4.7 Article

Negative porosity issue in the Heckel analysis: A possible solution

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DOI: 10.1016/j.ijpharm.2022.122205

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Heckel analysis; Modified Heckel equation; Negative porosity; Pycnometric tablet density; Pycnometric powder density; Relative density; True density

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This paper proposes a new approach to using pycnometric tablet density in the relative density calculations of Heckel analysis, which solves the problem of negative porosity in high-pressure regions. The new approach enables the evaluation of macroscopic compaction performance and saves time and costs.
A parameterization of compaction simulator generated dynamic compression profile with a few grams of powder provides important information about the material deformation and compact elasticity. The Heckel equation is by far the most popular choice among pharmaceutical scientists for such parametrization. A general approach of Heckel analysis uses pycnometric powder density (pP0) for relative density calculation. However, as 'in-die' tablet bulk density at applied compression pressure (pBP) becomes greater than or equal to the measured pP0, the general approach typically poses a negative porosity challenge at high compression pressure regions. It is only theoretically possible to have a tablet with zero or negative porosity. Negative porosity may be detected during 'in-die' compression analysis, but it will not exist after ejection of the tablet in practical aspect. Thus, the present work proposes a new approach to using pycnometric tablet density (pPP) in the relative density calculations of Heckel analysis. This pPP may be a better representation of actual tablet particle volume, as it is composed of non -accessible intra-particulate pores, which are broken under applied compression pressure. A new approach showed its immunity for Heckel high-pressure negative porosity. It enables the utilization of the compression and decompression phases of dynamic compression profiles to evaluate macroscopic compaction performance. The proposed approach was validated with a reported modified Heckel approach. The Heckel parameters computed with both methodologies for microcrystalline cellulose and lactose were not statistically different. However, a modified Heckel approach was unable to compute Heckel parameters of poorly compacting starch unlike the new approach. A modified Heckel approach became invalid during starch compaction at low compression pressures (below 400 MPa), where starch was forming weaker but still intact tablets. Certainly, a complete Heckel profiling with a new approach could save time and costs in an early development stage for designing and screening scientifically based lead prototype formulations.

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