Publications by authors named "Ramon Iniguez-Palomares"

In recent decades, the development and application of nonviral vectors, such as liposomes and lipidic nanoparticles, for gene therapy and drug delivery have seen substantial progress. The interest in the physicochemical properties and structures of the complexes liposome/DNA and liposome/RNA is due to their potential to substitute viruses as carriers of drugs or genetic material into cells with minimal cytotoxicity, which could lead to their use in gene therapy. Initially, cationic liposomes were utilized as nonviral DNA delivery vectors; subsequently, different molecules, such as polymers, were incorporated to enhance transfection efficiency.

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  • Idiopathic pulmonary fibrosis (IPF) is a severe lung disease with no effective treatments, characterized by abnormal lung tissue growth and scarring.
  • This study explored the potential of Allium sativum nanovesicles (AS-NV) in a mouse model of IPF and found that AS-NV reduced collagen levels and improved lung structure without harming healthy cells.
  • The results indicate that AS-NV may reduce key genes associated with fibrosis and inflammation, suggesting a promising avenue for future IPF treatments, though further research is necessary.
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This study presents a new procedure to condense DNA molecules and precipitate them onto a glass slide. The resulting DNA molecules undergo autonomous self-assembly, creating closed superstructures on the micrometer scale, which are called DNA hyperstructures. These structures can be observed using low-magnification (4×) light microscopy.

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The study, synthesis, and application of nanomaterials in medicine have grown exponentially in recent years. An example of this is the understanding of how nanomaterials activate or regulate the immune system, particularly macrophages. In this work, nanoparticles were synthesized using as a reducing agent (AgRhNPs).

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  • - The study investigates various bis-substituted tetrandrine derivatives and their binding properties to double-stranded DNA (dsDNA) using techniques like UV-vis and fluorescence, revealing their high affinity for dsDNA, especially the bis(methyl)anthraquinone (BAqT) and bis(ethyl)indole (BInT) derivatives, with binding constants around 10^-10 M.
  • - Utilizing viscometry, ethidium displacement assays, and molecular modeling, researchers identified that these compounds interact with dsDNA through a dual mechanism involving intercalation and major groove binding.
  • - Cytotoxicity tests showed low toxicity for most derivatives against various cell lines, except for the bis(methyl)pyrene (
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  • - A green method has been developed to synthesize gold nanoparticles using a hydroethanolic extract from fruit, serving as both a reducing and stabilizing agent (AuVmNPs).
  • - The synthesized nanoparticles are primarily spherical with two size populations averaging 12.5 and 22.5 nm, and their formation and characteristics were analyzed through various imaging techniques.
  • - AuVmNPs demonstrate low toxicity in human cell lines and significantly inhibit cell migration, suggesting their potential for use in antiangiogenic research.
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In this work, we used a sequential method of synthesis for gold-silver bimetallic nanoparticles with core@shell structure (Au@AgNPs). Rumex hymenosepalus root extract (Rh), which presents high content in catechins and stilbenes, was used as reductor agent in nanoparticles synthesis. Size distribution obtained by Transmission Electron Microscopy (TEM) gives a mean diameter of 36 ± 11 nm for Au@AgNPs, 24 ± 4 nm for gold nanoparticles (AuNPs), and 13 ± 3 nm for silver nanoparticles (AgNPs).

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In this work we use Mimosa tenuiflora (MtE) extracts as reducing agents to synthesize silver nanoparticles (AgMt NPs) which were characterized by DPPH and Total Polyphenols Assays, UV-visible, X-ray diffractometer (XRD), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS) and Thermogravimetric analysis (TGA). AgMt NPs possess average sizes of 21 nm and fcc crystalline structure, it was also confirmed that the MtE is present in the AgMt NPs even after the cleaning protocol applied. Subsequently, carbopol hydrogels were made and the MtE and the synthesized AgMt NPs were dispersed in different gels (MtE-G and AgMt NPs-G, respectively) at 100 µg/g concentration.

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Synthesis of gold nanoparticles (AuNPs) with plant extracts has gained great interest in the field of biomedicine due to its wide variety of health applications. In the present work, AuNPs were synthesized with Mimosa tenuiflora (Mt) bark extract at different metallic precursor concentrations. Mt extract was obtained by mixing the tree bark in ethanol-water.

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We synthesized silver nanoparticles using Rumex hymenosepalus root extract (Rh). Nanoparticles were subjected to a purification process and final product is a composite of Rh and silver nanoparticles (AgNPsC). Transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) were used to perform a microstructure study.

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We have synthesized silver nanoparticles in the non-polar phase of non-aqueous microemulsions. The nanocrystals have been grown by reducing silver ions in the microemulsion cylindrical micelles formed by the reducing agent (ethylene glycol). By a careful deposit of the microemulsion phase on a substrate, the micelles align in a hexagonal geometry, thus forming a 2D array of parallel strings of individual silver nanoparticles on the substrate.

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We have synthesized silver nanoparticles from silver nitrate solutions using extracts of Rumex hymenosepalus, a plant widely found in a large region in North America, as reducing agent. This plant is known to be rich in antioxidant molecules which we use as reducing agents. Silver nanoparticles grow in a single-step method, at room temperature, and with no addition of external energy.

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We have performed a dynamic light-scattering (DLS) investigation of the effect of a water-soluble polymer, polyethylene glycol (PEG), on the bending elastic modulus κ of surfactant membranes. The polymer, in concentrations ranging from 0 to 8 g/L (0 to 0.4 mM), was incorporated into the solvent of sponge phases of the sodium dodecyl sulfate (SDS)-hexanol-brine system.

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