A Programmable Five Qubit Quantum Computer Using Trapped Atomic Ions

Quantum computers can solve certain problems more efficiently compared to conventional classical methods. In the endeavor to build a quantum computer, several competing platforms have emerged that can implement certain quantum algorithms using a few qubits. However, the demonstrations so far have been done usually by tailoring the hardware to meet the requirements of a particular algorithm implemented for a limited number of instances. Although such proof of principal implementations are important to verify the working of algorithms on a physical system, they further need to have the potential to serve as a general purpose quantum computer allowing the flexibility required for running multiple algorithms and be scaled up to host more qubits. Here we demonstrate a small programmable quantum computer based on five trapped atomic ions each of which serves as a qubit. By optically resolving each ion we can individually address them in order to perform a complete set of single-qubit and fully connected two-qubit quantum gates and alsoperform efficient individual qubit measurements. We implement a computation architecture that accepts an algorithm from a user interface in the form of a standard logic gate sequence and decomposes it into fundamental quantum operations that are native to the hardware using a set of compilation instructions that are defined within the software. These operations are then effected through a pattern of laser pulses that perform coherent rotations on targeted qubits in the chain. The architecture implemented in the experiment therefore gives us unprecedented flexibility in the programming of any quantum algorithm while staying blind to the underlying hardware. As a demonstration we implement the Deutsch-Jozsa and Bernstein-Vazirani algorithms on the five-qubit processor and achieve average success rates of 95 and 90 percent, respectively. We also implement a five-qubit coherent quantum Fourier transform and examine its performance in the period finding and phase estimation protocol. We find fidelities of 84 and 62 percent, respectively. While maintaining the same computation architecture the system can be scaled to more ions using resources that scale favorably (O(N^2)) with the number of qubits N

Garcinol loaded vitamin E TPGS emulsified PLGA nanoparticles: preparation, physicochemical characterization, in vitro and in vivo studies

Garcinol (GAR) is a naturally occurring polyisoprenylated phenolic compound. It has been recently investigated for its biological activities such as antioxidant, anti-inflammatory, anti ulcer, and antiproliferative effect on a wide range of human cancer cell lines. Though the outcomes are very promising, its extreme insolubility in water remains the main obstacle for its clinical application. Herein we report the formulation of GAR entrapped PLGA nanoparticles by nanoprecipitation method using vitamin E TPGS as an emulsifier. The nanoparticles were characterized for size, surface morphology, surface charge, encapsulation efficiency and in vitro drug release kinetics. The MTT assay depicted a high amount of cytotoxicity of GAR-NPs in B16F10, HepG2 and KB cells. A considerable amount of cell apoptosis was observed in B16f10 and KB cell lines. In vivo cellular uptake of fluorescent NPs on B16F10 cells was also investigated. Finally the GAR loaded NPs were radiolabeled with technetium-99m with >95% labeling efficiency and administered to B16F10 melanoma tumor bearing mice to investigate the in vivo deposition at the tumor site by biodistribution and scintigraphic imaging study. In vitro cellular uptake studies and biological evaluation confirm the efficacy of the formulation for cancer treatmen

Multi-band Extension of the Wideband Timing Technique

The wideband timing technique enables the high-precision simultaneous estimation of Times of Arrival (ToAs) and Dispersion Measures (DMs) while effectively modeling frequency-dependent profile evolution. We present two novel independent methods that extend the standard wideband technique to handle simultaneous multi-band pulsar data incorporating profile evolution over a larger frequency span to estimate DMs and ToAs with enhanced precision. We implement the wideband likelihood using the libstempo python interface to perform wideband timing in the tempo2 framework. We present the application of these techniques to the dataset of fourteen millisecond pulsars observed simultaneously in Band 3 (300 - 500 MHz) and Band 5 (1260 - 1460 MHz) of the upgraded Giant Metrewave Radio Telescope (uGMRT) as a part of the Indian Pulsar Timing Array (InPTA) campaign. We achieve increased ToA and DM precision and sub-microsecond root mean square post-fit timing residuals by combining simultaneous multi-band pulsar observations done in non-contiguous bands for the first time using our novel techniques.Comment: Submitted to MNRA

Nanostructured polypyrrole: enhancement in thermoelectric figure of merit through suppression of thermal conductivity

Semi-crystalline polypyrrole (PPy) nanotubes were synthesized through a chemical polymerization route using methyl orange-ferric chloride (MO-FeCl3) as a template for growth. The thermoelectric properties of these PPy nanotubes have been studied in the temperature range 300-380 K after treatment with various dopants such as hydrochloric acid (HCl), p-toluene-sulphonic acid monohydrate (ToS), and tetrabutyl ammonium hexaflurophosphate (PF6). It has been observed that these dopants affect the electrical and thermal transport properties of PPy nanotubes in different ways. The temperature dependence of electrical resistivity suggests that pure PPy and ToS-doped PPy nanotubes exhibit a critical regime of metal-to-insulator transition, and doping with HCl drives them into the metallic regime. In contrast, PF6 doping of PPy nanotubes carries them into the insulating regime and these samples exhibited the highest figure of merit of similar to 3.4 x 10(-3) at 380 K, which was 240% higher than the value obtained in the case of pristine PPy nanotubes. Strongly repressed thermal conductivity along with moderately high Seebeck coefficient and electrical conductivity have been found to be responsible for the high figure of merit observed in PF6-doped PPy nanotubes. The suppression of thermal conductivity in PF6-doped PPy nanotubes is attributed to the scattering of the spectrum of phonons via hierarchical length-scale defect structures present in the sample

HMG-CoA Reductase Inhibitors as Drug Leads against Naegleria fowleri

Primary amebic meningoencephalitis (PAM), caused by the free-living ameba Naegleria fowleri, has a fatality rate of over 97%. Treatment of PAM relies on amphotericin B in combination with other drugs, but few patients have survived with the existing drug treatment regimens. Therefore, development of effective drugs is a critical unmet need to avert deaths from PAM. Since ergosterol is one of the major sterols in the membrane of N. fowleri, disruption of isoprenoid and sterol biosynthesis by small-molecule inhibitors may be an effective intervention strategy against N. fowleri. The genome of N. fowleri contains a gene encoding HMG-CoA reductase (HMGR); the catalytic domains of human and N. fowleri HMGR share <60% sequence identity with only two amino acid substitutions in the active site of the enzyme. Considering the similarity of human and N. fowleri HMGR, we tested well-tolerated and widely used HMGR inhibitors, known as cholesterol-lowering statins, against N. fowleri. We identified blood-brain-barrier-permeable pitavastatin as a potent amebicidal agent against the U.S., Australian, and European strains of N. fowleri. Pitavastatin was equipotent to amphotericin B against the European strain of N. fowleri; it killed about 80% of trophozoites within 16 h of drug exposure. Pretreatment of trophozoites with mevalonate, the product of HMGR, rescued N. fowleri from inhibitory effects of statins, demonstrating that HMGR of N. fowleri is the target of statins. Because of the good safety profile and availability for both adult and pediatric uses, consideration should be given to repurposing the fast-acting pitavastatin for the treatment of PAM

Exploring the Potential of 99mTc(CO)3-Labeled Triazolyl Peptides for Tumor Diagnosis

In recent years the authors have reported on 99mTc(CO)3-labeled peptides that serve as carriers for biomolecules or radiopharmaceuticals to the tumors. In continuation of that work they report the synthesis of a pentapeptide (Met-Phe-Phe-Gly-His; pep-1), a hexapeptide (Met-Phe-Phe-Asp-Gly-His; pep-2), and a tetrapeptide (Asp-Gly- Arg-His; pep-3) and the attachment of 3-amino-1,2,4-triazole to the b carboxylic function of the aspartic acid unit of pep-2 and pep-3. The pharmacophores were radiolabeled in high yields with [99mTc(CO)3(H2O)3]+ metal aqua ion, characterized for their stability in serum and saline, as well as in His solution, and found to be substantially stable. B16F10 cell line binding studies showed favorable uptake and internalization. In vivo behavior of the radiolabeled triazolyl peptides was assessed in mice bearing induced tumor. The 99mTc(CO)3- triazolyl pep-3 demonstrated rapid urinary clearance and comparatively better tumor uptake. Imaging studies showed visualization of the tumor using 99mTc(CO)3-triazolyl pep-3, but due to high abdominal background, low delineation occurred. Based on the results further experiments will be carried out for targeting tumor with triazolyl peptide

99mTc-Labeling of Ciprofloxacin and Nitrofuryl Thiosemicarbazone Using Fac-[99mTc(CO)3(H2O)3] Core: Evaluation of Their Efficacy as Infection Imaging Agents

The aim of this study was to radiolabel ciprofloxacin (Cip) and nitrofuryl thiosemicarbazone (NFT) with the fac-[99mTc(CO)3(H2O)3]+ core and to evaluate the ability of the radiopharmaceuticals as tracers in detecting sites of infection. Cip and NFT were radiolabeled with the fac-[99mTc(CO)3(H2O)3]+ core and characterized by RHPLC. The stabilities of the preparations were evaluated in saline and rat serum. In vitro binding studies of the radiopharmaceuticals with S. aureus were performed. Biodistribution studies were conducted at different time points after injecting (i.v.) the radiopharmaceuticals in rats (intramuscularly infected with S. aureus) as well as in rats with sterile inflammation. To assess the infection targeting capacity of 99mTc-tricarbonyl ciprofloxacin and nitrofuryl thiosemicarbazone, 99mTc(V)O-Cip and 99mTc(V)O-NFT were used as control. Scintigraphic imaging studies of tricarbonyl compounds and 99mTc(V)O-Cip were performed at 4 h after injection. The radiochemical purities of 99mTc(CO)3-Cip and 99mTc(CO)3-NFT were between 97–98% as determined by thin layer chromatography (TLRC) and RHPLC; no further purification is necessary before injection. The radiopharmaceuticals exhibited substantial stability when incubated in isotonic saline and serum up to 24 h. Biodistribution studies showed maximum uptake in the infected rat thigh muscle at 4 h post injection and washing out at slower rate from the infected site than the oxo technetium chelate. The mean ratios of uptake in infected/non–infected thighs were 3.87 : 1, 3.41 : 1 and 3.17 : 1 for 99mTc(CO)3-Cip, 99mTc(CO)3-NFT and 99mTc(V)O-Cip respectively. During scintigraphic studies, infection sites appeared quite distinctly with 99mTc(CO)3-Cip and 99mTc(CO)3-NFT, comparable to the behaviour with 99mTc(V)O-Cip. These results encouraged us for further development of infection imaging radiopharmaceuticals based on the 99mTc-tricarbonyl core