Self-Assembly of Lamellae-in-Lamellae by Double-Tail Cationic Surfactants.

The molecular structures of surfactants play a pivotal role in influencing their self-assembly behaviors. In this work, using simulations and experiments, an unconventional hierarchically layered structure in the didodecyldimethylammonium bromide (DDAB)/water binary system: lamellae-in-lamellae is revealed, a new self-assembly structure in surfactant system. This self-assembly structure refers to a lamellar structure with a shorter periodic length (inner lamellae) embedded in a lamellar phase with a longer periodic length (outer lamellae). The normal vectors of these two lamellar regions orient perpendicularly. In addition, it is observed that this lamellar-in-lamellar phase disappears when the two tails of the cationic surfactants become longer. The formation of the lamellar-in-lamellar architecture arises from multiple interacting factors. The key element is that the short tails of the DDAB surfactants enhance hydrophilicity and rigidity, which facilitates the formation of the inner lamellae. Moreover, the lateral monolayer of the inner lamellae provides shielding from the water and prompts the formation of the outer lamellae. These findings indicate that molecular structures and flexibility can profoundly redirect the hierarchical self-assembly behaviors in amphiphilic systems. More broadly, this work presents a new strategy to deliberately program hierarchical nanomaterials by designing specific surfactant molecules to act as tunable scaffolds, reactors, and carriers.

Phase Behaviors of Dialkyldimethylammonium Bromide Bilayers.

Dialkyldimethylammonium bromide (2CnBr) surfactants in bilayer exhibit polymorphic phases and rich self-assembly behaviors. However, the effects of alkyl chain length on the phase behavior of the 2CnBr bilayer are still not completely understood. Herein, we investigate the 2CnBr bilayers by performing all-atom molecular dynamics simulations, taking into consideration the influence of temperature and initial interdigitated degree. Our findings indicate that DOAB (2C8Br) is challenging to remain in a bilayer structure, while DDAB (2C12Br) and DPAB (2C16Br) maintain bilayers in different phases. DDAB bilayers exhibit an interdigitated gel phase, and this phase structure enhances the stability and rigidity of the bilayer membrane. In contrast, DPAB bilayers show a ripple gel phase, which has better softness and ductility. The differences in phase behaviors can be attributed to a competition between the rigidity of the 2CnBr surfactants and the hydrophobic interaction of the alkyl tails. The results reveal the crucial role of the bilayer phase in determining the rigidity of bilayer membranes.

Interactions in Aqueous Mixtures of Cationic Hydroxyethyl Cellulose and Different Anionic Bile Salts.

It is known that the reduction of blood cholesterol can be accomplished through foods containing a large number of dietary fibers; this process is partially related to the binding of bile salt to fibers. To gain new insights into the interactions between dietary fibers and bile salts, this study investigates the interactions between cationic hydroxyethyl cellulose (catHEC) and sodium deoxycholate (NaDC) or sodium cholate (NaC), which have a similar structure. Turbidity measurements reveal strong interactions between catHEC and NaDC, and under some conditions, macroscopic phase separation occurs. In contrast, the interactions with NaC are weak. At a catHEC concentration of 2 wt %, incipient phase separation is approached at concentrations of NaC and NaDC of 32.5 and 19.3 mM, respectively. The rheological results show strong interactions and a prominent viscosification effect for the catHEC/NaDC system but only moderate interactions for the catHEC/NaC system. Both cryogenic transmission electron microscopy and small-angle X-ray scattering results display fundamental structural differences between the two systems, which may explain the stronger interactions in the presence of NaDC. The surmise is that the extended structures formed in the presence of NaDC can easily form connections and entanglements in the network.

Noncovalent Bile Acid Oligomers as Facial Amphiphilic Antimicrobials.

New antimicrobial agents are needed to address the ever-growing risk of bacterial resistance, particularly for methicillin- and vancomycin-resistant Staphylococcus aureus (S. aureus). Here, we report a class of bile acid oligomers as facial amphiphilic antimicrobials, which are noncovalently fabricated by cholic acid (CA) and deoxycholic acid (DCA) with polyamines (e.g., diamines, diethylenetriamine, spermidine, and spermine). The antibacterial activities of these bile acid oligomers (CA/polyamines and DCA/polyamines) against S. aureus become stronger with increasing the amine group numbers of polyamines without obviously enhanced cytotoxicity and skin irritation. DCA/spermine, entirely composed of natural products, exhibits the best antibacterial activity but the lowest cytotoxicity and the weakest skin irritation. All CA/polyamines and DCA/polyamines form well-ordered ribbon-like aggregates, collecting numerous facial amphiphilic structures to significantly enhance the interactions with bacterial membranes. In particular, the biogenic polyamines with more than two amine groups provide extra positively charged sites, hence facilitating the binding of bile acid oligomers to the negatively charged outer membrane of the bacteria via electrostatic interaction. This in turn promotes more oligomeric bile acid units that can be inserted into the membrane through hydrophobic interaction between bile acids and lipid domains. The noncovalently constructed and separable amphiphilic antimicrobials can avoid the long-term coexistence of microorganisms and antibacterial molecules in different acting modes. Therefore, the noncovalent bile acid oligomers, especially those with higher oligomerization degrees, can be a potential approach to effectively enhance antibacterial activity, improve environmental friendliness, and reduce bacterial drug resistance.

Condensed Supramolecular Helices: The Twisted Sisters of DNA.

Condensation of DNA helices into hexagonally packed bundles and toroids represents an intriguing example of functional organization of biological macromolecules at the nanoscale. The condensation models are based on the unique polyelectrolyte features of DNA, however here we could reproduce a DNA-like condensation with supramolecular helices of small chiral molecules, thereby demonstrating that it is a more general phenomenon. We show that the bile salt sodium deoxycholate can form supramolecular helices upon interaction with oppositely charged polyelectrolytes of homopolymer or block copolymers. At higher order, a controlled hexagonal packing of the helices into DNA-like bundles and toroids could be accomplished. The results disclose unknown similarities between covalent and supramolecular non-covalent helical polyelectrolytes, which inspire visionary ideas of constructing supramolecular versions of biological macromolecules. As drug nanocarriers the polymer-bile salt superstructures would get advantage of a complex chirality at molecular and supramolecular levels, whose effect on the nanocarrier assisted drug efficiency is a still unexplored fascinating issue.

Block copolymers as bile salt sequestrants: intriguing structures formed in a mixture of an oppositely charged amphiphilic block copolymer and bile salt.

To study the formation and characterize the structure of mixed complexes of oppositely charged block copolymers and surfactants are of great significance for practical applications, e.g., in drug carrier formulations that are based on electrostatically assisted assembly. In this context, biocompatible block copolymers and biosurfactants (like bile salts) are particularly interesting. In this work, we report on the co-assembly in dilute aqueous solution between a cationic poly(N-isopropyl acryl amide) (PNIPAM) diblock copolymer and the oppositely charged bile salt surfactant sodium deoxycholate at ambient temperature. The cryogenic transmission electron microscopy (cryo-TEM) experiments revealed the co-existence of two types of co-assembled complexes of radically different morphology and inner structure. They are formed mainly as a result of the electrostatic attraction between the positively charged copolymer blocks and bile salt anions and highlight the potential of using linear amphiphilic block copolymers as bile salt sequestrants in the treatment of bile acid malabsorption and hypercholesterolemia. The first complex of globular morphology has a coacervate core of deoxycholate anions and charged copolymer blocks surrounded by a PNIPAM corona. The second complex has an intriguing tape-like supramolecular morphology of several micrometer in length that is striped in the direction of the long axis. A model is presented in which the stretched cationic blocks of several block copolymers interact electrostatically with the bile salt molecules that are associated to form a zipper-like structure. The tape is covered on both sides by the PNIPAM chains that stabilize the overall complex in solution. In addition to cryo-TEM, the mixed system was investigated in a range of molar charge fractions at a constant copolymer concentration by static light scattering, small angle X-ray scattering, and electrophoretic mobility measurements.

One-Step Synthesis of Hydrophobic Multicompartment Organosilica Microspheres with Highly Interconnected Macro-mesopores for the Stabilization of Liquid Marbles with Excellent Catalysis.

The combination of an emulsion template with polymerization is a very convenient approach to the one-step realization of both simple control porous structures via a change in emulsion formulation and easy functionalization via the concomitant choice of an on-demand monomer. A major challenge of this approach is the inherent instability of the oil/water interface in emulsions, especially the occurrence of chemical reactions in oil or aqueous phases. This study reports the pioneering preparation of highly interconnected macro-mesopores and multicompartment (HIMC) vinyl organosilica microspheres with hydrophobicity by the one-step formation of W/O/W emulsions acting as a template. The emulsion system consists of acidified deionized water, a stabilizer, and vinyltriethoxysilane (VTEO) in which VTEO can be used to produce an organosilica skeleton of the resultant microsphere by a sol-gel process. The study demonstrated that the marvelous stability of W/O/W emulsions aids the formation of multicompartment organosilica microspheres with highly interconnected macro-mesopores by emulsion droplets rather than single-compartment (SC) microspheres. Meanwhile, the internal porous structure and surface morphology of as-prepared organosilica microspheres could be largely tuned by a simple variation of the pH value, the volume fraction of the water phase, and the stabilizer concentration in the initiating multiemulsions. Benefiting from such a well-orchestrated structure and the existence of numerous vinyl groups on the surface, HIMC organosilica microspheres exhibit very high hydrophobicity (with a water contact angle larger than 160°), which allows them to stabilize liquid marbles with excellent stability and high mechanical robustness. Because of its strong catalyst, Ag nanoparticles within HIMC organosilica microspheres enable Ag/HIMC-vinyl organosilica microsphere-based liquid marbles to be an efficient catalytic microreactor, realizing the complete degradation of MB to leuco methylene blue by NaBH4 in 10 min. The result of this work could provide some guidance for the easy, low-cost, benign preparation of HIMC microspheres having the potential to be excellent supporter of metal nanoparticles or other functionalized compounds for applications in sensing, optoelectronics, and catalysis.

Smart magnetic ionic liquid-based Pickering emulsions stabilized by amphiphilic Fe3O4 nanoparticles: Highly efficient extraction systems for water purification.

This study presents the general method to formulate magnetically responsive ionic liquid (IL)-based Pickering emulsions that are stabilized by amphiphilic Fe3O4 nanoparticles. The magnetic nanoparticle stabilizer (MN-CHOL) was synthesized using the surface-initiated ATRP method with further modification that uses a specially designed cholesteryl derivative, and characterized by FT-IR, XPS, TGA, and magnetization measurements. It is confirmed that the resulting MN-CHOL shows a stronger interfacial activity, efficiently emulsifying C4mim [PF6] and water, and resultantly forming stable Pickering emulsions without the help of any co-surfactant. Due to its super paramagnetism and high saturation magnetization, MN-CHOL attached on the IL interface enables droplets of IL to be moved very conveniently on their target for as many times by an external magnetic field without demulsification, indicating high controllability and excellent stability. The resulting Pickering emulsion is a good extraction system that efficiently separates chlorobenzene, phenol, and methyl orange from aqueous solution. Subsequently, the simple magnetic separation was applied, to produce purified water due as a result of the rapid removal of organic pollutants from contaminated water.