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Controlled Microwave Processing Applied to the Pharmaceutical Formulation of Ibuprofen

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Abstract

The first successful development of controlled microwave processing for pharmaceutical formulations is presented and illustrated with a model drug (ibuprofen) and two excipients (stearic acid and polyvinylpyrrolidone). The necessary fine temperature control for formulation with microwave energy has been achieved using a uniquely modified microwave oven with direct temperature measurement and pulse-width modulation power control. In addition to comparing microwave and conventional heating, the effect of the presence of liquid (water) in aiding the mixing of the drug and excipient during formulation was also investigated. Analysis of the prepared formulations using differential scanning calorimetry and dissolution studies suggest that microwave and conventional heating produce similar products when applied to mixtures of ibuprofen and stearic acid. However, the differences were observed for the ibuprofen and polyvinylpyrrolidone formulation in terms of the dissolution kinetics. In all cases, the presence of water did not appear to influence the formulation to any appreciable degree. The application of controllable microwave heating is noteworthy as fine temperature control opens up opportunities for thermally sensitive materials for which microwave methods have not been feasible prior to this work.

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REFERENCES

  1. Metaxas AC, Meredith RJ. Industrial microwave heating. 2nd ed. London: P. Peregrinus Ltd.; 1988.

    Book  Google Scholar 

  2. National Research Council. Microwave processing of materials. Washington DC, USA: National Academy Press; 1994.

    Google Scholar 

  3. NMAB-473 Publication, Committee on microwave processing of materials: an emerging industrial technology. Microwave processing of materials. Washington DC, USA: National Academy Press; 1994.

    Google Scholar 

  4. Kingston HM, Haswell SJ. Microwave enhanced chemistry. Washington, USA: American Chemical Society; 1997.

    Google Scholar 

  5. Chee SN, Johansen AL, Gu L, Karlsen J, Heng PWS. Microwave drying of granules containing a moisture sensitive drug: a promising alternative to fluid bed and hot air oven drying. Chem Pharm Bull. 2005;53:770–5.

    Article  PubMed  CAS  Google Scholar 

  6. Loh ZH, Liew CV, Lee CC, Heng PWS. Microwave-assisted drying of pharmaceutical granules and its impact on drug stability. Int J Pharm. 2008;359:53–62.

    Article  PubMed  CAS  Google Scholar 

  7. Moneghini M, Zingone G, De Zordi N. Influence of the microwave technology on the physical–chemical properties of solid dispersion with nimesulide. Powder Technol. 2009;195:259–63.

    Article  CAS  Google Scholar 

  8. Bergese P, Colombo I, Gervasoni D, Depero LE. Microwave generated nanocomposites for making insoluble drugs soluble. Mat Sci Eng C. 2003;23:791–5.

    Article  Google Scholar 

  9. Moneghini M, Bellich B, Baxa P, Princivalle F. Microwave generated solid dispersions containing ibuprofen. Int J Pharm. 2008;361:125–30.

    Article  PubMed  CAS  Google Scholar 

  10. Moneghini M, De Zordi N, Grassi M, Zingone G. Sustained release solid dispersions of ibuprofen prepared by microwave irradiation. J Drug Del Sci Tech. 2008;18:327–33.

    CAS  Google Scholar 

  11. Dwivedi SK, Sattari S, Jamali F, Mitchell AG. Ibuprofen racemate and enantiomers: phase diagram, solubility and thermodynamic studies. Int J Pharm. 1992;87:95–104.

    Article  Google Scholar 

  12. Lavasanifar A, Samuel J, Kwon GS. The effect of fatty acid substitution on the in vitro release of amphotericin B from micelles composed of poly(ethylene oxide)-block-poly(N-hexyl stearate-L-aspartamide). J Control Rel. 2002;79:165–72.

    Article  CAS  Google Scholar 

  13. Robson HJ, Craig DQM, Deutsch D. An investigation into the release of cefuroxime axetil from taste-masked stearic acid microspheres Part 2: the effects of buffer composition on drug release. Int J Pharm. 2000;195:137–45.

    Article  PubMed  CAS  Google Scholar 

  14. Waters LJ, Pavlakis E. In vitro controlled drug release from loaded microspheres—dose regulation through formulation. Can J Pharm Pharm Sci. 2007;10:464–72.

    CAS  Google Scholar 

  15. Feldstein MM, Shandryuk GA, Kuptsov SA, Platé NA. Coherence of thermal transitions in poly(N-vinyl pyrrolidone)-poly(ethylene glycol) compatible blends 1. Interrelations among the temperatures of melting, maximum cold crystallization rate and glass transition. Polymer. 2000;41:5327–38.

    Article  CAS  Google Scholar 

  16. Serratoni M, Newton M, Booth S, Clarke A. Controlled drug release from pellets containing water-insoluble drugs dissolved in a self-emulsifying system. Eur J Pharm Biopharm. 2007;65:94–8.

    Article  PubMed  CAS  Google Scholar 

  17. O'Hara T, Dunne A, Butler J, Devane J. A review of methods used to compare dissolution profile data. Pharm Sci Tech Today. 1998;1:214–23.

    Article  Google Scholar 

  18. Albertini B, Cavallari C, Passerini N, Voinovich D, González-Rodríguez ML, Magarotto L, et al. Characterization and taste-masking evaluation of acetaminophen granules: comparison between different preparation methods in a high-shear mixer. Eur J Pharm Sci. 2004;21:295–303.

    Article  PubMed  CAS  Google Scholar 

  19. Zhu Y, Shi J, Li Y, Chen H, Shen W, Dong X. Storage and release of ibuprofen drug molecules in hollow mesoporous silica spheres with modified pore surface. Micropor Mesopor Mater. 2005;85:75–81.

    Article  CAS  Google Scholar 

  20. Furlanetto S, Cirri M, Maestrelli F, Corti G, Mura P. Study of formulation variables influencing the drug release rate from matrix tablets by experimental design. Eur J Pharm Biopharm. 2006;62:77–84.

    Article  PubMed  CAS  Google Scholar 

  21. Dürig T, Fassihi AR. Identification of stabilising and destabilising effects of excipient-drug interactions in solid dosage form design. Int J Pharm. 1993;9:161–70.

    Article  Google Scholar 

  22. Tomassetti M, Catalani A, Rossi V, Vecchio S. Thermal analysis study of the interactions between acetaminophen and excipients in solid dosage forms and in some binary mixtures. J Pharm Biomed Analysis. 2005;37:949–55.

    Article  CAS  Google Scholar 

  23. Lerdkanchanaporn S, Dollimore D, Evans SJ. Phase diagram for the mixtures of ibuprofen and stearic acid. Thermochim Acta. 2001;367:1–8.

    Article  Google Scholar 

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ACKNOWLEDGEMENTS

The authors would like to thank the University of Huddersfield for funding S. Bedford and Dr. G. Midgley for useful discussions.

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Correspondence to Laura J. Waters.

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Waters, L.J., Bedford, S. & Parkes, G.M.B. Controlled Microwave Processing Applied to the Pharmaceutical Formulation of Ibuprofen. AAPS PharmSciTech 12, 1038–1043 (2011). https://doi.org/10.1208/s12249-011-9671-5

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