Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.xphs.2018.10.007 http://hdl.handle.net/11449/189931 |
Resumo: | According to the most recent World Health Organization statistics, malaria infected approximately 219 million people in 2017, with an estimate of 435,000 deaths (World Health Organization, 2018). Communities isolated from cities are the most deprived of access to the necessary hospital facilities. Herein we report the development of a transdermal bioadhesive containing artemether (ART), an alternative, potentially lifesaving, treatment regimen for malaria in low-resource settings. Bioadhesives were prepared from an aqueous blend of hydroxyethylcellulose (4.5% w/w), ART, propoxylated-ethoxylated-cetyl-alcohol, polysorbate 80, propyleneglycol, glycerine, mineral oil, and oleic acid. In this study, the average pore size of bioadhesive 5.5b was 52.6 ± 15.31 μm. Differential scanning calorimetry and thermogravimetric analyses confirm the thermal stability of ART bioadhesives at room temperature. Tensile tests indicated good mechanical properties for bioadhesive 5.5b, when compared to 5.5a, where 5.5b showed elastic modulus 0.19 MPa, elongation at break 204%, tensile stress 0.31 MPa, tensile strength at break 0.23 MPa. Bioadhesion assays suggested that formulations containing surfactants had higher detachment forces. Permeation studies demonstrated that the best outcome was achieved with a bioadhesive containing 25 mg ART (5.5b) that after 24 h released 6971 ± 125 μg, which represents approximately 28% of drug permeation. Data reported presents a promising candidate for a new antimalarial transdermal formulation. |
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Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in ChildrenartemetherbioadhesiveshydroxyethylcellulosemalariaPlasmodium falciparumAccording to the most recent World Health Organization statistics, malaria infected approximately 219 million people in 2017, with an estimate of 435,000 deaths (World Health Organization, 2018). Communities isolated from cities are the most deprived of access to the necessary hospital facilities. Herein we report the development of a transdermal bioadhesive containing artemether (ART), an alternative, potentially lifesaving, treatment regimen for malaria in low-resource settings. Bioadhesives were prepared from an aqueous blend of hydroxyethylcellulose (4.5% w/w), ART, propoxylated-ethoxylated-cetyl-alcohol, polysorbate 80, propyleneglycol, glycerine, mineral oil, and oleic acid. In this study, the average pore size of bioadhesive 5.5b was 52.6 ± 15.31 μm. Differential scanning calorimetry and thermogravimetric analyses confirm the thermal stability of ART bioadhesives at room temperature. Tensile tests indicated good mechanical properties for bioadhesive 5.5b, when compared to 5.5a, where 5.5b showed elastic modulus 0.19 MPa, elongation at break 204%, tensile stress 0.31 MPa, tensile strength at break 0.23 MPa. Bioadhesion assays suggested that formulations containing surfactants had higher detachment forces. Permeation studies demonstrated that the best outcome was achieved with a bioadhesive containing 25 mg ART (5.5b) that after 24 h released 6971 ± 125 μg, which represents approximately 28% of drug permeation. Data reported presents a promising candidate for a new antimalarial transdermal formulation.Graduate School of Bioscience and Technology of Bioactive Products Biology Institute University of CampinasSchool of Pharmacy Queen's University BelfastCentro Pluridisciplinar de Pesquisas Químicas Biológicas e AgrícolasDepartamento de Botânica Instituto de Biociências Universidade de São PauloUNESP-Univ Estadual Paulista Faculdade de Ciências FarmacêuticasSchool of Mechanical Engineering University of CampinasUniversity of CalabarUNESP-Univ Estadual Paulista Instituto de BiociênciasFaculty of Pharmaceutical Science University at CampinasUNESP-Univ Estadual Paulista Faculdade de Ciências FarmacêuticasUNESP-Univ Estadual Paulista Instituto de BiociênciasUniversidade Estadual de Campinas (UNICAMP)Queen's University BelfastBiológicas e AgrícolasUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)University of CalabarUniversity at CampinasVolpe Zanutto, FabianaMcAlister, EmmaMarucci Pereira Tangerina, MarceloFonseca-Santos, Bruno [UNESP]Costa Salles, Taís HelenaOliveira Souza, Ilza MariaBrisibe, AndiVilegas, Wagner [UNESP]Chorilli, Marlus [UNESP]Akira d’Ávila, MarcosDonnelly, Ryan F.Foglio, Mary Ann2019-10-06T16:56:54Z2019-10-06T16:56:54Z2019-03-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1177-1188http://dx.doi.org/10.1016/j.xphs.2018.10.007Journal of Pharmaceutical Sciences, v. 108, n. 3, p. 1177-1188, 2019.1520-60170022-3549http://hdl.handle.net/11449/18993110.1016/j.xphs.2018.10.0072-s2.0-850574460651427125996716282Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Pharmaceutical Sciencesinfo:eu-repo/semantics/openAccess2024-06-24T13:46:23Zoai:repositorio.unesp.br:11449/189931Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:59:06.267542Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children |
title |
Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children |
spellingShingle |
Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children Volpe Zanutto, Fabiana artemether bioadhesives hydroxyethylcellulose malaria Plasmodium falciparum |
title_short |
Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children |
title_full |
Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children |
title_fullStr |
Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children |
title_full_unstemmed |
Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children |
title_sort |
Semisynthetic Derivative of Artemisia annua-Loaded Transdermal Bioadhesive for the Treatment of Uncomplicated Malaria Caused by Plasmodium falciparum in Children |
author |
Volpe Zanutto, Fabiana |
author_facet |
Volpe Zanutto, Fabiana McAlister, Emma Marucci Pereira Tangerina, Marcelo Fonseca-Santos, Bruno [UNESP] Costa Salles, Taís Helena Oliveira Souza, Ilza Maria Brisibe, Andi Vilegas, Wagner [UNESP] Chorilli, Marlus [UNESP] Akira d’Ávila, Marcos Donnelly, Ryan F. Foglio, Mary Ann |
author_role |
author |
author2 |
McAlister, Emma Marucci Pereira Tangerina, Marcelo Fonseca-Santos, Bruno [UNESP] Costa Salles, Taís Helena Oliveira Souza, Ilza Maria Brisibe, Andi Vilegas, Wagner [UNESP] Chorilli, Marlus [UNESP] Akira d’Ávila, Marcos Donnelly, Ryan F. Foglio, Mary Ann |
author2_role |
author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Campinas (UNICAMP) Queen's University Belfast Biológicas e Agrícolas Universidade de São Paulo (USP) Universidade Estadual Paulista (Unesp) University of Calabar University at Campinas |
dc.contributor.author.fl_str_mv |
Volpe Zanutto, Fabiana McAlister, Emma Marucci Pereira Tangerina, Marcelo Fonseca-Santos, Bruno [UNESP] Costa Salles, Taís Helena Oliveira Souza, Ilza Maria Brisibe, Andi Vilegas, Wagner [UNESP] Chorilli, Marlus [UNESP] Akira d’Ávila, Marcos Donnelly, Ryan F. Foglio, Mary Ann |
dc.subject.por.fl_str_mv |
artemether bioadhesives hydroxyethylcellulose malaria Plasmodium falciparum |
topic |
artemether bioadhesives hydroxyethylcellulose malaria Plasmodium falciparum |
description |
According to the most recent World Health Organization statistics, malaria infected approximately 219 million people in 2017, with an estimate of 435,000 deaths (World Health Organization, 2018). Communities isolated from cities are the most deprived of access to the necessary hospital facilities. Herein we report the development of a transdermal bioadhesive containing artemether (ART), an alternative, potentially lifesaving, treatment regimen for malaria in low-resource settings. Bioadhesives were prepared from an aqueous blend of hydroxyethylcellulose (4.5% w/w), ART, propoxylated-ethoxylated-cetyl-alcohol, polysorbate 80, propyleneglycol, glycerine, mineral oil, and oleic acid. In this study, the average pore size of bioadhesive 5.5b was 52.6 ± 15.31 μm. Differential scanning calorimetry and thermogravimetric analyses confirm the thermal stability of ART bioadhesives at room temperature. Tensile tests indicated good mechanical properties for bioadhesive 5.5b, when compared to 5.5a, where 5.5b showed elastic modulus 0.19 MPa, elongation at break 204%, tensile stress 0.31 MPa, tensile strength at break 0.23 MPa. Bioadhesion assays suggested that formulations containing surfactants had higher detachment forces. Permeation studies demonstrated that the best outcome was achieved with a bioadhesive containing 25 mg ART (5.5b) that after 24 h released 6971 ± 125 μg, which represents approximately 28% of drug permeation. Data reported presents a promising candidate for a new antimalarial transdermal formulation. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-10-06T16:56:54Z 2019-10-06T16:56:54Z 2019-03-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.xphs.2018.10.007 Journal of Pharmaceutical Sciences, v. 108, n. 3, p. 1177-1188, 2019. 1520-6017 0022-3549 http://hdl.handle.net/11449/189931 10.1016/j.xphs.2018.10.007 2-s2.0-85057446065 1427125996716282 |
url |
http://dx.doi.org/10.1016/j.xphs.2018.10.007 http://hdl.handle.net/11449/189931 |
identifier_str_mv |
Journal of Pharmaceutical Sciences, v. 108, n. 3, p. 1177-1188, 2019. 1520-6017 0022-3549 10.1016/j.xphs.2018.10.007 2-s2.0-85057446065 1427125996716282 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Pharmaceutical Sciences |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1177-1188 |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129380936843264 |