Development of spray freezer for production of freeze granulations


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Authors

  • DARSHAN M B Assistant Research Engineer, All India Coordinated Research Project on Post Harvest Technology, University of Agricultural Sciences, GKVK, Bengaluru, Karnataka 560 065
  • ABHIJIT KAR Senior Scientist, Division of Food Science and Post Harvest Technology, Indian Agricultural Research Institute, Pusa Campus, New Delhi
  • DEBABANDYA MOHAPATRA Senior Scientist, Agro-Produce Processing Division, Central Institute of Agricultural Engineering, Bhopal, Madhya Pradesh 462 038

https://doi.org/10.56093/ijas.v85i12.54230

Keywords:

Atomization, Encapsulation, Freeze granulation, Microspheres, Spray freezer

Abstract

Spray freezer is an essential component of spray freeze drying (SFD) technique to produce microspheres during encapsulation. In this study, a lab scale spray freezer unit was developed to produce freeze granulations, which could be used for encapsulation of bio-pigments and other useful bio-active compounds. The components of spray freezer were spray nozzle, freezing chamber, magnetic stirrer, feed reservoir, homogenizer, peristaltic pump, air compressor, liquid nitrogen tank and hose fittings. The maltodextrin ‘MD’ solution (10%) was atomized into liquid nitrogen using spray freezer to produce freeze granulations and these granulations were freeze dried to obtain spray freeze dried maltodextrin (SFDMD) particles. The produced SFDMD particles were characterized and compared with classical freeze dried maltodextrin (FDMD) particles to evaluate the performance of spray freezing unit. The drying period for producing maltodextrin granules in SFD and freeze drying (FD) technique was between 12 to 24 and 36 to 48 hr, and their % moisture absorption was found to be 2.37 and 2.17%, respectively. The SFD technique produced microspheres of maltodextrin with particle size ranging from 2 to 60 μm, whereas FD technique produced irregular macro-size flakes. The morphological studies revealed that SFD microstructure particles had smooth surface and freeze dried particles had rough surface; however, porous appearance was observed in both samples. There were no significant differences in colour values; however, the flow properties of SFDMD particles were relatively better than FDMD particles. The developed spray freezer can be used for production of freeze granulations during SFD technique.

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References

Alanazi F K, El-Bagory I M, Alsarra I A, Bayomi M A and Abdel-kawy M A. 2008. Saudi-corn starch as a tablet excipient compared with imported starch. Saudi Pharmaceutical Journal 16(2): 112–21.

Banker G S and Anderson N R. 1986. Tablets. (In) The Theory and Practice of Industrial Pharmacy, pp 293–345, 3rd Edn.Lachman L, Liberman H A and Kanig J L (Eds). Lea and Febiger, Philadelphia.

Burke P A, Klumb L A, Herberger J D, Nguyen X C, Harrell R A and Zordich M. 2004. Poly (Lactide-Co-Glycolide) microsphere formulations of Darbepoetinalfa, spray drying is an alternative to encapsulation by spray-freeze drying. Pharmaceutical Research 21(3): 500–6. DOI: https://doi.org/10.1023/B:PHAM.0000019305.79599.a5

Cain J. 2002. An alternative technique for determining ANSI/ CEMA Standard 550 flowability ratings for granular materials. Powder Handling and Processing 14: 218–20.

Costantino H R, Firouzabadian L, Hogeland K, Wu C, Beganski C, Carrasquillo K G, Co‘rdova M, Griebenow K, Zale S E and Tracy M A. 2000. Protein spray-freeze drying: Effect of atomization conditions on particle size and stability. Pharmceutical Research 17: 1 374–83. DOI: https://doi.org/10.1023/A:1007570030368

Costantino H R, Firouzabadian L, Hogeland K, Wu, Carrasquillo K G, Griebenow K, Zale S E and Tracy M A. 2002. Protein spray freeze drying: Effect of formulation variables on particle size and stability. Journal of Pharmaceutical Sciences 91: 388– 95. DOI: https://doi.org/10.1002/jps.10059

Djuris J, Medarevic D, Krstic M, Vasiljevic I, MasicI and Ibric S. 2012. Design space approach in optimization of fluid bed granulation and tablets compression process. Scientific World Journal 2012: 1–10. DOI: https://doi.org/10.1100/2012/185085

Ersus S and Yurdagel U. 2007. Microencapsulation of anthocyanin pigments of black carrot (Daucus carota L.) by spray drier. Journal of Food Engineering 80: 805–12. DOI: https://doi.org/10.1016/j.jfoodeng.2006.07.009

Fiese E F and Hagen T A. 1986.Preformulation.The Theory and Practice of Industrial Pharmacy, pp 171–94, 3rd Edn. Lachman L, Liberman H A and Kanig J L (Eds). Lea and Febiger, Philadelphia.

Maa Y F and Prestrelski S J. 2000. Biopharmaceutical powders, particle formation and formulation considerations. Current Pharmaceutical Biotechnology 1(3): 283–302. DOI: https://doi.org/10.2174/1389201003378898

Maa Y F, Nguyen P A, Sweeney T, Shire S J and Hsu C C. 1999. Protein inhalation powders spray drying vs spray freeze drying. Pharmaceutical Research 16(2): 249–54. DOI: https://doi.org/10.1023/A:1018828425184

Malamatris S, Karidas K and Goidas P. 1994. Effect of particle size and adsorbed moisture on the compression behavior of some hydroxypropyl methylcellulose (HPMC) polymers. International journal of pharmaceutics 103: 205–15. DOI: https://doi.org/10.1016/0378-5173(94)90170-8

Masters K. 1991.Spray Drying Handbook, 4thEdn. Longman Scientific & Technical, Harlow, UK.

Maury M, Murphy K, Kumar S, Shi L and Lee G. 2005. Effects of process variables on the powder yield of spray dried trehalose on a laboratory spray-dryer. European Journal of Pharmaceutics and Biopharmaceutic 59: 565–73. DOI: https://doi.org/10.1016/j.ejpb.2004.10.002

Musa H, Gambo A and Bhatia B G. 2011.Studies on some physicochemical properties of native and modified starches from Digitaria iburua and Zea mays. International Journal of Pharmacy and Pharmaceutical Sciences 3(1): 28–31.

Nyberg B, Carlstrom E and Carlsson R. 1993.Granulation of ceramic powders for pressing by spray-freezing and freezedrying. EuroCeramicsII,Deutsche Keramische Gesellschaft 1: 447–51.

Patel S S, Patel M S and Patel N M. 2008. Flowability and packability testing of directly compressible expedients. Indian Pharmacist 7(71): 9–65.

Phadke D S and Anderson N R. 1990. Effect of cross povidone on the wet granulation aspects of acetaminophen.Drug Development and Industrial Pharmacy 16: 983–94. DOI: https://doi.org/10.3109/03639049009114923

Schiffter H. 2007. Spray freeze drying in the manufacture of pharmaceuticals. European Pharmaceutical Review 12: 67– 71.

Staniforth J N. 2007. Powder flow.Pharmaceutics- the Science of Dosage form Design, pp 168–79, 3rd Edn. Aulton M E (Ed). Churchill Livingstone, London.

Stapley A and Rielly C. 2007. Advances in unconventional freeze drying technology.Chemical Engineer 790: 33–5.

Webb S D, Golledge S T, Cleland J L, Carpenter J F and Randolph T W. 2002.Surface adsorption of recombinant human interferon-g in lyophilized and spray-lyophilized formulations. Journal of Pharmaceutical Sciences 91: 1 474–87. DOI: https://doi.org/10.1002/jps.10135

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2015-12-11

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2015-12-11

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How to Cite

B, D. M., KAR, A., & MOHAPATRA, D. (2015). Development of spray freezer for production of freeze granulations. The Indian Journal of Agricultural Sciences, 85(12), 1523-1528. https://doi.org/10.56093/ijas.v85i12.54230
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