Thermodynamic Determination of the Metal/Semiconductor Separation of Carbon Nanotubes Using Hydrogels

The metal/semiconductor separation of single-wall carbon nanotubes (SWCNTs) using hydrogels, such as agarose gel and Sephacryl, together with sodium dodecyl sulfate is one of the most successful techniques necessary for industrial applications. Despite recent improvements in the technique, little is known about the separation mechanism. Here, we show that SWCNTs are reversibly adsorbed onto hydrogels in the presence of sodium dodecyl sulfate. The results enabled us to examine the thermodynamics of the adsorption reaction and thereby elucidate the separation mechanism. The adsorbability of SWCNTs onto the hydrogels was described by the standard Gibbs free energy for the adsorption, as well as the area of the hydrogels allowing the adsorption. We demonstrated, for the first time, that the free energy of adsorption for semiconducting SWCNTs was 0–12 kJ/mol lower than that for metallic SWCNTs in the temperature range of 290–320 K (<i>e.g.</i>, <i>ca</i>. −4 kJ/mol for the agarose gel and <i>ca</i>. −9 kJ/mol for Sephacryl at 300 K), which permits metal/semiconductor separation. Importantly, the difference in the free energy was attributed to the difference in the enthalpy of adsorption: the enthalpy of adsorption of metallic SWCNTs was <i>ca</i>. 70 kJ/mol higher than that of semiconducting SWCNTs. Thus, the enthalpy of adsorption was found to be an important parameter in the metal/semiconductor separation of SWCNTs using hydrogels. In addition, the thermodynamic parameters depended on the hydrogel type and the surfactant concentration, which is most likely why under certain conditions hydrogels and surfactants produce different separations, <i>e.g.,</i> chirality-selective or diameter-selective separation

Arginine-Assisted Solubilization System for Drug Substances: Solubility Experiment and Simulation

The poor aqueous solubility of drug substances hampers their broader applications. This paper describes a de novo strategy to increase the aqueous solubility of drug substances using an arginine-assisted solubilization system (AASS) with alkyl gallates as model drug substances. Solubility experiments of alkyl gallates showed that arginine greatly increases the aqueous solubility of different alkyl gallates, whose aqueous solubilities differ widely. In contrast, lysine showed marginal effects on alkyl gallates solubility. Molecular dynamic simulation indicated a greater interaction of arginine with alkyl gallates than that of lysine, which reflects favorable interaction between the guanidinium group of arginine and the aromatic ring of alkyl gallates. Such interaction apparently disrupts association of alkyl gallate molecules, leading to solubilization. These results indicate AASS as a promising approach to solubilize poorly soluble drug substances containing aromatic ring structures

Oxidative Stress of Carbon Nanotubes on Proteins Is Mediated by Metals Originating from the Catalyst Remains

Nanomaterials introduced into biological systems are immediately coated by proteins in vivo. They induce oxidative stress on adsorbed proteins and hence alter the protein structures, which determines the fate pathways and biological impacts of nanomaterials. Carbon nanotubes (CNTs) have been suggested to cause protein oxidation. In this work, we discovered that CNTs induce oxidative stress on proteins in cooperation with coexisting metals originating from catalyst remains. Protein sulfhydryl groups were readily oxidized by the coexistence of CNTs and metals. Numerical simulations of the reaction demonstrated that the metals effectively mediate electron transfer between the CNTs and protein sulfhydryl groups. Thus, the coexistence of CNTs and metals, even in low concentrations, generates oxidative stress on proteins with high reaction rates. Metal catalysts used for CNT growth, in turn, catalyze the oxidation reaction of proteins. The proposed protein oxidation mechanism will advance the fundamental understanding of the biological safety and toxicity of nanomaterials synthesized using metal catalysts

pH- and Solute-Dependent Adsorption of Single-Wall Carbon Nanotubes onto Hydrogels: Mechanistic Insights into the Metal/Semiconductor Separation

The gel separation of single-wall carbon nanotubes (SWCNTs) suspended in sodium dodecyl sulfate (SDS) is expected to be one of the most successful methods of large-scale and high-purity separation. Understanding the mechanism of the gel separation helps improve the quality and quantity of separation and reveals the colloidal behaviors of SWCNTs, which reflects their band structures. In this study, we characterize the pH- and solute-dependent adsorption of SWCNTs onto agarose and Sephacryl hydrogels and provide a mechanistic model of the metal/semiconductor separation. The adsorbability of SWCNTs is substantially reduced under acidic pH conditions. Importantly, the pH dependence differs between metallic and semiconducting species; therefore, the adsorbability is related to the band-structure-dependent oxidation of the SWCNTs. Oxidation confers positive charges on SWCNTs, and these charges enhance the electrostatic interactions of the SWCNTs with SDS, thereby leading to the condensation of SDS on the SWCNTs. This increase in SDS density reduces the interactions between the SWCNTs and hydrogels. Under highly basic conditions, such as pH ∼12.5, or in the presence of salts, the adsorption is dissociative because of the condensation of SDS on the SWCNTs through electrostatic screening by counterions. Desorption of the SWCNTs from the hydrogels due to the addition of urea implies a hydrophobic interface between SDS-dispersed SWCNTs and the hydrogels. These results suggest that the metal/semiconductor separation can be explained by the alteration of the interaction between SDS-dispersed SWCNTs and the hydrogels through changes in the conformation of SDS on the SWCNTs depending on the SWCNTs’ band structures

Additional file 1: of Destabilization of Surfactant-Dispersed Carbon Nanotubes by Anions

Experimental Results. (DOCX 636 kb

Purification of Single-Wall Carbon Nanotubes by Controlling the Adsorbability onto Agarose Gels Using Deoxycholate

One of the key challenges to the industrialization of single-wall carbon nanotubes (SWCNTs) is the commercial-scale production of highly purified SWCNTs separated into metallic and semiconducting species. In the present study, the purification of SWCNTs, i.e., the removal of amorphous carbon or bundled SWCNTs, was performed by quantifying and controlling their adsorbability onto agarose gel. The quantification of the adsorbability was achieved by assuming the Langmuir isotherm, and control over the adsorbability was exerted using 0.05–1% sodium deoxycholate (DOC). The results show that the adsorbability depends on the concentration of DOC. At a low DOC concentration (approximately 0.05%), impurities such as amorphous carbon or bundled SWCNTs were preferentially adsorbed onto the gels, whereas, at an intermediate DOC concentration (ca. 0.25%), high-purity SWCNTs were mainly adsorbed onto the gels. Thus, the impurities, which are difficult to remove by conventional methods, could be separated from unpurified SWCNTs by controlling the adsorbability, leading to the extraction of high-purity SWCNTs. In the purification, diameter-selective separation of SWCNTs was also observed. The purification method using a gel column can be conducted simply and continuously, so that it can be applied for the high-throughput production of high-purity SWCNTs

One-Dimensional Protein-Based Nanoparticles Induce Lipid Bilayer Disruption: Carbon Nanotube Conjugates and Amyloid Fibrils

Along with recent progress of nanotechnology, concern has risen about biological impacts of nanoparticles deriving from their interaction with cell membranes. Nanoparticles tend to adsorb proteins in vivo. Therefore, the physical properties of the conjugates to cell membranes must be investigated to elucidate and assess their properties. We examined whether one-dimensional protein-based nanoparticles induce liposome leakage in physiological saline. Carbon nanotube conjugates with adsorbed lysozyme interacted with the liposome through electrostatic interaction, leading to liposome leakage. Surprisingly, amyloid fibrils of lysozyme resembled the conjugate in terms of their effects on liposome leakage. Results described herein provide new insight into the interaction between nanoparticles and cell membranes in terms of their shape, mechanical properties, and noncovalent interactions

Protein’s Protein Corona: Nanoscale Size Evolution of Human Immunoglobulin G Aggregates Induced by Serum Albumin

Nanoparticles are readily coated by proteins in biological systems. The protein layers on the nanoparticles, which are called the protein corona, influence the biological impacts of the nanoparticles, including internalization into cells and cytotoxicity. This study expands the scope of the nanoparticle’s protein corona for exogenous artificial nanoparticles to that for exogenous proteinaceous nanoparticles. Specifically, this study addresses the formation of protein coronas on nanoscale human antibody aggregates with a radius of approximately 20–40 nm, where the antibody aggregates were induced by a pH shift from low to neutral pH. The size of the human immunoglobulin G (hIgG) aggregates grew to approximately 25 times the original size in the presence of human serum albumin (HSA). This size evolution was ascribed to the association of the hIgG aggregates, which was triggered by the formation of the hIgG aggregate’s protein corona, i.e., protein’s protein corona, consisting of the adsorbed HSA molecules. Because hIgG aggregate association was significantly reduced by the addition of 30–150 mM NaCl, it was attributed to electrostatic attraction, which was supported by molecular dynamics (MD) simulations. Currently, the use of antibodies as biopharmaceuticals is concerning because of undesired immune responses caused by antibody aggregates that are typically generated by a pH shift during the antibody purification process. The present findings suggest that nanoscale antibody aggregates form protein coronas induced by HSA and the resulting nanoscale antibody–HSA complexes are stable in blood containing approximately 150 mM salt ions, at least in terms of the size evolution. Mechanistic insights into protein corona formation on nanoscale antibody aggregates are useful for understanding the unintentional biological impacts of antibody drugs

Solubilization of Carbon Nanobelts in Aqueous Solutions: Optical and Colloidal Properties

Carbon nanobelts (CNBs) correspond to carbon nanotube (CNT) segments and are insoluble in most common aqueous solutions, posing challenges across diverse applications. In this study, [12] CNB, which corresponds to a (6,6) CNT segment, was solubilized by aliphatic surfactant micelles through host–guest complexation, which was confirmed by comprehensive analyses involving spectrophotometry, mass spectrometry, and molecular dynamics simulations. Through this solubilization, zero-Stokes shift emission of the CNB could occur, which could be ascribed to the symmetry-allowed transition. In contrast, CNB was insoluble in non-aliphatic surfactant solutions. The mechanism by which CNB is solubilized using aliphatic surfactants is completely distinct from that of the CNT dispersion mechanism. The present finding provides knowledge of the effectiveness of aliphatic compounds in solubilizing CNBs and their derivatives (carbon nanohoops), which show significant potential for various applications in aqueous systems, including biological applications

Molecular Dynamics Simulation of the Arginine-Assisted Solubilization of Caffeic Acid: Intervention in the Interaction

We have previously demonstrated that arginine increases the solubility of aromatic compounds that have poor water solubility, an effect referred to as the “arginine-assisted solubilization system (AASS)”. In the current study, we utilized a molecular dynamics simulation to examine the solubilization effects of arginine on caffeic acid, which has a tendency to aggregate in aqueous solution. Caffeic acid has a hydrophobic moiety containing a π-conjugated system that includes an aromatic ring and a hydrophilic moiety with hydroxyl groups and a carboxyl group. While its solubility increases at higher pH values due to the acquisition of a negative charge, the solubility was greatly enhanced by the addition of 1 M arginine hydrochloride at any pH. The results of the simulation indicated that the caffeic acid aggregates were dissociated by the arginine hydrochloride, which is consistent with the experimental data. The binding free energy calculation for two caffeic acid molecules in an aqueous 1 M arginine hydrochloride solution indicated that arginine stabilized the dissociated state due to the interaction between its guanidinium group and the π-conjugated system of the caffeic acid. The binding free energy of two caffeic acid molecules in the arginine hydrochloride solution exhibited a local minimum at approximately 8 Å, at which the arginine intervened between the caffeic acid molecules, causing a stabilization of the dissociated state of caffeic acid. Such stabilization by arginine likely led to the caffeic acid solubilization, as observed in both the experiment and the MD simulation. The results reported in this paper suggest that AASS can be attributed to the stabilization resulting from the intervention of arginine in the interaction between the aromatic compounds