Loredana Latterini

Plasmonic Nanobubbles as Transient Vapor Nanobubbles Generated Around Plasmonic Nanoparticles

We have used short laser pulses to generate transient vapor nanobubbles around plasmonic nanoparticles. The photothermal, mechanical, and optical properties of such bubbles were found to be different from those of plasmonic nanoparticle and vapor bubbles, as well. This phenomenon was considered as a new complex nanosystem-plasmonic nanobubble (PNB). Mechanical and optical scattering properties of PNB depended upon the nanoparticle surface and heat capacity, clusterization state, and the optical pulse length. The generation of the PNB required much higher laser pulse fluence thresholds than the explosive boiling level and was characterized by the relatively high lower threshold of the minimal size (lifetime) of PNB. Optical scattering by PNB and its diameter (measured as the lifetime) has been varied with the fluence of laser pulse, and this has demonstrated the tunable nature of PNB.

Photophysical Properties and Antibacterial Activity of Meso-substituted Cationic Porphyrins¶

A series of derivatives of 5,10,15,20‐tetrakis‐(4‐N‐methylpyridyl)‐porphine, where one N‐methyl group was replaced by a hydrocarbon chain ranging from C6 to C22, were characterized for their photophysical and photosensitizing properties. The absorption and fluorescence features of the various compounds in neutral aqueous solutions were typical of largely monomeric porphyrins, with the exception of the C22 derivative, which appeared to be extensively aggregated. This was confirmed by the very low triplet quantum yield and lifetime of the C22 derivative as compared with 0.2–0.7 quantum yields and 88–167 μs lifetimes for the other porphyrins. The photophysical properties and photosensitizing activity toward N‐acetyl‐l‐tryptophanamide of the C22 porphyrin became comparable to those typical of the other derivatives in 2% aqueous sodium dodecyl sulfate, where the C22 compound is fully monomerized. All the porphyrin derivatives exhibited at micromolar concentrations photoinactivation activity against both Staphylococcus aureus and Escherichia coli, even though the gram‐negative bacteria were markedly less photosensitive. The photosensitizing efficiency was influenced by (1) the amount of cell‐bound porphyrin, which increased with increasing length of the hydrocarbon chain; and (2) the tendency to undergo partial aggregation in the cell, which seems to be especially important for the C22 derivative.

Nano-biocomposite films with modified cellulose nanocrystals and synthesized silver nanoparticles

Ternary nano-biocomposite films based on poly(lactic acid) (PLA) with modified cellulose nanocrystals (s-CNC) and synthesized silver nanoparticles (Ag) have been prepared and characterized. The functionalization of the CNC surface with an acid phosphate ester of ethoxylated nonylphenol favoured its dispersion in the PLA matrix. The positive effects of the addition of cellulose and silver on the PLA barrier properties were confirmed by reductions in the water permeability (WVP) and oxygen transmission rate (OTR) of the films tested. The migration level of all nano-biocomposites in contact with food simulants were below the permitted limits in both non-polar and polar simulants. PLA nano-biocomposites showed a significant antibacterial activity influenced by the Ag content, while composting tests showed that the materials were visibly disintegrated after 15 days with the ternary systems showing the highest rate of disintegration under composting conditions.

Preparation and photo-physical characterisation of nanocomposites obtained by intercalation and co-intercalation of organic chromophores into hydrotalcite-like compounds

Several chromophores with donor–acceptor properties and containing a carboxylic or sulfonic group [coumarin-3-carboxylic acid (3-CCA), 9-anthracenecarboxylic acid (9-ACA), 4-benzoylbenzoic acid (4-BBA) and 2-naphthalenesulfonic acid (2-NSA)] have been intercalated into Mg–Al hydrotalcite-like compounds, both via anion exchange procedures and by using the “memory effect” of the hydrotalcites. The obtained intercalation compounds have been characterised by X-ray diffractometry, thermal analysis and chemical composition. Data obtained indicate that the guest species are accommodated in the interlayer region as a monofilm of interdigitaded anions with the C–COO− or C–SO3− bond almost perpendicular to the layer plane. The pairs of chromophores investigated, 3-CCA–9-ACA and 4-BBA–2-NSA, can give rise to energy transfer processes because of the characteristics of their excited states. Co-intercalation of the above-mentioned pairs of chromophores has been achieved with different synthetic procedures. The mono-intercalated and co-intercalated systems were investigated by absorption and emission spectroscopy and by laser flash photolysis. The absorption spectrum of MgAl-9-ACA shows an unexpected band around 490 nm that was attributed to an aggregate. The fluorescence characteristics of the various co-intercalated samples depend on the excitation wavelength and on the preparation methods, which control the relative amounts of the two fluorophores in the interlayer region. In all the samples containing 9-ACA excitation around 500 nm generates an emission attributed to the anthracene aggregate. In mono-intercalated and co-intercalated samples, the fluorescence decays satisfactorily fit bi-exponential and tri-exponential functions, respectively. Laser flash photolysis experiments showed that excitation of the intercalated chromophores produces transients which can be attributed to the guest triplets and, in the case of co-intercalated 4-BBA–2-NSA composite, the probable occurrence of an energy transfer process.

Ag/AgCl nanoparticle decorated layered double hydroxides: synthesis, characterization and antimicrobial properties

A layered double hydroxide (LDH) surface was employed as a substrate for growing silver nanoparticles (NPs). An efficient method to produce stable silver/silver chloride nanoparticles supported on the ZnAl-LDH surface was developed. NPs of AgCl were grown on the ZnAl-LDH surface by using AgNO3 as the silver source. The ZnAl-LDH in chloride form acts as a nucleating agent, and depending on the pH of the LDH dispersion, AgClNPs with different dimensions were obtained. In particular AgClNPs with a diameter of 60 nm were formed at pH 5. The AgClNPs supported on LDH sheets were partially reduced by different reducing agents (NaBH4 and formaldehyde) resulting in a Ag/AgCl-LDH nanocomposite. The silver chloride and silver NP dimensions were evaluated by X-ray powder diffraction, field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). UV-Vis spectra of the samples upon reduction showed a band centred at 415 nm due to the surface plasmon resonance of silver nanoparticles with a diameter of about 10 nm, in agreement with the TEM analysis. The AgCl-LDH and Ag/AgCl-LDH nanocomposites, subjected to antimicrobial tests, exhibited good antimicrobial activity against both Gram-negative (Pseudomonas aeruginosa) and Gram-positive (Staphylococcus epidermidis and S. aureus) bacteria and yeast (Candida albicans). The nanocomposites were also studied for their ability to release silver by obtaining release curves, under conditions of antibacterial assays. Finally, the nanocomposites antibacterial behavior, as a function of time, was investigated by performing time-kill experiments using S. aureus and Candida albicans.

Structure and catalytic behavior of myoglobin adsorbed onto nanosized hydrotalcites.

The adsorption of myoglobin (Mb) onto nanosized nickel aluminum hydrotalcite (NiAl-HTlc) surface was studied, and the structural properties of the resulting protein layer were analyzed by using FT-IR, Raman, and fluorescence spectroscopies. Upon adsorption onto the nanoparticle surface, the protein molecules maintained their secondary structure, while the tertiary structure was altered. The fluorescence spectra and anisotropy values of adsorbed Mb revealed that the emitting amino acid residues are affected by different microenvironments when compared to the native protein behavior. Moreover, the decrease of fluorescence decay times of tryptophan indicated the occurrence of interactions among the fluorophores and the constituents of the nanoparticles, such as the metal cations, which can take place when conformational changes of Mb occur. Raman spectra indicated that the interaction of Mb molecules with NiAl-HTlc nanoparticles modified the porphyrin core, changing the spin state of the heme iron from high spin (HS) to low spin (LS). The enzymatic activity of the nanostructured biocomposite was evaluated in the oxidation of 2-methoxyphenol by hydrogen peroxide and discussed on the basis of structural properties of adsorbed myoglobin.

Excited state properties and in vitro phototoxicity studies of three phenothiazine derivatives

Abstract This work concerns a combined photophysical, photochemical and photobiological study of three drugs (psychotherapeutic agents) of the phenothiazine series: perphenazine, fluphenazine hydrochloride and thioridazine hydrochloride. The excited-state properties were first investigated by stationary and time-resolved fluorimetry and by laser flash photolysis. The spectral description was assisted by quantum-mechanical calculations with the INDO/1-CI method. In organic media the lowest excited singlet state was found to decay by fluorescence (small quantum yield) and mainly by intersystem crossing to the lowest triplet state, which is responsible for oxygen photosensitization (high yields of singlet oxygen production) and photodegradation. A further decay pathway in aqueous solutions was the photoionization process, which led to the formation of the phenothiazine radical cations and the solvated electron. After the preliminary study of the photobehavior in organic solvents and in water, the phototoxicity of the three drugs was investigated on various biological substrates through a series of in vitro assays under UVA irradiation. Photohemolysis of mouse erythrocytes and phototoxicity on cultured murine fibroblasts were observed for all three compounds. Lipid photoperoxidation was then investigated using linoleic acid as the unsaturated lipid model and isolated red blood cell membranes. The drug-induced photodamage was also evaluated on proteins by measuring the photosensitizing cross-linking in erythrocyte ghosts. The combined approach proved to be useful in understanding the mechanism by which these phenothiazine derivatives induce skin photosensitization. In particular, the photophysical properties of the compounds under investigation and the results of the study on their phototoxicity are in agreement with a mechanism that involves the radical cation of the drugs as a main intermediate.

Sensing Proteins with Luminescent Silica Nanoparticles

Nanometer sized silica nanoparticles (SiO2-NP) were prepared in water and loaded with two organic compounds, namely perylene and 1,6-diphenyl-1,3,5-hexatriene, which have well-defined and known fluorescence properties. The size of void and dye-doped SiO2-NP were determined by both transmission electron microscopy and atomic force microscopy, which allowed determining the loading effects on the particle size and morphology. Differently loaded nanoparticles were characterized by both steady-state and time-resolved spectrofluorimetric techniques. The spectroscopic characterization allowed in the first place to establish where the dye molecules are localized within the particles and, later, to evaluate the sensing capability of the hybrid materials with respect to proteins. In particular, dye molecules resulted to have a bimodal distribution on the particle template, specifically (i) at the particle/water interphase and (ii) in close contact with the silica surface (in the inner particle). To prove the ability of the as-prepared and characterized particles to interact with proteins, BSA and RNA-si were used as models; the particle fluorescence was used as a sensitive tool to monitor the occurrence of such interactions. In all cases, proteins interact very efficiently with the SiO2-NP mainly through static interactions likely determined by electrostatic forces. A quantitative analysis of the steady-state fluorescence quenching experiments allowed to estimate the interaction radius, which is a useful parameter to sense and to discriminate proteins.

Chitosan films containing mesoporous SBA-15 supported silver nanoparticles for wound dressing

Chitosan films containing mesoporous SBA-15 supported silver nanoparticles (AgNPs) were prepared to be applied as a potential wound dressing material. First SBA-15-silver nanoparticle (SBA-15-Ag) composite materials were prepared by a controlled annealing process without the use of organic solvents and reagents. The SBA-15-AgNPs were characterized in detail by X-ray powder diffraction, field emission scanning electron microscopy and transmission electron microscopy which evidenced the presence of uniformly distributed silver nanostructures inside the silicate pores. UV-vis spectra of the sample showed a band at 430 nm characteristic of the surface plasmon resonance of silver nanoparticles with a diameter below 10 nm and X-ray photoemission spectra confirmed the formation of metal-nanoparticles on the silicate template. Then SBA-15-Ag was used to prepare chitosan films which were characterized in detail. In particular, they showed good hydration properties, water vapor transmission rate and mechanical properties. After hydration films exhibited good antimicrobial activity against both Gram-negative (Pseudomonas aeruginosa) and Gram-positive (Staphylococcus epidermidis and S. aureus) bacteria.

Modeling, Preparation, and Characterization of a Dipole Moment Switch Driven by Z/E Photoisomerization

We report the results of a multidisciplinary research effort where the methods of computational photochemistry and retrosynthetic analysis/synthesis have contributed to the preparation of a novel N-alkylated indanylidene-pyrroline Schiff base featuring an exocyclic double bond and a permanent zwitterionic head. We show that, due to its large dipole moment and efficient photoisomerization, such a system may constitute the prototype of a novel generation of electrostatic switches achieving a reversible light-induced dipole moment change on the order of 30 D. The modeling of a peptide fragment incorporating the zwitterionic head into a conformationally rigid side chain shows that the switch can effectively modulate the fluorescence of a tryptophan probe.