Literature DB >> 21782911

Comparison of HPMC based polymers performance as carriers for manufacture of solid dispersions using the melt extruder.

Indrajit Ghosh1, Jennifer Snyder, Radha Vippagunta, Marilyn Alvine, Ronak Vakil, Wei-Qin Tong, Sudha Vippagunta.   

Abstract

Preparation of amorphous solid dispersions using hot-melt extrusion process for poorly water soluble compounds which degrade on melting remains a challenge due to exposure to high temperatures. The aim of this study was to develop a physically and chemically stable amorphous solid dispersion of a poorly water-soluble compound, NVS981, which is highly thermal sensitive and degrades upon melting at 165 °C. Hydroxypropyl Methyl Cellulose (HPMC) based polymers; HPMC 3cps, HPMC phthalate (HPMCP) and HPMC acetyl succinate (HPMCAS) were selected as carriers to prepare solid dispersions using hot melt extrusion because of their relatively low glass transition temperatures. The solid dispersions were compared for their ease of manufacturing, physical stability such as recrystallization potential, phase separation, molecular mobility and enhancement of drug dissolution. Two different drug loads of 20 and 50% (w/w) were studied in each polymer system. It was interesting to note that solid dispersions with 50% (w/w) drug load were easier to process in the melt extruder compared to 20% (w/w) drug load in all three carriers, which was attributed to the plasticizing behavior of the drug substance. Upon storage at accelerated stability conditions, no phase separation was observed in HPMC 3cps and HPMCAS solid dispersions at the lower and higher drug load, whereas for HPMCP, phase separation was observed at higher drug load after 3 months. The pharmaceutical performance of these solid dispersions was evaluated by studying drug dissolution in pH 6.8 phosphate buffer. Drug release from solid dispersion prepared from polymers used for enteric coating, i.e. HPMCP and HPMCAS was faster compared with the water soluble polymer HPMC 3cps. In conclusion, of the 3 polymers studied for preparing solid dispersions of thermally sensitive compound using hot melt extrusion, HPMCAS was found to be the most promising as it was easily processible and provided stable solid dispersions with enhanced dissolution.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 21782911     DOI: 10.1016/j.ijpharm.2011.05.073

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  13 in total

Review 1.  Challenges and Strategies in Thermal Processing of Amorphous Solid Dispersions: A Review.

Authors:  Justin S LaFountaine; James W McGinity; Robert O Williams
Journal:  AAPS PharmSciTech       Date:  2015-08-26       Impact factor: 3.246

Review 2.  Use of Spray-Dried Dispersions in Early Pharmaceutical Development: Theoretical and Practical Challenges.

Authors:  Jinjiang Li; Dhaval Patel; George Wang
Journal:  AAPS J       Date:  2016-11-28       Impact factor: 4.009

3.  Thermal Processing of PVP- and HPMC-Based Amorphous Solid Dispersions.

Authors:  Justin S LaFountaine; Leena Kumari Prasad; Chris Brough; Dave A Miller; James W McGinity; Robert O Williams
Journal:  AAPS PharmSciTech       Date:  2015-10-13       Impact factor: 3.246

4.  Stable amorphous solid dispersions of fenofibrate using hot melt extrusion technology: Effect of formulation and process parameters for a low glass transition temperature drug.

Authors:  Venkata Raman Kallakunta; Sandeep Sarabu; Suresh Bandari; Amol Batra; Vivian Bi; Thomas Durig; Michael A Repka
Journal:  J Drug Deliv Sci Technol       Date:  2019-11-18       Impact factor: 3.981

5.  Controlled porosity solubility modulated osmotic pump tablets of gliclazide.

Authors:  Arti Banerjee; P R P Verma; Subhash Gore
Journal:  AAPS PharmSciTech       Date:  2014-11-07       Impact factor: 3.246

6.  Low-viscosity hydroxypropylcellulose (HPC) grades SL and SSL: versatile pharmaceutical polymers for dissolution enhancement, controlled release, and pharmaceutical processing.

Authors:  Ashish Sarode; Peng Wang; Catherine Cote; David R Worthen
Journal:  AAPS PharmSciTech       Date:  2012-12-19       Impact factor: 3.246

7.  Application of carrier and plasticizer to improve the dissolution and bioavailability of poorly water-soluble baicalein by hot melt extrusion.

Authors:  Yilan Zhang; Rui Luo; Yi Chen; Xue Ke; Danrong Hu; Miaomiao Han
Journal:  AAPS PharmSciTech       Date:  2014-02-26       Impact factor: 3.246

8.  Use of Polyvinyl Alcohol as a Solubility-Enhancing Polymer for Poorly Water Soluble Drug Delivery (Part 1).

Authors:  Chris Brough; Dave A Miller; Justin M Keen; Shawn A Kucera; Dieter Lubda; Robert O Williams
Journal:  AAPS PharmSciTech       Date:  2015-12-04       Impact factor: 3.246

9.  Improved dissolution and anti-inflammatory effect of ibuprofen by solid dispersion.

Authors:  Liyuan Chen; Qifeng Dang; Chengsheng Liu; Jun Chen; Lei Song; Xiguang Chen
Journal:  Front Med       Date:  2012-05-09       Impact factor: 4.592

10.  Mutual Effects of Hydrogen Bonding and Polymer Hydrophobicity on Ibuprofen Crystal Inhibition in Solid Dispersions with Poly(N-vinyl pyrrolidone) and Poly(2-oxazolines).

Authors:  Xiaoning Shan; Maryam A Moghul; Adrian C Williams; Vitaliy V Khutoryanskiy
Journal:  Pharmaceutics       Date:  2021-05-04       Impact factor: 6.321

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