Cargando…
Formulation and evaluation of butenafine loaded PLGA-nanoparticulate laden chitosan nano gel
The present research work is designed to prepare and optimize butenafine (BT) loaded poly lactic co glycolic acid (PLGA) nanoparticles (BT-NPs). BT-NPs were prepared by emulsification probe sonication method using PLGA (A), PVA (B) as polymer and stabilizer, respectively. The optimum composition of...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8583856/ https://www.ncbi.nlm.nih.gov/pubmed/34747275 http://dx.doi.org/10.1080/10717544.2021.1995078 |
_version_ | 1784597305039519744 |
---|---|
author | Alshehri, Sultan Imam, Syed Sarim |
author_facet | Alshehri, Sultan Imam, Syed Sarim |
author_sort | Alshehri, Sultan |
collection | PubMed |
description | The present research work is designed to prepare and optimize butenafine (BT) loaded poly lactic co glycolic acid (PLGA) nanoparticles (BT-NPs). BT-NPs were prepared by emulsification probe sonication method using PLGA (A), PVA (B) as polymer and stabilizer, respectively. The optimum composition of BT-NPs was selected based on the point prediction method given by the Box Behnken design software. The optimized composition of BT-NPop showed a particle size of 267.21 ± 3.54 nm with an entrapment efficiency of 72.43 ± 3.11%. The optimum composition of BT-NPop was further converted into gel formulation using chitosan as a natural polymer. The prepared topical gel formulation (BT-NPopG) was further evaluated for gel characterization, drug release, permeation study, irritation, and antifungal studies. The prepared BT-NPopG formulation showed optimum pH, viscosity, spreadability, and drug content. The release and permeation study results revealed slow BT release (42.76 ± 2.87%) with significantly enhanced permeation across the egg membrane. The irritation study data showed negligible irritation with a cumulative score of 0.33. The antifungal study results conclude higher activity than marketed as well as pure BT. The overall conclusion of the results revealed BT-NPopG as an ideal delivery system to treat topical fungal infection. |
format | Online Article Text |
id | pubmed-8583856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-85838562021-11-12 Formulation and evaluation of butenafine loaded PLGA-nanoparticulate laden chitosan nano gel Alshehri, Sultan Imam, Syed Sarim Drug Deliv Research Article The present research work is designed to prepare and optimize butenafine (BT) loaded poly lactic co glycolic acid (PLGA) nanoparticles (BT-NPs). BT-NPs were prepared by emulsification probe sonication method using PLGA (A), PVA (B) as polymer and stabilizer, respectively. The optimum composition of BT-NPs was selected based on the point prediction method given by the Box Behnken design software. The optimized composition of BT-NPop showed a particle size of 267.21 ± 3.54 nm with an entrapment efficiency of 72.43 ± 3.11%. The optimum composition of BT-NPop was further converted into gel formulation using chitosan as a natural polymer. The prepared topical gel formulation (BT-NPopG) was further evaluated for gel characterization, drug release, permeation study, irritation, and antifungal studies. The prepared BT-NPopG formulation showed optimum pH, viscosity, spreadability, and drug content. The release and permeation study results revealed slow BT release (42.76 ± 2.87%) with significantly enhanced permeation across the egg membrane. The irritation study data showed negligible irritation with a cumulative score of 0.33. The antifungal study results conclude higher activity than marketed as well as pure BT. The overall conclusion of the results revealed BT-NPopG as an ideal delivery system to treat topical fungal infection. Taylor & Francis 2021-11-08 /pmc/articles/PMC8583856/ /pubmed/34747275 http://dx.doi.org/10.1080/10717544.2021.1995078 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Alshehri, Sultan Imam, Syed Sarim Formulation and evaluation of butenafine loaded PLGA-nanoparticulate laden chitosan nano gel |
title | Formulation and evaluation of butenafine loaded PLGA-nanoparticulate laden chitosan nano gel |
title_full | Formulation and evaluation of butenafine loaded PLGA-nanoparticulate laden chitosan nano gel |
title_fullStr | Formulation and evaluation of butenafine loaded PLGA-nanoparticulate laden chitosan nano gel |
title_full_unstemmed | Formulation and evaluation of butenafine loaded PLGA-nanoparticulate laden chitosan nano gel |
title_short | Formulation and evaluation of butenafine loaded PLGA-nanoparticulate laden chitosan nano gel |
title_sort | formulation and evaluation of butenafine loaded plga-nanoparticulate laden chitosan nano gel |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8583856/ https://www.ncbi.nlm.nih.gov/pubmed/34747275 http://dx.doi.org/10.1080/10717544.2021.1995078 |
work_keys_str_mv | AT alshehrisultan formulationandevaluationofbutenafineloadedplgananoparticulateladenchitosannanogel AT imamsyedsarim formulationandevaluationofbutenafineloadedplgananoparticulateladenchitosannanogel |