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New miniaturised microfluidic biofilter (BF) devices based on silicon micropillars have been developed and tested regarding their ability to extract HBV (Hepatitis B Virus) bacterial DNA from biological sample solutions. The device is composed of a silicon microchannel in which the pillars are distributed at the bottom surface. The extracted DNA solutions were analysed by real time PCR amplification and the biofilter performance was evaluated. The results obtained show that the DNA binding to the biofilters and the elution efficiency strictly depend on the pillars' geometrical dimensions and increase proportionally with the surface/volume ratio. The device exhibiting the best extraction efficiency was then tested in combination with a silicon integrated real time PCR amplification chip as a preliminary step towards the development of genetic point-of-care devices.

We report herein a photoresponsive nanoplatform that delivers nitric oxide (NO) on demand, achieved by the covalent functionalization of graphene oxide (GO) with an amino-terminated nitric oxide (NO) photodonor (NOP1). The resulting GO-NOP1 hybrid nanomaterial is dispersible in water, is very stable in the dark and has been thoroughly characterized by SEM, TEM, AFM, XRD, FTIR and UV-Vis absorption spectroscopy. Photolysis experiments demonstrate that the photodecomposition of the NO photoreleaser integrated into the GO scaffold occurs with an efficiency similar to that observed for a free model compound, ruling out any significant quenching effect (i.e. photoinduced energy/electron transfer) and accounting for the excellent preservation of its photochemical properties upon grafting. A combination of direct amperometric detection and indirect measurements based on a fluorometric assay prove that the remote-controlled release of NO from the GO-NOP1 nanoplatform is exclusively regulated by visible light stimuli.

Background: Several microdevices have been developed to perform only a single step of a genotyping process, such as PCR or detection by probe hybridization. Here, we describe a Lab-on-Chip (LoC) platform integrating a PCR amplification microreactor with a customable microarray for the detection of sequence variations on human genomic DNA., Methods: Preliminary work was focused on developing the single analytical steps including PCR and labeling strategies of the amplified product by conventional reference systems. The optimized protocols included a 1:4 forward:reverse primer ratio for asymmetric PCR, and Cy5-dCTP multiple incorporation for the generation of a labeled PCR product to be hybridized to complementary probes bound to the chip surface., Results: Final conditions were applied to the fully integrated LoC platform for the detection of the IVSI-110 G > A mutation in the human beta-globin (HBB) gene associated with beta-thalassemia, used as a model of genetic application, allowing for correct genotyping of 25 samples that were heterozygous, homozygous or wild-type for this mutation., Conclusions: The overall results show that the present platform is very promising for rapid identification of DNA sequence variations in an integrated, cost effective and convenient silicon chip format.

Thin films of a newly synthesized iron(III) porphyrazine, LFeOESPz ( L = ClEtO, OESPz = ethylsulfanylporphyrazine), have been deposited by the Langmuir-Schafer (LS) technique (horizontal lifting) on ITO or gold substrates. Before deposition, the floating films have been investigated at the air-water interface by pressure/area per molecule (pi/ A) experiments, Brewster angle microscopy (BAM) and UV-vis reflection spectroscopy (RefSpec). The complex reacts with water subphase (pH 6.2) forming the mu-oxo dimer, which becomes the predominant component of the LS films ( LS-Fe) as indicated by optical, IR, XPS, and electrochemical data. LS-Fe multilayers exhibit, between open circuit potential (OCP) and +0.90 V (vs SCE), two independent peak pairs with formal potentials, E surf (I) and E surf(II) of +0.56 V and +0.78 V, respectively. According to dynamic voltammetric and coulometric experiments the peak pair at +0.56 V is attributed to one-electron process at the iron(III) centers on the monomer, while the peak pair at +0.78 V is associated to a four-electron process involving mu-oxo-dimer oligomers. LS-Fe films prove to be quite stable electrochemically between OCP and +0.90 V. The electrochemical stability decreases, however, when the potential range is extended both anodically and cathodically outside these limits, due to formation of new species. Upon incubation with TCA solutions, LS-Fe films show remarkable changes in the UV-vis spectra, which are consistent with a significant mu-oxo dimer --> monomer conversion. Addition of TCA to the electrochemical cell using a LS-Fe film as working electrode, results in a linear increase of a cathodic current peak near -0.40 V as the TCA concentration varies in the 0.1-2.0 mM range. This behavior is interpreted in terms of TCA inducing a progressive change in the composition of the LS-Fe films in favor of the monomeric iron(III) porphyrazine, which is responsible for the observed increase in the cathodic current near -0.40 V.

Thin films consisting of two fulleropyrrolidine derivatives 1 or 2 and a water-soluble porphyrin, TPPS4, were prepared by the Langmuir-Schäfer (LS, horizontal lifting) method. In particular, a solution of the fulleropyrrolidine in chloroform and dimethyl sulfoxide was spread on the water surface, while the porphyrin (bearing peripheral anionic sulfonic groups) was dissolved into the aqueous subphase. To the best of our knowledge, such a versatile method for film fabrication of fullerene/porphyrin mixed composite films has never been used by other researchers. Evidence of the effective interactions between the two components at the air-water interface was obtained from the analysis of the floating layers by means of surface pressure vs area per molecule Langmuir curves, Brewster angle microscopy, and UV-visible reflection spectroscopy. The characterization of the LS films by UV-visible spectroscopy reveals that in each case the two constituents behave as strongly interacting pi systems. The use of polarized light suggests the existence of a preferential direction of the TPPS4 macrocyclic rings with an edge-on arrangement with respect to the substrate surface, regardless which fulleropyrrolidine derivative is in the composite film. Atomic force microscopy investigations give evidence of morphologically flat layers even for LS transfer at low surface pressures. Photoaction spectra were recorded from films deposited by only one horizontal lifting onto indium-tin-oxide (ITO) electrodes, and the observed photocurrent increased notably with increasing transfer surface pressure for both 1/TPPS4 and 2/TPPS4 composite films. IPCE values are larger for 2/TPPS4 systems in comparison with 1/TPPS4 composite layers. Finally, a nonconventional approach to photoinduced phenomena is proposed by differential spectroscopy in the FT-IR attenuated total reflectance (ATR) mode.

This work reports on the structural and spectroscopic properties of ethane-bridged Zn porphyrin dimers (1) in Langmuir-Schäfer (LS) thin films by combining scanning force microscopy (SFM) with film balance, UV-vis absorption, fluorescence, and nanosecond laser flash photolysis measurements. Results show that depending on the surface pressure the Langmuir films of pure 1 can be arranged in two different condensed phases, whereas SFM of the LS films shows characteristic fractal networks constituted by nanoscopic aggregates. The spectral findings agree with a picture in which 1 is apparently present in the anti conformation but aggregated in a sort of H-type structure whose optical features resemble those of the syn conformer. This type of structure is not responsive to light stimuli. By diluting 1 in arachidic acid the porphyrin aggregation is significantly minimized with 1 exhibiting almost exclusively the anti conformation. As a result the LS films become photoresponsive, showing fluorescence emission and triplet-triplet transient absorption.

It is shown, for the first time, that small (ca. 2 nm) and stable platinum nanoparticles can be easily obtained in one step through visible light irradiation of a host-guest inclusion complex between beta-cyclodextrin and platinum acetylacetonate in a water solution. The exclusive control of the reaction by an external trigger, the removal of the undesired reaction products without any manipulation of the sample, and the absence of ionic repulsions between the metal nanoparticles represent the main remarkable advantages offered by this synthetic methodology.

The synthesis of a molecule, 1-(11-dodecylsulfanyl-undecyl)-[4,4']bipyridinium bromide (1), suitable at the same time to form a covalent bond with gold electrodes of a piezoelectric quartz crystal and to interact with heavy metal ions in aqueous solutions, has been successfully accomplished. A commercial quartz crystal microbalance instrument has been modified in order to perform a Flow-Injection Analysis. The behaviour of the system follows the Kanazawa-Gordon equation as demonstrated by measurements with glucose solutions. The self-assembled layer of 1 onto a gold electrode has been characterised by Atomic Force Microscopy before and after the sensing tests. The sensing performances of the modified gold electrode were investigated by monitoring the frequency variation induced by the presence of heavy metal ions, such as lead, cadmium and mercury, in aqueous media. The explored concentrations ranged between 10(-4) and 10(-2) M and the corresponding frequency variations ranged between 10 and 50 Hz. All responses observed were fast, reproducible and reversible. In particular, the response to mercury appears significantly higher in comparison with the other analytes. To the best of our knowledge, this contribution represents the first example of sensing layer based on bipyridinium receptor showing reversible and, at some extent, differentiated response towards heavy metal ions.

Thin films consisting of a fulleropyrrolidine derivative 1 and a novel water-soluble porphyrin 2 were prepared by the Langmuir-Shäfer (LS, horizontal lifting) method. In particular, a solution of 1 in chloroform and dimethyl sulfoxide was spread on the water surface, while porphyrin 2 (bearing peripheral anionic groups) was dissolved into the aqueous subphase. To the best of our knowledge, such a versatile method of film fabrication for fullerene/porphyrin mixed composite films has never been used before. Evidence of the effective interactions between the two moieties at the air-water interface was obtained from the analysis of the floating layers by means of surface pressure versus area per molecule Langmuir curves, Brewster angle microscopy and UV-visible reflection spectroscopy. The characterisation of the LS films by UV-visible spectroscopy reveals that the two constituents behave as discrete and weakly interacting pi systems. The use of polarised light suggests the existence of a preferential direction of the macrocyclic rings with an edge-on arrangement with respect to the substrate surface. Finally, photoaction spectra were recorded from films deposited by only one horizontal lifting onto indium-tin-oxide (ITO) electrodes and the observed photocurrent increased notably with increasing transfer surface pressure.

In this paper the preparation and characterization of Langmuir-Schäfer (LS) films of a novel amphiphilic dipolar complex, [Ru(II)(NH(3))(5)(N-dodecyl-4,4'-bpy)](PF(6))(3) (1), are reported. Preparation of these films, otherwise precluded utilizing standard Langmuir procedures, is achieved by using a subphase at relatively high ionic strength, by addition of NH(4)PF(6). The morphology and the spectroscopic features of the floating films are investigated by Brewster angle microscopy and UV-vis reflection spectroscopy at the water-air interface, respectively, whereas LS films are characterized by absorption spectroscopy and atomic force microscopy. The overall results indicate the existence of aggregates of 1 and formation of homogeneous, densely packed layers. The presented approach could represent a general method to achieve Langmuir-Blodgett films of amphiphilic metal complexes having an "almost naked" multicharged headgroup.

We report the first example of a reversible redox-molecular switch based on dipolar ruthenium(III/II) pentaammine(4,4'-bipyridinium) complexes self-assembled on an optically transparent metal electrode, whose change in molecular properties can be simply detected by transmission spectroscopy with a conventional spectrophotometer.

The cooperative attack of four (dipyrromethanyl)Sm(II) units on dinitrogen resulted in a novel tetranuclear samarium dinitrogen complex (shown schematically). The presence of halogen atoms inhibited reactivity with dinitrogen through the assembly of divalent samarium clusters. dipyrr=diphenylmethyldipyrrolide dianion.