Un método reproducible para obtener peg biramificado monofuncional de alta pureza

PEGylation has become a widely applied technique to enhancing in vitro and in vivo stability of therapeutic proteins and to increasing materials biocompatibility. PEG branched structures have proven useful for protein and peptide modification. Furthermore, they may be better than linear structures for many purposes. This paper describes an improved procedure for obtaining 2-arms PEG based on L-lysine. The efficiency of the synthesis was not related to moisture of the raw materials. This procedure does not use hazardous reagents as previous protocols do. It implemented a purification process for obtaining the desired structure with high purity ( > 99%). Finally, the procedure described here allows the obtaining of others PEGylation reagents.

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Main Authors: Ramón,José A., Peniche,Carlos, Castro,Fidel R., Sáez,Vivian M., Colás,Rosa M., Páez,Rolando
Format: Digital revista
Language:Spanish / Castilian
Published: Sociedade Brasileira de Química 2009
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422009000600012
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spelling oai:scielo:S0100-404220090006000122009-09-22Un método reproducible para obtener peg biramificado monofuncional de alta purezaRamón,José A.Peniche,CarlosCastro,Fidel R.Sáez,Vivian M.Colás,Rosa M.Páez,Rolando PEGylation branched PEG interferon PEGylation has become a widely applied technique to enhancing in vitro and in vivo stability of therapeutic proteins and to increasing materials biocompatibility. PEG branched structures have proven useful for protein and peptide modification. Furthermore, they may be better than linear structures for many purposes. This paper describes an improved procedure for obtaining 2-arms PEG based on L-lysine. The efficiency of the synthesis was not related to moisture of the raw materials. This procedure does not use hazardous reagents as previous protocols do. It implemented a purification process for obtaining the desired structure with high purity ( > 99%). Finally, the procedure described here allows the obtaining of others PEGylation reagents.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaQuímica Nova v.32 n.6 20092009-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422009000600012es10.1590/S0100-40422009000600012
institution SCIELO
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country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language Spanish / Castilian
format Digital
author Ramón,José A.
Peniche,Carlos
Castro,Fidel R.
Sáez,Vivian M.
Colás,Rosa M.
Páez,Rolando
spellingShingle Ramón,José A.
Peniche,Carlos
Castro,Fidel R.
Sáez,Vivian M.
Colás,Rosa M.
Páez,Rolando
Un método reproducible para obtener peg biramificado monofuncional de alta pureza
author_facet Ramón,José A.
Peniche,Carlos
Castro,Fidel R.
Sáez,Vivian M.
Colás,Rosa M.
Páez,Rolando
author_sort Ramón,José A.
title Un método reproducible para obtener peg biramificado monofuncional de alta pureza
title_short Un método reproducible para obtener peg biramificado monofuncional de alta pureza
title_full Un método reproducible para obtener peg biramificado monofuncional de alta pureza
title_fullStr Un método reproducible para obtener peg biramificado monofuncional de alta pureza
title_full_unstemmed Un método reproducible para obtener peg biramificado monofuncional de alta pureza
title_sort un método reproducible para obtener peg biramificado monofuncional de alta pureza
description PEGylation has become a widely applied technique to enhancing in vitro and in vivo stability of therapeutic proteins and to increasing materials biocompatibility. PEG branched structures have proven useful for protein and peptide modification. Furthermore, they may be better than linear structures for many purposes. This paper describes an improved procedure for obtaining 2-arms PEG based on L-lysine. The efficiency of the synthesis was not related to moisture of the raw materials. This procedure does not use hazardous reagents as previous protocols do. It implemented a purification process for obtaining the desired structure with high purity ( > 99%). Finally, the procedure described here allows the obtaining of others PEGylation reagents.
publisher Sociedade Brasileira de Química
publishDate 2009
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422009000600012
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