Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Pharmaceutical Sciences |
Texto Completo: | https://www.revistas.usp.br/bjps/article/view/181409 |
Resumo: | This study evaluated the incorporation of tetracaine into liposomes by RSM (Response Surface Methodology) and ANN (Artificial Neural Networks) based models. RCCD (rotational central composite design) and ANN were performed to optimize the sonication conditions of particles containing 100 % lipid. Laser light scattering was used to perform measure hydrodynamic radius and size distribution of vesicles. The liposomal formulations were analyzed by incorporating the drug into the hydrophilic phase or the lipophilic phase. RCCD and ANN were conducted, having the lipid/cholesterol ratio and concentration of tetracaine as variables investigated and, the encapsulation efficiency and mean diameter of the vesicles as response variables. The optimum sonication condition set at a power of 16 kHz and 3 minutes, resulting in sizes smaller than 800 nm. Maximum encapsulation efficiency (39.7 %) was obtained in the hydrophilic phase to a tetracaine concentration of 8.37 mg/mL and 79.5:20.5% lipid/cholesterol ratio. Liposomes were stable for about 30 days (at 4 °C), and the drug encapsulation efficiency was higher in the hydrophilic phase. The experimental results of RCCD-RSM and ANN techniques show ANN obtained more refined prediction errors that RCCD-RSM technique, therefore, ANN can be considered as an efficient mathematical method to characterize the incorporation of tetracaine into liposomes. |
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Brazilian Journal of Pharmaceutical Sciences |
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Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomesLocal anestheticsLiposomesResponse Surface MethodologyArtificial Neural NetworksThis study evaluated the incorporation of tetracaine into liposomes by RSM (Response Surface Methodology) and ANN (Artificial Neural Networks) based models. RCCD (rotational central composite design) and ANN were performed to optimize the sonication conditions of particles containing 100 % lipid. Laser light scattering was used to perform measure hydrodynamic radius and size distribution of vesicles. The liposomal formulations were analyzed by incorporating the drug into the hydrophilic phase or the lipophilic phase. RCCD and ANN were conducted, having the lipid/cholesterol ratio and concentration of tetracaine as variables investigated and, the encapsulation efficiency and mean diameter of the vesicles as response variables. The optimum sonication condition set at a power of 16 kHz and 3 minutes, resulting in sizes smaller than 800 nm. Maximum encapsulation efficiency (39.7 %) was obtained in the hydrophilic phase to a tetracaine concentration of 8.37 mg/mL and 79.5:20.5% lipid/cholesterol ratio. Liposomes were stable for about 30 days (at 4 °C), and the drug encapsulation efficiency was higher in the hydrophilic phase. The experimental results of RCCD-RSM and ANN techniques show ANN obtained more refined prediction errors that RCCD-RSM technique, therefore, ANN can be considered as an efficient mathematical method to characterize the incorporation of tetracaine into liposomes.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2020-12-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/18140910.1590/s2175-97902019000317808Brazilian Journal of Pharmaceutical Sciences; Vol. 56 (2020); e17808Brazilian Journal of Pharmaceutical Sciences; v. 56 (2020); e17808Brazilian Journal of Pharmaceutical Sciences; Vol. 56 (2020); e178082175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/181409/168343Copyright (c) 2020 Brazilian Journal of Pharmaceutical Scienceshttp://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessPereira, Ana Karina Vidal Barbosa, Raquel de Melo Fernandes, Marcelo Augusto Costa Finkler, Leandro Finkler, Christine Lamenha Luna 2021-06-12T19:46:54Zoai:revistas.usp.br:article/181409Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2021-06-12T19:46:54Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes |
title |
Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes |
spellingShingle |
Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes Pereira, Ana Karina Vidal Local anesthetics Liposomes Response Surface Methodology Artificial Neural Networks |
title_short |
Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes |
title_full |
Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes |
title_fullStr |
Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes |
title_full_unstemmed |
Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes |
title_sort |
Comparative analyses of response surface methodology and artificial neural networks on incorporating tetracaine into liposomes |
author |
Pereira, Ana Karina Vidal |
author_facet |
Pereira, Ana Karina Vidal Barbosa, Raquel de Melo Fernandes, Marcelo Augusto Costa Finkler, Leandro Finkler, Christine Lamenha Luna |
author_role |
author |
author2 |
Barbosa, Raquel de Melo Fernandes, Marcelo Augusto Costa Finkler, Leandro Finkler, Christine Lamenha Luna |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Pereira, Ana Karina Vidal Barbosa, Raquel de Melo Fernandes, Marcelo Augusto Costa Finkler, Leandro Finkler, Christine Lamenha Luna |
dc.subject.por.fl_str_mv |
Local anesthetics Liposomes Response Surface Methodology Artificial Neural Networks |
topic |
Local anesthetics Liposomes Response Surface Methodology Artificial Neural Networks |
description |
This study evaluated the incorporation of tetracaine into liposomes by RSM (Response Surface Methodology) and ANN (Artificial Neural Networks) based models. RCCD (rotational central composite design) and ANN were performed to optimize the sonication conditions of particles containing 100 % lipid. Laser light scattering was used to perform measure hydrodynamic radius and size distribution of vesicles. The liposomal formulations were analyzed by incorporating the drug into the hydrophilic phase or the lipophilic phase. RCCD and ANN were conducted, having the lipid/cholesterol ratio and concentration of tetracaine as variables investigated and, the encapsulation efficiency and mean diameter of the vesicles as response variables. The optimum sonication condition set at a power of 16 kHz and 3 minutes, resulting in sizes smaller than 800 nm. Maximum encapsulation efficiency (39.7 %) was obtained in the hydrophilic phase to a tetracaine concentration of 8.37 mg/mL and 79.5:20.5% lipid/cholesterol ratio. Liposomes were stable for about 30 days (at 4 °C), and the drug encapsulation efficiency was higher in the hydrophilic phase. The experimental results of RCCD-RSM and ANN techniques show ANN obtained more refined prediction errors that RCCD-RSM technique, therefore, ANN can be considered as an efficient mathematical method to characterize the incorporation of tetracaine into liposomes. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020-12-09 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/181409 10.1590/s2175-97902019000317808 |
url |
https://www.revistas.usp.br/bjps/article/view/181409 |
identifier_str_mv |
10.1590/s2175-97902019000317808 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/bjps/article/view/181409/168343 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2020 Brazilian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2020 Brazilian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Ciências Farmacêuticas |
dc.source.none.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences; Vol. 56 (2020); e17808 Brazilian Journal of Pharmaceutical Sciences; v. 56 (2020); e17808 Brazilian Journal of Pharmaceutical Sciences; Vol. 56 (2020); e17808 2175-9790 1984-8250 reponame:Brazilian Journal of Pharmaceutical Sciences instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Brazilian Journal of Pharmaceutical Sciences |
collection |
Brazilian Journal of Pharmaceutical Sciences |
repository.name.fl_str_mv |
Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
bjps@usp.br||elizabeth.igne@gmail.com |
_version_ |
1800222915057156096 |