Silica Nanoparticles Research Articles

Thrombin Immobilized on Magnetic Core-Shell Mesoporous Silica Nanoparticles for Screening of the Enzyme Inhibitors From Notopterygium Incisum.

Thrombin was immobilized on magnetic core-shell mesoporous silica nanoparticles (Fe3O4@nSiO2@mSiO2) for the first time and used to screen enzyme inhibitors from extracts of Notopterygium incisum. The immobilized thrombin was characterized by Fourier-transform infrared spectroscopy, transmission electronic microscopy, thermal gravimetric analysis, and vibrating sample magnetometry. The results demonstrated that the immobilized thrombin possessed good thermal stability and high-temperature resistance for feasible storage and reuse. Two ligands, notopterol (1) and isoimperatorin (2) were fished out from the extract of N. incisum using the immobilized thrombin. They inhibited thrombin with IC50 values of 59.35±1.420 and 107.8±1.660µM, respectively. This is the first report of thrombin-inhibitory activity associated with notopterol and isoimperatorin. Meanwhile, the inhibition mechanism of both compounds was investigated by enzyme kinetic analysis and molecular docking. The method used enables rapid screening for thrombin inhibitors from medicinal plants, providing an efficient tool for the discovery of anti-thrombotic active compounds.

An innovative biosensor utilizing aptamer-gated mesoporous silica nanoparticles for determination of aminoglycoside antibiotics through indirect-lateral flow

BackgroundAminoglycoside antibiotics (AGs) are commonly utilized in both human and veterinary medicine to treat and manage a range of infections. These antibiotics are recognized for their narrow therapeutic window, with an overdose potentially resulting in severe side effects like kidney and ear damage. Hence, the implementation of a quick, precise, and on-the-spot testing method is crucial in clinical settings. In the present investigation, we designed an innovative indirect lateral flow assay (LFA) utilizing aptamers to detect kanamycin, a type of aminoglycoside antibiotics. We prepared mesoporous silica nanoparticles (MSNs) functionalized with amino groups, loaded them with morphine (MOP), and then sealed them with aminoglycoside aptamers (Apt). The complex of gated-MSNs@Apt was tested using the MOP LFA in the presence or absence of kanamycin antibiotics. ResultsThe indirect LFA system displayed a single colored line in the test line for positive samples, whereas it exhibited double colored lines in both the control line and test line for negative samples. Our custom-designed LFA biosensors demonstrated two linear ranges, from 10 nM to 350 nM and 500 nM to 1500 nM, with a limit of detection (LOD) of 5 nM in serum media under optimized conditions. The introduced indirect LFA biosensor was effectively utilized to detect kanamycin, achieving a satisfactory recovery rate of 92.9-109.9% with RSD of 1.68-7.73% in serum samples. SignificanceIn general, the created LFA system offers a portable, straightforward, and affordable approach for point-of-care (POC) identification of kanamycin and other AGs.

Microfluidic-assisted synthesis of mesoporous silica nanoparticles as drug carriers: characterization and biocompatibility studies

Microfluidic-assisted synthesis of mesoporous silica nanoparticles as drug carriers: characterization and biocompatibility studies

Microstructure evolution of alite in-situ carbonated by aminated mesoporous silica nanoparticles

Microstructure evolution of alite in-situ carbonated by aminated mesoporous silica nanoparticles

Recent Approaches on Molecular Markers, Treatment and Novel Drug Delivery System Used for the Management of Colorectal Cancer: A Comprehensive Review.

Colorectal cancer affects 1 in 25 females and 1 in 24 males, making it the third most frequent cancer with over 6,08,030 deaths worldwide, despite advancements in detection and treatments, including surgery, chemotherapeutics, radiotherapy, and immune therapeutics. Novel potential agents have increased survival in acute and chronic disease conditions, with a higher risk of side effects and cost. However, metastatic disease has an insignificant long-term diagnosis, and significant challenges remain due to last-stage diagnosis and treatment failure. Early detection, survival, and treatment efficacy are all improved by biomarkers. The advancement of cancer biomarkers' molecular pathology and genomics during the last three decades has improved therapy. Clinically useful prognostic biomarkers assist clinical judgment, for example, by predicting the success of EGFR-inhibiting antibodies in the presence of KRAS gene mutations. Few biomarkers are currently used in clinical settings, so further research is still needed. Nanocarriers, with materials like Carbon nanotubes and gold nanoparticles, provide targeted CRC drug delivery and diagnostics. Light-responsive drugs with gold and silica nanoparticles effectively target and destroy CRC cells. We evaluate the potential use of the long non-coding RNA (non-coding RNA) oncogene plasmacytoma variant translocation 1 (PVT1) as a diagnostic, prognostic, and therapeutic biomarker, along with the latest nanotech breakthroughs in CRC diagnosis and treatment.

Fabrication of composite RGD-tagged poly(lactic acid)-graphene oxide nanofiber containing bone-forming peptide-3 loaded-dendritic silica nanoparticles for bone regeneration in rabbit

In the current study, polylactic acid (PLA)/graphene oxide (GO) based composite scaffolds were fabricated by electrospinning method and then covalently modified with bone-forming peptide-3 (BFP-3)-loaded thiol-functionalized dendritic mesoporous silica nanoparticles (BFP-3@HS-DMSNs) and RGD. In this regard, PLA electrospinning nanofibers and composite of PLA/GO electrospinning nanofibers containing 0.02, 0.01, 0.04, 0.1, 0.2 % of GO were prepared and characterized in terms of mechanical strength, nanofibers diameter, thermal stability, crystallinity, specific surface area, total pore volume and cell adhesion properties. Among the prepared composites, PLA nanofibers containing 0.02 % GO demonstrated superior mechanical and morphological characteristics along with better cell adhesion for mesenchymal stem cell. Then, the PLA/0.02 %GO nanofiber was treated with plasma and consequently modified with N-(2-aminoethyl)maleimide linker which was applied for Cys-RGD and BFP-3@HS-DMSNs conjugation. The obtained results showed desirable adhesion of PLA/0.02 %GO nanofiber after incorporation of RGD (5 % of maleimide groups of the linker) and DMSNs which significantly increase cell adhesion potency (1.53 folds). By incorporation of BFP-3@HS-DMSNs (equivalent to 0.1 µg of BFP-3) to the RGD-tagged PLA/0.02 %GO nanofiber, the scaffold demonstrated better cytocompatibility and MSC differentiation to osteoblast based on biomineralization assay via alizarin red (4.2 folds) and alkaline phosphatase activity (1.7 folds) tests. In preclinical stage, after skull defect creation in rabbits, 5 treatments groups comprising PLA/0.02 %GO nanofiber, PLA/0.02 %GO/DMSNs, PLA/0.02 %GO/DMSNs/Cys-RGD, PLA/0.02 %GO/BFP-3@DMSNs and PLA/0.02%GO/BFP-3@DMSNs/Cys-RGD were used for bone regeneration in skull defects. After 3 months, the implantation of PLA/0.02GO/BFP-3@DMSNs/Cys-RGD showed higher bone regeneration based on CBCT imaging (18.875 mm2 bone formed area) in comparison with other treatment groups. This hybrid multimodal platform is purposely organized interactive processes which lead to potential bone regeneration.

Engineered Biomimetic Nanoparticles-Mediated Targeting Delivery of Allicin Against Myocardial Ischemia-Reperfusion Injury by Inhibiting Ferroptosis.

Cardiac microvascular damage is substantially related with the onset of myocardial ischaemia-reperfusion (IR) injury. Reportedly, allicin (AL) effectively protects the cardiac microvascular system from IR injury. However, the unsatisfactory therapeutic efficacy of current drugs and insufficient drug delivery to the damaged heart are major concerns. Here, inspired by the natural interaction between neutrophils and inflamed cardiac microvascular endothelial cells (CMECs), a neutrophil membrane-camouflaged nanoparticle for non-invasive active-targeting therapy for IR injury by improving drug delivery to the injured heart is constructed. In this study, we engineered mesoporous silica nanoparticles (MSNs) coated with a neutrophil membrane to act as a drug delivery system, encapsulating AL. The potential of the nanoparticles (named AL@MSNs@NM) for specific targeting of infarcted myocardium was assessed using small animal vivo imaging system. The cardiac function of AL@MSNs@NM after treatment was evaluated by Animal Ultrasound Imaging system, HE staining, and Laser Speckle Imaging System. The therapeutic mechanism was analyzed by ELISA kits, immunofluorescence, and PCR. We discovered that AL@MSNs@NM significantly improves cardiac function index, reduced infarct size and fibrosis, increased vascular perfusion in ischemic areas, and also promoted the function of CMECs, including migration, tube formation, shear stress adaptation, and nitric oxide production. Further research revealed that AL@MSNs@NM have cardio-protective functions in IR rats by inhibiting CMEC ferroptosis and increasing platelet endothelial cell adhesion molecule-1 (PECAM-1) expression. Our results indicated that AL@MSNs@NM significantly reversed CMEC ferroptosis and increased PECAM-1 expression, enhanced cardiac function, and reduced myocardial infarction size. Therefore, this strategy demonstrates that engineered biomimetic nanotechnology effectively delivers AL for targeted therapy of myocardial infarction.

Bioactive hydrogel synergizes neuroprotection, macrophage polarization, and angiogenesis to improve repair of traumatic brain injury

Traumatic brain injury (TBI) can lead to severe neurotrauma, leading to long-term cognitive decline and even death. Massive neuronal loss and excessive neuroinflammation are critical issues in the treatment of secondary TBI. To tackle these challenges, we developed a GelMA and CSMA hydrogel loaded with Erythropoietin (EPO) and Interleukin-4 (IL-4), named GC/I/E. By directly loading the hydrogel with EPO, rapid neuroprotection and angiogenesis were achieved. Meanwhile, by loading Mesoporous silica nanoparticles (MSNs) with IL-4 (MSN@IL-4), sustained inflammation modulation during inflammation was attained. In vitro experiments demonstrated that GC/I/E hydrogel were biocompatible and could provide neuroprotection for HT22 cells in H2O2 environment, regulate RAW264.7 polarization from M1 to M2 phenotype and promote HUVEC angiogenesis. In vivo experiments demonstrated that GC/I/E hydrogel reduced brain oedema and Nissl body damage, inhibited inflammatory expression of G3-FFAP and neural scarring, improved microvascular and vascular function reconstruction, and facilitated neuronal and synaptogenesis, ultimately improving neurofunctional recovery in TBI. RNA sequencing results demonstrated that GC/I/E hydrogel treatment significantly correlated with the regulation of genes such as apoptosis, inflammation regulation, and neural regeneration. This bioactive hydrogel with neuroprotection, inflammation modulation and promotion of angiogenesis has great potential for TBI treatment.

Inhibition of Polyphenol Oxidase Activity by Mesoporous Silica Nanoparticles and Multiwalled Carbon Nanotubes Modified with Surfactants.

Polyphenol oxidase (PPO) is the culprit behind the browning of fruits and vegetables. Therefore, how to reduce the thermal deactivation temperature of PPO or use as few safe reagents as possible to inhibit enzymatic browning has practical significance. Mesoporous silica nanoparticles (MSNs) and multiwalled carbon nanotubes (MWCNTs) are stable and have high biosafety. In the present study, efficient PPO inhibitors were developed based on MSNs and MWCNTs. It is found that after modification with a very small amount of dodecyl trimethylammonium bromide (DTAB, ≥60 μg/mL), MSNs can significantly inhibit the activity of PPO although single MSNs and single DTAB show very limited effect on PPO activity. After modification with a very small amount of sodium dodecyl sulfate (SDS, 5.7-9.5 μg/mL), MWCNTs almost completely inactivate PPO. However, SDS@MSN and DTAB@MWCNT cannot decrease PPO activity significantly.

Doxorubicin- and Selenium-Incorporated Mesoporous Silica Nanoparticles as a Combination Therapy for Osteosarcoma

Doxorubicin- and Selenium-Incorporated Mesoporous Silica Nanoparticles as a Combination Therapy for Osteosarcoma

Multifunctional and novelty green composite film containing sodium alginate, chitosan, rice husk and curcumin

Foodborne diseases are a global public health issue, with their causes often originating from lapses in food production or transportation leading to food contamination. Therefore, food packaging plays a crucial role in preserving the safety and quality of food. In pursuit of sustainable development, this study aims to utilize agricultural waste-derived functional mesoporous silica nanoparticles in combination with biodegradable molecules to create food packaging films. Through recycling and the use of environmentally friendly green films, the goal is to achieve sustainability and the objectives of green chemistry. The study anticipates the production of biodegradable films and the testing of their antibacterial capabilities, antioxidant properties, biocompatibility, and film stress coefficients. This research will provide robust support for advancing green packaging technology to address the challenges of global food safety and environmental sustainability.The experiment is divided into two parts. The first part involves the synthesis of multifunctional mesoporous silica nanoparticles with antibacterial properties derived from rice husk (Rice husk mesoporous silica nanoparticles, rMSN) as nano-fillers. These nanoparticles are surface modified with a biodegradable polymer, chitosan (Chi), that interacts with the material. Natural extract curcumin (Cur), known for its antioxidant capabilities, is loaded into the pores, and the material's inherent antibacterial properties are utilized. The second part involves blending the material with the natural polymer sodium alginate (SA) to form a film (rMSN-Chi@Cur/Alg film). The film's thickness, stress strength, antibacterial, and antioxidant capabilities are tested to ensure the material possesses antibacterial and antioxidant properties.

TLR Agonist Nano Immune Therapy Clears Peritoneal and Systemic Ovarian Cancer.

Intraperitoneal (IP) administration of immunogenic mesoporous silica nanoparticles (iMSN) in a mouse model of metastatic ovarian cancer promotes the development of tumor-specific CD8+ T cells and protective immunity. IP delivery of iMSN functionalized with the Toll-like receptor (TLR) agonists polyethyleneimine (PEI), CpG oligonucleotide, and monophosphoryl lipid A (MPLA) stimulated rapid uptake by all peritoneal myeloid subsets. Myeloid cells quickly transported iMSN to milky spots and fat-associated lymphoid clusters (FALCs) present in tumor-burdened adipose tissues, leading to a reduction in suppressive T cells and an increase in activated memory T cells. Two doses of iMSN cleared or reduced ovarian and colorectal cancer and protected against future tumor engraftment. In contrast, subcutaneous (SC) and intravenous (IV) delivery of iMSN were without therapeutic effect in mice with peritoneal metastases, supporting the need for activation of regional immune cells. Remarkably, intraperitoneal delivery of iMSN cleared subcutaneously implanted ovarian cancer, supporting homing of antigen specific T cells to extraperitoneal tumor sites.

Silica/klucel nanocomposite as promising durable adsorbent for lead removal from industrial effluents

The removal of heavy metals, such as lead, from industrial wastewater is imperative due to their detrimental effects on both human health and the environment. This study delves into investigating the feasibility of employing a novel adsorbent, specifically a silica/klucel nanocomposite, for effectively extract lead from industrial effluents. The synthesis of this nanocomposite involved a simple and cost-effective method, combining silica nanoparticles with klucel. XRD, FTIR, E-SEM, Raman, and N2 gas adsorption at − 196 °C tools were employed to prospect the formation of silica/klucel nanocomposite. Outstandingly, treating 50 ml of 50 mg/l of lead with 10 mg of adsorbent exhibited rapid removal, which reached a maximum (95%) at 60 min contact time. The resulting composite demonstrated remarkable adsorption capabilities, primarily attributed to two factors: the expansive surface area of silica nanoparticles 139.1 m2/g and the porous structure provided by klucel. Through batch adsorption experiments, the nanocomposite’s proficiency in removing lead ions from aqueous solutions became evident. The kinetics of the adsorption process were found to adhere closely to a pseudo-second-order model, hinting at chemical adsorption as the rate-determining step. Langmuir isotherm model revealed that lead ions tend to form a monolayer on the surface of the nanocomposite and the maximum adsorption capacity (qm) was 63.938 mg/g. Additionally, the nanocomposite, exhibited notable stability and could be reused multiple times, where 65% removal efficiency was announced until the 7th cycle without significant degradation in performance. In summary, the silica/klucel nanocomposite emerges as a promising and eco-friendly adsorbent for removing lead from industrial effluents. Its efficient performance and sustainability offer a compelling solution to combat heavy metal contamination, thereby contributing to environmental preservation and human well-being.

Organic and Inorganic Modifications to Increase the Efficiency in Immobilization of Heavy Metal (Zn) in Cementitious Composites-The Impact of Cement Matrix Pore Network Characteristics.

This research investigated the properties of modified cementitious composites including water purification from heavy metal-zinc. A new method for characterizing the immobilization properties of tested modifiers was established. Several additions had their properties investigated: biochar (BC), active carbon (AC), nanoparticulate silica (NS), copper slag (CS), iron slag (EAFIS), crushed hazelnut shells (CHS), and lightweight sintered fly ash aggregate (LSFAA). The impact of modifiers on the mechanical and rheological properties of cementitious composites was also studied. It was found that considered additions had a significantly different influence over the investigated properties. The addition of crushed hazelnut shells, although determined as an effective immobilization modifier, significantly deteriorated the mechanical performance of the composite as well as its rheological properties. Modification by iron slag allowed for a significant increase in immobilization properties (five-fold compared to the reference series) without a substantial impact on other properties. The negative effect on immobilization efficiency was observed for nanoparticulate silica modification due to its sealing effect on the pore network of the cement matrix. The capillary pore content in the cement matrix was identified as a parameter significantly influencing the immobilization potential of most considered modifications, except biochar and active carbon.

Silicon dioxide incorporated cellulose acetate-mixed matrix membranes for Safranin-O removal from aqueous solutions.

Nanoparticle incorporated-mixed matrix membranes are renowned for their multifaceted advantages, including improved hydrophilicity, elevated solute rejection, enhanced mechanical robustness, and augmented chemical and thermal stability. The inherent hydrophilicity of silicon dioxide (SiO2) nanoparticles, due to silanol groups (Si-OH), along with their high porosity and surface area, renders them an ideal reinforcing filler within polymer matrices, significantly strengthening structural integrity of membranes. In this work, SiO2 nanoparticles were incorporated in a cellulose acetate (CA) matrix to prepare CA/SiO2 adsorptive membranes using phase inversion method. The performance of the membranes was assessed on the removal of Safranin-O (Sf-O) from aqueous solution. The physicochemical characterization of the synthesized membranes was assessed using contact angle, XRD, FE-SEM, EDS, FTIR, TGA, and tensile strength studies. The optimization studies on novel CA/SiO2 membrane revealed that the membrane with 2.5 wt.% of SiO2 in the CA matrix was the best in terms of Sf-O removal (approximately 100% dye removal) when the operating pH, initial dye concentration, and operating pressure were 9, 50 ppm, and 1 bar respectively. It is also found that 2.5 wt.% CA/SiO2 membrane has higher water permeability than other membranes. Incorporating SiO2 nanoparticles into a polymer matrix augments the structural, mechanical, and thermal properties of the resulting membranes while also enhancing water permeability, selectivity, and dye removal efficacy.

Incorporating silica nanoparticles with silver patches into alginate-based bioinks for 3D bioprinting

Abstract Alginate dialdehyde-gelatin (ADA-GEL) hydrogels are being studied in bioprinting for their combination of cell adhesion and printability. To incorporate specific functionalities and to improve printability, different additives to ADA-GEL inks are being proposed. Here, a novel type of functional nanoparticles comprising silver patches on silica cores was incorporated into ADA-GEL bioinks. Silver patchy particles (SPPs) were present both on the surface and interior of printed structures. Incorporation of SPPs improved printability of ADA-GEL inks and supported osteosarcoma (MG-63) cells over 7 days of culture. SPPs represent a valuable additive for ADA-GEL hydrogels, being attractive to develop bioinks with advanced functionalities. Graphical abstract

Glycocalyx Interactions Modulate the Cellular Uptake of Albumin-Coated Nanoparticles.

Albumin-based nanoparticles (ABNPs) represent promising drug carriers in nanomedicine due to their versatility and biocompatibility, but optimizing their effectiveness in drug delivery requires understanding their interactions with and uptake by cells. Notably, albumin interacts with the cellular glycocalyx, a phenomenon particularly studied in endothelial cells. This observation suggests that the glycocalyx could modulate ABNP uptake and therapeutic efficacy, although this possibility remains unrecognized. In this study, we elucidate the critical role of the glycocalyx in the cellular uptake of a model ABNP system consisting of silica nanoparticles (NPs) coated with native, cationic, and anionic albumin variants (BSA, BSA+, and BSA-). Using various methodologies-including fluorescence anisotropy, dynamic light scattering, microscale thermophoresis, surface plasmon resonance spectroscopy, and computer simulations─we found that both BSA and BSA+, but not BSA-, interact with heparin, a model glycosaminoglycan (GAG). To explore the influence of albumin-GAG interactions on NP uptake, we performed comparative uptake studies in wild-type and GAG-mutated Chinese hamster ovary cells (CHO), along with complementary approaches such as enzymatic GAG cleavage in wild-type cells, chemical inhibition, and competition assays with exogenous heparin. We found that the glycocalyx enhances the cell uptake of NPs coated with BSA and BSA+, while serving as a barrier to the uptake of NPs coated with BSA-. Furthermore, we showed that harnessing albumin-GAG interactions increases cancer cell death induced by paclitaxel-loaded albumin-coated NPs. These findings underscore the importance of albumin-glycocalyx interactions in the rational design and optimization of albumin-based drug delivery systems.

Antimicrobial and Antioxidant Properties of Photodegraded Amorphous Curcumin on Silica Nanoparticles

Antimicrobial and Antioxidant Properties of Photodegraded Amorphous Curcumin on Silica Nanoparticles

Basalt Fiber-Reinforced Epoxy Laminates: Improvement in Quasi-Static and Fatigue Properties with Modified Matrices and Fiber Surfaces Using Silica Nanoparticles

Basalt Fiber-Reinforced Epoxy Laminates: Improvement in Quasi-Static and Fatigue Properties with Modified Matrices and Fiber Surfaces Using Silica Nanoparticles

Application of micro and nano modifying additives in road construction materials

The need for stronger and more sustainable road infrastructure has stimulated research into innovative materials, including micro- and nano-additives, to improve the performance of asphalt and bitumen. This paper aims to summarize the advances in the application of these additives with a focus on improving mechanical, thermal, and environmental properties. The study provides a detailed review of traditional micro-additives such as elastomers and resins, as well as advanced nanomaterials including nano silica, nano clay, and carbon nanoparticles. Methods include analyzing experimental data from recent studies on bitumen modification with biopolymeric materials such as polylactic acid (PLA), which show an increase in molecular weight, softening point, and ductility. The main results show that the use of nano additives improves the durability of the road surface, increases its resistance to cracking, and increases the service life of the material under different climatic conditions. For example, roads modified with nano silica showed a 20-30% improvement in tensile strength and a 15% reduction in deformation. In addition, PLA bitumen modification increased the softening point by 10°C and improved the overall elasticity by 25%. These results emphasize the potential of micro- and nano-additives to create more durable, environmentally friendly, high-performance road materials.