Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process

Detalhes bibliográficos
Autor(a) principal: Yoshida, Valquíria M. H.
Data de Publicação: 2015
Outros Autores: Balcão, V. M., Vila, Marta M. D. C., Oliveira Júnior, J. M., Aranha, Norberto, Chaud, Marco V., Gremião, Maria P. D.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/35310
Resumo: A supercritical antisolvent (SAS) process for obtaining zidovudine-poly(l-lactic acid) (PLLA) solid dispersions (SDs) was used to attain a better intestinal permeation of this drug. A 32 factorial design was used, having as independent variables the ratio 3-azido-23-dideoxythymidine (AZT)PLLA and temperature/pressure conditions, as dependent variables the process yield and particle macroscopic morphology. AZTPLLA production batches were carried out by the SAS process, and the resulting products evaluated via scanning electron microscope, X-ray diffraction, differential scanning calorimetry, and Fourier transform infrared analyses. From the nine possible combinations of tests performed experimentally, only one combination did not produced a solid. The L3 batch of SD, produced with 1:2 (AZTPLLA) ratio, resulted in a 91.54% yield, with 40% AZT content. Intestinal permeability studies using the AZTPLLA from L3 batch led to an AZT permeability of approximately 9.87%, which was higher than that of pure AZT (3.84%). AZT remained in crystalline form, whereas PLLA remained in semicrystalline form. AZT release is controlled by a diffusion mechanism. It has been demonstrated that it is possible to use PLLA carrier and SAS process to obtain SD, in a single step.
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spelling Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent processsupercritical antisolvent processsupercritical fluidszidovudinepoly(l-lactic acid)solid dispersionoral absorptiongastrointestinal transiteverted rat intestinal sacspermeabilityCiências Médicas::Biotecnologia MédicaScience & TechnologyA supercritical antisolvent (SAS) process for obtaining zidovudine-poly(l-lactic acid) (PLLA) solid dispersions (SDs) was used to attain a better intestinal permeation of this drug. A 32 factorial design was used, having as independent variables the ratio 3-azido-23-dideoxythymidine (AZT)PLLA and temperature/pressure conditions, as dependent variables the process yield and particle macroscopic morphology. AZTPLLA production batches were carried out by the SAS process, and the resulting products evaluated via scanning electron microscope, X-ray diffraction, differential scanning calorimetry, and Fourier transform infrared analyses. From the nine possible combinations of tests performed experimentally, only one combination did not produced a solid. The L3 batch of SD, produced with 1:2 (AZTPLLA) ratio, resulted in a 91.54% yield, with 40% AZT content. Intestinal permeability studies using the AZTPLLA from L3 batch led to an AZT permeability of approximately 9.87%, which was higher than that of pure AZT (3.84%). AZT remained in crystalline form, whereas PLLA remained in semicrystalline form. AZT release is controlled by a diffusion mechanism. It has been demonstrated that it is possible to use PLLA carrier and SAS process to obtain SD, in a single step.Cristalia (Itapira, Brazil) for the kind supply of the reference substance used throughout the research work. Financial support from Fundação de Amparo á Pesquisa do Estado de São Paulo (2013-19300-4; 2012/01333-0; 2011/21219-5), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (PROSUP/CAPES) and Finep Inovação e Pesquisa (Finep, Brazil; 01.13.0286.00).John Wiley and SonsUniversidade do MinhoYoshida, Valquíria M. H.Balcão, V. M.Vila, Marta M. D. C.Oliveira Júnior, J. M.Aranha, NorbertoChaud, Marco V.Gremião, Maria P. D.2015-052015-05-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/35310engYoshida, Valquíria M. H.; Balcão, V. M.; Vila, Marta M. D. C.; Oliveira Júnior, José M.; Aranha, Norberto; Chaud, Marco V.; Gremião, Maria P. D., Zidovudinepoly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process. Journal of Pharmaceutical Sciences, 104(5), 1691-1700, 20150022-35491520-601710.1002/jps.2437725676038http://onlinelibrary.wiley.com/doi/10.1002/jps.24377/abstractinfo: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:RCAAP2023-07-21T12:24:34Zoai:repositorium.sdum.uminho.pt:1822/35310Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:18:36.353514Repositório 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 Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process
title Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process
spellingShingle Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process
Yoshida, Valquíria M. H.
supercritical antisolvent process
supercritical fluids
zidovudine
poly(l-lactic acid)
solid dispersion
oral absorption
gastrointestinal transit
everted rat intestinal sacs
permeability
Ciências Médicas::Biotecnologia Médica
Science & Technology
title_short Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process
title_full Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process
title_fullStr Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process
title_full_unstemmed Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process
title_sort Zidovudine-poly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process
author Yoshida, Valquíria M. H.
author_facet Yoshida, Valquíria M. H.
Balcão, V. M.
Vila, Marta M. D. C.
Oliveira Júnior, J. M.
Aranha, Norberto
Chaud, Marco V.
Gremião, Maria P. D.
author_role author
author2 Balcão, V. M.
Vila, Marta M. D. C.
Oliveira Júnior, J. M.
Aranha, Norberto
Chaud, Marco V.
Gremião, Maria P. D.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Yoshida, Valquíria M. H.
Balcão, V. M.
Vila, Marta M. D. C.
Oliveira Júnior, J. M.
Aranha, Norberto
Chaud, Marco V.
Gremião, Maria P. D.
dc.subject.por.fl_str_mv supercritical antisolvent process
supercritical fluids
zidovudine
poly(l-lactic acid)
solid dispersion
oral absorption
gastrointestinal transit
everted rat intestinal sacs
permeability
Ciências Médicas::Biotecnologia Médica
Science & Technology
topic supercritical antisolvent process
supercritical fluids
zidovudine
poly(l-lactic acid)
solid dispersion
oral absorption
gastrointestinal transit
everted rat intestinal sacs
permeability
Ciências Médicas::Biotecnologia Médica
Science & Technology
description A supercritical antisolvent (SAS) process for obtaining zidovudine-poly(l-lactic acid) (PLLA) solid dispersions (SDs) was used to attain a better intestinal permeation of this drug. A 32 factorial design was used, having as independent variables the ratio 3-azido-23-dideoxythymidine (AZT)PLLA and temperature/pressure conditions, as dependent variables the process yield and particle macroscopic morphology. AZTPLLA production batches were carried out by the SAS process, and the resulting products evaluated via scanning electron microscope, X-ray diffraction, differential scanning calorimetry, and Fourier transform infrared analyses. From the nine possible combinations of tests performed experimentally, only one combination did not produced a solid. The L3 batch of SD, produced with 1:2 (AZTPLLA) ratio, resulted in a 91.54% yield, with 40% AZT content. Intestinal permeability studies using the AZTPLLA from L3 batch led to an AZT permeability of approximately 9.87%, which was higher than that of pure AZT (3.84%). AZT remained in crystalline form, whereas PLLA remained in semicrystalline form. AZT release is controlled by a diffusion mechanism. It has been demonstrated that it is possible to use PLLA carrier and SAS process to obtain SD, in a single step.
publishDate 2015
dc.date.none.fl_str_mv 2015-05
2015-05-01T00:00:00Z
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 http://hdl.handle.net/1822/35310
url http://hdl.handle.net/1822/35310
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Yoshida, Valquíria M. H.; Balcão, V. M.; Vila, Marta M. D. C.; Oliveira Júnior, José M.; Aranha, Norberto; Chaud, Marco V.; Gremião, Maria P. D., Zidovudinepoly(l-lactic acid) solid dispersions with improved intestinal permeability prepared by supercritical antisolvent process. Journal of Pharmaceutical Sciences, 104(5), 1691-1700, 2015
0022-3549
1520-6017
10.1002/jps.24377
25676038
http://onlinelibrary.wiley.com/doi/10.1002/jps.24377/abstract
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 John Wiley and Sons
publisher.none.fl_str_mv John Wiley and Sons
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
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