Modal analysis of holey fiber mode-selective couplers

Mode Division Multiplexing is currently investigated as a possible way to increase fiber system capacity. With this approach, different modes of the same fiber carry distinct information. One of the problems to be solved in these systems concerns coupling/decoupling of the various modes to/from the same fiber. In this presentation, the mode features of a mode mux/demux based on holey fibers are investigated, with particular emphasis on optimal device design. Some preliminary experimental results will also be presented

Control of planar nonlinear guided waves and spatial solitons with a left-handed medium

The evidence that double negative media, with an effective negative permittivity, and an effective negative permeability, can be manufactured to operate at frequencies ranging from microwave to optical is ushering in a new era of metamaterials. They are referred to here as 'left-handed', even though a variety of names is evident from the literature. In anticipation of a demand for highly structured integrated practical waveguides, this paper addresses the impact of this type of medium upon waveguides that can be also nonlinear. After an interesting historical overview and an exposure of some straightforward concepts, a planar guide is investigated, in which the waveguide is a slab consisting of a left-handed medium sandwiched between a substrate and cladding that are simple dielectrics. The substrate and cladding display a Kerr-type nonlinear response. Because of the nonlinear properties of the Kerr media, the power flow direction can be controlled by the intensity of the electric field. A comprehensive finite-difference-time-domain (FDTD) analysis is presented that concentrates upon spatial soliton behaviour. An interesting soliton-lens arrangement is investigated that lends itself to a novel cancellation effect.Comment: 19 pages, 11 figure

Investigating the use of a hybrid plasmonic–photonic nanoresonator for optical trapping using finite-difference time-domain method

We investigate the use of a hybrid nanoresonator comprising a photonic crystal (PhC) cavity coupled to a plasmonic bowtie nanoantenna (BNA) for the optical trapping of nanoparticles in water. Using finite difference time-domain simulations, we show that this structure can confine light to an extremely small volume of ~30,000 nm3 (~30 zl) in the BNA gap whilst maintaining a high quality factor (5400–7700). The optical intensity inside the BNA gap is enhanced by a factor larger than 40 compared to when the BNA is not present above the PhC cavity. Such a device has potential applications in optical manipulation, creating high precision optical traps with an intensity gradient over a distance much smaller than the diffraction limit, potentially allowing objects to be confined to much smaller volumes and making it ideal for optical trapping of Rayleigh particles (particles much smaller than the wavelength of light)

Globally prevalent PfMDR1 mutations modulate Plasmodium falciparum susceptibility to artemisinin-based combination therapies

Antimalarial chemotherapy, globally reliant on artemisinin-based combination therapies (ACTs), is threatened by the spread of drug resistance in Plasmodium falciparum parasites. Here we use zinc-finger nucleases to genetically modify the multidrug resistance-1 transporter PfMDR1 at amino acids 86 and 184, and demonstrate that the widely prevalent N86Y mutation augments resistance to the ACT partner drug amodiaquine and the former first-line agent chloroquine. In contrast, N86Y increases parasite susceptibility to the partner drugs lumefantrine and mefloquine, and the active artemisinin metabolite dihydroartemisinin. The PfMDR1 N86 plus Y184F isoform moderately reduces piperaquine potency in strains expressing an Asian/African variant of the chloroquine resistance transporter PfCRT. Mutations in both digestive vacuole-resident transporters are thought to differentially regulate ACT drug interactions with host haem, a product of parasite-mediated haemoglobin degradation. Global mapping of these mutations illustrates where the different ACTs could be selectively deployed to optimize treatment based on regional differences in PfMDR1 haplotypes.This work was funded in part by the National Institutes of Health (R01 AI50234, AI124678 and AI109023) and a Burroughs Wellcome Fund Investigator in Pathogenesis of Infectious Diseases award to D.A.F. This research also received funding from the Portuguese Fundacao para a Ciencia e Tecnologia (FCT), cofunded by Programa Operacional Regional do Norte (ON.2-O Novo Norte); from the Quadro de Referencia Estrategico Nacional (QREN) through the Fundo Europeu de Desenvolvimento Regional (FEDER) and from the Projeto Estrategico - LA 26 - 2013-2014 (PEst-C/SAU/LA0026/2013). M.I.V. is the recipient of a postdoctoral fellowship from FCT/Ministerio da Ciencia e Ensino Superior, Portugal-MCES (SFRH/BPD/76614/2011). A.M.L. was supported by an Australian National Health and Medical Research Council (NHMRC) Overseas Biomedical Fellowship (585519). R.E.M. was supported by an NHMRC RD Wright Biomedical Fellowship (1053082). A.C.U. was supported by an Irving scholarship from Columbia University. We thank Dr Andrea Ecker for her help with plasmid design and Pedro Ferreira for his expert help with Fig. 6.info:eu-repo/semantics/publishedVersio