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    <title>Colibri Colección : Incluye artículos, objetos de conferencias, seminarios y jornadas, reportes técnicos, comunicaciones y otros</title>
    <link>https://hdl.handle.net/20.500.12008/26173</link>
    <description>Incluye artículos, objetos de conferencias, seminarios y jornadas, reportes técnicos, comunicaciones y otros</description>
    <pubDate>Tue, 07 Jul 2026 18:33:04 GMT</pubDate>
    <dc:date>2026-07-07T18:33:04Z</dc:date>
    <item>
      <title>Echinococcus granulosus antigen B acts as an LPS-scavenging lipoprotein in vitro, preventing TLR4-mediated activation of dendritic cells</title>
      <link>https://hdl.handle.net/20.500.12008/55730</link>
      <description>Título: Echinococcus granulosus antigen B acts as an LPS-scavenging lipoprotein in vitro, preventing TLR4-mediated activation of dendritic cells
Autor: Lagos Magallanes, S.; Beasley Lomazzi, A.; Zamarreño, F.; Carrión, F.; Fló, M.; Dutto, J.; Julve, J.; Costabel, M.; Maccioni, M.; Folle, A.M.; Ferreira, A.M.
Resumen: Echinococcus granulosus sensu lato antigen B (EgAgB) is a major parasite lipoprotein, produced by the hydatid and released at the host-parasite interface. Accumulating evidence supports that EgAgB may exert immunomodulatory effects on myeloid cells; however, the underlying molecular mechanisms remain poorly understood. We examined the impact of native EgAgB (nEgAgB) and recombinant EgAgB8/1 (rEgAgB) in lipopolysaccharide (LPS)-induced activation of bone marrow-derived dendritic cells (BMDC) to help elucidate these mechanisms. Both immunoaffinity-purified nEgAgB or rEgAgB induced modest BMDC activation, indicated by the production of IL-6, IL-12p40, and nitric oxide, but not IFN-β. This activation was primarily attributed to LPS traces in EgAgB preparations since it was nearly abolished by a specific TLR4 inhibitor and in Tlr4−/− BMDC, while EgAgB binding to BMDC was TLR4 independent. Notably, both nEgAgB and rEgAgB inhibited LPS-induced cytokine and nitric oxide production and disrupted TLR4 dimerization and endocytosis. Competitive binding assays showed that EgAgB and human high-density lipoprotein (hHDL) similarly inhibited LPS binding to macrophages and BMDC; however, EgAgB more effectively suppressed LPS-induced cytokine secretion. Contrastingly, EgAgB did not modulate BMDC responses to lipoteichoic acid, unlike hHDL. Using a lipoprotein capture and an ELISA-like assay, we demonstrated a higher potential of EgAgB to bind LPS than hHDL. Additionally, docking analyzes suggest the presence of a defined LPS-binding interface in EgAgB8/1 subunit. Overall, these findings reveal a novel binding property of EgAgB, which enables it to act as an extracellular LPS scavenger, interfering with TLR4-mediated LPS recognition and downstream proinflammatory responses in myeloid cells.</description>
      <pubDate>Thu, 01 Jan 2026 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://hdl.handle.net/20.500.12008/55730</guid>
      <dc:date>2026-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Computational study of carbon-doped TiO2(B) nanomaterials for improved dye-sensitized solar cells</title>
      <link>https://hdl.handle.net/20.500.12008/55702</link>
      <description>Título: Computational study of carbon-doped TiO2(B) nanomaterials for improved dye-sensitized solar cells
Autor: Heffner, Herman; Marchetti, Jorge M.; Faccio, Ricardo; López-Corral, Ignacio
Resumen: Surface doping has emerged as a promising approach to enhance the reactivity and optoelectronic&#xD;
properties of titanium dioxide (TiO2) and other inorganic oxide semiconductors. This strategy has&#xD;
significant potential to improve the efficiency and long-term stability of dye-sensitized solar cells&#xD;
(DSSCs). The present study employs density functional theory (DFT) calculations to investigate,&#xD;
for the first time, the adsorption behavior of the organometallic N719 dye on pristine and carbondoped&#xD;
ultrathin TiO2(B) films. Initially, the interaction between the N719 dye and the pristine TiO2(B)&#xD;
(100) surface is examined, considering various molecular orientations and anchoring configurations.&#xD;
The adsorption energies and the resultant changes in the semiconductor’s electronic structure are&#xD;
determined. Subsequently, the impact of carbon doping on the preferential adsorption configurations&#xD;
is analyzed. The results reveal that the adsorption of the N719 dye is energetically favorable on&#xD;
both the pristine and C-doped TiO2(B) (100) surfaces. Notably, all adsorption-related properties are&#xD;
significantly enhanced after carbon doping, with the adsorption energy increasing by up to 300%&#xD;
compared to the undoped surface. This substantial increase in adsorption performance is critical for&#xD;
achieving highly efficient and long-lasting DSSCs.</description>
      <pubDate>Thu, 01 Jan 2026 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://hdl.handle.net/20.500.12008/55702</guid>
      <dc:date>2026-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Molecular insights into soy protein–lupin flour meat analogues through FTIR spectrochemical analysis</title>
      <link>https://hdl.handle.net/20.500.12008/55689</link>
      <description>Título: Molecular insights into soy protein–lupin flour meat analogues through FTIR spectrochemical analysis
Autor: Kadam, Aayushi; Rodriguez Elhordoy, Matías; Vazquez, Daniel; Medrano, Alejandra; Gough, Kathleen M.; Koksel, Filiz
Resumen: Fourier transform infrared (FTIR) spectroscopy and spectrochemical imaging were used to investigate the structural and compositional changes in extruded high-moisture meat analogues (HMMAs) produced from soy protein isolate and lupin flour (LF) blends. Extrusion induced shifts in the amide I band (~1637 cm−1 in raw blends to ~1650 cm−1 in HMMAs), indicating protein denaturation and structural rearrangement associated with fibrous structure formation. Changes in carbohydrate- and lipidassociated bands further reflected extrusion-driven molecular reorganization. FTIR spectrochemical analysis revealed distinct HMMA regions, including aligned protein-rich domains and lipid−starch-rich domains appearing as polygonal grids. Increasing the LF content from 15 to 45% progressively increased lipid- and carbohydrate-associated spectral features (i.e., areas of the fatty acid ester peak at 1744 cm−1 and the carbohydrate peak around 1060 cm−1) relative to proteins. These insights advance the understanding of structure−function relationships in HMMAs and highlight the value of FTIR spectrochemical imaging for optimizing texture and the effective design of meat analogues.</description>
      <pubDate>Thu, 01 Jan 2026 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://hdl.handle.net/20.500.12008/55689</guid>
      <dc:date>2026-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Rate –limiting steps of the oxygen reduction reaction in REBa2Cu3O6+ẟ (RE = La, Nd, Sm, Gd and Y) layered perovskites as IT-SOFC cathodes</title>
      <link>https://hdl.handle.net/20.500.12008/55554</link>
      <description>Título: Rate –limiting steps of the oxygen reduction reaction in REBa2Cu3O6+ẟ (RE = La, Nd, Sm, Gd and Y) layered perovskites as IT-SOFC cathodes
Autor: Grassi, J.; Montenegro-Hernandez, A.; Serquis, A.C.; Basbus, J.F.; Suescun, L
Resumen: The classical high-temperature superconductor YBa2Cu3O6+δ (YBCO) with an oxygen-vacant triple perovskite&#xD;
structure has been proposed as a potential cathode for Intermediate Temperature Solid Oxide Fuel Cells (ITSOFCs),&#xD;
and REBa2Cu3O6+ẟ (RE = La, Nd, Sm, Gd and Y) triple perovskites synthesized by a self-combustion&#xD;
method were evaluated. The total substitution of Y by lanthanide ions (RE3+) proved to modify relevant bulk&#xD;
and surface properties, thus changing performance under operating conditions, i.e., the incorporation–diffusion&#xD;
mechanism by oxygen vacancies and oxide anion transport. Electrochemical Impedance Spectroscopy (EIS)&#xD;
under different oxygen partial pressure (pO2) and temperature (T) conditions allowed elucidating a co-limited&#xD;
oxygen incorporation/diffusion mechanism as Oxygen-Reduction Reaction (ORR) limiting steps. Ionic radii&#xD;
(ri) variation from Y3+ to La3+ impacts the kinetics of the two steps, thereby modifying the overall cathode&#xD;
performance. The results provide evidence of the complex relationship between crystallography, point defect&#xD;
concentration, chemical composition and electrochemical properties in REBCO cathodes. Data suggest that the&#xD;
Cu–O bond distance in cuprates may be critical for shifting the rate-limiting step and improving ORR activity.&#xD;
Overall, this research advances the comprehension of ORR kinetics in cobalt-free materials with layered&#xD;
diffusion.</description>
      <pubDate>Thu, 01 Jan 2026 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://hdl.handle.net/20.500.12008/55554</guid>
      <dc:date>2026-01-01T00:00:00Z</dc:date>
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