Nanocarrier systems loaded with IR780, iron oxide nanoparticles and chlorambucil for cancer theragnostics.

Theragnostics has become a popular term nowadays, since it enables both diagnosis and therapy at the same time while only using one carrier platform. Therefore, formulating a nanocarrier system that could serve as theragnostic agent by using simple techniques would be an advantage during production. In this project, we aimed to develop a nanocarrier that can be loaded with the chemotherapeutic medication chlorambucil and magnetic resonance imaging agents (e.g., iron oxide nanoparticles and near-infrared fluorophore IR780) for theragnostics. Poly(lactic-co-glycolic acid) was combined with the aforementioned ingredients to generate poly(vinyl alcohol)-based nanoparticles (NPs) using the single emulsion technique. Then the NPs were coated with F127 and F127-folate by simple incubation for five days. The nanoparticles have the hydrodynamic size of approx. 250 nm with negative charge. Similar to chlorambucil and IR780, iron oxide loadings were observed for all three kinds of NPs. The release of chlorambucil was quicker at pH 5.4 than at pH 7.4 at 37 °C. The F127@NPs and F127-folate@NPs demonstrated much greater cell uptake and toxicity up to 72 h after incubation. Our in vitro results of F127@NPs and F127-folate@NPs have demonstrated the ability of these systems to serve as medication and imaging agent carriers for cancer treatment and diagnostics, respectively.

Development of alginate-based film incorporated with anthocyanins of red cabbage and zinc oxide nanoparticles as freshness indicator for prawns.

The objective of this study was to develop pH-sensitive film indicators for intelligent food packaging by incorporating red cabbage anthocyanins (RCA) and zinc oxide nanoparticles (ZnO NPs) into an alginate (Alg) film, aiming to mitigate the risk of foodborne illnesses. The films were fabricated using a solvent-casting method and crosslinked with a calcium chloride (CaCl2) solution. Thorough evaluations of the films' physical, mechanical, and structural properties demonstrated significant improvements in elastic modulus and UV/vis light barrier characteristics, reduced water vapor permeability (WVP), and moisture content attributed to integrating RCA and ZnO NPs. The resulting film displayed discernible color changes when exposed to various pH buffer solutions and ammonia vapor, indicating heightened sensitivity to pH fluctuations due to the presence of ZnO NPs. Visual assessment using prawns as test specimens revealed a color shift from violet (indicating satisfactory condition) to blue-greenish (indicating spoilage), corroborated by colorimetric analysis. Moreover, the Alg/ZnO/RCA film exhibited antioxidant and antibacterial properties, demonstrated biodegradation activity, and showed no toxic effects on RSC96 cells, further underscoring its potential as an effective freshness indicator for food products.

Covalently Functionalized Graphene with Molecularly Imprinted Polymers for Selective Adsorption and Electrochemical Detection of Chloramphenicol.

In this report, we have presented a novel route to attach molecularly imprinted polymers (MIPs) on the surface of reduced graphene oxide (rGO) through covalent bonding. First, the surface of rGO was modified with maleic anhydride (MA) via a Diels-Alder reaction using a deep eutectic solvent (DES). Next, 3-propyl-1-vinylimidazolium molecular units were anchored and polymerized in the presence of ethylene glycol dimethacrylate (EGDMA) using chloramphenicol (CAP) as the template. Primarily, we investigated the effect of the molar ratio of individual precursors on the adsorption capacity of synthesized materials and accordingly fabricated the electrochemical sensor for CAP detection. Electrochemical results evidenced that the covalent bonding of MIP units enhanced the sensitivity of the respective sensor toward CAP in water as well as in real honey samples with high selectivity, stability, and reproducibility. This synthesis strategy involves the covalent binding of MIP on rGO materials via click chemisty under sonication power excluding harmful solvents and energy-intensive processes and thus could be a motivation for developing future electrochemical sensors through similar "green" routes.

Click-Chemistry-Mediated Synthesis of Silver Nanoparticle-Supported Polymer-Wrapped Carbon Nanotubes: Glucose Sensor and Antibacterial Material.

We report a novel approach for the synthesis of silver nanoparticles (NPs) stabilized on polymer-wrapped carbon nanotubes (Ag@polymer/CNTs) for the non-enzymatic glucose sensing and antibacterial activity applications. Poly(styrene-alt-maleic anhydride) (PSM) was functionalized with amino furan to obtain furan-modified poly(styrene-alt-maleic anhydride) (PSMF), which was later grafted onto the surface of CNTs by Diels-Alder "click" reaction to afford a polymer/CNTs hybrid material. The photo-deposition technique was applied to immobilized small-sized (∼10 nm) AgNPs on the surface of the polymer/CNTs hybrid material using visible light irradiation. The resulting material, Ag@polymer/CNTs, showed promising electrocatalytic activity for the non-enzymatic glucose sensing and antibacterial activity in vitro assays toward Escherichia coli, Staphylococcus aureus, and Bacillus cereus bacteria strains. Covalent-bonded polymer layer-bearing carboxylic pendent groups to the CNTs might be playing a pivot role in not only stabilizing AgNPs but also facile electron-transfer reaction, thus demonstrating better activity.

Novel biogenic gold nanoparticles stabilized on poly(styrene-co-maleic anhydride) as an effective material for reduction of nitrophenols and colorimetric detection of Pb(II).

Biogenic gold nanoparticles (AuNPs) have been extensively studied for the catalytic conversion of nitrophenols (NP) into aminophenols and the colorimetric quantification of heavy metal ions in aqueous solutions. However, the high self-agglomeration ability of colloidal nanoparticles is one of the major obstacles hindering their application. In the present study, we offered novel biogenic AuNPs synthesized by a green approach using Cistanche deserticola (CD) extract as a bioreducing agent and stabilized on poly(styrene-co-maleic anhydride) (PSMA). The prepared Au@PSMA nanoparticles were characterized by various techniques (HR-TEM, SEAD, FE-SEM, DLS, TGA, XRD, and FTIR) and studied for two applications: the catalytic reduction of 3-NP by NaBH4 and the sensing detection of Pb2+ ions. The optimal conditions for the synthesis of AuNPs were investigated and established at 60 °C, 20 min, pH of 9, and 0.5 mM Au3+. Morphological studies showed that AuNPs synthesized by CD extract were mostly spherical with a mean diameter of 25 nm, while the size of polymer-integrated AuNPs was more than two-fold larger. Since PSMA acted as a matrix keeping the nanoparticles from coagulation and maintaining the optimal surface area, AuNPs integrated with PSMA showed higher catalytic efficiency with a faster reaction rate and lower activation energy than conventional nanoparticles. Au@PSMA could completely reduce 3-NP within 10 min with a rate constant of 0.127 min-1 and activation energy of 9.96 kJ/mol. The presence of PSMA also improved the stability and recyclability of AuNPs. Used as a sensor, Au@PSMA exhibited excellent sensitivity and selectivity for Pb2+ ions with a limit of detection of 0.03 µM in the linear range of 0-100 µM. The study results suggested that Au@PSMA could be used as a promising catalyst for the reduction of NP and the colorimetric sensor for detection of Pb2+ ions in aqueous environmental samples.

Roles of Chitosan in Green Synthesis of Metal Nanoparticles for Biomedical Applications.

Chitosan (CS) is a well-known stabilizer for metal nanoparticles in biomedical engineering. However, very few studies have explored other important roles of CS including reducing, shape-directing, and size-controlling. This review aims to provide the latest and most comprehensive overview of the roles of CS in the green synthesis of metal nanoparticles for biomedical applications. To the best of our knowledge, this is the first review that highlights these potentialities of CS. At first, a brief overview of the properties and the bioactivity of CS is presented. Next, the benefits of CS for enhancing the physicochemical behaviors of metal nanoparticles are discussed in detail. The representative biomedical applications of CS-metal nanoparticles are also given. Lastly, the review outlines the perceptual vision for the future development of CS-metal nanoparticles in the biomedicine field.

Ultrasound-promoted direct functionalization of multi-walled carbon nanotubes in water via Diels-Alder "click chemistry".

A facile and environmentally friendly strategy for grafting polymers onto the surface of multi-walled carbon nanotubes (CNTs) was demonstrated by Diels-Alder "click chemistry". Firstly, the copolymers of poly(styrene-alt-maleic anhydride) (PSM) were prepared by the reversible addition-fragmentation chain transfer (RAFT) polymerization and subsequently functionalized with furfuryl amine to introduce anchoring groups. The copolymers were then grafted on CNTs via the Diels-Alder reaction in water through a conventional heating-stirring route and ultrasound-assisted method. The obtained nanocomposite materials were characterized by thermogravimetric analysis, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, Raman spectroscopy and transmission electron microscopy. The results indicated that the reaction rate under ultrasound irradiation was accelerated about 12 times than the one under the conventional heating-stirring condition without losing the grafting efficiency. The direct functionalization of CNTs formed a stably dispersed solution in water, promising a green and effective method for industrial process.

Beta-Cyclodextrin Multi-Conjugated Magnetic Graphene Oxide as a Nano-Adsorbent for Methylene Blue Removal.

The composites of graphene oxide and magnetic nanoparticles multi-conjugated with beta-cyclodextrin (MNPs/GO-betaCD) were prepared by a facile route and their properties were investigated. First, poly(glycidyl methacrylate) was covalently wrapped onto the surface of magnetic nanoparticles (MNPs) by the reversible addition-fragmentation chain transfer polymerization. The mixture of modified MNPs and graphene oxide (GO) was then functionalized with beta-cyclodextrin to produce MNPs/GO-betaCD. The composites were characterized by FT-IR, XRD, TGA, SEM, and TEM. The MNPs/GO-betaCD owned a superparamagnetic character and showed remarkable methylene blue (MB) adsorption capacity from aqueous solution in comparison with GO. The adsorbent could be recycled and maintained about 64.4% of its initial adsorption capacity for MB after five regeneration cycles.

Synthesis and Characterization of Multiwalled Carbon Nanotubes/Poly(HEMA-co-MMA) by Utilizing Click Chemistry.

The hybrid material consisting of multi walled carbon nanotubes (MWNTs) and poly(2-hydroxyethylmethacrylate-co-methylmethacrylate) [poly(HEMA-co-MMA)] was synthesized by a combination of RAFT and Click chemistry. In the primary stage, the copolymer poly(HEMA-co-MMA) was prepared by applying RAFT technique. Alkynyl side groups were incorporated onto the poly(HEMA-co-MMA) backbone by esterification reaction. Then, MWNTs-N3 was prepared by treating MWNTs with 4-azidobutylamine. The click coupling reaction between azide-functionalized MWNTs (MWNTs-N3) and the alkyne-functionalized random copolymer ((HEMA-co-MMA)-Alkyne) with the Cu(I)-catalyzed [3+2] Huisgen cycloaddition afforded the hybrid compound. The structure and properties of poly(MMA-co-HEMA)-g-MWNTs were investigated by FT-IR, EDX and TGA measurements. The copolymer brushes were observed to be immobilized onto the functionalized MWNTs by SEM and TEM analysis.

Combination of Surface Initiated Reversible Addition Fragmentation Chain Transfer Polymerization, Thiol-Ene Click Chemistry and Coordination Chemistry for the Fabrication of a Novel Photoluminescent Hydroxyapatite Nanohybrids.

Hydroxyapatite nanocrystals (HAPs) were encapsulated by poly(allyl methacrylate) (PAMA) employing controlled surface-initiated reversible addition-fragmentation chain transfer polymerization of allyl methacrylate to give HAP-PAMA nanohybrids. The subsequent thiol-ene coupling of nanohybrids with 2-mercaptosuccinic acid resulted in HAP-PAMA-COOH possessing multicarboxyl functionality. The coordination of the nanohybrids with Tb3+ ions in the presence of 1,10-phenanthroline (Phen) afforded photoluminescent Tb3+ tagged HAPs-PAMA nanohybrid complexes (HAP-PAMA-Tb3+-Phen). The structure, morphology, and fluorescence properties of the Tb3+ coordinated nanohybrid complexes were investigated by respective physical and spectral studies.

Preparation of ß-Cyclodextrin Multi-Decorated Halloysite Nanotubes as a Catalyst and Nanoadsorbent for Dye Removal.

Hybrid materials of ß-cyclodextrin multi-decorated halloysite nanotubes (HNTs-g-ßCD) were prepared by a facile route, which showed high efficiency for catalysis and dye adsorption. Initially, the surface of halloysite nanotubes (HNTs) was modified with poly(glycidyl methacrylate) by the reversible addition fragmentation chain transfer (RAFT) polymerization of glycidyl methacrylate having epoxy groups as a monomer. Subsequently, ß-cyclodextrin was conjugated with the modified HNTs to produce HNTs-g-ßCD by the epoxide ring-opening reaction of mono-6-deoxy-6-hexanediamine-ß-cyclodextrin. The nanocomposites were characterized by FT-IR, TGA, SEM, and TEM. The HNTs-g-ßCD composites could be used as a nano adsorbent for methylene blue and a catalyst in the oxidation reaction of benzyl alcohol owing to the unique structure of ß-cyclodextrin. The HNTs-g-ßCD shows promiseas potential multi-functional materials by a combination of ß-cyclodextrin and HNTs properties.