Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process

Detalhes bibliográficos
Autor(a) principal: Oliveira, Rafaela Santos de
Data de Publicação: 2023
Outros Autores: Funk, Nadine Lysyk, Santos, Juliana dos, Oliveira, Thayse Viana de, Oliveira, Edilene Gadelha de, Petzhold, Cesar Liberato, Benvenutti, Edilson Valmir, Deon, Monique, Beck, Ruy Carlos Ruver
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/264095
Resumo: The alliance between 3D printing and nanomaterials brings versatile properties to pharmaceuticals, but few studies have explored this approach in the development of skin delivery formulations. In this study, clobetasol propionate (CP) was loaded (about 25% w/w) in mesoporous silica nanomaterial (MSN) to formulate novel bioadhesive and hydrophilic skin delivery films composed of pectin (5% w/v) and carboxymethylcellulose (5% w/v) by 3D printing. As a hydrophobic model drug, CP was encapsulated in MSN at a 3:1 (w/w) ratio, resulting in a decrease of CP crystallinity and an increase of its dissolution efficiency after 72 h (65.70 6.52%) as compared to CP dispersion (40.79 4.75%), explained by its partial change to an amorphous form. The CP-loaded MSN was incorporated in an innovative hydrophilic 3D-printable ink composed of carboxymethylcellulose and pectin (1:1, w/w), which showed high tensile strength (3.613 0.38 N, a homogenous drug dose (0.48 0.032 mg/g per film) and complete CP release after 10 h. Moreover, the presence of pectin in the ink increased the skin adhesion of the films (work of adhesion of 782 105 mN mm). Therefore, the alliance between MSN and the novel printable ink composed of carboxymethylcellulose and pectin represents a new platform for the production of 3D-printed bioadhesive films, opening a new era in the development of skin delivery systems.
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spelling Oliveira, Rafaela Santos deFunk, Nadine LysykSantos, Juliana dosOliveira, Thayse Viana deOliveira, Edilene Gadelha dePetzhold, Cesar LiberatoBenvenutti, Edilson ValmirDeon, MoniqueBeck, Ruy Carlos Ruver2023-08-30T03:59:59Z20231999-4923http://hdl.handle.net/10183/264095001170129The alliance between 3D printing and nanomaterials brings versatile properties to pharmaceuticals, but few studies have explored this approach in the development of skin delivery formulations. In this study, clobetasol propionate (CP) was loaded (about 25% w/w) in mesoporous silica nanomaterial (MSN) to formulate novel bioadhesive and hydrophilic skin delivery films composed of pectin (5% w/v) and carboxymethylcellulose (5% w/v) by 3D printing. As a hydrophobic model drug, CP was encapsulated in MSN at a 3:1 (w/w) ratio, resulting in a decrease of CP crystallinity and an increase of its dissolution efficiency after 72 h (65.70 6.52%) as compared to CP dispersion (40.79 4.75%), explained by its partial change to an amorphous form. The CP-loaded MSN was incorporated in an innovative hydrophilic 3D-printable ink composed of carboxymethylcellulose and pectin (1:1, w/w), which showed high tensile strength (3.613 0.38 N, a homogenous drug dose (0.48 0.032 mg/g per film) and complete CP release after 10 h. Moreover, the presence of pectin in the ink increased the skin adhesion of the films (work of adhesion of 782 105 mN mm). Therefore, the alliance between MSN and the novel printable ink composed of carboxymethylcellulose and pectin represents a new platform for the production of 3D-printed bioadhesive films, opening a new era in the development of skin delivery systems.application/pdfengPharmaceutics. Basel. Vol. 15, n. 1 (2023), 20, 18 p.Impressão tridimensionalClobetasolNanoestruturasNanotecnologia3D printingClobetasol propionateDrugNanomaterialSemisolid extrusionMesoporous silicaBioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing processEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001170129.pdf.txt001170129.pdf.txtExtracted Texttext/plain87020http://www.lume.ufrgs.br/bitstream/10183/264095/2/001170129.pdf.txt6b37c0a4de93a0b1088979b2e3496cecMD52ORIGINAL001170129.pdfTexto completo (inglês)application/pdf4028747http://www.lume.ufrgs.br/bitstream/10183/264095/1/001170129.pdf2fe2fec402a0d7351ff48c4cd1061582MD5110183/2640952023-08-31 03:34:04.898359oai:www.lume.ufrgs.br:10183/264095Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-08-31T06:34:04Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process
title Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process
spellingShingle Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process
Oliveira, Rafaela Santos de
Impressão tridimensional
Clobetasol
Nanoestruturas
Nanotecnologia
3D printing
Clobetasol propionate
Drug
Nanomaterial
Semisolid extrusion
Mesoporous silica
title_short Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process
title_full Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process
title_fullStr Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process
title_full_unstemmed Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process
title_sort Bioadhesive 3D-printed skin drug delivery polymeric films : from the drug loading in mesoporous silica to the manufacturing process
author Oliveira, Rafaela Santos de
author_facet Oliveira, Rafaela Santos de
Funk, Nadine Lysyk
Santos, Juliana dos
Oliveira, Thayse Viana de
Oliveira, Edilene Gadelha de
Petzhold, Cesar Liberato
Benvenutti, Edilson Valmir
Deon, Monique
Beck, Ruy Carlos Ruver
author_role author
author2 Funk, Nadine Lysyk
Santos, Juliana dos
Oliveira, Thayse Viana de
Oliveira, Edilene Gadelha de
Petzhold, Cesar Liberato
Benvenutti, Edilson Valmir
Deon, Monique
Beck, Ruy Carlos Ruver
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Oliveira, Rafaela Santos de
Funk, Nadine Lysyk
Santos, Juliana dos
Oliveira, Thayse Viana de
Oliveira, Edilene Gadelha de
Petzhold, Cesar Liberato
Benvenutti, Edilson Valmir
Deon, Monique
Beck, Ruy Carlos Ruver
dc.subject.por.fl_str_mv Impressão tridimensional
Clobetasol
Nanoestruturas
Nanotecnologia
topic Impressão tridimensional
Clobetasol
Nanoestruturas
Nanotecnologia
3D printing
Clobetasol propionate
Drug
Nanomaterial
Semisolid extrusion
Mesoporous silica
dc.subject.eng.fl_str_mv 3D printing
Clobetasol propionate
Drug
Nanomaterial
Semisolid extrusion
Mesoporous silica
description The alliance between 3D printing and nanomaterials brings versatile properties to pharmaceuticals, but few studies have explored this approach in the development of skin delivery formulations. In this study, clobetasol propionate (CP) was loaded (about 25% w/w) in mesoporous silica nanomaterial (MSN) to formulate novel bioadhesive and hydrophilic skin delivery films composed of pectin (5% w/v) and carboxymethylcellulose (5% w/v) by 3D printing. As a hydrophobic model drug, CP was encapsulated in MSN at a 3:1 (w/w) ratio, resulting in a decrease of CP crystallinity and an increase of its dissolution efficiency after 72 h (65.70 6.52%) as compared to CP dispersion (40.79 4.75%), explained by its partial change to an amorphous form. The CP-loaded MSN was incorporated in an innovative hydrophilic 3D-printable ink composed of carboxymethylcellulose and pectin (1:1, w/w), which showed high tensile strength (3.613 0.38 N, a homogenous drug dose (0.48 0.032 mg/g per film) and complete CP release after 10 h. Moreover, the presence of pectin in the ink increased the skin adhesion of the films (work of adhesion of 782 105 mN mm). Therefore, the alliance between MSN and the novel printable ink composed of carboxymethylcellulose and pectin represents a new platform for the production of 3D-printed bioadhesive films, opening a new era in the development of skin delivery systems.
publishDate 2023
dc.date.accessioned.fl_str_mv 2023-08-30T03:59:59Z
dc.date.issued.fl_str_mv 2023
dc.type.driver.fl_str_mv Estrangeiro
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/264095
dc.identifier.issn.pt_BR.fl_str_mv 1999-4923
dc.identifier.nrb.pt_BR.fl_str_mv 001170129
identifier_str_mv 1999-4923
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url http://hdl.handle.net/10183/264095
dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Pharmaceutics. Basel. Vol. 15, n. 1 (2023), 20, 18 p.
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