Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos
Autor(a) principal: | |
---|---|
Data de Publicação: | 2003 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | LOCUS Repositório Institucional da UFV |
Texto Completo: | http://locus.ufv.br/handle/123456789/5172 |
Resumo: | Was evaluated the immunological response of synthetic peptide SBm7462 emulsified with the adjuvant saponin or encapsulated in biodegradable PLGA microspheres; as well as, the response of synthetic peptide SPf66 encapsulated on cited delivery system. Mice Balb/c, female, were utilized on study, with a dose of 100mg of peptide for each animal. The mice were separated in six groups of twenty: group I: animals inoculated with 75mg of saponin; group II: inoculated with 100mL of water milliQ; group III: immunized with the peptide SBm7462 emulsified on saponin, 75mg of saponin for 100mg of peptide; group IV: inoculated with empty microspheres; group V: immunized with the peptide SBm7462 enclausured in PLGA microspheres; group VI: immunized with the synthetic peptide SPf66 enclausured in PLGA microspheres. The three inoculations was executed on day zero and latter on third and sixth weeks after the first inoculation. The mice were bled prior of first immunisation and at periodic intervals (of seven days) until week 21. The serum was assayed by indirect ELISA for detection of specific IgGs anti-SBm7462, and for realization of tests of hepatic function. The synthetic peptide SBm7462 showed a better immune response emulsified with saponin adjuvant. The peptide SPf66 showed a similar response when compared with the obtained for others authors when encapsulated in PLGA microspheres and utilized in mice. The tests of hepatic function were realized in equipament multiparametric of bioquimic Alisé, and no evidence of hepatotoxic effects was viewed, when was evaluated the parameters: total proteins, albumin, AST and ALT. In order to verification of histologic alterations post-immunization, were colleted spleen of mice, for each treatment, on day zero, three, six and nine days post the second inoculation and two, four and six days post the third inoculation. The results obtained showed the saponin potentiate a better immune response of peptide SBm7462, and this response was more precoce than the obtained with the PLGA microspheres. This delivery system show itself as a good approach for utilization with the synthetic peptide SBm7462, nevertheless more studies are necessary for promotion of a better efficacy of encapsulation. |
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Sales Junior, Policarpo Ademarhttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4764903E9Salcedo, Joaquín Hernán Patarroyohttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4783313T4Viloria, Marlene Isabel Vargashttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4781964E6Guimarães, Antonio Marcoshttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4786353E2Afonso, Luis Carlos Croccohttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4789739U0Santos, Tomaz Aroldo da Motahttp://lattes.cnpq.br/22150793357716202015-03-26T13:47:21Z2007-07-202015-03-26T13:47:21Z2003-12-19SALES JUNIOR, Policarpo Ademar. Utilization of biodegradable PLGA microspheres as a delivery system for synthetic vaccine SBm7462 on control of the Boophilus microplus (Canestrini, 1887): experimental model in mice. 2003. 94 f. Dissertação (Mestrado em Biotecnologia, diagnóstico e controle de doenças; Epidemiologia e controle de qualidade de prod. de) - Universidade Federal de Viçosa, Viçosa, 2003.http://locus.ufv.br/handle/123456789/5172Was evaluated the immunological response of synthetic peptide SBm7462 emulsified with the adjuvant saponin or encapsulated in biodegradable PLGA microspheres; as well as, the response of synthetic peptide SPf66 encapsulated on cited delivery system. Mice Balb/c, female, were utilized on study, with a dose of 100mg of peptide for each animal. The mice were separated in six groups of twenty: group I: animals inoculated with 75mg of saponin; group II: inoculated with 100mL of water milliQ; group III: immunized with the peptide SBm7462 emulsified on saponin, 75mg of saponin for 100mg of peptide; group IV: inoculated with empty microspheres; group V: immunized with the peptide SBm7462 enclausured in PLGA microspheres; group VI: immunized with the synthetic peptide SPf66 enclausured in PLGA microspheres. The three inoculations was executed on day zero and latter on third and sixth weeks after the first inoculation. The mice were bled prior of first immunisation and at periodic intervals (of seven days) until week 21. The serum was assayed by indirect ELISA for detection of specific IgGs anti-SBm7462, and for realization of tests of hepatic function. The synthetic peptide SBm7462 showed a better immune response emulsified with saponin adjuvant. The peptide SPf66 showed a similar response when compared with the obtained for others authors when encapsulated in PLGA microspheres and utilized in mice. The tests of hepatic function were realized in equipament multiparametric of bioquimic Alisé, and no evidence of hepatotoxic effects was viewed, when was evaluated the parameters: total proteins, albumin, AST and ALT. In order to verification of histologic alterations post-immunization, were colleted spleen of mice, for each treatment, on day zero, three, six and nine days post the second inoculation and two, four and six days post the third inoculation. The results obtained showed the saponin potentiate a better immune response of peptide SBm7462, and this response was more precoce than the obtained with the PLGA microspheres. This delivery system show itself as a good approach for utilization with the synthetic peptide SBm7462, nevertheless more studies are necessary for promotion of a better efficacy of encapsulation.Foi avaliada a resposta imunológica do peptídeo sintético SBm7462 emulsificado com o adjuvante saponina ou encapsulado em microesferas biodegradáveis PLGA; bem como, a do peptídeo sintético SPf66 encapsulado no referido sistema de liberação. O estudo foi realizado com camundongos Balb/c, fêmeas, utilizando-se uma dose de 100 mg de peptídeo por animal. Os camundongos foram separados em seis grupos de vinte: grupo I: animais em que foram inoculados 75mg de saponina; grupo II: inoculados com 100 mL de água milli Q; grupo III: imunizados com o peptídeo SBm7462 emulsificado com o adjuvante saponina (75mg de saponina para 100mg de peptídeo); grupo IV: inoculados com as microesferas vazias; grupo V: imunizados com o peptídeo SBm7462 encapsulado nas microesferas PLGA; grupo VI: imunizados com o peptídeo sintético SPf66 encapsulado nas microesferas PLGA. As três inoculações foram efetuadas no dia zero e depois a cada três semanas. Os camundongos foram sangrados antes da primeira imunização e a intervalos periódicos (a cada sete dias) até 21ª semana, sendo o soro utilizado para a realização de ELISA indireto para detecção de IgGs anti-SBm7462, como também para a realização de testes de função hepática. O peptídeo sintético SBm7462 mostrou uma melhor resposta humoral quando emulsificado com o adjuvante saponina. Já o SPf66 mostrou uma resposta similar à encontrada por outros autores quando encapsulado em microesferas PLGA e utilizado em camundongos. Os testes de função hepática foram realizados em equipamento multiparamétrico de bioquímica Alisé e, não se observou evidências de efeitos hepatotóxicos quando foram avaliados parâmetros como proteínas totais, albumina, AST e ALT. Foram também coletados baços de camundongos para verificação das alterações histológicas pós-imunização, para cada tratamento, no dia zero, três, seis e nove dias após a segunda e dois, quatro e seis dias após a terceira inoculação. Os resultados obtidos revelam que a saponina potencializa uma melhor resposta imune do peptídeo SBm7462, tendo sido também esta resposta mais precoce e que, as microesferas PLGA mostram-se viáveis a serem utilizadas como sistema de liberação para este peptídeo, necessitando-se, porém, de estudos adicionais para promoção de uma melhor eficácia de encapsulação.Fundação Oswaldo Cruzapplication/pdfporUniversidade Federal de ViçosaMestrado em Medicina VeterináriaUFVBRBiotecnologia, diagnóstico e controle de doenças; Epidemiologia e controle de qualidade de prod. deBoophilus microplusVacina sintéticaAdjuvantesBoophilus microplusSynthetic vaccineAdjuvantsCNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA::MEDICINA VETERINARIA PREVENTIVAUtilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongosUtilization of biodegradable PLGA microspheres as a delivery system for synthetic vaccine SBm7462 on control of the Boophilus microplus (Canestrini, 1887): experimental model in miceinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFVORIGINALtexto completo.pdfapplication/pdf876611https://locus.ufv.br//bitstream/123456789/5172/1/texto%20completo.pdfa2f759bb57143bd8beafaa8f6d9a9652MD51TEXTtexto completo.pdf.txttexto completo.pdf.txtExtracted texttext/plain142942https://locus.ufv.br//bitstream/123456789/5172/2/texto%20completo.pdf.txt2ecb80247bfe636965357ffe0cc78296MD52THUMBNAILtexto completo.pdf.jpgtexto completo.pdf.jpgIM Thumbnailimage/jpeg3661https://locus.ufv.br//bitstream/123456789/5172/3/texto%20completo.pdf.jpg0a07fdbdace2f0081f39098b52dd1dcfMD53123456789/51722016-04-11 23:09:44.922oai:locus.ufv.br:123456789/5172Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452016-04-12T02:09:44LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false |
dc.title.por.fl_str_mv |
Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos |
dc.title.alternative.eng.fl_str_mv |
Utilization of biodegradable PLGA microspheres as a delivery system for synthetic vaccine SBm7462 on control of the Boophilus microplus (Canestrini, 1887): experimental model in mice |
title |
Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos |
spellingShingle |
Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos Sales Junior, Policarpo Ademar Boophilus microplus Vacina sintética Adjuvantes Boophilus microplus Synthetic vaccine Adjuvants CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA::MEDICINA VETERINARIA PREVENTIVA |
title_short |
Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos |
title_full |
Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos |
title_fullStr |
Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos |
title_full_unstemmed |
Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos |
title_sort |
Utilização de microesferas biodegradáveis PLGA como sistema de liberação para a vacina sintética SBm7462 no controle do Boophilus microplus (Canestrini, 1887): modelo experimental em camundongos |
author |
Sales Junior, Policarpo Ademar |
author_facet |
Sales Junior, Policarpo Ademar |
author_role |
author |
dc.contributor.authorLattes.por.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4764903E9 |
dc.contributor.author.fl_str_mv |
Sales Junior, Policarpo Ademar |
dc.contributor.advisor1.fl_str_mv |
Salcedo, Joaquín Hernán Patarroyo |
dc.contributor.advisor1Lattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4783313T4 |
dc.contributor.referee1.fl_str_mv |
Viloria, Marlene Isabel Vargas |
dc.contributor.referee1Lattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4781964E6 |
dc.contributor.referee2.fl_str_mv |
Guimarães, Antonio Marcos |
dc.contributor.referee2Lattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4786353E2 |
dc.contributor.referee3.fl_str_mv |
Afonso, Luis Carlos Crocco |
dc.contributor.referee3Lattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4789739U0 |
dc.contributor.referee4.fl_str_mv |
Santos, Tomaz Aroldo da Mota |
dc.contributor.referee4Lattes.fl_str_mv |
http://lattes.cnpq.br/2215079335771620 |
contributor_str_mv |
Salcedo, Joaquín Hernán Patarroyo Viloria, Marlene Isabel Vargas Guimarães, Antonio Marcos Afonso, Luis Carlos Crocco Santos, Tomaz Aroldo da Mota |
dc.subject.por.fl_str_mv |
Boophilus microplus Vacina sintética Adjuvantes |
topic |
Boophilus microplus Vacina sintética Adjuvantes Boophilus microplus Synthetic vaccine Adjuvants CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA::MEDICINA VETERINARIA PREVENTIVA |
dc.subject.eng.fl_str_mv |
Boophilus microplus Synthetic vaccine Adjuvants |
dc.subject.cnpq.fl_str_mv |
CNPQ::CIENCIAS AGRARIAS::MEDICINA VETERINARIA::MEDICINA VETERINARIA PREVENTIVA |
description |
Was evaluated the immunological response of synthetic peptide SBm7462 emulsified with the adjuvant saponin or encapsulated in biodegradable PLGA microspheres; as well as, the response of synthetic peptide SPf66 encapsulated on cited delivery system. Mice Balb/c, female, were utilized on study, with a dose of 100mg of peptide for each animal. The mice were separated in six groups of twenty: group I: animals inoculated with 75mg of saponin; group II: inoculated with 100mL of water milliQ; group III: immunized with the peptide SBm7462 emulsified on saponin, 75mg of saponin for 100mg of peptide; group IV: inoculated with empty microspheres; group V: immunized with the peptide SBm7462 enclausured in PLGA microspheres; group VI: immunized with the synthetic peptide SPf66 enclausured in PLGA microspheres. The three inoculations was executed on day zero and latter on third and sixth weeks after the first inoculation. The mice were bled prior of first immunisation and at periodic intervals (of seven days) until week 21. The serum was assayed by indirect ELISA for detection of specific IgGs anti-SBm7462, and for realization of tests of hepatic function. The synthetic peptide SBm7462 showed a better immune response emulsified with saponin adjuvant. The peptide SPf66 showed a similar response when compared with the obtained for others authors when encapsulated in PLGA microspheres and utilized in mice. The tests of hepatic function were realized in equipament multiparametric of bioquimic Alisé, and no evidence of hepatotoxic effects was viewed, when was evaluated the parameters: total proteins, albumin, AST and ALT. In order to verification of histologic alterations post-immunization, were colleted spleen of mice, for each treatment, on day zero, three, six and nine days post the second inoculation and two, four and six days post the third inoculation. The results obtained showed the saponin potentiate a better immune response of peptide SBm7462, and this response was more precoce than the obtained with the PLGA microspheres. This delivery system show itself as a good approach for utilization with the synthetic peptide SBm7462, nevertheless more studies are necessary for promotion of a better efficacy of encapsulation. |
publishDate |
2003 |
dc.date.issued.fl_str_mv |
2003-12-19 |
dc.date.available.fl_str_mv |
2007-07-20 2015-03-26T13:47:21Z |
dc.date.accessioned.fl_str_mv |
2015-03-26T13:47:21Z |
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info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
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masterThesis |
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publishedVersion |
dc.identifier.citation.fl_str_mv |
SALES JUNIOR, Policarpo Ademar. Utilization of biodegradable PLGA microspheres as a delivery system for synthetic vaccine SBm7462 on control of the Boophilus microplus (Canestrini, 1887): experimental model in mice. 2003. 94 f. Dissertação (Mestrado em Biotecnologia, diagnóstico e controle de doenças; Epidemiologia e controle de qualidade de prod. de) - Universidade Federal de Viçosa, Viçosa, 2003. |
dc.identifier.uri.fl_str_mv |
http://locus.ufv.br/handle/123456789/5172 |
identifier_str_mv |
SALES JUNIOR, Policarpo Ademar. Utilization of biodegradable PLGA microspheres as a delivery system for synthetic vaccine SBm7462 on control of the Boophilus microplus (Canestrini, 1887): experimental model in mice. 2003. 94 f. Dissertação (Mestrado em Biotecnologia, diagnóstico e controle de doenças; Epidemiologia e controle de qualidade de prod. de) - Universidade Federal de Viçosa, Viçosa, 2003. |
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http://locus.ufv.br/handle/123456789/5172 |
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Universidade Federal de Viçosa |
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Mestrado em Medicina Veterinária |
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UFV |
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BR |
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Biotecnologia, diagnóstico e controle de doenças; Epidemiologia e controle de qualidade de prod. de |
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Universidade Federal de Viçosa |
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