The Effect of Microcrystalline Cellulose-CaHPO<sub>4</sub> Mixtures in Different Volume Ratios on the Compaction and Structural-Mechanical Properties of Tablets

Using microcrystalline cellulose (MCC) with plastic behaviour and calcium phosphate anhydrous (CaHPO<sub>4</sub>) with brittle behaviour under compaction is very popular in the pharmaceutical industry for achieving desirable structural-mechanical properties of tablet formulations. Thus,...

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Main Authors: Valentyn Mohylyuk (Author), Artūrs Paulausks (Author), Oskars Radzins (Author), Liga Lauberte (Author)
Format: Book
Published: MDPI AG, 2024-03-01T00:00:00Z.
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Summary:Using microcrystalline cellulose (MCC) with plastic behaviour and calcium phosphate anhydrous (CaHPO<sub>4</sub>) with brittle behaviour under compaction is very popular in the pharmaceutical industry for achieving desirable structural-mechanical properties of tablet formulations. Thus, mixtures of specific grades of MCC and CaHPO<sub>4</sub> were tested in volume proportions of 100-0, 75-25, 50-50, 25-75, and 0-100 at a constant weight-by-weight concentration of sodium stearyl fumarate lubricant, utilizing a state-of-the-art benchtop compaction simulator (STYL'One Nano). Tablet formulations were prepared at 100, 150, 250, 350, 450, and 500 MPa, and characterized by tabletability profile, ejection force profile, proportion-tensile strength relationship, proportion-porosity relationship, pressure-displacement, and elastic recovery profiles, as well as by in-/out-of-die Heckel plots and yield pressures. Interestingly, the 25-75 formulation demonstrated a two-stage out-of-die Heckel plot and was additionally investigated with X-ray micro-computed tomography (µCT). By post-processing the µCT data, the degree of brittle CaHPO<sub>4</sub> particles falling apart, along with the increasing compression pressure, was quantified by means of the surface area to volume (S/V) ratio. For the 25-75 formulation, the first stage (up to 150 MPa) and second stage (above the 150 MPa) of the out-of-die Heckel plot could be attributed to predominant MCC and CaHPO<sub>4</sub> deformation, respectively.
Item Description:10.3390/pharmaceutics16030362
1999-4923