Search results for "Kinetic"

"Figure 9a-1" of "Deviation from quark-number scaling of the anisotropy parameter v_2 of pions, kaons, and protons in Au+Au collisions at sqrt(s_NN) …

2023

The quark-number-scaled $v_2$ ($v_2/n_q$) of identified hadrons are shown as a function of the kinetic energy per quark, KE$_T/n_q$ in 10–20% centrality [panel (b)] in Au + Au collisions at $\sqrt{s_{NN}}$ = 200 GeV. The error bars (shaded boxes) represent the statistical (systematic) uncertainties. The systematic uncertainties shown are type A and B only.

"Figure 9c-3" of "Deviation from quark-number scaling of the anisotropy parameter v_2 of pions, kaons, and protons in Au+Au collisions at sqrt(s_NN) …

2023

The quark-number-scaled $v_2$ ($v_2/n_q$) of identified hadrons are shown as a function of the kinetic energy per quark, KE$_T/n_q$ in 0–10% centrality [panel (a)] in Au + Au collisions at $\sqrt{s_{NN}}$ = 200 GeV. The error bars (shaded boxes) represent the statistical (systematic) uncertainties. The systematic uncertainties shown are type A and B only.

"Figure 10b-3" of "Deviation from quark-number scaling of the anisotropy parameter v_2 of pions, kaons, and protons in Au+Au collisions at sqrt(s_NN)…

2023

The quark-number-scaled $v_2$ ($v_2/n_q$) of identified hadrons are shown as a function of the kinetic energy per quark, KE$_T/n_q$ in 10–40% centrality [panel (b)] in Au + Au collisions at $\sqrt{s_{NN}}$ = 200 GeV. The $v_2$ of $\Lambda$ and K$^0_S$ are measured by STAR collaboration [21]. The error bars (open boxes) represent the statistical (systematic) uncertainties. The systematic uncertainties shown on the results from this study are type A and B only.

"Figure 8b-3" of "Deviation from quark-number scaling of the anisotropy parameter v_2 of pions, kaons, and protons in Au+Au collisions at sqrt(s_NN) …

2023

Identified hadron $v_2$ in central (0–20% centrality, left panels) Au + Au collisions at $\sqrt{s_{NN}}$ = 200 GeV. Panels (a) and (b) show $v_2$ as a function of transverse momentum $p_T$. The $v_2$ of all species for centrality 0–20% has been scaled up by a factor of 1.6 for better comparison with results of 20–60% centrality. The error bars (shaded boxes) represent the statistical (systematic) uncertainties. The systematic uncertainties shown are type A and B only.

Dipeptidyl Enoates As Potent Rhodesain Inhibitors That Display a Dual Mode of Action

2015

Dipeptidyl enoates were prepared through a high-yielding two-step synthetic route. They have a dipeptidic structure with a 4-oxoenoate moiety as a warhead with multiple reactive sites. Dipeptidyl enoates were screened against rhodesain and human cathepsins B and L, and were found to be potent and selective inhibitors of rhodesain. Among them (S,E)-ethyl 5-((S)-2-{[(benzyloxy)carbonyl]amino}-3-phenylpropanamido)-7-methyl-4-oxooct-2-enoate (6) was the most potent, with an IC50 value of 16.4 nm and kinact/Ki=1.6×106 m−1 s−1 against rhodesain. These dipeptidyl enoates display a reversible mode of inhibition at very low concentrations and an irreversible mode at higher concentrations. Inhibition…

The effects of locomotor pattern diversity and ageing on the lower limb joint mechanics and loading during human walking and running

2015

Aportación de la monitorización farmacocinética de vancomicina a la calidad farmacoterapéutica y seguridad del paciente neonato prematuro

2014

Vancomicina es un antibiótico utilizado con gran frecuencia en pacientes neonatos prematuros ingresados en las Unidades de Cuidados Intensivos Neonatales. La elevada variabilidad en los parámetros farmacocinéticos en este grupo de población representa la mayor barrera en el desarrollo y en la optimización de regímenes de dosificación. Esta situación favorece el desarrollo de diversas recomendaciones basadas en modelos farmacocinéticos poblacionales y nomogramas de dosificación, que consideran, para el cálculo de la dosis, variables como la edad postconcepcional, postnatal, creatinina sérica o el peso de los pacientes. Sin embargo, la experiencia clínica ha puesto de relieve que las concentr…

Modelling the effect of ethanol on growth rate of food spoilage moulds

2005

The effect of ethanol (E) on the radial growth rate (mu) of food spoilage moulds (Aspergillus candidus, Aspergillus flavus, Aspergillus niger, Cladosporium cladosporioides, Eurotium herbariorum, Mucor circinelloides, Mucor racemosus, Paecilomyces variotii, Penicillium chrysogenum, Penicillium digitatum, Rhizopus oryzae and Trichoderma harzianum) was assessed in Potato Dextrose Agar (PDA) medium at a(w) 0.99, 25 degrees C. In order to model this effect, the Monod type equation described previously by Houtsma et al. (Houtsma, P.C., Kusters, B.J.M., de Wit, J.C., Rombouts, F.M., Zwietering, M.H., 1994. Modelling growth rates of Listeria monocytogenes as a function of lactate concentration. Int…

Numerical Simulations of the Flow Field of a Submerged Hydraulic Jump over Triangular Macroroughnesses

2021

The submerged hydraulic jump is a sudden change from the supercritical to subcritical flow, specified by strong turbulence, air entrainment and energy loss. Despite recent studies, hydraulic jump characteristics in smooth and rough beds, the turbulence, the mean velocity and the flow patterns in the cavity region of a submerged hydraulic jump in the rough beds, especially in the case of triangular macroroughnesses, are not completely understood. The objective of this paper was to numerically investigate via the FLOW-3D model the effects of triangular macroroughnesses on the characteristics of submerged jump, including the longitudinal profile of streamlines, flow patterns in the cavity regi…

Kinetic evidence for the incorporation of the [(pentamethylcyclopentadienyl) (2,2′-bipyridyl)(aquo)rhodium(III)] complex into DPPC vesicles

2008

Abstract The binding of the [(pentamethylcyclopentadienyl) (2,2′-bipyridyl)(aquo)rhodium(III)] complex [Cp*RhIII(bpy)H2O]2+, to l -α-dipalmitoylphosphatidyl choline (DPPC) vesicles has been estimated by studying the kinetics of the electron transfer reaction between the rhodium(III) complex and formiate ions. Kinetic measurements carried out under anaerobic conditions in absence and presence of DPPC show that the total reaction is composed of two steps. The rate of the first reaction increases with the phospholipid concentration, while that of the second process is independent of the concentration of DPPC. This is consistent with a reaction, where the two reacting species are partitioned be…