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dc.contributor.author
Samelo, Jaime
dc.contributor.author
Mora, Maria Julia
dc.contributor.author
Granero, Gladys Ester
dc.contributor.author
Moreno, Maria João
dc.date.available
2018-12-05T12:51:57Z
dc.date.issued
2017-02
dc.identifier.citation
Samelo, Jaime; Mora, Maria Julia; Granero, Gladys Ester; Moreno, Maria João; Partition of Amphiphilic Molecules to Lipid Bilayers by ITC: LowAffinity Solutes; American Chemical Society; ACS Omega; 2; 10; 2-2017; 6863-6869
dc.identifier.issn
2470-1343
dc.identifier.uri
http://hdl.handle.net/11336/65828
dc.description.abstract
A protocol is developed to allow the accurate characterization of partition to lipid bilayers for solutes with low affinity, using isothermal titration calorimetry. The methodology proposed is suitable for studies using complex membranes, such as intact biomembranes or whole cells. In the method developed, the association is characterized at increasing solute concentrations. This allows the characterization of solute partition into unperturbed membranes, as well as effects induced by high solute concentrations. Most druglike molecules are expected to interact with lowto-moderate affinity with relevant cell membranes. This is due to both the need for a relatively high aqueous solubility of the drug and the poor binding properties of the cell membranes. The methodology is applied to characterize the interaction of antibiotic Rifampicin with 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine and with lipid bilayers representative of bacterial membranes.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
American Chemical Society
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Partition of Amphiphilic Molecules
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Lipid Bilayers
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Isothermal Titration Calorimetry
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Rifampicin
dc.subject.classification
Nano-materiales
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Nanotecnología
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INGENIERÍAS Y TECNOLOGÍAS
dc.title
Partition of Amphiphilic Molecules to Lipid Bilayers by ITC: LowAffinity Solutes
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-10-22T19:36:32Z
dc.journal.volume
2
dc.journal.number
10
dc.journal.pagination
6863-6869
dc.journal.pais
Estados Unidos
dc.description.fil
Fil: Samelo, Jaime. CQC-Biological Chemistry Group; Portugal
dc.description.fil
Fil: Mora, Maria Julia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica; Argentina
dc.description.fil
Fil: Granero, Gladys Ester. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica; Argentina
dc.description.fil
Fil: Moreno, Maria João. CQC-Biological Chemistry Group; Portugal
dc.journal.title
ACS Omega
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/pdf/10.1021/acsomega.7b01145
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1021/acsomega.7b01145
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