Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets
This study focuses on the combination of three-dimensional printing (3DP) and amorphous solid dispersion (ASD) technologies for the manufacturing of gastroretentive floating tablets. Employing hot melt extrusion (HME) and fused deposition modeling (FDM), the study investigates the development of dru...
| Autores: | , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2024 |
| País: | España |
| Institución: | Universidad de Sevilla (US) |
| Repositorio: | idUS. Depósito de Investigación de la Universidad de Sevilla |
| OAI Identifier: | oai:idus.us.es:11441/165146 |
| Acceso en línea: | https://hdl.handle.net/11441/165146 https://doi.org/10.1016/j.ijpharm.2024.124215 |
| Access Level: | acceso abierto |
| Palabra clave: | 3D printing Amorphous solid dispersion Drug-loaded filaments Fused deposition modeling Gastroretentive floating tablets Zero-order release |
| id |
ES_2d810b0df4e70341c4e893597950471d |
|---|---|
| oai_identifier_str |
oai:idus.us.es:11441/165146 |
| network_acronym_str |
ES |
| network_name_str |
España |
| repository_id_str |
|
| spelling |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating TabletsMora Castaño, GloriaMillán Jiménez, MónicaNiederquell, AndreasSchonenberger, MonicaShojaie, FatemehKuentz, MartinCaraballo Rodríguez, Isidoro3D printingAmorphous solid dispersionDrug-loaded filamentsFused deposition modelingGastroretentive floating tabletsZero-order releaseThis study focuses on the combination of three-dimensional printing (3DP) and amorphous solid dispersion (ASD) technologies for the manufacturing of gastroretentive floating tablets. Employing hot melt extrusion (HME) and fused deposition modeling (FDM), the study investigates the development of drug-loaded filaments and 3D printed (3DP) tablets containing felodipine as model drug and hydroxypropyl methylcellulose (HPMC) as the polymeric carrier. Prior to fabrication, solubility parameter estimation and molecular dynamics simulations were applied to predict drug-polymer interactions, which are crucial for ASD formation. Physical bulk and surface characterization complemented the quality control of both drug-loaded filaments and 3DP tablets. The analysis confirmed a successful amorphous dispersion of felodipine within the polymeric matrix. Furthermore, the low infill percentage and enclosed design of the 3DP tablet allowed for obtaining low-density systems. This structure resulted in buoyancy during the entire drug release process until a complete dissolution of the 3DP tablets (more than 8 h) was attained. The particular design made it possible for a single polymer to achieve a zero-order controlled release of the drug, which is considered the ideal kinetics for a gastroretentive system. Accordingly, this study can be seen as an advancement in ASD formulation for 3DP technology within pharmaceutics.Ministerio de Ciencia e Innovación RTI2018-095041-B-C31Junta de Andalucía US-1380923Ministerio de Ciencia, Innovación y Universidades FPU18/05665, EST22/00038Premio Mensual Publicación Científica Destacada de la US. Facultad de FarmaciaElsevierFarmacia y Tecnología FarmacéuticaMinisterio de Ciencia e Innovación (MICIN). EspañaJunta de AndalucíaMinisterio de Ciencia, Innovación y Universidades (MICINN). España2024info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttps://hdl.handle.net/11441/165146https://doi.org/10.1016/j.ijpharm.2024.124215reponame:idUS. Depósito de Investigación de la Universidad de Sevillainstname:Universidad de Sevilla (US)InglésInternational Journal of Pharmaceutics, 658, 124215.RTI2018-095041-B-C31US-1380923FPU18/05665EST22/00038https://doi.org/10.1016/j.ijpharm.2024.124215info:eu-repo/semantics/openAccessoai:idus.us.es:11441/1651462026-06-17T12:51:07Z |
| dc.title.none.fl_str_mv |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets |
| title |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets |
| spellingShingle |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets Mora Castaño, Gloria 3D printing Amorphous solid dispersion Drug-loaded filaments Fused deposition modeling Gastroretentive floating tablets Zero-order release |
| title_short |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets |
| title_full |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets |
| title_fullStr |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets |
| title_full_unstemmed |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets |
| title_sort |
Amorphous Solid Dispersion of a Binary Formulation with Felodipine and HPMC for 3D Printed Floating Tablets |
| dc.creator.none.fl_str_mv |
Mora Castaño, Gloria Millán Jiménez, Mónica Niederquell, Andreas Schonenberger, Monica Shojaie, Fatemeh Kuentz, Martin Caraballo Rodríguez, Isidoro |
| author |
Mora Castaño, Gloria |
| author_facet |
Mora Castaño, Gloria Millán Jiménez, Mónica Niederquell, Andreas Schonenberger, Monica Shojaie, Fatemeh Kuentz, Martin Caraballo Rodríguez, Isidoro |
| author_role |
author |
| author2 |
Millán Jiménez, Mónica Niederquell, Andreas Schonenberger, Monica Shojaie, Fatemeh Kuentz, Martin Caraballo Rodríguez, Isidoro |
| author2_role |
author author author author author author |
| dc.contributor.none.fl_str_mv |
Farmacia y Tecnología Farmacéutica Ministerio de Ciencia e Innovación (MICIN). España Junta de Andalucía Ministerio de Ciencia, Innovación y Universidades (MICINN). España |
| dc.subject.none.fl_str_mv |
3D printing Amorphous solid dispersion Drug-loaded filaments Fused deposition modeling Gastroretentive floating tablets Zero-order release |
| topic |
3D printing Amorphous solid dispersion Drug-loaded filaments Fused deposition modeling Gastroretentive floating tablets Zero-order release |
| description |
This study focuses on the combination of three-dimensional printing (3DP) and amorphous solid dispersion (ASD) technologies for the manufacturing of gastroretentive floating tablets. Employing hot melt extrusion (HME) and fused deposition modeling (FDM), the study investigates the development of drug-loaded filaments and 3D printed (3DP) tablets containing felodipine as model drug and hydroxypropyl methylcellulose (HPMC) as the polymeric carrier. Prior to fabrication, solubility parameter estimation and molecular dynamics simulations were applied to predict drug-polymer interactions, which are crucial for ASD formation. Physical bulk and surface characterization complemented the quality control of both drug-loaded filaments and 3DP tablets. The analysis confirmed a successful amorphous dispersion of felodipine within the polymeric matrix. Furthermore, the low infill percentage and enclosed design of the 3DP tablet allowed for obtaining low-density systems. This structure resulted in buoyancy during the entire drug release process until a complete dissolution of the 3DP tablets (more than 8 h) was attained. The particular design made it possible for a single polymer to achieve a zero-order controlled release of the drug, which is considered the ideal kinetics for a gastroretentive system. Accordingly, this study can be seen as an advancement in ASD formulation for 3DP technology within pharmaceutics. |
| publishDate |
2024 |
| dc.date.none.fl_str_mv |
2024 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/11441/165146 https://doi.org/10.1016/j.ijpharm.2024.124215 |
| url |
https://hdl.handle.net/11441/165146 https://doi.org/10.1016/j.ijpharm.2024.124215 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
International Journal of Pharmaceutics, 658, 124215. RTI2018-095041-B-C31 US-1380923 FPU18/05665 EST22/00038 https://doi.org/10.1016/j.ijpharm.2024.124215 |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf application/pdf |
| dc.publisher.none.fl_str_mv |
Elsevier |
| publisher.none.fl_str_mv |
Elsevier |
| dc.source.none.fl_str_mv |
reponame:idUS. Depósito de Investigación de la Universidad de Sevilla instname:Universidad de Sevilla (US) |
| instname_str |
Universidad de Sevilla (US) |
| reponame_str |
idUS. Depósito de Investigación de la Universidad de Sevilla |
| collection |
idUS. Depósito de Investigación de la Universidad de Sevilla |
| repository.name.fl_str_mv |
|
| repository.mail.fl_str_mv |
|
| _version_ |
1869405325131513856 |
| score |
15.811543 |