Quantum computation with optical coherent states

We show that quantum computation circuits using coherent states as the logical qubits can be constructed from simple linear networks, conditional photon measurements and "small" coherent superposition resource states

The statistical strength of experiments to reject local realism with photon pairs and inefficient detectors

Because of the fundamental importance of Bell's theorem, a loophole-free demonstration of a violation of local realism (LR) is highly desirable. Here, we study violations of LR involving photon pairs. We quantify the experimental evidence against LR by using measures of statistical strength related to the Kullback-Leibler (KL) divergence, as suggested by van Dam et al. [W. van Dam, R. Gill and P. Grunwald, IEEE Trans. Inf. Theory. 51, 2812 (2005)]. Specifically, we analyze a test of LR with entangled states created from two independent polarized photons passing through a polarizing beam splitter. We numerically study the detection efficiency required to achieve a specified statistical strength for the rejection of LR depending on whether photon counters or detectors are used. Based on our results, we find that a test of LR free of the detection loophole requires photon counters with efficiencies of at least 89.71%, or photon detectors with efficiencies of at least 91.11%. For comparison, we also perform this analysis with ideal unbalanced Bell states, which are known to allow rejection of LR with detector efficiencies above 2/3.Comment: 18 pages, 3 figures, minor changes (add more references, replace the old plots, etc.)

Orthotopic xenografts of human melanoma and colonic and ovarian carcinoma in sheep to evaluate radioimmunotherapy.

Extrapolation to humans from experimental radioimmunotherapy in nude mouse xenograft models is confounded by large relative tumour size and small volume of distribution in mice allowing tumour uptake of radiolabelled antibodies unattainable in patients. Our large animal model of human tumours in cyclosporin-immunosuppressed sheep demonstrated tumour uptake of targeted radiolabelled monoclonal antibodies comparable with uptakes reported in clinical trials. Sheep immunosuppression with daily intravenous cyclosporin augmented by oral ketoconazole maintained trough blood levels of cyclosporin within the range 1000-1500 ng ml(-1). Human tumour cells were transplanted orthotopically by inoculation of 10(7) cells: SKMEL melanoma subcutaneously; LS174T and HT29 colon carcinoma into bowel, peritoneum and liver; and JAM ovarian carcinoma into ovary and peritoneum. Tumour xenografts grew at all sites within 3 weeks of inoculation, preserving characteristic morphology without evidence of necrosis or host rejection. Lymphatic metastasis was demonstrated in regional nodes draining xenografts of melanoma and ovarian carcinoma. Colonic LS1 74T xenografts produced mucin and carcinoembryonic antigen (CEA). The anti-CEA IgG1 monoclonal antibody A5B7 was radiolabelled with iodine-131 and administered intravenously to sheep. Peak uptake at 5 days in orthotopic human tumour transplants in gut was 0.027% DI g(-1) (percentage of injected dose per gram) and 0.034% DI g(-1) in hepatic metastases with tumour to blood ratios of 2-2.5. Non-specific tumour uptake in melanoma was 0.003% DI g(-1). Uptake of radiolabelled monoclonal antibody in human tumours in our large animal model is comparable with that observed in patients and may be more realistic than nude mice xenografts for prediction of clinical efficacy of radioimmunotherapy

Calcium Activation of Mitochondrial Respiration is Maintained in Heart Failure Despite Altered Mitochondrial Membrane Potential

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