9 research outputs found
Additional file 2: of l-carnitine in critically ill patients—a case series study
Figure S2. Distribution of carnitine concentrations on ICU admission. (a) The distribution of t-Carnitine on ICU admission is shown in the histogram. The mean t-Carnitine was 94.9 ± 79.6 nmol/mL, and the median t-Carnitine was 64.2 (50.5–102.3) nmol/mL. (b) The distribution of f-Carnitine on ICU admission is shown in the histogram. The mean f-Carnitine was 68.6 ± 51.2 nmol/mL, and the median f-Carnitine was 50.5 (36.8–80.3) nmol/mL. (ZIP 160 kb
Additional file 3: of l-carnitine in critically ill patients—a case series study
Figure S3. Comparison of f-Carnitine transition among the patients with f-Carnitine increased and decreased. The transition of f-Carnitine area for 14 days plotted at each sampling point. The round and square signs within the figure indicate the medians for f-Carnitine, and the error bars indicate 25th and 75th percentile range. The dotted lines indicate the upper and lower reference values for f-Carnitine. The patients whose data are lacking at day 7 or day 14 were excluded from this analysis. (TIFF 123 kb
Additional file 5: of l-carnitine in critically ill patients—a case series study
Table S1. Clinical outcomes according to f-carnitine levels at ICU admissiona. (DOCX 21 kb
Additional file 1: of l-carnitine in critically ill patients—a case series study
Figure S1. Flowchart of study enrollment. (TIFF 117 kb
Additional file 4: of l-carnitine in critically ill patients—a case series study
Figure S4. Correlation of BMI and SOFA score with the change in f-Carnitine from day 0 to day 14. (a) Each plot depicts a relationship between the BMI on the x-axis, and the change of f-Carnitine from day 0 to day 14 (Δ f-Carnitine) on the y-axis. There was a significant negative correlation between the BMI and the Δf-Carnitine (r = − 0.47, p = 0.01), which suggests an association between lower BMI and larger decrease of f-Carnitine. (b) Each plot depicts a relationship between the SOFA score at the time of ICU admission on the x-axis, and the change of f-Carnitine from day 0 to day 14 (Δ f-Carnitine) on the y-axis. There was a significant correlation between the SOFA score on ICU admission and the Δf-Carnitine (r = 0.46, p = 0.01), which suggests an association between high SOFA score and larger decrease of f-Carnitine. (ZIP 188 kb
Dispersion of Rod-like Particles of Nafion in Salt-Free Water/1-Propanol and Water/Ethanol Solutions
The
dispersion of perfluorinated sulfonic acid ionomers in catalyst
inks is an important factor controlling the performance of catalyst
layers in membrane electrode assemblies of proton exchange membrane
fuel cells (PEMFCs). The effect of water/alcohol composition on the
dispersion of H-Nafion in water/1-propanol and water/ethanol solutions
was studied by dynamic light scattering (DLS), small-angle X-ray scattering
(SAXS), and <sup>19</sup>F nuclear magnetic resonance (<sup>19</sup>F NMR) spectroscopy. Hydrodynamic radii calculated from DLS decay
profiles and the radii and interparticle distance of rod-like particles
derived from SAXS profiles showed almost the same dependence on alcohol
concentration. 1-Propanol was more effective than ethanol to induce
changes in the characteristic lengths of the rod-like particles. The
motional narrowing in the <sup>19</sup>F NMR spectra by addition of
1-propanol indicates selective solvation of the rod-like particles.
We suppose this might have decreased their radii and induced their
elongation, which eventually led to extension of the ordered regions
as observed in the hydrodynamic radii. Our study helps to clarify
the dispersion of Nafion in aqueous alcohol solutions, which has implications
for the performance of PEMFCs
In Situ Hard X‑ray Photoelectron Study of O<sub>2</sub> and H<sub>2</sub>O Adsorption on Pt Nanoparticles
To improve the efficiency of Pt-based
cathode catalysts in polymer
electrolyte fuel cells, understanding of the oxygen reduction process
at surfaces and interfaces in the molecular level is essential. In
this study, H<sub>2</sub>O and O<sub>2</sub> adsorption and dissociation
as the first step of the reduction process were investigated by in
situ hard X-ray photoelectron spectroscopy (HAXPES). Pt 5d valence
band and Pt 3d, Pt 4f core HAXPES spectra of Pt nanoparticles upon
H<sub>2</sub>O and O<sub>2</sub> adsorption revealed that H<sub>2</sub>O adsorption has a negligible effect on the electronic structure
of Pt, while O<sub>2</sub> adsorption has a significant effect, reflecting
the weak and strong chemisorption of H<sub>2</sub>O and O<sub>2</sub> on the Pt nanoparticle, respectively. Combined with ab initio theoretical
calculations, it is concluded that Pt 5d states responsible for Pt–O<sub>2</sub> bonding reside within 2 eV from the Fermi level
Patient and healthy subject characteristics.
<p>p-values, when shown in italics such as <i>p<0.01</i>, indicate that there are significant differences. Values are shown as mean ± SD (standard deviation). BMI; Body Mass Index, AST; Aspartate transaminase, ALT; Alanine transaminase, CHO; cholesterol, TG; triglyceride.</p
Scatter plots of serum total TG, VLDL-TG, non-VLDL-TG levels, and VLDL-TG/non-VLDL-TG ratios.
<p>P-values are indicated as the values between groups with bars. The mean value of each group is indicated at the bottom of each diagram. P-values, when indicated in bold with an asterisk (such as <b>0.025*)</b>, indicate significant differences. SD; standard deviation.</p