Carboxymethyl Cellulose Hydrogel Research Articles

Wood-inspired anisotropic hydrogel electrolyte with large modulus and low tortuosity realizing durable dendrite-free zinc-ion batteries

While aqueous zinc-ion batteries exhibit great potential, their performance is impeded by zinc dendrites. Existing literature has proposed the use of hydrogel electrolytes to ameliorate this issue. Nevertheless, the mechanical attributes of hydrogel electrolytes, particularly their modulus, are suboptimal, primarily ascribed to the substantial water content. This drawback would severely restrict the dendrite-inhibiting efficacy, especially under large mass loadings of active materials. Inspired by the structural characteristics of wood, this study endeavors to fabricate the anisotropic carboxymethyl cellulose hydrogel electrolyte through directional freezing, salting-out effect, and compression reinforcement, aiming to maximize the modulus along the direction perpendicular to the electrode surface. The heightened modulus concurrently serves to suppress the vertical deposition of the intermediate product at the cathode. Meanwhile, the oriented channels with low tortuosity enabled by the anisotropic structure are beneficial to the ionic transport between the anode and cathode. Comparative analysis with an isotropic hydrogel sample reveals a marked enhancement in both modulus and ionic conductivity in the anisotropic hydrogel. This enhancement contributes to significantly improved zinc stripping/plating reversibility and mitigated electrochemical polarization. Additionally, a durable quasi-solid-state Zn//MnO2 battery with noteworthy volumetric energy density is realized. This study offers unique perspectives for designing hydrogel electrolytes and augmenting battery performance.

Assessment of the ability of Pseudomonas aeruginosa and Staphylococcus aureus to create biofilms during wound healing in a rat model treated with carboxymethyl cellulose/carboxymethyl chitosan hydrogel containing EDTA.

The primary objective of this study was to develop a carboxymethyl cellulose (CMC) and carboxymethyl chitosan (CMCS) hydrogel containing ethylene diamine tetra acetic acid (EDTA) as the materials for wound healing. CMC and CMCS solutions were prepared with a concentration of 4% (w/v). These solutions were made using normal saline serum with a concentration of 0.5% (v/v). Additionally, EDTA with the concentrations of 0.01%, 0.05%, 0.1%, 0.5%, 1%, and 2% (w/v) was included in the prepared polymer solution. The analysis of the hydrogels revealed that they possess porous structures with interconnected pores, with average in size 88.71 ± 5.93 μm. The hydrogels exhibited a swelling capacity of up to 60% of their initial weight within 24 h, as indicated by the weight loss and swelling measurements. The antibacterial experiments showed that the formulated CMC/CMCS/EDTA 0.5% hydrogel inhibited the growth of Staphylococcus aureus and Pseudomonas aeruginosa. Moreover, the produced hydrogels were haemocompatible and biocompatible. At the last stage, the evaluation of wound healing in the animal model demonstrated that the use of the produced hydrogels significantly improved the process of wound healing. Finally, the findings substantiated the effectiveness of the formulated hydrogels as the materials for promoting wound healing and antibacterial agents.

Enhancing storage and gastroprotective viability of Lactiplantibacillus plantarum encapsulated by sodium caseinate-inulin-soy protein isolates composites carried within carboxymethyl cellulose hydrogel

Probiotics are subjected to various edible coatings, especially proteins and polysaccharides, which serve as the predominant wall materials, with ultrasound, a sustainable green technology. Herein, sodium caseinate, inulin, and soy protein isolate composites were produced using multi-frequency ultrasound and utilized to encapsulateLactiplantibacillus plantarumto enhance its storage, thermal, and gastrointestinal viability. The physicochemical analyses revealed that the composites with 5 % soy protein isolate treated with ultrasound at 50 kHz exhibited enough repulsion forces to maintain stability, pH resistance, and the ability to encapsulate larger particles and possessed the highest encapsulation efficiency (95.95 %). The structural analyses showed changes in the composite structure at CC, CH, CO, and amino acid residual levels. Rheology, texture, and water-holding capacity demonstrated the production of soft hydrogels with mild chewing and gummy properties, carried the microcapsules without coagulation or sedimentation. Moreover, the viability attributes ofL. plantarumevinced superior encapsulation, protecting them for at least eight weeks and against heat (63 °C), reactive oxidative species (H2O2), and GI conditions.

Facile in situ synthesis of CuO nanoparticles through the copper-crosslinked carboxymethylcellulose hydrogel bead: a potential implantable anticancer drug delivery system

Facile in situ synthesis of CuO nanoparticles through the copper-crosslinked carboxymethylcellulose hydrogel bead: a potential implantable anticancer drug delivery system

A Novel Nanofiber Hydrogel Adhesive Based on Carboxymethyl Cellulose Modified by Adenine and Thymine.

Natural polymer-based adhesive hydrogels have garnered significant interest for their outstanding strength and versatile applications, in addition to being eco-friendly. However, the adhesive capabilities of purely natural products are suboptimal, which hampers their practical use. To address this, we engineered carboxymethyl cellulose (CMC) surfaces with complementary bases, adenine (A) and thymine (T), to facilitate the self-assembly of adhesive hydrogels (CMC-AT) with a nanofiber configuration. Impressively, the shear adhesive strength reached up to 6.49 MPa with a mere 2% adhesive concentration. Building upon this innovation, we conducted a comparative analysis of the shear adhesion properties between CMC and CMC-AT hydrogel adhesives when applied to delignified and non-delignified wood chips. We examined the interplay between the adhesives and the substrate, as well as the role of mechanical interlocking in overall adhesion performance. Our findings offer a fresh perspective on the development of new biodegradable polymer hydrogel adhesives.

Curcumin Targeted Drug Delivery Using Iron Oxide Nanoparticle Incorporated Magnetic Responsive Carboxymethyl Cellulose Hydrogel

Curcumin Targeted Drug Delivery Using Iron Oxide Nanoparticle Incorporated Magnetic Responsive Carboxymethyl Cellulose Hydrogel

Formulation of double nanoemulsions based on pH-sensitive carboxymethyl cellulose /Starch copper doped carbon quantum dots for quercetin controlled release

Nanocomposite Hydrogels are versatile and adaptable in drug delivery, suitable for various administrations. They offer prolonged and regulated drug release which makes them valuable in targeting cancer treatments. This study used the water/oil/water approach to construct a drug nanocarrier. It encapsulated hazelnut oil, serving as a protective and organic membrane that enveloped the nanocarrier and regulated drug release. Quercetin (QC), a potent flavonoid with potential therapeutic applications, faces challenges due to its hydrophobic nature and poor solubility. This approach presents a novel approach to enhance QC's solubility and stability by integrating it with copper carbon quantum dots (Cu-CQDs) into a pH-sensitive carboxymethyl cellulose (CMC) and starch-based hydrogel nanocomposite. This system aims to improve QC delivery while minimizing adverse effects. The nanocomposite exhibited exceptional drug loading and encapsulation efficiencies of 47.00 % ± 0.45 and 86.25 % ± 0.75, respectively, ranking among the top-reported values for similar systems. Fourier-transform infrared spectroscopy (FTIR) was used to examine molecular interactions. X-ray diffraction (XRD) assessment demonstrated the presence of components beneficial for drug solubility enhancement at 2Θ = 17–24°, where QC's crystalline peaks are absent from the CMC/Starch/Cu-CQDs@QC XRD pattern. A particle size of 151.57 ± 37 nm is optimized for selectively targeting cancer cells, minimizing interaction with healthy cells, as revealed through DLS assessment. Morphological characteristics analyzed by FE-SEM support this observation as well. Zeta potential measurement (+38.8 mV) highlights nanocarrier stability. CMC/Starch/Cu-CQDs@QC displayed remarkable cytotoxicity against cancerous cells, reducing U87-MG cell viability to 48 % while maintaining high cell viability (92 %) for normal L929 cells. These results emphasize the promise of this nanocomposite as a QC drug delivery system by indicating improved anticancer efficacy with fewer adverse effects.

Carboxymethyl cellulose and gelatin composite hydrogel for environmentally friendly urea delivery

The global agricultural expansion drives a rising demand for urea-based fertilizers, yet the widespread issue of rapid leaching challenges farmers, diminishing efficacy. This study aimed to develop a hybrid hydrogel from carboxymethyl cellulose (CMC) and pharmaceutical waste gelatin (GE), using glutaraldehyde (GA) as a cross-linking agent for slow release of urea fertilizer. The effects of CMC to GE mass ratios, GA concentration, and urea loading methods on hydrogel production were studied. CMC and GE solutions were mixed, cross-linked for 24 h at room temperature, and dried at 60 °C for 48 h. SEM analysis revealed increased urea particles in the hydrogel with higher urea content. FT-IR spectroscopy confirmed CMC, GE, and urea presence, with the urea functional group becoming more apparent as the urea content increased. Higher GA concentrations resulted in slower urea release in water. The best sample was the 1:3 CMC:GE-5 G/6 U, with a CMC to GE ratio of 1:3, a GA concentration of 5% by volume, and the direct addition of 6 g of urea during hydrogel formation. This sample had a urea loading of 51.25% and cumulative release of 80.71%. Notably, it exhibited sustained urea release over 17 cycles compared to commercial urea’s three cycles.

Fabrication of CMC/PVA/Dextrin-Based Polymeric Membrane for Controlled Release of Cefixime With Enhanced Antibacterial Activity.

This study focuses on the investigation of the significance of polymers in drug delivery approaches. The carboxymethyl cellulose (CMC), polyvinyl alcohol (PVA) and dextrin-based hydrogel membrane were prepared and employed for the sustained release of third-generation oral antibiotic (cefixime). Different proportions of CMC, PVA and dextrin were blended and hydrogel membranes were fabricated via solvent casting method. The prepared membrane was characterized by FTIR, SEM, UV-visible, TGA and swelling analysis. Cefixime drug was incorporated in the CMC/PVA/dextrin matrix and drug release was investigated. The sustained release of the tested drug (cefixime) was investigated and the drug was released in 120 min in the phosphate-buffered saline (PBS) solution. The antibacterial activity of the prepared membrane was promising against Proteus vulgaris, salmonella typhi, Escherichia coli and Bacillus subtilis strains. The swelling capabilities, thermal stability and non-toxic nature of the prepared CMC/PVA/dextrin membrane could have potential applications for cefixime drug in delivery in a controlled way for the treatment of infectious diseases.

Construction of strain responsive Ti-containing carboxymethyl cellulose hydrogel with transitional coordination precursor

Due to marvelous sensitivity and flexibility, conductive hydrogels are popularly used as strain sensors in intelligent skin and wearable electronic devices fields. However, hydrogel tends to be destroyed after long-term use or in accident, leading to performance degradation. Herein, we developed an environmental-friendly Ti-containing conductive hydrogel. The hydrogel network was constructed via a simple two-step method with coordination reaction and amidation reaction based on a metal ion precursor from transitional coordination. The synergies of reversible metal coordination bonds and dynamic hydrogen bonds endowed the hydrogel with excellent self-healing properties (3 h, 93.66 %), tensile properties (136.46 kPa), compression properties (1.122 MPa), and anti-fatigue performance. At the same time, the hydrogel showed excellent self-adhesion, even underwater. Due to Ti4+, electrical conductivity of the hydrogel was visibly enhanced (σ = 25.64 mS·cm−1), which resulted in fast response (TS [time sensitivity] = 24.78 s−1) and short recovery time (153 ms). As a flexible strain sensor, the hydrogel with stable conductivity and high sensitivity could precisely detect and distinguish a series of human motions, even different letter pronunciations. These remarkable features make it a promising application in the fields of intelligent skin and wearable electronic devices.

NIR-responsive carboxymethyl-cellulose hydrogels containing thioketal-linkages for on-demand drug delivery system

Near-infrared (NIR) light-responsive hydrogels have emerged as a highly promising strategy for effective anticancer therapy owing to the remotely controlled release of chemotherapeutic molecules with minimal invasive manner. In this study, novel NIR-responsive hydrogels were developed from reactive oxygen species (ROS)-cleavable thioketal cross-linkers which possessed terminal tetrazine groups to undergo a bio-orthogonal inverse electron demand Diels Alder click reaction with norbornene modified carboxymethyl cellulose. The hydrogels were rapidly formed under physiological conditions and generated N2 gas as a by-product, which led to the formation of porous structures within the hydrogel networks. A NIR dye, indocyanine green (ICG) and chemotherapeutic doxorubicin (DOX) were co-encapsulated in the porous network of the hydrogels. Upon NIR-irradiation, the hydrogels showed spatiotemporal release of encapsulated DOX (>96 %) owing to the cleavage of thioketal bonds by interacting with ROS generated from ICG, whereas minimal release of encapsulated DOX (<25 %) was observed in the absence of NIR-light. The in vitro cytotoxicity results revealed that the hydrogels were highly cytocompatible and did not induce any toxic effect on the HEK-293 cells. In contrast, the DOX + ICG-encapsulated hydrogels enhanced the chemotherapeutic effect and effectively inhibited the proliferation of Hela cancer cells when irradiated with NIR-light.

Insitu synthesis of gold nanospheres immobilised carboxymethyl cellulose-based conductive hydrogel bioink for 3D bioprinting technology

Electrically conductive bioink (ECB) improves the cellular electrical coupling which increases the propagation of cells in bioprinted 3D scaffolds for developing biomimetic architectures. The preparation of ECB predominantly relies on synthetic organic polymers and inorganic nanomaterials, which have certain limitations such as cytotoxicity, weak mechanical stability, and non-biodegradability. The current study focuses on synthesising an ECB immobilised with gold nanospheres (GNS) within the carboxymethyl cellulose (CMC) polymer to eliminate the drawbacks of ECB preparation. Insitu reduction of gold into stable gold nanoparticles within the CMC hydrogel polymer matrix imparted better conductivity without compromising the bioink properties for 3D bioprinting technology.

Expression of concern: Decoration of graphene oxide nanosheets with carboxymethylcellulose hydrogel, silk fibroin and magnetic nanoparticles for biomedical and hyperthermia applications

Expression of concern for ‘Decoration of graphene oxide nanosheets with carboxymethylcellulose hydrogel, silk fibroin and magnetic nanoparticles for biomedical and hyperthermia applications’ by Mostafa Ghafori Gorab et al., Nanoscale Adv., 2023, 5, 153–159, https://doi.org/10.1039/D2NA00394E.

L-Carnosine loaded on carboxymethyl cellulose hydrogels for promoting wound healing.

Wound management remains a challenge in clinical practice. Nowadays, patients have an increasing demand for wound repair with enhanced speed and quality; therefore, there is a great need to seek therapeutic strategies that can promote rapid and effective wound healing. In this study, we developed a carboxymethyl cellulose hydrogel loaded with l-carnosine (CRN@hydrogel) for potential application as a wound dressing. In vitro experiments confirmed that CRN@hydrogel can release over 80% of the drug within 48 h and demonstrated its favorable cytocompatibility and blood compatibility, thus establishing its applicability for safe utilization in clinical practice. Using a rat model, we found that this hydrogel could promote and accelerate wound healing more effectively. These results indicate that the novel hydrogel can serve as an efficient therapeutic strategy for wound treatment.

Injectable multifunctional hydrogel containing Sphingosine 1-phosphate and human acellular amniotic membrane for skin wound healing.

The skin serves as the main defense barrier, protecting against injuries, and preventing infection and water loss. Consequently, wound healing and skin regeneration are crucial aspects of wound management. A novel hydrogel scaffold was developed by incorporating carboxymethyl cellulose (CMC) and gelatin (Gel) hydrogels cross-linked with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) containing Sphingosine 1-phosphate (S1P). This hydrogel is applied topically to treat acute wounds and is covered with a human acellular amniotic membrane (hAAM) as a secondary dressing. The scaffold was subjected to in vitro cell viability, red blood cell hemolysis, blood clotting index, and in vivo assays. Real-time PCR was implemented to verify the expression of genes involved in skin wounds. The physical and chemical properties of the scaffolds were also tested using weight loss, swelling ratio, scanning electron microscopy (SEM), Fourier transform infrared (FTIR), and mechanical tensile analysis. The synthetic scaffold is biocompatible as evidenced by the high percentage of 3T3 cell viability (127%) after 72 hr. Additionally, excellent hemocompatibility with a low hemolytic effect (2.26%) was observed. Our in vivo wound healing assay demonstrated that CMC/Gel/S1P/hAAM wound dressing led to faster wound healing in treated rats compared to the control group over 14.Also, the mechanical tests showed that the amniotic membrane and the hAAM had very different Young's modulus and elongation at break values. This study demonstrates the effectiveness of the CMC/Gel/EDC hydrogel with S1P as a wound dressing. Additionally, hAAM exhibits excellent characteristics as a protective layer for the treatment of acute wounds.

Sustainable bioelectronics fabrication through photo-induced swelling of green hydrogels

Electrical circuit manufacture for flexible electronics is a very specialized printing process in which electrically functional inks are printed onto a substrate. In almost all cases, the substrate assumes a passive role in ink distribution, which has been the conventional methodology used up until now. Herein we have discovered that a sodium carboxymethyl cellulose (CMCNa) hydrogel substrate demonstrates heightened susceptibility to UV photo-irradiating and because of molecular-level bond lability that leads to a macroscopic improved swelling (“writing” action). The localized photo-activated events lead to temporary 3D contours on the hydrogel substrate where conductive ink is held in valleys to allow the formation of conductive traces. A self-distribution of ink in the valleys is achieved which, moreover, is a type of mask-based photolithography or digital image generation. The process can be employed for polymeric inks such as PEDOT:PSS to obtain ink patterns without need of complex inkjet printers or other conventional printers. The drying causes recession of the temporary swollen hydrogel contours and returns the surface to flattened format. The process works at lower ink solids of 0.125 % and has shown that 1.15 J/mm2 of UV energy is capable of creating an electrically isolated conductive pattern. Initial water content of the system plays an important role in which 20 g/g of absorbed water/substrate is sufficient for acceptable pattern generation.

Tailoring the rheological properties of biosynthesized Copper oxide nanoparticles decorated Carboxymethyl cellulose hydrogels for biomedical applications

Nanoparticle-decorated hydrogels have seized substantial momentum in recent years, exclusively in biomedical research. In this investigation, Copper oxide nanoparticles decorated carboxymethyl cellulose hydrogels were prepared in an eco-friendly approach without using toxic cross-linkers. Initially, Copper oxide nanoparticles were prepared by biosynthesis approach to diminish the harmful effects of chemicals and to improve the biological activities using the leaf extract of Justicia adhatoda. The prepared nanoparticles were incorporated into the Carboxymethyl solution and carbopol to form a hydrogel by non-covalent interactions. X-ray diffraction analysis of CuO nanoparticles revealed a monoclinic crystalline structure without impurity. Rheological investigation of the pure hydrogel and CuO-decorated hydrogels revealed that CuO contributed to the enhancement of the hydrogel's mechanical performance. All the hydrogels demonstrated shear thinning behavior and better flow behavior index with the addition of CuO nanoparticles. The yield stress of the hydrogels was improved and found to be in the range of 61–79 Pa, which matches the ideal yield stress values in transdermal drug delivery. Storage moduli of hydrogels as a function of frequency was doubled (14–47.5 Pa), endorsing the involvement of CuO nanoparticles in crosslinking the polymeric matrix. Temperature and time sweep measurements revealed that the stability of the hydrogels also improved with the addition of CuO nanoparticles. The antibacterial activity of the hydrogels was evaluated using biofilm inhibition and showed better inhibition of 70 ± 0.5%, 75 ± 0.9%, 86 ± 0.8%, and 83 ± 0.8% against Escherichia coli, Klebsiella pneumonia, Staphylococcus aureus, and Enterococcus faecalis, respectively with increased concentration of CuO nanoparticles. The cell viability of the CuO-decorated hydrogels against MCF-7 and A431 was found to be 39% and 42%, respectively. Therefore, the eco-friendly biosynthesized CuO nanoparticles decorated hydrogels with improved mechanical properties can be employed in injectable and transdermal drug delivery systems.

Phytic acid-modified carboxymethyl cellulose hydrogel for uranium adsorption from aqueous solutions

Phytic acid-modified carboxymethyl cellulose (CMC-PA) has been investigated as a promising adsorbent for the removal of uranium from aqueous solutions. The synthesis of CMC-PA involves the hydrogen bonding interaction between CMC and PA, resulting in the incorporation of PA groups onto the cellulose backbone. The hydrophilicity, reusability and adsorption capacity of the prepared CMC-PA hydrogel have improved with the increase of PA content. Moreover, the adsorption experiments were conducted by varying parameters such as pH, initial uranium concentration, and contact time. The results showed that CMC-PA exhibited excellent uranium adsorption performance, with a theoretical maximum adsorption capacity of 436 mg/g. In addition, the material exhibits excellent reusability, and the reusability improves with the increase of crosslinking density, indicating that the crosslinking structure of the polymer gel can effectively enhance the structural stability of the material. Furthermore, CMC-PA also exhibits high selective adsorption performance towards uranium ions in the presence of various competing ions. Its high adsorption capacity, reusability, and selectivity make it a promising candidate for high-performance uranium ion adsorbents.

Application of cathodic protection method on steel structures using sacrificial anode and sodium polyacrylate-sodium carboxymethyl cellulose (PANa–CMC) hydrogel electrolyte

An ionically conductive sodium polyacrylate-sodium carboxymethyl cellulose (PANa–CMC) hydrogel electrolyte was developed for the sacrificial anode cathodic protection (SACP) of carbon steel in high-humidity environments. The incorporation of varying ratios of CMC into hydrogel formulation enhanced the water retention capacity, adhesion strength, and electrochemical performance, making it suitable for SACP applications. Particularly, PANa-5% CMC hydrogels demonstrated a current density of approximately 3 μA/cm², inhibited passive corrosion product formation, and sequestered metal ions from anodes, thus minimizing contamination. These findings highlight the substantial potential of PANa–CMC hydrogels as electrolytes, expanding the application of the SACP method to atmospheric environments.

Carboxymethylcellulose hydrogels with stable carbon quantum dots: Enabling dynamic fluorescence modulation, automatic erasure, and secure information encryption

Inspired by “disappear after reading”, a time-modulated encryption hydrogel was synthesized by carboxymethyl cellulose with carbon quantum dots. Carboxymethyl cellulose in this system stabilized carbon quantum dots, which ensured the whole hydrogel worked well. The encryption/decryption of information depended on pH adjustment, application of EDTA and Cr (VI). Furthermore, an in-depth analysis of the fluorescence change mechanism uncovered that fluorescence quenching was potentially influenced by internal filtering effects and static quenching, which involved the amino, carboxyl, and hydroxyl groups present within the hydrogel.