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Significant progress in fabricating new multifunctional soft materials and the advances of additive manufacturing technologies have given birth to a new generation of soft robots with complex capabilities, such as crawling, swimming, jumping, gripping, and releasing. Within this vast array of responsive soft materials, hydrogels receive considerable attention due to their fascinating properties, including biodegradable, self-healing, stimuli-responsive, and large volume transformation. Konjac glucomannan (KGM) is an edible polysaccharide that forms a pH-responsive, self-healing hydrogel when crosslinked with borax, and it is the focus of this study. A novel KGM-Borax ink for three-dimensional (3D) printing of free-form structures and soft robots at room temperature is presented. A complete process from ink preparation to the fabrication of a completely cross-linked part is demonstrated. Print setting parameters, rheological properties of the ink and crosslinked gels were characterized. Print quality was found to be consistent across a wide range of print settings. The minimum line width achieved is 650 μm. Tensile testing was carried out to validate the self-healing capability of the KGM-Borax gel. Results show that KGM-Borax has a high self-healing efficiency of 98%. Self-healing underwater was also demonstrated, a rarity for crosslinked gels. The means to form complex structures via 3D printing, reacting to environmental stimuli and the resilience against damage, make this new KGM-Borax gel a promising candidate for the fabrication of the next generation of soft robots.

Programmable materials have artificially designed physical shapes responding to external stimuli, as well as high design capability and high flexibility. Here, we propose a microfiber-shaped programmable material with an axial pattern of stimuli-responsive (SR) and nonresponsive hydrogels. The SR pre-gel solution was mixed to sodium alginate pre-gel solution for instantaneous gelation with ionic crosslinking and solidified on a nonresponsive hydrogel microfiber with a valve-controlled microfluidic system. A design of microfiber-shaped programmable material (patterned position of SR regions) could be flexibly altered by changing a coded sequence program. We confirmed that the three-dimensional (3D) coil-like structures were self-folded at the patterned SR regions responding to the thermal stimulus and that the chirality of the self-folded 3D coil-like structures depends on the condition of the stimulus to the microfiber. Finally, interaction with objects using the programmable microfiber as a soft actuator was demonstrated. Our microfiber-shaped programmable materials expand possibilities of fiber-based materials in biomimetics and soft robotics fields.

Responsive emulsions are the emulsions that can be reversibly switched on-demand between “stable” and “unstable” by environmental stimulus or trigger, which allows a simple and effective adjustment approach to achieve emulsification and demulsification. In recent years, stimuli-responsive emulsions acting as smart soft material are received considerable attention with the advantages of simple manipulation, good reversibility, low cost, easy treatment, and little effect on the system. In this paper, the recent research progress of emulsions that can respond to external stimuli, including pH, light, magnetic field, CO2/N2 and dual responsive are reviewed. Also, the potential applications based on responsive emulsion are discussed, such as catalytic reactions, heavy oil recovery, polymer particles synthesis and optical sensor, aiming to summarize the latest achievements and put forward the possible development trends of responsive emulsions.

The hybridization of mechanically responsive molecular crystals with polymers has proven to be an efficient approach to fabricate smart hybrid materials that can produce multiple motions upon exter...

A judicious strategy was utilized to envision the substantial regio-positional effects of substituents on the photophysical properties of the 2H-chromen-2-one-3-benzothiazole scaffold-based push-pull framework, named 6-X-CUMs. Among them, 6-NEt2-CUM reveals prominent excited-state intramolecular charge transfer with a large change of dipole moment (Δμ ∼ 18.23 D), hence displaying remarkable emission solvatochromism from the green (536 nm in cyclohexane) to far-red region (714 nm in dimethyl sulfoxide) and a high-temperature sensitivity (-0.23 nm °C-1). These, together with unique basicity and acido-/vaporchromism upon acidification elucidated by NMR and photospectroscopic studies, show stark contrast to the conventional 7-NEt2-CUM. The new series of these tailored 6-X-CUMs represents a new dimension in tailoring the photophysical properties for the development of a promising class of multistimuli-responsive materials.

Circularly polarized luminescence (CPL) materials have potential applications in 3D optical displays, information security encryption, sensors, and photoelectric devices because of their inherent a...

Biomimetic membrane materials have been widely explored and developed for drug loading and tissue engineering applications due to their excellent biocompatibility and abundant reaction sites. However, novel cytomembrane mimics have been lacking for a long time. In this study, black phosphorus (BP) was used as the foundation for a new generation of promising cytomembrane mimics due to its multiple similarities to cytomembranes. Inspired by the dual function of endotoxins on membranes, we prepared a BP-based cytomembrane mimic with controllable antibacterial ability via electrostatic interaction between BP and [1-pentyl-1-quaternary ammonium-3-vinyl-imidazole]Br ([PQVI]Br). The release of PQVI could be manipulated in different conditions by adjusting the electrostatic force, thereby achieving controllable antibacterial ability. This report confirms the possibility of using BP as a new material to mimic cytomembranes and provides a new concept of controllable antibacterial action based on endotoxins.

Stimuli-responsive fibers are highly desirable for their potential applications in areas such as anti-counterfeiting, optical memory systems, colorimetric sensing, and bioimaging sensors. An iridescent luminescent fibers that can achieve multi-color with long afterglow and photochromic properties is always required in color-on-demand applications. Here, a set of distinct three-primary colors luminescent fibers based on red-green-blue (RGB) system. Y2O2S:Eu3+, Mg2+, Ti4+ (red), SrAl2O4:Eu2+, Dy3+ (green), Sr2MgSi2O7: Eu2+, Dy3+ (blue) are successfully synthesized. Spiropyran and as-prepared luminescent materials are introduced into PAN fibers by a one-step extrusion wet-spinning process to achieve distinct three-primary colors luminescent photochromic fiber. These as-prepared fibers emit bright lights under excitation of ultraviolet with long afterglow. These fibers exhibit outstanding tensile properties which allow knitting or weaving them into demonstrated functional designs for aesthetic designs and encryption/decryption protocols. Comparing with previous studied stimuli-responsive fibers, our research focus on distinct three-primary colors luminescent photochromic fibers present enormous potential in 3D printing, information encryption, and next generation smart fibers.

Electrospun nanofibrous membranes offer superior properties over other polymeric membranes not only due to their high membrane porosity but also due to their high surface-to-volume ratio. A plethor...

Liquid crystalline epoxy networks (LCENs) are a class of materials that combine the useful benefits of both liquid crystals and epoxy networks exhibiting fascinating thermal, mechanical, and stimuli-responsive properties. They have emerged as a new platform for developing functional materials suitable for various applications, such as sensors, actuators, smart coatings and adhesives, tunable optical systems, and soft robotics. This article provides an overview of LCENs and their composites as functional materials, including their synthesis and characterisation, focusing on structure-processing–property relationships. We provide objective analyses on how materials engineers can use these relationships to develop LCENs with desired functionalities for targeted applications. Emerging areas, including advanced manufacturing and multi-functional design of LCENs are covered to show the overall progress in this field. We also survey the forward-looking status of LCEN research in designing novel materials for future technologies.

Nano- and microgels are promising soft polymer materials for different application fields: stabilizers, sensors, catalysts, selective sorbents, drug delivery carriers etc. They are composed of cross-linked polymer chains swollen with a solvent. The building blocks, synthesis approaches and architecture of nano- and microgels are reviewed. The mechanisms of responsiveness to various stimuli are described, examples of applications are provided. Micro- and nanogels are good objects for learning projects and the ideas for learning projects with microgels are described.

Background: Development of controlled drug delivery systems can improve the pharmacokinetic characteristics of drug molecules in the human body, thereby significantly improving the utilization rate of drugs and reducing toxicity and side effects caused by their high concentrations, which can occur when delivery is not controlled. Metal organic frameworks are a new class of very promising crystalline microporous materials, especially when the size is reduced to the nanometer range. Metal-organic frameworks exhibit large specific surface areas, tunable compositions, and easy functionalization. In recent years, an increasing number of studies have reported the remarkable advances in multifunctional nanoscale metal-organic frameworks in drug delivery. Objective: To review the latest research involving advances in stimuli-responsive nanoscale metal organic frameworks as drug delivery systems in controlled-release drugs. Discussion: We first introduce the two main strategies associated with nanoscale metal organic frameworks used in drug loading: direct assembly and post-encapsulation. We next focus on the latest discoveries of nanoscale metal-organic framework-based stimulus response systems for drug delivery, including pH, magnetics, light, ion, temperature, and other stimuli, as well as multiple stimulus- responsive drug delivery systems. Finally, we discuss the challenges and future developmental directions of nanoscale metal-organic framework-based controlled drug release.

Soft photonic materials formed from nanoscale colloidal crystals are versatile platforms for sensing and signaling in biomedical, chemical, and mechanical application scenarios. A particularly leve...

Inspired by the coloring mechanism of insects, we demonstrated the preparation of metallic luster materials by a combination of dye absorption and specular reflection from layered microcrystals. Me...

Development of smart switchable surfaces to solve the inevitable bacteria attachment and colonization has attracted much attention; however, it proves very challenging to achieve on-demand regeneration for noncontaminated surfaces. We herein report a smart, host-guest interaction-mediated photo/temperature dual-controlled antibacterial surface, topologically combining stimuli-responsive polymers with nanobactericide. From the point of view of long-chain polymer design, the peculiar hydration layer generated by hydrophilic poly(2-hydroxyethyl methacrylate) (polyHEMA) segments severs the route of initial bacterial attachment and subsequent proliferation, while the synergistic effect on chain conformation transformation poly(N-isopropylacrylamide) (polyNIPAM) and guest complex dissociation azobenzene/cyclodextrin (Azo/CD) complex greatly promotes the on-demand bacterial release in response to the switch of temperature and UV light. Therefore, the resulting surface exhibits triple successive antimicrobial functions simultaneously: (i) resists ∼84.9% of initial bacterial attachment, (ii) kills ∼93.2% of inevitable bacteria attack, and (iii) releases over 94.9% of killed bacteria even after three cycles. The detailed results not only present a potential and promising strategy to develop renewable antibacterial surfaces with successive antimicrobial functions but also contribute a new antimicrobial platform to biomedical or surgical applications.

With the incessant improvement of requirements for optical anti-counterfeiting technology, it is essential to develop multifunctional luminescent materials with multiple models and adjustable lumin...

This study presents dual-responsive colloidal microgels to repair nonwoven fiber mats (NWFs) and recover their native morphological and functional properties. The formulation comprises poly(N-isopr...

Stimuli-responsive emulsifiers have emerged as a class of smart agents that can permit regulated stabilization and destabilization of emulsions, which is essential for food, cosmetic, pharmaceutical, and petroleum industries. Here, we report the synthesis of novel "smart" hydroxyapatite (HaP) magnetic nanoparticles and their corresponding stimuli-responsive Pickering emulsions and explore their movement under confined spaces using a microfluidic platform. Pickering emulsions prepared with our magnetic stearic acid-functionalized Fe2O3@HaP nanoparticles exhibited pronounced pH-responsive behavior. We observed that the diameter of emulsion droplets decreases with an increase in pH. Swift demulsification was achieved by lowering the pH, whereas the reformation of emulsions was achieved by increasing the pH; this emulsification-demulsification cycling was successful for at least ten cycles. We used a microfluidic platform to test the stability of the emulsions under flowing conditions and their response to a magnetic field. We observed that the emulsion stability was diminished and droplet coalescence was enhanced by the application of the magnetic field. The smart nanoparticles we developed and their HaP-based emulsions present promising materials for pharmaceutical and petroleum industries, where responsive emulsions with controlled stabilities are required.

Metal substrates beneath polymeric coatings are susceptible to localized corrosion, which could result in lifetime reduction and catastrophic failure without timely repair treatment. In situ detection of corrosion and repair coating defects are in high demand yet challenging to fulfill so far. Herein, we report a smart polymeric coating by integrating nanosensors into the coating matrix, which is capable of efficient corrosion sensing and active anticorrosion protecting. The nanosensors were constructed by zeolitic imidazolate framework encapsulated with the polyethylene glycol-tannic acid complex. The morphology, chemical constitution, and stimulus responsiveness of nanosensors were systematically analyzed. The generation of local corrosion beneath coating can be promptly sensed and reported by a conspicuous purple color derived from tannic-iron ion coordinates. Meanwhile, local electrochemical impedance spectroscopy results proved that the metal degradation process at the defected interface can be largely inhibited, exhibiting active anticorrosion property. Furthermore, the constructed smart coating possessed superior impermeability and long-term protective performance under simulated seawater and harsh salts spray conditions. This feasible and effective strategy based on simple nanosensors to engineer smart coatings paves a new way to develop high environmental adaptability protective materials with protecting, corrosion sensing, and self-healing functions.

Targeted release of drugs is important for precision treatment at the desired site and preventing the indiscriminate release of drugs. Incorporating stimuli-responsiveness into drug carriers has been proposed to enable the carriers to have the ability to perform targeted release at specific sites. However, a vast majority of the many established carriers are not stimuli-responsive. The current methods used for the synthesis of stimuli-responsive carriers are mostly highly specific and ineffective (e.g., they either leak or cannot release completely). This manuscript describes a novel class of stimuli-responsive attachments that can be attached flexibly onto any type of soft carrier (i.e., loaded with chemicals or drugs), thus transforming the non-responsive carrier into a stimuli-responsive carrier. The attachment consists of a layer of stimuli-responsive hydrogel around the carrier and a partial rigid coating on the exterior. The attachment is general: non-responsive carrier materials of different types (e.g., liposomes and polymeric carriers) and different sizes (e.g., nanoscale and macroscopic) are shown to become stimuli-responsive for different types of stimuli. Importantly, the attachment is capable of exerting a large pressure for rupturing carriers with rigid and impermeable shells (e.g., highly crosslinked shells). Hence, these carriers with stimuli-responsive attachment effectively exhibit a full range of stimuli-responsiveness: they are not leaky due to their rigid shells, but can release their contents completely via rupture of their shells under the influence of the stimulus. The approach of using this novel class of stimuli-responsive attachments is thus general, simple, and effective. The large number and diverse range of well-established soft non-responsive drug carriers can be transformed into stimuli-responsive carriers conveniently without the constant need to find specific methods for different types of carriers.

Stimuli-responsive crystals have aroused tremendous interest due to their potential as smart materials. However, endowing mono-component crystals with multiple stimuli-responsive and multifunction properties is still a great challenge. Here, we report an anthracene derivative, 9-anthraldehyde, which can respond to mechanical force and light. It possesses two-dimensional (2D) elastic bending, plastic twisting and photoinduced bending properties. Unusual elastic bending of the plastic twisted crystal was achieved in one crystal. The crystal obtained in this work is a multi-dimensional elastic crystal, which is different from reported twistable materials. To reveal the mechanisms of the properties of 2D elastic bending, plastic twisting and photoinduced bending, nanoindentation tests, energy framework analysis and Hirshfeld surface analysis were used to study the property–structure relationship at the molecular level. It was found that these properties can be ascribed to the unique intermolecular interactions and types of molecular arrangement.

Stimuli-responsive luminescent materials have received much attention as next-generation smart materials for various applications, including their use as biomedical probes, for the visualization of pollutants and sensing toxic gases. Boron-containing luminophores have been widely utilized to achieve such sensing materials because of their vacant 2pz orbital, which is responsible for their Lewis acidity, electron-accepting properties, and ability to form complexes. In addition, polymeric structures often enhance stimuli-responsivity because slight environmental changes around the molecules can dramatically affect their molecular motions, shapes and physical properties. This review describes the development of stimuli-responsive materials using various kinds of luminescent boron compounds, focusing on the mechanisms of the sensing abilities and the molecular designs.

Smart fibers with reversible optical properties have received extensive attention due to their wide potential for application in human health monitoring and wearable devices. However, achieving multi-stimuli-responsive luminescent fibers via a facile manufacturing process is challenging. Herein, novel independent multi-stimuli-responsive luminescent fibers are successfully fabricated via a facile wet-spinning process. The color of the fibers responds to ultraviolet (UV) and heat independently and in combination. The fibers emit bright red light emission (λem = 627 nm) after excitation (λex = 330 nm) which is attributed to Y2O2S:Eu3+,Mg2+,Ti4+ ceramics. The as-prepared fibers possess a tensile strength of around 9.39 MPa. The experimental results demonstrate that the multi-stimuli-responsive persistent luminescent fibers coupled with the facile preparation process make the multi-stimuli-responsive luminescent fibers a potential candidate for application in anti-counterfeiting and UV/heat detection devices.

Multifunctional nanocomposites have drawn great attention in clinical applications because of their ability to integrate diagnostic and therapeutic functions. Manganese dioxide (MnO2), owing to its biocompatibility and magnetic resonance imaging (MRI) properties, has been widely applied in biomedical research. Our previous work on biogenic MnO2 nanoparticles (Bio-MnO2 NPs) revealed that intrinsic photothermal properties and stimuli-responsive MRI imaging are particularly promising for the development of theranostic systems. However, further improvement in the photothermal therapy (PTT) performance of Bio-MnO2 NPs is still required. Herein, we have improved the PTT efficiency of Bio-MnO2 NPs by in situ synthesis of fluorescent polydopamine (PDA) while generating additional stimuli responsive fluorescence properties in this system, thus further broadening the scope of their theranostic functions. These synthesis conditions are mild and green. The fluorescence of PDA was quenched by capping Bio-MnO2 NPs and could be recovered upon degradation of Bio-MnO2 NPs inside tumour cells. Additionally, Mn2+ released from the nanoparticles can support T1-weighted MR imaging. Compared to the Bio-MnO2 NPs alone, the integration of Bio-MnO2 NPs and PDA significantly enhances the photothermal performance in vitro and in vivo. With their high biocompatibility, these multifunctional composite nanodevices hold great potential for fluorescence imaging and MRI-guided photothermal therapy.

A method for the synthesis of DNA-based acrylamide hydrogel microcapsules loaded with quantum dots as a readout signal is introduced. The shell of DNA-acrylamide hydrogel microcapsules is encoded with microRNA-responsive functionalities, being capable of the detection of cancer-associated microRNA. The microRNA-141 (miR-141), a potential biomarker in prostate cancer, was employed as a model target in the microcapsular biosensor. The sensing principle of the microcapsular biosensor is based on the competitive sequence displacement of target miR-141 with the bridging DNA in the microcapsule's shell, leading to the unlocking of DNA-acrylamide hydrogel microcapsules and the release of the readout signal provided by fluorescent quantum dots. The readout signal is intensified as the concentration of miR-141 increases. While miR-141 was directly measured by DNA-acrylamide hydrogel microcapsules, the linear range for the detection of miR-141 is 2.5 to 50 μM and the limit of detection is 1.69 μM. To improve the sensitivity of the microcapsular biosensor for clinical needs, the isothermal strand displacement polymerization/nicking amplification machinery (SDP/NA) process was coupled to the DNA-acrylamide hydrogel microcapsule sensor for the microRNA detection. The linear range for the detection of miR-141 is improved to the range of 102 to 105 pM and the limit of detection is 44.9 pM. Compared to direct microcapsular biosensing, the detection limit for miR-141 by microcapsules coupled with strand-displacement amplification is enhanced by four orders of magnitude.

Gels prepared from low-molecular-weight gelators (LMWGs) represent versatile soft materials. Self-assembly of LMWGs forms nanofibers and above critical gelation concentrations, the entanglement of which leads to self-supporting gels. Owing to the dynamic properties of the self-assembly process, stimuli-responsive LMWGs have prospered in the last decade. In addition, incorporating multiple LMWGs into one system brings the opportunity to achieve sophisticated designs and functions. This review covers recent advances in the field of supramolecular gels, from stimuli-responsive gelators to multicomponent systems that are self-sorting and/or co-assembling.

Herein, we report the first example of two pure organic polymorphs with stimuli-responsive single/dual phosphorescence transformation. By analyzing the crystal structures and theoretical results, it could be understood that efficient intermolecular interactions could restrict the molecular movements and lock distinct molecular conformations, leading to different phosphorescence behaviors. Besides, single/dual phosphorescence could transform into each other by heating or under solvent vapor conditions. Considering such unique properties, logical sensors (AND gate and OR gate) were built by providing different emission colors as inputs. Our work provides not only important information for understanding the dual RTP mechanism but also unique stimuli-responsive pure organic phosphorescent materials to enrich material fields.

The vinyl caprolactam (VCL) based microgel system has become the center of great attention due to its versatile properties. Copolymerization of VCL with an ionic monomer imparts pH responsive properties into the microgel system in addition to thermo-sensitivity. Stimuli responsive behavior of VCL-based microgels makes them prospective and appealing candidates for practical applications covering the fields of drug delivery, catalysis and optical devices. In the last few years, VCL-based microgels have been used as microreactors and stabilizers for the synthesis and stabilization of inorganic nanoparticles to obtain hybrid microgels. The present review article provides a summary of the present-day progress of fabrication, stabilization, categorization and analysis of VCL-based microgels and their hybrids with different morphologies. The stimuli responsive properties and applications of VCL-based hybrid microgels have been reviewed critically. The remaining problems which need to be addressed have been pointed out for further advancement in this field.

Graphene possesses a set of unique physicochemical properties including exceptional mechanical, thermal, and electrical properties, making it an excellent candidate for constructing materials for a wide range of applications including the vast field of separation technology using membranes. Separation membranes based on graphene and its derivatives have shown satisfactory results over the years when applied to environmental systems such as wastewater treatment and gas purification, which is a great contribution in sustainable development. However, membrane separation research is generally performed using conventional membranes with fixed driving force and separation properties that suffer from fouling and decline in performance upon long-term use or when a change in the environmental conditions occur. These issues can be solved by employing an emerging technology that makes use of graphene and its derivatives combined with polymeric materials to construct stimuli-responsive or “smart” membranes that respond to the changes in their environment such as chemical cues, temperature, pressure, and external fields, and have a self-regulated separation performance due to reversible physicochemical properties. In this review, we present a report on the recent advancements on graphene-based separation technology including a concise discussion on the basic structure and properties of graphene and its derivatives, various membrane fabrication methods, and their employment on the different areas of membrane separation. More importantly, the main focus of this paper is to evaluate the design and utilization of graphene-based smart separation membranes.

Responsive polymers with properties designed to interact with their surrounding environment are enabling “smart” design features for custom biomaterials. Numerous applications are being innovated, ranging from diagnostics and imaging to tissue engineering and drug delivery. Herein, I feature a collection of research articles published in ACS Macro Letters that highlight an array of innovative chemical attributes such as pH-triggered hydrolytic degradation, reduction-based release, photomodulation, glucose responsiveness, thermal sensitivity, and membrane permeating peptides. The chemical, physical, mechanical, and morphological properties of polymeric structures can be custom tailored to enhance numerous features such as biological delivery, pharmaceutical potency and safety, disease diagnosis, and antigen/biomaker detection.

Herein, we report the synthesis and application of a smart polymeric acrylic syntan (synthetic tanning material), which can respond to temperature and pH. Behavior of polymer at different pH (1-10) at room temperature (28°C) was studied. Also interactions with collagen were ascertained in order to understand the polymers’ response towards secondary structures of collagen. Leather made using the experimental syntan demonstrated higher temperature resistance of 3±0.5°C compared to control syntan treated leathers (1±0.5°C) when exposed to heat under artificial simulation. Experimental leathers exhibited better strength and organoleptic properties. These smart leathers find its application in extreme climatic conditions of heat or cold.

In the past few years four-dimensional (4D) printing technologies have attained worldwide interest and they are now considered the "next big thing". The aim of this research is to provide three selected examples of stimuli-responsive polymer (SRP) applications additively manufactured (AM) by the fused filament fabrication (FFF) technique. To that end, a CCT BLUE filament of thermo-responsive polymer was chosen to produce a water temperature indicator, which changes colour from blue to white when temperature increases; a CCU RED filament of photo-responsive polymer was used to produce a sunlight / UV indicator bracelet; a transparent PLA CLEAR polymer, a CCU RED photo-responsive polymer, and an electrical conductive PLA polymer were selected to produce a smart business card stand. The temperature indicator capability was analysed based on examining colour changes as a function of temperature changes. The sunlight/UV indicator capability was analysed based on the inspection of colour change as a function of absorbed sun/ultraviolet light. The electrical conductivity of the conductive PLA polymer was examined by performing resistance measurements. All three objects were successfully produced and their functionality was demonstrated. We hope that these examples will catalyse the expansion of FFF 4D printed SRP applications, as much work remains to be done in designing the parts and developing FFF printing parameters that take advantage of the stimuli-responsive materials currently being developed for FFF technology.

Carbon nanotubes (CNTs) have high photothermal conversion efficiency and hence can be used to prepare light-absorbing nanocomposites with polymers. In this study, an interesting type of nanocomposi...

Smart materials possess a high potential for application in process engineering. Among these smart materials, stimuli-responsive hydrogels exhibit the chemically inherent characteristic to signific...

We demonstrate a new fabrication technology to realize “intelligent”, transdermal, minimally invasive microneedle array ( i $\mu $ NA) by crosslinking a hydrogel, Polyethylene Glycol Diacrylate (PEGDA) by photo-polymerization using Digital Light Processing (DLP) based 3D printing. The photo-polymerization conditions have been optimized so that the mutually exclusive requirements of excellent mechanical strength while retaining hydrogel properties of PEGDA are met which would allow swelling/delivery of therapeutic cargo of diclofenac sodium via diffusion. An array having 100 microneedles arranged in a $10\times 10$ array was successfully 3D printed which efficiently penetrated human skin during ex vivo characterization. In vitro drug release studies demonstrated that the PEGDA based i $\mu $ NA behaves as a stimuli responsive device showing distinct release characteristics from external stimuli such as temperature and pH. [2020-0133]

Over the last decade, stimuli-responsive microemulsions, that is, those that switch between stable and unstable states in response to certain stimuli, have attracted considerable attention because of their unique properties and potential for diverse applications. Herein, we highlight the recent advances in the development of microemulsions responsive to external triggers such as pH, redox reactions, light, CO2 gas, magnetic field and temperature; discuss the corresponding responses; and reveal important composition–microstructure–macroscopic property relationships to suggest future research directions and potential applications.