Stimuli-responsive Behavior Research Articles

Sequential Stimuli-Response System of Eu-MOF Isomers.

Multiple stimuli-responsive materials hold excellent potential for the next generation smart materials owing to their unique response to external stimuli, providing a powerful impetus for the development of intelligent optical devices. The stimuli-responsive behavior of common multiple stimuli-responsive materials are independent of each other, causing the lack of multiplicity and identification for information technology, which is easy to decode. Herein, QIPA-Eu-1 and QIPA-Eu-2 isomers were prepared from QIPA and EuCl3·6H2O in different solvent thermal conditions for building sequential stimuli-response (SSR) system. Solvent-driven structural transformations of the isomers into QIPA-Eu-3 occurred, along with color change and fluorescence emission variation ascribed to the generation of QIPA aggregates. Furthermore, QIPA-Eu-3 displayed excellent photochromic behaviors. Combining theoretical calculation with well-defined experiments to reveal the mechanism, it was found that light drove the change in the dihedral angles between the quinoline nucleus and adjacent benzene rings in QIPA aggregates. Finally, on the basis of sequential stimuli-induced stepwise responsive behavior of QIPA-Eu-1, the sequential logic gate and time-dependent fluorescence dynamic anti-counterfeiting pattern were successfully constructed. This study provided a new perspective for design and construction of SSR system, which showed promising potential in the fields of data transmission and information encryption.

Preparation, Coating, and Multimodal Therapeutic Properties of an Anticancer System Based on UiO-66(Ce).

UiO-66(Ce) was prepared from cerium metal, which could trigger Fenton-like reactions. A system DOX@UiO-66(Ce)@TA-Fe was constructed by coating a metal polyphenol layer (TA-Fe) on the surface of DOX@UiO-66(Ce), which was loaded with the anticancer drug doxorubicin hydrochloride (DOX). It could produce reactive oxygen species to realize chemodynamic therapy and show stimuli-responsive drug release behaviors to realize chemotherapy. In addition, the system displayed biocompatibility to normal cells (L929 cells) and toxicity to cancer cells (MCF-7 cells), implying an ideal effect for multimodal cancer therapy.

Nitroxide-Containing Poly(2-oxazoline)s Show Dual-Stimuli-Responsive Behavior and Radical-Trapping Activity.

2,2,6,6-Tetramethylpiperidine-N-oxyl (TEMPO) structures possess potent antioxidant activities for biomedical applications. TEMPO immobilization on hydrophilic polymers is a powerful strategy to improve its properties; however, it is mostly limited to reversible-deactivation radical polymerizations or postpolymerization approaches. Here, we immobilized TEMPO units on a hydrophilic poly(2-ethyl-2-oxazoline) (PEtOx) backbone through cationic ring-opening polymerization (CROP) of a new 2-oxazoline monomer bearing a methoxy-protected TEMPO 2-substituent with 2-ethyl-2-oxazoline (EtOx). The ratios of EtOx/TempOx were adjusted to optimize the nitroxide content while maintaining suitable water solubility of the resulting P(EtOxx-stat-TempOx-Oy•) copolymers upon deprotection. P(EtOx40-stat-TempOx-O10•) and P(EtOx33-stat-TempOx-O17•) showed a dual stimuli-responsive behavior and demonstrated significant radical-trapping activities in aqueous media. Particularly, a meaningful augmentation in the activity of TempOx-O• was observed when it was immobilized as P(EtOxx-stat-TempOx-Oy•). The P(EtOx40-stat-TempOx-O10•) system exhibited a longer-lasting activity in water, statistically comparable to that of the antioxidant ferrostatin-1 (Fer-1). Overall, this study introduces a biocompatible polymeric platform for TEMPO immobilization that augments its radical-trapping activity and offers controllable stimuli-responsive properties.

Acid-Vapor-Responsive Supramolecular Gels of Hydrogen-Bonding D–A type Fluorenones

Abstract In this study, we investigated the gelation properties and stimulus-responsive behavior of donor–acceptor–donor-type (D–A–D-type) fluorenone derivatives bearing urethane units. The fluorenone derivatives exhibited characteristic photophysical properties that originate from π–π* and intramolecular charge-transfer (ICT) transitions, and dilute solutions exhibited fluorescence solvatofluorochromic behavior. In addition, the D–A–D-type fluorenone derivatives formed supramolecular gels in appropriate organic solvents; these gels also exhibited acid-vapor-responsive functional variations.

K+-Responsive Nanoparticles with Charge Reversal and Gating Synergistic Effects for Targeted Intracellular Bacteria Eradication.

Intracellular bacteria can evade the attack of the immune system and the bactericidal effects of most antibiotics due to the protective effect of the host cells. Herein, inspired by the stimuli-responsive behaviors of biological ion channels, a kind of synergistic cascade potassium ion (K+)-responsive nanoparticles gated with K+-responsive polymers is ingeniously designed to target intracellular bacteria and then control drug release. Due to the cooperative interaction of host-guest complexation and conformational transition of K+-responsive polymers, the grafted gates based on these polymers could recognize high K+ concentration to reverse the negatively charged nanoparticles into positively charged ones for targeting bacteria and subsequently inducing a switch from the hydrophobic shrinking "off" state to the hydrophilic stretching "on" state for drug release. The K+-responsive nanoparticles can effectively load antibiotics and be endocytosed into the infected cells, and K+-responsive gates can be actuated by a high intracellular K+ concentration. With the efficient synergistic cascade strategy, these K+-responsive nanocarriers can deliver antibiotics to the subcellular region where intracellular bacteria reside and show superior elimination efficiencies in vitro and in vivo than the free drug in delivering vancomycin. The K+-responsive nanocarriers are expected to improve the bioavailability of drugs and enhance their antibacterial efficacy.

Dissipative particle dynamics simulations on the self-assembly of rod-coil asymmetric diblock molecular brushes bearing responsive side chains.

The self-assembly behaviors of rod-coil asymmetric diblock molecular brushes (ADMBs) bearing responsive side chains in a selective solvent are investigated via dissipative particle dynamics simulations. By systematically varying the polymerization degree, copolymer concentration, and side chain length, several morphological phase diagrams were constructed. ADMB assemblies exhibited a rich variety of morphologies, including cylindrical micelles, spherical micelles, nanowires, polyhedral micelles, ellipsoid micelles, and large compound micelles. The structures of the representative nanowires were analyzed in detail. A kinetics study revealed that the one-dimensional growth of nanowires follows the step-growth polymerization mechanism. Besides, by calculating the local order parameter of the rigid chains, we found that increasing the lengths of A and C side chains can promote the ordered arrangement of the rigid chains. Moreover, the rod-to-coil conformation transitions were simulated to explore the stimuli-responsive behaviors of ADMBs with responsive rigid side chains. The simulation results indicated that the volume of the assemblies expanded without the support of the rigid chains. The present work not only provides a comprehensive understanding of the self-assembly behaviors of ADMBs but also provides meaningful theoretical support for the development of novel molecular brush materials.

Dimer Is Not Double: The Unexpected Behavior of Two-Floor Peptide Nanosponge.

Using the framework of an investigation of the stimuli-responsive behavior of peptide assembly on a solid surface, this study on the behavior of a chemisorbed peptide on a gold surface was performed. The studied peptide is a dimeric form of the antimicrobial peptide Trichogin GAIV, which was also modified by substituting the glycine with lysine residues, while the N-terminus octanoyl group was replaced by a lipoic one that was able to bind to the gold surface. In this way, a chemically linked peptide assembly that is pH-responsive was obtained because of the protonation/deprotonation of the sidechains of the Lys residues. Information about the effect of protonation/deprotonation equilibria switching the pH from acid (pH = 3) to basic (pH = 11) conditions was obtained macroscopically by performing Quartz crystal microbalance with dissipation monitoring (QCM-D), Surface Plasmon Resonance (SPR), Nanoplasmonic Sensing (NPS), and FTIR techniques. Using molecular dynamics (MD) simulations, it is possible to explain, at the molecular level, our main experimental results: (1) pH changes induce a squeezing behavior in the system, consisting in thickness and mass variations in the peptide layer, which are mainly due to the pH-driven hydrophilic/hydrophobic character of the lysine residues, and (2) the observed hysteresis is due to small conformational rearrangements from helix to beta sheets occurring mainly on the first half of the peptide, closer to the surface, while the second half remains almost unaffected. The latter result, together with the evidence that the layer thickness is not simply double the assembly of the monomeric analog, indicates that the dimeric peptide does not behave as a double monomer, but assumes very peculiar features.

Raman Imaging of Targeted Drug Delivery with DNA-Based Nano-Optical Devices.

Raman spectroscopy (RS) has emerged as a novel optical imaging modality by identifying molecular species through their bond vibrations, offering high specificity and sensitivity in molecule detection. However, its application in intracellular molecular probing has been limited due to challenges in combining vibrational tags with functional probes. DNA nanostructures, known for their high programmability, have been instrumental in fields like biomedicine and nanofabrication. So far, their ability to customize Raman signals remains largely untapped. In this study, a new class of Raman active DNA origami-based hybrid nanodevice (ND) for targeted cancer cell drug delivery and imaging is engineered. The ND is specifically engineered for metastatic prostate cancer treatment, featuring a legumain enzyme-responsive sequence for the controlled release of the chemotherapeutic agent doxorubicin. Integrating RS with precise targeting, the ND enables imaging of aggressive cancer cells and efficient drug delivery with minimal off-target effects. The developed device offers stimuli-responsive behavior, enhanced stability, exceptional tunability, and potent targeting abilities, positioning it as a highly promising strategy for advancing precision cancer imaging and therapy.

Regioregular Poly(p-phenylene iminoborane): A Strictly Alternating BN-Isostere of Poly(p-phenylene vinylene) with Stimuli-Responsive Behavior.

Incorporation of BN units into π-conjugated organic compounds, as substitutes for specific CC couples, often leads to new hybrid materials with modified physical and chemical properties. Poly(p-phenylene iminoborane)s are derived from well-known poly(p-phenylene vinylene) (PPV) by replacement of the vinylene groups by B=N linking units. Herein, an unprecedented poly(p-phenylene iminoborane) is presented that features a strictly alternating sequence of BN units along the main chain. The synthesis thereof was achieved by AB-type polymerization of a monomer featuring an N and a B terminus. Monodisperse oligomers with up to three BN units in the chain were additionally prepared and structurally characterized. Associated with the introduction of a dipole in the regioregular backbone structure, they display notable fluorescence already in solution and large Stokes shifts, distinct from their previously reported BBNN-sequenced congeners. All compounds show aggregation-induced emission enhancement (AIEE) properties. Computational studies provided evidence for emission from either locally excited (LE) or twisted intramolecular charge transfer (TICT) states. These processes can be optionally addressed by various stimuli, giving rise to dual emission, solvatochromic, thermochromic, and reversible mechanochromic behavior.

Quadruple Stimuli-Responsive Behaviour of Acylhydrazone Crystals: Mechanical, Photomechanical, Thermomechanical, and Optical Waveguide Properties.

As society advances, the demand for high-performance crystal materials with versatile stimuli-responsive capabilities has increased. However, there remains a notable shortage of simple molecular crystals that exhibit stable and swift responses to various stimuli. In this study, we synthesized a novel acylhydrazone crystal by integrating benzene-fused heterocycles and halogens, achieving a crystal material with multiple stimuli-responsive behaviours. The crystal demonstrates good mechanical flexibility, capable of with standing a strain of 2.3 % under applying mechanical force and recovering its original shape after force removal. Crystal structure analysis reveals this property is due to the strong and flexible intermolecular interactions. It also exhibits rapid photomechanical bending away from light source under UV irradiation, which could be attributed to the facile photoisomerization. Moreover, the crystal undergoes significant thermomechanical transitions, including cracking and jumping, upon heating. Additionally, the prepared crystal exhibits passive optical waveguide of red light at 640 nm, which, combining the photomechanical bending, can achieve controllable light output direction. These multi-stimuli-responsive behaviors make the acylhydrazone crystal a promising candidate for applications in multifunctional sensors, optoelectronic devices, and thermal switches. This work provides a helpful reference for the study of potential crystal material design and functionality of advanced responsive systems.

Circularly polarized luminescence in chiral nematic liquid crystals based on photochromic molecules

Circularly polarized luminescence (CPL) has emerged as a focal point in luminescent materials research, reflecting a growing field of study. Responding to the demand for practical applications across diverse sectors, there is a critical need for CPL materials with high luminescence dissymmetry factors (g lum) and adjustable optical performance, driving the development of novel materials and methodological approaches. Chiral nematic liquid crystals (N*-LCs) have attracted significant attention as promising candidates for producing high-performance CPL materials due to their ability to exhibit enhanced g lum and modulate circularly polarized light. This review comprehensively presents the stimuli-responsive CPL properties, utilizing N*-LCs as chiral templates doped with various photochromic compounds, particularly azobenzene, spiropyran (SP), diarylethene and overcrowded alkene. By elucidating the dynamic interplay between molecular structure, supramolecular organization, and optical response, it offers a profound understanding of the stimuli-responsive CPL behaviors. Additionally, the review also explores the multifaceted applications of photochromic N*-LCs materials, spanning advanced display technologies, optical data storage, and beyond. By examining diverse avenues for leveraging their unique optical properties, it highlights their pivotal role in driving innovation across photonic applications, facilitating transformative advancements in the field.

High contrast stimuli-responsive fluorescence emitters based on carbazole-cyanostilbene derivatives with aggregation induced emission properties

Due to the aggregation induced emission (AIE) materials exhibiting obvious fluorescent emission changes under the external stimuli of heat, solvent, force and so on, significant efforts have been directed toward developing AIE-active materials with high contrast stimuli-responsive fluorescence behaviors. Herein, three electron-donor(D)-electron-acceptor(A) and D-A-D type organic fluorescence emitters of Cz-DC-tBu, Cz-DC-CN and Cz-DC-OMe were facilely synthesized using carbazole group as D unit and cyano group as A unit. They showed typical AIE features and exhibited remarkable color changes under mechanical force and in different polarity solvents, respectively. The stimuli-responsive mechanism of the compounds were investigated by powder X-ray Diffraction (PXRD) and density functional theory calculations (DFT), which revealed that the mechanofluorochromic behaviors were associated with the molecular packing modes, and the solvatochromic effects were caused by the intramolecular charge-transfer transition (ICT) effect. Significantly, it was found that Cz-DC-tBu showed high contrast stimuli-responsive behaviors through adjusting the substituent groups on the cyanostilbene unit with CN, OMe, and tBu groups, respectively. This study provided a new strategy for the design of AIE-active stimuli-responsive fluorescence emitters, and made them possible using in stress sensors, chemical detection, memory storage, anti-counterfeiting applications.

Biocompatible PVAc-g-PLLA Acrylate Polymers for DLP 3D Printing with Tunable Mechanical Properties.

The technological advancement of Additive Manufacturing has enabled the fabrication of various customized artifacts and devices, which has prompted a huge demand for multimaterials that can cater to stringent mechanical, chemical, and other functional property requirements. Photocurable formulations that are widely used for Digital Light Processing (DLP)/Stereolithography (SLA) 3D printing applications are now expected to meet these new challenges of hard and soft or stretchable structural requirements in addition to good resolution in multiple scales. Here we present a biocompatible photocurable resin formulation with tunable mechanical properties that can produce hard or stretchable elastomeric 3D printed materials in a graded manner. Acrylate poly(lactic acid) (PLA) grafted polyvinyl acetate (PVAc) polymer was mixed with hydroxyl ethyl methacrylate (HEMA) and hydroxyl ethyl acrylate (HEA) as reactive diluents (50-70 wt %) in various compositions to form a series of photocurable resin formulations. Depending on the nature of the reactive diluent (HEMA or HEA) and their weight percentage, the mechanical properties of the 3D printed parts could be fine-tuned from hard (Tensile strength 20.6 ± 2 MPa, elongation 2 ± 1%) to soft (Tensile strength 1.1 ± 0.2 MPa, elongation 62 ± 8%) materials. The printed materials displayed remarkable dye absorption (95%), showing stimuli-responsive behavior for dye release (with respect to both pH and enzyme), while also demonstrating high cell viability (>90%) for mouse embryonic (WT-MEF) cells and degradability in PBS solution. These biobased 3D printing resins have the potential for a variety of applications, including tissue engineering, soft robotics, dye absorption, and elastomeric actuators.

Antisense oligonucleotide facilitate the photothermal therapy of Mxene-based nanoplatform for drug-resistant breast cancer

Breast cancer has become the most common form of cancer worldwide. Chemotherapy failure, primarily due to drug resistance, necessitates the development of new therapeutic strategies. In this study, ultrathin Ti3C2 nanosheets are utilized as photothermal agents and nanocarriers. We developed a multifunctional Ti3C2-based nanoplatform (214.7 nm) through layer-by-layer absorption of HSP90 antisense oligonucleotide (ASO) and doxorubicin (DOX), with surface modification using hyaluronic acid (HA). In a simulated acidic tumor microenvironment in vitro, 90 % of the drug was released within 36 hours. Additionally, Under 808 nm irradiation (2.0 W/cm²), MCF-7/ADM cell viability assays revealed the following results: HA-Ti3C2 (57 %), HA-Ti3C2@ASO (HT@A) (41 %), and HA-Ti3C2@ASO/DOX (HT@AD) (26 %), which shown the synergistic inhibitory effects of this multifunctional nanoplatform. Herein, this nanosystem exhibits enhanced biocompatibility, superior photothermal performance, and stimuli-responsive drug release behavior, making it a promising candidate for effective inhibition of cancer cell proliferation and migration.

Fiber complex-stabilized high-internal-phase emulsion for allicin encapsulation: microstructure, stability, and thermal-responsive properties.

Stimuli-responsive emulsions have garnered significant attention for their ability to enhance sensory qualities and control the release of encapsulated nutrient in emulsion-based products. However, the characteristics of synthetic materials of fabricating stimuli-responsive emulsions have been a crucial limitation in the food industry. Regulating the behavior of molecules at the interface could potentially achieve the desired stimuli-responsive behavior, but currently there is limited information available. High-internal-phase emulsions (HIPEs) were fabricated for the encapsulation of allicin, stabilized by a complex of 20 g kg-1 whey protein amyloid fibrils (WPF) and 20 g kg-1 glycyrrhizin fibers (GA). The intermolecular interactions between WPF and GA in the fiber complexes were predominantly governed by hydrophobic and electrostatic forces. These complexes adsorbed and stacked around the oil droplets, forming a protective interfacial film that enhanced droplet stability. An increased proportion of WPF (WPF = 3:1 or 4:1) surrounding the oil droplets enhanced the accelerated storage stability of HIPEs, with instability indexes approaching 0.2. Additionally, HIPEs displayed a temperature-dependent modulus, with the emulsion stabilized by a WPF ratio of 3:1 showing the highest modulus at 85 °C. The encapsulation efficiency of allicin in HIPEs ranged from 88.69 ± 6.62% to 101 ± 1.37% at 25 °C, and from 31.95 ± 1.92% to 78.69 ± 4.63% after incubation at 85 °C for 8 h. The release profile of allicin from the HIPEs exhibited thermal responsiveness, depending on the interfacial content of GA. These findings indicated that the thermal-responsive properties of HIPEs can be strategically engineered by manipulating their interfacial characteristics. © 2024 Society of Chemical Industry.

Designing Stimuli-Responsive Supramolecular Gels by Tuning the Non-Covalent Interactions of the Functional Groups.

The physical characteristics of a supramolecular gel are greatly influenced by the nature and arrangement of functional groups in the gelator. This work focuses on the impact of the functional groups, specifically the hydroxyl group, on the stimuli-responsive properties of a gel. We used a C3-symmetric benzene-1,3,5-tricarboxamide (BTA) platform, which was attached to the methyl ester of phenylalanine (MPBTA) and tyrosine (MTBTA). The gelation studies revealed that MPBTA gelled in alcohols, non-polar aromatic solvents, and aqueous mixtures (1:1, v/v) of high-polar solvents, whereas MTBTA gelled only in an aqueous mixture of DMF (1:1, v/v). The mechanical and thermal strength of the gels were evaluated by rheological and Tgel studies, and the results indicated that MPBTA gels were stronger than MTBTA gels. The gels were characterized by powder X-ray diffraction and scanning electron microscopy (SEM). The analysis of stimuli-responsive properties revealed that MPBTA gels were intact in the presence of sodium/potassium salts, but the MTBTA gel network was disrupted. These results indicate that the elegant choice of functional groups could be used to tune the constructive or destructive stimuli-responsive behavior of gels. This study highlights the significant role of functional groups in modulating the stimuli-responsive properties of supramolecular gels.

Fabrication of albumin-Ti3C2 MXene quantum dots-based nanohybrids for breast cancer imaging and synergistic photo/chemotherapeutics

Advancement in the development of new materials with theranostic and phototherapeutic potential along with receptiveness to external stimuli has been persistently inspiring oncology research. Herein, titanium carbide-based MXene quantum dots (FHMQDs) have been synthesized and modified to take advantage of stimuli-responsive behavior and target specificity for breast cancer cells. With a size of around 3 nm, the developed FHMQDs demonstrate high fluorescent emission at around 460 nm. With ∼90 % encapsulation efficiency of doxorubicin (DOX), the developed system also offers rapid DOX release behavior when encountering an acidic pH (5.4). Further, the in vitro assessment of the developed FHMQDs on MDA-MB 231 breast cancer cells presents excellent target specificity to cancer cells which was reflected by its high cytotoxicity against cancer cells. Additionally, the outstanding photodynamic efficiency of FHMQDs due to excessive Reactive Oxygen Species (ROS) generating ability along with apoptosis promoting capability of FHMQDs in cancer cells demonstrates a synergistic approach in cancer theranostics. Encouragingly, the fabricated FHMQDs also exhibited fluorescent labelling and bioimaging capacity which makes it an incredible platform that ensures theranostic excellence in breast cancer research.

Zirconium-based nanoclusters as molecular robots for water decontamination

Water contamination owing to anionic pollutants is a persisting and ubiquitous global threat. The current remediation technologies are mostly low in efficiency, expensive in materials and often associated with complicated processes. Herein, we report a characteristic zirconium-based nanocluster that can work as molecular robots for the efficient remediation of anions-contaminated water with great effectiveness and molecular-level accuracy. It exhibits a stimuli-responsive behavior to facilitate the water treatment process: dissolve in acidic aqueous solutions for molecular-level decontamination and quickly aggregate for post-remediation collection. It can precisely capture the representative anionic pollutants, whilst featuring satisfactory capacities (ca. 175 mg-arsenic/g, 60 mg-chromium/g, 45 mg-fluoride/g, 70 mg-phosphorus/g, respectively), super-fast kinetics (finishing uptake within seconds, which is two to four orders of magnitude faster than typical sorbents), as well as multi-cycle applications without appreciable loss of activity. The coexisting common ions show no effect on the target uptake. The responsible active site investigation shows that four active sites are responsible for the monovalent pollutant removal, and the active sites work in pairs to capture divalent chromate species. Cost analysis shows its economical applicability in practical applications. This work would lead to the development of effective water decontamination with higher effectiveness, more convenience, lower cost and more practical application value.

Competence of Carbonaceous Fibers/Nanofillers (Graphene, Carbon Nanotube) Reinforced Shape Memory Composites/Nanocomposites Towards Aerospace—Existent Status and Expansions

Abstract Shape memory or stimuli responsive polymers have established a unique grouping of smart materials. The technical merit of these polymers has been evaluated in aerospace sector, since last few decades. Particularly, the stimuli responsive polymers render inherent competences to recuperate the structural damages in exterior/interior space architectures. In this context, both the thermoplastics as well as thermosetting polymers depicted essential stimuli responsive behaviour. As interpreted in this state-of the-art review, the carbonaceous reinforcement like carbon fibers and nano-reinforcements including nanocarbons (graphene, carbon nanotube) have been employed in the shape recovering matrices. The performance of ensuing shape retrieving aerospace materials was seemed to be reliant on the polymer chain crosslinking effects, filler/nanofiller dispersal/alignment, microstructural specs, interfacial contour and interactions, and processing techniques used. Consequently, the shape actuations of polymer/carbon fiber composites were found to be instigated and upgraded through the inclusion of nanocarbon nano-additives. The ensuing high-tech shape memory composites/nanocomposites have anomalous significance for various aero-structural units (fuselage, wings, antennas, engines, etc.) due to prevention of possible thermal/shock/impact damages. Future implications of carbonaceous shape memory composites/nanocomposites in aerospace demands minimizing the structure-property-performance challenges and large scale fabrication for industrial scale utilizations. In this way, deployment of carbonaceous nanofiller/filler based composites revealed enormous worth due to low density, anti-fatigue/wear, anti-corrosion, non-flammability, self-healing, and extended durability and long life operations. However, there are certain challenges associated with the use of nanocarbons and ensuing nanocomposites in this field markedly the adoption of appropriate carbon fiber coating technique, aggregation aptitude of nanocarbons, additional processing steps/cost, nanoparticle initiated invisible defects/voids, difficulty in machinability operations due to presence of nanoparticles, and corrosion risk of composite structures in contact with metal surfaces. By overcoming these hinderances, nanoparticles modified carbon fiber based composites can be promising towards a new look of upcoming modernized aerospace industry.

Stimuli-Responsive Phosphate Hydrogel: A Study on Swelling Behavior, Mechanical Properties, and Application in Expansion Microscopy.

Phosphorus-based stimuli-responsive hydrogels have potential in a wide range of applications due to their ionizable phosphorus groups, biocompatibility, and tunable swelling capacity utilizing hydrogel design parameters and external stimuli. In this study, poly(2-methacryloyloxyethyl phosphate) (PMOEP) hydrogels were synthesized via aqueous activators regenerated by electron transfer atomic transfer radical polymerization using ascorbic acid as the reducing agent. Swelling and deswelling behaviors of PMOEP hydrogels were examined in different salt solutions, pH conditions, and temperatures. The degree of swelling in salt solutions followed CaCl2 < MgCl2 < KCl < NaCl with a decrease in swelling rate at higher concentrations until reaching a saturation point. In water, the degree of swelling increased significantly around neutral pH and remained constant at basic pH values. The effects of polymerization conditions, including pH, temperature (30, 40, 50 °C), and MOEP concentration (40, 50, 60% v/v MOEP/H2O), on the hydrogel swelling behavior in various salt solutions were also investigated. PMOEP hydrogels showed a decrease in the degree of swelling as the pH was increased above the native pH of the monomer solution. Scanning electron microscopy and energy-dispersive spectroscopy were utilized to examine the microstructure and chemical composition of the dried hydrogel after salt solution swelling. Cytotoxicity testing using rat bone marrow stem cells confirmed the biocompatibility of the PMOEP hydrogels. A unique feature of this effort was evaluation of these phosphate hydrogels for use in expansion microscopy where a significant twofold enhancement in cellular expansion capacity was showcased utilizing 4T1 mouse breast cancer cells. This comprehensive study provides valuable insights into the stimuli-responsive behavior and expansion characteristics of phosphate hydrogels, highlighting their potential in diverse biomedical applications.