Search Results (62)

Clays, historically employed in traditional medical practices, have recently gained prominence within contemporary biomedical science, especially in the context of wound healing, due to advancements in nanotechnology and materials science. This review article investigates the physicochemical characteristics, biological processes, and therapeutic functions of clay materials—including bentonite, halloysite nanotubes, palygorskite, sepiolite, and synthetic clays like Laponite—in diverse wound-healing applications. These materials play a crucial role in the wound-healing process, including stopping bleeding, controlling inflammation, protecting against infection, and rebuilding tissue. They work through both passive and active methods. The layered or fibrous structure of these materials allows for efficient drug loading, controlled release, and mechanical support when used in hydrogels, films, and advanced drug delivery systems. Preclinical and initial clinical investigations have substantiated the biocompatibility, antimicrobial properties, and regenerative capabilities of these systems, although they have also revealed several challenges concerning toxicity, regulatory categorization, and standardization. Consequently, clay-based systems present a potentially valuable multifunctional platform for advancing next-generation wound-treatment therapies, necessitating additional translational and clinical research. Full article

Kaolinite-group minerals and kaolin rock occupy a distinct position in cultural heritage conservation. They occur both as original constituent materials and as components of conservation treatments. This review critically synthesizes the scattered literature on their use in the conservation of cultural heritage objects. It highlights the structure–property–performance relationships, including composition, particle morphology, pore structure, water retention, sorption properties, moisture transport, and residue formation on heritage substrates. Kaolin-based poultices are useful for desalination and cleaning where pore-size distribution, drying conditions, and application parameters can be controlled. Kaolinite and metakaolinite are mainly used in consolidation, the first acting as mineral filler/scaffold and the second as a reactive pozzolanic component, while halloysite is a potential nanocontainer for controlled release. This review highlights that kaolinite-group minerals should not be treated as generic clays, inert fillers, or automatically sustainable additives and particular attention should be given to issues of reversibility, formulation design, performance testing, long-term durability, and residue assessment, as well as to emerging data on toxicity and environmental impact. Future research should prioritize comparative testing, long-term field monitoring, and predictive modelling, alongside clearer assessment of health, environmental and sustainability impacts, to support evidence-based, sustainable use of kaolinite-group minerals in cultural heritage conservation practice. Full article

Halloysite nanotubes (HNTs), composed of an aluminosilicate framework, are naturally abundant, biocompatible, and sustainable clay minerals with a tubular morphology and tunable surface chemistry, making them attractive platforms for targeted, multifunctional drug delivery systems. In this study, a zinc ferrite integrated halloysite nanocomposite (ZnFe₂O₄/HNT) was developed via a one-pot synthesis approach for sustained release of cisplatin (Cp), aiming to reduce systemic toxicity and enhance cell-specific activity. The nanocomposites were further functionalized by integrating Cp (Cp: ZnFe₂O₄/HNT ratio 0.05) and folic acid (ZnFe₂O₄/HNT/Cp: FA ratio 0.05), followed by PEGylation (0.17 µL/mg of ZnFe₂O₄/HNT/Cp/FA/PEG). The structural and surface characteristics, phase, interfacial interactions (FA and Cp), and colloidal stability of nanoformulations were systematically investigated using powder X-ray diffraction analysis (XRD), Fourier transformed infrared (FT-IR) spectroscopy, zeta potential analysis, scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS), high-resolution transmission electron microscopy (HRTEM), and diffuse reflectance UV–visible (DRS-UV-Vis) spectroscopy. The results confirmed that ZnFe₂O₄ integration preserved the clay’s tubular framework while inducing nanocrystallization of both ferrite and cisplatin, indicating molecular dispersion within the clay matrix. Functionalization with FA (ZnFe₂O₄/HNT/Cp/FA) promoted amide bond linkage, modulated Cp-FA interactions, and significantly enhanced cumulative Cp release compared to the non-functionalized system ZnFe₂O₄/HNT/Cp (10.3% at 72 h vs. 34.4% at 72 h) under tumor acidic conditions (pH 6.6). PEGylation maintained the controlled release profile while improving dispersion stability. In vitro cytotoxicity studies revealed that FA-conjugated nanocomposites exhibited enhanced, time-dependent anticancer activity against HeLa cervical cancer cells, with reduced toxicity toward normal fibroblasts, indicating preferential cellular uptake via folate receptor-mediated mechanism. Overall, this work demonstrates that FA-functionalized ZnFe₂O₄/HNT nanocomposite provides an effective clay-based platform for modulating Cp release and enhancing folate receptor protein-mediated targeted therapy for cervical cancer. Full article

This study reports the preparation of alginate (Alg) beads incorporating different amounts of halloysite nanotubes (HNTs) and kaolin (K) in the presence of Ca²⁺ ions to compare their drug loading and release behaviors. The resulting composites, HNTs@Alg and K@Alg, were characterized using FTIR, SEM–EDS, XRD, and XPS analyses. Chlortetracycline hydrochloride (CTC) was employed as a model antibiotic to evaluate their drug delivery performance. The concentration of Alg and the incorporation of HNTs or K markedly influenced the adsorption capacity and release profile. The maximum drug loading capacities were 48.12 ± 1.4 mg/g for HNTs, 40.1 ± 1.2 mg/g for K, 59.85 ± 2.3 mg/g for HNTs@Alg-1 (1 g HNTs and 1% Alg), and 68.74 ± 2.1 mg/g for K@Alg-1 (1 g K and 1% Alg). The inclusion of Alg enhanced sustained release, extending beyond 100 h. Among the composite beads, HNTs@Alg-1 showed superior CTC release behavior compared to K@Alg-1. Furthermore, antibacterial assays confirmed that the CTC-loaded beads effectively inhibited E. coli and S. aureus, demonstrating maintained drug activity after encapsulation. Both systems effectively prolonged CTC release and exhibited antibacterial efficacy, highlighting their potential as controlled drug delivery matrices for wound treatment applications. Full article

The development of advanced wound dressings that integrate favorable physico-mechanical properties with the ability to support physiological healing processes remains a critical challenge in biomaterials science. An ideal dressing should modulate the wound microenvironment, prevent infection, maintain hydration, and possess adequate strength and elasticity. This study aimed to fabricate and characterize electrospun chitosan (CS)-based 3D scaffolds dual-reinforced with halloysite nanotubes (HNTs) and cerium oxide nanoparticles (CeONPs) to enhance material properties and biological performance. HNTs were incorporated to improve electrospinnability and provide mechanical reinforcement, while CeONPs were added for their redox-modulating and anti-inflammatory activities. Composite mats were fabricated via non-capillary electrospinning. The individual and synergistic effects of HNTs and CeONPs were systematically evaluated using physico-chemical methods (SEM, EDX, WAXS, TGA, mechanical testing) and biological assays (in vitro cytocompatibility with mesenchymal stem cells, in vivo biocompatibility, and wound healing efficacy in a rat model). Scaffolds containing only HNTs exhibited defect-free nanofibers with an average diameter of 151 nm, whereas the dual-filler (CS-PEO-HNT-CeONP) composites showed less uniform fibers with a rough surface and a larger average diameter of 233 nm. The dual-filler system demonstrated significantly enhanced mechanical properties, with a Young’s modulus nearly double that of pure CS mats (881 MPa vs. 455 MPa), attributed to strong interfacial interactions. In vivo, the CS-PEO-HNT-CeONP scaffolds degraded more slowly, promoted earlier formation of a connective tissue capsule, and elicited a reduced inflammatory response compared to single-filler systems. Although epithelialization was temporarily delayed, the dual-filler composite ultimately facilitated superior tissue regeneration, characterized by a more organized, native-like collagen architecture. The synergistic combination of HNTs and CeONPs within a CS matrix yields a highly promising scaffold for wound management, offering a unique blend of tailored biodegradability, enhanced mechanical strength, and the ability to guide healing towards a regenerative rather than a fibrotic outcome, particularly for burns and traumatic injuries. Full article

Background: Poor water solubility is a major limitation for the therapeutic use of many anticancer drugs. In this study, we report the design and development of two halloysite-based hybrid nanomaterials for the encapsulation and delivery of hydrophobic and positively charged drugs. Methods: A novel multicavity platform was obtained by covalently grafting calix[5]arene macrocycles onto the external surface of halloysite nanotubes (HNTs), combining lumen encapsulation with supramolecular host–guest recognition. PB4, a planar and hydrophobic pyridinium salt with significant antiproliferative activity, was selected as a model compound. Both PB4-loaded HNTs (HNTs/PB4) and calixarene-functionalized HNTs (HNTs-Calix/PB4) were incorporated into Laponite^®-based thixotropic hydrogels to obtain injectable and biocompatible systems. Results: The nanomaterials were thoroughly characterized, and their loading efficiency, release behavior, and aqueous dispersibility were evaluated. Antiproliferative tests on MCF-7 cells demonstrated that both hydrogels retained PB4 activity, with distinct release profiles: the pristine HNTs allowed faster drug availability, while calix[5]arene-functionalized systems promoted sustained release. Conclusions: This work introduces the first example of covalently calixarene-functionalized halloysite and presents a versatile drug delivery platform adaptable to different therapeutic contexts and combination strategies. Full article

Lung cancer is the leading cause of cancer mortality worldwide, with a poor prognosis driven by late diagnosis, systemic toxicity of existing therapies, and rapid development of multidrug resistance (MDR) to agents such as paclitaxel and cisplatin. MDR arises through multiple mechanisms, including overexpression of efflux transporters, alterations in apoptotic pathways, and tumour microenvironment-mediated resistance. The application of nanotechnology offers a potential solution to the aforementioned challenges by facilitating the enhancement of drug solubility, stability, bioavailability, and tumour-specific delivery. Additionally, it facilitates the co-loading of agents, thereby enabling the attainment of synergistic effects. Halloysite nanotubes (HNTs) are naturally occurring aluminosilicate nanocarriers with unique dual-surface chemistry, allowing hydrophobic drug encapsulation in the positively charged lumen and functionalisation of the negatively charged outer surface with targeting ligands or MDR modulators. This architecture supports dual-delivery strategies, enabling simultaneous administration of phytocannabinoids and chemotherapeutics or efflux pump inhibitors to enhance intracellular retention and cytotoxicity in resistant tumour cells. HNTs offer additional advantages over conventional nanocarriers, including mechanical and chemical stability and low production cost. Phytocannabinoids such as cannabidiol (CBD) and cannabigerol (CBG) show multitarget anticancer activity in lung cancer models, including apoptosis induction, proliferation inhibition, and oxidative stress modulation. However, poor solubility, instability, and extensive first-pass metabolism have limited their clinical use. Encapsulation in HNTs can overcome these barriers, protect against degradation, and enable controlled, tumour-targeted release. This review examined the therapeutic potential of HNT-based phytocannabinoid delivery systems in the treatment of lung cancer, with an emphasis on improving therapeutic selectivity, which represents a promising direction for more effective and patient-friendly treatments for lung cancer. Full article

Supported Pd-based catalysts have been widely applied in the hydrogenation of specific functional groups. Recent trends have focused on employing Pd-based heterogeneous catalysts supported on inorganic nanotubes, wherein inner surface functionalization modulates both palladium nanoparticle (Pd-NP) dispersion and the interaction between reactants and the catalyst surface, thereby influencing catalytic properties. This study aims to develop a catalytic system using amine-lumened halloysite nanotubes immobilizing Pd-NPs (Pd/HNTA) as catalysts for hydrogenation reactions. The formation of Pd-NPs within the organo-functionalized lumen—modified by 3-aminopropyltrimethoxysilane—is confirmed by transmission electron microscopy (TEM) imaging, which reveals a particle size of 2.2 ± 0.4 nm. For comparison, Pd-NPs supported on pristine halloysite (Pd/HNTP) were used as control catalysts, displaying a metal particle size of 2.8 ± 0.8 nm and thereby demonstrating the effect of organic functionalization on the halloysite nanotubes. Both catalysts were employed in the hydrogenation of furfural (FUR) and nitrobenzene (NB) as model reactions. Pd/HNTA demonstrated superior catalytic performance for both substrates, with TOF values of 880 h⁻¹ for FUR and 946 h⁻¹ for NB, and selectivities exceeding 98% for tetrahydrofurfuryl alcohol (THFOH) and aniline (AN), respectively. However, recyclability studies displayed that Pd/HNTA was deactivated at the 10 catalytic cycles during the hydrogenation of FUR, whereas, in the hydrogenation of NB, 5 catalytic cycles were achieved with maximum conversion and selectivity at 360 min. These results revealed that the liquid-phase environment plays a pivotal role in catalyst stability. In the hydrogenation of NB, the coproduction of H₂O adversely affects the interaction between the Pd particles and the inner amine-modified surface, increasing the deactivation of the catalyst with reuse. Thus, the Pd/HNTA catalyst holds significant promise for the development of noble-metal-based catalysts and their application in the transformation of other reducible organic functional groups via hydrogenation reaction. Full article

The wastewater from Chemical Mechanical Polishing (CMP) generated in the semiconductor industry contains a significant concentration of suspended particles and necessitates rigorous treatment to meet environmental standards. Ceramic ultrafiltration membranes offer significant advantages in treating such high-solid wastewater, including a high separation efficiency, environmental friendliness, and straightforward cleaning and maintenance. However, the preparation of high-precision ceramic ultrafiltration membranes with a smaller pore size (usually <20 nm) is very complicated, requiring the repeated construction of transition layers, which not only increases the time and economic costs of manufacturing but also leads to an elevated transport resistance. In this work, halloysite nanotubes (HNTs), characterized by their high aspect ratio and lumen structure, were utilized to create a high-porosity transition layer using a spray-coating technique, onto which a γ-Al₂O₃ ultrafiltration selective layer was subsequently coated. Compared to the conventional α-Al₂O₃ transition multilayers, the HNTs-derived transition layer not only had an improved porosity but also had a reduced pore size. As such, this strategy tended to simplify the preparation process for the ceramic membranes while reducing the transport resistance. The resulting high-flux γ-Al₂O₃ ultrafiltration membranes were used for the high-efficiency treatment of CMP wastewater, and the fouling behaviors were investigated. As expected, the HNTs-mediated γ-Al₂O₃ ultrafiltration membranes exhibited excellent water flux (126 LMH) and high rejection (99.4%) of inorganic particles in different solvent systems. In addition, such membranes demonstrated good operation stability and regeneration performance, showing promise for their application in the high-efficiency treatment of CMP wastewater in the semiconductor industry. Full article

This study presents a sustainable strategy to enhance polymer encapsulation, adsorption, and functional properties by chemically modifying sodium alginate with hydrophobic groups. Hydrophobic alginate derivatives were synthesized via a solvent-free method using hexadecyl trimethylammonium bromide, resulting in nanoparticles capable of effectively capturing non-polar compounds. To further improve compatibility within alginate-based biocomposites, halloysite nanotubes were modified through ball milling and surfactant-assisted treatments. The resulting nanocomposites (MBHA and MHHA) exhibited significantly enhanced adsorption and controlled release behavior, as confirmed by FTIR analysis of hexadecyl alginate ester conjugation. Vitamin D₃ adsorption followed the Langmuir isotherm, with high correlation coefficients (R² = 0.998 for MBHA and R² = 0.991 for MHHA), indicating monolayer adsorption on a homogenous surface. Kinetic modeling revealed that the adsorption process adhered to a pseudo-second-order model (R² = 0.9969 for MBHA and R² = 0.999 for MHHA), suggesting that chemisorption was the dominant rate-controlling mechanism. These results demonstrate the critical role of surface modification in designing nano-engineered biopolymers with superior adsorption, stability, and release profiles, offering sustainable applications in medicine, agriculture, and environmental remediation. Full article

In multi-layered wood materials, varying rates of dimensional changes can easily lead to cracking, which can have a negative impact on their structure and functionality. This study focuses on cracking issues of decorated blockboard caused by moisture content changes. First, surface cracks on the decorated blockboard were observed and classified using optical microscopy and scanning electron microscopy (SEM). Second, from modeling perspectives, the critical tensile strength of the surface of the decorated blockboard was predicted to be 16.93 MPa, providing guidance for crack-resistant modification. Subsequently, halloysite nanotubes (HNTs) were incorporated into MF-resin-impregnated paper, achieving a Grade 5 crack resistance for decorated blockboard. The interaction between HNTs and MF resin forms a multiscale stress–dispersion system, as confirmed by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD), indicating hydrogen and covalent bonding between HNTs and the MF resin. With a 5% HNTs addition, the tensile strength and strain break of the MF-resin-impregnated paper reached 36.60 MPa and 1.12%, respectively, representing increases of 97.39% and 60.00%, respectively, effectively preventing surface cracking. This has significant implications for improving the durability and performance of decorated blockboard in practical applications. Full article

The application of electrospinning technologies for the preparation of mats based on mucoadhesive polysaccharides, such as chitosan (CS), is an attractive strategy for the development of biopolymeric delivery systems for topical corticosteroids. In this work, an electrospinning technique is described for the preparation of CS-based mats doped with halloysite nanotubes (HNTs) with modified release of clobetasol propionate (CP). The optimized composition of the electrospinning solution was determined: 2.4% solution of CS in 46% acetic acid with addition of PEO (10% of CS mass) and HNTs (5% of CS mass); CP was introduced as an ethanol solution at the rate of 2 mg CP per 1 g of the obtained nonwoven material. The process parameters (the electrospinning voltage of 50–65 kV, the rotation speed of the spinning electrode of 10 min⁻¹, and the distance between the electrodes of 24 cm) were also optimized. The developed technology allowed us to obtain homogeneous nanofiber mats with excellent mechanical properties and biphasic drug release patterns (66% of CP released within 0.5 h and 88% of CP released within 6 h). The obtained nanofiber mats maintained the anti-inflammatory activity of corticosteroid at the level of free CP and showed no cytotoxicity. Full article

Background/Objectives: The development of therapies targeting unregulated Src signaling through selective kinase inhibition using small-molecule inhibitors presents a significant challenge for the scientific community. Among these inhibitors, pyrazolo[3,4-d]pyrimidine heterocycles have emerged as potent agents; however, their clinical application is hindered by low solubility in water. To overcome this limitation, some carrier systems, such as halloysite nanotubes (HNTs), can be used. Methods: Herein, we report the development of HNT-based nanomaterials as carriers for pyrazolo[3,4-d]pyrimidine molecules. To achieve this objective, the clay was modified by two different approaches: supramolecular loading into the HNT lumen and covalent grafting onto the HNT external surface. The resulting nanomaterials were extensively characterized, and their morphology was imaged by high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM). In addition, the kinetic release of the molecules supramolecularly loaded into the HNTs was also evaluated. QSAR studies were conducted to elucidate the physicochemical and pharmacokinetic properties of these inhibitors, and structure-based virtual screening (SBVS) was performed to analyze their binding poses in protein kinases implicated in cancer. Results: The characterization methods demonstrate successful encapsulation of the drugs and the release properties under physiological conditions. Furthermore, QSAR studies and SBVS provide valuable insights into the physicochemical, pharmacokinetic, and binding properties of these inhibitors, reinforcing their potential efficacy. Conclusions: The cytotoxicity of these halloysite-based nanomaterials, and of pure molecules for comparison, was tested on RT112, UMUC3, and PC3 cancer cell lines, demonstrating their potential as effective agents for prostate and bladder cancer treatment. Full article

Controlled drug delivery is a key strategy aimed at reducing both the frequency of therapeutic dosages and potential systemic side effects, particularly in the case of high drug concentrations. The nanocomposite hydrogel systems presented in this study were synthesized by combining carboxymethyl cellulose, polyvinyl alcohol, and (3-aminopropyl)triethoxysilane-functionalized halloysite nanotubes (fHNTs). This hydrogel system is a potential candidate for the controlled release of cefadroxil monohydrate. These hydrogels are analyzed by Fourier transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, and rheological measurements. Additionally, swelling properties, porosity, hydrophilicity, drug release, and in vitro and in vivo analyses were also evaluated. The observed trends in swelling and drug release demonstrated that the outcomes are dependent on the presence of fHNTs in the hydrogel matrix. Notably, fHNTs-loaded hydrogels displayed sustained drug release patterns. This innovative approach eliminates the need for traditional encapsulation and presents promising and translatable strategies for achieving more effective drug release. Full article

This study explores the use of Halloysite NanoTubes (HNTs) as photocatalysts capable of decomposing organic dyes under exposure to visible or ultraviolet light. Through a systematic series of photocatalytic experiments, we unveil that the photodegradation of Rhodamine B, used as a model cationic dye, is significantly accelerated in the presence of HNTs. We observe that the extent of RhB photocatalytic degradation in 100 min in the presence of the HNTs is ~four times higher compared to that of bare RhB. Moreover, under optimized conditions, the as-extracted photodegradation rate of RhB (~0.0022 min⁻¹) is comparable to that of the previously reported work on the photodegradation of RhB in the presence of tubular nanostructures. A parallel effect is observed for anionic Coumarin photodegradation, albeit less efficiently. Our analysis attributes this discrepancy to the distinct charge states of the two dyes, influencing their attachment sites on HNTs. Cationic Rhodamine B molecules preferentially attach to the outer surface of HNTs, while anionic Coumarin molecules tend to attach to the inner surface. By leveraging the unique properties of HNTs, a family of naturally occurring nanotube structures, this research offers valuable insights for optimizing photocatalytic systems in the pursuit of effective and eco-friendly solutions for environmental remediation. Full article