Understanding the Processing Window of Hypromellose Acetate Succinate for Hot-Melt Extrusion, Part I: Polymer Characterization and Hot-Melt Extrusion

The aims of this study were to assess the processing window of hypromellose acetate succinate (HPMCAS) as a polymeric carrier for hot-melt extrusion, and to investigate the effect of screw configuration and processing parameters on the physicochemical properties of HPMCAS extrudates. The processability was investigated using a Brabender® mixer and a Pharma 11 Twin Screw Extruder. HPMCAS extrudates were characterized with regard to glass transition temperature, true density, yellowness index, crystallinity, morphology, and free succinic acid/acetic acid/succinoyl group/acetyl group content. The specific energy input and mean residence time were also calculated and correlated to the physicochemical properties of final extrudates. Additionally, the effect of the die opening size of the twin screw extruder was investigated. The glass transition temperature of HPMCAS was found to be 137 and 133°C, using dynamic mechanical analyzer and oscillatory rheometer, respectively. HPMCAS demonstrated a shear thinning behavior at all temperatures tested (150, 160, and 170°C). The process conditions, screw configurations, as well as the diameter of die opening significantly affect the amount of free acetic acid and succinic acid. With a modified screw configuration and 1-mm die, the amounts of free acetic acid and succinic acid from the material processed at 180°C were 0.114% and 0.337%, respectively. Moreover, when the die was removed, the amounts of free acetic acid and succinic acid were further reduced to 0.084% and 0.294%, respectively. In conclusion, we successfully extruded HPMCAS at a temperature as low as 130°C and up to 180°C without any significant thermal degradation.

[1]  M. Repka,et al.  Solid-state characterization of Felodipine–Soluplus amorphous solid dispersions , 2016, Drug development and industrial pharmacy.

[2]  Jukka Rantanen,et al.  Rheology as a tool for evaluation of melt processability of innovative dosage forms. , 2015, International journal of pharmaceutics.

[3]  S. Majumdar,et al.  Investigation of phase diagrams and physical stability of drug–polymer solid dispersions , 2015, Pharmaceutical development and technology.

[4]  S. Majumdar,et al.  The effects of screw configuration and polymeric carriers on hot-melt extruded taste-masked formulations incorporated into orally disintegrating tablets. , 2015, Journal of pharmaceutical sciences.

[5]  N. Shah,et al.  Stability assessment of hypromellose acetate succinate (HPMCAS) NF for application in hot melt extrusion (HME). , 2014, Carbohydrate polymers.

[6]  M. Repka,et al.  Influence of Processing Parameters and Formulation Factors on the Bioadhesive, Temperature Stability and Drug Release Properties of Hot-Melt Extruded Films Containing Miconazole , 2014, AAPS PharmSciTech.

[7]  Beom-Jin Lee,et al.  Current trends and future perspectives of solid dispersions containing poorly water-soluble drugs. , 2013, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[8]  G. Amidon,et al.  The impact of hot melt extrusion and spray drying on mechanical properties and tableting indices of materials used in pharmaceutical development. , 2013, Journal of pharmaceutical sciences.

[9]  Damir E Zecevic,et al.  Rational development of solid dispersions via hot-melt extrusion using screening, material characterization, and numeric simulation tools. , 2013, Journal of pharmaceutical sciences.

[10]  H. Zia,et al.  Hot melt extrusion (HME) for amorphous solid dispersions: predictive tools for processing and impact of drug-polymer interactions on supersaturation. , 2013, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[11]  Peng Wang,et al.  Effects of screw configuration on indomethacin dissolution behavior in Eudragit E PO , 2012 .

[12]  E. O'Mara,et al.  Single-Dose Phase I Study To Evaluate the Pharmacokinetics of Posaconazole in New Tablet and Capsule Formulations Relative to Oral Suspension , 2012, Antimicrobial Agents and Chemotherapy.

[13]  Sejal Shah,et al.  Melt extrusion: process to product , 2012, Expert opinion on drug delivery.

[14]  Anant Paradkar,et al.  Characterization of thermal and rheological properties of zidovudine, lamivudine and plasticizer blends with ethyl cellulose to assess their suitability for hot melt extrusion. , 2011, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[15]  C. Gogos,et al.  Rheological study of the mixture of acetaminophen and polyethylene oxide for hot-melt extrusion application. , 2011, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[16]  Peter J. Halley,et al.  Mechanism of Degradation of Starch, a Highly Branched Polymer, during Extrusion , 2010 .

[17]  G. Van den Mooter,et al.  Review: physical chemistry of solid dispersions , 2009 .

[18]  P. York,et al.  Shear and extensional rheology of hydroxypropyl cellulose melt using capillary rheometry. , 2009, Journal of pharmaceutical and biomedical analysis.

[19]  Zedong Dong,et al.  Hydroxypropyl Methylcellulose Acetate Succinate: Potential Drug–Excipient Incompatibility , 2008, AAPS PharmSciTech.

[20]  James S. Taylor,et al.  Ideal copolymers and the second‐order transitions of synthetic rubbers. i. non‐crystalline copolymers , 2007 .

[21]  Patrick J. Marsac,et al.  Theoretical and Practical Approaches for Prediction of Drug–Polymer Miscibility and Solubility , 2006, Pharmaceutical Research.

[22]  Lorenzo Donati,et al.  The effect of die design on the production and seam weld quality of extruded aluminum profiles , 2005 .

[23]  Feng Zhang,et al.  Stability of polyethylene oxide in matrix tablets prepared by hot-melt extrusion. , 2002, Biomaterials.

[24]  Tomio Nakano,et al.  The role of the kneading paddle and the effects of screw revolution speed and water content on the preparation of solid dispersions using a twin-screw extruder. , 2002, International journal of pharmaceutics.

[25]  L Yu,et al.  Amorphous pharmaceutical solids: preparation, characterization and stabilization. , 2001, Advanced drug delivery reviews.

[26]  R. Shishoo,et al.  Influence of processing parameters on the degradation of poly(L‐lactide) during extrusion , 2001 .

[27]  J Dressman,et al.  Improving drug solubility for oral delivery using solid dispersions. , 2000, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[28]  A. Serajuddin,et al.  Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. , 1999, Journal of pharmaceutical sciences.

[29]  S. Ablett,et al.  The glass transition of amylopectin measured by DSC, DMTA and NMR , 1992 .

[30]  J. Pauquet,et al.  Degradation of polyolefins during melt processing , 1991 .

[31]  J. White,et al.  Flow in a Modular Intermeshing Co-rotating Twin Screw Extruder , 1989 .

[32]  H. Henning Winter,et al.  Design of dies for the extrusion of sheets and annular parisons: The distribution problem , 1986 .

[33]  Keiji Sekiguchi,et al.  Studies on Absorption of Eutectic Mixture. I. A Comparison of the Behavior of Eutectic Mixture of Sulfathiazole and that of Ordinary Sulfathiazole in Man. , 1961 .