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Optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design

The objective of this study was to examine extensively the influences of formulation and process variables on the microparticles. The microparticles were generated by the spray-drying technique using polymer chitosan, mannitol along with L-leucine. The effects of various experimental parameters such...

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Detalles Bibliográficos
Autores principales: Patel, P. V., Soni, T. G., Thakkar, V. T., Gandhi, T. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467832/
https://www.ncbi.nlm.nih.gov/pubmed/23066204
http://dx.doi.org/10.4103/0975-7406.94136
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author Patel, P. V.
Soni, T. G.
Thakkar, V. T.
Gandhi, T. R.
author_facet Patel, P. V.
Soni, T. G.
Thakkar, V. T.
Gandhi, T. R.
author_sort Patel, P. V.
collection PubMed
description The objective of this study was to examine extensively the influences of formulation and process variables on the microparticles. The microparticles were generated by the spray-drying technique using polymer chitosan, mannitol along with L-leucine. The effects of various experimental parameters such as polymer concentration, inlet temperature, and feed flow rate on particle size and production yields were evaluated by means of experimental box-behnken design. Multiple regression analysis was carried out and response surfaces were obtained. Optimized formulation and check points batches were selected by feasibility and grid search. Experimental design it was evaluated that inlet temperature and polymer concentration influence on the production yield. Feed flow rate impact on particle size. Results showed that spray drying technique yield 985 to 4060 nm indicate micro size range and production yield was found in between 27.01-52.96%. The selection of appropriate parameters yielded spray-dried microparticles characterized by narrow dimensional distribution. In our present work, prepared microparticles using the spray-drying technique and systematically estimated their feasibility for the pulmonary delivery of microparticles by careful investigations of their characteristics and aerosolization properties. Spray drying technique yield optimum size for deposition beyond the narrow airway into the alveoli and suitable for respiratory deposition.
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spelling pubmed-34678322012-10-12 Optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design Patel, P. V. Soni, T. G. Thakkar, V. T. Gandhi, T. R. J Pharm Bioallied Sci Original/Brief The objective of this study was to examine extensively the influences of formulation and process variables on the microparticles. The microparticles were generated by the spray-drying technique using polymer chitosan, mannitol along with L-leucine. The effects of various experimental parameters such as polymer concentration, inlet temperature, and feed flow rate on particle size and production yields were evaluated by means of experimental box-behnken design. Multiple regression analysis was carried out and response surfaces were obtained. Optimized formulation and check points batches were selected by feasibility and grid search. Experimental design it was evaluated that inlet temperature and polymer concentration influence on the production yield. Feed flow rate impact on particle size. Results showed that spray drying technique yield 985 to 4060 nm indicate micro size range and production yield was found in between 27.01-52.96%. The selection of appropriate parameters yielded spray-dried microparticles characterized by narrow dimensional distribution. In our present work, prepared microparticles using the spray-drying technique and systematically estimated their feasibility for the pulmonary delivery of microparticles by careful investigations of their characteristics and aerosolization properties. Spray drying technique yield optimum size for deposition beyond the narrow airway into the alveoli and suitable for respiratory deposition. Medknow Publications & Media Pvt Ltd 2012-03 /pmc/articles/PMC3467832/ /pubmed/23066204 http://dx.doi.org/10.4103/0975-7406.94136 Text en Copyright: © Journal of Pharmacy and Bioallied Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original/Brief
Patel, P. V.
Soni, T. G.
Thakkar, V. T.
Gandhi, T. R.
Optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design
title Optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design
title_full Optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design
title_fullStr Optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design
title_full_unstemmed Optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design
title_short Optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design
title_sort optimization of the experimental parameters of fluticasone propionate microparticles for pulmonary delivery using a box behenken design
topic Original/Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3467832/
https://www.ncbi.nlm.nih.gov/pubmed/23066204
http://dx.doi.org/10.4103/0975-7406.94136
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