Mussel-Inspired Antimicrobial and Antifouling Coating Constructed by the Combination of Zwitterionic Copolymers and Silver Nanoparticles.

Biofouling and bacterial infections are significant challenges in biomedical devices. In this study, a biocompatible dual-functional coating with antimicrobial and antifouling properties is developed by co-depositing the zwitterionic copolymer and silver nanoparticles via a dopamine-assisted strategy. Inspired by mussel adhesion, the coating exhibits substrate-independent adhesion as a result of the formation of irreversible covalent bonds. The zwitterionic copolymer in the dual coating plays a crucial role in improving surface wettability and reducing protein adsorption and platelet and bacterial adhesion, thereby improving its antifouling property significantly. The silver nanoparticles reduced by self-polymerized polydopamine without the addition of any chemical reductants can effectively improve the antimicrobial activity. Furthermore, as the zwitterion content in the zwitterion polymer increases, the antibacterial and antifouling properties of the coating can be further advanced. The simple and effective approach presented here provides a promising pathway for constructing potent antibacterial and antifouling surfaces, demonstrating great potential for clinical applications in implanted materials.

Controlling high-speed droplet splashing and superspreading behavior on anisotropic superhydrophobic leaf surfaces by ecofriendly Pseudogemini surfactants.

BACKGROUND: Efficient deposition of high-speed droplets on superhydrophobic leaf surfaces remains an important challenge. For anisotropic wired superhydrophobic leaf surfaces, the splashing phenomenon is especially serious because it leads to the low effective utilization of pesticides by biological targets. The lost pesticides cause serious ecological environment pollution, therefore there is an urgent need to develop a green and sustainable cost-effective strategy to achieve efficient deposition of high-speed droplets on anisotropic superhydrophobic leaf surfaces at low dosage. RESULTS: One type of green pseudogemini surfactant is constructed based on fatty acids and hexamethylenediamine by electrostatic interaction to control the splashing and spreading of high-speed droplets on superhydrophobic surfaces. The formed surfactant can not only achieve complete inhibition of the bouncing of droplets, but also promote rapid spreading on superhydrophobic leaf surfaces at very low usage. The efficient deposition and superspreading phenomenon are attributed to the rapid migration and adsorption of the surfactant from the dynamic spherical micelles at the newly formed solid-liquid interface, the network-like aggregated spherical micelles, and the Marangoni effect caused by the surface tension gradient. Moreover, the surfactant shows an excellent synergistic effect with herbicides to control weeds by inhibiting droplet splashing. CONCLUSION: This work provides a simpler, more effective and sustainable approach to utilize aggregated spherical micelles rather than conventional vesicles or wormlike micelles to improve the droplet deposition on superhydrophobic leaf surfaces and reduce the impact of surfactants and pesticides on the ecological environment. © 2023 Society of Chemical Industry.

Recent Advances of Organ-on-a-Chip in Cancer Modeling Research.

Although many studies have focused on oncology and therapeutics in cancer, cancer remains one of the leading causes of death worldwide. Due to the unclear molecular mechanism and complex in vivo microenvironment of tumors, it is challenging to reveal the nature of cancer and develop effective therapeutics. Therefore, the development of new methods to explore the role of heterogeneous TME in individual patients' cancer drug response is urgently needed and critical for the effective therapeutic management of cancer. The organ-on-chip (OoC) platform, which integrates the technology of 3D cell culture, tissue engineering, and microfluidics, is emerging as a new method to simulate the critical structures of the in vivo tumor microenvironment and functional characteristics. It overcomes the failure of traditional 2D/3D cell culture models and preclinical animal models to completely replicate the complex TME of human tumors. As a brand-new technology, OoC is of great significance for the realization of personalized treatment and the development of new drugs. This review discusses the recent advances of OoC in cancer biology studies. It focuses on the design principles of OoC devices and associated applications in cancer modeling. The challenges for the future development of this field are also summarized in this review. This review displays the broad applications of OoC technique and has reference value for oncology development.

Electroinduced Reconfiguration of Complex Emulsions for Fabrication of Polymer Particles with Tunable Morphology.

Continuous morphological control of anisotropic particles is always an important challenge in the field of materials. In this study, a new strategy for continuous fabrication of polymer particles with various morphologies induced by electricity is reported using complex emulsions as template. A synthetic electro-responsive surfactant containing ferrocene group is used to prepare complex emulsions, which contain a polymerizable monomer as inner phase. With the increasing time of electrical stimulation on the complex emulsions, hollow, hemispherical, mushroom-like, and spherical particles are constructed successively after photopolymerization. The Marangoni effect caused by the heterogeneity in the interfacial tension at the droplet surface is the reason for the reconfigurable morphology of the complex emulsion. The controllable complex emulsions by electricity present a versatile platform for constructing fine control of the microstructure and shape anisotropy of particles having customized shapes and functionalities, opening a new possibility for designing sophisticated architectures.

pH-Responsive Pickering emulsions stabilized solely by surface-inactive nanoparticles via an unconventional stabilization mechanism.

Using solely highly hydrophilic particles to stabilize emulsions, especially high internal phase emulsions, has always been an important challenge. Here pH-responsive Pickering emulsions stabilized by a low concentration of bare highly hydrophilic Ludox CL nanoparticles without surface modification or addition of surfactants are developed at neutral pH. The dispersed nanoparticles can be transformed into an aggregate state with a network-like structure near the isoelectric point, which contributes to the stabilization of the emulsions. Moreover, the vdW attraction between particles and droplets also plays a key role in the formation of emulsions, which can make the aggregated nanoparticles adsorb tightly around the droplets rather than penetrate the oil-water interface. The formed protective armor and network-like aggregates separate droplets from each other to prevent coalescence. At a low nanoparticle concentration (0.5 wt%), a high internal phase emulsion can be formed and can last up to half a year. This system can emulsify not only the hydrocarbon oil but also the fluoroalkane oil phase. Finally, organic-inorganic composite particles are fabricated using the template action of the Pickering emulsions. The method of preparing composite particles is more convenient than the traditional Pickering emulsion polymerization which often requires the modification of the surface of the hydrophilic particles or the addition of auxiliary monomers. This study provides a simple green strategy for the preparation of a more stable Pickering emulsion stabilized by surface-inactive nanoparticles and will broaden the scope of applications.

Photoinduced Reconfiguration of Complex Emulsions Using a Photoresponsive Surfactant.

Photoresponsive complex emulsions are prepared in a three-phase system consisting of two oils: hexane (H) and perfluorooctane (F). An aqueous solution of a mixed surfactant of fluorosurfactant, F(CF2) x(CH2CH2O) yH (Zonyl FS-300), and a synthesized light-responsive surfactant, 2-(4-(4-butylphenyl)diazenylphenoxy)ethyltrimethylammonium bromide (C4AZOC2TAB) was employed as the continuous phase. Complex emulsions with various geometries were prepared by one-step vortex mixing and a temperature-induced phase-separation method. It was noticed that the topology of the complex emulsion was highly dependent on the mass ratio of Zonyl FS-300/C4AZOC2TAB. Light microscopy images showed that phase inversion from an H/F/W- to an F/H/W-type double emulsion via a Janus emulsion was achieved by gradually increasing the mass ratio of C4AZOC2TAB/Zonyl FS-300. Upon UV/blue light irradiation, the topology of complex emulsions was turned to switch from an F/H/W double emulsion to a Janus emulsion to an entirely inverted H/F/W double emulsion. Dynamic interfacial tension measurements showed that UV irradiation of the interface between an aqueous trans-C4AZOC2TAB solution and hexane brings about an increase in the interfacial tension, suggesting the nature of photoinduced morphological changes in complex emulsions. The reconfiguration process of complex emulsions was illustrated by the Marangoni effect based on heterogeneity in the interfacial tension at the complex emulsion surface induced by controlling the molecular conversion of C4AZOC2TAB using light irradiation. Finally, we used the complex emulsions structure to form an on-off switch to start and shut off the evaporation of one volatile phase to achieve process monitoring. This could be used to initiate and quench a reaction, which offers a novel idea for achieving switchable and reversible reaction control in multiple-phase reactions.

Light-responsive multillamellar vesicles in coumaric acid/alkyldimethylamine oxide binary systems: Effects of surfactant and hydrotrope structures.

Herein, we report a series of novel light-responsive multilamellar vesicles based on the surfactant/hydrotrope binary systems. The phase behaviors of alkyldimethylamine oxide (CmDMAO, m=10, 12, 14) and trans-coumaric acid (trans-CA) isomerides, including trans-ortho-coumaric acid (trans-OCA), trans-meta-coumaric acid (trans-MCA) and trans-para-coumaric acid (trans-PCA), show that the multilamellar vesicle (MLV) formation region is commonly presented in the trans-CA/CmDMAO systems except trans-PCA/C12DMAO. Moreover, the molecular structures of CmDMAO and trans-CA affect the multilamellar vesicle formation region significantly. Generally speaking, the bigger the m, the larger the MLV region. Various techniques such as rheology, polarized optical microscopy (POM), (1)H NMR, (2)H NMR, cryogen transmission electron microscopy (cryo-TEM) and freeze-fracture transmission electron microscopy (FF-TEM) are used to characterize the aggregate structures. The multilamellar vesicles can transform into a homogeneous and transparent micelle phase or a two-phase system in the trans-OCA/CmDMAO binary systems under UV light irradiation, which depends on the chain length of CmDMAO and the molar ratio of [trans-OCA]/[CmDMAO]. Specifically, the light-stimuli response of multilamellar vesicles in the trans-OCA/C12DMAO system is representatively studied in detail. UV-vis spectra and (1)H NMR measurements illustrate that the light-induced trans-OCA to cis-OCA isomerization is essential during the transitions and the light-induced two-phase formation is attributed to the enrichment of surfactants, because the trans-cis isomerization can not only strengthen the hydrophilicity of cis-OCA but also increase the steric hindrance between cis-OCA and C12DMAO, and thereby altering the morphology of aggregate and the rheological response of bulk phase significantly.

Multiple Responsive Fluids Based on Vesicle to Wormlike Micelle Transitions by Single-Tailed Pyrrolidone Surfactants.

We report a new family of multiple responsive fluids based on the single-tailed pyrrolidone surfactants, N-ethyl-2-pyrrolidone N-alkyl amine (C(m)NP, where m = 10, 12, 14, 16, and 18). These surfactants are highly sensitive to solution pH as a result of the presence of the N-amino group in the molecules. Equilibrium surface tension results indicate that both the surface activity and micellization ability of C(m)NPs decrease with the increase of the protonation degree; i.e., they exhibit a higher critical micelle concentration (cmc) and higher surface tension at the cmc (γ(cmc)) at the acidic conditions than those at the basic conditions. The cmc values of C(m)NPs follow the well-known Klevens equation, which decrease linearly with the increase of the hydrocarbon chain length m at a given pH. More importantly, the self-assemblies of C(m)NPs are highly sensitive to pH, CO2, and CuCl2, as identified by turbidity and viscosity. The transitions between vesicles and wormlike micelles are further confirmed by rheology, static and dynamic light scattering (SLS and DLS), cryogenic transmission electron microscopy (cryo-TEM), and nuclear magnetic resonance (NMR) techniques systematically. Although the aggregate transitions induced by different factors are similar, however, the mechanisms are different. The pH- and CO2-induced transitions are attributed to variation in the protonation degree of the N-amino group; however, CuCl2-induced transitions are a result of the formation of C(m)NP and CuCl2 coordination complexes as revealed by two-dimensional (2D) nuclear Overhauser effect spectrometry (NOESY) NMR and ultraviolet-visible (UV-vis) spectra.