scholarly journals Alumina Membrane with Hour-Glass Shaped Nanochannels: Tunable Ionic Current Rectification Device Modulated by Ions Gradient

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Shengnan Hou ◽  
Qinqin Wang ◽  
Xia Fan ◽  
Zhaoyue Liu ◽  
Jin Zhai

A new alumina membrane with hour-glass shaped nanochannels is reported using the double-side anodization method and the subsequently in situ pore opening procedure, which is applied to develop the tunable ionic current rectification devices that were modulated by ions gradient. By regulating the pH gradient, tunable ionic current rectification properties which are mainly dependent on the asymmetric surface charge density or polarity distribution on the inner walls of the nanochannels can be obtained. The enhanced ionic current rectification properties were presented due to the synergistic effect of the voltage driven ion flow and diffusion driven ion flow with the application of pH and electrolyte concentration gradients. Therefore, such specific alumina nanochannels would be considered as a promising candidate for building bioinspired artificial ion channel systems.

Nanoscale ◽  
2020 ◽  
Vol 12 (22) ◽  
pp. 11899-11907 ◽  
Author(s):  
Fei-Fei Liu ◽  
Ye-Chang Guo ◽  
Wei Wang ◽  
Yu-Ming Chen ◽  
Chen Wang

A MOFs/PAA hybrid exhibits excellent ionic rectification, which creates an ideal experimental and theoretical platform for precise ion transport.


1996 ◽  
Vol 39 (1) ◽  
pp. 71-78 ◽  
Author(s):  
A.J. Hoogstraate ◽  
C. Cullander ◽  
J.F. Nagelkerke ◽  
F. Spies ◽  
J. Verhoef ◽  
...  

2019 ◽  
Vol 1 (1) ◽  
Author(s):  
Baayla D C Boon ◽  
Petra J W Pouwels ◽  
Laura E Jonkman ◽  
Matthijs J Keijzer ◽  
Paolo Preziosa ◽  
...  

Abstract Post-mortem in situ MRI has been used as an intermediate between brain histo(patho)logy and in vivo imaging. However, it is not known how comparable post-mortem in situ is to ante-mortem imaging. We report the unique situation of a patient with familial early-onset Alzheimer’s disease due to a PSEN1 mutation, who underwent ante-mortem brain MRI and post-mortem in situ imaging only 4 days apart. T1-weighted and diffusion MRI was performed at 3-Tesla at both time points. Visual atrophy rating scales, brain volume, cortical thickness and diffusion measures were derived from both scans and compared. Post-mortem visual atrophy scores decreased 0.5–1 point compared with ante-mortem, indicating an increase in brain volume. This was confirmed by quantitative analysis; showing a 27% decrease of ventricular and 7% increase of whole-brain volume. This increase was more pronounced in the cerebellum and supratentorial white matter than in grey matter. Furthermore, axial and radial diffusivity decreased up to 60% post-mortem whereas average fractional anisotropy of white matter increased approximately 10%. This unique case study shows that the process of dying affects several imaging markers. These changes need to be taken into account when interpreting post-mortem MRI to make inferences on the in vivo situation.


1986 ◽  
Vol 250 (5) ◽  
pp. C663-C675 ◽  
Author(s):  
D. P. Jones

Endogenous enzymes with different subcellular localizations provide in situ probes to study O2 and ATP concentration at various sites within cells. Results from this approach indicate that substantial intracellular concentration gradients occur under some O2- and ATP-limited conditions. These studies, along with electron microscopic analyses and mathematical modeling, indicate that clustering and distribution of mitochondria are major factors in determining the magnitude and location of the concentration gradients. The mitochondria appear to be clustered in sites of high ATP demand to maximize ATP supply under conditions of limited production. The size of such clusters is limited by the magnitude of the O2 gradient needed to provide adequate O2 concentrations for mitochondrial function within the clusters. Thus microheterogeneity of metabolite concentrations can occur in cells without membranal compartmentation and may be important in determining the rates of various high-flux processes.


2019 ◽  
Author(s):  
Dawson B.H. Livingston ◽  
Hirva Patel ◽  
Andrew Donini ◽  
Heath A. MacMillan

AbstractUnder conditions of stress, many animals suffer from epithelial barrier disruption that can cause molecules to leak down their concentration gradients, potentially causing a loss of organismal homeostasis, further injury or death. Drosophila is a common insect model, used to study barrier disruption related to aging, traumatic injury, or environmental stress. Net leak of a non-toxic dye (Brilliant blue FCF) from the gut lumen to the hemolymph is often used to identify barrier failure under these conditions, but Drosophila are capable of actively transporting structurally-similar compounds. Here, we examined whether cold stress (like other stresses) causes Brilliant blue FCF (BB-FCF) to appear in the hemolymph of flies fed the dye, and if so whether Drosophila are capable of clearing this dye from their body following chilling. Using in situ midgut leak and transport assays as well as Ramsay assays of Malpighian tubule transport, we tested whether these ionoregulatory epithelia can actively transport BB-FCF. In doing so, we found that the Drosophila midgut and Malpighian tubules can mobilize BB-FCF via an active transcellular pathway, suggesting that elevated concentrations of the dye in the hemolymph may occur from increased paracellular permeability, reduced transcellular clearance, or both.Summary StatementDrosophila are able to actively secrete Brilliant blue FCF, a commonly used marker of barrier dysfunction


2009 ◽  
Vol 329 (2) ◽  
pp. 376-383 ◽  
Author(s):  
Shizhi Qian ◽  
Sang W. Joo ◽  
Ye Ai ◽  
Marcos A. Cheney ◽  
Wensheng Hou

2019 ◽  
Vol 21 (44) ◽  
pp. 24740-24748 ◽  
Author(s):  
Anna S. Tolkacheva ◽  
Sergey N. Shkerin ◽  
Natalia M. Porotnikova ◽  
Mikhail V. Kuznetsov ◽  
Sergey V. Naumov ◽  
...  

Oxygen surface exchange and diffusion in Ca12Al14O33±δ single crystal were studied by a unique in situ method based on isotope equilibration in the gas phase.


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