cryo-TEM Experiments Research Articles

Mechanisms and kinetics of C-S-H nucleation approaching the spinodal line: Insights into the role of organics additives

Wet chemistry C-S-H precipitation experiments were performed under controlled conditions of solution supersaturation in the presence and absence of gluconate and three hexitol molecules. Characterization of the precipitates with SAXS and cryo-TEM experiments confirmed the presence of a multi-step nucleation pathway. Induction times for the formation of the amorphous C-S-H spheroids were determined from light transmittance. Analysis of those data with the classical nucleation theory revealed a significant increase of the kinetic prefactor in the same order as the complexation constants of calcium and silicate with each of the organics. Finally, two distinct precipitation regimes of the C-S-H amorphous precursor were identified: i) a nucleation regime at low saturation indexes (SI) and ii) a spinodal nucleation regime at high SI where the free energy barrier to the phase transition is found to be of the order of the kinetic energy or less.

Phosphates form spectroscopically dark state assemblies in common aqueous solutions

Phosphates and polyphosphates play ubiquitous roles in biology as integral structural components of cell membranes and bone, or as vehicles of energy storage via adenosine triphosphate and phosphocreatine. The solution phase space of phosphate species appears more complex than previously known. We present nuclear magnetic resonance (NMR) and cryogenic transmission electron microscopy (cryo-TEM) experiments that suggest phosphate species including orthophosphates, pyrophosphates, and adenosine phosphates associate into dynamic assemblies in dilute solutions that are spectroscopically "dark." Cryo-TEM provides visual evidence of the formation of spherical assemblies tens of nanometers in size, while NMR indicates that a majority population of phosphates remain as unassociated ions in exchange with spectroscopically invisible assemblies. The formation of these assemblies is reversibly and entropically driven by the partial dehydration of phosphate groups, as verified by diffusion-ordered spectroscopy (DOSY), indicating a thermodynamic state of assembly held together by multivalent interactions between the phosphates. Molecular dynamics simulations further corroborate that orthophosphates readily cluster in aqueous solutions. This study presents the surprising discovery that phosphate-containing molecules, ubiquitously present in the biological milieu, can readily form dynamic assemblies under a wide range of commonly used solution conditions, highlighting a hitherto unreported property of phosphate's native state in biological solutions.

Biocompatible Chemically Fueled Transient Polymer Nanoparticles for Temporally Programmable in Vivo Imaging

Biocompatible Chemically Fueled Transient Polymer Nanoparticles for Temporally Programmable in Vivo Imaging

PH-responsive worm-based viscoelastic fluid formed by a dynamic covalent gemini surfactant

Responsive viscoelastic fluids based on wormlike micelles have attracted significant interest both in laboratory research and industrial applications due to their intelligent rheological response. However, pH-responsive worm-based viscoelastic fluids based on a dynamic imine surfactant remain a significant challenge. Herein, a novel worm-based viscoelastic fluid that can response to pH was fabricated utilizing a dynamic covalent gemini surfactant featuring a imine-type spacer. This unique gemini imine surfactant could be expediently obtained in situ by simply mixing an aldehyde-containing cationic surfactant (HOBAB) and hexyldiamine (C6DA) in water at a stoichiometric ratio of 2:1. Rheology and cryo-TEM experiments both demonstrated the formation of elongated wormlike micelles, responsible for the viscoelastic fluid. Because of its pH-sensitivity, the gemini imine surfactant could be damaged under acidic conditions and reformed under alkali conditions. Consequently, the solution of HOBAB and C6DA can be switched between a water-like fluid and worm-based viscoelastic fluid. Changing the precursors, such as the alkyldiamine or length of the hydrophobic chain, can also tailor the worm-based viscoelastic fluid based on a dynamic imine surfactant. For the C2-C6 spacer precursors, the viscoelastic fluid mainly resulted from the WLMs-based network, but for the C8 spacer precursor, it mainly originated from the densely packed of vesicles.

Adsorption-Inhibition of Clathrate Hydrates by Self-Assembled Nanostructures.

The mechanism by which safranine O (SFO), an ice growth inhibitor, halts the growth of single crystal tetrahydrofuran (THF) clathrate hydrates was explored using microfluidics coupled with cold stages and fluorescence microscopy. THF hydrates grown in SFO solutions exhibited morphology changes and were shaped as truncated octahedrons or hexagons. Fluorescence microscopy and microfluidics demonstrated that SFO binds to the surface of THF hydrates on specific crystal planes. Cryo-TEM experiments of aqueous solutions containing millimolar concentrations of SFO exhibited the formation of bilayered lamellae with an average thickness of 4.2±0.2 nm covering several μm2 . Altogether, these results indicate that SFO forms supramolecular lamellae in solution, which might bind to the surface of the hydrate and inhibit further growth. As an ice and hydrate inhibitor, SFO may bind to the surface of these crystals via ordered water molecules near its amine and methyl groups, similar to some antifreeze proteins.

Abstract P-42: Structure of Hydrogels of an Anionic Polysaccharide Studied by Freeze-Fracture Transmission Electron Microscopy

Background: Polysaccharide hydrogels draw attention due to the ability to form mechanically tough gels at low concentrations (typically 1 wt% or lower), combined with biocompatibility and biodegradability. Biopolymer hydrogels can be used as a matrix for cell growth, in order to obtain materials for the replacement of damaged tissues. “Physical” gels with macromolecules cross-linked by dynamic reversible cross-links are of great interest due to their self-healing ability. However, investigation of the native un-perturbed structure of such hydrogels presents a challenge, since they collapse upon drying, and present a difficulty for preparing a thin specimen for cryo-TEM experiments due to very high viscosity. The aim of this work is to study the native structure of hydrogels of an anionic polysaccharide – carboxymethyl hydroxypropyl guar (CMHPG) – cross-linked by borax. Methods: Freeze-fracture transmission electron microscopy (FF-TEM) was conducted on a Phillips EM-301 microscope. A small volume of the sample (100 μl) was put into the copper cell and cooled down by liquid nitrogen, put under vacuum (10−5 torr) at continuous cooling with liquid nitrogen, and fractured. The surface was etched for 10–20 min at 10−5 torr and then replicated by spraying platinum and carbon. Results: The gels have a microphase-separated microstructure – a rather thick (several nm) polymer backbone is seen, which is presumably formed by multiple aggregated macromolecules, and meshes between the backbone do not contain polymer and are filled with solvent. Mesh size determined from the micrographs qualitatively coincides with the value determined from the elastic modulus of the gels. Upon increasing the concentrations of cross-linker, the network becomes denser: the mesh size becomes lower, and the thickness of the backbone increases. Thus, the addition of cross-linker favors the aggregation of polymer chains forming the backbone. Conclusion: It was shown by FF-TEM that cross-linked CMHPG gels have a microphase-separated structure with a dense backbone formed by polymer chains and rather large meshes between them.

Janus Vitrification of Droplet via Cold Leidenfrost Phenomenon.

Janus particles with asymmetric crystals show great importance in optoelectronics and photocatalysis, but their synthesis usually requires complicated procedures. Here, an unexpected Janus vitrification phenomenon is observed in a droplet caused by the Leidenfrost effect at a cryogenic temperature, which is commonly regarded as symmetric. The Leidenfrost phenomenon levitates the droplet when it comes in contact with liquid nitrogen causing different cooling conditions on the droplet's top and bottom surfaces. It induces asymmetric crystallization in the droplet, forming a Janus vitrified particle with an asymmetric crystallization borderline after cooling, as further evidenced by cryotransmission electron microscopy (cryo-TEM) experiments. Theoretical analysis and experimental study indicate that the position of the asymmetric crystallization borderline is determined by the droplet radius and density, and the observation window of asymmetric crystallization borderline is determined by the chemical concentration. The finding reveals the asymmetric crystallization phenomenon in droplet vitrification for the first time, and provides a new insight for creating Janus particles through the Leidenfrost phenomenon.

Physicochemical characterization of green sodium oleate-based formulations. Part 1. Structure and rheology

HypothesisThe structure, rheology and other physicochemical properties of dilute aqueous dispersions of sodium oleate (NaOL) are well known. This paper is the first report in which a moderately concentrated (13% w/w) dispersion of NaOL in water is investigated. In fact, at this concentration the phase and rheology behavior of the surfactant remarkably deviates from those of its dilute solutions in water and a significant effect is imparted by the addition of potassium chloride. ExperimentalThe structural, thermal and rheological properties of a 13% w/w dispersion of NaOL in water were investigated by cryo-TEM, rheology, and DSC experiments with and without the addition of potassium chloride. The system is comprised of elongated wormlike micelles that turn into a gel-like more disordered viscous material upon addition of small amounts of KCl (4% w/w). FindingsThis paper illustrates the multifaceted behavior of sodium oleate dispersions at intermediate concentrations that depends on the presence of other cosolutes (such as KCl). The results show that viscoelastic aqueous dispersions of NaOL are excellent candidates for the preparation of stimuli-responsive green materials to be used in a number of different applications. We also discuss the genesis of wormlike micelles (WLMs) in terms of the general theory of self-assembly.

Foaming behavior of fluorocarbon surfactant used in fire-fighting: The importance of viscosity and self-assembly structure

In this work, we systematically investigated the foaming behavior of a zwitterionic fluorocarbon surfactant (FC1157) used in fire-fighting. Two different foaming methods were used to generate foam, and the foaming behaviors of the fluorocarbon surfactant and typical hydrocarbon surfactants were compared. Multiscale approaches including cryogenic-transmission electron microscopy (cryo-TEM), surface tension measurements, viscosity and turbidity measurements were employed. Our results revealed that the foaming behavior of FC1157 is different from that of the hydrocarbon surfactants, which is not only related to the surfactant adsorption dynamics but also to the solution viscosity. We confirmed that the increased viscosity leads to a decrease in foaming ability and FC1157 is the only surfactant which exhibits viscous behavior in solution. The viscosity change is due to the variation in solution turbidity which comes from the formation of large aggregates in bulk. Cryo-TEM experiments indicated that FC1157 molecules tend to self-assemble in solution into vesicles. The presence of the vesicle phase strongly affects the solution viscosity and thus the foaming ability, which is different from that observed in the systems containing hydrocarbon surfactants. This study provided insight into the basic factors affecting the foaming behavior of the fluorocarbon surfactant used in fire-fighting, highlighting the crucial role of viscosity and self-assembly structure in determining the foaming behavior.

Fibril Charge Affects α-Synuclein Hydrogel Rheological Properties.

In this paper, we have investigated the interactions between α-synuclein fibrils at different pH values and how this relates to hydrogel formation and gel properties. Using a combination of rheology, small-angle X-ray scattering, Raman spectroscopy, and cryo-transmission electron microscopy (cryo-TEM) experiments, we have been able to investigate the relationship between protein net charge, fibril-fibril interactions, and hydrogel properties, and have explored the potential for α-synuclein to form hydrogels at various conditions. We have found that α-synuclein can form hydrogels at lower concentrations (50-300 μM) and over a wider pH range (6.0-7.5) than previously reported. Over this pH range and at 300 μM, the fibril network is electrostatically stabilized. Decreasing the pH to 5.5 results in the precipitation of fibrils. A maximum in gel stiffness was observed at pH 6.5 (∼1300 Pa), which indicates that significant attractive interactions operate at this pH and cause an increase in the density of hydrophobic contacts between the otherwise negatively charged fibrils. We conclude that fibril-fibril interactions under these conditions involve both long-range electrostatic repulsion and a short-range hydrophobic attractive (sticky) component. These results may provide a basis for potential applications and add to the understanding of amyloids.

PEGylation and surface functionalization of liposomes containing drug nanocrystals for cell-targeted delivery

Liposomal formulations have important therapeutic applications in anti-cancer treatments but current formulations suffer from serious side effects, high dosage requirements and prolonged treatment. In this study, PEGylated azide-functionalized liposomes containing drug nanocrystals were investigated with the aim of increasing the drug payload and achieving functionalization for targeted delivery. Liposomes were characterized using cryogenic transmission electron microscopy (cryo-TEM), dynamic light scattering (DLS), small and ultra-small angle neutron scattering (SANS/USANS) and small and wide angle X-ray scattering (SAXS/WAXS). Cryo-TEM experiments revealed the dimensions of the nanocrystal-loaded liposomes and the change of shape from spherical to elongated after the formation of nanocrystals. Results from SANS/USANS experiments confirmed the asymmetric particle shape. SAXS/WAXS experiments confirmed that the crystalline drug only occurred in freeze-thawed samples and correlated with a new unidentified polymorphic form of ciprofloxacin. Using a small molecule dye, dibenzocyclooctyne (DBCO)-cy5, specific conjugation between DBCO groups and surface azide groups on the liposomes was confirmed; this indicates the promise of this system for tumour-targeted delivery.

(Invited) Lithium Plating – Understanding of a Very Complicated Phenomenon

Lithium metal electrode (LME) poises as the best candidate for truly high-energy designs for rechargeable lithium batteries (RLB) when coupled with high-voltage, high-capacity cathode materials. To enable LME function well in such designs, very dense lithium (Li) deposition without dendrite growth is essential. To achieve this goal, acquiring fundamental understanding of Li nucleation and growth during deposition and the subsequent pathways toward stability during cycling at very negative, reducing potentials; is vital. It is well known that Li reacts with electrolyte to form solid electrolyte interphases (SEI). Putting the complicated SEI issues aside, understanding Li nucleation fundamentals is still very critical to ultimate Li deposition. Currently Li electrodeposition is limited by non-uniform behavior that leads to volume expansion due to pore generation, poor Li utilization (e.g. forming inactive or “dead” Li), and accelerated SEI formation and electrolyte decomposition due to increased interfacial area, just to name a few. The key question is, “Are these undesirable consequences come from the same origin or not?” Here, multi-scale observations by cryogenic-transmission electron microscopy (cryo-TEM) and advanced reactive-molecular dynamics (r-MD) simulations were used to understand the kinetic progression of Li nucleation. The cryo-TEM imaging revealed that amorphous metal deposits can be obtained at room temperature with very slow deposition rates, traditionally only possible with very high quenching rates (e.g. >106 K s-1) on Li nucleation and reveals the transition from amorphous disordered states to crystalline ordered ones as a function of current density and deposition time. The r-MD simulations provide additional understanding of the driving forces and kinetic pathways for the nucleation and the associated amorphous-to-crystalline (disorder-order or second-order) phase transition. The incubation time for the phase transition varies with the Li canonical ensemble size, mass and energy transfer rate between an ensemble and the neighboring ones, and as a function of current density (i.e. Li deposition rate). It is important to note that this is the first time the r-MD was used to simulate kinetic pathway in a discrete manner with canonical ensembles to assess the impacts from the kinetic regime, which is very different from the conventional temporal or spatial averaging methods according to the statistical thermodynamics. Although the r-MD results were developed independently from cryo-TEM experiments, i.e. without any empirical correlation; there is a high degree of agreement with experimental observations.

Transfection of plasmid DNA by nanocarriers containing a gemini cationic lipid with an aromatic spacer or its monomeric counterpart

This study performed a biophysical characterization (electrochemistry, structure and morphology) and assessment of the biological activity and cell biocompatibility of GCL/DOPE-pDNA lipoplexes comprised of plasmid DNA and a mixed lipid formed by a DOPE zwitterionic lipid and a gemini cationic lipid N-N′-(1,3-phenylene bis (methylene)) bis (N,N-dimethyl-N-(1-dodecyl) ammonium dibromide (12PH12) containing an aromatic spacer or its monomeric counterpart surfactant, N-benzyl-N,N-dimethyl-N-(1-dodecyl) ammonium bromide (12PH). Electrochemical results reveal that i) the gemini cationic lipid (12PH12) and the plasmid pDNA yield effective charges less than their nominal charges (+2 and −2/bp, respectively) and that ii) both vectors (12PH12/DOPE and 12PH/DOPE) could compact pDNA and protect it from DNase I degradation. SAXS and cryo-TEM experiments indicate the presence of a lamellar lyotropic liquid crystal phase represented as alternating layers of mixed lipid and plasmid. Transfection efficiency (by FACS and luminometry) and cell viability assay in COS-7 cells, performed with two plasmid DNAs (pEGFP-C3 and pCMV-Luc VR1216), confirm the goodness of the proposed formulations (12PH12/DOPE and 12PH/DOPE) to transport genetic material, with efficiencies and biocompatibilities comparable to or better than those exhibited by the control Lipofectamine 2000*. In conclusion, although major attention has been paid to gemini cationic lipids in the literature, due to the large variety of modifications that their structures may support to improve the biological activity of the resulting lipoplexes, it is remarkable that the monomeric counterpart surfactant with an aromatic group analyzed in the present work also exhibits good biological activity. The in vitro results reported here indicate that the optimum formulations of the gene vectors studied in this work efficiently transfect plasmid DNA with very low toxicity levels and, thus, may be used in forthcoming in vivo experiments.

A new method for the formulation of double nanoemulsions.

Double emulsions are very attractive systems for many reasons; the most important of these are their capacity to encapsulate hydrophilic and lipophilic molecules simultaneously in a single particle and their potentiality to protect fragile hydrophilic molecules from the continuous phase. Double emulsions represent a technology that is widely present down to the micrometer scale; however, double nanoemulsions, with their new potential applications as nanomedicines or diagnosis agents, currently present a significant challenge. In this study, we propose an original two-step approach for the fabrication of double nanoemulsions with a final size below 200 nm. The process consists of the formulation of a primary water-in-oil (w1/O) nanoemulsion by high-pressure homogenization, followed by the re-emulsification of this primary emulsion by a low-energy method to preserve the double nanostructure. Various characterization techniques were undertaken to confirm the double structure and to evaluate the encapsulation efficiency of a small hydrophilic probe in the inner aqueous droplets. Complementary fluorescence confocal and cryo-TEM microscopy experiments were conducted to characterize and confirm the double structure of the double nanoemulsion.

Formation and Reversible Morphological Transition of Bicontinuous Nanospheres and Toroidal Micelles by the Self-Assembly of a Crystalline-b-Coil Diblock Copolymer.

We herein report the formation of two complex nanostructures, toroidal micelles and bicontinuous nanospheres, by the self-assembly of the single structurally simple crystalline-b-coil diblock copolymer poly[bis(trifluoroethoxy)phosphazene]-b-poly(styrene), PTFEP-b-PS, in one solvent (THF) and without additives. The nature of these nanostructures in solution was confirmed by DLS and cryo-TEM experiments. The two morphologies are related by means of a new type of reversible morphological evolution, bicontinuous-to-toroidal, triggered by changes in the polymer concentration. WAXS experiments showed that the degree of crystallinity of the PTFEP chains located at the core of the toroids was higher than that in the bicontinuous nanospheres, thus indicating that the final morphology of the aggregates is mostly determined by the ordering of the PTFEP core-forming blocks.

Design of Ionizable Lipids To Overcome the Limiting Step of Endosomal Escape: Application in the Intracellular Delivery of mRNA, DNA, and siRNA.

The intracellular delivery of nucleic acid molecules is a complex process involving several distinct steps; among these the endosomal escape appeared to be of particular importance for an efficient protein production (or inhibition) into host cells. In the present study, a new series of ionizable vectors, derived from naturally occurring aminoglycoside tobramycin, was prepared using improved synthetic procedures that allow structural variations on the linker and hydrophobic domain levels. Complexes formed between the new ionizable lipids and mRNA, DNA, or siRNA were characterized by cryo-TEM experiments and their transfection potency was evaluated using different cell types. We demonstrated that lead molecule 30, bearing a biodegradable diester linker, formed small complexes with nucleic acids and provided very high transfection efficiency with all nucleic acids and cell types tested. The obtained results suggested that the improved and "universal" delivery properties of 30 resulted from an optimized endosomal escape, through the lipid-mixing mechanism.

Thermodynamics of self-assembling of mixture of a cationic gemini surfactant and sodium dodecylsulfate in aqueous solution: Calorimetry, conductivity and surface pressure measurements

The thermodynamics and phase behavior of mixtures of cationic gemini surfactant decanediyl-α,ω-bis(dodecyldimethylammonium bromide) (12-10-12) and sodium dodecylsulfate (SDS) were studied in the dilute SDS-rich region. The enthalpy of interaction between both surfactant monomers before the critical micelle concentration for the mixture (cmcmix) was determined by isothermal titration calorimetry (ITC). After the cmcmix, ITC results exhibited a first process associated with a large endothermic enthalpy change followed by a second one with a very small exothermic enthalpy change. In the same regions, the conductivity curves show an increase in slope after the break, followed by a plateau region, respectively for the two processes. The combined results from the various methodologies used lead us to propose that the first process reflects the formation of non-spherical micelles and the second one the vesicle formation. The area per catanionic complex was obtained through surface pressure measurements, leading to an apparent packing parameter ⩾1. The observed behavior may be rationalized on the basis of the hypothesis that both surfactants distribute asymmetrically in the vesicle bilayers and unevenly in the non-spherical micelle. In order to get structural information Cryo-TEM experiments were performed, which provided images that support this interpretation. From all the information gathered a phase diagram was mapped, including three one-phase regions of spherical micelles, non-spherical micelles and vesicles.

Exploiting Conjugated Polyelectrolyte Photophysics toward Monitoring Real-Time Lipid Membrane-Surface Interaction Dynamics at the Single-Particle Level.

Herein we report the real-time observation of the interaction dynamics between cationic liposomes flowing in solution and a surface-immobilized charged scaffolding formed by the deposition of conjugated polyanion poly[5-methoxy-2-(3-sulfopropoxy)-1,4-phenylenevinylene (MPS-PPV) onto 100-nm-diameter SiO2 nanoparticles (NPs). Contact of the freely floating liposomes with the polymer-coated surfaces led to the formation of supported lipid bilayers (SLBs). The interaction of the incoming liposomes with MPS-PPV adsorbed on individual SiO2 nanoparticles promoted the deaggregation of the polymer conformation and led to large emission intensity enhancements. Single-particle total internal reflection fluorescence microscopy studies exploited this phenomenon as a way to monitor the deformation dynamics of liposomes on surface-immobilized NPs. The MPS-PPV emission enhancement (up to 25-fold) reflected on the extent of membrane contact with the surface of the NP and was correlated with the size of the incoming liposome. The time required for the MPS-PPV emission to reach a maximum (ranging from 400 to 1000 ms) revealed the dynamics of membrane deformation and was also correlated with the liposome size. Cryo-TEM experiments complemented these results by yielding a structural view of the process. Immediately following the mixing of liposomes and NPs the majority of NPs had one or more adsorbed liposomes, yet the presence of a fully formed SLB was rare. Prolonged incubation of liposomes and NPs showed completely formed SLBs on all of the NPs, confirming that the liposomes eventually ruptured to form SLBs. We foresee that the single-particle studies we report herein may be readily extended to study membrane dynamics of other lipids including cellular membranes in live cell studies and to monitor the formation of polymer-cushioned SLBs.

Polymersome Shape Transformation at the Nanoscale

Polymer vesicles, also named polymersomes, are valuable candidates for drug delivery and micro- or nanoreactor applications. As far as drug delivery is concerned, the shape of the carrier is believed to have a strong influence on the biodistribution and cell internalization. Polymersomes can be submitted to an osmotic imbalance when injected in physiological media leading to morphological changes. To understand these osmotic stress-induced variations in membrane properties and shapes, several nanovesicles made of the graft polymer poly(dimethylsiloxane)-g-poly(ethylene oxide) (PDMS-g-PEO) or the triblock copolymer PEO-b-PDMS-b-PEO were osmotically stressed and observed by light scattering, neutron scattering (SANS), and cryo-transmission electron microscopy (cryo-TEM). Hypotonic shock leads to a swelling of the vesicles, comparable to optically observable giant polymersomes, and hypertonic shock leads to collapsed structures such as stomatocytes and original nested vesicles, the latter being only observed for bilayers classically formed by amphiphilic copolymers. Complementary SANS and cryo-TEM experiments are shown to be in quantitative agreement and highlight the importance of the membrane structure on the behavior of these nanopolymersomes under hypertonic conditions as the final morphology reached depends whether or not the copolymers assemble into a bilayer. The vesicle radius and membrane curvature are also shown to be critical parameters for such transformations: the shape evolution trajectory agrees with theoretical models only for large enough vesicle radii above a threshold value around 4 times the membrane thickness.

Transformation of micelles into supramolecular vesicles triggered by the formation of [4]pseudorotaxanes

Spontaneous formation of supramolecular vesicles which are triggered by the formation of [4]pseudorotaxane B was demonstrated, whereas both Guest and [2]pseudorotaxane A, the precursors of [4]pseudorotaxane B, only assemble into micelles in DMF/water solution. The remarkable transformation of Guest from micelles to supramolecular vesicles was confirmed through DLS, TEM, and Cryo-TEM experiments. The cumulative release of a model drug, 5-carboxyfluorescein (CF), was used to determine the permeability of the supramolecular vesicles. No leakage of entrapped CF was observed within 48h by fluorescence measurement, indicating the high stability of supramolecular vesicles. The formation mechanism of supramolecular vesicles self-assembled by [4]pseudorotaxane B was also discussed. In [4]pseudorotaxane B, CB[6] is used to increase the hydrophobic property of site β, which acts as hydrophobic “tail.” Meanwhile, CB[7] plays the role of increasing “head area” of site α, which acts as hydrophilic “head.” The synergistic effect of CB[6] and CB[7] induces the formation of supramolecular vesicles. Moreover, the effect of DMF content was investigated by TEM observations. It was found that the [4]pseudorotaxane B can self-assemble into regular supramolecular vesicles when the DMF content is in the range of 50–70%.