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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  
dc.subject
Lipid Bilayers  
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Isothermal Titration Calorimetry  
dc.subject
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