Improved tableting behavior of paracetamol in the presence of polyvinylpyrrolidone additive: Effect of mixing conditions

Monoclinic paracetamol (PA) is notorious as a poorly compactible model drug. Polyvinylpyrrolidone (PVP) is a polymer that can act as an effective binder to improve the mechanical properties of PA. It is surprising however that the role of mixing conditions on the physicochemical and mechanical properties of PA–PVP mixtures has not been reported previously. The results of this work showed that PA–PVP mixtures containing 5% (w/w) PVP prepared using high energy mixing conditions had considerably smaller particle size distributions and higher cohesivities than mixtures prepared using low energy mixing conditions. Solid-state analysis did not detect any change in the monoclinic crystalline form of PA after mixing with PVP. The following rank order of tabletability for PA–PVP mixtures was obtained according to the mixing condition: low shear ∼ medium shear < dry high shear < wet high shear < high-speed homogenization. A higher level of hydrogen bonding was detected in the mixtures prepared via high energy mixing conditions than in those prepared using low energy mixing conditions. Mixing is therefore a critical process that needs to be optimized during the preparation of interactive mixtures for tableting.



The effects of mixing conditions on the micrometric and mechanical properties of PA–PVP mixture should not be ignored.In contrast to low energy mixing conditions, high energy mixing conditions promoted hydrogen bonding between PA and PVP with consequent improvements in the mechanical properties of the resultant mixtures. High energy mixing conditions were therefore successfully applied to produce PA with improved tensile strength in the presence of 5% (w/w) PVP additive. This method should have general applicability to many poorly compactible drug entities. Cooperative research and development between mixing equipment providers and pharmaceutical manufacturers is required in the future to optimize the quality of interactive mixtures for tableting. Future studies should also concentrate on the application ofvarious mixing methods to improve the functional properties of awide range of drugs including chemical drugs and Chinese drugsand herbal extracts that are prepared using direct compression.


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Photo of the crystalline structure of paracetamol with new additive
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