Continuous-flow production of a pharmaceutical nanoemulsion by high-amplitude ultrasound: Process scale-up

a b s t r a c t High-pressure homogenization (HPH, including microfluidization) and high-amplitude ultrasonic processing are currently the leading two methods used to produce nanoemulsions of superior qual- ity. Despite suffering from multiple important drawbacks, HPH is currently the technology of choice for the industrial manufacture of pharmaceutical nanoemulsions. The ultrasonic nanoemulsification tech- nology is free from most of these drawbacks and frequently used in laboratory studies. The challenge for the ultrasonic method, however, has been bridging the gap between laboratory research and its indus- trial implementation. Due to limitations of conventional ultrasonic technology, scaling up has not been possible without a significant reduction in ultrasonic amplitudes, which compromises product quality. This limitation has been overcome by Barbell Horn Ultrasonic Technology (BHUT), which permits con- structing bench and industrial-scale processors capable of operating at high ultrasonic amplitudes. In the present study, a high-quality MF59®-analog pharmaceutical nanoemulsion has been successfully manu- factured using laboratory, bench and industrial-scale high-amplitude ultrasonic processors. The overall laboratory-to-industrial scale-up factor achieved by using BHUT was approximately 55. The ultrasonic amplitude and the resulting product quality were maintained identical at all three scales. To our knowl- edge, this work is the first reported instance of a successful and systematic industrial scale-up of any high-amplitude ultrasonic process.

[1]  S. Tamilvanan Formulation of multifunctional oil-in-water nanosized emulsions for active and passive targeting of drugs to otherwise inaccessible internal organs of the human body. , 2009, International journal of pharmaceutics.

[2]  C. Gourdon,et al.  Emulsification by ultrasound: drop size distribution and stability. , 1999, Ultrasonics sonochemistry.

[3]  Seid Mahdi Jafari,et al.  Production of sub-micron emulsions by ultrasound and microfluidization techniques , 2007 .

[4]  D. Novicki,et al.  Safety of MF59 adjuvant. , 2008, Vaccine.

[5]  M. Hora,et al.  The Adjuvant MF59: A 10-Year Perspective Gary Ott, Ramachandran Radhakrishnan, , 2000 .

[6]  Parag R. Gogate,et al.  A review of applications of cavitation in biochemical engineering/biotechnology , 2009 .

[7]  G. Ott,et al.  Enhancement of humoral response against human influenza vaccine with the simple submicron oil/water emulsion adjuvant MF59. , 1995, Vaccine.

[8]  M. Ashokkumar,et al.  The use of ultrasonics for nanoemulsion preparation , 2008 .

[9]  M. Ashokkumar,et al.  The use of ultrasonics for nanoemulsion preparation , 2008 .

[10]  Y. Maa,et al.  Performance of sonication and microfluidization for liquid-liquid emulsification. , 1999, Pharmaceutical development and technology.

[11]  Alexey S. Peshkovsky,et al.  Acoustic cavitation theory and equipment design principles for industrial applications of high-intensity ultrasound , 2010 .

[12]  Kuniaki Tanaka,et al.  Formation and Charaterization of Submicrometer Oil-in-Water (O/W) Emulsions, Using High-Energy Emulsification , 2006 .

[13]  S. Bystryak,et al.  Scalable high-power ultrasonic technology for the production of translucent nanoemulsions , 2013 .

[14]  R. Rappuoli,et al.  New adjuvants for human vaccines. , 2010, Current opinion in immunology.

[15]  Parag R. Gogate,et al.  Design aspects of sonochemical reactors: Techniques for understanding cavitational activity distribution and effect of operating parameters , 2009 .

[16]  M. Ashokkumar,et al.  Minimising oil droplet size using ultrasonic emulsification. , 2009, Ultrasonics sonochemistry.

[17]  R. Coler,et al.  Physicochemical characterization and biological activity of synthetic TLR4 agonist formulations. , 2010, Colloids and surfaces. B, Biointerfaces.

[18]  T. Tadros,et al.  Formation and stability of nano-emulsions. , 2004, Advances in colloid and interface science.

[19]  A. del Pozo,et al.  Use of ultrasound to prepare lipid emulsions of lorazepam for intravenous injection. , 2001, International journal of pharmaceutics.

[20]  Sergei L Peshkovsky,et al.  Matching a transducer to water at cavitation: acoustic horn design principles. , 2007, Ultrasonics sonochemistry.

[21]  S. Davis,et al.  The production of parenteral feeding emulsions by microfluidizer , 1988 .

[22]  A. Peshkovsky,et al.  Shock-wave model of acoustic cavitation. , 2008, Ultrasonics sonochemistry.

[23]  D. Driscoll,et al.  Lipid Injectable Emulsions: Pharmacopeial and Safety Issues , 2006, Pharmaceutical Research.

[24]  Keiche Meleson,et al.  The formation and stability of nanoemulsions , 2008 .

[25]  Parag R Gogate,et al.  Mapping the efficacy of new designs for large scale sonochemical reactors. , 2007, Ultrasonics sonochemistry.

[26]  A. Wilhelm,et al.  Ultrasound Emulsification—An Overview , 2002 .

[27]  T. Tsai MF59 adjuvanted seasonal and pandemic influenza vaccines. , 2011, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan.

[28]  K. Eberth,et al.  Ultrasonic preparation of pharmaceutical emulsions. Droplet size measurements by quasi-elastic light scattering , 1984 .

[29]  Rainer H Müller,et al.  Drug nanocrystals of poorly soluble drugs produced by high pressure homogenisation. , 2006, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[30]  S. Bertholet,et al.  The Importance of Adjuvant Formulation in the Development of a Tuberculosis Vaccine , 2012, The Journal of Immunology.

[31]  Aniruddha B. Pandit,et al.  Sonochemical reactors: important design and scale up considerations with a special emphasis on heterogeneous systems , 2011 .