Cargando…

Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release

In this study, gellan gum (GG), a natural polysaccharide, was used to fabricate spherical porous beads suitable as sustained drug delivery systems for oral administration. GG was cross-linked with calcium ions to prepare polymeric beads. Rheological studies and preliminary experiments of beads prepa...

Descripción completa

Detalles Bibliográficos
Autores principales: Adrover, Alessandra, Paolicelli, Patrizia, Petralito, Stefania, Di Muzio, Laura, Trilli, Jordan, Cesa, Stefania, Tho, Ingunn, Casadei, Maria Antonietta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523394/
https://www.ncbi.nlm.nih.gov/pubmed/30999609
http://dx.doi.org/10.3390/pharmaceutics11040187
_version_ 1783419324152676352
author Adrover, Alessandra
Paolicelli, Patrizia
Petralito, Stefania
Di Muzio, Laura
Trilli, Jordan
Cesa, Stefania
Tho, Ingunn
Casadei, Maria Antonietta
author_facet Adrover, Alessandra
Paolicelli, Patrizia
Petralito, Stefania
Di Muzio, Laura
Trilli, Jordan
Cesa, Stefania
Tho, Ingunn
Casadei, Maria Antonietta
author_sort Adrover, Alessandra
collection PubMed
description In this study, gellan gum (GG), a natural polysaccharide, was used to fabricate spherical porous beads suitable as sustained drug delivery systems for oral administration. GG was cross-linked with calcium ions to prepare polymeric beads. Rheological studies and preliminary experiments of beads preparation allowed to identify the GG and the CaCl(2) concentrations suitable for obtaining stable and spherical particles. GG beads were formed, through ionotropic gelation technique, with and without the presence of the synthetic clay laponite. The resultant beads were analyzed for dimensions (before and after freeze-drying), morphological aspects and ability to swell in different media miming biological fluids, namely SGF (Simulated Gastric Fluid, HCl 0.1 M) and SIF (Simulated Intestinal Fluid, phosphate buffer, 0.044 M, pH 7.4). The swelling degree was lower in SGF than in SIF and further reduced in the presence of laponite. The GG and GG-layered silicate composite beads were loaded with two model drugs having different molecular weight, namely theophylline and cyanocobalamin (vitamin B12) and subjected to in-vitro release studies in SGF and SIF. The presence of laponite in the bead formulation increased the drug entrapment efficiency and slowed-down the release kinetics of both drugs in the gastric environment. A moving-boundary swelling model with “diffuse” glassy-rubbery interface was proposed in order to describe the swelling behavior of porous freeze-dried beads. Consistently with the swelling model adopted, two moving-boundary drug release models were developed to interpret release data from highly porous beads of different drugs: drug molecules, e.g., theophylline, that exhibit a typical Fickian behavior of release curves and drugs, such as vitamin B12, whose release curves are affected by the physical/chemical interaction of the drug with the polymer/clay complex. Theoretical results support the experimental observations, thus confirming that laponite may be an effective additive for fabricating sustained drug delivery systems.
format Online
Article
Text
id pubmed-6523394
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-65233942019-06-04 Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release Adrover, Alessandra Paolicelli, Patrizia Petralito, Stefania Di Muzio, Laura Trilli, Jordan Cesa, Stefania Tho, Ingunn Casadei, Maria Antonietta Pharmaceutics Article In this study, gellan gum (GG), a natural polysaccharide, was used to fabricate spherical porous beads suitable as sustained drug delivery systems for oral administration. GG was cross-linked with calcium ions to prepare polymeric beads. Rheological studies and preliminary experiments of beads preparation allowed to identify the GG and the CaCl(2) concentrations suitable for obtaining stable and spherical particles. GG beads were formed, through ionotropic gelation technique, with and without the presence of the synthetic clay laponite. The resultant beads were analyzed for dimensions (before and after freeze-drying), morphological aspects and ability to swell in different media miming biological fluids, namely SGF (Simulated Gastric Fluid, HCl 0.1 M) and SIF (Simulated Intestinal Fluid, phosphate buffer, 0.044 M, pH 7.4). The swelling degree was lower in SGF than in SIF and further reduced in the presence of laponite. The GG and GG-layered silicate composite beads were loaded with two model drugs having different molecular weight, namely theophylline and cyanocobalamin (vitamin B12) and subjected to in-vitro release studies in SGF and SIF. The presence of laponite in the bead formulation increased the drug entrapment efficiency and slowed-down the release kinetics of both drugs in the gastric environment. A moving-boundary swelling model with “diffuse” glassy-rubbery interface was proposed in order to describe the swelling behavior of porous freeze-dried beads. Consistently with the swelling model adopted, two moving-boundary drug release models were developed to interpret release data from highly porous beads of different drugs: drug molecules, e.g., theophylline, that exhibit a typical Fickian behavior of release curves and drugs, such as vitamin B12, whose release curves are affected by the physical/chemical interaction of the drug with the polymer/clay complex. Theoretical results support the experimental observations, thus confirming that laponite may be an effective additive for fabricating sustained drug delivery systems. MDPI 2019-04-17 /pmc/articles/PMC6523394/ /pubmed/30999609 http://dx.doi.org/10.3390/pharmaceutics11040187 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Adrover, Alessandra
Paolicelli, Patrizia
Petralito, Stefania
Di Muzio, Laura
Trilli, Jordan
Cesa, Stefania
Tho, Ingunn
Casadei, Maria Antonietta
Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release
title Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release
title_full Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release
title_fullStr Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release
title_full_unstemmed Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release
title_short Gellan Gum/Laponite Beads for the Modified Release of Drugs: Experimental and Modeling Study of Gastrointestinal Release
title_sort gellan gum/laponite beads for the modified release of drugs: experimental and modeling study of gastrointestinal release
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523394/
https://www.ncbi.nlm.nih.gov/pubmed/30999609
http://dx.doi.org/10.3390/pharmaceutics11040187
work_keys_str_mv AT adroveralessandra gellangumlaponitebeadsforthemodifiedreleaseofdrugsexperimentalandmodelingstudyofgastrointestinalrelease
AT paolicellipatrizia gellangumlaponitebeadsforthemodifiedreleaseofdrugsexperimentalandmodelingstudyofgastrointestinalrelease
AT petralitostefania gellangumlaponitebeadsforthemodifiedreleaseofdrugsexperimentalandmodelingstudyofgastrointestinalrelease
AT dimuziolaura gellangumlaponitebeadsforthemodifiedreleaseofdrugsexperimentalandmodelingstudyofgastrointestinalrelease
AT trillijordan gellangumlaponitebeadsforthemodifiedreleaseofdrugsexperimentalandmodelingstudyofgastrointestinalrelease
AT cesastefania gellangumlaponitebeadsforthemodifiedreleaseofdrugsexperimentalandmodelingstudyofgastrointestinalrelease
AT thoingunn gellangumlaponitebeadsforthemodifiedreleaseofdrugsexperimentalandmodelingstudyofgastrointestinalrelease
AT casadeimariaantonietta gellangumlaponitebeadsforthemodifiedreleaseofdrugsexperimentalandmodelingstudyofgastrointestinalrelease