6 results match your criteria: "National Nanotechnology Laboratory (NNL)-Institute of Nanoscience (NANO)[Affiliation]"

mRNA delivery using non-viral PCL nanoparticles.

Biomater Sci

January 2015

National Nanotechnology Laboratory, Institute Nanoscience CNR (NNL, CNR-NANO), via Arnesano, Lecce, Italy.

Messenger RNA (mRNA) provides a promising alternative to plasmid DNA as a genetic material for delivery in non-viral gene therapy strategies. However, it is difficult to introduce mRNA in vivo mainly because of the instability of mRNA under physiological conditions. Here, mRNA-protamine complex encapsulated poly(ε-caprolactone) (PCL) nanoparticles (NPs) are proposed for the intracellular delivery of mRNA molecules.

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Unconventional tailorable patterning by solvent-assisted surface-tension-driven lithography.

J Colloid Interface Sci

May 2015

National Nanotechnology Laboratory-Institute Nanoscience-CNR (NNL-CNR NANO), via Arnesano, 73100 Lecce, Italy; Department of Physics, University Sapienza, P. le A. Moro 2, 00185 Rome, Italy. Electronic address:

Unconventional nanopatterning methods are emerging as powerful tools for the development of controlled shapes and ordered morphology of nanostructured materials with novel properties and tailorable functions. Here, we report a simple yet straightforward and efficient approach for patterning through unconventional dewetting that involves surface tension driven process. Using this innovative approach, we have successfully demonstrated to be able to prepare surface micro-patterns over large areas deposited through Eu(3+):TiO2 nanoparticles providing rational control over the local nucleation of nanoparticles.

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Experimental evidence of replica symmetry breaking in random lasers.

Nat Commun

January 2015

1] Department of Physics, La Sapienza University, Piazzale Aldo Moro 5, I-00185 Rome, Italy [2] Institute for Complex Systems, CNR (CNR-ISC), Via dei Taurini 19, I-00185 Rome, Italy.

Spin-glass theory is one of the leading paradigms of complex physics and describes condensed matter, neural networks and biological systems, ultracold atoms, random photonics and many other research fields. According to this theory, identical systems under identical conditions may reach different states. This effect is known as replica symmetry breaking and is revealed by the shape of the probability distribution function of an order parameter named the Parisi overlap.

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Cationic liposomes formulated with DMPC and a gemini surfactant traverse the cell membrane without causing a significant bio-damage.

Biochim Biophys Acta

October 2014

Dipartimento di Biologia e Biotecnologie, Sapienza Università di Roma, P.le Aldo Moro 5, 00185 Roma, Italy. Electronic address:

Cationic liposomes have been intensively studied both in basic and applied research because of their promising potential as non-viral molecular vehicles. This work was aimed to gain more information on the interactions between the plasmamembrane and liposomes formed by a natural phospholipid and a cationic surfactant of the gemini family. The present work was conducted with the synergistic use of diverse experimental approaches: electro-rotation measurements, atomic force microscopy, ζ-potential measurements, laser scanning confocal microscopy and biomolecular/cellular techniques.

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We have recently reported initial results concerning an original approach to introduce additional properties into fibrillar proteins produced by live fibroblasts and extruded into the ECM. The key to such an approach was biocompatible, fluorescent and semiconducting synthetic molecules which penetrated spontaneously the cells and were progressively encompassed via non-bonding interactions during the self-assembly process of the proteins, without altering cell viability and reproducibility. In this paper we demonstrate that the intracellular secretion of fluorescent microfibers can be generalized to living primary and immortalized human/mouse fibroblasts.

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We have developed an integrated microfluidic platform for producing 2-[(18)F]-fluoro-2-deoxy-D-glucose ((18)F-FDG) in continuous flow from a single bolus of radioactive isotope solution, with constant product yields achieved throughout the operation that were comparable to those reported for commercially available vessel-based synthesisers (40-80%). The system would allow researchers to obtain radiopharmaceuticals in a dose-on-demand setting within a few minutes. The flexible architecture of the platform, based on a modular design, can potentially be applied to the synthesis of other radiotracers that require a two-step synthetic approach, and may be adaptable to more complex synthetic routes by implementing additional modules.

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