Continuous variable entanglement on a chip

Encoding quantum information in continuous variables (CV)---as the quadrature of electromagnetic fields---is a powerful approach to quantum information science and technology. CV entanglement---light beams in Einstein-Podolsky-Rosen (EPR) states---is a key resource for quantum information protocols; and enables hybridisation between CV and single photon discrete variable (DV) qubit systems. However, CV systems are currently limited by their implementation in free-space optical networks: increased complexity, low loss, high-precision alignment and stability, as well as hybridisation, demand an alternative approach. Here we show an integrated photonic implementation of the key capabilities for CV quantum technologies---generation and characterisation of EPR beams in a photonic chip. Combined with integrated squeezing and non-Gaussian operation, these results open the way to universal quantum information processing with light

Impact of polyplex micelles installed with cyclic RGD peptide as ligand on gene delivery to vascular lesions

Gene therapy is expected to open a new strategy for the treatment of refractory vascular diseases, so the development of appropriate gene vectors for vascular lesions is needed. To realize this requirement with a non-viral approach, cyclo(RGDfK) peptide (cRGD) was introduced to block copolymer, poly(ethylene glycol)-block-polycation carrying ethylenediamine units (PEG-PAsp(DET)). cRGD recognizes αvβ3 and αvβ5 integrins, which are abundantly expressed in vascular lesions. cRGD-conjugated PEG-PAsp(DET) (cRGD-PEG-PAsp(DET)) formed polyplex micelles through complexation with plasmid DNA (pDNA), and the cRGD-PEG-PAsp(DET) micelles achieved significantly more efficient gene expression and cellular uptake as compared with PEG-PAsp(DET) micelles in endothelial cells and vascular smooth muscle cells. Intracellular tracking of pDNA showed that cRGD-PEG-PAsp(DET) micelles were internalized via caveolae-mediated endocytosis, which is associated with a pathway avoiding lysosomal degradation, and that PEG-PAsp(DET) micelles were transported to acidic endosomes and lysosomes via clathrin-mediated endocytosis. Further, in vivo evaluation in rat carotid artery with a neointimal lesion revealed that cRGD-PEG-PAsp(DET) micelles realized sustained gene expression, while PEG-PAsp(DET) micelles facilitated rapid but transient gene expression. These findings suggest that introduction of cRGD to polyplex micelles might create novel and useful functions for gene transfer and contribute to the establishment of efficient gene therapy for vascular diseases