Publications by authors named "Jose Antonio Lebron"

The goal of this work is to investigate if the synergistic antifungal activity between cyclosporine A, CsA, and voriconazole, VRZ, increases when both drugs are encapsulated in a nanocarrier as compared when they are free. The preparation and characterization of blank and VRZ and CsA loaded polymeric based PLGA nanoparticles (PLGA, PLGA-PEG, and PLGA+PEG) was a necessary previous step. Using the more suitable NPs, those of PLGA, the antifungal susceptibility tests performed with VRZ-loaded PLGA NPs, show no significant increase of the antifungal activity in comparison to that of free VRZ.

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  • Research on flavonoids, dating back to 1937, shows they can help treat various diseases like cancer and AIDS due to their effectiveness against free radicals, but their medical use is limited by poor absorption and solubility.
  • * Recent studies focus on using nanocarriers, specifically carbon nanotubes (CNTs), to enhance the oral absorption and stability of 7-hydroxyflavone (7-HF) by protecting it from degradation and facilitating its transport in the body.
  • * The interactions between 7-HF and different types of CNTs were examined, including their release profiles at varying pH levels to understand how they might behave in the human body.*
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  • The study focused on creating calixarene-based liposomes and characterizing them using various techniques, employing four different amphiphilic calixarenes with varying hydrophobic chain lengths and polar groups.
  • The liposomes were formed using one calixarene and DOPE phospholipid, followed by cytotoxicity assessments across different cell lines.
  • The least toxic calixarene (TEAC) was successfully utilized to deliver nucleic acids and the cancer drug doxorubicin, showing improved transfection efficiency with extra DOPE and demonstrating high encapsulation and controlled release of the drug.
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The interaction between calf-thymus DNA, ctDNA, and various single-chained surfactants with different functional groups at the end of hydrophobic tail was studied with the goal of investigating the influence of the functional group nature on surfactant DNA compacting efficiency. The surfactants investigated were dodecyltriethylammonium bromide (DTEABr), triethyl(1-phenoxydodecyl)ammonium bromide (12PhBr), triethyl(2-naphthoxydodecyl)ammonium bromide (12NBr) and 11-(isonicotinoyloxy)-,,-triethyl-1-undecanaminium bromide (11PyBr). Results made evident that the surfactants' tendencies to self-aggregation is the key factor determining their efficiency to compact the nucleic acid.

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The interaction (adsorption process) of commercial ionic surfactants with non-functionalized and functionalized carbon nanotubes (CNTs) has been studied by potentiometric measurements based on the use of ion-selective electrodes. The goal of this work was to investigate the role of the CNTs' charge and structure in the CNT/surfactant interactions. Non-functionalized single- (SWCNT) and multi-walled carbon nanotubes (MWCNT), and amine functionalized SWCNT were used.

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Gene therapy is a therapeutic process consisting of the transport of genetic material into cells. The design and preparation of novel carriers to transport DNA is an important research line in the medical field. Hybrid compounds such as metallo-liposomes, containing a mixture of lipids, were prepared and characterized.

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Article Synopsis
  • The study examines how different types of surfactants, specifically oligomeric ones, interact with calf thymus DNA (ctDNA) and how varying their structures affects this interaction.
  • It highlights that dimeric surfactants are particularly effective in changing the nucleic acid's charge and provides insights into how the arrangement of positive charges and hydrophobic tails in surfactants influences ctDNA condensation.
  • The findings suggest that designing better cationic surfactants could enhance their use as non-viral gene therapy vectors.
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Cefepime is an antibiotic with a broad spectrum of antimicrobial activity. However, this antibiotic has several side effects and a high degradation rate. For this reason, the preparation and characterization of new liposomes that are able to encapsulate this antibiotic seem to be an important research line in the pharmaceutical industry.

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The goal of this work was to understand the key factors determining the DNA compacting capacity of single-chained cationic surfactants. Fluorescence, zeta potential, circular dichroism, gel electrophoresis and AFM measurements were carried out in order to study the condensation of the nucleic acid resulting from the formation of the surfactant-DNA complexes. The apparent equilibrium binding constant of the surfactants to the nucleic acid, K, estimated from the experimental results obtained in the ethidium bromide competitive binding experiments, can be considered directly related to the ability of a given surfactant as a DNA compacting agent.

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