Magnetic Mesoporous Nanoparticles Research Articles

Efficient defluoridation of drinking water using mesoporous magnetic malachite nanocomposites

The study evaluated the efficacy of magnetic mesoporous Malachite nanoparticles (NPs) in eliminating fluoride (F−) from drinking water. Screening experiments were conducted to gauge the F− adsorption capabilities of the synthesized material under different Fe3O4 loading conditions. Among the various nanomaterials examined, 0.25-Fe-M demonstrated optimal performance, exhibiting consistent Fe3O4 distribution with a crystal size of 16.66 nm with revealed irregular morphology exhibiting magnetic properties, a surface area of 13.595 m2/g and a pore size of 1.6574 nm. The optimized reaction conditions determined were: 10 min of contact time, a NC dose of 0.5 mg/mL, and an F− concentration of 10 mg/L. The maximum adsorption capacities recorded were 6.57 mg/g for Fe3O4 NPs and 7.87 mg/g for malachite NPs. Notably, the optimal adsorption capacity for F− removal was achieved with 0.25 Fe-M-NCs, reaching 8.44 mg/g, demonstrating superior performance compared to other NCs. The interplay between surface area, pore volume, and adsorption is intricate and contingent upon the unique properties of the adsorbent and adsorbate, with specific interactions governing the adsorption process. Furthermore, this study unveiled accelerated adsorption with shorter contact time and high adsorption capacity at the working pH.

Development of mesoporous magnetic nanoparticles supported idarubicin and investigation of apoptotic and cytotoxic effects on cancer cell lines.

Many methods are used for cancer treatment, especially chemotherapy. In addition to the their therapeutic effects, chemotherapeutic drugs also have serious disadvantages, such as not being cell and tissue-specific, causing toxicity in many tissues, and developing drug resistance. Many methods, especially nanocarriers, have been designed to overcome these disadvantages. In this study, we synthesized mesoporous silica iron oxide nanoparticles with different pore diameters and loaded idarubicin (6MFe3O4-NH2-IDA and 35MFe3O4-NH2-IDA). The synthesized molecules were characterized using FT-IR, XRD, and SEM methods. The cytotoxic effects of unbound idarubicin and idarubicin-loaded nanoparticles on MCF7 and HL-60 cell lines were examined by MTT test. Additionally, the expression of anti-apoptotic (Survivin and BCL-2) and apoptotic (BAX, PUMA, and NOXA) genes of the nanoparticles were measured by PCR method. As a result of the analyses, it was seen that nanoparticles with the desired properties and sizes were synthesized. In MTT analysis, it was observed that both nanoparticles dramatically decreased the IC50 value in cell lines. However, the 35MFe3O4-NH2-IDA molecule was found to have lower IC50 values. IC50 values ​​for pristine IDA, 6MFe3O4-NH2, and 35MFe3O4-NH2 at 24h were found to be 3.56, 1.24 and 0.25 µM in the MCF7 cell line and 4.15, 1.16 and 0.34 µM in the HL-60 cell line, respectively. Additionally, apoptotic gene expression increased, and anti-apoptotic gene expression decreased. Our study demonstrates that the effectiveness of idarubicin can be significantly enhanced by its application with mesoporous nanocarriers. This enhancement is attributed to the controlled release of idarubicin from the nanocarrier, which circumvents drug resistance mechanisms, improves drug solubility, and increases the drug-carrying capacity per unit volume due to the porous structure of the carrier. These findings underscore the potential of the synthesized nanocarrier in cancer treatment and provide a clear direction for future research in this field.

Theranostic Nanoplatform Based on Polydopamine-Coated Magnetic Mesoporous Silicon for Precise Cancer Triplex Nanotherapy and Multimodal Imaging.

Although targeted therapy has revolutionized oncotherapy, engineering a versatile oncotherapy nanoplatform integrating both diagnostics and therapeutics has always been an intractable challenge to overcome the limitations of monotherapy. Herein, a theranostics platform based on DI/MP-MB has successfully realized the fluorescence detection of disease marker miR-21 and the gene/photothermal/chemo triple synergetic cancer therapy, which can trace the tumor through photothermal and fluorescence dual-mode imaging and overcome the limitations of monotherapy to improve the treatment efficiency of tumors. DI/MP-MB was prepared by magnetic mesoporous silicon nanoparticles (M-MSNs) loaded with doxorubicin (Dox) and new indocyanine green (IR820), and subsequently coating polydopamine as a "gatekeeper", followed by the surface adsorbed with molecular beacons capable of targeting miR-21 for responsive imaging. Under the action of enhanced permeability retention and external magnetic field, DI/MP-MB were targeted and selectively accumulated in the tumor. MiR-21 MB hybridized with miR-21 to form a double strand, which led to the desorption of miR-21 MB from the polydopamine surface and the fluorescence recovery to realize gene silencing and fluorescence imaging for tracking the treatment process. Meanwhile, with the response to the near-infrared irradiation and the tumor's microacid environment, the outer layer polydopamine will decompose, releasing Dox and IR820 to realize chemotherapy and photothermal therapy. Finally, the ability of DI/MP-MB to efficiently suppress tumor growth was comprehensively assessed and validated both in vitro and in vivo. Noteworthily, the excellent anticancer efficiency by the synergistic effect of gene/photothermal/chemo triple therapy of DI/MP-MB makes it an ideal nanoplatform for tumor therapy and imaging.

Highly Efficient Separation of Ethanol Amines and Cyanides via Ionic Magnetic Mesoporous Nanomaterials.

Simple and efficient sample pretreatment methods are important for analysis and detection of chemical warfare agents (CWAs) in environmental and biological samples. Despite many commercial materials or reagents that have been already applied in sample preparation, such as SPE columns, few materials with specificity have been utilized for purification or enrichment. In this study, ionic magnetic mesoporous nanomaterials such as poly(4-VB)@M-MSNs (magnetic mesoporous silicon nanoparticles modified by 4-vinyl benzene sulfonic acid) and Co2+@M-MSNs (magnetic mesoporous silicon nanoparticles modified by cobalt ions) with high absorptivity for ethanol amines (EAs, nitrogen mustard degradation products) and cyanide were successfully synthesized. The special nanomaterials were obtained by modification of magnetic mesoporous particles prepared based on co-precipitation using -SO3H and Co2+. The materials were fully characterized in terms of their composition and structure. The results indicated that poly(4-VB)@M-MSNs or Co2+@M-MSNs had an unambiguous core-shell structure with a BET of 341.7 m2·g-1 and a saturation magnetization intensity of 60.66 emu·g-1 which indicated the good thermal stability. Poly(4-VB)@M-MSNs showed selective adsorption for EAs while the Co2+@M-MSNs were for cyanide, respectively. The adsorption capacity quickly reached the adsorption equilibrium within the 90 s. The saturated adsorption amounts were MDEA = 35.83 mg·g-1, EDEA = 35.00 mg·g-1, TEA = 17.90 mg·g-1 and CN-= 31.48 mg·g-1, respectively. Meanwhile, the adsorption capacities could be maintained at 50-70% after three adsorption-desorption cycles. The adsorption isotherms were confirmed as the Langmuir equation and the Freundlich equation, respectively, and the adsorption mechanism was determined by DFT calculation. The adsorbents were applied for enrichment of targets in actual samples, which showed great potential for the verification of chemical weapons and the destruction of toxic chemicals.

Advanced magnetic adsorbents for enhanced phosphorus and fluoride removal from wastewater: Mechanistic insights and applications

A novel mesoporous magnetic nanoparticle adsorbent, Fe3O4@CSH-AAO, was synthesized using the atomization-precipitation method, effectively removing phosphorus (P) and fluoride (F) from wastewater, particularly from the recirculating water of wet-process phosphoric acid. The adsorbent achieved removal efficiencies of 99.6 % for P and 73.5 % for F under conditions of 20 g/L adsorbent dosage, pH ≈ 4, with initial P and F concentrations at 115 mg/L and 38 mg/L, respectively. Equilibrium adsorption data indicated that the adsorption kinetics followed the pseudo-second-order model for F and the pseudo-first-order model for P. The adsorption isotherms fitted the Langmuir model for P and the Freundlich model for F, with maximum adsorption capacities of 37.86 mg P/g and 6.764 mg F/g at pH 4 and 298 K. The surface properties, functionality, and crystallinity were analyzed using BET, SEM, TEM, XRD, and XRF. Furthermore, XPS analyses and molecular dynamics (MD) simulations elucidated that surface Ca in CSH and the exposed Al atoms on the γ-Al2O3 (110) surface serve as optimal adsorption sites for P and F. The steric hindrance imposed by phosphorus contributes to its preferentially higher adsorption capacity over fluoride. This study not only presents an effective method for the removal of phosphorus and fluoride suitable for practical applications but also provides deep insights into the adsorption mechanism, highlighting the pivotal role of steric hindrance in facilitating ion adsorption.

Magnetic natural lipid nanoparticles for oral treatment of colorectal cancer through potentiated antitumor immunity and microbiota metabolite regulation

The therapeutic efficacy of oral nanotherapeutics against colorectal cancer (CRC) is restricted by inadequate drug accumulation, immunosuppressive microenvironment, and intestinal microbiota imbalance. To overcome these challenges, we elaborately constructed 6-gingerol (Gin)-loaded magnetic mesoporous silicon nanoparticles and functionalized their surface with mulberry leaf-extracted lipids (MLLs) and Pluronic F127 (P127). In vitro experiments revealed that P127 functionalization and alternating magnetic fields (AMFs) promoted internalization of the obtained P127-MLL@Gins by colorectal tumor cells and induced their apoptosis/ferroptosis through Gin/ferrous ion-induced oxidative stress and magneto-thermal effect. After oral administration, P127-MLL@Gins safely passed to the colorectal lumen, infiltrated the mucus barrier, and penetrated into the deep tumors under the influence of AMFs. Subsequently, the P127-MLL@Gin (+ AMF) treatment activated antitumor immunity and suppressed tumor growth. We also found that this therapeutic modality significantly increased the abundance of beneficial bacteria (e.g., Bacillus and unclassified-c-Bacilli), reduced the proportions of harmful bacteria (e.g., Bacteroides and Alloprevotella), and increased lipid oxidation metabolites. Strikingly, checkpoint blockers synergistically improved the therapeutic outcomes of P127-MLL@Gins (+ AMF) against orthotopic and distant colorectal tumors and significantly prolonged mouse life spans. Overall, this oral therapeutic platform is a promising modality for synergistic treatment of CRC.

Magnetic Fe3O4@SiO2 study on adsorption of methyl orange on nanoparticles

Magnetic core–shell Fe3O4@SiO2 nanoparticles were synthesized by sol–gel method. Based on the characterization and experimental results, the adsorbent was found to have an average particle size of approximately 120 nm, a pore size range of 2–5 nm and superparamagnetic properties. It exhibited electrostatic and hydrogen bonding interactions during adsorption of methyl orange (MO). The adsorption of MO on the magnetic Fe3O4@SiO2 nanoparticles exhibited pseudo-second-order kinetics, the adsorption process is a spontaneous endothermic adsorption process, which conforms to the Langmuir adsorption isotherm model. he maximum amount of MO was adsorbed at pH = 2, T = 45 °C and t = 30 min, and the highest adsorption capacity was 182.503 mg/g; The unit adsorption capacity of the Fe3O4@SiO2 nanoparticles still reached 83% of the original capacity after 5 cycles, so the material was reusable and met the requirements of environmental protection. This study reveals the great potential of magnetic mesoporous nanoparticles for removal of dyes from wastewater.

Magnetic mesoporous Fe3O4@nSiO2@mSiO2 nanoparticles for high-throughput mass spectrometry detection of hydrolyzed products of organophosphorus nerve agents.

Rapid and accurate detection of hydrolyzed products of organophosphorus nerve agents (OPNAs) is an important method to effectively confirm the use of these agents. OPNAs are rapidly hydrolyzed to the methyl phosphonates (MPs) in the environment, which can be used as environmental traceability marker for OPNAs. Herein, magnetic mesoporous materials combined with real-time in situ mass spectrometry (MS) were used to achieve high-throughput detection of MPs. Novel magnetic mesoporous nanoparticles Fe3O4@nSiO2@mSiO2 were synthesized via co-condensation of tetraethyl orthosilicate and cetyltrimethylammonium bromide (CTAB) on the surface of nonporous silica-coated Fe3O4 under alkaline conditions. CTAB templates were removed by the reflux of ethanol (0.0375 mM ammonium nitrate) to form mesoporous SiO2, which has a large specific surface area of 549 m2 g-1 and an excellent magnetization strength of 59.6 emu g-1. A quick, cost-effective, rugged, and safe magnetic preparation method, magnetic QuEChERS, was established with magnetic mesoporous nanoparticles (Fe3O4@nSiO2@mSiO2) as adsorption materials for direct analysis in real-time and tandem MS (DART-MS/MS) of MPs in environmental samples. The method exhibits good linearity (R2 > 0.992) in the range of 20.0-4.00 μg mL-1, the limits of detection were <5.00 ng mL-1, the limits of quantification were <20.0 ng mL-1, and the extraction recoveries were 70.2-98.1%, with relative standard deviations (RSDs) in the range of 1.97-10.6%. Additionally, using this method, analysis of 70 environmental samples could be completed within 20 min. Then, the M-QuEChERS-DART-MS/MS method was applied to the 52nd Organisation for the Prohibition of Chemical Weapons (OPCW) environmental spiked samples analysis, where the accuracy was 95.2-116%, and the RSD was 1.16-7.83%. The results demonstrated that Fe3O4@nSiO2@mSiO2 based on the QuEChERS method can quickly and efficiently remove the matrix of environmental samples and when coupled with the DART-MS/MS can achieve high-throughput determination of MPs in environmental samples.

Fabrication and characterization of magnetic mesoporous nanoparticles for efficient determination and magnetic separation of sulfonamides in food samples.

A magnetic, mesoporous core/shell structured Fe3O4@SiO2@mSiO2 nanocomposite was synthesized and employed as a magnetic solid phase extraction (MSPE) sorbent for the determination of trace sulfonamides (SAs) in food samples. The synthesized nanocomposite was characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis, X-ray diffraction, N2 sorption analysis and vibrating sample magnetometry. The results showed that Fe3O4@SiO2@mSiO2 possessed a mesoporous structure with a large surface area. Batch experiments were carried out to investigate the adsorption ability for SAs. Fe3O4@SiO2@mSiO2 showed fast kinetics and high adsorption capacity, and the pseudo-second-order model and Langmuir adsorption isotherm are well fitted with the experimental data, indicating that chemical adsorption might be the rate-limiting step. Moreover, the high adsorption capacity can be maintained for at least 8 runs, indicating excellent stability and reusability. The proposed method exhibited good linearity in the range of 0.2-500 μg L-1, the R2 values of all the analytes were greater than 0.99 and the LODs were all lower than 0.2 μg L-1. Furthermore, real food samples were successfully analyzed with Fe3O4@SiO2@mSiO2 and high recoveries varying from 89.7% and 110.6% were obtained with low relative standard deviations ranging from 1.78% to 6.91%. The Fe3O4@SiO2@mSiO2 magnetic nanocomposite is a promising sorbent for the efficient extraction of SAs from complex food samples.

Upscale Synthesis of Magnetic Mesoporous Silica Nanoparticles and Application to Metal Ion Separation: Nanosafety Evaluation.

The synthesis of core-shell magnetic mesoporous nanoparticles (MMSNs) through a phase transfer process is usually performed at the 100-250 mg scale. At the gram scale, nanoparticles without cores or with multicore systems are observed. Iron oxide core nanoparticles (IO) were synthesized through a thermal decomposition procedure of α-FeO(OH) in oleic acid. A phase transfer from chloroform to water was then performed in order to wrap the IO nanoparticles with a mesoporous silica shell through the sol-gel procedure. MMSNs were then functionalized with DTPA (diethylenetriaminepentacetic acid) and used for the separation of metal ions. Their toxicity was evaluated. The phase transfer procedure was crucial to obtaining MMSNs on a large scale. Three synthesis parameters were rigorously controlled: temperature, time and glassware. The homogeneous dispersion of MMSNs on the gram scale was successfully obtained. After functionalization with DTPA, the MMSN-DTPAs were shown to have a strong affinity for Ni ions. Furthermore, toxicity was evaluated in cells, zebrafish and seahorse cell metabolic assays, and the nanoparticles were found to be nontoxic. We developed a method of preparing MMSNs at the gram scale. After functionalization with DTPA, the nanoparticles were efficient in metal ion removal and separation; furthermore, no toxicity was noticed up to 125 µg mL-1 in zebrafish.

Mesoporous magnetic nanoparticles conjugated aptamers for exosomes capture and detection of Alzheimer's disease

Mesoporous magnetic nanoparticles conjugated aptamers for exosomes capture and detection of Alzheimer's disease

Development of a new method for the preparation of mesoporous magnetic nanoparticles of cobalt ferrite (CoFe2O4) with applied parameters for magnetic hyperthermia

This study introduces a novel method for preparing mesoporous magnetic cobalt ferrite nanoparticles (CoFe2O4) for magnetic hyperthermia and other applications. The synthesis of nanoparticles was carried out using the solvo thermal method assisted by Cetyltrimethylammonium Bromide. TEM results revealed a spherical and mesoporous shape, and according to the histogram, the average particle size distribution is uniform, with a diameter of 132 ± 21 nm. This study provides a new platform for the application of magnetic mesoporous nanoparticles in magnetic hyperthermia therapy. The methodology is relevant because it allows the formation of mesoporous structures.

Synthesis and Characterization of Core-Shell Mesoporous Iron oxide Magnetic Nanoparticles using Modified Co-Precipitation Method

In recent era, development of nanotechnology is an art of delivery of drug by improving its compatibility, effectiveness and efficacy. Among all nanoparticles, magnetic nanoparticles play a predominant role to shows their targeted drug delivery using a magnetic field, also helps to diagnose the diseases like cancer. The present study included preparation of four different mesoporous nanoparticles using the Pluronic block copolymer P123 as a surfactant template, then insert iron oxides using co-precipitation method. The resulted formed mesoporous magnetic nanoparticles are examined for structural characters by using FTIR, XRD, HRSEM and Elemental Mapping techniques. The results of X-ray diffraction (XRD) showed that the formed composites conserved ordered mesoporous structure after the formation of iron oxide nanoparticles in the pores. FTIR results indicated that the surface contains silanol group and Fe–O on the surface of the materials at 1060 cm-1 and 1020 cm-1 peaks respectively. Scanning electron microscopy (SEM) results showed that all mesoporous magnetic nanoparticles within the range of size from 50 to 100nm also possessed a regular spherical shape. These particles possessed high surface area, high pore volume and showed magnetic response sufficient for drug targeting in the presence of an external magnetic field. Elemental mapping data indicated about the percentage of all elements present in the mesoporous materials. We concluded that all four types of magnetic nanoparticles are structurally arranged in their structure with sufficient percentage of elements on their particle surface along with good size range. Further loading of drug into all types of magnetic nanoparticles decides the loading efficiency, stability and drug release nature.

Direct coupling of CO2 with epoxides catalyzed by lanthanum(III) supported on magnetic mesoporous organosilica nanoparticles

Lanthanum(III) supported on the magnetic mesoporous organosilica nanoparticle (La@MON) has been described as an efficient, simple, and durable heterogeneous catalyst for the synthesis of 5-membered cyclic carbonates from carbon dioxide (CO2) and epoxides. Under optimized reaction conditions, various terminal epoxides have been converted to the corresponding carbonates in the presence of 0.3 mol% La@MON and 0.5 mol% tetrabutylammonium iodide (TBAI) as co-catalyst at relatively mild reaction conditions. It was also found that La@MON catalysts had significantly higher catalytic activity than some selected reference catalysts, which can be explained by the abundance of lanthanum(III) species acting as Lewis acidic sites for activating both carbon dioxide and epoxide molecules, along with the fact that the catalyst channels are short and provided facile mass transfer. The catalyst showed good reusability for at least five reaction cycles while the magnetic core of the catalyst helps the easy separation of the catalyst by just using an external magnet.

Synergistic Pro-Apoptotic Effect of a Cyclic RGD Peptide-Conjugated Magnetic Mesoporous Therapeutic Nanosystem on Hepatocellular Carcinoma HepG2 Cells.

Numerous nanocarriers have been developed to deliver drugs for the treatment of hepatocellular carcinoma. However, the lack of specific targeting ability, the low administration efficiency, and insufficient absorption by hepatocellular carcinoma cells, severely limits the therapeutic effect of the current drugs. Therefore, it is still of great clinical significance to develop highly efficient therapies with few side effects for the treatment of hepatocellular carcinoma. Herein, we developed a highly effective nanocarrier, cyclic RGD peptide-conjugated magnetic mesoporous nanoparticles (RGDSPIO@MSN NPs), to deliver the chemotherapeutic drug doxorubicin (DOX) to human hepatocellular carcinoma HepG2 cells, and further explored their synergistic apoptosis-promoting effects. The results showed that the prepared RGDSPIO@MSN NPs had good stability, biosafety and drug-loading capacity, and significantly improved the absorption of DOX by HepG2 cells, and that the RGDSPIO@MSN@DOX NPs could synergistically promote the apoptosis of HepG2 cells. Thus, this cyclic RGD peptide-modified magnetic mesoporous silicon therapeutic nanosystem can be regarded as a potentially effective strategy for the targeted treatment of hepatocellular carcinoma.

Accelerated and simplified synthesis of magnetic mesoporous nanoparticles in a continuous multistep microfluidic system

Here a fully continuous flow strategy for the preparation of Fe3O4@nSiO2@mSiO2 nanocomposites starting from ferrous and ferric ions was established for the first time. The three synthetic steps for Fe3O4 core, nonporous silica middle shell and mesoporous silica outer shell were connected and integrated into a single flow sequence with a total residence time of approximately 3 min. Moreover, the multistep continuous flow system was simplified with smaller footprint and increased safety by feeding all the ammonia needed by the three synthetic steps only once at the starting point of the system. The final product Fe3O4@nSiO2@mSiO2 nanoparticles with a specific surface area 378 m2 g−1 and saturation magnetization 19.3 emu g−1 showed great potential as a catalyst support with easy and excellent recyclability. Proved to be capable of achieving fast and accurate parameter optimization, the uninterrupted continuous flow system proposed in this work holds great prospects to mediate multistep synthesis of complex nanoparticles with hierarchical structures in an efficient and controllable manner.

High-Efficient Anionic Dyes Removal from Water by Cationic Polymer Brush Functionalized Magnetic Mesoporous Silica Nanoparticles

High efficiency removal of methyl orange (MO) and bromothymol blue (BT) dyes from contaminated water has been reported using magnetic mesoporous nanoparticles modified with cationic polymer brush (poly(2-methacryloyloxy)ethyl] trimethylammonium chloride solution) (Fe3O4-MSNs-PMETAC). Atom transfer radical polymerization (ATRP) was utilized to grow the polymer chains on the magnetic mesoporous silica nanoparticles. The chemical surface modifications were confirmed using IR, TGA, SEM and TEM. The results show that the obtained Fe3O4-MSNs-PMETAC materials were nearly spherical in shape with approximately 30 nm magnetic core, and silica shell thicknesses ranged from 135 to 250 nm. The adsorption performance of the material was found to be unaffected by the pH (3-9) of the media, with a removal efficiency of 100% for both dyes. The adsorption of BT and MO on the surface of Fe3O4-MSNs-PMETAC was found to follow Freundlich and Langmuir models, respectively. Since the synthesized nanocomposite materials exhibit an enhanced properties such as large maximum adsorption capacity, rapid synthesis process, and easy separation from solution, it could be an effective sorbent for the removal of other pollutants such as potentially toxic anionic elements (e.g., arsenate and chromate ions) from water and wastewater.

Polyethyleneimine Functionalized Mesoporous Magnetic Nanoparticles with Enhanced Antibacterial and Antibiofilm Activity in an Alternating Magnetic Field.

Despite a lot of research on the antibacterial effect of Fe3O4 nanoparticles, their interactions with biofilm matrix have not been well understood. The surface charge of nanoparticles mainly determines their ability to adhere on the biofilm. In this work, negatively charged Fe3O4 nanoparticles were synthesized via a trisodium citrate-assisted solvothermal method and then the surfaces were functionalized using polyethyleneimine (PEI) to obtain positively charged Fe3O4 nanoparticles. The antibacterial and antibiofilm activities of both negatively and positively charged Fe3O4 nanoparticles in an alternating magnetic field were then systematically investigated. The positively charged Fe3O4 nanoparticles showed a strong self-adsorbed attachment ability to the planktonic and sessile cells, resulting in a better antibacterial activity and enhanced biofilm eradication performance compared to the conventional Fe3O4 nanoparticles with negative charges. Fe3O4@PEI nanoparticles produced physical stress and thermal damage in response to an alternating magnetic field, inducing the accumulation of intracellular reactive oxygen species into live bacterial cells, bacterial membrane damage, and biofilm dispersion. Utilizing an alternating magnetic field along with positively charged nanoparticles leads to a synergistic antibacterial approach to improve the antibiofilm performance of magnetic nanoparticles.

Preparation of Folic Conjugated Magnetic Silica Mesoporous Nanoparticles and Their Encapsulated 10-HCPT Anticancer Behavior

Preparation of Folic Conjugated Magnetic Silica Mesoporous Nanoparticles and Their Encapsulated 10-HCPT Anticancer Behavior

Magnetic mesoporous silica nanoparticles as a theranostic approach for breast cancer: Loading and release of the poorly soluble drug exemestane

Exemestane has a limited aqueous solubility that leads to a very high variability in absorption when administrated orally. It is crucial to develop strategies to increase the solubility and bioavailability of this drug. To overcome these issues, the aim of the present work was the development of magnetic silica mesoporous nanoparticles (IOMSNs) to carry and release exemestane. Furthermore, these nanoparticles could be also used as Magnetic Resonance Imaging (MRI) contrast agents for treatment monitorization and tumor detection. MRI analysis showed that IOMSNs present a concentration dependent contrast effect, revealing their potential for MRI applications. Also, IOMSNs present a very good polydispersity (0.224) and nanometric range size (137.2 nm). It was confirmed that the nucleus is composed by magnetite and the silica coating presents tubes with MCM-41-like hexagonal structure. Both iron oxide nanoparticles and iron oxide mesoporous silica nanoparticles were not toxic in cell culture for 24 h. Exemestane was successful released for 72 h following a typical sustained release pattern, achieving a very high loading capacity (37.7%) and in vitro release of 98.8%. Taking into account the results it is possible to conclude that IOMSNs have a high potential to be used as theranostic for intravenous breast cancer treatment with exemestane.