353 research outputs found

    Density Matrix Renormalization Group of Gapless Systems

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    We investigate convergence of the density matrix renormalization group (DMRG) in the thermodynamic limit for gapless systems. Although the DMRG correlations always decay exponentially in the thermodynamic limit, the correlation length at the DMRG fixed-point scales as ξ∼m1.3\xi \sim m^{1.3}, where mm is the number of kept states, indicating the existence of algebraic order for the exact system. The single-particle excitation spectrum is calculated, using a Bloch-wave ansatz, and we prove that the Bloch-wave ansatz leads to the symmetry E(k)=E(π−k)E(k)=E(\pi -k) for translationally invariant half-integer spin-systems with local interactions. Finally, we provide a method to compute overlaps between ground states obtained from different DMRG calculations.Comment: 11 pages, RevTex, 5 figure

    Clustering in mixing flows

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    We calculate the Lyapunov exponents for particles suspended in a random three-dimensional flow, concentrating on the limit where the viscous damping rate is small compared to the inverse correlation time. In this limit Lyapunov exponents are obtained as a power series in epsilon, a dimensionless measure of the particle inertia. Although the perturbation generates an asymptotic series, we obtain accurate results from a Pade-Borel summation. Our results prove that particles suspended in an incompressible random mixing flow can show pronounced clustering when the Stokes number is large and we characterise two distinct clustering effects which occur in that limit.Comment: 5 pages, 1 figur

    In Vitro Evaluation of Non-Protein Adsorbing Breast Cancer Theranostics Based on 19F-Polymer Containing Nanoparticles

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    Eight fluorinated nanoparticles (NPs) are synthesized, loaded with doxorubicin (DOX), and evaluated as theranostic delivery platforms to breast cancer cells. The multifunctional NPs are formed by self-assembly of either linear or star-shaped amphiphilic block copolymers, with fluorinated segments incorporated in the hydrophilic corona of the carrier. The sizes of the NPs confirm that small circular NPs are formed. The release kinetics data of the particles reveals clear hydrophobic core dependence, with longer sustained release from particles with larger hydrophobic cores, suggesting that the DOX release from these carriers can be tailored. Viability assays and flow cytometry evaluation of the ratios of apoptosis/necrosis indicate that the materials are non-toxic to breast cancer cells before DOX loading; however, they are very efficient, similar to free DOX, at killing cancer cells after drug encapsulation. Both flow cytometry and confocal microscopy confirm the cellular uptake of NPs and DOX-NPs into breast cancer cells, and in vitro 19F-MRI measurement shows that the fluorinated NPs have strong imaging signals, qualifying them as a potential in vivo contrast agent for 19F-MRI

    Unmixing in Random Flows

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    We consider particles suspended in a randomly stirred or turbulent fluid. When effects of the inertia of the particles are significant, an initially uniform scatter of particles can cluster together. We analyse this 'unmixing' effect by calculating the Lyapunov exponents for dense particles suspended in such a random three-dimensional flow, concentrating on the limit where the viscous damping rate is small compared to the inverse correlation time of the random flow (that is, the regime of large Stokes number). In this limit Lyapunov exponents are obtained as a power series in a parameter which is a dimensionless measure of the inertia. We report results for the first seven orders. The perturbation series is divergent, but we obtain accurate results from a Pade-Borel summation. We deduce that particles can cluster onto a fractal set and show that its dimension is in satisfactory agreement with previously reported in simulations of turbulent Navier-Stokes flows. We also investigate the rate of formation of caustics in the particle flow.Comment: 39 pages, 8 figure

    The Density Matrix Renormalization Group technique with periodic boundary conditions

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    The Density Matrix Renormalization Group (DMRG) method with periodic boundary conditions is introduced for two dimensional classical spin models. It is shown that this method is more suitable for derivation of the properties of infinite 2D systems than the DMRG with open boundary conditions despite the latter describes much better strips of finite width. For calculation at criticality, phenomenological renormalization at finite strips is used together with a criterion for optimum strip width for a given order of approximation. For this width the critical temperature of 2D Ising model is estimated with seven-digit accuracy for not too large order of approximation. Similar precision is reached for critical indices. These results exceed the accuracy of similar calculations for DMRG with open boundary conditions by several orders of magnitude.Comment: REVTeX format contains 8 pages and 6 figures, submitted to Phys. Rev.

    Recurrent Variational Approach to the Two-Leg Hubbard Ladder

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    We applied the Recurrent Variational Approach to the two-leg Hubbard ladder. At half-filling, our variational Ansatz was a generalization of the resonating valence bond state. At finite doping, hole pairs were allowed to move in the resonating valence bond background. The results obtained by the Recurrent Variational Approach were compared with results from Density Matrix Renormalization Group.Comment: 10 pages, 14 Postscript figure

    A class of ansatz wave functions for 1D spin systems and their relation to DMRG

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    We investigate the density matrix renormalization group (DMRG) discovered by White and show that in the case where the renormalization eventually converges to a fixed point the DMRG ground state can be simply written as a ``matrix product'' form. This ground state can also be rederived through a simple variational ansatz making no reference to the DMRG construction. We also show how to construct the ``matrix product'' states and how to calculate their properties, including the excitation spectrum. This paper provides details of many results announced in an earlier letter.Comment: RevTeX, 49 pages including 4 figures (macro included). Uuencoded with uufiles. A complete postscript file is available at http://fy.chalmers.se/~tfksr/prb.dmrg.p

    Heterogeneity in Blood Pressure Response to 4 Antihypertensive Drugs: A Randomized Clinical Trial

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    Importance: Hypertension is the leading risk factor for premature death worldwide. Multiple blood pressure-lowering therapies are available but the potential for maximizing benefit by personalized targeting of drug classes is unknown. Objective: To investigate and quantify the potential for targeting specific drugs to specific individuals to maximize blood pressure effects. Design, Setting, and Participants: A randomized, double-blind, repeated crossover trial in men and women with grade 1 hypertension at low risk for cardiovascular events at an outpatient research clinic in Sweden. Mixed-effects models were used to assess the extent to which individuals responded better to one treatment than another and to estimate the additional blood pressure lowering achievable by personalized treatment. Interventions: Each participant was scheduled for treatment in random order with 4 different classes of blood pressure-lowering drugs (lisinopril [angiotensin-converting enzyme inhibitor], candesartan [angiotensin-receptor blocker], hydrochlorothiazide [thiazide], and amlodipine [calcium channel blocker]), with repeated treatments for 2 classes. Main Outcomes and Measures: Ambulatory daytime systolic blood pressure, measured at the end of each treatment period. Results: There were 1468 completed treatment periods (median length, 56 days) recorded in 270 of the 280 randomized participants (54% men; mean age, 64 years). The blood pressure response to different treatments varied considerably between individuals (P <.001), specifically for the choices of lisinopril vs hydrochlorothiazide, lisinopril vs amlodipine, candesartan vs hydrochlorothiazide, and candesartan vs amlodipine. Large differences were excluded for the choices of lisinopril vs candesartan and hydrochlorothiazide vs amlodipine. On average, personalized treatment had the potential to provide an additional 4.4 mm Hg-lower systolic blood pressure. Conclusions and Relevance: These data reveal substantial heterogeneity in blood pressure response to drug therapy for hypertension, findings that may have implications for personalized therapy. Trial Registration: ClinicalTrials.gov Identifier: NCT02774460

    Staggered flux and stripes in doped antiferromagnets

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    We have numerically investigated whether or not a mean-field theory of spin textures generate fictitious flux in the doped two dimensional t−Jt-J-model. First we consider the properties of uniform systems and then we extend the investigation to include models of striped phases where a fictitious flux is generated in the domain wall providing a possible source for lowering the kinetic energy of the holes. We have compared the energetics of uniform systems with stripes directed along the (10)- and (11)-directions of the lattice, finding that phase-separation generically turns out to be energetically favorable. In addition to the numerical calculations, we present topological arguments relating flux and staggered flux to geometric properties of the spin texture. The calculation is based on a projection of the electron operators of the t−Jt-J model into a spin texture with spinless fermions.Comment: RevTex, 19 pages including 20 figure
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