528.  https://doi.org/10.18004/Mem.iics/1812-9528/2016.014(02)53-060.

Epilepsy is the most common neurologic disease in the world, this situation boosts the development of new anticonvulsant drugs (AEDs) as lamotrigine (LMT) having, the latter, a high economic cost for the population with seizures. The aim of the study was to compare the dissolution profiles of LMT tablets of 25 mg (Test) marketed in Paraguay and the Reference or innovator (Lamictal®). LMT 25mg tablets were chosen with the current health register sold in Paraguay and performing the quality controls according to general criteria of the official pharmacopoeia. Subsequently, the kinetics of dissolution of the Test and Reference products were determined in the three recommended dissolution media (pH 1,2 ; 4,5 and 6,8). The dissolution profiles of LMT products evaluated presented similar behavior at the three different pHs, releasing more than 85% within 15 minutes in the three dissolution media. No comparison with the f1 and f2 test was necessary. The kinetics of dissolution of the tablets of LMT 25 mg analyzed showed a similar in vitro behavior between the formulations. These results constitute only a guide for the implementation of bioequivalence studies between the Test and the Reference assayed in vitro. These tests carried out with LMT could emerge as an initial step in order to study the behavior of dissolution profiles of the Test product and the corresponding references in the Paraguayan market.

Palabras clave : Epilepsy; lamotrigine; in vitro dissolution tests.

        · resumen en Español     · texto en Español     · Español ( pdf )

 

Creative Commons License Todo el contenido de esta revista, excepto dónde está identificado, está bajo una Licencia Creative Commons