1,628 research outputs found
Quasi-static aberrations induced by laser guide stars in adaptive optics
Laser Guide Star Adaptive Optics (LGS AO) systems use the return from an artificial guide star to measure the wavefront aberrations in the direction of the science object. We observe quasi-static differences between the measured wavefront and the wavefront aberration of the science object. This paper quantifies and explains the source of the difference between the wavefronts measured using an LGS and a natural guide star at the W. M. Keck Observatory, which can be as high as 1000 nm RMS
Expectation Values from the Single-Layer Quantum Approximate Optimization Algorithm on Ising Problems
We report on the energy-expectation-value landscapes produced by the
single-layer () Quantum Approximate Optimization Algorithm (QAOA) when
being used to solve Ising problems. The landscapes are obtained using an
analytical formula that we derive. The formula allows us to predict the
landscape for any given Ising problem instance and consequently predict the
optimal QAOA parameters for heuristically solving that instance using the
single-layer QAOA. We have validated our analytical formula by showing that it
accurately reproduces the landscapes published in recent experimental reports.
We then applied our methods to address the question: how well is the
single-layer QAOA able to solve large benchmark problem instances? We used our
analytical formula to calculate the optimal energy-expectation values for
benchmark MAX-CUT problems containing up to vertices and
edges. We also calculated the optimal energy expectations for general Ising
problems with up to vertices and edges. Our results
provide an estimate for how well the single-layer QAOA may work when run on a
quantum computer with thousands of qubits. In addition to providing performance
estimates when optimal angles are used, we are able to use our analytical
results to investigate the difficulties one may encounter when running the QAOA
in practice for different classes of Ising instances. We find that depending on
the parameters of the Ising Hamiltonian, the expectation-value landscapes can
be rather complex, with sharp features that necessitate highly accurate
rotation gates in order for the QAOA to be run optimally on quantum hardware.
We also present analytical results that explain some of the qualitative
landscape features that are observed numerically.Comment: 24 pages, 15 figure
Increased Cerebrospinal Fluid Production as a Possible Mechanism Underlying Caffeine's Protective Effect against Alzheimer's Disease
Alzheimer's disease (AD), the most common type of dementia among older people, is characterized by the accumulation of β-amyloid (Aβ) senile plaques and neurofibrillary tangles composed of hyperphosphorylated tau in the brain. Despite major advances in understanding the molecular etiology of the disease, progress in the clinical treatment of AD patients has been extremely limited. Therefore, new and more effective therapeutic approaches are needed. Accumulating evidence from human and animal studies suggests that the long-term consumption of caffeine, the most commonly used psychoactive drug in the world, may be protective against AD. The mechanisms underlying the suggested beneficial effect of caffeine against AD remain to be elucidated. In recent studies, several potential neuroprotective effects of caffeine have been proposed. Interestingly, a recent study in rats showed that the long-term consumption of caffeine increased cerebrospinal fluid (CSF) production, associated with the increased expression of Na+-K+ ATPase and increased cerebral blood flow. Compromised function of the choroid plexus and defective CSF production and turnover, with diminished clearance of Aβ, may be one mechanism implicated in the pathogenesis of late-onset AD. If reduced CSF turnover is a risk factor for AD, then therapeutic strategies to improve CSF flow are reasonable. In this paper, we hypothesize that long-term caffeine consumption could exert protective effects against AD at least in part by facilitating CSF production, turnover, and clearance. Further, we propose a preclinical experimental design allowing evaluation of this hypothesis
Are Costs of Robot-Assisted Surgery Warranted for Gynecological Procedures?
The exponential use of robotic surgery is not the result of evidence-based benefits but mainly driven by the manufacturers, patients and enthusiastic surgeons. The present review of the literature shows that robot-assisted surgery is consistently more expensive than video-laparoscopy and in many cases open surgery. The average additional variable cost for gynecological procedures was about 1600 USD, rising to more than 3000 USD when the amortized cost of the robot itself was included. Generally most robotic and laparoscopic procedures have less short-term morbidity, blood loss, intensive care unit, and hospital stay than open surgery. Up to now no major consistent differences have been found between robot-assisted and classic video-assisted procedures for these factors. No comparative data are available on long-term morbidity and oncologic outcome after open, robotic, and laparoscopic gynecologic surgery. It seems that currently only for very complex surgical procedures, such as cardiac surgery, the costs of robotics can be competitive to open surgical procedures. In order to stay viable, robotic programs will need to pay for themselves on a per case basis and the costs of robotic surgery will have to be reduced
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Rapid, efficient, and economical synthesis of PET tracers in a droplet microreactor: application to O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET).
BackgroundConventional scale production of small batches of PET tracers (e.g. for preclinical imaging) is an inefficient use of resources. Using O-(2-[18F]fluoroethyl)-L-tyrosine ([18F]FET), we demonstrate that simple microvolume radiosynthesis techniques can improve the efficiency of production by consuming tiny amounts of precursor, and maintaining high molar activity of the tracers even with low starting activity.ProceduresThe synthesis was carried out in microvolume droplets manipulated on a disposable patterned silicon "chip" affixed to a heater. A droplet of [18F]fluoride containing TBAHCO3 was first deposited onto a chip and dried at 100 °C. Subsequently, a droplet containing 60 nmol of precursor was added to the chip and the fluorination reaction was performed at 90 °C for 5 min. Removal of protecting groups was accomplished with a droplet of HCl heated at 90 °C for 3 min. Finally, the crude product was collected in a methanol-water mixture, purified via analytical-scale radio-HPLC and formulated in saline. As a demonstration, using [18F]FET produced on the chip, we prepared aliquots with different molar activities to explore the impact on preclinical PET imaging of tumor-bearing mice.ResultsThe microdroplet synthesis exhibited an overall decay-corrected radiochemical yield of 55 ± 7% (n = 4) after purification and formulation. When automated, the synthesis could be completed in 35 min. Starting with < 370 MBq of activity, ~ 150 MBq of [18F]FET could be produced, sufficient for multiple in vivo experiments, with high molar activities (48-119 GBq/μmol). The demonstration imaging study revealed the uptake of [18F]FET in subcutaneous tumors, but no significant differences in tumor uptake as a result of molar activity differences (ranging 0.37-48 GBq/μmol) were observed.ConclusionsA microdroplet synthesis of [18F]FET was developed demonstrating low reagent consumption, high yield, and high molar activity. The approach can be expanded to tracers other than [18F]FET, and adapted to produce higher quantities of the tracer sufficient for clinical PET imaging
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