USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN
Autor(a) principal: | |
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Data de Publicação: | 1997 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Chemical Engineering |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66321997000400011 |
Resumo: | The self-assembly technique is employed for producing alternating ultra-thin films of lysozyme and poly(styrene sulfonate) (PSS). The influence of important parameters in the self-assembly process, namely immersion time, drying method, solution pH and ionic strength, on adsorption kinetics is investigated by ultraviolet (UV) spectroscopy. The absorbance increases rapidly in the initial stages of adsorption for all pHs studied, before reaching a plateau indicative of complete adsorption. Adsorption is considerably more effective when the proton concentration in the solution increases, which is attributed to the increase in the positive charge density within the protein molecules. Furthermore, UV absorbance increases linearly with the number of bilayers (lysozyme/PSS), indicating that a constant amount of material is being adsorbed at each deposition process. These results are highly promising as the self-assembled films are of great interest for biotechnology and molecular electronic applications |
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Brazilian Journal of Chemical Engineering |
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USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEINUltra-thin filmsadsorption kineticsself-assemblyproteinsThe self-assembly technique is employed for producing alternating ultra-thin films of lysozyme and poly(styrene sulfonate) (PSS). The influence of important parameters in the self-assembly process, namely immersion time, drying method, solution pH and ionic strength, on adsorption kinetics is investigated by ultraviolet (UV) spectroscopy. The absorbance increases rapidly in the initial stages of adsorption for all pHs studied, before reaching a plateau indicative of complete adsorption. Adsorption is considerably more effective when the proton concentration in the solution increases, which is attributed to the increase in the positive charge density within the protein molecules. Furthermore, UV absorbance increases linearly with the number of bilayers (lysozyme/PSS), indicating that a constant amount of material is being adsorbed at each deposition process. These results are highly promising as the self-assembled films are of great interest for biotechnology and molecular electronic applicationsBrazilian Society of Chemical Engineering1997-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66321997000400011Brazilian Journal of Chemical Engineering v.14 n.4 1997reponame:Brazilian Journal of Chemical Engineeringinstname:Associação Brasileira de Engenharia Química (ABEQ)instacron:ABEQ10.1590/S0104-66321997000400011info:eu-repo/semantics/openAccessBorato,C.E.Herrmann,P.S.P.Colnago,L.A.Oliveira Jr.,O.N.Mattoso,L. H. C.eng1998-10-06T00:00:00Zoai:scielo:S0104-66321997000400011Revistahttps://www.scielo.br/j/bjce/https://old.scielo.br/oai/scielo-oai.phprgiudici@usp.br||rgiudici@usp.br1678-43830104-6632opendoar:1998-10-06T00:00Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ)false |
dc.title.none.fl_str_mv |
USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN |
title |
USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN |
spellingShingle |
USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN Borato,C.E. Ultra-thin films adsorption kinetics self-assembly proteins |
title_short |
USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN |
title_full |
USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN |
title_fullStr |
USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN |
title_full_unstemmed |
USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN |
title_sort |
USING THE SELF-ASSEMBLY TECHNIQUE FOR THE FABRICATION OF ULTRA-THIN FILMS OF A PROTEIN |
author |
Borato,C.E. |
author_facet |
Borato,C.E. Herrmann,P.S.P. Colnago,L.A. Oliveira Jr.,O.N. Mattoso,L. H. C. |
author_role |
author |
author2 |
Herrmann,P.S.P. Colnago,L.A. Oliveira Jr.,O.N. Mattoso,L. H. C. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Borato,C.E. Herrmann,P.S.P. Colnago,L.A. Oliveira Jr.,O.N. Mattoso,L. H. C. |
dc.subject.por.fl_str_mv |
Ultra-thin films adsorption kinetics self-assembly proteins |
topic |
Ultra-thin films adsorption kinetics self-assembly proteins |
description |
The self-assembly technique is employed for producing alternating ultra-thin films of lysozyme and poly(styrene sulfonate) (PSS). The influence of important parameters in the self-assembly process, namely immersion time, drying method, solution pH and ionic strength, on adsorption kinetics is investigated by ultraviolet (UV) spectroscopy. The absorbance increases rapidly in the initial stages of adsorption for all pHs studied, before reaching a plateau indicative of complete adsorption. Adsorption is considerably more effective when the proton concentration in the solution increases, which is attributed to the increase in the positive charge density within the protein molecules. Furthermore, UV absorbance increases linearly with the number of bilayers (lysozyme/PSS), indicating that a constant amount of material is being adsorbed at each deposition process. These results are highly promising as the self-assembled films are of great interest for biotechnology and molecular electronic applications |
publishDate |
1997 |
dc.date.none.fl_str_mv |
1997-12-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66321997000400011 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0104-66321997000400011 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0104-66321997000400011 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Brazilian Society of Chemical Engineering |
publisher.none.fl_str_mv |
Brazilian Society of Chemical Engineering |
dc.source.none.fl_str_mv |
Brazilian Journal of Chemical Engineering v.14 n.4 1997 reponame:Brazilian Journal of Chemical Engineering instname:Associação Brasileira de Engenharia Química (ABEQ) instacron:ABEQ |
instname_str |
Associação Brasileira de Engenharia Química (ABEQ) |
instacron_str |
ABEQ |
institution |
ABEQ |
reponame_str |
Brazilian Journal of Chemical Engineering |
collection |
Brazilian Journal of Chemical Engineering |
repository.name.fl_str_mv |
Brazilian Journal of Chemical Engineering - Associação Brasileira de Engenharia Química (ABEQ) |
repository.mail.fl_str_mv |
rgiudici@usp.br||rgiudici@usp.br |
_version_ |
1754213170315001856 |