Core@Satellite Janus Nanomotors with pH‐Responsive Multi‐phoretic Propulsion

We report core@satellite Janus mesoporous silica‐Pt@Au (JMPA) nanomotors with pH‐responsive multi‐phoretic propulsion. The JMPA nanomotors first undergo self‐diffusiophoretic propulsion in 3.0 % H₂O₂ due to the isolation of the Au nanoparticles (AuNPs) from the PtNPs layer. Then the weak acidity of H₂O₂ can trigger the disassembly and reassembly of the AuNPs, resulting in the Janus distribution of large AuNPs aggregates. Such reconstruction of JMPA leads to the contact between PtNPs and AuNPs aggregates, thus changing the propulsion mechanism to self‐electrophoresis. The asymmetric and aggregated AuNPs also enable the generation of a thermal gradient under laser irradiation, which propels the JMPA nanomotors by self‐thermophoresis. Such multi‐phoretic propulsion offers considerable promise for developing advanced nanomachines with a stimuli‐responsive switch of propulsion modes in biomedical applications.     

Photoactivated Polymersome Nanomotors: Traversing Biological Barriers

Synthetic nanomotors are appealing delivery vehicles for the dynamic transport of functional cargo. Their translation toward biological applications is limited owing to the use of non‐degradable components. Furthermore, size has been an impediment owing to the importance of achieving nanoscale (ca. 100 nm) dimensions, as opposed to microscale examples that are prevalent. Herein, we present a hybrid nanomotor that can be activated by near‐infrared (NIR)‐irradiation for the triggered delivery of internal cargo and facilitated transport of external agents to the cell. Utilizing biodegradable poly(ethylene glycol)‐b‐poly(d,l ‐lactide) (PEG‐PDLLA) block copolymers, with the two blocks connected via a pH sensitive imine bond, we generate nanoscopic polymersomes that are then modified with a hemispherical gold nanocoat. This Janus morphology allows such hybrid polymersomes to undergoing photothermal motility in response to thermal gradients generated by plasmonic absorbance of NIR irradiation, with velocities ranging up to 6.2±1.10 μm s^?1. These polymersome nanomotors (PNMs) are capable of traversing cellular membranes allowing intracellular delivery of molecular and macromolecular cargo.     

Chemically Powered Micro‐ and Nanomotors

Chemically powered micro‐ and nanomotors are small devices that are self‐propelled by catalytic reactions in fluids. Taking inspiration from biomotors, scientists are aiming to find the best architecture for self‐propulsion, understand the mechanisms of motion, and develop accurate control over the motion. Remotely guided nanomotors can transport cargo to desired targets, drill into biomaterials, sense their environment, mix or pump fluids, and clean polluted water. This Review summarizes the major advances in the growing field of catalytic nanomotors, which started ten years ago.     

Systematic Research and Evaluation Models of Nanomotors for Cancer Combined Therapy

Limited tumor permeability of therapeutic agents is a great challenge faced by current cancer therapy methods. Herein, a kind of near infrared light (NIR)‐driven nanomotor with autonomous movement, targeted ability, hierarchical porous structure, multi‐drugs for cancer chemo/photothermal therapy is designed, prepared and characterized. Further, we establish a method to study the interaction between nanomotors and cells, along with their tumor permeability mechanism, including 2D cellular models, 3D multicellular tumor spheroids and in vivo models. In vivo tumor elimination results verify that the movement behaviour of the nanomotors can greatly facilitate them to eliminate tumor through multiple therapeutic methods. This work tries to establish systematic research and evaluation models, providing strategies to understand the relationship between motion behaviour and tumor permeation efficiency of nanomotors in depth.     

Noncontinuous Super‐Diffusive Dynamics of a Light‐Activated Nanobottle Motor

We report a carbonaceous nanobottle (CNB) motor for near infrared (NIR) light‐driven jet propulsion. The bottle structure of the CNB motor is fabricated by soft‐template‐based polymerization. Upon illumination with NIR light, the photothermal effect of the CNB motor carbon shell causes a rapid increase in the temperature of the water inside the nanobottle and thus the ejection of the heated fluid from the open neck, which propels the CNB motor. The occurrence of an explosion, the on/off motion, and the swing behavior of the CNB motor can be modulated by adjusting the NIR light source. Moreover, we simulated the physical field distribution (temperature, fluid velocity, and pressure) of the CNB motor to demonstrate the mechanism of NIR light‐driven jet propulsion. This NIR light‐powered CNB motor exhibits fuel‐free propulsion and control of the swimming velocity by external light and has great potential for future biomedical applications.     

Self‐Guided Supramolecular Cargo‐Loaded Nanomotors with Chemotactic Behavior towards Cells

Delivery vehicles that are able to actively seek and precisely locate targeted tissues using concentration gradients of signaling molecules have hardly been explored. The directed movement toward specific cell types of cargo‐loaded polymeric nanomotors along a hydrogen peroxide concentration gradient (chemotaxis) is reported. Through self‐assembly, bowl‐shaped poly(ethylene glycol)‐b‐polystyrene nanomotors, or stomatocytes, were formed with platinum nanoparticles entrapped in the cavity while a model drug was encapsulated in the inner compartment. Directional movement of the stomatocytes in the presence of a fuel gradient (chemotaxis) was first demonstrated in both static and dynamic systems using glass channels and a microfluidic flow. The highly efficient response of these motors was subsequently shown by their directional and autonomous movement towards hydrogen peroxide secreting neutrophil cells.     

Biocompatible and pH-Responsive Colloidal Surfactants with Tunable Shape for Controlled Interfacial Curvature

Molecular-surfactant-stabilized emulsions are susceptible to coalescence and Ostwald ripening. Amphiphilic particles, which have a much stronger anchoring strength at the interface, could effectively alleviate these problems to form stable Pickering emulsions. Herein, we describe a versatile method to fabricate biocompatible amphiphilic dimer particles through controlled coprecipitation and phase separation. The dimer particles consist of a hydrophobic PLA bulb and a hydrophilic shellac–PEG bulb, thus resembling nonionic molecular surfactants. The size and diameter ratio of the dimer particles are readily tunable, providing flexible control over the water/oil interfacial curvature and thus the type of emulsion. The particle-stabilized emulsions were stable for a long period of time and could be destabilized through a pH-triggered response. The biocompatible amphiphilic dimer particles with tunable morphology and functionality are thus ideal colloidal surfactants for various applications.     

Self‐Propelled Janus Mesoporous Silica Nanomotors with Sub‐100 nm Diameters for Drug Encapsulation and Delivery

The synthesis of an innovative self‐propelled Janus nanomotor with a diameter of about 75 nm that can be used as a drug carrier is described. The Janus nanomotor is based on mesoporous silica nanoparticles (MSNs) with chromium/platinum metallic caps and propelled by decomposing hydrogen peroxide to generate oxygen as a driving force with speeds up to 20.2 μm s^?1 (about 267 body lengths per second). The diffusion coefficient (D) of nanomotors with different H₂O₂ concentrations is calculated by tracking the movement of individual particles recorded by means of a self‐assembled fluorescence microscope and is significantly larger than free Brownian motion. The traction of a single Janus MSN nanomotor is estimated to be about 13.47×10^?15 N. Finally, intracellular localization and drug release in vitro shows that the amount of Janus MSN nanomotors entering the cells is more than MSNs with same culture time and particle concentrations, meanwhile anticancer drug doxorubicin hydrochloride loaded in Janus MSNs can be slowly released by biodegradation of lipid bilayers in cells.     

pH-Responsive Phase Transition of Supramolecular Hydrogel Consisting of Glycosylated Amino Acetate and Carboxylic Acid Derivative

By addition of a carboxylated amino acetate (2) to a low-molecular-weight hydrogel (1) which has a unique thermally induced volume-phase transition character, a macroscopic pH-responsive feature is newly conferred on the supramolecular hydrogel. The direct observation of temperature-dependent behavior of the mixed hydrogel clearly showed that the thermally induced swelling-shrinkage type of the volume phase transition at pH 4 is shifted to the gel–sol transition at pH 7 by 10?mol% addition of 2 to the hydrogel 1. On the basis of the measurements by TEM, SEM, XRD and FT-IR, it is conceivable that incorporation of the anionic carboxylate of 2 slightly disturbs the packing of the hydrogen bond belt of the mixed hydrogel. Such a slight disturbance greatly leads to the sol–gel transition by elevating temperature, instead of the volume-phase transition. Introduction of dynamic characteristics to supramolecular systems in a macroscopic level may extend the potential of these materials in various fields.     

pH-Responsive shrinkage/swelling of a supramolecular hydrogel composed of two small amphiphilic molecules

A pH-responsive volume-change function was successfully introduced into a supramolecular hydrogel that contained GalNAc-appended (GalNAc=N-acetylgalactosamine) glutamate ester 1 by the simple mixing of it with an appropriate amount of 2 a or 2 b amphiphilic carboxylic acid. In the 1:1 mixture (1:2), the hydrogel swelled under neutral pH conditions, but shrank to almost half of its original volume under acidic pH conditions. The structure and pH response of the mixed hydrogel were characterized by using X-ray diffraction (XRD), confocal laser scanning microscopy (CLSM), transmission or scanning electron microscopy (TEM, SEM), and Fourier transform IR (FTIR) spectroscopy. Well-developed fibers formed a stable hydrogel by self-assembly, and under acidic conditions the charge of the carboxylic acid terminal (from the carboxylate anion) was neutralized and then these fibers became densely packed. This macroscopic pH response was also applied to the pH-triggered release of bioactive substances. In this mixed supramolecular hydrogel, the hydrogelator 1 provides a stable hydrogel structure and the additive 2 acts as a commander that is sensitive to an environmental pH signal. The present supramolecular copolymerization strategy should be useful for the construction of novel, stimuli-responsive, soft materials.     

光响应Janus粒子体系的构建与应用

Janus粒子通常由两种或两种以上不同物理或化学性质的部分组成,其结构的不对称性导致了粒子形貌和性质具有不对称性。与“静态”Janus粒子相比,具有刺激响应性的“动态”Janus粒子能够与环境发生相互作用,在外界刺激下表达特殊功能。光响应Janus粒子是一类可以在光刺激下发生特定响应的Janus粒子,其两侧不同的组成不仅可以结合多种类型的光响应性,也能与其他类型的刺激响应进行配合,从而实现对特定体系的精确调控。由于光能易于调节的特性,光响应Janus粒子可以与无机纳米团簇或有机官能团产生特定反应,具有光热效应、色彩调节、光动力治疗等独特特性。它们还可以应用于药物递送、生物传感与成像、微纳米马达和光致发光等领域,为解决生物医学和光学器件相关的问题提供了新的方法。本文主要介绍光响应Janus粒子近期发展的制备方法,并着重阐述其独特调控机理以及其在生物医药、发光材料等领域的突出应用,最后对目前该领域的发展前景做出展望。     

Harvesting Light To Produce Heat: Photothermal Nanoparticles for Technological Applications and Biomedical Devices

The photothermal properties of nanoparticles (NPs), that is, their ability to convert absorbed light into heat, have been studied since the end of the last century, mainly on gold NPs. In the new millennium, these studies have developed into a burst of research dedicated to the photothermal ablation of tumors. However, beside this strictly medical theme, research has also flourished in the connected areas of photothermal antibacterial surface coatings, gels and polymers, of photothermal surfaces for cell stimulation, as well as in purely technological areas that do not involve medical biotechnology. These include the direct conversion of solar light into heat, a more efficient sun-powered generation of steam and the use of inkjet-printed patterns of photothermal NPs for anticounterfeit printing based on temperature reading, to cite but a few. After an analysis of the photothermal effect (PTE) and its mechanism, this minireview briefly considers the antitumor-therapy theme and takes an in-depth look at all the other technological and biomedical applications of the PTE, paying particular attention to photothermal materials whose NPs have joined those based on Au.     

Template‐Free Synthesis and Selective Filling of Janus Nanocups

We report on the formation of shape‐ and surface‐anisotropic Janus nanocups (JNCs) by evaporation‐induced confinement assembly (EICA) of ABC triblock terpolymers. During microphase separation in spherical confinement, the triblock terpolymer spontaneously adopted a hemispherical shape with an inner concentric lamella–lamella (ll) morphology. Cross‐linking and disassembly of the microparticles resulted in well‐defined JNCs with different chemistry on the inside and outside. By synthesizing polymers with increasing length of the cross‐linkable block, we tuned the mechanical stability of the nanocups, which is relevant to control opening and closing of the cup cavity. We utilize the Janus properties for selective uptake of cargo exemplified by the filling of JNCs with polymer or gold nanoparticles. The directional properties of JNCs suggest applications in locomotion, oil‐spill recovery, storage and release, templating, and as nanoreactors with attoliter volume.     

Superparamagnetic Nanoparticles with Efficient Near-Infrared Photothermal Effect at the Second Biological Window

Superparamagnetic nanoparticles (iron oxide nanoparticles—IONs) are suitable for hyperthermia after irradiating with radiofrequency radiation. Concerning the suitability for laser ablation, IONs present a low molar absorption coefficient in the near-infrared region close to 800 nm. For this reason, they are combined with other photothermal agents into a hybrid composite. Here, we show that IONs absorb and convert into heat the infrared radiation characteristic of the so-called second-biological window (1000–1350 nm) and, in consequence, they can be used for thermal ablation in such wavelengths. To the known excellent water solubility, colloidal stability and biocompatibility exhibited by IONs, an outstanding photothermal performance must be added. For instance, a temperature increase of 36 °C was obtained after irradiating at 8.7 W cm⁻² for 10 min a suspension of IONs at iron concentration of 255 mg L⁻¹. The photothermal conversion efficiency was ~72%. Furthermore, IONs showed high thermogenic stability during the whole process of heating/cooling. To sum up, while the use of IONs in the first bio-window (700–950 nm) presents some concerns, they appear to be good photothermal agents in the second biological window.     

Magnetic-controllable Janus fibrous membranes with wind-resistant floatability for airflow-enhanced solar evaporation

Interfacial solar evaporation has been widely regarded as a promising pathway to desalinate seawater without secondary pollution and additional carbon emission. However, one of the challenges rarely considered is the floating stability and remote controllability of the evaporator in the face of wind and waves at the seawater surface. Herein, we demonstrate magnetic Janus membranes (MJMs) with remotely magnetic controllability and wind-resistant floatation for enhanced interfacial solar evaporation in airflow condition. These membranes are fabricated by sequential electrospinning of a hydrophobic Fe₃O₄-embedded polyvinylidene fluoride (PVDF) layer and a hydrophilic polyacrylonitrile (PAN) layer. Due to the superparamagnetism of Fe₃O₄, our MJMs can be remotely manipulated by a magnet and can float in situ with the aid of a magnetic field, even facing the blast of airflow with a speed of 1.75 m/s. Moreover, the MJMs realize an enhanced vapor diffusion under airflow (v = 0.5 m/s) and show a water evaporation rate of 1.39 ± 0.06 kg∙m⁻²∙h⁻¹ under one sun, which is 40.4% higher than that in windless condition. This work provides a promising material solution with magnetic design for the practical offshore application of Janus membranes in interfacial solar evaporation.