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ABSTRACT: Objectives
The aim of the study was to develop and characterize an optimal ODF formulation containing equivalent hydrocortisone at 0.5 mg/cm2 using the solvent-casting method. A stability-indicating assay for the simultaneous quantification of hydrocortisone and hydrocortisone 21-hemissucinate (HMS) was developed. ODFs were characterized by organoleptic properties and by testing for uniformity of mass, content, stability, thickness, and dissolution.Results
When optimized, ODF is thin, flexible, and transparent, making it suitable for production in hospital ph
SUBMITTER: Boisseillier C
PROVIDER: S-EPMC11768698 | biostudies-literature | 2025 Jan
REPOSITORIES: biostudies-literature