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Eur J Pharm Biopharm ; 201: 114370, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38880402

ABSTRACT

The difficulty in swallowing is a frequent problem when oral solid dosage forms (conventional tablets or capsules) are administered to paediatric population or patients with dysphagia. An interesting alternative to overcome these problems are non-conventional formulations like chewable gels, commonly known as 'gummies'. Therefore, this work addresses the design, development and characterization of gummies using gelatine and pectin, for the vehiculization of the antiarrhythmic amiodarone (AMIO). Applying a Design of Experiments (DoE) approach, four gelatine (GG1-GG4) and eight pectin formulations (PG1-PG8) were developed. Considering the obtained results for responses during DoE evaluation (i.e., volume, syneresis, hardness, and gumminess), GG3 and PG8 were selected for complete characterization. Water activity, pH, drug content, texture parameters (adhesiveness, springiness, cohesiveness, and fracturability), disintegration time, in vitro dissolution, and microbiological features were evaluated. The obtained results were within the expected values for this type of formulation. The dissolution profiles showed a 94 % - 99 % of the AMIO content released for GG3 and PG8, respectively, so they could be considered suitable as immediate release dosage forms. In conclusion, the chewable gels were successfully developed and characterised, suggesting a potential means to accomplish a final prototype for the improvement of congenital cardiopathies treatment.


Subject(s)
Amiodarone , Anti-Arrhythmia Agents , Gels , Heart Defects, Congenital , Pectins , Amiodarone/administration & dosage , Amiodarone/chemistry , Humans , Pectins/chemistry , Anti-Arrhythmia Agents/administration & dosage , Anti-Arrhythmia Agents/chemistry , Heart Defects, Congenital/drug therapy , Gelatin/chemistry , Animals , Child , Administration, Oral , Drug Liberation , Drug Compounding/methods , Solubility , Chemistry, Pharmaceutical/methods
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