Excellent Self-healing Properties Research Articles

A self-healing composite solid electrolyte with dynamic three-dimensional inorganic/organic hybrid network for flexible all-solid-state lithium metal batteries

Composite solid electrolytes (CSEs), which combine the advantages of solid polymer electrolytes and inorganic solid electrolytes, are considered to be promising electrolytes for all-solid-state lithium metal batteries. However, the current CSEs suffer from defects such as poor inorganic/organic interface compatibility, lithium dendrite growth, and easy damage of electrolyte membrane, which hinder the practical application of CSEs. Herein, a CSE (PBHL@LLZTO@DDB) with polyurethane (PBHL) as the polymer matrix and Li6.4La3Zr1.4Ta0.6O12 (LLZTO) modified by silane coupling agent (DDB) as inorganic fillers (LLZTO@DDB) has been prepared. Disulfide bond exchange reactions between PBHL and LLZTO@DDB enable PBHL@LLZTO@DDB to form a dynamic three-dimensional (3D) inorganic/organic hybrid network, which promotes the uniform dispersion of LLZTO in PBHL@LLZTO@DDB, improves the Li+ conductivity (1.24 ± 0.08 × 10−4 S cm−1 at 30 ℃), and broadens the electrochemical stability window (5.16 V vs. Li+/Li). Moreover, a combination of hydrogen bonds and disulfide bonds endows PBHL@LLZTO@DDB with excellent self-healing properties. As such, both all-solid-state symmetric and full cells exhibit excellent cycle performance at ambient temperature. More importantly, the healed PBHL@LLZTO@DDB can almost completely restore its original electrochemical properties, indicating its application potential in flexible electronic products.

A Self-Healing and Sweat-Chargeable Hydrogel Electrolyte for All-in-One Flexible Supercapacitors.

Flexible solid-state supercapacitors (SCs) with hydrogel as an electrolyte and separator combine the advantages of wearability and energy storage and exhibit a broad application prospect in wearable energy textiles. However, irreversible electrolyte damage and unstable electrode-electrolyte interfaces during mechanical deformations remain bottlenecks in realizing truly wearable applications. Herein, poly(acrylic acid) (PAA)-Fe hydrogels were prepared through a simple thermal polymerization strategy. The dynamic reversible metal coordination bonds between Fe3+ and carboxylic acids confers the hydrogels with excellent self-healing properties. As expected, the prepared hydrogels exhibited superior mechanical strength (tensile stress of 45.80 kPa), ionic conductivity (0.076 S cm-1), and self-healing properties. Subsequently, the SCs were constructed using composite hydrogel electrodes (MnO2@CC embedded in the PAA-Fe hydrogels) as symmetrical electrodes (marked as MSCs). The reversible metal coordination bonds between composite hydrogel electrodes formed an ultrastable electrode/electrolyte interface in the all-in-one MSCs, thus revealing excellent mechanical durability. The all-in-one MSCs delivered a remarkable specific capacitance (30.98 F g-1 at 0.2 A g-1), excellent cyclic stability (87.24% after 5000 cycles), outstanding mechanical deformation stability, and impressive electrochemical output stability after self-healing (capacitance retention of 85.34% after five cycles of cutting/self-healing). It is noteworthy that the all-in-one MSCs employed NaCl as an electrolyte, which can be obtained from human sweat. As a proof of the self-charged concept, the all-in-one MSCs can be reused in sweat, whose capacitance was maintained at 90.05% of the initial state after three repetitions. This work is expected to shine light into the design of all-in-one and fabric-based SCs and the development of wearable energy textiles.

Preparation and properties of double-layer phenolic/polyurethane coated isophorone diisocyanate self-healing microcapsules

Single-layer isophorone diisocyanate (IPDI) are one of the most popular self-healing microcapsules but suffers from low shell strength, poor heat resistance, stability and aging properties. In this paper, IPDI microcapsules were encapsulated into double-layer phenolic (PF)/polyurethane (PU) by a two-step process involving interfacial polymerization and in-situ polymerization. The prepared microcapsule composites were comprehensively characterized for their physical and chemical properties using optical microanalysis, scanning electron microscope, Fourier transform infrared spectroscopy, thermal gravimetric analysis and depth-sensing indentation analysis. Compared with the single-layer PU-IPDI microcapsule counterpart, the mechanical performance, thermal resistance, aging property and environmental stability of double-layer PF/PU-IPDI microcapsules were significantly improved. The epoxy coating was enhanced with the incorporation of 10 wt.% PF/PU-IPDI microcapsules, whose self-healing performance was evaluated by scratch corrosion test. The results demonstrated successful repair of coating scratches, along with the absence of corrosion on the coated steel substrate soaked in a 10 wt.% NaCl solution for 7 days. By comparing the tensile strength of epoxy coating before and after crack formation, it could be found that the self-healing efficiency was 57.9% when loaded with 10 wt.% of PF/PU-IPDI microcapsules in coating. This study highlights that the rational design of double-layer microcapsules integrated into the epoxy coating matrix could provide excellent anti-corrosion and self-healing properties.

Design of self-healing nanocomposite hydrogels and the application to the detection of human exercise and ascorbic acid in sweat

Hydrogel sensors have broad application prospects in human motion monitoring and sweat composition detection. However, hydrogel-based sensors are faced with challenges such as low accuracy and poor mechanical properties of analytes detection. Based on mussel-inspired chemistry, we synthesized mesoporous silica@polydopamine-Au (MPS@PDA-Au) nanomaterials and designed a self-healing nanocomposite hydrogel to monitor human movement and ascorbic acid detection in sweat. Mesoporous silica (MPS) possess orderly mesoporous structure. Dopamine (DA) polymerized on the surface of MPS to generate polydopamine (PDA), forming the composite material MPS@PDA-Au. This composite was then embedded into polyvinyl alcohol (PVA) hydrogels through a simple freeze-thaw cycle process. The hydrogels have achieved excellent deformable ability (508.6%), self-healing property (90.5%) and mechanical strength (2.9 MPa). The PVA/MPS@PDA-Au hydrogel sensors had the characteristics of fast response time (123.2 ms), wide strain sensing range (0–500%), excellent fatigue resistance and stability in human detection. The detection range of ascorbic acid (AA) in sweat was wide (8.0 μmol/L-100.0 μmol/L) and the detection limit was low (3.3 μmol/L). Therefore, these hydrogel sensors have outstanding application prospects in human motion monitoring and sweat composition detection.

A robust bio-based polyurethane employed as surgical suture with help to promote skin wound healing

Designing bio-based polyurethane materials with excellent mechanical, biocompatibility, and self-healing properties simultaneously is currently a significant challenge due to the increasing demands for high-performance materials. In this study, we propose an asymmetric backbone strategy utilizing bio-based polycarbonate as the soft segment, equimolar ratios of lysine diisocyanate and isophorone diisocyanate as asymmetric hard segments, and isophorone diamine as the chain extender. The resulting polyurethane elastomers exhibit excellent mechanical properties, including high tensile stress (46.1 MPa), toughness (213.9 MJ/m3), and fracture energy (98.47 kJ/m3). The polyurethane elastomers demonstrate good self-healing and recyclable properties under simple heat treatment. Furthermore, biological experiments confirm the degradability and bio-safety of the bio-based polyurethane elastomers, which have shown potential in accelerating wound healing in mice when used as surgical sutures. These findings highlight the promising prospects of the obtained polyurethane elastomers in various applications, including biomedicine, flexible sensing, and electronic components.

Eco-friendly development of intrinsically antibacterial and mechanically robust self-healing hydrogels using alginate and oval proteins: Advancing periodontitis treatment

A novel approach for fabricating self-healing, intrinsically antibacterial hydrogels for potential periodontitis treatment is presented in this study. Self-healable hydrogels are promising substitutes for brittle hydrogels due to their excellent durability and stability. Drug-loaded regenerative hydrogels have shown good outcomes but face challenges, specifically in managing the development of drug resistance. The hydrogels were prepared by incorporating bioactive oval proteins and hydroxyapatite into polyvinyl alcohol using a simple synthesis method with eco-friendly crosslinkers (oxidized alginate, borax, and divalent metal salts). The synthesized hydrogels exhibited excellent self-healing properties, mechanical robustness, and malleability. Furthermore, characterization techniques confirmed successful crosslinking and interactions within the network. The hydrogels demonstrated significant water absorption, tunable degradation, and potent antibacterial activity against E. coli, S. aureus and P. gingivalis. In vitro studies confirmed good cytocompatibility with epithelial and fibroblasts cells. Wound healing assays further supported the potential of these hydrogels for tissue regeneration applications. This approach offers a promising alternative to traditional drug-loaded hydrogels, overcoming limitations of cost and potential for resistance.

Enhancing long-segmental tracheal restoration: A self-repairing hydrogel loaded with chondrocytokines for sutureless anastomosis and cartilage regeneration

Artificial tracheal substitutes encounter significant challenges during long-segmental tracheal defects (LSTD) reconstruction, notably early postoperative anastomotic stenosis and tracheal chondromalacia. Mitigating early anastomotic stenosis by creating a compliant sutureless substitute is pivotal. Enhancing its chondrogenic capacity is equally critical for sustained healthy tracheal cartilage regeneration. This study proposes a self-healing hydrogel for sutureless tracheal anastomosis to mitigate anastomotic stenosis, enriched with kartogenin (KGN) and transforming growth factor-β1 (TGFβ1) to bolster chondrogenic properties. Initially, two precursor solutions were prepared: 1) aldehyde-modified hyaluronic acid with sulfonation and β-cyclodextrin-CHO loaded with KGN; 2) hydrazide-grafted gelatin loaded with TGFβ1. Coextrusion of these solutions resulted in a gelated G + TGFβ1/sH-CD + KGN hydrogel, characterized by a robust covalent bonding network of acylhydrazones between hydrazide and aldehyde groups, imparting excellent self-healing properties. The G + TGFβ1/sH-CD + KGN hydrogels, showcasing favorable cytocompatibility, excellent injectability, and rapid gelation, were loaded with bone marrow stem cells. These were customized into O-shaped rings and assembled into a malleable tracheal substitute using our established ring-to-tube method. This resultant compliant substitute facilitated sutureless anastomosis of LSTD in a rabbit model, attributed to the Schiff base reaction between the hydrogel's carbonyl group and the tissue's amino group. Notably, the tracheal substitute reduced early postoperative anastomotic stenosis, maintained tracheal patency, alleviated sputum blockage, promoted reepithelization, and increased the survival rate of the experimental rabbits. The sustained release of chondrocytokines resulted in excellent tracheal cartilage regeneration. Employing chondrocytokines-loaded hydrogels with self-healing properties represents a significant advancement in sutureless tracheal anastomosis and tracheal cartilage regeneration, holding promising potential in inhibiting early postoperative anastomotic stenosis and tracheal chondromalacia when treating LSTD.

Rapid preparation of injectable dual-network hydrogels for biomedical applications using UV-triggered sulfhydryl click reactions

The use of hydrogels to mimic natural cartilage implantation can effectively solve the current problems of insufficient cartilage donors and low rate of injury healing. In particular, injectable hydrogels are less invasive in clinical applications and better able to fill uneven injury surfaces. Here, we prepared NorCS and CS-SH by modifying chitosan with 5-norbornene-2-carboxylic acid and N-Acetyl-L-cysteine, respectively. Dual-network hydrogels were prepared by using UV-triggered thiol-ene click reaction between NorCS and CS-SH and the metal coordination between SA and Ca2+. The prepared hydrogels can be cross-linked quickly and exhibit excellent degradability, self-healing and injectable properties. At the same time, the hydrogel also showed good cytocompatibility and could significantly restore the motor function of mice. This study provides an effective strategy for preparing injectable hydrogels capable of rapid cross-linking.

Fabrication of anti-freezing and self-healing hydrogel sensors based on carboxymethyl guar gum and poly(ionic liquid)

As classical soft materials, conductive hydrogels have attracted wide attention in the field of strain sensors due to their unique flexibility and conductivity. However, there are still challenges in developing conductive hydrogels with comprehensive mechanical strength, self-healing ability and sensitive sensing properties. In this paper, a novel PAV/CMGG hydrogel was prepared by a simple one-pot method through the introduction of 1-vinyl-3-butylimidazolium bromide (VBIMBr), acrylic acid (AA), carboxymethyl guar gum (CMGG) and AlCl3. The coordination bond between Al3+ and –COO− groups on PAA and CMGG, the hydrogen bond between PAA and CMGG, and the electrostatic interaction between [VBIM]+ and –COO− endow the hydrogel with good mechanical properties, self-recovery ability, fatigue resistance and great self-healing properties. PAV/CMGG hydrogel had good conductivity of 2.31 S/m which could successfully light up the bulb. The hydrogel as the strain sensor had not only a wide strain sensing capability (strain ranging from 0 to 800 %), but also a high strain sensitivity (gauge factor (GF) = 28.50 for the strain ranging from 600 to 800 %). This study can provide inspiration for the construction of new high-performance flexible sensors.

A simple and universal approach for fabricating bioactive self-stacked hydrogels with enhanced therapeutic efficacy

Despite significant advancements in self-stacked hydrogels of herbal small molecules in recent years, the emergence of new pharmacological small molecule self-stacked hydrogel systems remains largely reliant on serendipity and painstaking efforts. To address this challenge, we proposed a ‘bioactive bivalent metal ions-coordinated pharmacological small molecules’ strategy. This approach enabled the preparation of triterpenoid betulinic acid-based self-stacked hydrogels with excellent injectable and self-healing properties via a simple two-step method. We extended this strategy to self-stacking hydrogels based on other pentacyclic triterpene small molecules, anthraquinone small molecules, flavonoid small molecules and synthetic steroid small molecules. This universal strategy is capable of extracting hydrophobic pharmacological small molecules to construct novel self-stacked biomaterials in a cost-effective, efficient, large-scale, and environmentally friendly manner. Importantly, we successfully synthesized Mg2+-coordinated betulinic acid (BA-Mg) self-stacked hydrogel at low concentrations in the bacterial cellulose (termed BC) hydrogel network, overcoming the mechanical limitations of self-stacked hydrogels for biomedical applications. The BA-Mg/BC hybrid hydrogel demonstrated exceptional biocompatibility, anti-inflammatory, and angiogenic properties, significantly accelerating the skin wound healing process through the synergistic pharmacological effects of Mg2+ and BA.

Improvement in adhesion and corrosion resistance of Ce-based coating on micro-arc oxidized AZ31B Mg alloy via employing graphene oxide as an effective interlayer

Ce-based coatings are often used as protective coatings on Mg alloy because of their excellent self-healing and anticorrosion properties. However, poor adhesion of Ce coating can easily cause it peel off and thus lose its protective effect. In this work, for the first time, the graphene oxide (GO) was employed as an interlayer between micro-arc oxidation (MAO) and Ce-based coatings to improve their adhesion strength. The results show that the addition of GO layer can effectively improve the adhesion strength and hardness of the composite coating. The MAO/GO/Ce composite coating not only significantly enhance the corrosion resistance of the substrate, but also has self-healing ability. According to the molecular dynamics calculations, the GO interlayer can form a good bond with the inner MgO layer and the outer CeO2 layer. The MAO/GO/Ce composite coating with high adhesion and self-healing property may extend the practical application of Mg alloys.

Self-Repairing Humidity-Adjustable Anisotropic Adhesion Switch for Smart Manipulation.

Stimuli-responsive surface adhesion regulation is widely used in automated assembly systems, intelligent pick-up and placement systems, and soft crawling robots. However, in the actual separation process, it tends to produce separation residue or excessive adhesion. Therefore, how to regulate surface adhesion on demand is a significant challenge. Herein, inspired by the anisotropic adhesion behavior of butterflies and the controlled adhesion behavior of octopuses, based on molecular conformational rearrangement and anisotropic structures, a humidity-responsive PES-PI/PDMS composite surface is achieved to meet the needs of controllable adhesion orientation and strength, which could be used for an intelligent transfer system (grasping and releasing and anisotropic transporting). Humidity can effectively tune the hydrogen bonding and the interaction between polymers, resulting in excellent self-healing and durability properties of the composite surface. Moreover, humidity could adjust the surface transmittance as well, making it possible to be used in humidity sensing and in a detection and encryption/decryption system to enhance environmental monitoring and information protection capabilities. This work not only establishes a method for the fabrication of innovative "high-flexibility" adhesive materials but also provides approaches for the design and development of intelligent response devices.

Design of Cellulose Nanocrystal-Based Self-Healing Nanocomposite Hydrogels and Application in Motion Sensing and Sweat Detection.

Hydrogels, as flexible materials, have been widely used in the field of flexible sensors. Human sweat contains a variety of biomarkers that can reflect the physiological state of the human body. Therefore, it is of great practical significance and application value to realize the detection of sweat composition and combine it with human motion sensing through a hydrogel. Based on mussel-inspired chemistry, polydopamine (PDA) and gold nanoparticles (AuNPs) were coated on the surface of cellulose nanocrystals (CNCs) to obtain CNC-based nanocomposites (CNCs@PDA-Au), which could simultaneously enhance the mechanical, electrochemical, and self-healing properties of hydrogels. The CNCs@PDA-Au was composited with poly(vinyl alcohol) (PVA) hydrogel to obtain the nanocomposite hydrogel (PVA/CNCs@PDA-Au) by freeze-thaw cycles. The PVA/CNCs@PDA-Au has excellent mechanical strength (7.2 MPa) and self-healing properties (88.3%). The motion sensors designed with PVA/CNCs@PDA-Au exhibited a fast response time (122.9 ms), wide strain sensing range (0-600.0%), excellent stability, and fatigue resistance. With the unique electrochemical redox properties of uric acid, the designed hydrogel sensor successfully realized the detection of uric acid in sweat with a wide detection range (1.0-100.0 μmol/L) and low detection limit (0.42 μmol/L). In this study, the dual detection of human motion and uric acid in sweat was successfully realized by the designed PVA/CNCs@PDA-Au nanocomposite hydrogel.

Injectable Self-Healing Antibacterial Hydrogels with Tailored Functions by Loading Peptide Nanofiber-Biomimetic Silver Nanoparticles.

Polymer hydrogels find extensive application in biomedicine, serving specific purposes such as drug delivery, biosensing, bioimaging, cancer therapy, tissue engineering, and others. In response to the growing threat of bacterial infections and the escalating resistance to conventional antibiotics, this research introduces a novel injectable, self-healing antimicrobial hydrogel comprising bioactive aldolized hyaluronic acid (AHA) and quaternized chitosan (QCS). This designed QCS/AHA hydrogel incorporates self-assembling peptide nanofibers (PNFs) and small-sized silver nanoparticles (AgNPs) for tailored functionality. The resulting hybrid QCS/AHA/PNF/AgNPs hydrogel demonstrates impressive rheological characteristics, broad-spectrum antimicrobial efficacy, and high biocompatibility. Notably, its antimicrobial effectiveness against Escherichia coli and S. aureus surpasses 99.9%, underscoring its potential for treating infectious wounds. Moreover, the rheological analysis confirms its excellent shear-thinning and self-healing properties, enabling it to conform closely to irregular wound surfaces. Furthermore, the cytotoxicity assessment reveals its compatibility with human umbilical vein endothelial cells, exhibiting no significant adverse effects. The combined attributes of this bioactive QCS/AHA/PNF/AgNPs hydrogel position it as a promising candidate for antimicrobial applications and wound healing.

Rosin-based self-healing functionalized composites with two-dimensional polyamide for antimicrobial and anticorrosion coatings

The design of polymer-based composites possessing good mechanical and self-healing properties remains a challenge in the development of high-performance self-healing materials. In this study, we used two-dimensional polyamide (2DPA), biomass rosin ester, and a dynamic crosslinking agent poly (urethane-urea) as raw materials, and prepared biomass rosin-based composites via in situ polymerization. The composites with 1 wt% 2DPA exhibited excellent self-healing properties (self-healing efficiency of 94 % after 24 h at 80 °C) and mechanical properties (tensile strength = 7.8 MPa). Moreover, the composites were applied to anticorrosion and antimicrobial coatings, which possessed excellent anticorrosion and antimicrobial properties. This study provides a new strategy for developing high-performance bio-based self-healing composites.

Ligand Dissociation of Metal-Complex Photocatalysts toward pH-Photomanipulation in Dynamic Covalent Hydrogels for Printing Reprocessable and Recyclable Devices.

Dynamic covalent hydrogels are gaining attention for their potential in smart materials, soft devices, electronics, and more thanks to their impressive mechanical properties, biomimetic structures, and dynamic behavior. However, a significant challenge lies in designing precise and efficient dynamic photochemistry for their preparation, allowing for complex structures and control over the dynamic process. Herein, we propose a general and straightforward orthogonal dynamic covalent photochemistry strategy for preparing high-performance printable dynamic covalent hydrogels, thereby broadening their advanced applications. This photochemical strategy uses a bifunctional photocatalyst to initiate radical polymerization and release ligands through a rapid light-mediated dissociation mechanism. This process leads to a controlled increase in system pH from mildly acidic to alkaline conditions within one hundred seconds, which in turn triggers the pH-sensitive model reactions of boronic acid/diol complexation and Knoevenagel condensation. The orthogonal photochemistry enables the formation of interpenetrated and conjoined networks, significantly enhancing the mechanical properties of the hydrogels. The reversible bonds formed during the process, i.e., boronic ester and unsaturated ketone bonds, confer excellent self-healing, reprocessable, and recyclable properties on the hydrogels through photochemical pH variations. Furthermore, this rapid, controlled fabrication process and dynamic behavior are highly compatible with printing techniques, enabling the design of adaptive and recyclable sensors with different structures. These advancements are promising for various material science, medicine, and engineering applications.

Self-healing glassy hybrids based on imidazole-functionalized silica nanoparticles with zinc complexes using dynamic and reversible cross-linking

Self-healing glass materials can potentially overcome the inherent limitations of glass, such as brittleness and difficulties in repairing broken sections while maintaining its critical properties. This paper reports a structural design and synthetic strategy for preparing glassy self-healing hybrids with high silica contents. The developed hybrids exhibited excellent self-healing properties based on dynamic and reversible crosslinking owing to the high density of zinc/imidazole units on the silica surface. First, core–shell silica nanoparticles with small multifunctional imidazole/butyl units (diameter: approximately10 nm) and good processability (homogeneous colloidal dispersions in common organic solvents) were synthesized. Afterwards, imidazole-functionalized silica nanoparticles were fabricated using Zn species to obtain self-healing hybrids with high silica contents (>60 wt%). These nanoparticles served as multifunctional and reversible crosslinking sites that dissipated energy, resulting in excellent mechanical, thermal, and healing characteristics. The obtained zinc/imidazole-based silica hybrids remain solid with high storage elasticity in the temperature range of 25–160 °C and high thermal stability corresponding to a 5 wt% weight loss above 280 °C, which were critical for self-healing glass applications. They also exhibited a moderate Young’s modulus of 330 MPa and a self-healing recovery efficiency of 87%. The findings of this study provide new insights into the roles of reversible interactions (metal/ligand exchange reactions) at particle–particle interfaces and high surface functionalities that serve as non-covalent crosslinking points. The prepared hybrids with high silica contents remain solid over a wide temperature range, which can open new avenues for self-healing glass materials.

Smart reconfigurable electromagnetic metamaterials based on thermadapt shape memory Poly(ethylene–vinyl acetate)

Smart reconfigurable metamaterials can better adapt to changing electromagnetic environments and broaden the range of applications. However, constructing electromagnetic reconfigurable metamaterials, especially those with large areas or applied to complex surfaces via a universal approach, is still a challenge. Here, we introduce a smart reconfigurable metamaterial consisting of a thermadapt shape memory polymer ethylene vinyl acetate copolymer (EVA) matrix and a flowable liquid–metal resonant unit. Based on the excellent self-healing properties of EVA, large-area metamaterials can be constructed by thermal assembly of metamaterial units. In addition, the original shape of the metamaterial can be reprogrammed to apply to complex three-dimensional surfaces with the reprocessing properties of EVA. Moreover, by utilizing the shape memory performance of the EVA, the temporary resonant frequency of the metamaterial can be set by programming and the resonant frequency tuning of the metamaterial can be controlled under external temperature stimulation, achieving noncontact tuning. In the future, this concept can be broadly applied in fields such as complex structure stealth layers and multifunction filters.

Rapid self-healing nanocomposite gel crosslinked by LDH for lost circulation control

Lost circulation presents a complex challenge in drilling operations. Ascribed to the favorable remaining in fracture, strong resistance to efflux, and entire gel block rather than individual particles, the self-healing gels have been broadly applied as lost circulation material (LCM). In this study, we utilized layered bimetallic hydroxide (LDH) as a dynamic crosslinking agent to synthesize a novel nanocomposite (NC) gel through in-situ polymerization following the stripping of LDH in acrylic acid (AA) solution. LDH/PAA NC gels exhibit excellent self-healing properties, rheological strength, mechanical properties and adhesion properties, with these attributes being influenced by the LDH content. At 110 °C, the optimal LDH/PAA NC gel rapidly self-healed in bentonite mud within 1 h, revealing storage modulus (G′) of 4041 Pa, tensile strength of 8.04 kPa, and adhesion strength of 2.1 kPa. Visual plugging tests revealed that the LDH/PAA NC gel could withstand pressures up to 4 MPa, surpassing the capabilities of MA gel, which lacked self-healing properties. These findings highlight the potential of LDH/PAA NC gels as efficient LCM, offering a promising solution for controlling lost circulation during drilling operations.

Biodegradable chitin nanofiber-alginate dialdehyde hydrogel: An injectable, self-healing scaffold for anti-tumor drug delivery

Injectable hydrogels fabricated from natural polymers have attracted increasing attentions for their potential in biomedical application owing to the biocompatibility and biodegradability. A new class of natural polymer based self-healing hydrogel is constructed through dynamic covalent bonds. The injectable self-healing hydrogels are fabricated by introducing alginate aldehyde to form Schiff base bonds with the chitin nanofibers. These hydrogels demonstrate excellent self-healing properties, injectability, and pH-responsive sol-gel transition behaviors. As a result, they can serve as carriers to allow an effective encapsulation of doxorubicin (DOX) for drug delivery. Furthermore, these hydrogels exhibit excellent biocompatibility and degradability in vitro and in vivo. The sustained release of DOX from the hydrogels effectively suppresses tumor growth in animal models without causing significant systemic toxicity, suggesting their potential application in anti-tumor therapies.