Publications by authors named "Maria Vittoria Russo"

Gold nanoparticles, capped by 3-mercapto propane sulfonate (Au-3MPS), were synthesized inside a swollen sulfonated poly(ether ether ketone) membrane (sPEEK). The formation of the Au-3MPS nanoparticles in the swollen sPEEK membrane was observed by spectroscopic and microscopic techniques. The nanocomposite containing the gold nanoparticles grown in the sPEEK membrane, showed the plasmon resonance λ at about 520 nm, which remained stable over a testing period of three months.

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Gold nanoparticles (AuNPs) represent an effective choice for topical drug delivery systems thanks to their small size, general non-toxicity, ease of functionalization and high surface to volume ratio. Even if systemic, methotrexate still plays an important role in psoriasis treatment: its topical use shows insufficient percutaneus penetration owing to limited passive diffusion, high molecular weight and dissociation at physiological pH. The aim of our study was to design a new drug delivery nanocarrier for Methotrexate and to improve its solubility, stability and biodistribution.

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In this work, a simple and versatile methodology to obtain two different bioconjugated systems has been developed by the immobilization of Candida rugosa lipase (CRL) on hydrophilic gold nanoparticles functionalized with 2-diethylaminoethanethiol hydrochloride (DEA) or with sodium 3-mercapto-1-propanesulfonate (3MPS), namely Au-DEA@CRL and Au-3MPS@CRL. Both spectroscopic and morphological properties of metal nanoparticles have been deeply investigated. The enzyme loading and lipolytic activity of AuNPs@CRL bioconjugates have been studied with respect to different surface functionalization and compared with the free enzyme.

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The hidden structural properties of semicrystalline polymer films are revealed by nanofocused X-ray scattering studies. X-ray cross-correlation analysis (XCCA) is employed to diffraction patterns from blends of poly(3-hexylthiophene) (P3HT) with gold nanoparticles (AuNPs). Spatially resolved maps of orientational distribution of crystalline domains allow us to distinguish sample regions of predominant face-on morphology, with a continuous transition to edge-on morphology.

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Water-soluble gold nanoparticles functionalized by sodium 3-mercapto-1-propansulfonate (Au-3MPS) were synthesized with different Au/thiol molar ratios for their ability to interact with biomolecules. In particular, a synthetic glucocorticoid steroid, i.e.

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Nanostructured composite materials based on polyaniline (PANI) and gold nanoparticles have been prepared by means of an osmosis based method. Several morphologies have been obtained for the pristine nanoPANI and for nanoPANI-Au composite, ranging from amorphous to sponge-like and spherical shapes. On the basis of this morphological investigation, different materials with high surface area have been selected and tested as chemical interactive materials for room temperature gas and vapor sensing.

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The effect of (60)Co gamma rays irradiation on the polymetallayne [-Pt(PBu(3))-C≡C-C(6)H(4)-C(6)H(4)-C≡C-](n) (Pt-DEBP) of defined chain length corresponding to 10 repeat units, has been studied in detail. The UV-vis absorption spectra of Pt-DEBP have been recorded in solution upon exposure of the polymetallayne at increasing radiation doses in the range up to 90 Gy, with special care to the features related to low doses. Complex modifications of the chemical structure of Pt-DEBP could be accessed through NMR, FTIR, GPC, and XPS characterizations, which support the attack of Cl and H radicals coming from the radiolysis of the solvent, CHCl(3), to the triple C≡C bonds of the backbone, leading to the formation of chlorinated double and single C-C bonds, with a concomitant increase of the molecular weight due to a recombinant effect of oligomer fragments upon irradiation.

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Stable gold nanoparticles stabilized by different mono and bi-functional arenethiols, namely, benzylthiol and 1,4-benzenedimethanethiol, have been prepared by using a modified Brust's two-phase synthesis. The size, shape, and crystalline structure of the gold nanoparticles have been determined by high-resolution electron microscopy and full-pattern X-ray powder diffraction analyses. Nanocrystals diameters have been tuned in the range 2 ÷ 9 nm by a proper variation of Au/S molar ratio.

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Noble metal nanoparticles of different sizes and shapes combined with conjugated functional polymers give rise to advanced core shell hybrids with interesting physical characteristics and potential applications in sensors or cancer therapy. In this paper, a versatile and facile synthesis of core shell systems based on noble metal nanoparticles (AuNPs, AgNPs, PtNPs), coated by copolymers belonging to the class of substituted polyacetylenes has been developed. The polymeric shells containing functionalities such as phenyl, ammonium, or thiol pending groups have been chosen in order to tune hydrophilic and hydrophobic properties and solubility of the target core shell hybrids.

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Synthesis and properties of bioconjugates based on functionalized polymeric nanoparticles (PNs) and monoclonal anti-Integrin αV CD51 (aI) antibody were investigated. Polymeric and co-polymeric colloidal nanoparticles with different functionalities, i.e.

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The effect of (60)Co γ irradiation on the absorption and emission spectra of the organometallic polymer [-Pt(PBu(3))(2)-C≡C-C(6)H(4)-C(6)H(4)-C≡C-](n) (Pt-DEBP) in chloroform and toluene solutions for dosimetry applications has been studied. The system Pt-DEBP/chloroform can be used for dosimetric applications in two different ways: (i) monitoring of absorption spectra changes for higher doses (higher than 1 Gy), and (ii) monitoring of emission spectra changes for low doses (below 1 Gy). The response of the polymer solution to γ ray doses has been interpreted with the aid of theoretical studies based on time dependent density functional theory (TD-DFT) calculations on the absorption bands of a model complex and of the possible fragments coming from the degradation of the polymer backbone.

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A modified emulsion copolymerization of phenylacetylene (PA) with hydrophilic monomers having different functions, i.e., acrylic acid (AA) and N,N-dimethylpropargylamine (DMPA) respectively, yields functionalized polymeric P(PA-co-AA) and P(PA-co-DMPA) nanoparticles.

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Multilayers and self-assembled monolayers of on-purpose-prepared organometallic thiolates, trans-[Pd(PBu(3))(2)(SCOCH(3))(2)], trans-[(C(6)H(5)C[triple bond]C)Pd(PBu(3))(2)(SCOCH(3))], and trans,trans-[(CH(3)COS)Pd(PBu(3))(2)(C[triple bond]C-C(6)H(4)-C(6)H(4)-C[triple bond]C)(PBu(3))(2)Pd(SCOCH(3))] were deposited onto gold surfaces. High-resolution X-ray photoelectron spectroscopy and near-edge X-ray absorption fine structure measurements allowed us to assess the anchoring of the organometallic thiols onto gold substrates; the interaction occurring at the interface; and their molecular orientation on the surface with tilt angles of about 30 degrees-40 degrees, depending on the investigated molecule. The molecule packing density/coverage was also assessed.

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In this work the synthesis and characterization of gold nanoparticles functionalized by a novel thiol-organometallic complex containing Pd(II) centers is presented. Pd(II) thiol, trans, trans-[dithiolate-dibis(tributylphosphine)dipalladium(II)-4,4'-diethynylbiphenyl] was synthesized and linked to Au nanoparticles by the chemical reduction of a metal salt precursor. The new hybrid made of organometallic Pd(II) thiol-gold nanoparticles, shows through a single S bridge a direct link between Pd(II) and Au nanoparticles.

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The interaction between gaseous H2S and the surface of several metal-containing oligomers, investigated by emission and absorption spectroscopies, is presented and discussed. The polymetallayne trans-{Cl-[Pt(PBu3)2(CC-C6H4-C6H4-CC)]9Pt(PBu3)2Cl} and related model molecules, i.e.

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Nanostructured polystyrene (PS) and polymethylmethacrylate (PMMA) were used as carriers for the preparation of bioconjugates with lipolytic enzymes, such as Candida rugosa lipase (CRL) and Pseudomonas cepacia lipase (PCL). Simple addition of the lipase solution to the polymeric nanoparticles under protein-friendly conditions (pH 7.6) led to the formation of polymer-enzyme bioconjugates.

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