Influence of basket mesh size on the hydrodynamics in the USP rotating basket dissolution testing Apparatus 1
[Display omitted] •Velocity profiles with baskets of different mesh sizes were obtained using PIV.•Small deviations from perfect symmetry result in asymmetries in velocity profiles.•All velocities in USP Apparatus 1 increase using baskets with larger mesh openings.•Baskets with larger mesh openings...
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Veröffentlicht in: | International journal of pharmaceutics 2021-09, Vol.607, p.120976-120976, Article 120976 |
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Sprache: | eng |
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•Velocity profiles with baskets of different mesh sizes were obtained using PIV.•Small deviations from perfect symmetry result in asymmetries in velocity profiles.•All velocities in USP Apparatus 1 increase using baskets with larger mesh openings.•Baskets with larger mesh openings promote stronger flow through the basket.•The selection of the basket mesh must be considered during drug product development.
The USP Apparatus 1 (rotating basket), typically used to assess drug product reproducibility and evaluate oral solid dosage forms performance, consists of a cylindrical glass vessel with a hemispherical bottom and a wire basket rotating at constant speed. Baskets with different wire openings can be used in alternative to the standard mesh opening (40-mesh) in order to discriminate between drug formulations during early stage of drug product development. Any changes introduced by different basket geometries can potentially and significantly impact the system hydrodynamics and cause variability of results, thus affecting product quality. In this work, Particle Image Velocimetry (PIV) was used to experimentally quantify the velocity distribution in the USP rotating basket Apparatus 1 using baskets of different mesh sizes (10-, 20-, and 40-mesh size) under the typical operating conditions described in dissolution testing procedures. Similar flow patterns were observed in all cases. However, the radial and axial velocities in the USP Apparatus 1 generally increased with increasingly larger openings of the basket mesh. Increasing the basket agitation speed also resulted in an overall increase in the velocities, especially below in the innermost core region below the basket, where drug fragments typically reside. More importantly, the flow entering and leaving the baskets was quantified from the velocity profiles in the immediate vicinity of the baskets. It was found that the flow increased significantly with increasingly larger mesh openings, which can, in turn, promote faster dissolution of the oral solid dosage forms, thus affecting drug dissolution profiles. Hence, the selection of the basket mesh size must be carefully considered during drug product development. |
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ISSN: | 0378-5173 1873-3476 |
DOI: | 10.1016/j.ijpharm.2021.120976 |