Cargando…
Development of Risperidone PLGA Microspheres
The aim of this study was to design and evaluate biodegradable PLGA microspheres for sustained delivery of Risperidone, with an eventual goal of avoiding combination therapy for the treatment of schizophrenia. Two PLGA copolymers (50 : 50 and 75 : 25) were used to prepare four microsphere formulatio...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927762/ https://www.ncbi.nlm.nih.gov/pubmed/24616812 http://dx.doi.org/10.1155/2014/620464 |
_version_ | 1782304173965967360 |
---|---|
author | D'Souza, Susan Faraj, Jabar A. Giovagnoli, Stefano DeLuca, Patrick P. |
author_facet | D'Souza, Susan Faraj, Jabar A. Giovagnoli, Stefano DeLuca, Patrick P. |
author_sort | D'Souza, Susan |
collection | PubMed |
description | The aim of this study was to design and evaluate biodegradable PLGA microspheres for sustained delivery of Risperidone, with an eventual goal of avoiding combination therapy for the treatment of schizophrenia. Two PLGA copolymers (50 : 50 and 75 : 25) were used to prepare four microsphere formulations of Risperidone. The microspheres were characterized by several in vitro techniques. In vivo studies in male Sprague-Dawley rats at 20 and 40 mg/kg doses revealed that all formulations exhibited an initial burst followed by sustained release of the active moiety. Additionally, formulations prepared with 50 : 50 PLGA had a shorter duration of action and lower cumulative AUC levels than the 75 : 25 PLGA microspheres. A simulation of multiple dosing at weekly or 15-day regimen revealed pulsatile behavior for all formulations with steady state being achieved by the second dose. Overall, the clinical use of Formulations A, B, C, or D will eliminate the need for combination oral therapy and reduce time to achieve steady state, with a smaller washout period upon cessation of therapy. Results of this study prove the suitability of using PLGA copolymers of varying composition and molecular weight to develop sustained release formulations that can tailor in vivo behavior and enhance pharmacological effectiveness of the drug. |
format | Online Article Text |
id | pubmed-3927762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-39277622014-03-10 Development of Risperidone PLGA Microspheres D'Souza, Susan Faraj, Jabar A. Giovagnoli, Stefano DeLuca, Patrick P. J Drug Deliv Research Article The aim of this study was to design and evaluate biodegradable PLGA microspheres for sustained delivery of Risperidone, with an eventual goal of avoiding combination therapy for the treatment of schizophrenia. Two PLGA copolymers (50 : 50 and 75 : 25) were used to prepare four microsphere formulations of Risperidone. The microspheres were characterized by several in vitro techniques. In vivo studies in male Sprague-Dawley rats at 20 and 40 mg/kg doses revealed that all formulations exhibited an initial burst followed by sustained release of the active moiety. Additionally, formulations prepared with 50 : 50 PLGA had a shorter duration of action and lower cumulative AUC levels than the 75 : 25 PLGA microspheres. A simulation of multiple dosing at weekly or 15-day regimen revealed pulsatile behavior for all formulations with steady state being achieved by the second dose. Overall, the clinical use of Formulations A, B, C, or D will eliminate the need for combination oral therapy and reduce time to achieve steady state, with a smaller washout period upon cessation of therapy. Results of this study prove the suitability of using PLGA copolymers of varying composition and molecular weight to develop sustained release formulations that can tailor in vivo behavior and enhance pharmacological effectiveness of the drug. Hindawi Publishing Corporation 2014 2014-01-28 /pmc/articles/PMC3927762/ /pubmed/24616812 http://dx.doi.org/10.1155/2014/620464 Text en Copyright © 2014 Susan D'Souza et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article D'Souza, Susan Faraj, Jabar A. Giovagnoli, Stefano DeLuca, Patrick P. Development of Risperidone PLGA Microspheres |
title | Development of Risperidone PLGA Microspheres |
title_full | Development of Risperidone PLGA Microspheres |
title_fullStr | Development of Risperidone PLGA Microspheres |
title_full_unstemmed | Development of Risperidone PLGA Microspheres |
title_short | Development of Risperidone PLGA Microspheres |
title_sort | development of risperidone plga microspheres |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927762/ https://www.ncbi.nlm.nih.gov/pubmed/24616812 http://dx.doi.org/10.1155/2014/620464 |
work_keys_str_mv | AT dsouzasusan developmentofrisperidoneplgamicrospheres AT farajjabara developmentofrisperidoneplgamicrospheres AT giovagnolistefano developmentofrisperidoneplgamicrospheres AT delucapatrickp developmentofrisperidoneplgamicrospheres |