scholarly journals Theory of the Interaction of Colloidal Particles with Constant Surface Charge Density and Its Application to the Cell Inteeraction

1973 ◽  
Vol 13 (6) ◽  
pp. 262-270
Author(s):  
Hiroyuki OHSHIMA
Keyword(s):  
Charge Density ◽  
Surface Charge ◽  
Surface Charge Density ◽  
Colloidal Particles

scholarly journals Some modification of cellulose nanocrystals for functional Pickering emulsions

2016 ◽  
Vol 374 (2072) ◽  
pp. 20150139 ◽  
Author(s):  
Dorra Saidane ◽  
Emilie Perrin ◽  
Fanch Cherhal ◽  
Florian Guellec ◽  
Isabelle Capron
Keyword(s):  
Charge Density ◽  
Surface Charge ◽  
Cellulose Nanocrystals ◽  
Surface Charge Density ◽  
Colloidal Particles ◽  
Hydroxyl Groups ◽  
Layer By Layer ◽  
Pickering Emulsions ◽  
Simple Method ◽  
Oil Emulsions

Cellulose nanocrystals (CNCs) are negatively charged colloidal particles well known to form highly stable surfactant-free Pickering emulsions. These particles can vary in surface charge density depending on their preparation by acid hydrolysis or applying post-treatments. CNCs with three different surface charge densities were prepared corresponding to 0.08, 0.16 and 0.64 e nm −2 , respectively. Post-treatment might also increase the surface charge density. The well-known TEMPO-mediated oxidation substitutes C 6 -hydroxyl groups by C 6 -carboxyl groups on the surface. We report that these different modified CNCs lead to stable oil-in-water emulsions. TEMPO-oxidized CNC might be the basis of further modifications. It is shown that they can, for example, lead to hydrophobic CNCs with a simple method using quaternary ammonium salts that allow producing inverse water-in-oil emulsions. Different from CNC modification before emulsification, modification can be carried out on the droplets after emulsification. This way allows preparing functional capsules according to the layer-by-layer process. As a result, it is demonstrated here the large range of use of these biobased rod-like nanoparticles, extending therefore their potential use to highly sophisticated formulations. This article is part of the themed issue ‘Soft interfacial materials: from fundamentals to formulation’.

Interaction Of Dilute Colloidal Particles In A Mixed Solvent

1995 ◽  
Vol 407 ◽  
Author(s):  
James V. Maher ◽  
M. Levent Kurnaz
Keyword(s):  
Charge Density ◽  
Surface Charge ◽  
Surface Charge Density ◽  
Colloidal Particles ◽  
Mixed Solvents ◽  
Phase Region ◽  
Polystyrene Latex ◽  
Two Phase ◽  
Rich Phase ◽  
The One

IntroductionColloidal particles in mixed solvents can show reversible aggregation in the one-phase regime of the mixture near the mixture's phase separation temperature [1–5]. This aggregation condition has been shown to be related to the affinity of the colloidal surfaces for one of the solvent components. In particular, for a 2,6 lutidine plus water (LW) mixture with colloidally dispersed polystyrene latex spheres (PLS) in a temperature range near the critical temperature, Tc, in the mixture's two-phase region, the particles will partition into one of the solvent phases, with the meniscus between the liquid phases clear to the eye and showing no sign of population by colloidal particles. Which phase of the solvent attracts the particles depends on the surface charge density of the particles, with high surface charge density particles preferring the water-rich phase and low charge density particles preferring the lutidine rich phase. As temperature is advanced deeper into the two-phase region (all effects discussed here are equilibrium effects), there is a temperature, Tw, at which particles appear on the meniscus (most particles remain in the preferred phase, whose population depletion is too small to measure). Tw changes with the surface charge density of the particles [4], but not with radius or with number density of the particles in the sample. The aggregation observed in the one-phase region [5] is then restricted to the side of the solvent's coexistence curve poor in the component which is rich in the partitioning-favored phase.

scholarly journals Mapping Surface Charge Distribution of Single-Cell via Charged Nanoparticle

Cells ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 1519
Author(s):  
Leixin Ouyang ◽  
Rubia Shaik ◽  
Ruiting Xu ◽  
Ge Zhang ◽  
Jiang Zhe
Keyword(s):  
Cell Surface ◽  
Charge Density ◽  
Surface Charge ◽  
Charge Distribution ◽  
Surface Charge Density ◽  
Single Cells ◽  
Fluorescent Light ◽  
Fluorescent Nanoparticles ◽  
Cell Surface Charge ◽  
Surface Charge Distribution

Many bio-functions of cells can be regulated by their surface charge characteristics. Mapping surface charge density in a single cell’s surface is vital to advance the understanding of cell behaviors. This article demonstrates a method of cell surface charge mapping via electrostatic cell–nanoparticle (NP) interactions. Fluorescent nanoparticles (NPs) were used as the marker to investigate single cells’ surface charge distribution. The nanoparticles with opposite charges were electrostatically bonded to the cell surface; a stack of fluorescence distribution on a cell’s surface at a series of vertical distances was imaged and analyzed. By establishing a relationship between fluorescent light intensity and number of nanoparticles, cells’ surface charge distribution was quantified from the fluorescence distribution. Two types of cells, human umbilical vein endothelial cells (HUVECs) and HeLa cells, were tested. From the measured surface charge density of a group of single cells, the average zeta potentials of the two types of cells were obtained, which are in good agreement with the standard electrophoretic light scattering measurement. This method can be used for rapid surface charge mapping of single particles or cells, and can advance cell-surface-charge characterization applications in many biomedical fields.

Triboelectrification of nanocomposites using identical polymer matrixes with different concentrations of nanoparticle fillers

2021 ◽  
Author(s):  
Linards Lapčinskis ◽  
Artis Linarts ◽  
Kaspars Mālnieks ◽  
Hyunseung Kim ◽  
Kristaps Rubenis ◽  
...  
Keyword(s):  
Charge Density ◽  
Surface Charge ◽  
Surface Charge Density ◽  
Polymer Layers

In this study, we investigate triboelectrification in polymer-based nanocomposites using identical polymer matrixes containing different concentrations of nanoparticles (NPs). The triboelectric surface charge density on polymer layers increased as the...

scholarly journals Effect of Selected Anionic and Cationic Drugs Affecting the Central Nervous System on Electrical Properties of Phosphatidylcholine Liposomes: Experiment and Theory

2021 ◽  
Vol 22 (5) ◽  
pp. 2270
Author(s):  
Joanna Kotyńska ◽  
Monika Naumowicz
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Charge Density ◽  
Surface Charge ◽  
Surface Charge Density ◽  
Barbituric Acid ◽  
Membrane Surface ◽  
Adsorption Equilibria ◽  
Two Component ◽  
The Central Nervous System

Interactions between phospholipid membranes and selected drugs affecting the central nervous system (CNS) were investigated. Small, unilamellar liposomes were used as biomimetic cell membrane models. Microelectrophoretic experiments on two-component liposomes were performed using the electrophoretic light scattering technique (ELS). The effect of both positively (perphenazine, PF) and negatively (barbituric acid, BA) charged drugs on zwitterionic L-α-phosphatidylcholine (PC) membranes were analyzed. Experimental membrane surface charge density (d) data were determined as a function of pH. Quantitative descriptions of the adsorption equilibria formed due to the binding of solution ions to analyzed two-component membranes are presented. Binding constants of the solution ions with perphenazine and barbituric acid-modified membranes were determined. The results of our research show that both charged drugs change surface charge density values of phosphatidylcholine membranes. It can be concluded that perphenazine and barbituric acid are located near the membrane surface, interacting electrostatically with phosphatidylcholine polar heads.

Surface charging parameters of charged particles in symmetrical electrolyte solutions

2020 ◽  
Vol 22 (35) ◽  
pp. 20123-20142
Author(s):  
Hadi Saboorian-Jooybari ◽  
Zhangxin Chen
Keyword(s):  
Charge Density ◽  
Surface Charge ◽  
Electrolyte Solution ◽  
Surface Charge Density ◽  
Potential Surface ◽  
Research Work ◽  
Charged Particles ◽  
Electrolyte Solutions ◽  
Surface Charging ◽  
Curvature Dependence

This research work is directed at development of accurate physics-based formulas for quantification of curvature-dependence of surface potential, surface charge density, and total surface charge for cylindrical and spherical charged particles immersed in a symmetrical electrolyte solution.

A multi-dielectric-layered triboelectric nanogenerator as energized by corona discharge

Nanoscale ◽  
2017 ◽  
Vol 9 (27) ◽  
pp. 9668-9675 ◽  
Author(s):  
Jia Jia Shao ◽  
Wei Tang ◽  
Tao Jiang ◽  
Xiang Yu Chen ◽  
Liang Xu ◽  
...  
Keyword(s):  
Charge Density ◽  
Surface Charge ◽  
Corona Discharge ◽  
Surface Charge Density ◽  
High Surface ◽  
Cycling Stability ◽  
Triboelectric Nanogenerator ◽  
Excellent Cycling Stability ◽  
Vertical Contact ◽  
High Surface Charge Density

A multi-dielectric-layered vertical contact-separation mode TENG through a corona discharge approach results in outstanding output performances, i.e., a high surface charge density of 283 μC m−2 and excellent cycling stability (92.6% retention after 200 000 cycles).

Modelling soil surface charge density using mineral composition

Geoderma ◽  
2004 ◽  
Vol 121 (1-2) ◽  
pp. 123-133 ◽  
Author(s):  
C. Taubaso ◽  
M. Dos Santos Afonso ◽  
R.M. Torres Sánchez
Keyword(s):  
Charge Density ◽  
Surface Charge ◽  
Mineral Composition ◽  
Surface Charge Density ◽  
Soil Surface
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