FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states
Interactions of L-cysteine ethyl ester hydrochloride (CE), a bioactive cysteine derivative, with dipalmitoylphosphatidylcholine (DPPC) were investigated. To gain a deeper insight into analyzing L-cysteine ethyl ester HCl interaction with liposomes of DPPC in anhydrous and hydrated states, we perform...
| Autores: | , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2015 |
| País: | Argentina |
| Institución: | Consejo Nacional de Investigaciones Científicas y Técnicas |
| Repositorio: | CONICET Digital (CONICET) |
| Idioma: | inglés |
| OAI Identifier: | oai:ri.conicet.gov.ar:11336/77843 |
| Acceso en línea: | http://hdl.handle.net/11336/77843 |
| Access Level: | acceso abierto |
| Palabra clave: | Raman Ftir Dppc Bilayers Phospholipid Hydrations https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
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FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated statesArias, Juan MarceloTuttolomondo, María EugeniaDíaz, Sonia BeatrizBen Altabef, AídaRamanFtirDppc BilayersPhospholipid Hydrationshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Interactions of L-cysteine ethyl ester hydrochloride (CE), a bioactive cysteine derivative, with dipalmitoylphosphatidylcholine (DPPC) were investigated. To gain a deeper insight into analyzing L-cysteine ethyl ester HCl interaction with liposomes of DPPC in anhydrous and hydrated states, we performed experimental studies by infrared (Fourier transform infrared spectroscopy) and Raman spectroscopies. The results revealed that the interaction of CE with the phospholipid head groups was the same in absence or presence of water. In both states, the wavenumber of the PO2 group and C?N bond of the choline group decreased. This behavior can be ascribed to the replacement of hydration water and binding to the phosphate group. In the Raman spectrum results for the anhydrous and gel states, the S?H stretching band of the CE shifted to lower frequencies with a decrease in its force constant. Biologically active lipophilicmolecules such as CE should be studied in terms of their interaction with lipid bilayers prior to the development of advanced lipid carrier systems such as liposomes. The results of these studies provide information onmembrane integrity and physicochemical properties that are essential for the rational design of lipidic drug delivery systems.Fil: Arias, Juan Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; ArgentinaFil: Tuttolomondo, María Eugenia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; ArgentinaFil: Díaz, Sonia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; ArgentinaFil: Ben Altabef, Aída. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; ArgentinaWiley2015-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/77843Arias, Juan Marcelo; Tuttolomondo, María Eugenia; Díaz, Sonia Beatriz; Ben Altabef, Aída; FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states; Wiley; J. Raman Spectroscopy; 46; 4; 3-2015; 369-3761097-4555CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1002/jrs.4659info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/jrs.4659info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2024-05-08T13:43:20Zoai:ri.conicet.gov.ar:11336/77843instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982024-05-08 13:43:20.532CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states |
| title |
FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states |
| spellingShingle |
FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states Arias, Juan Marcelo Raman Ftir Dppc Bilayers Phospholipid Hydrations https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| title_short |
FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states |
| title_full |
FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states |
| title_fullStr |
FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states |
| title_full_unstemmed |
FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states |
| title_sort |
FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states |
| dc.creator.none.fl_str_mv |
Arias, Juan Marcelo Tuttolomondo, María Eugenia Díaz, Sonia Beatriz Ben Altabef, Aída |
| author |
Arias, Juan Marcelo |
| author_facet |
Arias, Juan Marcelo Tuttolomondo, María Eugenia Díaz, Sonia Beatriz Ben Altabef, Aída |
| author_role |
author |
| author2 |
Tuttolomondo, María Eugenia Díaz, Sonia Beatriz Ben Altabef, Aída |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
Raman Ftir Dppc Bilayers Phospholipid Hydrations https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| topic |
Raman Ftir Dppc Bilayers Phospholipid Hydrations https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| description |
Interactions of L-cysteine ethyl ester hydrochloride (CE), a bioactive cysteine derivative, with dipalmitoylphosphatidylcholine (DPPC) were investigated. To gain a deeper insight into analyzing L-cysteine ethyl ester HCl interaction with liposomes of DPPC in anhydrous and hydrated states, we performed experimental studies by infrared (Fourier transform infrared spectroscopy) and Raman spectroscopies. The results revealed that the interaction of CE with the phospholipid head groups was the same in absence or presence of water. In both states, the wavenumber of the PO2 group and C?N bond of the choline group decreased. This behavior can be ascribed to the replacement of hydration water and binding to the phosphate group. In the Raman spectrum results for the anhydrous and gel states, the S?H stretching band of the CE shifted to lower frequencies with a decrease in its force constant. Biologically active lipophilicmolecules such as CE should be studied in terms of their interaction with lipid bilayers prior to the development of advanced lipid carrier systems such as liposomes. The results of these studies provide information onmembrane integrity and physicochemical properties that are essential for the rational design of lipidic drug delivery systems. |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015-03 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/77843 Arias, Juan Marcelo; Tuttolomondo, María Eugenia; Díaz, Sonia Beatriz; Ben Altabef, Aída; FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states; Wiley; J. Raman Spectroscopy; 46; 4; 3-2015; 369-376 1097-4555 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/77843 |
| identifier_str_mv |
Arias, Juan Marcelo; Tuttolomondo, María Eugenia; Díaz, Sonia Beatriz; Ben Altabef, Aída; FTIR an d Raman analysis of L - cysteine ethyl ester.HCl interaction with dipalmitoylphosphatidylcholine in anhydrous and hydrated states; Wiley; J. Raman Spectroscopy; 46; 4; 3-2015; 369-376 1097-4555 CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1002/jrs.4659 info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/jrs.4659 |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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openAccess |
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https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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application/pdf application/pdf |
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Wiley |
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Wiley |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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15,812429 |