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Application of melt granulation technology to enhance tabletting properties of poorly compactible high-dose drugs.
J Pharm Sci. 2011 Apr; 100(4):1553-65.JP

Abstract

Using metformin HCl as the model drug and hydroxypropylcellulose (HPC) as the polymeric excipient, a melt granulation (MG) process that employs a twin-screw extruder has been developed to enhance compactibility of poorly compactible high-dose drug substances. A high (90%) drug-load tablet formulation, containing 1025 mg of active pharmaceutical ingredients and 109 mg of excipients, was produced. Drug-polymer-powder mixtures were melt granulated at a temperature above glass transition of HPC (130°C) but below melting point of metformin HCl (224°C). MG was compared with modified wet granulation (WG) and solvent granulation (SG) processes. Under identical compression force, the hardness of tablets produced was MG>SG>WG and the friability was MG<SG<WG. The hardness of WG tablets was highly sensitive to moisture content both during compression and subsequent storage, and, although not to the same extent, the hardness of SG tablets was also affected by loss-on-drying levels. MG provided a robust manufacturing process with highest compactibility and lowest friability that were not sensitive to changes in atmospheric moisture level. The process can decrease tablet sizes of high-dose drugs and combination products by decreasing the need for relatively large amounts of excipients generally used to overcome physicochemical limitations of drug substances. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 100:1553-1565, 2011.

Authors+Show Affiliations

Pharmaceutical and Analytical Development, Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936. jay.lakshman@novartis.com.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

24081475

Citation

Lakshman, Jay P., et al. "Application of Melt Granulation Technology to Enhance Tabletting Properties of Poorly Compactible High-dose Drugs." Journal of Pharmaceutical Sciences, vol. 100, no. 4, 2011, pp. 1553-65.
Lakshman JP, Kowalski J, Vasanthavada M, et al. Application of melt granulation technology to enhance tabletting properties of poorly compactible high-dose drugs. J Pharm Sci. 2011;100(4):1553-65.
Lakshman, J. P., Kowalski, J., Vasanthavada, M., Tong, W. Q., Joshi, Y. M., & Serajuddin, A. T. (2011). Application of melt granulation technology to enhance tabletting properties of poorly compactible high-dose drugs. Journal of Pharmaceutical Sciences, 100(4), 1553-65. https://doi.org/10.1002/jps.22369
Lakshman JP, et al. Application of Melt Granulation Technology to Enhance Tabletting Properties of Poorly Compactible High-dose Drugs. J Pharm Sci. 2011;100(4):1553-65. PubMed PMID: 24081475.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Application of melt granulation technology to enhance tabletting properties of poorly compactible high-dose drugs. AU - Lakshman,Jay P, AU - Kowalski,James, AU - Vasanthavada,Madhav, AU - Tong,Wei-Qin, AU - Joshi,Yatindra M, AU - Serajuddin,Abu T M, Y1 - 2010/12/03/ PY - 2009/10/26/received PY - 2010/08/13/revised PY - 2010/09/16/accepted PY - 2013/10/2/entrez PY - 2011/4/1/pubmed PY - 2014/12/30/medline KW - extrusion KW - formulation KW - granulation KW - solid dosage form KW - tableting KW - water in solids SP - 1553 EP - 65 JF - Journal of pharmaceutical sciences JO - J Pharm Sci VL - 100 IS - 4 N2 - Using metformin HCl as the model drug and hydroxypropylcellulose (HPC) as the polymeric excipient, a melt granulation (MG) process that employs a twin-screw extruder has been developed to enhance compactibility of poorly compactible high-dose drug substances. A high (90%) drug-load tablet formulation, containing 1025 mg of active pharmaceutical ingredients and 109 mg of excipients, was produced. Drug-polymer-powder mixtures were melt granulated at a temperature above glass transition of HPC (130°C) but below melting point of metformin HCl (224°C). MG was compared with modified wet granulation (WG) and solvent granulation (SG) processes. Under identical compression force, the hardness of tablets produced was MG>SG>WG and the friability was MG<SG<WG. The hardness of WG tablets was highly sensitive to moisture content both during compression and subsequent storage, and, although not to the same extent, the hardness of SG tablets was also affected by loss-on-drying levels. MG provided a robust manufacturing process with highest compactibility and lowest friability that were not sensitive to changes in atmospheric moisture level. The process can decrease tablet sizes of high-dose drugs and combination products by decreasing the need for relatively large amounts of excipients generally used to overcome physicochemical limitations of drug substances. © 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 100:1553-1565, 2011. SN - 1520-6017 UR - https://www.unboundmedicine.com/medline/citation/24081475/Application_of_melt_granulation_technology_to_enhance_tabletting_properties_of_poorly_compactible_high_dose_drugs_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0022-3549(15)32202-4 DB - PRIME DP - Unbound Medicine ER -