Simple Method For Preparation Research Articles

Facile One-Pot Preparation of Polypyrrole-Incorporated Conductive Hydrogels for Human Motion Sensing.

Conductive hydrogels have been widely used in soft robotics, as well as skin-attached and implantable bioelectronic devices. Among the candidates of conductive fillers, conductive polymers have become popular due to their intrinsic conductivity, high biocompatibility, and mechanical flexibility. However, it is still a challenge to construct conductive polymer-incorporated hydrogels with a good performance using a facile method. Herein, we present a simple method for the one-pot preparation of conductive polymer-incorporated hydrogels involving rapid photocuring of the hydrogel template followed by slow in situ polymerization of pyrrole. Due to the use of a milder oxidant, hydrogen peroxide, for polypyrrole synthesis, the photocuring of the hydrogel template and the growing of polypyrrole proceeded in an orderly manner, making it possible to prepare conductive polymer-incorporated hydrogels in one pot. The preparation process is facile and extensible. Moreover, the obtained hydrogels exhibit a series of properties suitable for biomedical strain sensors, including good conductivity (2.49 mS/cm), high stretchability (>200%), and a low Young's modulus (~30 kPa) that is compatible with human skin.

Fabrication of a Hydrophilic Al2O3/AlN EP Coating with Self‐Cleaning and High‐Efficiency Anti‐Corrosion Properties

AbstractCurrently, with the gradual development of anticorrosive coatings, the pursuit of simple preparation methods and the improvement of anticorrosive coatings’ properties have become the major research trends. This study successfully prepared a hydrophilic super anticorrosive coating through a simple mixing method. The coating has a contact Angle of 67.8° and a rolling Angle greater than 20°. This coating can withstand 180 days of salt spray test with no bubble or rust formation when placed on a Q 235 substrate in a 3.5 wt % NaCl solution, demonstrating the excellent corrosion resistance of the AO0.4AN0.6EP coating. Furthermore, after being immersed in a 3.5 wt % NaCl solution for 3 days, the AO0.4AN0.6EP coating exhibited the largest impedance diameter (2.07×108 Ω⋅cm2), almost three times larger than other coatings, and possessed the highest Bode modulus value, one order of magnitude higher than other coatings. After immersion in a 3.5 wt % NaCl solution for 7 days, the AO0.4AN0.6EP coating had the largest Ecorr and the smallest icorr, indicating its superior corrosion resistance. In addition to corrosion resistance, the AO0.4AN0.6EP coating showed no signs of cracking, discoloration, or decomposition after being exposed to ultraviolet aging lights for 30 days, demonstrating its excellent UV resistance. Moreover, neither dry soil particles nor muddy water could adhere to the coating surface, proving its good self‐cleaning ability. Therefore, this coating holds promising applications in the field of super corrosion‐resistant coatings.

Mesenchymal Stem Cell-Based Biomimetic Liposome for Targeted Treatment of Rheumatoid Arthritis.

Rheumatoid arthritis (RA) is a systemic autoimmune disorder that severely compromises joint health. The primary therapeutic strategy for advanced RA aims to inhibit joint inflammation. However, the nonspecific distribution of pharmacological agents has limited therapeutic efficacy and heightens the risks associated with RA treatment. To address this issue, we developed mesenchymal stem cell (MSC)-based biomimetic liposomes, termed MSCsome, which were composed of a fusion between MSC membranes and liposomes. MSC some with relatively simple preparation method effectively enhanced the targeting efficiency of drug to diseased joints. Interaction between lymphocyte function-associated antigen-1 and intercellular adhesion molecule-1 enhanced the affinity of the MSCsome for polarized macrophages, thereby improving its targeting capability to affected joints. The effective targeted delivery facilitated drug accumulation in joints, resulting in the significant inhibition of the inflammation, as well as protection and repair of the cartilage. In conclusion, this study introduced MSCsome as a promising approach for the effective treatment of advanced RA, providing a novel perspective on targeted drug delivery therapy for inflammatory diseases.

Supramolecular Composite Hydrogel Loaded with CaF2 Nanoparticles Promotes the Recovery of Periodontitis Bone Resorption.

Treatments to reduce periodontal inflammation and rescue periodontitis bone resorption have been of interest to researchers. Bone tissue engineering materials have been gradually used in the treatment of bone defects, but periodontal bone tissue regeneration still faces challenges. Considering the biocompatibility factor, constructing bionic scaffolds with natural extracellular matrix properties is an ideal therapeutic pathway. Based on the pathological mechanism of periodontitis, in this study, short peptide and nanometer inorganic particles were comingled to construct NapKFF-nano CaF2 supramolecular composite hydrogels with different ratios. Material characterization experiments confirmed that the composite hydrogel had suitable mechanical properties and a three-dimensional structure that can function in the resorption region of the alveolar bone and provide spaces for cell proliferation and adhesion. The release of low concentrations of fluoride and calcium ions has been shown to have positive biological effects in both in vivo and in vitro experiments. Vitro experiments confirmed that the composite hydrogel had good biocompatibility and promoted osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs). Microbiological experiments confirmed that the composite hydrogel inhibited the activity of periodontal pathogenic bacteria. In animal studies, composite hydrogel applied to periodontitis rats in vivo can effectively repair alveolar bone resorption. This composite hydrogel has a simple preparation method and is inexpensive to produce, yet it has antibacterial and osteogenesis-promoting incremental effects, which makes it well suited for the treatment of periodontitis bone resorption, providing a new strategy for periodontal bone tissue engineering.

Wavelength Modulation and Fast Response of Mixed-Phase β-Ga2O3:Zn/SnO2 in-Plane Heterojunction Ultraviolet Photodetectors.

Ultraviolet photodetectors based on wide bandgap mixed-phase β-Ga2O3:Zn/SnO2 thin films formed through doping on the c-sapphire substrate (c-Al2O3) are prepared to construct in-plane heterojunctions employing a low-cost and simple preparation method. The mixed-phase thin film photodetectors have a low dark current of 0.74 nA, and the photo-to-dark current ratio ranges from 36.43 to 642.38 at 10 V. The photodetectors also have wavelength modulation, with response peaks ranging from 260 nm (4 mA/W) to 295 nm (1.63 A/W). Furthermore, the photodetectors have a fast response time with a rise time of 0.07 s/0.22 s and a decay time of 0.04 s/0.22 s at 1 V. The excellent performance of the devices is attributed to the reduction of VO and the establishment of multiple electric fields in the mixed-phase films, which indicates the feasibility of implementing wavelength-modulated and fast-response β-Ga2O3 photodetectors using the sol-gel method.

Application of N-doped NiCo2O4/NiO/Co3O4 composites rich in oxygen vacancies in electromagnetic wave absorption

In this work, N-doped and oxygen vacancy-rich NiCo2O4/NiO/Co3O4composites are synthesized by the direct calcination method. Noticeably, by changing the additive concentrations of urea dissolved in DMF (N-N dimethylformamide), the electromagnetic wave (EMW) absorption abilities of NiCo2O4/NiO/Co3O4composite effectively. A maximum reflection loss (RLmax) value at 12.94 GHz for a 2.8 mm thick sheet is -29.76 dB, while its effective absorption bandwidth (RL < -10 dB) reaches 4.21 GHz. In-depth research of possible mechanisms of EMW absorption enhancement. Owing to its simple preparation method and superb EMW absorption properties, the NiCo2O4/NiO/Co3O4composites have a chance to be suitable candidates for high-property EMW absorbers.

Access to 1,3- and 1,5-Disubstituted 1,2,4-Triazoles by Condensation of Acyl Hydrazides with Formamidinium Acetate

AbstractA simple redox-neutral method for the regioselective preparation of 1,3- and 1,5-disubstituted 1,2,4-triazoles from the corresponding unactivated acyl hydrazides and the inexpensive, non-toxic, and shelf-stable formamidinium acetate was developed. The addition of zinc salts proved to be pivotal to ensure full regioselectivity for the 1,3-disubstitution pattern, while 1,5-disubstituted 1,2,4-triazoles could be accessed without. A variety of sensitive functional groups were tolerated, and [1,2,4]triazolo[4,3-a]pyridines were obtained from the corresponding 2-hydrazopyridines without Dimroth rearrangement.

Preparation of Paper-Based Fluorescent Sensors and Their Application for the Detection of Cu2+ in Water.

Excessive copper (Cu2+) causes adverse effects on human health and the ecological environment. Traditional methods for detecting Cu2+ have drawbacks such as high detection costs, complex operating conditions, and being time consuming. Therefore, there is an urgent need to develop simple detection methods to better meet specific health and environment quality needs. In this work, a paper-based fluorescence sensor was prepared (herein referred to as the as-prepared method) by immersing filter paper in aqueous polyethyleneimine (PEI) solution, and its potential use in Cu2+ detection was investigated. The results showed that the as-prepared paper samples, with fluorescence properties obtained by aggregation-induced luminescence of PEI, have selective recognition of Cu2+ based on the internal filtration effect, and the lowest detection limit is 0.03 μM. In addition, the relative error of this method is in the range of 1.80~2.23%, which is relatively comparable to the national standard method (0.63~630 μM), demonstrating high accuracy. Therefore, paper-based sensors with a simple preparation method have potential applications in the detection of Cu2+ in water.

In-situ immobilization of ZIF-67/ZIF-8 on wood biomass for degradation of methylene blue and formaldehyde

Metal-organic frameworks (MOFs) have been extensively studied for the removal of pollutants in wastewater and air. However, the existence of MOF materials in powder form with easy agglomeration and difficult separation has greatly confined their application potential. To address this challenge, ZIF-67/ZIF-8 composites were in-situ grown on wood biomass, with its porous structure providing channels for the growth of MOFs and active sites for MOFs catalysis. The structure, i.e., morphology, crystallinity and chemical components, and optical properties were characterized. The degradation efficiency of methylene blue (MB) by the ZIF-67/ZIF-8@wood composites photocatalyst was more than 85.7 % under visible light irradiation within 90 mins, reflecting the good photocatalytic activity of the composites. The ZIF-67/ZIF-8@wood composites completely adsorbed and decomposed HCHO (22.3 ppm) within 30 mins. The high catalytic performance of the ZIF-67/ZIF-8@wood composites can be attributed to the high surface area of wood that results in a high absorption of contaminants. This simple, low-cost, and green preparation method has promoted the sustainable utilization of biomass resources with great significance for practical environmental remediation.

Enhanced electrochemical nitrate removal from groundwater by simply calcined Ti nanopores with modified surface characters

Simple and convenient preparation method with high catalytic reduction activity is crucial for the remediation of nitrate contamination. In this study, the innovation for fabricating a nanoelectrode was developed by calcinating the anodized plate to alter the surface crystalline phase of the material. The prepared calcined Ti nano-pores (TNPs) electrode could effectively remove up to 95.1% nitrate from simulated groundwater at 30 mA·cm–2 electrolysis for 90 min, while under the same conditions, the removal efficiency of nano electrode prepared by conventional methods was merely 52.5%. SEM images indicated that the calcined-TNPs nanoelectrode was porous with different pore sizes. The higher nitrate removal efficiency of TNPs-500 (95.1%) than TNPs-400 (77.5%) and TNPs-550 (93.4%) may resulted from the positive nonlinear response of the larger ECSA, the improved electron transfer and suitable surface structure, and not the “anatase-to-rutile” of surface TiO2 nanotubes. After 90 min of electrolysis, by using RuO2 as an anode and adding 0.3 g·L–1 NaCl solution, 87.5% nitrate was removed, and the by-products (ammonia and nitrite) were negligible. Increased temperature and alkaline conditions can enhance the nitrate removal, while higher initial nitrate concentration only improved the nitrate removal slightly. Moreover, The TNPs-500 electrode also exhibited excellent nitrate removal performance in real groundwater with the efficiency at 82.9% and 92.1% after 90 and 120 min, which were 0.87 (removal efficiency=95.1%), 0.92 (removal efficiency=100%) of the efficiency for simulated groundwater, indicating the widely applicable conditions of the TNPs-500 electrode. This approach of surface bonded elements and structure modification through calcination significantly improves catalytic activity, and will guide the simple designing of functional nanostructured electrodes with wide application conditions.

High sensitivity and low noise photodetector based on topological crystalline insulator SnTe/Si heterostructure

Topological insulators, as a class of materials with narrow bulk bandgap and gapless surface states with response wavelengths covering infrared to terahertz, have great potential for application in new generation photodetector, but the large dark current and small photocurrent limit their application, so the device performance is generally improved by the method of heterogeneous integration. SnTe, as a topological crystalline insulator with multiple surface states, has a narrower forbidden bandwidth, it is suitable for the fabrication of infrared photodetector. In this work, SnTe thin films were deposited on Si substrates by magnetron sputtering, and SnTe/n-Si heterostructure photodetectors were fabricated on this basis. The photodetector exhibited good photoresponses in the visible near-infrared (532–1400 nm), with the responsivity (R) and normalized detectivity (D*) reaching 1.12 A/W, 5.17 × 1011 Jones. Thanks to the formation of the built-in electric field at the SnTe/Si interface, the photogenerated carriers can be rapidly separated and transported, and the switching ratio reaches 103. In addition, the rise time and fall time of the device are 218 μs and 174 μs, respectively. The good performance and simple preparation method make the device have a wide application prospect in the new generation of photodetector.

Ultrasensitive carbon nanotube-bridged MXene conductive network arrays for one-step homogeneous electrochemical immunosensing of tumor markers

Developing non-passivating and fully integrated electrode arrays for point-of-care testing of carcinoembryonic antigen (CEA) is crucial, as the serum level of CEA is closely associated with colorectal cancer. Herein, we propose a simple, low-cost, and eco-friendly template-assisted filtration method for the scalable preparation of carbon nanotube-bridged Ti3C2Tx MXene (MX@CNT) electrode arrays with a conductive network. Furthermore, we fabricate a homogeneous electrochemical (HEC) sensor for CEA detection by integrating a magnetic-bead-based alkaline phosphatase-linked immunoassay (MB-aElisa), which enables the in-situ generation of the electroactive substance 1-naphthol (1-NP). Benefiting from the unique electrochemical characteristics of a MX@CNT electrode array, such as ultra-low background signal and superior electrocatalytic activity towards the hydrolyzed 1-NP, the MB-aElisa-based HEC sensor specifically measures CEA within a detection range spanning from 0.005 to 1.0 ng mL−1, achieving a detection limit of 1.6 pg mL−1. Subsequently, this biosensing prototype is successfully utilized for the detection of CEA in serum specimens obtained from colorectal cancer patients. More importantly, the integration of MB-aElisa with a MX@CNT electrode array not only marks a significant advancement but also enables the creation of a one-step homogeneous electrochemical immunosensing platform, serving as a paradigm for the highly sensitive and selective measurement of trace tumor markers in complex biological samples.

Composite antibacterial hydrogels based on two natural products pullulan and ε-poly-l-lysine for burn wound healing

Antibacterial hydrogels as burn wound dressings are capable of efficaciously defending against bacterial infection and accelerating burn wound healing. Thus far, a large plethora of antibacterial hydrogels have adopted numerous components and intricate preparation processes, yet restricting their practical industrialization applications. Simple and effective preparation methods of antibacterial hydrogels are hence urgently needed. Herein, an easy but efficacious strategy with the employment of two natural products pullulan and ε-poly-l-lysine (ε-PL) was designed to fabricate composite antibacterial hydrogels for burn wound healing for the first time. The hydrogel crosslinking networks were formed through amidation reactions between carboxylated pullulan derivative (CP) and ε-poly-l-lysine hydrochloride (ε-PL·HCl). The resulting hydrogels possessed high transparency, porous structures, tunable gelation time and gel content, relatively low swelling ratios, appropriate self-degradability, proper mechanical properties, strong in vitro bacteriostatic activities, non-cytotoxicity, capacities of facilitating cell migration and excellent hemocompatibility. In the infected burn model of mice, the hydrogels were observed to display prominent in vivo antibacterial activities and enable the acceleration of burn wound healing. We opine the simply and effectively prepared antibacterial hydrogels as promising dressings for burn wound recovery have broad industrialization prospects.

In Situ Formation of Compound Eye-like SAN-OSB Composite Microspheres by Melt-Blending Method: Enhancing Multiple-Scattering Effect.

The preparation of novel structures of light-diffusing particles is currently a research focus in the field of light-diffusing materials. This study, conducted by the common melt-blending process, controlled thermodynamic and kinetic factors to distribute smaller-sized organic silica bead (OSB) particles at the interface between a polycarbonate (PC) matrix and spherical island-phase styrene-acrylonitrile copolymer (SAN) for the in situ formation of compound eye-like microspheres with SAN as "large eyes" and OSBs as "small eyes". Through the multiple-scattering effects of these compound eye-like microspheres, these light-diffusing materials significantly improved the haze, scattering range, and light-shielding capabilities while maintaining high transmittance. Specifically, the PC/SAN-OSB light-scattering materials achieved a haze of 100% with an OSB content of only 0.17%, maintaining a transmittance of 88%. Compared with the PC/OSB system with the same level of haze, the addition of OSB was reduced by 88%. Therefore, this study achieved exceptionally effective light-diffusing materials through a simple, environmentally friendly, and low-cost preparation method, suitable for the scalable production of light-diffusing materials in new display and lighting fields.

A novel magnetoelastic biosensor consisting of carbon quantum dots/nitrocellulose membranes and NiFe2O4/ polylactic acid based on 3D printing for α2-macroglobulin detection

α2-macroglobulin (α2-M) have crucial clinical significance as a potent biomarker for diabetes nephropathy (DN). There is an increasing demand for rapid detection of α2-M. Herein, a magnetoelastic (ME) biosensor with a layered composite structure is developed for α2-M detection. Based on 3D printing, the basal layer of the biosensor is prepared as a grid structure fabricated by polylactic acid (PLA) doped with NiFe2O4. The conductivity of the biosensor was improved significantly due to the addition of multi-walled carbon nanotubes (MWCNTs). The biological site for capturing α2-M antigen was provided by the carbon quantum dots (CDs) coupled with anti-α-2M (anti-α2-M@CDs) in the nitrocellulose filter (NC) membrane. Meanwhile, the distribution of antibodies on the biosensor surface can be observed more directly due to the fluorescence characteristics of CDs. The biosensor in this work can realize multi-pattern recognition of fluorescent signal and electromagnetic signal. The results show that the limit of detection (LOD) was 0.506 ng/mL in the linear range from 10 ng/mL to 100 µg/mL and the linear equation of fitting curve is: y = 0.21 x - 0.15. The ME biosensors with a simple preparation method have advantages of high sensitivity, good stability and low LOD, showing the great potential for α2-M detection.

Development and antioxidant evaluation of mango leaf (Mangifera indica L.) extract loaded silk fibroin nanoparticles

The main antioxidant polyphenol compounds in the mango (Mangifera indica L.) leaf extract are susceptible to environmental degradations. Thus, in biomedical applications, the mango leaf extract is commonly encapsulated in a carrier. However, most studies employed the synthetic carrier materials that could affect the human health, and the complicated formulation procedure that could hinder the scalability. Therefore, this work, for the first time, explored the use of silk fibroin (an FDA-approved biomaterial), in nanoparticles platform, to encapsulate and deliver the mango leaf extract, utilizing the simple coacervation preparation method. Initially, the mango leaf ethanolic extract was obtained through maceration, resulting in a total phenolic content of 76.39 ± 0.14 mg GAE/g DPW and a notably high antioxidant activity (IC50 = 6.872 ± 0.512 μg/mL). Subsequently, silk fibroin nanoparticles loaded with the extract were developed by the coacervation technique. Depending on the fibroin content, these nanoparticles exhibited an appropriate size range of 500–800 nm with narrow size distributions, a spherical shape with smooth surfaces, a dominant silk-II crystalline structure, a drug entrapment efficiency exceeding 70%, and retained the main biomarker mangiferin. Moreover, the phenolic-compounds release profiles from the particles followed the three-step process, the first burst-release step, the second sustained-release step, and the third degradation step. The particles were also non-toxic to the erythrocytes and the human embryonic kidney HEK-293 cell line. Lastly, the 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay demonstrated that the antioxidant activity of the mango leaf extract was preserved within the extract-loaded nanoparticles. The results suggested that the silk fibroin nanoparticles could be a potential platform to effectively encapsulate and deliver the mango leaf extract for biomedical purposes.

DNA aptamer-functionalized PDA nanoparticles: from colloidal chemistry to biosensor applications.

Polydopamine nanoparticles (PDA NPs) are widely utilized in the field of biomedical science for surface functionalization because of their unique characteristics, such as simple and low-cost preparation methods, good adhesive properties, and ability to incorporate amine and oxygen-rich chemical groups. However, challenges in the application of PDA NPs as surface coatings on electrode surfaces and in conjugation with biomolecules for electrochemical sensors still exist. In this work, we aimed to develop an electrochemical interface based on PDA NPs conjugated with a DNA aptamer for the detection of glycated albumin (GA) and to study DNA aptamers on the surfaces of PDA NPs to understand the aptamer-PDA surface interactions using molecular dynamics (MD) simulation. PDA NPs were synthesized by the oxidation of dopamine in Tris buffer at pH 10.5, conjugated with DNA aptamers specific to GA at different concentrations (0.05, 0.5, and 5μM), and deposited on screen-printed carbon electrodes (SPCEs). The charge transfer resistance of the PDA NP-coated SPCEs decreased, indicating that the PDA NP composite is a conductive bioorganic material. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) confirmed that the PDA NPs were spherical, and dynamic light scattering (DLS), Fourier transform infrared spectroscopy (FTIR), and Raman spectroscopy data indicated the successful conjugation of the aptamers on the PDA NPs. The as-prepared electrochemical interface was employed for the detection of GA. The detection limit was 0.17μg/mL. For MD simulation, anti-GA aptamer through the 5'terminal end in a single-stranded DNA-aptamer structure and NH2 linker showed a stable structure with its axis perpendicular to the PDA surface. These findings provide insights into improved biosensor design and have demonstrated the potential for employing electrochemical PDA NP interfaces in point-of-care applications.

Harnessing photocatalytic activity of mesoporous graphitic carbon nitride decorated by copper single-atom catalysts for oxidative dehydrogenation of N-heterocycles

This work describes the application of Cu single-atom catalysts (SACs) for photocatalytic oxidative dehydrogenation of N-heterocyclic amines to the respective N-heteroaromatics through environmentally benign and sustainable pathways. The mesoporous graphitic carbon nitride (mpg-C3N4), prepared by the one-step pyrolysis method, possesses a lightweight material with a high surface area (95 m2 g−1) and an average pore diameter (3.6 nm). A simple microwave-assisted preparation method was employed to decorate Cu single-atom over mpg-C3N4 support. The Cu single-atom decorated on mpg-C3N4 support (Cu@mpg-C3N4) is characterized by various characterization techniques, including XRD, UV–visible spectrophotometry, HRTEM, HAADF-STEM with elemental mapping, AC-STEM, ICP-OES, XANES, EXAFS, and BET surface area. These characterization studies confirmed that the Cu@mpg-C3N4 catalyst exhibited high surface area, mesoporous nature, medium band gap, and low metal loading. The as-synthesized and well-characterized Cu@mpg-C3N4 single-atom photocatalyst is then evaluated for its efficacy in converting N-heterocycles into corresponding N-heteroaromatic compounds with excellent conversion and selectivity (>99 %). This transformation is achieved using water as a green solvent and a 30 W white light as a visible light source, demonstrating the catalyst's potential for sustainable and environmentally benign reactions.

Application of a Green Deep Eutectic Solvent for Preconcentration and Determination of Copper and Cadmium in Food, Cosmetic, and Water Samples

Background:: Determination of environmental pollutants is important due to their harmful effects on the health of living organisms. However, direct measurement of many of these pollutants is not possible due to their low concentrations, which necessitates the need for sample preparation methods. One of the rapid and simple sample preparation methods is the Air-Agitated Liquid-Liquid Microextraction (AALLME) method, which requires toxic organic solvents that can lead to environmental pollution. Therefore, finding green solvents like Deep Eutectic Solvents (DESs) to replace them can be investigated. Methods:: A novel Deep Eutectic Solvent (DES) was synthesized from a combination of choline chloride and 2-phenylethanol with a molar ratio of 1:4, and it was examined using FT-IR analysis. This solvent was used in an AALLME method for measuring copper and cadmium heavy metal ions in complex real samples with Flame Atomic Absorption Spectroscopy (FAAS). Results:: The influential parameters of this method, such as solution pH (5.4), extraction cycles (12), and extraction solvent volume (440 μL), were optimized utilizing central composite design (CCD). Underneath the optimized circumstances, the detection limits for Cu2+ and Cd2+ were 0.14 and 0.09 ng mL-1, and the linear dynamic range was 0.47-50.0 and 0.32-22.5 ng mL-1, respectively. The preconcentration factors for these cations were 139.7 and 133.4, respectively. Conclusion:: Combining this novel green solvent and rapid sample preparation method for the preconcentration and determination of the studied heavy metal ions has shown promising results in terms of enrichment factors and detection limit values.

An overview on cubic liquid crystalline nanoparticles-trig lipid drug delivery system

This type of complex structure allows them greater drug loading ability, because of increased surface area and cuboidal structures, they have simple method of preparation and have ability to encapsulate hydrophilic, hydrophobic and amphiphilic substances. Cubosomes increases the solubility of poorly soluble drugs. Cubosomal dispersions are bioadhesive and biocompatible in nature. These are versatile systems, administered by different ways such as oral, perctuneous and parental routes. Cubosomes have broad vast applications in many areas and are characterized by various parameters consequently cubosomes are in move forward of awareness by pharmaceutical development division. Cubosomes, sometimes referred to as bicontinuous cubic phase liquid crystals, are spherical, quadruple nanoparticles with an interior cubic lattice mostly composed of certain amphiphilic lipids in a particular proportion. Cubosomes often arise when a solid-like phase is dispersed into smaller particles after a surfactant or polar lipid is hydrated to form a cubic phase. With distinct qualities of practical interest, they exhibit solid like rheology. They are thermodynamically stable, self-assembling drug delivery devices. Water and lipid bicontinuous domains give cubosomes their carvenous structure. Three-dimensional bilayers are formed by tightly twisted honeycomb arrangements.