Cargando…

Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion

This study aimed to demonstrate the feasibility of hot-melt extrusion in the development of extended-release formulations of Fenbendazole (Fen) dispersed in PEO/PCL blend-based matrices. Their thermal, physical, chemical and viscosity properties were assessed by differential scanning calorimetry, th...

Descripción completa

Detalles Bibliográficos
Autores principales: Bezerra, Gilberto S. N., de Lima, Tielidy A. de M., Colbert, Declan M., Geever, Joseph, Geever, Luke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573241/
https://www.ncbi.nlm.nih.gov/pubmed/36236135
http://dx.doi.org/10.3390/polym14194188
_version_ 1784810819234562048
author Bezerra, Gilberto S. N.
de Lima, Tielidy A. de M.
Colbert, Declan M.
Geever, Joseph
Geever, Luke
author_facet Bezerra, Gilberto S. N.
de Lima, Tielidy A. de M.
Colbert, Declan M.
Geever, Joseph
Geever, Luke
author_sort Bezerra, Gilberto S. N.
collection PubMed
description This study aimed to demonstrate the feasibility of hot-melt extrusion in the development of extended-release formulations of Fenbendazole (Fen) dispersed in PEO/PCL blend-based matrices. Their thermal, physical, chemical and viscosity properties were assessed by differential scanning calorimetry, thermogravimetric analysis/derivative thermogravimetry, Fourier transform infrared spectroscopy, X-ray diffraction spectroscopy, and melt flow index. Drug dispersion was analyzed by scanning electron microscopy with electron dispersive X-ray spectroscopy, and drug release was evaluated by ultraviolet-visible spectroscopy. A thermal analysis indicated the conversion of the drug to its amorphous state. FTIR analysis endorsed the thermal studies pointing to a decrease in the drug’s crystallinity with the establishment of intermolecular interactions. XRD analysis confirmed the amorphous nature of Fen. MFI test revealed that PCL acts as a plasticizer when melt-processed with PEO. SEM images displayed irregular surfaces with voids and pores, while EDX spectra demonstrated a homogeneous drug distribution throughout the polymeric carrier. Dissolution testing revealed that PCL retards the drug release proportionally to the content of such polymer incorporated. These melt-extruded matrices showed that the drug release rate in a PEO/PCL blend can easily be tailored by altering the ratio of PCL to address the issues related to the multiple-dosing regimen of Fen in ruminants.
format Online
Article
Text
id pubmed-9573241
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-95732412022-10-17 Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion Bezerra, Gilberto S. N. de Lima, Tielidy A. de M. Colbert, Declan M. Geever, Joseph Geever, Luke Polymers (Basel) Article This study aimed to demonstrate the feasibility of hot-melt extrusion in the development of extended-release formulations of Fenbendazole (Fen) dispersed in PEO/PCL blend-based matrices. Their thermal, physical, chemical and viscosity properties were assessed by differential scanning calorimetry, thermogravimetric analysis/derivative thermogravimetry, Fourier transform infrared spectroscopy, X-ray diffraction spectroscopy, and melt flow index. Drug dispersion was analyzed by scanning electron microscopy with electron dispersive X-ray spectroscopy, and drug release was evaluated by ultraviolet-visible spectroscopy. A thermal analysis indicated the conversion of the drug to its amorphous state. FTIR analysis endorsed the thermal studies pointing to a decrease in the drug’s crystallinity with the establishment of intermolecular interactions. XRD analysis confirmed the amorphous nature of Fen. MFI test revealed that PCL acts as a plasticizer when melt-processed with PEO. SEM images displayed irregular surfaces with voids and pores, while EDX spectra demonstrated a homogeneous drug distribution throughout the polymeric carrier. Dissolution testing revealed that PCL retards the drug release proportionally to the content of such polymer incorporated. These melt-extruded matrices showed that the drug release rate in a PEO/PCL blend can easily be tailored by altering the ratio of PCL to address the issues related to the multiple-dosing regimen of Fen in ruminants. MDPI 2022-10-06 /pmc/articles/PMC9573241/ /pubmed/36236135 http://dx.doi.org/10.3390/polym14194188 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bezerra, Gilberto S. N.
de Lima, Tielidy A. de M.
Colbert, Declan M.
Geever, Joseph
Geever, Luke
Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion
title Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion
title_full Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion
title_fullStr Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion
title_full_unstemmed Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion
title_short Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion
title_sort formulation and evaluation of fenbendazole extended-release extrudes processed by hot-melt extrusion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573241/
https://www.ncbi.nlm.nih.gov/pubmed/36236135
http://dx.doi.org/10.3390/polym14194188
work_keys_str_mv AT bezerragilbertosn formulationandevaluationoffenbendazoleextendedreleaseextrudesprocessedbyhotmeltextrusion
AT delimatielidyadem formulationandevaluationoffenbendazoleextendedreleaseextrudesprocessedbyhotmeltextrusion
AT colbertdeclanm formulationandevaluationoffenbendazoleextendedreleaseextrudesprocessedbyhotmeltextrusion
AT geeverjoseph formulationandevaluationoffenbendazoleextendedreleaseextrudesprocessedbyhotmeltextrusion
AT geeverluke formulationandevaluationoffenbendazoleextendedreleaseextrudesprocessedbyhotmeltextrusion