2026-04-13T01:14:22Zhttps://recercat.cat/oai/request

oai:recercat.cat:2445/2219102025-12-05T14:12:34Zcom_2072_1057col_2072_478815col_2072_478916col_2072_478917

00925njm 22002777a 4500 dc Canadell Heredia, Ricard author Rouaz El Hajoui, Khadija author Franco-Piedrahita, Natalia author Pérez Lozano, Pilar author Suñé Pou, Marc author Suñé i Negre, Josep M. (Josep Maria) author García Montoya, Encarna author 2025-06-30T12:22:32Z 2025-06-30T12:22:32Z 2025-05-08 2025-06-30T12:22:32Z Background/Objectives:</strong><span style="color:rgb( 34 , 34 , 34 )"> Carbamazepine is widely used as a first-line treatment for pediatric patients with benign epilepsy. However, most commercial formulations have doses of 100 mg or higher, limiting their suitability for pediatric use. The aim of this study was to develop mini orally disintegrating tablets (ODTs) containing 50 mg of carbamazepine, utilizing direct compression technology, specifically tailored to meet the unique needs of pediatric patients. </span><strong style="color:rgb( 34 , 34 , 34 )">Methods:</strong><span style="color:rgb( 34 , 34 , 34 )"> The development was carried out following a Quality by Design (QbD) approach, beginning with preformulation studies using the SeDeM expert system. Various co-processed excipients (PROSOLV® ODT and PARTECK® ODT) and non-co-processed excipients (L-HPC LH11 and L-HPC NBD-022) were evaluated. Additionally, modifications to the radius parameter of the SeDeM expert system were investigated to improve formulation design. </span><strong style="color:rgb( 34 , 34 , 34 )">Results:</strong><span style="color:rgb( 34 , 34 , 34 )"> Optimized Formulations 13 and 14 achieved disintegration times below 1 min, hardness values between 25 and 60 N, and friability under 1%, fulfilling the predefined Critical Quality Attributes (CQAs). Tablets were successfully produced with a diameter of 5 mm and a weight below 100 mg. Moreover, reducing the SeDeM incidence radius from 5.0 to values between 4.0 and 3.5 proved viable, enabling the inclusion of excipients previously considered unsuitable and broadening formulation options without compromising quality. </span><strong style="color:rgb( 34 , 34 , 34 )">Conclusions:</strong><span style="color:rgb( 34 , 34 , 34 )"> This study demonstrates the feasibility of producing small, fast-disintegrating, and mechanically robust 50 mg carbamazepine ODTs tailored for pediatric patients. It also validates the adjustment of SeDeM parameters as an effective strategy to expand excipient selection and enhance formulation flexibility in pediatric drug development. Farmacologia pediàtrica Epilèpsia en els infants Pediatric pharmacology Epilepsy in children Preformulation Study of Carbamazepine Orally Disintegrating Tablets for Pediatric Patients Using Direct Compression and the SeDeM Diagram Tool: A Quality by Design Approach.