Search Results (1,572)

Heparin-based delivery platforms have gained increasing attention in regenerative medicine due to their exceptional affinity for growth factors and versatility in structural and functional design. This review first introduces the molecular biosynthesis and physicochemical diversity of heparin, which underpin its binding selectivity and degradability. It then categorizes the delivery platforms into microspheres, nanofibers, and hydrogels, with detailed discussions on their fabrication techniques, biofunctional integration of heparin, and release kinetics. Special focus is given to stimuli-responsive systems—including pH-, enzyme-, redox-, thermal-, and ultrasound-sensitive designs—which allow spatiotemporal control over growth factor release. The platform applications are organized by tissue types, encompassing soft tissue regeneration, bone and cartilage repair, neuroregeneration, cardiovascular regeneration, wound healing, anti-fibrotic therapies, and cancer microenvironment modulation. Each section provides recent case studies demonstrating how heparin enhances the bioactivity, localization, and therapeutic efficacy of pro-regenerative or anti-pathologic growth factors. Collectively, these insights highlight heparin’s dual role as both a carrier and modulator, positioning it as a pivotal component in next-generation, precision-targeted delivery systems. Full article

The growing challenge of biofilm-associated infections in dentistry necessitates advanced solutions. This review highlights the potential of smart bioactive and antibacterial materials—bioactive glass ceramics (BGCs), silver nanoparticle (AgNP)-doped polymers, and pH-responsive chitosan coatings—in transforming restorative dentistry. BGCs reduce biofilms by >90% while promoting bone integration. AgNP-polymers effectively combat S. mutans and C. albicans but require controlled dosing (<0.3 wt% in PMMA) to avoid cytotoxicity. Chitosan coatings enable pH-triggered drug release, disrupting acidic biofilms. Emerging innovations like quaternary ammonium compounds, graphene oxide hybrids, and 4D-printed hydrogels offer on-demand antimicrobial and regenerative functions. However, clinical translation depends on addressing cytotoxicity, standardizing antibiofilm testing (≥3-log CFU/mL reduction), and ensuring long-term efficacy. These smart materials pave the way for self-defending restorations, merging infection control with tissue regeneration. Future advancements may integrate AI-driven design for multifunctional, immunomodulatory dental solutions. Full article

In this work, ethyl cellulose nanoparticles loaded with rosemary extract (RCL-NPs) were synthesized and utilized to reinforce high-density polyethylene (HDPE) packaging bags as a nanotechnological alternative for rabbit meat preservation. The synthesized RCL-NPs were characterized by DLS and for their stability. The analyzed variables of rabbit meat packaged samples included drained liquid, weight loss, color, pH, texture, and hardness. The total phenolic content (TPC) and antioxidant capacity of rosemary extract were also investigated. The results demonstrated that RCL-NPs were 117.30 nm in size with a negative surface charge (−24.59 mV) and low PDI (0.12). According to the Higuchi model, the release rate of RCL-NPs was sustained from 0 to 24 h. The encapsulation efficiency of the implemented synthesis route was 99.97%. The TPC of rosemary extract was 566.13 ± 1.72 mg GAE/L, whereas their antioxidant activity utilizing the DPPH and FRAP assays was 27.86 ± 0.32 mM Trolox/L and 0.31 mM Trolox/L, respectively. Contrary to control samples, rabbit meat samples conserved in HDPE packaging bags reinforced with RCL-NPs prevent drained liquid and weight loss, while preserving *L (60 ± 2.5–66.10 ± 2.0) and *b (10.67 ± 2.28–11.62 ± 2.39), pH (5.22 ± 0.05–5.80 ± 0.03), and texture (10.37 ± 0.82–0.70 ± 0.50). In the same regard, the developed material conserved the hardness of rabbit meat samples, exhibiting values that ranged from 27.79 ± 7.23 to 27.60 ± 3.05 N during the evaluated period (0–13 days). The retrieved data demonstrate the efficacy of RCL in preserving the quality of rabbit meat when integrated with additional food packaging materials. Full article

Straw return is widely adopted to promote agricultural sustainability, but it can also increase cadmium (Cd) bioavailability in contaminated paddy soils, potentially leading to higher Cd accumulation in rice grains. Although numerous studies have investigated straw incorporation, the specific differences between early- and late-season straw return regarding Cd dynamics within double-cropping rice systems remain inadequately characterized. To address this knowledge gap, we conducted a two-year field experiment comparing early-rice (ER) and late-rice (LR) straw return, complemented by controlled pot experiments simulating ER (ER-S, ER-CK; July–September 2023) and LR (LR-S, LR-CK; December 2022–March 2023) straw incorporation. The results revealed that the Total-Cd exhibited an upward trend following both ER and LR straw incorporation. The ER treatment caused a rapid yet short-lived increase in CaCl₂-extractable Cd (CaCl₂-Cd) concentration, peaking around 60 days following straw return and exhibiting a 28.83% increase compared to the LR treatment. In contrast, the LR treatment induced a slower but more prolonged Cd release, with CaCl₂-Cd concentration peaking around 210 days and exhibiting a 34.89% increase relative to the ER treatment. Additionally, at the late-rice stage, grain Cd concentration in the ER treatment increased by 23.64% relative to the LR treatment. In the subsequent year, grain Cd concentrations in the LR treatment increased significantly by 32.12% to 45.08% compared to the ER treatment for both early- and late-rice crops. These differences were attributed to variations in straw decomposition rates, soil pH, and redox potential between warm, aerobic summer–autumn conditions and cooler, anaerobic winter–spring conditions. This suggests that returning late-rice straw constitutes an elevated hazard to soil health and rice safety compared to early-rice straw return. Full article

The quest for sustainable agriculture demands nutrient delivery systems that align productivity with environmental responsibility. This review critically evaluates stimuli-responsive starch-based biopolymer coatings for controlled-release fertilizers (CRFs), highlighting their structure, functionality, and agronomic relevance. Starch, an abundant and biodegradable polysaccharide, offers intrinsic advantages such as modifiability, film-forming ability, and compatibility with green chemistry. The paper discusses starch’s physicochemical characteristics, its functionalization to achieve responsiveness to environmental triggers (pH, moisture, temperature, ionic strength), and coating strategies like in situ polymerization, grafting, and nanocomposite integration. A comprehensive analysis of release kinetics, swelling behavior, biodegradability, and water retention is provided, followed by evaluations under simulated field conditions, encompassing various soil types, environmental stressors, and crop responses. Comparative insights with other smart biopolymers such as chitosan, alginate, and cellulose underscore starch’s unique position in CRF technology. Despite promising developments, the review identifies critical research gaps, including limitations in scalability, coordination of multi-stimuli responses, and the need for extensive field validation. This work serves as a consolidated platform for researchers, policy makers, and agro-industrial stakeholders aiming to design smart, eco-friendly fertilizers that address global food security while minimizing ecological footprints. Full article

In this work, alkylammonium-functionalized hollow mesoporous silica as a nonocarrier of drugs was synthesized to realize enhanced cancer therapy by pH stimuli for sustained drug release. First, functionalized hollow mesoporous silica nanoparticles (Hollow MSNs) were synthesized using dodecyl dimethyl(3-sulfopropyl)ammonium hydroxide (DDAPS), sodium dodecyl sulfate (SDS), and triethanolamine as structure-directing agents, while tetraethyl orthosilicate (TEOS) and N-trimethoxysilypropyl-N,N,N-trimethylammonium chloride (TMAPS) were used as silica sources under basic condition via the sol–gel process. The structure and morphology of the alkylammonium-functionalized hollow mesoporous silica nanoparticles (Hollow MSN-N⁺CH₃) were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N₂ adsorption–desorption analysis, and Fourier transform infrared (FT-IR) spectroscopy. The functionalized hollow MSNs had a particle size of about 450 nm and a shell thickness of about 60 nm with uniform size. The nanoparticle had a surface area of 408 m²g⁻¹, pore volume of 0.8 cm³g⁻¹, and a uniform pore diameter of 45.9 Å. In the cancer cell viability test with a MCF-7 cell, fludarabine-incorporated and alkylammonium-functionalized hollow mesoporous silica nanoparticles (Flu/Hollow MSN-N⁺CH₃) showed excellent cancer cell death comparable with pure fludarabine drug with the controlled drug release by pH stimuli. It is suggested that our current materials have potential applicability as pH-responsive nanocarriers in the field of cancer therapy. Full article

Graphene, owing to its exceptionally high specific surface area, abundant surface functional groups, and outstanding biocompatibility, exhibits tremendous potential in the development of nanodrug delivery systems. This review systematically outlines the latest research advancements regarding graphene and its derivatives in drug loading, targeted delivery, and smart release. It covers delivery strategies and mechanisms for various types of drugs, including small molecules and macromolecules, with a particular emphasis on their applications in major diseases such as cancer, neurological disorders, and infection control. The article also discusses stimulus-responsive release mechanisms, such as pH-responsiveness and photothermal responsiveness, and highlights the critical role of surface functionalization of graphene and its derivatives in enhancing therapeutic efficacy while reducing systemic toxicity. Furthermore, the review evaluates key challenges to the clinical translation of graphene-based materials, including safety, toxicity, and metabolic uncertainties. It points out that future research should focus on integrating structural modulation of materials with biological behavior to construct intelligent nanoplatforms featuring biodegradability, low immunogenicity, and precise therapeutic targeting. The aim of this paper is to provide theoretical insights and technical guidance for the customized design and precision medicine applications of graphene and its derivative-based drug delivery systems. Full article

Cellulose nanofibril (CNF)-based hydrogels, owing to their sustainability, biocompatibility, and versatile mechanical properties, are promising for biomedical applications. This review analyzes the recent advances and biomedical applications of CNF hydrogels. CNF hydrogels can be prepared via physical and chemical crosslinking. Physical crosslinking involves surface charge density control, pH manipulation, and flow-based processing to generate stable networks, whereas chemical crosslinking employs agents such as epichlorohydrin and citric acid to form permanent covalent bonds. These approaches enable precise control over hydrogel properties, including mechanical strength, porosity, and stimuli responsiveness. CNF hydrogels are particularly promising in drug delivery systems and tissue engineering. CNFs as drug delivery vehicles offer enhanced bioavailability and drug loading capacity owing to their open pore structure and large surface area. Recent developments in stimuli-responsive and injectable CNF hydrogels have enabled controlled drug release and improved targeting capabilities. Moreover, CNF hydrogels serve as effective scaffolds for cell growth and tissue regeneration, with applications in cartilage engineering and wound healing. Integrating CNF hydrogels with 3D bioprinting technology has generated complex tissue structures. However, several challenges remain, including the need for the standardization of toxicology assessments, optimization of large-scale production processes, and development of sophisticated control mechanisms for drug delivery. Future research should advance manufacturing technologies, improve long-term stability, and develop standardized testing protocols for regulatory compliance. Full article

We present a straightforward emulsion-induced interfacial anisotropic assembly method for in- situ synthesis of bowl-shaped, self-encapsulated mesoporous polydopamine (BMPDA) nanocontainers (M-M@P) loaded with 2-mercaptobenzimidazole (2-MBI). Results showed that the loading capacity of the bowl-shaped mesoporous polydopamine reaches 24 wt.%. The M-M@P exhibits a cumulative MBI release of 91.61% after immersion in a 3.5 wt.% NaCl solution at pH = 2 for 24 h, accompanied by a corrosion inhibition efficiency of 95.54%. Additionally, the acid-responsive M-M@P not only enables controlled release of MBI but also synergistically promotes the formation of a protective film on the carbon steel substrate via the chelation of PDA-Fe³⁺, thereby enhancing the self-healing performance of waterborne epoxy coatings. Full article

Stimuli-responsive, cell-mediated drug delivery systems represent a dynamic interface between biological functionality and engineered control. Leveraging the inherent targeting properties of erythrocytes, immune cells, stem cells, and exosomes, these systems offer a promising strategy for precise therapeutic delivery. In this review, we provide a comprehensive analysis of the design principles and biological underpinnings of stimuli-responsive carriers that release payloads in response to endogenous triggers (e.g., pH, redox, enzymatic activity) or external stimuli (e.g., light, ultrasound, magnetic fields). We further examine current strategies for loading and functionalizing cellular carriers, highlight key therapeutic applications across oncology and regenerative medicine, and assess translational progress and regulatory challenges. This review underscores the emerging clinical potential of intelligent cell-based delivery vehicles and outlines future directions for their optimization and implementation. Full article

Hepatocellular carcinoma (HCC) is a leading cause of cancer-related death worldwide, and treatment remains challenging due to high recurrence rates, resistance to chemotherapy, and severe side effects. Dasatinib (Das) has shown therapeutic potential against HCC, but its clinical use is limited by poor bioavailability and short half-life (~3–4 h). Here, we developed a hyaluronic acid (HA)-coated sterosome for targeted and sustained delivery of Das to CD44-overexpressing HCC cells. Sterosomes composed of octadecylamine and cholesterol at a 5:5 (v/v) ratio were prepared via thin-film hydration and sonication, yielding stable particles (~90 nm) with high encapsulation efficiency (EE ~72%) for uncoated vesicles and ~58% after HA coating. HA-sterosomes (HA-St-Das) exhibited a uniform size (≈200 nm) and negative surface charge (–26 mV), with improved storage stability and resistance to lyophilization. In vitro release studies demonstrated pH-responsive Das release accelerated under acidic conditions (pH 6.0–5.0), mimicking tumor and lysosomal environments. In HepG2 cells, HA-St-Das exhibited enhanced cytotoxicity (IC50 ~7.0 μM) and prolonged intracellular retention compared to free Das and uncoated carriers. Fluorescence microscopy confirmed receptor-mediated uptake via CD44, leading to gradual and sustained intracellular delivery. Overall, the HA-St-Das system provides biocompatible, targeted, and controlled Das delivery, addressing key limitations of current liver cancer therapies and representing a promising nanomedicine platform for further development. Full article

If untreated, skin wounds can lead to severe complications. Depending on the type of injury, long-term antibiotic administration is often required, and this decreases patient compliance. This limitation could be addressed by applying dressings capable of preventing infections by controlling drug release to the wound site. In this research, biodegradable wound dressings were investigated, based on natural polymers chitosan and alginate and incorporating the broad-spectrum gentamicin as antibiotic. Specifically, gentamicin was loaded into alginate nanoparticles, which were then loaded into chitosan-based films. This approach aimed at obtaining a system capable of modulating antibiotic release. The obtained nanoparticles had an average diameter of 86 nm and polydispersity index of 0.15. Antibiotic loading was around 600 µg/mg, with loading efficiency close to 100%. Films incorporating nanoparticles were compared to control films, which contained only gentamicin. Results showed that nanoparticles incorporation decreased film’s swelling in phosphate buffer saline, thus leading to a decrease in burst release while cytocompatibility for human dermal fibroblasts was maintained. Antibacterial activity was confirmed against both gram-positive and gram-negative bacteria. Moreover, the antibiotic was released as a function of pH, with distinct behavior at pHs ranging from 7.4 to 5.5. This indicates that alginate nanoparticles dispersed in chitosan films effectively release gentamicin on demand. Full article

When desalinated water enters the existing drinking water distribution systems (DWDSs), the balance between water and scale will be destroyed, resulting in the release of iron and water quality problems, causing “yellow water”. This study investigated the inhibitory effects of pH, alkalinity, and phosphate on iron release and the optimal control condition using pipe section reactors with a response surface. For steel pipe, the optimal condition for iron release control was pH = 8.5, alkalinity = 250 mg/L CaCO₃, and phosphate = 0.1 mg/L. For cast iron pipe, the optimal condition was pH = 8.0, alkalinity = 250 mg/L CaCO₃, and phosphate = 0.1 mg/L. This study can provide theoretical support for subsequent water supply safety and lay a foundation for the water supply safety of the municipal pipe network. Full article

Background: Excessive formation of neutrophil extracellular traps (NETs) leads to NETosis, accompanied by the release of citrullinated histone H3 (CitH3), a key mediator of septic inflammation. However, the role of CitH3 in sterile inflammation, such as acute myocardial infarction (MI) and post-MI heart failure, remains incompletely understood. Methods and Results: We investigated the role of CitH3, a byproduct of NETosis, in myocardial ischemia/reperfusion (I/R) injury using a murine MI model. C57BL/6J mice were subjected to left coronary artery (LCA) occlusion followed by reperfusion and treated with either a humanized anti-CitH3 monoclonal antibody (hCitH3-mAb) or control human IgG. In mice undergoing 40 min of LCA occlusion and 24 h of reperfusion, hCitH3-mAb administered 10 min before reperfusion significantly reduced infarct size by 36% compared to control (p < 0.05). Plasma levels of CitH3, IL-1β, and interferon-β were significantly elevated following MI but were attenuated by hCitH3-mAb. In addition, plasma and cardiac tissue from treated mice showed significantly lower levels of citrate synthase, a marker of mitochondrial injury, suggesting that hCitH3-mAb preserved mitochondrial integrity after MI. In mice undergoing 50 min of LCA occlusion and 21 days of reperfusion, longitudinal echocardiography revealed preservation of left ventricular ejection fraction (LVEF) in hCitH3-mAb-treated mice, with significant improvement observed on days 7, 14, and 21 post-MI (p < 0.05 vs. control). hCitH3-mAb also mitigated myocardial fibrosis and preserved tissue architecture. Conclusions: These findings demonstrated CitH3 as a critical mediator of myocardial injury and adverse remodeling following acute MI. Neutralization of CitH3 via hCitH3-mAb attenuates I/R injury and preserves cardiac function by mitigating inflammation and protecting mitochondrial integrity. Targeting CitH3 represents a promising therapeutic strategy to prevent heart failure following MI. Full article

Harmful cyanobacterial blooms pose significant threats to lake ecosystems, and the stocking of filter-feeding fish has often been used for their control. However, filter-feeding fish like silver carp excrete feces that not only retain viable cyanobacterial cells but also increase nutrient loading to the sediment. Furthermore, the quantity and frequency of fecal input vary depending on the biomass of algae and fish and the stocking strategy. In this study, a two-by-two factorial microcosm experiment was carried out to investigate the effects of silver carp feces on P release in shallow lakes. Results showed that fecal input quantity was the key determinant of P release. The peak flux reached 8.82 mg m⁻² d⁻¹ in high input treatments, compared to 1.01 mg m⁻² d⁻¹ in low input treatments. Phased-input exacerbated these effects compared to single-input. The dominant mechanisms of sediment P release varied with input levels. Microbial reduction was strongly associated with P release at low fecal input, while high-input scenarios showed concurrent hypoxia, an increase in sediment pH (from 7.28 to 7.46), and competition for adsorption sites by dissolved organic matter (DOM up to 38.57 mg L⁻¹). These results indicate that stocking of filter-feeding fish for cyanobacterial bloom control substantially altered P flux dynamics, with high input treatments exhibiting fluxes from −6.02 to 8.82 mg m⁻² d⁻¹ compared to −0.007 to 0.33 mg m⁻² d⁻¹ in controls, depending on the patterns of fecal input. For the prevention and control of cyanobacterial blooms and to ensure the sustainability of lakes, the stocking of filter-feeding fish should be carried out before the outbreak of blooms to avoid the impact of large amounts of fish feces input on P release and water quality during the blooms. Full article