Literature DB >> 27113866

Hydrophilic thermoplastic polyurethanes for the manufacturing of highly dosed oral sustained release matrices via hot melt extrusion and injection molding.

G Verstraete1, J Van Renterghem2, P J Van Bockstal2, S Kasmi1, B G De Geest1, T De Beer2, J P Remon1, C Vervaet3.   

Abstract

Hydrophilic aliphatic thermoplastic polyurethane (Tecophilic™ grades) matrices for high drug loaded oral sustained release dosage forms were formulated via hot melt extrusion/injection molding (HME/IM). Drugs with different aqueous solubility (diprophylline, theophylline and acetaminophen) were processed and their influence on the release kinetics was investigated. Moreover, the effect of Tecophilic™ grade, HME/IM process temperature, extrusion speed, drug load, injection pressure and post-injection pressure on in vitro release kinetics was evaluated for all model drugs. (1)H NMR spectroscopy indicated that all grades have different soft segment/hard segment ratios, allowing different water uptake capacities and thus different release kinetics. Processing temperature of the different Tecophilic™ grades was successfully predicted by using SEC and rheology. Tecophilic™ grades SP60D60, SP93A100 and TG2000 had a lower processing temperature than other grades and were further evaluated for the production of IM tablets. During HME/IM drug loads up to 70% (w/w) were achieved. In addition, Raman mapping and (M)DSC results confirmed the homogenous distribution of mainly crystalline API in all polymer matrices. Besides, hydrophilic TPU based formulations allowed complete and sustained release kinetics without using release modifiers. As release kinetics were mainly affected by drug load and the length of the PEO soft segment, this polymer platform offers a versatile formulation strategy to adjust the release rate of drugs with different aqueous solubility.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  High drug load; Hot melt extrusion; Injection molding; Rheology; Sustained release; Thermoplastic polyurethanes

Mesh:

Substances:

Year:  2016        PMID: 27113866     DOI: 10.1016/j.ijpharm.2016.04.057

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


  6 in total

Review 1.  Hot-Melt Extrusion: a Roadmap for Product Development.

Authors:  Marta F Simões; Rui M A Pinto; Sérgio Simões
Journal:  AAPS PharmSciTech       Date:  2021-06-17       Impact factor: 3.246

2.  PVP VA64 as a novel release-modifier for sustained-release mini-matrices prepared via hot melt extrusion.

Authors:  Yongcheng Li; Ming Lu; Chuanbin Wu
Journal:  Drug Deliv Transl Res       Date:  2018-12       Impact factor: 4.617

3.  Chronotherapeutic Drug Delivery of Ketoprofen and Ibuprofen for Improved Treatment of Early Morning Stiffness in Arthritis Using Hot-Melt Extrusion Technology.

Authors:  Nagi Reddy Dumpa; Sandeep Sarabu; Suresh Bandari; Feng Zhang; Michael A Repka
Journal:  AAPS PharmSciTech       Date:  2018-07-02       Impact factor: 3.246

4.  Development of Porous Polyurethane Implants Manufactured via Hot-Melt Extrusion.

Authors:  Ioannis Koutsamanis; Martin Spoerk; Florian Arbeiter; Simone Eder; Eva Roblegg
Journal:  Polymers (Basel)       Date:  2020-12-10       Impact factor: 4.329

Review 5.  Sustained Release Drug Delivery Applications of Polyurethanes.

Authors:  Michael B Lowinger; Stephanie E Barrett; Feng Zhang; Robert O Williams
Journal:  Pharmaceutics       Date:  2018-05-09       Impact factor: 6.321

Review 6.  Advanced Pharmaceutical Applications of Hot-Melt Extrusion Coupled with Fused Deposition Modelling (FDM) 3D Printing for Personalised Drug Delivery.

Authors:  Deck Khong Tan; Mohammed Maniruzzaman; Ali Nokhodchi
Journal:  Pharmaceutics       Date:  2018-10-24       Impact factor: 6.321

  6 in total

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