Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo

Detalhes bibliográficos
Autor(a) principal: Querino, Marcelo Vargas
Data de Publicação: 2004
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFSCAR
Texto Completo: https://repositorio.ufscar.br/handle/ufscar/4007
Resumo: The use of the technology of animal cell culture for the expression of recombinant proteins has been gaining major interest within biotechnology due the obtation of recent efficient medicaments in the chronic diseases. In this work was utilized the recombinant lineage CHO-K1, denominate CHOZMD, anchorage-dependent. It is capable of expressing a disintegrin with antimetastics properties. Knowing the precedent of well performance of fixed bed bioreactors with utilization of microcarriers in large scale animals cells cultures. It was fixed as purpose of this work the definition of a method to prepare of inoculum to this bioreactor utilizing Cytoline 1 commercial macroporous microcarrier in spinner flask. The cultures realized in spinner flasks of 500 mL with Cytoline 1 microcarriers with DMEM medium in range of pH in 7.0 to 7.4. It showed that the electrostatic incompatibility between the cell and the microcarrier matrix composed of polyethylene and silica was responsible by decreased adhesion cell and, consequently, by intense cell death for firsts hours of experiments. In function this was necessary to utilize an inoculum with high cell concentration and a better pH medium control to reach satisfactory results in the culture. Following this strategy was possible to achieve highest maximum specific growth cell rate (μmáx) for the CHOZMD cell of 0.24d-1 while for wild CHO-K1 cell was obtained 0.36d-1, both comparable with other works encounter in the literature. The best value obtained of cell productivity with recombinant cell was of 6,096 cel/mL·h and for wild cell was of 10,596 cel/mL·h The lager concentrations of adherents cells on microcarriers were obtained in this experiments that utilized concentrated inoculums, in the case of recombinant cell was obtained 1.39·106 cel/mL and in the case with wild cell of 1.65·106 cel/mL. For the preparation of an inoculum for a fixed bed bioreactor when prepared in spinner with Cytoline 1 microcarrier recommend: adoption of an inoculum approximate of 2.0·106 cel/mL in exponential growth phase and with rigorous control of pH medium in 7.3.
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spelling Querino, Marcelo VargasSuazo, Cláudio Alberto Torreshttp://genos.cnpq.br:12010/dwlattes/owa/prc_imp_cv_int?f_cod=K4783900Z9http://lattes.cnpq.br/2775887824019811ffb8ed82-de17-458a-ba7b-1dcc204b3f592016-06-02T19:56:33Z2009-07-072016-06-02T19:56:33Z2004-08-20QUERINO, Marcelo Vargas. Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo. 2004. 125 f. Dissertação (Mestrado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2004.https://repositorio.ufscar.br/handle/ufscar/4007The use of the technology of animal cell culture for the expression of recombinant proteins has been gaining major interest within biotechnology due the obtation of recent efficient medicaments in the chronic diseases. In this work was utilized the recombinant lineage CHO-K1, denominate CHOZMD, anchorage-dependent. It is capable of expressing a disintegrin with antimetastics properties. Knowing the precedent of well performance of fixed bed bioreactors with utilization of microcarriers in large scale animals cells cultures. It was fixed as purpose of this work the definition of a method to prepare of inoculum to this bioreactor utilizing Cytoline 1 commercial macroporous microcarrier in spinner flask. The cultures realized in spinner flasks of 500 mL with Cytoline 1 microcarriers with DMEM medium in range of pH in 7.0 to 7.4. It showed that the electrostatic incompatibility between the cell and the microcarrier matrix composed of polyethylene and silica was responsible by decreased adhesion cell and, consequently, by intense cell death for firsts hours of experiments. In function this was necessary to utilize an inoculum with high cell concentration and a better pH medium control to reach satisfactory results in the culture. Following this strategy was possible to achieve highest maximum specific growth cell rate (μmáx) for the CHOZMD cell of 0.24d-1 while for wild CHO-K1 cell was obtained 0.36d-1, both comparable with other works encounter in the literature. The best value obtained of cell productivity with recombinant cell was of 6,096 cel/mL·h and for wild cell was of 10,596 cel/mL·h The lager concentrations of adherents cells on microcarriers were obtained in this experiments that utilized concentrated inoculums, in the case of recombinant cell was obtained 1.39·106 cel/mL and in the case with wild cell of 1.65·106 cel/mL. For the preparation of an inoculum for a fixed bed bioreactor when prepared in spinner with Cytoline 1 microcarrier recommend: adoption of an inoculum approximate of 2.0·106 cel/mL in exponential growth phase and with rigorous control of pH medium in 7.3.O uso da tecnologia de cultivo de célula animal para a expressão de proteínas recombinantes vem ganhando interesse crescente dentro da biotecnologia em função da obtenção de novos medicamentos eficientes no tratamento de doenças crônicas. Neste trabalho foi utilizada a linhagem recombinante CHO-K1 (Chinese Hamster Ovary), denominada CHOZMD, dependente de ancoramento. Capaz de expressar uma desintegrina com propriedades antimetastáticas. Conhecendo os precedentes de bom desempenho do biorreator de leito fixo com utilização de microcarregadores no cultivo de células animais em larga escala fixou-se como objetivo deste trabalho a definição de um método para preparo de inóculo para esse biorreator utilizando o microcarregador macroporoso comercial Cytoline 1 em frasco spinner. Os cultivos realizados em frasco spinner de 500 mL com microcarregadores Cytoline 1 em meio DMEM em pH variando entre 7,0 e 7,4 mostraram que a baixa compatibilidade entre a célula e a matriz do microcarregador composta de polietileno e sílica foi responsável pela baixa adesão celular. Em função disso foi necessário utilizar um inóculo com alta concentração celular e um melhor controle do pH do meio para alcançar resultados satisfatórios nos cultivos. Seguindo essa estratégia foi possível conseguir velocidades específicas máximas de crescimento celular (μmáx) para a célula CHOZMD de 0,24d-1 enquanto que para a célula CHO-K1 selvagem obteve-se 0,36d-1, ambas comparáveis as de outros trabalhos encontrados na literatura. O melhor valor obtido de produtividade celular com célula recombinante foi de 6.096 células/mL·h e para a célula selvagem foi de 10.569 células/mL·h. As maiores concentrações de células aderidas aos microcarregadores foram obtidas nos experimentos que utilizaram inóculos concentrados, no caso da célula recombinante obteve-se 1,39·106 células/mL e no caso com célula selvagem 1,65·106 células/mL. Para o preparo de um inóculo adequado para um biorreator de leito fixo quando preparado no spinner com microcarregador Cytoline 1 recomenda-se a adoção de um inóculo em torno de 2,0·106 células/mL na fase exponencial de crescimento e controle rigoroso do pH do meio em 7,3.Universidade Federal de Sao Carlosapplication/pdfporUniversidade Federal de São CarlosPrograma de Pós-Graduação em Engenharia Química - PPGEQUFSCarBRCélula CHO - K1MicrocarregadoresCélula animalBiorreatoresENGENHARIAS::ENGENHARIA QUIMICADesenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixoinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis-1-1a35fad8c-e6aa-4839-b89a-4a1eb6fcd885info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINAL2151.pdfapplication/pdf1524860https://repositorio.ufscar.br/bitstream/ufscar/4007/1/2151.pdf6ed528476d44762b88988e6b1ca76146MD51THUMBNAIL2151.pdf.jpg2151.pdf.jpgIM Thumbnailimage/jpeg6231https://repositorio.ufscar.br/bitstream/ufscar/4007/2/2151.pdf.jpg60959dc4e4666344c9fef17aa684bd96MD52ufscar/40072023-09-18 18:30:59.195oai:repositorio.ufscar.br:ufscar/4007Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-09-18T18:30:59Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo
title Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo
spellingShingle Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo
Querino, Marcelo Vargas
Célula CHO - K1
Microcarregadores
Célula animal
Biorreatores
ENGENHARIAS::ENGENHARIA QUIMICA
title_short Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo
title_full Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo
title_fullStr Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo
title_full_unstemmed Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo
title_sort Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo
author Querino, Marcelo Vargas
author_facet Querino, Marcelo Vargas
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/2775887824019811
dc.contributor.author.fl_str_mv Querino, Marcelo Vargas
dc.contributor.advisor1.fl_str_mv Suazo, Cláudio Alberto Torres
dc.contributor.advisor1Lattes.fl_str_mv http://genos.cnpq.br:12010/dwlattes/owa/prc_imp_cv_int?f_cod=K4783900Z9
dc.contributor.authorID.fl_str_mv ffb8ed82-de17-458a-ba7b-1dcc204b3f59
contributor_str_mv Suazo, Cláudio Alberto Torres
dc.subject.por.fl_str_mv Célula CHO - K1
Microcarregadores
Célula animal
Biorreatores
topic Célula CHO - K1
Microcarregadores
Célula animal
Biorreatores
ENGENHARIAS::ENGENHARIA QUIMICA
dc.subject.cnpq.fl_str_mv ENGENHARIAS::ENGENHARIA QUIMICA
description The use of the technology of animal cell culture for the expression of recombinant proteins has been gaining major interest within biotechnology due the obtation of recent efficient medicaments in the chronic diseases. In this work was utilized the recombinant lineage CHO-K1, denominate CHOZMD, anchorage-dependent. It is capable of expressing a disintegrin with antimetastics properties. Knowing the precedent of well performance of fixed bed bioreactors with utilization of microcarriers in large scale animals cells cultures. It was fixed as purpose of this work the definition of a method to prepare of inoculum to this bioreactor utilizing Cytoline 1 commercial macroporous microcarrier in spinner flask. The cultures realized in spinner flasks of 500 mL with Cytoline 1 microcarriers with DMEM medium in range of pH in 7.0 to 7.4. It showed that the electrostatic incompatibility between the cell and the microcarrier matrix composed of polyethylene and silica was responsible by decreased adhesion cell and, consequently, by intense cell death for firsts hours of experiments. In function this was necessary to utilize an inoculum with high cell concentration and a better pH medium control to reach satisfactory results in the culture. Following this strategy was possible to achieve highest maximum specific growth cell rate (μmáx) for the CHOZMD cell of 0.24d-1 while for wild CHO-K1 cell was obtained 0.36d-1, both comparable with other works encounter in the literature. The best value obtained of cell productivity with recombinant cell was of 6,096 cel/mL·h and for wild cell was of 10,596 cel/mL·h The lager concentrations of adherents cells on microcarriers were obtained in this experiments that utilized concentrated inoculums, in the case of recombinant cell was obtained 1.39·106 cel/mL and in the case with wild cell of 1.65·106 cel/mL. For the preparation of an inoculum for a fixed bed bioreactor when prepared in spinner with Cytoline 1 microcarrier recommend: adoption of an inoculum approximate of 2.0·106 cel/mL in exponential growth phase and with rigorous control of pH medium in 7.3.
publishDate 2004
dc.date.issued.fl_str_mv 2004-08-20
dc.date.available.fl_str_mv 2009-07-07
2016-06-02T19:56:33Z
dc.date.accessioned.fl_str_mv 2016-06-02T19:56:33Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
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status_str publishedVersion
dc.identifier.citation.fl_str_mv QUERINO, Marcelo Vargas. Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo. 2004. 125 f. Dissertação (Mestrado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2004.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/ufscar/4007
identifier_str_mv QUERINO, Marcelo Vargas. Desenvolvimento de processo de inoculação com microcarregador Cytoline 1 visando o cultivo de célula CHO-K1 em biorreator de leito fixo. 2004. 125 f. Dissertação (Mestrado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2004.
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