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Nanotechnology and materials science are highly developing sectors where several new materials are investigated. One area includes iron oxide nanoparticles with superparamagnetic behavior. Since nanomaterials are prone to be associated with high levels of intrinsic toxicity and can have adverse effects if not properly guided. So, toxic mechanisms associated with nanomaterials are like that of a therapeutic drug or any other toxic compound. In that way, by ignoring the general pathways of cell death followed by the nanomaterials, the present report covers the points to control the growth of cancer cells by employing engineered nanoparticles (NPs) to induce therapeutic toxicity. We discuss the pathways for the induction of toxicity to the cancer cells using the superparamagnetic iron oxide nanoparticles (SPIONs) with and without surface ligands, and the ligand efficiency towards controlling toxicity is covered. Also, the therapeutic means of controlling the cancer cells, such as generating heat and releasing anticancer drugs in an externally organized manner, are also discussed. Overall, the report links the physical properties of SPIONs related to their natural or therapeutical toxicity by connecting physicochemical and toxicology principles.

Due to the complexity of high temperature and cutting tool wear, most machined components are still facing problems in terms of harder functional fillers that reinforce aluminium matrix composites. Conversely, abrasive water jet machining (AWJM) incredibly useful for the cutting of anisotropic and non-homogeneous metal matrix composites. In this research article, silicon carbide (SiC) particulates were utilized as reinforcement in the AA6026 matrix material (AA6026/SiC) and machined using AWJM under different process parameters namely SiC loading, traverse speed and stand-off distance. Two different compositions of SiC (4, and 8 wt%) were considered to fabricate AA6026 composites using the stir casting. In addition, outputs have been examined, e.g., surface roughness, material removal rate, and kerf angle. An optical microscope, scanning electron microscope, Brinell hardness tester and universal testing machine have been used to characterize the matrix material AA6026 and its composites. Microstructural analysis revealed that the inclusion of SiC particulates in AA6026 affects the very fine grain size of the composite. Furthermore, the 8 wt% composite exhibits the evolution of the Al-Si eutectic phase during solidification. Processing of these composites was performed using the L _27 orthogonal geometry, successfully improving the parameters of the abrasive water jet process. The output response shows that reducing the SiC load improves the surface roughness under the key parameters of traverse speed and stand-off distance. However, increasing the SiC loading increases the material removal rate and kerf angle under the key parameters, namely traverse speed, and stand-off distance.

The objective of this research is to investigate the extraction and characterization of a particular kind of Indian bamboo family plant known as Bambusa bambos . The fibres were extracted from the bamboo plant in the form of strips using the retting process and separated as thin fibres after the stamping process. The extracted raw bamboo fibres were chemically modified in a 5% alkali solution. The thermogravimetric analysis (TGA), x-ray diffraction (XRD), and scanning electron microscopy (SEM) were used to investigate the thermal, crystalinity, and morphological properties of untreated and alkali (NaOH) treated bamboo fibres. The ASTM standard was followed for the chemical composition and tensile testing of raw and chemically treated bamboo fibres. In contrast to raw bamboo fibres, alkali-treated bamboo fibres had a 5% drop in hemicellulose concentration. In the alkali-treated state, weakly bonded containments were removed from the fiber's surface, exposing the cellulose over a wider surface area. As a result, the thermal stability of the alkali-treated fibres was enhanced as compared to raw bamboo fibres. The increased amount of cellulose content and decreasing aspect ratio of the alkali-treated bamboo fibers lead to increased tensile strength. A significant improvement in the crystallinity index (broad band width of the second peak) was observed in the alkali-treated condition, which may occur due to the removal of hemicelluloses. Based on their performance, the chemically treated bamboo fibres can be used as effective reinforcement elements for the development of polymer matrix composites in the automobile and construction industries.

In this present investigation, Sansevieria cylindrica fiber was used as a reinforcement in a natural rubber matrix. Various biocomposite samples with different fiber contents (lengths and loadings) were fabricated, using compression molding process and vulcanizing technique by maintaining the temperature around 150 °C. From the results obtained, mechanical properties: tensile strength, modulus elongation at break and tear strength of 10.44 MPa, 2.36 MPa, 627.59% and 34.99 N respectively, were obtained from the optimum composite sample with length and loading of 6 mm and 20 wt% composition, respectively. The maximum hardness was observed at 76.85 Shore A from the composite sample of 6 mm and 40 wt%. The optimum properties can be attributed to the presence of strong interfacial adhesion between the Sansevieria cylindrica fiber and the natural rubber matrix. The mechanisms of failure of the biocomposites at their interfaces were examined and analyzed, using scanning electron microscopy (SEM). The micrographs obtained from SEM further confirmed that the Sansevieria cylindrica fibers were surrounded with more amount of natural rubber which can exhibit strong interfacial bonding between fiber and matrix. The optimal composites of this work can be used in general, abrasion resistant conveyor belt.

The increasing global need to achieve sustainability in product development demands the use of biodegradable materials from renewable resources in many engineering applications. Accordingly, various natural fibers were explored as suitable reinforcement in polymer matrixes due to their low density and biodegradability. Hence, in this present work, a novel fiber reinforcement was extracted from the stem of the Cryptostegia grandiflora (CG) plant through a retting process and manual intervention. The extracted Cryptostegia grandiflora fibers (CGFs) were chemically treated using NaOH and silane. Various properties like crystal structure, chemical composition, surface morphology, and thermal degradation were studied using x-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR) Scanning electron Microscopy (SEM) and Thermogravimetric analysis (TGA). The increasing cellulose content and the removal of hemicellulose after the chemical treatment indicate the potential for this CG fiber as a better reinforcement element in polymers. The increasing trend of tensile strength was observed for the CG fiber in the following order: silane > NaOH > untreated conditions. Two-stage thermal degradation was observed in all the cases where the maximum thermal degradation was found at the silane-treated CG fibers. Based on their performance, the chemically treated CG fibres can be made into composites and used for structural applications.

In the present study, ion imprinted polymer monoliths (IIPMs) were developed to overcome the limitations of ion imprinted polymer particles (IIPPs) used for the removal of Hg(II) ions from waste water samples. The adsorbents preparation, characterization and Hg(II) removal were very well reported. The IIPMs on porogen optimization was prepared using the molding technique with Hg(II) as a template ion, [2-(methacryloyloxy)ethyl]trimethylammonium cysteine (MAETC) as ligand, methacrylic acid (MAA) as functional monomer, ethylene glycol dimethacrylamide (EGDMA) as cross-linker, benzoyl peroxide as an initiator and methanol and acetonitrile as porogen in the polypropylene tube (drinking straw) as mold. The IIPMs prepared with higher volumes of porogen were indicated to have a good adsorption rate for the Hg(II) removal along with good water permeability and larger porosity as compared to a lower volume of porogen. The IIPMs prepared using the binary porogen were able to improve the porosity and surface area of the monolithic polymers as compared to the single porogen added IIPMs. Finally, we indicate from our analysis that the IIPM having the efficient capacity for the Hg(II) ions is easy to prepare, and has higher water permeability along with high porosity and high adsorption capacity and all these factors making it one of the suitable adsorbent for the successful removal of Hg(II) ions.

This work addresses manufacture, testing and simulation of foot valve lever (FVL) for monoblock pump industry, using a cost-effective casting design process. The impact of different types of sands, such as air-set, dry and sodium silicate as well as gating designs, namely H-, U- and O-type, were studied with respect to surface roughness and porosity. The mold pattern was produced using additive manufacturing (AM) technology. Both experimental and numerical investigations were performed on the temperature distribution of molten metal at random locations for the different gating configurations or designs, considering mold filling and solidification. It was evident from the experimental investigation that contribution of air-set sand and O-type gating architecture showed limited consistency effects. Importantly, gating architecture was the most influential parameter to determine all specified quality outcomes, independent of sand mold. An order of O

Fibre reinforced polymer (FRP) hybrid composites builds vertically due to the achievement of custom-made properties with lightweight. However, these materials have finding limitations in exceptional circumstances due to the unpredicted sustainability. Hence, it is necessary to create the database for the durable and sustainable low-density FRP hybrid composites with the support of significant experimental investigations. This review paper is mainly covers durability studies of various FRP hybrid composites under different environmental conditions. The thermal ageing, hydrothermal ageing, sea water, acid and alkali environment, ultraviolet radiation and stress cycle effects were extensively discussed with suitable scientific evidence in this work. Further, most of the FRP composites are rapidly degraded by underwater conditions at high temperatures. The failure mechanisms such as delamination, degradation of fibre and matrix, poor interfacial adhesion, matrix surface cracking, etc. are found to be dominant in the FRP composites under the hydrothermal and acid environment conditions also covered. The combination of natural/synthetic hybrid composites and addition of some nano fillers enhance the durability performance of hybrid composites significantly. However, ageing properties of hybrid polymer composites in different environment conditions need to study for various applications. The review process revealed that the life cycles of hybrid FRP composites mainly affected by stress cycle based on continuous usage.

The objective of this work is to develop cost-effective, reliable, and large-scale production of metallic nanoparticles (NPs) by adopting green chemistry principles for industrial applications. In that view, we have studied the phytochemical reducibility of silver nitrate by making use of Calotropis Procera (Ait.) R. Br root extract, and based on its medicinal properties, an attempt was made to evaluate the therapeutic potentials of silver (Ag) NPs containing this plant extract towards the clinical strains of bacteria. The optimization studies on reducing the potentials were done considering the concentration, pH, temperature, and reaction period of both the extract and the metal precursor. The nanoarchitecture elements were interpreted using visual, spectroscopic, and microscopic analyses cohorting the antibacterial potentials towards the clinically significant strains. The antimicrobial activity exercised by these Ag NPs towards 10 different strains of medically important bacteria at a given concentration was proved to be significant. The antimicrobial potential was further validated quantitatively, and the MIC/MBC concentration values were determined. Finally, the cytotoxicity of Ag NPs when tested against the HEPK cell line indicated that the metal-phytochemical moiety exhibited the maximum therapeutic efficacy and thereby paving the way for the development of disruptive technologies in the field of nanomedicine.

Titanium oxide (TiO2) is one of the most scrutinized material because of its in-built fundamental properties and has been developed as an outstanding photo-catalytic material intended for many different industrial applications. In order to further explore the properties of TiO2, we prepared Copper-loaded TiO2 (Cu-TiO2) nanoparticles (NPs) for inhibiting the growth of bacterial cells and also to serve as a chemical sensor. The physico-chemical characteristics of the synthesized Cu-TiO2 NPs were characterized by many different techniques for the crystallinity, bonding and functionality, morphology, elemental composition, and absorption characteristics. From the results, we confirm for the formation of anatase phase of TiO2 having a tetragonal crystal system, while the morphology studies indicated that the Cu dope TiO2 has spherical morphology. The elemental analysis confirmed for the inclusion of Cu into TiO2 crystal lattice and the absorption spectroscopic analysis helped for the bandgap calculation and visible light absorption property of Cu-TiO2 NPs. The metal nanoclusters of Cu are observed to be deposited on different phases and sites of TiO2 resulting in the inter-band transitions. Further, the sensitivity of Cu-TiO2 as a chemical sensor is determined by fabricating the electrode at the FTO glass substrate where the ethanol sensitivity was found to be little increased/enhanced with Cu loading. Finally, the antibacterial activity of Cu-TiO2 NPs was confirmed by its activity against various bacterial cultures and are found to be efficient.

The present study deals with Plectranthus amboinicus (Lour.), multiple potential herbs perceived as a medicinal and culinary adjunct has been used to fabricate gold (Au) nanoparticles (NPs) in an eco-benign fashion. We have primly reported the antioxidant and anticarcinogenic effects of phytofabricated Au NPs towards lung adenocarcinoma (LAC) cells (A549 cell line) in vitro. The herbal concentrate, size and dosage of Au NPs were the key variables that determined the anticarcinogenic efficacy. Results indicated that the herbal concentrate encompassing flavonoids, alkaloids and polyphenolics aided reduction and stabilisation of Au NPs supported by spectral (λmax @ 550 nm) and quantitative analyses. The Fourier transform-infrared spectra anticipated distinct phenolics and protein frequencies involved in Au NPs capping in the course of fabrication. The manipulated Au NPs of 15 nm size has significantly influenced the radical scavenging (48.1 μg) and proliferation pattern of LAC cells (A549) associated with cytotoxic characteristics and IC50 (Au NPs concentration linked with 50% mortality) defined at 16.3 μg/mL in 48 h. This nanotoxicological prospect on the use of nanomaterials as an anticancer agent would be an alternative for the emerging intrinsic resistance of cells to the drug; a great challenge pertaining to safer environmental and biological outcomes.

Pollution with oil spills, a major contributor to water contamination, has a remarkable effect on the economy, biodiversity, and environment. To protect marine species and environment, efforts should be undertaken for developing efficient ways to remove oil spills. The current work discusses the oil spill removal using magnetite nanoparticles (MNPs) functionalized with hydrophobic polyethyleneimine (HPEA). In this respect, nonylphenol pentaethylenehexamine (NTEPA) and nonylphenol triethylenetetramine (NDETA) were prepared by a simple one-step method and used as capping agents in the synthesis of hydrophobically modified magnetite nanoparticles designated as NDETA/Fe3O4 (magnetite as a core and NDETA as a shell) and NTEPA/Fe3O4 (magnetite as a core and NTEPA as a shell). The prepared MNPs were characterized using FTIR, XRD, TEM, DLS, TGA, and DSA to determine their physical and chemical properties. Additionally, MNPs were applied as oil spill collectors with high efficiencies that reached 93% and 90% for NDETA/Fe3O4 and NTEPA/Fe3O4, respectively, at low magnetite to oil ratios.

The present study develops on insulin-release studies from the chitosan-amide-modified stimuli-responsive polymers formed from various fatty acids including stearic acid, oleic acid, linoleic acid, and linolenic acid. This is the continuation of an earlier reported study that investigates the insulin-release profiles of chitosan-modified fatty acid amides (without stimuli responsive polymers). Following the synthesis and characterization of many different fatty acid amides with a varying amount of unsaturation, the insulin drug loading and release effects were compared among N-isopropylacrylamide (NIPAm), a thermo-responsive polymer, and 2-acrylamide-2-methylpropane sulfonic acid (AMPS), a pH-responsive polymer-modified hydrogel that is expected to enhance environmental response and the controllability of release. Finally, drug release effects were studied to investigate the drug release mechanisms with the help of five different pharmacokinetic models including the zero-order, first-order, Higuchi, Korsmeyers–Peppas, and Hixson models. The results indicate that the Higuchi and Hixson models are valid in terms of the operation of the NIPAm and AMPS matrices during the delivery of insulin.

This work aimed to use abietic acid (AA), as a widely available natural product, as a precursor for the synthesis of two new amphiphilic ionic liquids (AILs) and apply them as effective demulsifiers for water-in-crude oil (W/O) emulsions. AA was esterified using tetraethylene glycol (TEG) in the presence of p-toluene sulfonic acid (PTSA) as a catalyst obtaining the corresponding ester (AATG). AATG was reacted with 1-vinylimidazole (VIM) throughout the Diels–Alder reaction, forming the corresponding adduct (ATI). Following this, ATI was quaternized using alkyl iodides, ethyl iodide (EI), and hexyl iodide (HI) to obtain the corresponding AILs, ATEI-IL, and ATHI-IL, respectively. The chemical structure, surface activity, thermal stability, and relative solubility number (RSN) were investigated using different techniques. The efficiency of ATEI-IL and ATHI-IL to demulsify W/O emulsions in different crude oil: brine volumetric ratios were evaluated. ATEI-IL and ATHI-IL achieved promising results as demulsifiers. Their demulsification efficiency increased as the brine ratios decreased where their efficiency reached 100% at the crude oil: brine ratio (90:10), even at low concentrations.

The interaction of common anticancer drug gemcitabine with human serum albumin (HSA) has been studied in detail. The effect of an omnipresent nonsteroidal anti-inflammatory drug ibuprofen was also seen on the binding of HSA and gemcitabine. A slight hyperchromic shift in the difference UV-visible absorption spectra of HSA on the addition of gemcitabine gave a primary idea of the possible complex formation between them. The inner filter effect, which happens due to the significant absorbance of the ligand at the excitation and/or emission wavelengths, played an important role in the observed fluorescence quenching of HSA by gemcitabine that can be understood by comparing the observed and corrected fluorescence intensities obtained at λex = 280 nm and 295 nm. Gemcitabine showed weak interaction with HSA, which took place via a dynamic quenching mechanism with 1:1 cooperative binding between them. Secondary structural analysis, based on circular dichroism (CD) spectroscopy, showed that low concentrations of gemcitabine did not affect the native structure of protein; however, higher concentrations affected it slightly with partial unfolding. For understanding the binding site of gemcitabine within HSA, both experimental (using site markers, warfarin and ibuprofen) as well as computational methods were employed, which revealed that the gemcitabine binding site is located between the interface of subdomain IIA and IIB within the close proximity of the warfarin site (drug site 1). The effect of ibuprofen on the binding was further elaborated because of the possibility of its coexistence with gemcitabine in the prescription given to the cancer patients, and it was noticed that, ibuprofen, even present in high amounts, did not affect the binding efficacy of gemcitabine with HSA. DFT analyses of various conformers of gemcitabine obtained from its docking with various structures of HSA (free and bounded with site markers), show that the stability of the gemcitabine molecule increased slightly after binding with ibuprofen-complexed HSA. Both experimental as well as computational results were in good agreement with each other.

In this work, new crosslinked pyridinium poly ionic liquid and its magnetite hybrid structured composite were prepared and applied to remove the toxic dye Coomassie Brilliant Blue (CBB-R250) from aqueous solutions. In this respect, vinyl pyridine, maleic anhydride, and dibromo nonane were used to prepare crosslinked quaternized vinyl pyridinium/maleic anhydride ionic liquid (CQVP-MA). Furthermore, a linear copolymer was prepared by the reaction of vinyl pyridine with bromo nonane followed by its copolymerization with maleic anhydride in order to use it as a capping agent for magnetite nanoparticles. The monodisperse MNPs were incorporated into the crosslinked PIL (CQVP-MA) by ultrasonication to prepare CQVP-MA/Fe3O4 composite to facilitate its recovery using an external magnetic field and enhance its adsorption capacity. The chemical structures, thermal stabilities, zeta potential, particle size, EDS, and SEM of the prepared CQVP-MA and CQVP-MA/Fe3O4 were investigated. Adsorption kinetics, isotherms, and mechanisms of CB-R250 elimination from aqueous solutions using CQVP-MA and CQVP-MA/Fe3O4 were also studied, and the results revealed that the pseudo second-order kinetic model and the Langmuir isotherm model were the most suitable to describe the CBB adsorption from an aqueous solution. The adsorption capacities of CQVP-MA and CQVP-MA/Fe3O4 were found to be 1040 and 1198, respectively, which are more than those for previously reported material in the literature with reasonable stability for five cycles.

Lysozyme is often used as a model protein to study interaction with drug molecules and to understand biological processes which help in illuminating the therapeutic effectiveness of the drug. In the present work, in vitro interaction studies of 1-{(2-hydroxyethyl)amino}-2-amino-1,2-dideoxy-d-glucose triphenyl tin (IV) (GATPT) complex with lysozyme were carried out by employing various biophysical methods such as absorption, fluorescence, and circular dichroism (CD) spectroscopies. The experimental results revealed efficient binding affinity of GATPT with lysozyme with intrinsic binding (Kb) and binding constant (K) values in the order of 105 M−1. The number of binding sites and thermodynamic parameters ΔG, ΔH, and ΔS at four different temperatures were also calculated and the interaction of GATPT with lysozyme was found to be enthalpy and entropy driven. The CD spectra revealed alterations in the population of α–helical content within the secondary structure of lysozyme in presence of GATPT complex. The morphological analysis of the complex with lysozyme and lysozyme-DNA condensates was carried out by employing confocal and SEM studies. Furthermore, the molecular docking studies confirmed the interaction of GATPT within the larger hydrophobic pocket of the lysozyme via several non-covalent interactions.

Over the past few decades, there has been an increased trend for the use of natural compounds and their derivatives as alternatives to traditional chemicals and is due to their renewability, green character, and wide availability. This work aims to convert sodium alginate (S.ALG), a natural polysaccharide, into amides through its conversion to alginic acid (H.ALG). The formed H.ALG was esterified using methanol, followed by a reaction with octadecylamine (OA) and dodecylamine (DA) to produce corresponding amides, OA-ALG, and DA-ALG, respectively. The synthesized OA-ALG and DA-ALG were used as capping agents to further form hydrophobic magnetite nanoparticles (MNPs), OA-MNPs and DA-MNPs, respectively. The chemical structures, morphology, hydrophobicity, and magnetic properties of OA-MNPs and DA-MNPs were investigated using different instrumental techniques. Furthermore, the efficacy of as-synthesized MNPs as oil spill collectors were also evaluated using different ratios of MNPs:crude oil. From the analysis of results, the OA-MNPs and DA-MNPs exhibited high efficiency in the collection of oil spill even at low ratios of MNPs:crude oil.

In the last few decades, there has been an increasing trend for the usage of natural products and their derivatives as green and renewable oil-filed chemicals. Use of these compounds or their derivatives contributes to reducing the use of traditional chemicals, and enhances green chemistry principles. Curcumin (CRC) is one of the most popular natural products and is widely available. The green character, antioxidant action, and low cost of CRC prompt its use in several applications. In the present study, Curcumin was used to synthesize two new amphiphilic ionic liquids (AILs) by reacting with 1,3-propanesultone or bromoacetic acid to produce corresponding sulfonic and carboxylic acids, CRC-PS and CRC-BA, respectively. Following this, the formed CRC-PS and CRC-BA were allowed to react with 12-(2-hydroxyethyl)-15-(4-nonylphenoxy)-3,6,9-trioxa-12-azapentadecane-1,14-diol (HNTA) to form corresponding AILs, GCP-IL and GRB-IL, respectively. The chemical structures, surface tension, interfacial tension, and relative solubility number (RSN) of the synthesized AILs were investigated. The efficiency of GCP-IL and GRB-IL to demulsify water in heavy crude oil (W/O) emulsions was also investigated, where we observed that both GCP-IL and GRB-IL served as high-efficiency demulsifiers and the efficiency increased with a decreased ratio of water in W/O emulsion. Moreover, the data showed an increased efficiency of these AILs with an increased concentration. Among the two AILs, under testing conditions, GCP-IL exhibited a higher efficiency, shorter demulsification time, and cleaner demulsified water.

A portable electrochemical aptamer-antibody based sandwich biosensor has been designed and successfully developed using an aptamer bioreceptor immobilized onto a screen-printed electrode surface for Mycobacterium tuberculosis (M. tuberculosis) detection in clinical sputum samples. In the sensing strategy, a CFP10-ESAT6 binding aptamer was immobilized onto a graphene/polyaniline (GP/PANI)-modified gold working electrode by covalent binding via glutaraldehyde linkage. Upon interaction with the CFP10-ESAT6 antigen target, the aptamer will capture the target where the nano-labelled Fe3O4/Au MNPs conjugated antibody is used to complete the sandwich format and enhance the signal produced from the aptamer–antigen interaction. Using this strategy, the detection of CFP10-ESAT6 antigen was conducted in the concentration range of 5 to 500 ng/mL. From the analysis, the detection limit was found to be 1.5 ng/mL, thereby demonstrating the efficiency of the aptamer as a bioreceptor. The specificity study was carried out using bovine serum albumin (BSA), MPT64, and human serum, and the result demonstrated good specificity that is 7% higher than the antibody–antigen interaction reported in a previous study. The fabricated aptasensor for M. tuberculosis analysis shows good reproducibility with an relative standard deviation (RSD) of 2.5%. Further analysis of M. tuberculosis in sputum samples have shown good correlation with the culture method with 100% specificity and sensitivity, thus making the aptasensor a promising candidate for M. tuberculosis detection considering its high specificity and sensitivity with clinical samples.

Nanotechnology-based drug delivery systems are an emerging technology for the targeted delivery of chemotherapeutic agents in cancer therapy with low/no toxicity to the non-cancer cells. With that view, the present work reports the synthesis, characterization, and testing of Mn:ZnS quantum dots (QDs) conjugated chitosan (CS)-based nanocarrier system encapsulated with Mitomycin C (MMC) drug. This fabricated nanocarrier, MMC@CS-Mn:ZnS, has been tested thoroughly for the drug loading capacity, drug encapsulation efficiency, and release properties at a fixed wavelength (358 nm) using a UV–Vis spectrophotometer. Followed by the physicochemical characterization, the cumulative drug release profiling data of MMC@CS-Mn:ZnS nanocarrier (at pH of 6.5, 6.8, 7.2, and 7.5) were investigated to have the highest release of 56.48% at pH 6.8, followed by 50.22%, 30.88%, and 10.75% at pH 7.2, 6.5, and 7.5, respectively. Additionally, the drug release studies were fitted to five different pharmacokinetic models including pesudo-first-order, pseudo-second-order, Higuchi, Hixson–Crowell, and Korsmeyers–Peppas models. From the analysis, the cumulative MMC release suits the Higuchi model well, revealing the diffusion-controlled mechanism involving the correlation of cumulative drug release proportional to the function square root of time at equilibrium, with the correlation coefficient values (R2) of 0.9849, 0.9604, 0.9783, and 0.7989 for drug release at pH 6.5, 6.8, 7.2, and 7.5, respectively. Based on the overall results analysis, the formulated nanocarrier system of MMC synergistically envisages the efficient delivery of chemotherapeutic agents to the target cancerous sites, able to sustain it for a longer time, etc. Consequently, the developed nanocarrier system has the capacity to improve the drug loading efficacy in combating the reoccurrence and progression of cancer in non-muscle invasive bladder diseases.

Two novel amphiphilic polyethylene amine terephthalate have been prepared via the glycolsis of polyethylene terephthalate (PET). The product, bis (2-hydroxyethyl terephthalate) (BHET), was converted to the corresponding dialkyl halide, bis(2-chloroethyl) terephthalate (BCET), using thionyl chloride (TC). This dialkyl compound was used for alkylation of dodecyl amine (DOA) and tetraethylenepentamine (TEPA) or pentaethylenehexamine (PEHA) to form the corresponding polyethylene amine terephthalate, i.e., DOAT and DOAP, respectively. Their chemical structure, surface tension, interfacial tension (IFT), and dynamic light scattering (DLS) were determined using different techniques. The efficiency of the prepared polyethylene amine terephthalate to demulsify water in heavy crude (W/O) emulsions was also determined and found to increase as their concentrations increased. Moreover, DOAT showed faster and higher efficiency, and cleaner separation than DOAP.

New magnetic imidazolium ionic liquid (IIL) was synthesized to improve the curing, mechanical, and thermal characteristics of the epoxy/polyamine system. In this respect, 2-(4-minophenyl)-1.3-bis(triethoxysilyl)-1H-imidazol-3-ium acetate as IIL was synthesized and characterized by different spectroscopy tools. The IIL was used as capping to prepare Fe3O4 nanoparticles (NPs) as new Fe3O4-IIL NPs. The thermal stability, morphology, crystal lattice structures, and magnetic properties were evaluated to confirm the formation of uniform, thermal, stable, and superparamagnetic Fe3O4-IIL NPs. The prepared Fe3O4-IIL NPs were mixed with an epoxy/polyamine system to improve the curing, thermal, and mechanical properties of epoxy through chemical reactions. The dynamic mechanical analyzer and differential scanning calorimeter were used to investigate the flexibility and storage modulus of the cured epoxy/polyamine system in the absence and presence of Fe3O4-IIL NPs. The atomic force microscope and scanning electron microscope were used to evaluate the dispersion and embedding of Fe3O4-IIL NPs into epoxy matrix. The thermal, mechanical, and surface morphologies data confirmed that the incorporation of Fe3O4-IIL NPs using 3 wt. % during the curing of an epoxy/polyamine system produces superior epoxy films without cracks, holes, and NPs agglomeration.

The theme of this work is to highlight the significance of green plant extracts in the synthesis of nanostructures. In asserting this statement, herein, we report our obtained results on the synthesis of hexagonal CdSe nanorods preferably oriented along (0002) plane through henna leaf extract-mediated reaction along with a discussion about the structural, morphological and optical properties of the synthesized nanorods. The possible mechanism for the synthesis of CdSe nanorods was explored. The formation of nanorods along (0002) plane was confirmed by the relatively high intensity of the (0002) peak in X-ray diffraction pattern. To account for the experimentally realistic condition, we have calculated the surface energies of hexagonal CdSe surface slabs along the low indexed (0002), (101¯0) and (112¯0) plane surfaces using density functional theory approach and the calculated surface energy value for (0002) surface is 802.7 mJ m−2, which is higher than (112¯0) and (101¯0) surfaces. On realizing the calculated surface energies of these slabs, we determined that the combination of (112¯0) and (101¯0) planes with lower surface energies will lead to the formation of CdSe nanorods growth along (0002) orientation. Finally, we argue that the design of new greener route for the synthesis of novel functional nanomaterials is highly desired.