Search Results (1,024)

Polymer gels are essential functional materials for subsurface energy operations, playing a critical role in conformance control, fluid diversion, hydraulic fracturing, and leakage mitigation. As reservoirs become increasingly complex and the demand for sustainable energy grows, continued innovation in gel technologies is crucial. This editorial introduces a Special Issue titled “Advances and Applications of Polymer Gels for Subsurface Energy and Storage,” which compiles seven original research articles exploring recent developments in gel synthesis, characterization, and applications. The featured studies highlight the versatility of polymer gels, including nanoparticle-reinforced composites, foam–gel hybrids, recrosslinkable preformed particle gels, and advanced fracturing fluids. The contributions address key challenges across CO₂-enhanced oil recovery, heavy oil production, low-permeability reservoir fracturing, and combined enhanced oil recovery strategies. The findings demonstrate ongoing efforts to tailor gel systems for harsh reservoir conditions, improve sweep efficiency, and reduce formation damage, fostering more efficient and sustainable subsurface engineering practices. This Special Issue serves as a valuable resource for researchers and practitioners advancing polymer gel technologies for energy and storage applications. Full article

Cancer nanomedicine has generated extensive preclinical evidence of improved drug delivery, pharmacokinetics, and tolerability, yet its clinical impact has often remained modest. This narrative review examines the interconnected biological, pharmacokinetic, manufacturing, regulatory, and clinical factors underlying this translational paradox. A structured literature search was conducted primarily in PubMed and Google Scholar, focusing on studies published between 2022 and 2026 while retaining seminal earlier reports. Major biological barriers include protein corona formation, mononuclear phagocyte system clearance, heterogeneous enhanced permeability and retention, complex tumor microenvironments, and intratumoral heterogeneity. These factors limit circulation, tumor accumulation, tissue penetration, drug release, and interpatient reproducibility. Translation is further constrained by off-target accumulation, uncertain long-term toxicity, non-standardized experimental methods, batch-to-batch variability, scale-up challenges, and fragmented regulatory pathways. Clinical experience shows that successful products are dominated by relatively established platforms and reformulations of known anticancer agents, whereas many actively targeted or structurally complex systems have failed to demonstrate sufficient efficacy or safety. Future progress will require mechanism-driven design, human-relevant preclinical models, harmonized characterization, quality-by-design manufacturing, early regulatory integration, biomarker-guided patient selection, and adaptive clinical trials. Aligning nanoparticle engineering with biological and clinical realities is essential for achieving meaningful patient benefit. Full article

This study reports a systematic, single-additive investigation of biodegradable films based on polylactic acid (PLA) and polybutylene adipate terephthalate (PBAT) blends (T2308 and F2332) from Ecovio^® for packaging applications by incorporating additives such as nisin, essential oils (tea tree, lemongrass, eucalyptus, clove leaves), curcumin, and zinc oxide nanoparticles. Their effects on structure, morphology, thermal behavior, mechanical properties, barrier performance, and optical properties were evaluated by FTIR, SEM with EDX, TGA, DSC, DMA, XPS, mechanical testing, water vapor permeability, moisture absorption, contact angle measurements and UV/visible transmittance. FTIR confirmed additive incorporation with bonding interactions. SEM revealed matrix-dependent morphologies, with T2308 being denser and more heterogeneous, F2332 being more homogeneous and flexible. DSC/TGA showed curcumin markedly reduces crystallinity and melting enthalpy in T2308 (weaker effects in F2332), while oils generally decrease crystallinity and shift Tg depending on molecular structure. Mechanical testing indicated modulus is highly matrix-dependent: curcumin, nisin, and ZnO decrease stiffness in T2308, whereas F2332 shows smaller or opposite trends. UV shielding increases with curcumin and ZnO, and clove oil improves barrier performance. Biodegradation was assessed only for neat films: weight loss averaged ~4–6% after 49 days, with PET/HDPE remaining largely inert. These results illustrate the importance of matrix–additive interactions in enabling tailored biodegradable packaging materials. Full article

Background/Aims: Type 2 diabetes mellitus (T2DM) is characterized by hyperglycemia and is a risk factor for stroke. Our previous studies demonstrated that adipocyte-derived exosomes (Ad-EXs) mediate adipose–brain communication. This study investigated the effects of hyperglycemic subcutaneous and visceral Ad-EXs on brain microvascular endothelial cell (BMEC) dysfunction during ischemic injury. Hypothesis: Hyperglycemic Ad-EXs exacerbate stroke injury via inducing oxidative stress and lipid peroxidation in BMECs. Methods: EXs were isolated from primary human subcutaneous and visceral adipocytes cultured in normal glucose (NG): NG-S-Ad-EXs and NG-V-Ad-EXs, or high-glucose (HG, 25 mM) media: HG-S-Ad-EXs and HG-V-Ad-EXs by ultracentrifugation and characterized by a nanoparticle tracking analysis system. PKH26-labeled Ad-EXs were used to evaluate uptake mechanisms in human BMECs (HBMECs). Functional effects were assessed in hypoxia/reoxygenation (H/R)-injured HBMECs treated with different Ad-EXs. Oxidative stress and lipid peroxidation markers (NOX2/4, MDA, 4-HNE, and GPX4) were analyzed. Results: HG increased Ad-EX release from both adipocyte depots. HG-derived Ad-EXs increased HBMEC cytotoxicity and permeability while reducing angiogenesis after H/R injury. Mechanistically, HG-Ad-EXs promoted oxidative stress through increased NOX2/4 and lipid peroxidation via elevated MDA/4-HNE and reduced GPX4 expression. Conclusion: Hyperglycemic Ad-EX triggered oxidative stress via NOX2/4 and lipid peroxidation via MDA/4HNE/GPX4, leading to impaired HBMEC functioning, which was exacerbated in the H/R injury condition. Full article

Phytol, an acyclic diterpene alcohol and a key lipophilic side-chain moiety of chlorophyll, is widely distributed in nature. It exhibits potent antioxidant, anti-inflammatory, analgesic and broad-spectrum antibacterial activities. Notably, phytol can also effectively inhibit melanin production, repair the skin barrier, and exert profound anti-aging effects, making it a highly promising ingredient for daily skincare with substantial industrial application value. The skincare benefits of phytol are primarily achieved by constructing a multi-dimensional regulatory network involving defense, modulation and repair. Compared to conventional retinol-based skincare ingredients, phytol exhibits superior biocompatibility, mild irritation, and remarkable safety advantages. Nevertheless, its application is hindered by inherent limitations, including strong hydrophobicity, spontaneous aggregation tendency, and poor photothermal stability. These drawbacks severely restrict its dispersibility, storage stability and percutaneous bioavailability in aqueous cosmetic formulations. To address these deficiencies, nanodrug delivery systems (NDDS), such as liposomes, nanoemulsions, solid lipid nanoparticles and PLGA nanoparticles, have been widely employed. These nanocarriers can penetrate the skin barrier via the size effect, enabling targeted skin delivery and long-term controlled release of phytol. This review systematically summarizes the biological sources and metabolic fate of phytol, as well as its multi-mechanistic pharmacological effects on the skin. Furthermore, we outline the current application status and industrial development trends of phytol in mainstream cosmetics worldwide. This work aims to provide theoretical basis and forward-looking references for the development of high-efficiency, safe and stable phytol-derived skincare raw materials and topical formulations. Highlights: (1) Phytol, a natural acyclic diterpene alcohol, exerts multi-dimensional skincare effects including antioxidant, anti-inflammatory, whitening, anti-aging, and skin barrier repair activities via a defense–modulation–repair regulatory network. (2) Phytol may act as a mild, non-irritating functional alternative to retinoids, targeting PPAR/RXR pathways and avoiding TRPV1-mediated irritation, making it suitable for sensitive skin. (3) Poor water solubility and instability hinder phytol’s translation; nanodelivery systems effectively improve solubility, permeability, and sustained release. Full article

Carbon nanoparticles (CNPs) have attracted considerable attention for biomedical applications owing to their excellent biocompatibility, tunable optical properties, and low toxicity. In this study, we report a simple, rapid, and cost-effective one-pot bottom-up synthesis of fluorescent carbon nanoparticles using propanoic acid as a novel liquid carbon precursor. Unlike conventional approaches that often require high temperatures, lengthy reaction times, or complex procedures, the proposed method enables efficient nanoparticle synthesis under mild thermal conditions. The use of propanoic acid enabled carbonization under relatively mild conditions, yielding nanoparticles with excellent aqueous dispersibility. Following the synthesis of CNPs using propanoic acid as the carbon precursor, the nanoparticles were treated with ethylenediamine (EDA) as a nitrogen source and surface-passivating agent, yielding nitrogen-doped carbon nanoparticles (NCNPs). The resulting NCNPs exhibited approximately fourfold higher fluorescence intensity than the undoped CNPs. The NCNPs exhibited strong visible photoluminescence with a dominant emission band in the green spectral region (490–540 nm), which is advantageous for cellular imaging due to reduced background interference and improved imaging selectivity. Furthermore, the NCNPs demonstrated high aqueous solubility, cellular permeability, and excellent photostability under the in vitro imaging conditions investigated. The bioimaging capability of the NCNPs was evaluated using human lung fibroblasts and lung cancer cells. Confocal fluorescence microscopy revealed efficient cellular uptake and successful nuclear labeling without observable photobleaching and morphological alterations. These findings demonstrate the feasibility of using propanoic acid-derived NCNPs as fluorescent probes for cellular imaging and suggest their potential for future applications in bioimaging, biosensing, and related biomedical research. Further studies are warranted to evaluate their long-term biological safety and performance. Full article

To overcome the limitations of conventional biopolymer films and reduce reliance on petroleum-based plastics, a nacre-inspired film was developed via 3D printing. During printing process, shear-induced alignment of mica flakes was achieved within a sodium alginate/xanthan gum matrix. Additionally, zinc oxide nanoparticles (ZnO NPs) were incorporated to achieve a synergistic reinforcement effect. Structural analysis revealed that the mica flakes within the film exhibited an oriented distribution, with ZnO NPs uniformly embedded in the interlayer voids, and hydrogen bonding assisted in forming a dense network of the components. Performance testing showed that the tensile strength rose from 13.8 MPa to 62.9 MPa. Improvements in water resistance and thermal stability were also observed. Furthermore, the material exhibited outstanding comprehensive protective properties, including a low water vapor permeability value of 7.587 × 10⁻¹¹ g·m/m²·Pa·s, an ultraviolet blocking rate of 99.37% at a wavelength of 280 nm, and the ability to completely inhibit target bacterial strains, while also possessing good biodegradability and recyclability. Shelf-life tests indicated that the film fabricated in this work could notably prolong the shelf life of strawberries. Biocompatibility test results indicated that the film was safe and non-toxic, and showed no significant cytotoxicity. Full article

Background/Objectives: Combining chemotherapy with local magnetic hyperthermia (MHT) is promising because heating tumor tissue can increase cell damage, sensitize cells to cytostatic drugs, impair DNA repair, and change tumor microenvironment permeability. This creates conditions for enhancing the antitumor efficacy of chemotherapy while potentially reducing systemic toxicity. The aim of this study was to evaluate the efficacy of MHT with Zn_0.2Mn_0.8Fe₂O₄@OA nanoparticles alone and in combination with cisplatin in a Lewis lung carcinoma model. Methods: Four types of magnetic nanoparticles were synthesized and characterized: Fe₃O₄ and Zn_0.2Mn_0.8Fe₂O₄ coated with oleic acid (OA) or SiO₂-NH₂. Their physicochemical and magnetothermal properties, cytotoxicity, reactive oxygen species generation, and biodegradation in vivo were evaluated. Antitumor efficacy was studied in C57Bl/6 mice with LLC tumors after intratumoral administration of nanoparticles and two MHT sessions (100 kHz, 8 kA/m, 30 min). In combination therapy, ZnMn@OA and cisplatin at doses of 9 or 18 mg/kg were used. Results/Conclusions: Zn_0.2Mn_0.8Fe₂O₄@OA combined efficient heating, biodegradation, and the most pronounced effect among the MHT-alone groups, although MHT without chemotherapy did not provide sustained inhibition of tumor growth or a significant increase in survival. The combination of Zn_0.2Mn_0.8Fe₂O₄@OA-MHT with cisplatin 9 mg/kg produced the best therapeutic outcome: median survival increased significantly by two fold compared with the control group and by 1.8-fold compared with the chemotherapy-alone group at the comparable cisplatin dose. This regimen also stabilized body weight, reduced systemic toxicity, and restored RBC, HGB, and HCT parameters to the level of healthy animals by day 7 of the experiment. These data confirm the potential of MHT as a chemosensitizing approach that improves the efficacy and tolerability of cisplatin therapy. Full article

As critical infrastructure for carbon capture, utilization, and storage (CCUS) and large-scale energy storage, subsurface salt caverns are seriously challenged by fluid-induced sediment mobilization during the supplementary debrining. Conventional bulk resin consolidation often causes severe viscous fingering, uneven consolidation, and pore clogging under hypersaline conditions. Here, we develop a foam-templated hybrid polymer gel co-stabilized by silica nanoparticles, polyvinyl alcohol, and the zwitterionic surfactant. The key novelty is the use of foam as a transient transport template that redistributes the resin phase and promotes selective cementation at grain-contact points instead of indiscriminate pore filling. This nano-reinforced gel system remained stable under hypersaline conditions (24% NaCl), and temperatures ranging from 20–80 °C. Micro-CT analysis showed that this selective templating preserved an interconnected pore network with a porosity above 45% and a CT-derived permeability of approximately 1.18 D, while reducing binder consumption by 55.6% relative to bulk resin injection. Crucially, a 1:200 geometrically scaled, velocity-matched pilot model demonstrated that this gel strategy limited sediment entrainment below 0.5% and reduced fluid discharge by 45.9%. These results establish a material-efficient consolidation strategy that combines sediment stabilization with permeability preservation, providing a promising solution for safer supplementary debrining in salt-cavern CCUS and energy-storage operations. Full article

Maintaining the rheological performance of wormlike micellar fluids at elevated temperatures remains challenging. Conventional viscoelastic surfactant (VES) systems may undergo thermally induced micellar scission and loss of gel-like viscoelasticity at elevated temperatures. In this study, we investigate the size-dependent reinforcement of long-chain C22⁺ wormlike micellar systems by silica nanoparticles under a temperature-ramp protocol reaching 160 °C. Under the applied temperature-ramp protocol, the formulation containing 0.10 wt% of 15 nm SiO₂ nanoparticles exhibited the highest measured rheological response among the tested formulations, retaining an apparent viscosity of approximately 210 mPa·s and a plateau storage modulus of approximately 18.5 Pa during the 20 min isothermal holding period at 160 °C, compared with a plateau storage modulus of approximately 11 Pa for the corresponding VES system. At equal nanoparticle mass loading, the 15 nm particles produced approximately 18% and 6% higher G′ and G″, respectively, than the 500 nm particles. The rheological results, together with qualitative electrokinetic measurements after dilution, are consistent with nanoparticle-surfactant association that may promote micellar entanglement and network reinforcement. The nanoparticle-enhanced viscoelastic surfactant (N-EVES) formulation reduced the acid-rock reaction rate to approximately 25% of that measured for conventional HCl while showing an apparent effective H⁺ diffusion coefficient of the same order. Scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM–EDS) detected Si- and N-containing species on the treated carbonate surface, suggesting that surface adsorption or deposition may contribute to reaction retardation. Parallel dual-core flooding under a permeability contrast of approximately 13 showed fluid redistribution toward the low-permeability core. Based on the axial wormhole penetration length obtained from the CT reconstruction, the normalized axial wormhole penetration fraction of the low-permeability core was approximately 70% for the 0.10 wt% formulation. These results provide experimental evidence of nanoparticle-size-dependent rheological reinforcement, acid-rock reaction retardation, and core-scale flow redistribution under strongly acidic and high-temperature conditions. Full article

Background/objectives: Delayed wound healing, along with excessive scar formation, is the major clinical drawback due to the presence of stubborn bacteria, oxidative stress, prolonged inflammation, and irregular tissue regeneration. Utilizing nanomaterial-based wound dressings offers significant advancements and minimal cytotoxicity, but also presents issues such as poor biocompatibility, low solubility, and reduced permeability. These factors limit the effectiveness of nanomaterial-based wound dressings in promoting complete tissue regeneration. To overcome these limitations, plant-derived bioactives are integrated with nanomaterials within a hydrogel cage to enhance antibacterial activity, mitigate oxidative stress and inflammation, and promote tissue regeneration. Methods: A multifunctional alginate–gelatin hydrogel incorporating silver nanoparticles and plant extracts (AG-AgNP-PE) was developed to promote scar-free wound healing, alongside a plant extract-free silver nanoparticles-loaded hydrogel for comparative evaluation of the functional contribution of plant bioactives. The biological performance of the formulated hydrogels was systematically evaluated through antioxidant, antimicrobial, and antibiofilm assays, while in vitro cytocompatibility and proregenerative activity were assessed using MTT and Alamar Blue assays, live/dead cell imaging, and a scratch-wound assay, complemented by in vivo evaluation in zebrafish embryos. Results: Pro-angiogenic activity was further investigated using the CAM model, and therapeutic efficacy was validated in an in vivo rat burn wound model through microscopic wound assessment, histopathological examination, and biochemical assays. Conclusions: Among the hydrogels, AG-AgNP-PE exhibited superior performance across all key properties, highlighting the synergistic effect of the nanomaterial combined with plant extracts within hydrogel cages and positioning it as a promising multifunctional wound dressing for rapid tissue regeneration and scar-free wound healing, suitable for advanced wound management. Full article

Hybrid structural materials (HSMs), such as nanoparticle-treated fabrics, have been shown to enhance acoustic and ballistic performance in multifunctional protective structures. They offer a promising means for low-frequency (<~1000 Hz) noise mitigation, which remains a critical challenge in aerospace and defense applications. The measurement and modeling of their sound transmission loss (TL) behavior using a coupled acoustic–poroelastic approach is explored in this study. A colloid-based soaking and drying process is used to impregnate nanoparticles into the fabric. Previous studies using SEM imaging have established that at low (<~20 wt.%) treatment levels, the nanoparticles agglomerate in the interstitial spaces between yarn crossover points, whereas at higher levels, they begin to coat the yarn bundle tops. TL was measured experimentally using normal-incidence impedance tube tests. Further, parameters such as static flow resistivity, porosity, flexural modulus, and density required to model the neat and treat samples as fluid-filled porous solids using the Biot–Allard model were obtained from experiments for a limited set of neat and treated cases. Static flow resistivity was measured using an air permeability tester as per ISO 9237, and a modified version of the Peirce’s cantilever beam test was used to obtain the flexural modulus for neat and treated samples. Porosity was estimated using digital image analytics. The poroelastic fabric model was implemented in finite element simulations, and the predicted TL was compared with experiments including those for uncalibrated treated cases. The model shows close alignment with measured TL at low frequencies (<~600 Hz) for all cases but deviates closer towards the theoretical mass law at higher frequencies, where flanking effects and the influence of the hierarchy of pores are expected to be dominant in experiments. Further studies are underway to incorporate such higher-order effects to improve predictions at higher frequencies. The development of this model provides a means to capture the influence of nanoparticle addition on the acoustic performance of Kevlar, enabling fast and efficient virtual design iterations. The approach helps optimize HSMs for noise mitigation in multifunctional applications for the aerospace, defense, and infrastructural sectors. Full article

Kaempferol is a natural flavonol compound widely present in various single-herb remedies and compound formulations used for the treatment of ocular diseases. Despite its inherent pharmaceutical limitations, accumulating evidence indicates that kaempferol exerts broad protective effects against diverse ocular disorders through multiple biological pathways, highlighting its potential as a multi-target therapeutic candidate in ophthalmology. However, current evidence regarding kaempferol-based ophthalmic applications remains fragmented across different ocular diseases and mechanistic investigations, and a comprehensive evaluation of its therapeutic potential, translational challenges, and existing limitations is still lacking. This review systematically summarizes the research progress on kaempferol in the treatment of eye diseases, encompassing its source distribution, structural characteristics, ocular delivery strategies, disease spectrum coverage, molecular mechanisms, and safety profile. By critically evaluating currently available evidence, this review further identifies unresolved issues and translational barriers that hinder the clinical application of kaempferol in ophthalmology. Regarding delivery strategies, carriers such as gelatin nanoparticles, porous bovine serum albumin membranes, platelet-derived extracellular vesicles, and polyvinylpyrrolidone-based nanocomposites have preliminarily improved ocular surface retention and corneal permeability of kaempferol in models of corneal neovascularization and alkali burns. In terms of therapeutic indications, kaempferol has demonstrated protective effects in diverse experimental models, including age-related macular degeneration (AMD), diabetic retinopathy, diabetic cataract, dry eye disease, fungal keratitis, corneal transplant rejection, acute glaucoma, and retinoblastoma. At the mechanistic level, kaempferol exerts comprehensive pharmacological actions—anti-inflammatory, antioxidant, metabolic regulation, anti-angiogenic, and immunomodulatory—by modulating multiple signaling pathways, including MAPK, NF-κB, STAT1/IRF7, Nrf2/HO-1, VEGF/PI3K/Src/Akt/ERK, aldose reductase, estrogen-related receptor alpha (ERRα), and the NOD-like receptor family pyrin domain-containing protein 3 (NLRP3) inflammasome. Available safety assessments suggest that kaempferol exhibits a generally favorable safety profile across ocular, cellular, systemic, and genetic evaluations. Despite these advances, the clinical translation of kaempferol in ophthalmology remains limited by insufficient clinical and pharmacokinetic evidence, underdeveloped targeted delivery strategies, and a lack of integrated understanding of its molecular basis in ocular protection. By systematically integrating evidence from ocular disease models, molecular mechanisms, delivery strategies, and safety evaluations, this review bridges fragmented knowledge regarding kaempferol-based ophthalmic applications and provides an integrated framework for understanding its therapeutic potential and translational prospects. Overall, this review highlights kaempferol as a promising multi-target therapeutic candidate for ocular diseases and provides insights into its future translational development. Full article

Cancer therapy is increasingly focused on manipulating the tumor microenvironment rather than directly eradicating malignant cells. Vascular-targeting strategies are emerging, and calcium-mediated vascular disruption is an exciting approach through which rapid and irreversible blood flow shutdown can be achieved. Here, we overview the molecular and physiological basis of calcium signaling in vascular homeostasis and outline how unregulated calcium dysfunctions in endothelial cells compromise their functionality and represent therapeutic opportunities. Elevation of intracellular calcium concentrations in endothelial cells promotes their dysfunction, coagulation, mitochondrial collapse, oxidative stress, and ultimately apoptosis, resulting in catastrophic vascular depletion and secondary necrosis that follows such collapse. A promising area of calcium-mediated attack is the emergence of exciting nanotechnologies that result in the development of calcium phosphate, calcium carbonate, and calcium peroxide nanoparticles, exploiting the enhanced permeability and retention effect of nanoparticle therapeutics to achieve selective tumor accumulation and controlled calcium release. Indeed, hybrid therapeutic platforms that couple calcium dysregulation with chemotherapy, photodynamic therapy, sonodynamic therapy, immunotherapy, or thermal ablation can exhibit pronounced antitumor effects through synergistic means. There is good preclinical evidence for the feasibility of vascular collapse mediated via calcium dysregulation. The transition of calcium to the clinic faces hurdles in relation to biosafety, how to achieve precise delivery, pharmacokinetics, and regulatory harmonization. Compared to traditional vascular disrupting agents and anti-angiogenic therapies, calcium modalities can provide rapid occlusion of vessels, are less prone to resistance development, and potentially have less systemic toxicity. Overall, calcium-mediated vascular collapse is thus an exciting next-generation technology for the vascular-targeted treatment of cancer, and likely to play an important role in precision oncology therapeutics. Full article

Background: Colorectal cancer (CRC) is a major clinical challenge due to high metastasis and therapy resistance. Photodynamic therapy (PDT) offers precise tumor ablation but lacks sustained anti-metastatic activity. Peptidic urokinase-type plasminogen activator (uPA) inhibitors suppress metastasis but suffer from short half-life and poor tumor retention. This study aimed to develop a dual-functional self-assembled nanoplatform integrating PDT and selective uPA inhibition for synergistic CRC treatment. Methods: We designed and synthesized a conjugate by linking pyropheophorbide-a (PPA) with uPA-targeted cyclic peptide IG2, which self-assembled into nanoparticles (PINPs). Physicochemical properties, reactive oxygen species (ROS) generation, and uPA inhibitory activity were characterized. In vitro studies included cellular uptake, cytotoxicity, and invasion assays. In vivo therapeutic efficacy was evaluated in subcutaneous CT26 tumor models and lung metastasis models, with biosafety assessed by body weight monitoring. Results: PINPs exhibited uniform spherical nanostructure, prolonged blood circulation, and enhanced tumor accumulation via the enhanced permeability and retention (EPR) effect. Under 680 nm irradiation, PINPs generated robust ROS and induced tumor cell apoptosis. PINPs potently inhibited uPA activity and suppressed tumor cell invasion. In vivo, PINPs plus PDT achieved significant tumor growth inhibition (73.6%) and strong anti-metastatic efficacy (60.7%), superior to free IG2. No obvious systemic toxicity was observed. Conclusions: The dual-functional PINPs achieve short-term acute tumor ablation via PDT and sustained anti-metastatic potential via uPA inhibition within the tested observation windows, with favorable biosafety. This carrier-free self-assembly strategy provides proof-of-concept validation and a generalizable design paradigm for developing synergistic anti-metastatic nanotherapeutics against metastatic CRC. Full article