A Review: Novel Granulation Technology
Abstract
All the pharmaceutical Active pharmaceutical Ingredients (API) and Pharmaceutical excipients will have different particle size. While formulating a dosage form, particles from raw materials will tend to separate from other due to their rheological properties. There could be a condition where fine particles separate from the larger particles causing demixing or uneven distribution of active with its excipients leading to tablet content uniformity issue. To overcome this problem, particle enlargement or particle cohesiveness with or without additional aid is necessary, which could be achieved by granulation. Hence granulation technology is important in the formulation of pharmaceutical oral solid dosage form. Granulation is the process of adhering fine particles agglomerate into a large particle using two most common methods i.e. wet granulation and dry granulation/compaction. Day by day technological innovation is happening in all fields and pharmaceutical granulation process is also not an exemption. The objective of present review is to focus the novel granulation technology and how it is differing from the conventional granulation technology.
References
Bhaskar V, Bala krishnan. Veliparuthi (Pergularia daemia (Forsk.) Chiov) -As a phytomedicine: A review: International Journal of PharmTech Research 2009;1:1305-1313.
Hardik P, Viral Shah and Umaesh U: New pharmaceutical excipients in solid dosage form- A Review. International Journal of Pharmaceutical and Life Sciences 2011;2:1006-1019.
Faure A, York P and Rowe RC. Process control and scale-up of pharmaceutical wet granulation processes: a review. European journal of pharmaceutics and biopharmaceutics 2001:52;269-277.
Thejaswini P, Suguna B, Sumalatha N, Umasankar K and Jeyachandra Reddy. Advanced granulation techniques for pharmaceutical formulations – overview. International Journal of Research in Pharmaceutical and Nano Sciences 2013;6:723-732.
Hansuld E M, Briens L. A review of monitoring methods for pharmaceutical wet granulation. International Journal of Pharmaceutics 2014:472;192-201.
Himanshu K, Tarashankar B, Jalaram H and Chirag A. Recent advances in granulation technology. International Journal of Pharmaceutical Sciences Review and Research 2010:5;48-54.
Balakrishna K, Venkatareddy K and Venkateswara Rao T. advanced granulation technologies: a review. Indian Journal of Research in Pharmacy and Biotechnology 2010:6;1507-1511.
Rodriguez L, Cavallari C, Passerini N and Albertini B. Preparation, and characterization by morphological analysis of diclofenac/PEG 4000 granules obtained using three different techniques. International Journal of Pharmaceutics 2002:242;285–289.
Srinivasan Shanmugam. Granulation techniques and technologies: recent progresses. BioImpacts 2015:5;55-63.
Keleb E I, Vermeire A, Vervaet C and Remon J P. Twin screw granulation as a simple, and efficient tool for continuous wet granulation. International Journal of Pharmaceutics.2004:273;183–194.
Jonathan B W, Gary P M and David F L. The development of a growth regime map for a novel reverse-phase wet granulation process. International Journal of Pharmaceutics 2016:512;224–233.
Wade J B, Martin G P and Long D F. Controlling granule size through breakage in a novel reverse-phase wet granulation process; the effect of impeller speed and binder liquid Viscosity. International Journal of Pharmaceutics 2015:478;439-446.
Jonathan Wade. The development and characterisation of a novel reverse-phase wet granulation process. Institute of Pharmaceutical Science, King’s College London. 2013.
Nidhi P S, Vaishali A K, Minal N B and Anwar S D. Application of a convenient and cost-effective granulation technology for the formulation of tablets using conventional excipients. Asian Journal of Pharmacology 2014:1;183-189.
Himanshu K, Tarashankar B, Jalaram H and Chirag A. Recent advances in granulation technology. International journal of pharmaceutical sciences review and research 2010:5;48-54.
Venkateswara B R, Navaneetha K and Venkata R K. Process development, and optimization for moisture activated dry granulation method for losartan potassium tablets. International Journal of Pharmacy and Pharmaceutical Sciences 2014:6;312-317.
Hong L L, Hsiu O H, Chia C C, Ta Shuong Y and Ming T S. Process, and formulation characterizations of the thermal adhesion granulation (TAG) process for improving granular properties. International Journal of Pharmaceutics 2008:357;206-212.
Ying C C, Hsiu O H, Jiun D C and Ming T S. Physical, and dissolution characterization of cilostazol solid dispersions prepared by hot melt granulation (HMG) and thermal adhesion granulation (TAG) methods. International Journal of Pharmaceutics 2014:473;458-468.
Viapandom M, Albertini B, Passerini N, Vander H Y, Rombaut P, Martens JA and Van Den Mooter G. Agglomeration of mesoporous silica by melt and steam granulation.Part-II; Screening of steam granulation process variable using a factorial design. Journal of Pharmaceutical Sciences 2013:102;3978-3986.
Subhash P G, Srilatha K S, Ajay Kumar, Madhusudhan P, Jamal Shariff, Shaik and Jayanth Kumar Reddy G. Emphasis on novel granulation technologies: An overview. Indo American Journal of Pharmaceutical Research 2011:1;305-316.
Cristina C, Beatrice A, Marisa L G and Lorenzo R. Improved dissolution behavior of steam-granulated piroxicam. European Journal of Pharmaceutics and Biopharmaceutics 2002:54;65-73.
Passerini N, Calogera G, Albertini B and Rodriguez L. Melt granulation of pharmaceutical powders: A comparison of high-shear mixer and fluidised bed processes International Journal of Pharmaceutics 2010:391;177–186.
Kowalski J, Kalb O, Joshi Y M and Abu T M. Application of melt granulation technology to enhance stability of a moisture sensitive immediate-release drug product. International Journal of Pharmaceutics 2009:38;56–61.
Melvin X L, Hapgood K P. Foam granulation: Binder dispersion and nucleation in mixture granulator. Chemical Engineering Research and Design 2011:89;526-536.
www.pharmatech.com/Foamgranulation. (Assessed on 12-Sep-2016)
Thompson M R, Veatherley S, Pukadyil R N and Sheskey P J. Foam granulation: New development in pharmaceutical oral solid dosage form using twin screw extrusion machinery. Drug Development and Industrial Pharmacy 2011:38;771-784.
www.ceramicindustry.com/article/804941-ppt-Improving-powder-with-Freeze-granulation. (Assessed on 05-Sep-2016)
Vasiliki T, Kagias G and Vassilions Z. Freeze granulation: A novel technique for loss Mn-Zn ferrities. International magnetics conference, Madrid, Spain.2008.
www.swerea.se/en/File/1068/download?token=lrRPM2cl (Assessed on 01-Sep-2016)
Sandler N, Lammens R F. Pneumatic dry granulation: Potential to improve roller compaction technology in drug manufacture. Expert Opinion on Drug Delivery 2011:8;225-236.
Manmaya Mishra: Handbook of encapsulation and controlled release. CRL Press, Second Edition 2015.
Amol P S, Dattatraya M S and Saudagar R B. Granulation techniques. Asian Journal of Pharmaceutical Sciences 2015:5; 203-215.
Ranjit M D, Richard S F, James J C, David G D, et al. Twin screw wet granulation: Granule properties. Chemical Engineering.2010:164;322-32.
El Hagrasy A S, Hennenkamp A R, Burke M D, Cartwright J J, Michael J. H and Agba D.S. Twin screw wet granulation: Influence of formulation parameters on granule properties and growth behavior. Powder Technology 2013:238;108-115.
Dhenge R M, James J C, Michael J H and Agba D S. Twin screw granulation: Steps in granule growth. International Journal of Pharmaceutics 2012:438;20-32.
Patil H, Tiwari RV, Upadhye SB, Vladyka RS and Repka MA. Formulation and development of pH-independent/dependent sustained release matrix tablets of ondansetron HCl by a continuous twin-screw melt granulation process. International Journal of Pharmaceutics 2015:496;33-41.
Vanhoorne V, Vanbillemont B, Vercruysse J, Vervaet F C, Leersnyder F, Gomes P, Beer TD, Remon JP, Vervaet C. Development of a controlled release formulation by continuous twin screw granulation: Influence of process and formulation parameters. International Journal of Pharmaceutics 2016:505;61-68.
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