Effect of processing conditions and excipients on dehydration kinetics of sodium naproxen hydrate in formulation.

Int J Pharm

Upsher Smith Laboratories LLC., 6701 Evenstad Dr., Maple Grove, MN 55369, United States.

Published: February 2019

AI Article Synopsis

  • The manufacturing process of oral dosage forms can change the physical state of active pharmaceutical ingredients (APIs), exemplified by naproxen sodium dihydrate (DH) transitioning to anhydrous form during granulation and drying.
  • Different processing conditions (ambient air, inert gas flow, low pressure, and high pressure) were tested to understand the dehydration kinetics of DH, revealing that dehydration occurred fastest with inert gas flow and slowest in closed environments.
  • The study also highlighted how excipients like polyvinyl pyrrolidone (PVP) and microcrystalline cellulose (MCC) influenced the dehydration rates, with PVP slowing down and MCC facilitating the transition, showcasing the importance of excipient selection in formulating APIs.

Article Abstract

The manufacture of oral dosage form may induce changes in the physical form of an active pharmaceutical ingredient. One such example includes formation of hydrate during granulation followed by the reverse transition to the anhydrous form during drying. We used naproxen sodium dihydrate (DH) as the model compound and studied its dehydration at elevated temperature under different processing conditions, (i) in ambient air, (ii) in flow of inert gas (iii) under low pressure environment, and (iv) under 'high' pressure in closed environments. In situ variable temperature X-ray diffraction was used to monitor kinetics of phase transformation under these processing conditions. The DH dehydration was fastest under the flow of inert gas and slowest in closed environment. Polyvinyl pyrrolidone (PVP) and microcrystalline cellulose (MCC), commonly used hygroscopic solids, were used as the model excipients to monitor influence of excipients in modulating DH dehydration behavior under different processing conditions. Both the excipients altered the kinetics as well as the extent of DH dehydration, with PVP delaying and MCC facilitating the transformation under all processing conditions studied. The results indicate that the physical form of API, such as hydrate or anhydrous in the present case, in the formulation may be modulated by rational excipient selection.

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Source
http://dx.doi.org/10.1016/j.ijpharm.2018.12.058DOI Listing

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