# Multivariate Data Analysis to Assess Process Evolution and Systematic Root Causes Investigation in Tablet Manufacturing at an Industrial Scale—A Case Study Focused on Improving Tablet Hardness

**Authors:** Rita Mathe, Tibor Casian, Ioan Tomuta

PMC · DOI: 10.3390/pharmaceutics17020213 · Pharmaceutics · 2025-02-07

## TL;DR

This study uses multivariate analysis to improve tablet hardness in industrial manufacturing by identifying key process variables and optimizing them for consistent quality.

## Contribution

The study introduces multivariate methods to analyze real industrial data and identify root causes of tablet hardness variability.

## Key findings

- Four key variables affecting tablet hardness were identified: API particle size, nozzle type, wet discharge, and drying intensity.
- Optimized process conditions increased tablet hardness by 15–20% and reduced batch variability.
- The new control strategy achieved decent sigma quality levels (2.5) for production batches.

## Abstract

Background/Objectives: Only a few studies performed at industrial scale in non-simulated conditions have investigated the effect of input variability from the product’s lifecycle on product quality. The purpose of this work was to identify the root causes for the low and variable hardness of core tablets prepared using high-shear wet granulation through batch statistical modeling and to verify the short- and long-term effectiveness of the improvement actions. Methods: The novelty of this study is the use of multivariate methods for the complex assessment of a wide data set belonging to two proportional composition strengths, manufactured at an industrial scale, with different tablet shapes and sizes, with the aim of identifying inter-related active ingredient and process variables with the highest impact on hardness value and for defining optimal processing conditions leading to a robust product. Results: Four main variables affecting the output variable were identified: API particle size, nozzle type used for granulation, wet discharge, and drying intensity. These were included in an updated control strategy (3 out of 4 variables having to be within the desired ranges: API d0.5 < 45 microns; granulation nozzle that ensures liquid dispersion into droplets; gentle wet discharge and drying processes). In the case of the product studied, the newly defined process conditions could even accommodate d0.5 up to 70 microns and still ensure adequate core tablet hardness (at least 30% above the lower specification limit) for the successive film-coating step. Conclusions: Besides the beneficial impact of reducing the risk for out-of-specification hardness results, this study also offered the benefit of cost avoidance and yield improvement. The improvement was confirmed through the significant average hardness increase (15–20%) and between-batch variability decrease, leading to decent sigma quality levels (2.5) for the control phase batches.

## Full-text entities

- **Genes:** TNP2 (transition protein 2) [NCBI Gene 7142] {aka TP2}, TNP1 (transition protein 1) [NCBI Gene 7141] {aka TP1}
- **Diseases:** Waste reduction (MESH:D019282), injury to people or property (MESH:C000719191)
- **Chemicals:** microcrystalline cellulose (MESH:C109691), silicon dioxide (MESH:D012822), magnesium stearate (MESH:C031183), water (MESH:D014867), starch (MESH:D013213), sodium lauryl sulfate (MESH:D012967), sodium starch glycolate (MESH:C048390)
- **Mutations:** Q2, R2X, A to F
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11858851/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC11858851/full.md

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Source: https://tomesphere.com/paper/PMC11858851