A Literature Review on Extrusion/Spheronisation-A Pelletization Technology


Year : 2025 | Volume : 16 | Issue : 01 | Page : 61-71
    By

    Nandlal B. Savaliya,

  • Chetan H.Borkhataria,

  • Chintankumar J. Tank,

  • Harshal A. Sadhariya,

  1. Research Scholar, Department of Pharmacy, Dr. Subhash University, Junagadh, Gujarat, India
  2. Assistant Professor, B.K. Mody Government Pharmacy College, Rajkot, Gujarat, India
  3. Professor, School of Pharmacy, Dr. Subhash University, Junagadh, Gujarat, India
  4. Trainee Officer, Formulation and Development, Troikaa Pharmaceuticals Ltd, Gujarat, India

Abstract

Extrusion-spheronization is a leading pelletization technology, widely favored for its economic and commercial viability. It is a cost-effective method suitable for large-scale production, making it the most efficient approach for oral drug delivery. This process provides multiple benefits, such as improved flow characteristics, lower friability, a narrow particle size range, easier coating, consistent packing, reduced likelihood of dose dumping, and more predictable gastric emptying. Pellets usually measure between 0.5 and 1.5 mm in size. The formation of these pellets involves several stages, including nucleation, coalescence, layering, and abrasion transfer. Additionally, processes like attrition, breakage, and fragmentation contribute to the size reduction of pellets. Pelletization techniques include agitation (balling), compaction (compression, extrusion-spheronization), layering (powder or solution/suspension), and globulation (spray drying and spray congealing). Among these, extrusion-spheronization is the most prominent due to its versatility and process efficiency. Extrusion-spheronization involves distinct steps: it comprises dry mixing, wet massing, extrusion, spheronization, and drying. Various formulation factors (moisture content, granulating fluid, excipients, drugs), process parameters (spheronization time, speed, temperature), and equipment variables (mixer, extruder, extrusion screen) influence pellet quality. Pellet characterization is crucial and includes particle size distribution (PSD), surface area, sphericity, friability, and dissolution. This technology not only ensures efficient drug delivery but also facilitates the production of robust, high-quality pellets for pharmaceutical applications. Extrusion/spheronization is the most promising pelletization technology because it is both economic and commercial. Due to its affordability for large-scale production, extrusion spheronization is currently the most efficient method for oral drug delivery. Numerous benefits are available, including improved flow characteristics, a less friable dosage form, a narrow particle size distribution, ease of coating, and uniform packing. Pellets usually range in size from 0.5 to 1.5 mm. The mechanism of pellet formation involves nucleation, coalescence, layering, and abrasion transfer. Mechanisms and techniques for pelletization include agitation (balling), compaction (compression, extrusion spheronization) layering (powder, solution/suspension), and globulation (spray drying, spray congealling) described in the next section of this literature. It outlines the procedures involved in extrusion spheronization (dry mixing, wet massing, extrusion, spheronization, and drying). It also discusses the variables, such as formulation, process (moisture content, granulating fluid, excipients, drugs) equipment parameters (spheronization time, spheronization speed, spheronization temperature), and equipment parameters. (Mixer, extruder, extrusion screen that affects pellet formation. The description of pellet characterization, including PSD, surface area, sphericity, friability, and dissolution is given at last.

Keywords: Pelletization, Spheronisation, Extrusion, Pelletization Technique, Characterization of pellets.

[This article belongs to Research and Reviews: A Journal of Pharmaceutical Science (rrjops)]

How to cite this article:
Nandlal B. Savaliya, Chetan H.Borkhataria, Chintankumar J. Tank, Harshal A. Sadhariya. A Literature Review on Extrusion/Spheronisation-A Pelletization Technology. Research and Reviews: A Journal of Pharmaceutical Science. 2025; 16(01):61-71.
How to cite this URL:
Nandlal B. Savaliya, Chetan H.Borkhataria, Chintankumar J. Tank, Harshal A. Sadhariya. A Literature Review on Extrusion/Spheronisation-A Pelletization Technology. Research and Reviews: A Journal of Pharmaceutical Science. 2025; 16(01):61-71. Available from: https://journals.stmjournals.com/rrjops/article=2025/view=196707


References

1. Muley, S., Nandgude, T., & Poddar, S. (2016). Extrusion–spheronization: A promising pelletization technique—In-depth review. Asian Journal of Pharmaceutical Sciences, 11(6), 684–699. https://doi.org/10.1016/j.ajps.2016.08.001
2. Roy, P., & Shahiwala, A. (2009). Multiparticulate formulation approach to pulsatile drug delivery: Current perspectives. Journal of Controlled Release, 134(2), 74–80. https://doi.org/10.1016/j.jconrel.2008.11.011
3. Supriya, P., & Rajni, B. (2012). Pelletization techniques: A literature review. International Research Journal of Pharmacy Online. Retrieved from www.irjponline.com
4. Kleinebudde, P., & Lindner, H. (1993). Experiments with an instrumented twin-screw extruder using a single-step granulation/extrusion process. Volume 94 ,(Issue 1-3)P49-58.
5. Hell, L., Yliruusi, J., Merkku, P., & Kristoffersson, E. (1993). Process variables of instant granulator and spheroniser: I. Physical properties of granules, extrudate and pellets. Volume 96, Issue 1-3 P197-204 https://doi.org/10.1016/0378-5173(93)90228-8 .
6. Mehta KA, Rekhi GS, Parikh DM. Extrusion/spheronization as a granulation technique. InHandbook of Pharmaceutical Granulation Technology 2005 Aug 30 2nd Editions (pp. 361-392). CRC Press . https://www.researchgate.net/publication/329322142
7. Vervaet, C., Baert, L., & Remon, J. P. (1995). Extrusion-spheronization: A literature review. International Journal of Pharmaceutics, 116,(2) 131–136 https://doi.org/10.1016/0378-5173(94)00311-R .
8. O’Connor, R. E., & Schwartz, J. B. (1985). Spheronization II: Drug Release from Drug-Diluent Mixtures. Drug Development and Industrial Pharmacy, 11(9–10), 1837–1857. https://doi.org/10.3109/03639048509057702 .
9. Lustig-Gustafsson, C., Johal, H. K., Podczeck, F., & Newton, J. M. (1999). The influence of water content and drug solubility on the formulation of pellets by extrusion and spheronization, European Journal of Pharmaceutical Sciences. Volume 8, Issue 2 P.147-152.
10. Tomer, G., & Newton, J. M. (1999). Water movement evaluation during extrusion of wet powder masses by collecting extrudate fractions. International Journal of Pharmaceutics, Volume 182, issue 1,p 71-77 https://doi.org/10.1016/S0378-5173(99)00061-7 .
11. Dreu, R., Širca, J., Pintye-Hodi, K., Burjan, T., Planinšek, O., & Srčič, S. (2005). Physicochemical properties of granulating liquids and their influence on microcrystalline cellulose pellets obtained by extrusion-spheronization technology. International Journal of Pharmaceutics, 291, Issue 1-2, 99–111. https://doi.org/10.1016/j.ijpharm.2004.07.047
12. Law, M. F. L., & Deasy, P. B. (1997). Effect of common classes of excipients on extrusion-spheronization. Journal of Microencapsulation, 14(5), 647–657. https://doi.org/10.3109/02652049709006817
13. Ghali, E. S., Klinger, G. H., & Schwartz, J. B. (1989). Modified Drug Release From Beads Prepared with Combinations of Two Grades of Microcrystalline Cellulose. Drug Development and Industrial Pharmacy, 15(9), 1455–1473. https://doi.org/10.3109/03639048909062757
14. Nejati, L., Kalantari, F., Bavarsad, N., Saremnejad, F., Moghaddam, P. T., & Akhgari, A. (2018). Investigation of using pectin and chitosan as natural excipients in pellet formulation. International Journal of Biological Macromolecules, 120, Part A, 1208–1215. https://doi.org/10.1016/j.ijbiomac.2018.08.129
15. Wang, Z., Chen, B., Quan, G., et al. (2012). Increasing the oral bioavailability of poorly water-soluble carbamazepine using immediate-release pellets supported on SBA-15 mesoporous silica. International Journal of Nanomedicine, 7, 5807–5818. https://doi.org/10.2147/IJN.S37650
16. Dukić-Ott, A., Remon, J. P., Foreman, P., & Vervaet, C. (2007). Immediate release of poorly soluble drugs from starch-based pellets prepared via extrusion/spheronization. European Journal of Pharmaceutics and Biopharmaceutics, 67 (3), 715–724. https://doi.org/10.1016/j.ejpb.2007.04.014
17. Singh, S. K., Dodge, J., Durrani, M. J., & Khan, M. A. (1995). Optimization and characterization of controlled release pellets coated with an experimental latex: I. Anionic drug. International Journal of Pharmaceutics, 125, Issue 243-255 https://doi.org/10.1016/0378-5173(95)00135-6 .
18. Vishal Gupta N, Gowda D, Balamuralidhara V, Mohammed Khan S. Formulation and evaluation of olanzapine matrix pellets for controlled release. Daru. 2011;19(4):249-56.
19. Sawicki, W. (n.d.). Pharmacokinetics of verapamil and norverapamil from controlled release floating pellets in humans. European Journal of Pharmaceutics and Biopharmaceutics vol 53, P 29-35 https://doi.org/10.1016/S0939-6411(01)00189-8
20. Sinchaipanid, N., Junyaprasert, V., & Mitrevej, A. (2004). Application of hot-melt coating for controlled release of propranolol hydrochloride pellets. Powder Technology, 141(3), 203–209. https://doi.org/10.1016/j.powtec.2004.02.008
21. Yang, C., Ji, X., Pan, W., et al. (2018). Paliperidone ascending controlled-release pellets with osmotic core and driven by delayed osmotic pressure. Journal of Drug Delivery Science and Technology, 48, 193–199. https://doi.org/10.1016/j.jddst.2018.09.018
22. Kan, S. L., Li, J., Liu, J. P., & Zhao, Y. (2015). Preparation and IVIVC evaluation of salvianolic acid B micro-porous osmotic pump pellets. Drug Development and Industrial Pharmacy, 41(3), 476–481. https://doi.org/10.3109/03639045.2013.879722
23. Patel, S., Patel, N., Misra, M., & Joshi, A. (2018). Controlled-release domperidone pellets compressed into fast disintegrating tablets forming a multiple-unit pellet system (MUPS). Journal of Drug Delivery Science and Technology, 45, 220–229. https://doi.org/10.1016/j.jddst.2017.12.015
24. Szewczyk, A., Skwira, A., Konopacka, A., Sądej, R., Walker, G., & Prokopowicz, M. (2020). Mesoporous silica pellets as bifunctional bone drug delivery system for cefazolin. International Journal of Pharmaceutics, 588. https://doi.org/10.1016/j.ijpharm.2020.119718
25. Bryan, M. P., Kent, M. D., Rickenbach, J., Rimmer, G., Wilson, D. I., & Rough, S. L. (2015). The effect of mixing on the extrusion-spheronisation of a micro-crystalline cellulose paste. International Journal of Pharmaceutics, 479(1), 1–10. https://doi.org/10.1016/j.ijpharm.2014.12.028
26. Baert, J. P., Remon, L., & Newton, J. (1992). A comparison between the extrusion forces and sphere quality of a gravity feed extruder and a ram extruder, Int Journ of Pharmaceutics Volume 86 issue 2-3, 187-192 https://doi.org/10.1016/0378-5173(92)90196-9 .
27. Baert, L., Rernon, P., Elbers, J. A. C., & van Bommel, E. M. G. (1993). Comparison between a gravity feed extruder and a twin screw extruder, International Journal of Pharmaceutics, Volume 99, Issue 1, P 7-12, https://doi.org/10.1016/0378-5173(93)90316-8
28. Vervaet, C., Baert, L., Risha, P. A., & Remon, J. P. (1994). The influence of the extrusion screen on pellet quality using an instrumented basket extruder. International Journal of Pharmaceutics, 107,Issue 1,P29-39 https://doi.org/10.1016/0378-5173(94)90299-2 .
29. Bölcskei, E., Regdon, G., Sovány, T., Kleinebudde, P., & Pintye-Hódi, K. (2012). Optimization of preparation of matrix pellets containing Eudragit® NE 30D. Chemical Engineering Research and Design, 90(5), 651–657. https://doi.org/10.1016/j.cherd.2011.09.005
30. Baert, L., Vermeersch, H., Remon, J. P., Smeyers-Verbeke, J., & Massart, D. L. (1993). Study of parameters important in the spheronization Process, International Journal of Pharmaceutics, Volume 96, Issues 1–3, Pages 225-229, https://doi.org/10.1016/0378-5173(93)90231-4
31. Wilson, D. L., & Rough, S. L. (1995). Extrusion-spheronization. Pharmaceutica Acta Helvetiae, 70(5), 259–268.

32. Fielden, K. E., Newton, J. M., O’Brien, P., & Rowe, R. C. (1988). Thermal studies on the interaction of water and microcrystalline cellulose. Journal of Pharmacy and Pharmacology, 40(10), 674–678.

33. Fielden, K. E., Newton, J. M., & Rowe, R. C. (1991). The influence of lactose particle size on spheronization of extrudate processed by a ram extruder. Volume 810992.

34. Sarkar, S., & Liew, C. V. (2014). Moistening liquid-dependent de-aggregation of microcrystalline cellulose and its impact on pellet formation by extrusion-spheronization. AAPS Pharm SciTech, 15(3), 753–761. https://doi.org/10.1208/s12249-014-0098-7

35. Chamsai, B., & Sriamornsak, P. (2013). Novel disintegrating microcrystalline cellulose pellets with improved drug dissolution performance. Powder Technology, 233, 278–285. https://doi.org/10.1016/j.powtec.2012.08.019

36. Schroder, M., & Kleinebudde, P. (1995). A novel extrusion-spheronization technique: The development of pharmaceutical pellets with controlled release properties. Pharmaceutical Research, 12, 1612–1617.

37. Lundqvist, A. B., Podczeck, F., & Newton, J. M. (1997). The influence of disintegrant type and proportion on the properties of tablets produced from mixtures of pellets. International Journal of Pharmaceutics, 147(2), 127–137.

38. Sousa, J. J., Sousa, A., Moura, M. J., Podczeck, F., & Newton, J. M. (2002). The influence of core materials and film coating on the drug release from coated pellets. International Journal of Pharmaceutics, 233, 227–238. https://doi.org/10.1016/S0378-5173(02)00342-9


Regular Issue Subscription Review Article
Volume 16
Issue 01
Received 24/12/2024
Accepted 27/01/2025
Published 01/02/2025


Loading citations…