Formulation-dependent stability mechanisms affecting dissolution performance of directly compressed griseofulvin tablets

Maclean, Natalie and Khadra, Ibrahim and Mann, James and Abbott, Alexander and Mead, Heather and Markl, Daniel (2023) Formulation-dependent stability mechanisms affecting dissolution performance of directly compressed griseofulvin tablets. International Journal of Pharmaceutics, 631. 122473. ISSN 1873-3476 (https://doi.org/10.1016/j.ijpharm.2022.122473)

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Abstract

During drug product development, stability studies are used to ensure that the safety and efficacy of a product are not affected during storage. Any change in the dissolution performance of a product must be investigated, as this may indicate a change in the bioavailability. In this study, three different griseofulvin formulations were prepared containing microcrystalline cellulose (MCC) with either mannitol, lactose monohydrate, or dibasic calcium phosphate anhydrous (DCPA). The tensile strength, porosity, contact angle, disintegration time, and dissolution rate were measured after storage under five different accelerated temperature and humidity conditions for 1, 2, and 4 weeks. The dissolution rate was found to decrease after storage for all three batches, with the change in dissolution rate strongly correlating with the storage humidity. The changes in physical properties of each formulation were found to relate to either the premature swelling (MCC/DCPA, MCC/lactose) or dissolution (MCC/mannitol) of particles during storage. These results are also discussed with consideration of the performance- and stability-controlling mechanisms of placebo tablets of the same formulations [1, 2].

ORCID iDs

Maclean, Natalie ORCID logoORCID: https://orcid.org/0000-0003-0768-1673, Khadra, Ibrahim ORCID logoORCID: https://orcid.org/0000-0002-9846-1520, Mann, James, Abbott, Alexander, Mead, Heather and Markl, Daniel ORCID logoORCID: https://orcid.org/0000-0003-0411-733X;
CORE (COnnecting REpositories)