Literature DB >> 26511936

Investigation of Thermal and Viscoelastic Properties of Polymers Relevant to Hot Melt Extrusion, IV: Affinisol™ HPMC HME Polymers.

Simerdeep Singh Gupta1,2, Nayan Solanki1, Abu T M Serajuddin3.   

Abstract

Most cellulosic polymers cannot be used as carriers for preparing solid dispersion of drugs by hot melt extrusion (HME) due to their high melt viscosity and thermal degradation at high processing temperatures. Three HME-grade hydroxypropyl methylcelluloses, namely AffinisolHPMC HME 15 cP, AffinisolHPMC HME 100 cP, and AffinisolHPMC HME 4 M, have recently been introduced by The Dow Chemical Co. to enable the preparation of solid dispersion at lower and more acceptable processing temperatures. In the present investigation, physicochemical properties of the new polymers relevant to HME were determined and compared with that of Kollidon(®) VA 64. Powder X-ray diffraction (PXRD), modulated differential scanning calorimetry (mDSC), thermogravimetric analysis (TGA), moisture sorption, rheology, and torque analysis by melt extrusion were applied. PXRD and mDSC showed that the Affinisolpolymers were amorphous in nature. According to TGA, the onset of degradation for all polymers was >220°C. The Affinisolpolymers exhibited less hygroscopicity than Kollidon(®) VA 64 and another HPMC polymer, Methocel™ K100LV. The complex viscosity profiles of the Affinisolpolymers as a function of temperature were similar. The viscosity of the Affinisolpolymers was highly sensitive to the shear rate applied, and unlike Kollidon(®) VA 64, the viscosity decreased drastically when the angular frequency was increased. Because of the very high shear rate encountered during melt extrusion, Affinisolpolymers showed capability of being extruded at larger windows of processing temperatures as compared to that of Kollidon(®) VA 64.

Entities:  

Keywords:  Affinisol™ HPMC HME; hot melt extrusion; hydroxypropyl methylcellulose; solid dispersion; thermal analysis; viscosity

Mesh:

Substances:

Year:  2015        PMID: 26511936      PMCID: PMC4766120          DOI: 10.1208/s12249-015-0426-6

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  11 in total

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Authors:  A T Serajuddin
Journal:  J Pharm Sci       Date:  1999-10       Impact factor: 3.534

2.  Crystal structure and hydrogen bonding system in cellulose I(alpha) from synchrotron X-ray and neutron fiber diffraction.

Authors:  Yoshiharu Nishiyama; Junji Sugiyama; Henri Chanzy; Paul Langan
Journal:  J Am Chem Soc       Date:  2003-11-26       Impact factor: 15.419

Review 3.  Melt extrusion: from process to drug delivery technology.

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Journal:  Eur J Pharm Biopharm       Date:  2002-09       Impact factor: 5.571

Review 4.  IV-IVC considerations in the development of immediate-release oral dosage form.

Authors:  Shoufeng Li; Handan He; Lakshman J Parthiban; Hequn Yin; Abu T M Serajuddin
Journal:  J Pharm Sci       Date:  2005-07       Impact factor: 3.534

Review 5.  Pharmaceutical applications of hot-melt extrusion: part I.

Authors:  Michael M Crowley; Feng Zhang; Michael A Repka; Sridhar Thumma; Sampada B Upadhye; Sunil Kumar Battu; James W McGinity; Charles Martin
Journal:  Drug Dev Ind Pharm       Date:  2007-09       Impact factor: 3.225

6.  Application of melt extrusion in the development of a physically and chemically stable high-energy amorphous solid dispersion of a poorly water-soluble drug.

Authors:  Jay P Lakshman; Yu Cao; James Kowalski; Abu T M Serajuddin
Journal:  Mol Pharm       Date:  2008 Nov-Dec       Impact factor: 4.939

Review 7.  Melt extrusion with poorly soluble drugs.

Authors:  Sejal Shah; Sindhuri Maddineni; Jiannan Lu; Michael A Repka
Journal:  Int J Pharm       Date:  2012-11-20       Impact factor: 5.875

8.  Effect of carbamazepine on viscoelastic properties and hot melt extrudability of Soluplus ®.

Authors:  Simerdeep Singh Gupta; Tapan Parikh; Anuprabha K Meena; Nidhi Mahajan; Imre Vitez; Abu T M Serajuddin
Journal:  Int J Pharm       Date:  2014-11-13       Impact factor: 5.875

9.  Application of film-casting technique to investigate drug-polymer miscibility in solid dispersion and hot-melt extrudate.

Authors:  Tapan Parikh; Simerdeep Singh Gupta; Anuprabha K Meena; Imre Vitez; Nidhi Mahajan; Abu T M Serajuddin
Journal:  J Pharm Sci       Date:  2015-04-27       Impact factor: 3.534

Review 10.  Salt formation to improve drug solubility.

Authors:  Abu T M Serajuddin
Journal:  Adv Drug Deliv Rev       Date:  2007-05-29       Impact factor: 15.470

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  18 in total

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Journal:  AAPS PharmSciTech       Date:  2016-02-09       Impact factor: 3.246

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4.  Investigation of Polymer-Surfactant and Polymer-Drug-Surfactant Miscibility for Solid Dispersion.

Authors:  Suhas G Gumaste; Simerdeep Singh Gupta; Abu T M Serajuddin
Journal:  AAPS J       Date:  2016-06-14       Impact factor: 4.009

5.  Development of Fast-Dissolving Amorphous Solid Dispersion of Itraconazole by Melt Extrusion of its Mixture with Weak Organic Carboxylic Acid and Polymer.

Authors:  Tapan Parikh; Abu T M Serajuddin
Journal:  Pharm Res       Date:  2018-04-25       Impact factor: 4.200

6.  Electrospinning Optimization of Eudragit E PO with and without Chlorpheniramine Maleate Using a Design of Experiment Approach.

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Journal:  Mol Pharm       Date:  2019-05-07       Impact factor: 4.939

Review 7.  Polymers for Extrusion-Based 3D Printing of Pharmaceuticals: A Holistic Materials-Process Perspective.

Authors:  Mohammad A Azad; Deborah Olawuni; Georgia Kimbell; Abu Zayed Md Badruddoza; Md Shahadat Hossain; Tasnim Sultana
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8.  Influence of Plasdone S630 Ultra-an Improved Copovidone on the Processability and Oxidative Degradation of Quetiapine Fumarate Amorphous Solid Dispersions Prepared via Hot-Melt Extrusion Technique.

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Review 9.  Hot Melt Extrusion: Highlighting Physicochemical Factors to Be Investigated While Designing and Optimizing a Hot Melt Extrusion Process.

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10.  Processing of Polyvinyl Acetate Phthalate in Hot-Melt Extrusion-Preparation of Amorphous Solid Dispersions.

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