Phosphorylated silk fibroin matrix for methotrexate release

Detalhes bibliográficos
Autor(a) principal: Volkov, Vadim
Data de Publicação: 2015
Outros Autores: Sárria, M. P., Gomes, Andreia C, Paulo, Artur Cavaco
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/1822/32905
Resumo: Silk-based matrix was produced for delivery of a model anticancer drug, methotrexate (MTX). The calculation of net charge of silk fibroin and MTX was performed to better understand the electrostatic interactions during matrix formation upon casting. Silk fibroin films were cast at pH 7.2 and pH 3.5. Protein kinase A was used to prepare phosphorylated silk fibroin. The phosphorylation content of matrix was controlled by mixing at specific ratios the phosphorylated and unphosphorylated solutions. In vitro release profiling data suggest that the observed interactions are mainly structural and not electrostatical. The release of MTX is facilitated by use of proteolytic enzymes and higher pHs. The elevated -sheet content and crystallinity of the acidified-cast fibroin solution seem not to favor drug retention. All the acquired data underline the prevalence of structural interactions over electrostatical interactions between methotrexate and silk fibroin.
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spelling Phosphorylated silk fibroin matrix for methotrexate releaseSilk fibroinPhosphorylationMethotrexateDLSNet chargesilk fibroinScience & TechnologySilk-based matrix was produced for delivery of a model anticancer drug, methotrexate (MTX). The calculation of net charge of silk fibroin and MTX was performed to better understand the electrostatic interactions during matrix formation upon casting. Silk fibroin films were cast at pH 7.2 and pH 3.5. Protein kinase A was used to prepare phosphorylated silk fibroin. The phosphorylation content of matrix was controlled by mixing at specific ratios the phosphorylated and unphosphorylated solutions. In vitro release profiling data suggest that the observed interactions are mainly structural and not electrostatical. The release of MTX is facilitated by use of proteolytic enzymes and higher pHs. The elevated -sheet content and crystallinity of the acidified-cast fibroin solution seem not to favor drug retention. All the acquired data underline the prevalence of structural interactions over electrostatical interactions between methotrexate and silk fibroin.The authors would like to acknowledge the support, granted by European NOVO Project, Contract No. FP7-HEALTH 2011-two-stage 278402. This work was partially supported by FEDER through POFC-COMPETE and by national funds from FCT through the projects PEst-C/BIA/UI4050/2011 (CBMA). V.V. also wants to thank Dr. Claudia Botelho for her helpful discussion and comments made during the critical reading of the manuscript.American Chemical SocietyUniversidade do MinhoVolkov, VadimSárria, M. P.Gomes, Andreia CPaulo, Artur Cavaco20152015-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/32905engVolkov, Vadim; Sárria, M. P.; Gomes, Andreia C.; Paulo, Artur Cavaco, Phosphorylated silk fibroin matrix for methotrexate release. Molecular Pharmaceutics, 12(1), 75-86, 20151543-83921543-838410.1021/mp500433825435334info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-05-11T06:25:22Zoai:repositorium.sdum.uminho.pt:1822/32905Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-05-11T06:25:22Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Phosphorylated silk fibroin matrix for methotrexate release
title Phosphorylated silk fibroin matrix for methotrexate release
spellingShingle Phosphorylated silk fibroin matrix for methotrexate release
Volkov, Vadim
Silk fibroin
Phosphorylation
Methotrexate
DLS
Net charge
silk fibroin
Science & Technology
title_short Phosphorylated silk fibroin matrix for methotrexate release
title_full Phosphorylated silk fibroin matrix for methotrexate release
title_fullStr Phosphorylated silk fibroin matrix for methotrexate release
title_full_unstemmed Phosphorylated silk fibroin matrix for methotrexate release
title_sort Phosphorylated silk fibroin matrix for methotrexate release
author Volkov, Vadim
author_facet Volkov, Vadim
Sárria, M. P.
Gomes, Andreia C
Paulo, Artur Cavaco
author_role author
author2 Sárria, M. P.
Gomes, Andreia C
Paulo, Artur Cavaco
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Volkov, Vadim
Sárria, M. P.
Gomes, Andreia C
Paulo, Artur Cavaco
dc.subject.por.fl_str_mv Silk fibroin
Phosphorylation
Methotrexate
DLS
Net charge
silk fibroin
Science & Technology
topic Silk fibroin
Phosphorylation
Methotrexate
DLS
Net charge
silk fibroin
Science & Technology
description Silk-based matrix was produced for delivery of a model anticancer drug, methotrexate (MTX). The calculation of net charge of silk fibroin and MTX was performed to better understand the electrostatic interactions during matrix formation upon casting. Silk fibroin films were cast at pH 7.2 and pH 3.5. Protein kinase A was used to prepare phosphorylated silk fibroin. The phosphorylation content of matrix was controlled by mixing at specific ratios the phosphorylated and unphosphorylated solutions. In vitro release profiling data suggest that the observed interactions are mainly structural and not electrostatical. The release of MTX is facilitated by use of proteolytic enzymes and higher pHs. The elevated -sheet content and crystallinity of the acidified-cast fibroin solution seem not to favor drug retention. All the acquired data underline the prevalence of structural interactions over electrostatical interactions between methotrexate and silk fibroin.
publishDate 2015
dc.date.none.fl_str_mv 2015
2015-01-01T00:00:00Z
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 https://hdl.handle.net/1822/32905
url https://hdl.handle.net/1822/32905
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Volkov, Vadim; Sárria, M. P.; Gomes, Andreia C.; Paulo, Artur Cavaco, Phosphorylated silk fibroin matrix for methotrexate release. Molecular Pharmaceutics, 12(1), 75-86, 2015
1543-8392
1543-8384
10.1021/mp5004338
25435334
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv mluisa.alvim@gmail.com
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