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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...

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Autores principales: D'Souza, Susan, Faraj, Jabar A., Giovagnoli, Stefano, DeLuca, Patrick P.
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
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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.
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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
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