Preparation and Properties of GO/ZnO/nHAp Composite Microsphere Bone Regeneration Material.

The purpose of this study is to explore the possibility of using graphene-zinc oxide-hydroxyapatite (GO/ZnO/nHAp) composite microspheres as bone regeneration materials by making use of the complementary advantages of nanocomposites, so as to provide reference for the clinical application of preventing and solving bacterial infection after implantation of synthetic materials. Firstly, GO/ZnO composites and hydroxyapatite nanoparticles were synthesized using the hydrothermal method, and then GO/ZnO/nHAp composite microspheres were prepared via high-temperature sintering. The graphene-zinc oxide-calcium phosphate composite microspheres were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), energy dispersion spectroscopy (EDS), water contact angle measurement, degradation and pH determination, and differential thermal analysis (DiamondTG/DTA). The biocompatibility, osteogenic activity, and antibacterial activity of GO/ZnO/nHAp composite microspheres were further studied. The results of the cell experiment and antibacterial experiment showed that 0.5% and 1% GO-ZnO-nHAp composite microspheres not only had good biocompatibility and osteogenic ability but also inhibited Escherichia coli and Staphylococcus aureus by more than 45% and 70%. Therefore, GO/ZnO/nHAp composite microspheres have good physical and chemical properties and show good osteogenic induction and antibacterial activity, and this material has the possibility of being used as a bone regeneration material.

Analysis of Photocatalytic Properties of NS-CQDs/g-C3N4 Composites.

N- and S-doped CQDs were prepared using L-cysteine as a precursor. Different NS-CQDs/g-C3N4 composite photocatalysts were formed by modifying graphite-phase carbon nitride with different contents of NS-CQDs using a hydrothermal method. The morphology, constituent elements and functional groups of the composite photocatalysts were analyzed by SEM, EDS, TEM, Mapping, XRD and FT-IR as a proof of its successful preparation. Meanwhile, it was characterized by PL, UV-Vis DRS and electrochemical impedance, which proved that the CQDs could be used as an electronic memory in the composite system to accelerate the electron transfer induced by the photo-excitation of g-C3N4 and effectively inhibit the recombination of e--h+ improvement of the photocatalytic activity of g-C3N4. The stability of the composite photocatalysts under different conditions and the photodegradation activity of Rh B under visible light were investigated. It was found that the photocatalytic degradation efficiency of rhodamine B by NS-CQDS-modified g-C3N4 was significantly higher than that of pure g-C3N4, which could reach 90.82%, and its degradation rate was 3.5 times higher than that of pure g-C3N4. It was demonstrated by free radical trapping experiments that ·OH and ·O2- were the main active species in the photocatalytic degradation process, in which ·O2- played a guiding role.

Synthesis and Catalytic Degradation of PEF, ENR, and CIP by g-C3N4/TCNQ/Eu Composite.

By using melamine as a precursor for the copolymerization process, g-C3N4 and g-C3N4/TCNQ/Eu complexes with various amounts of doping were created. These complexes were then examined using XRD, FT-IR, SEM, TEM, XPS, PL, UV-vis, and I-T. The degradation rates of pefloxacin (PEF), enrofloxacin (ENR), and ciprofloxacin (CIP) were 91.1%, 90.8%, and 93.2% under visible light (λ > 550 nm). The photocatalytic performance of the composite was analyzed, and the best effect was obtained for CIP photocatalysis when Eu doping was 3 mg at 20 °C and pH 7. Kinetic analysis showed that there was a linear relationship between the sample and the photocatalytic time, and the degradation rate was about 5 times that of g-C3N4. The cyclic stability of the g-C3N4/TCNQ/Eu composite sample was found to be good through repeated experiments. UPLC-MS visualizes the degradation process of CIP. The extremely low stability of piperazine ring induced subsequent degradation, followed by the fracture of quinolone ring promoting the complete decomposition of CIP.

ZnO QDs/GO/g-C3N4 Preparation and Photocatalytic Properties of Composites.

Using an ultrasound-assisted chemical technique, ZnO quantum dot and ZnO composites were created. The optical characteristics and structural details of these composites were examined using TEM, XRD, XPS, FT-IR, UV-vis, and BET. The results revealed that both the ZnO quantum dot composite and ZnO composite exhibited outstanding optical properties, making them suitable for photocatalytic reactions. In order to analyze the photocatalytic performance, a degradation experiment was conducted using Rhodamine B solution as the simulation dye wastewater. The experiment demonstrated that the degradation of Rhodamine B followed the first-order reaction kinetics equation when combined with the photocatalytic reaction kinetics. Moreover, through cyclic stability testing, it was determined that the ZnO QDs-GO-g-C3N4 composite sample showed good stability and could be reused. The degradation rates of Rhodamine B solution using ZnO-GO-g-C3N4 and ZnO QDs-GO-g-C3N4 reached 95.25% and 97.16%, respectively. Furthermore, free-radical-trapping experiments confirmed that ·O2- was the main active species in the catalytic system and its photocatalytic mechanism was elucidated. The photocatalytic oxidation of ZnO quantum dots in this study has important reference value and provides a new idea for the subsequent research.

Fluorescence Properties of ZnOQDs-GO-g-C3N4 Nanocomposites.

In this paper, the fluorescence properties of ZnOQD-GO-g-C3N4 composite materials (ZCGQDs) were studied. Firstly, the addition of a silane coupling agent (APTES) in the synthesis process was explored, and it was found that the addition of 0.04 g·mL-1 APTES had the largest relative fluorescence intensity and the highest quenching efficiency. The selectivity of ZCGQDs for metal ions was also investigated, and it was found that ZCGQDs showed good selectivity for Cu2+. ZCGQDs were optimally mixed with Cu2+ for 15 min. ZCGQDs also had good anti-interference capability toward Cu2+. There was a linear relationship between the concentration of Cu2+ and the fluorescence intensity of ZCGQDs in the range of 1~100 µM. The regression equation was found to be F0/F = 0.9687 + 0.12343C. The detection limit of Cu2+ was about 1.74 µM. The quenching mechanism was also analyzed.

Study of a Fluorescent System Based on the Naphthalene Derivative Fluorescent Probe Bound to Al3.

The naphthalene derivative fluorescent probe F6 was synthesized and a 1 × 10-3 mol/L solution of Al3+ and other metals to be tested was prepared for the subsequent experiments. The Al3+ fluorescence system of the naphthalene derivative fluorescent probe F6 was successfully constructed as demonstrated by fluorescence emission spectroscopy. The optimal time, temperature and pH of the reaction were investigated. The selectivity and anti-interference ability of the probe F6 for Al3+ were investigated by fluorescence spectroscopy in a methanol solution. The experiments showed that the probe has high selectivity and anti-interference ability for Al3+. The binding ratio of F6 to Al3+ was 2:1, and the binding constant was calculated to be 1.598 × 105 M-1. The possible mechanism of the binding of the two was speculated. Different concentrations of Al3+ were added to Panax Quinquefolium and Paeoniae Radix Alba. The results showed that the recoveries of Al3+ were 99.75-100.56% and 98.67-99.67%, respectively. The detection limit was 8.73 × 10-8 mol/L. The experiments demonstrated that the formed fluorescence system can be successfully adapted for the determination of Al3+ content in two Chinese herbal medicines, which has good practical application.

Preparation of g-C3N4/TCNQ Composite and Photocatalytic Degradation of Pefloxacin.

g-C3N4 and g-C3N4/TCNQ composites with different doping levels were prepared using the copolymerization thermal method with melamine as a precursor. XRD, FT-IR, SEM, TEM, DRS, PL, and I-T characterized them. The composites were successfully prepared in this study. The photocatalytic degradation of pefloxacin (PEF), enrofloxacin (ciprofloxacin), and ciprofloxacin (ciprofloxacin) under visible light (λ > 550 nm) showed that the composite material had the best degradation effect on PEF. When TCNQ doping is 20 mg and catalyst dosage is 50 mg, the catalytic effect is the best, and the degradation rate reaches 91.6%, k = 0.0111 min-1, which is four times that of g-C3N4. Repeated experiments found that the cyclic stability of the g-C3N4/TCNQ composite was good. The XRD images were almost unchanged after five reactions. The radical capture experiments revealed that ·O2- was the main active species in the g-C3N4/TCNQ catalytic system, and h+ also played a role in PEF degradation. And the possible mechanism for PEF degradation was speculated.

Photodegradation of fleroxacin by g-C3N4/PPy/Ag and HPLC-MS/MS analysis of degradation pathways.

To improve the photocatalytic activity of g-C3N4, graphitic phase carbon nitride was prepared using melamine as the substrate and modified with PPy and Ag nanoparticles. The structure, morphology, and optical properties of the photocatalysts were investigated using various characterization methods such as XRD, FT-IR, TEM, XPS, and UV-vis DRS. The degradation of fleroxacin, a common quinolone antibiotic, was isolated and measured using the HPLC-MS/MS technique to trace its intermediates and deduce the main degradation pathways. The results showed that g-C3N4/PPy/Ag had high photocatalytic activity and a degradation rate of more than 90%. The fleroxacin degradation reactions were primarily oxidative ring opening of the N-methyl piperazine ring structure, defluorination reactions on fluoroethyl, HCHO, and N-methyl ethylamine removal reactions.

Study on g-C3N4/BiVO4 Binary Composite Photocatalytic Materials.

Recent studies have shown that the composite of semiconductor photocatalytic materials and g-C3N4 can effectively inhibit photocatalytic carrier recombination and enhance the adsorption performance of the composite photocatalytic materials, so that the composite photocatalyst has stronger photocatalytic activity. In this paper, three kinds of graphitic carbon nitride photocatalyst g-C3N4 with different morphologies were prepared using the same precursor system by the chemical cracking method. After characterization and application, the sample with the most significant photocatalytic activity was selected and the g-C3N4/BiVO4 heterostructure was synthesized by the simple solvent evaporation method, then the photocatalytic experiment was carried out. The results show that, when the content of BiVO4 in the composite sample is 1%, the photocatalytic activity of RhB was the highest, and the degradation rate could reach 90.4%. The kinetic results showed that the degradation of RhB was consistent with the quasi-primary degradation kinetic model. The results of the photocatalytic cycle experiment show that the photocatalytic performance remains unchanged and stable after four photocatalytic cycles. The existence of a g-C3N4/BiVO4 binary heterojunction was confirmed by UV/Visible diffuse reflection (UV-DRS) and photoluminescence (PL) experiments. Owing to the Z-type charge process between BiVO4 and g-C3N4, efficient carrier separation was achieved, thus enhancing the photocatalytic capacity. This work provides a new idea for the study of heterojunction photocatalytic materials based on g-C3N4.

Deep-Eutectic-Solvent-Assisted Synthesis of a Z-Scheme BiVO4/BiOCl/S,N-GQDS Heterojunction with Enhanced Photocatalytic Degradation Activity under Visible-Light Irradiation.

Z-scheme heterojunction photocatalytic nanomaterial designs have attracted attention due to their high catalytic performance. Deep eutectic solvents (DESs) have been used as green, sustainable media, acting as solvents and structure inducers in the synthesis of nanomaterials. In this work, a novel visible-light-absorption-enhanced bismuth vanadate/bismuth oxychloride/sulfur, nitrogen co-doped graphene quantum dot (BiVO4/BiOCl/S,N-GQDS) heterojunction photocatalyst was prepared in a deep eutectic solvent. The photosynthetic activity of the BiVO4/BiOCl/S,N-GQDS composite was determined by the photocatalytic degradation of rhodamine B (RhB) under visible-light irradiation. The results showed that the highest photocatalytic activity of BiVO4/BiOCl/S,N-GQDS was achieved when the doping amount of S,N-GQDS was 3%, and the degradation rate of RhB reached 70% within 5 h. The kinetic and photocatalytic cycles showed that the degradation of Rhb was in accordance with the quasi-primary degradation kinetic model, and the photocatalytic performance remained stable after four photocatalytic cycles. Ultraviolet-visible diffuse reflectance (UV-DRS) and photoluminescence (PL) experiments confirmed that BiVO4/BiOCl/S,N-GQDS ternary heterojunctions have a narrow band gap energy (2.35 eV), which can effectively improve the separation efficiency of the photogenerated electron-hole pairs and suppress their complexation. This is due to the construction of a Z-scheme charge process between the BiVO4/BiOCl binary heterojunction and S,N-GQDS, which achieves effective carrier separation and thus a strong photocatalytic capability. This work not only provides new insights into the design of catalysts using a green solvent approach but also provides a reference for the study of heterojunction photocatalytic materials based on bismuth vanadate, as well as new ideas for other photocatalytic materials.

Felodipine Determination by a CdTe Quantum Dot-Based Fluorescent Probe.

In this work, a CdTe quantum dot-based fluorescent probe was synthesized to determine felodipine (FEL). The synthesis conditions, structure, and interaction conditions with FEL of CdTe quantum dots were analysed by fluorescence spectrophotometry, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), UV-visible spectroscopy, and TEM. The CdTe QD concentration was 2.0 × 10-4 mol/L. The amount of quantum dots controlled in the experiment was 0.8 mL. The controlled feeding ratio of N (Cd2+):N (Te2-):N (TGA) was 2:1:4, the heating temperature was 140 °C, the heating time was 60 min, and the pH of the QD precursor was adjusted to 11 for subsequent experiments. The UV-visible spectrum showed that the emission wavelength of CdTe quantum dots at 545 nm was the strongest and symmetric. The particle size of the synthesized quantum dots was approximately 5 nm. In the interaction of CdTe quantum dots with FEL, the FEL dosage was 1.0 mL, the optimal pH value of Tris-HCl buffer was 8.2, the amount of buffer was 1.5 mL, and the reaction time was 20 min. The standard curve of FEL was determined under the optimal synthesis conditions of CdTe quantum dots and reaction of CdTe quantum dots with FEL. The linear equation was Y = 3.9448x + 50.068, the correlation coefficient R2 was 0.9986, and the linear range was 5 × 10-6-1.1 × 10-4 mol/L. A CdTe quantum dot-based fluorescent probe was successfully constructed and could be used to determine the FEL tablet content.

Pt-Substituted polyoxometalate modification on the surface of low-cost TiO2 with highly efficient H2 evolution performance.

In this study, Pt-substituted polyoxometalate was first modified on the surface of commercially available TiO2, forming an efficient photocatalyst with high reactivity for hydrogen evolution. During the photocatalytic process, Pt-polyoxometalates not only increase the mobility rate of electrons but also improve the separation efficiency of photoinduced electrons and holes. After photoreduction, the in situ generated Pt0 species are anchored on the surface of polyoxometalate anion, which prevents further agglomeration. Then, the in situ formed Pt0 species and polyoxometalates synergistically promote the efficiency of photoinduced electron transfer from TiO2 to the protons adsorbed on the Pt0 surface. Although the content of Pt0 in the nanocomposite is only 0.6%, the photocatalytic hydrogen production rate reaches 5.6 mmol g-1 h-1 and remains stable at 4.5 mmol g-1 h-1 after the continuous catalytic process. Due to the modification of TiO2 by Pt-substituted polyoxometalate, this nanocomposite represents a practical model that possesses highly efficient photoelectric conversion performance. The presented work not only extends the family of new TiO2-polyoxometalate-based materials but also takes a further step toward the practical application of commercial TiO2 in photocatalytic hydrogen production.

Caproyl-Modified G2 PAMAM Dendrimer (G2-AC) Nanocomplexes Increases the Pulmonary Absorption of Insulin.

We aimed to investigate the absorption-enhancing effect (AEE) of caproyl-modified G2 PAMAM dendrimer (G2-AC) on peptide and protein drugs via the pulmonary route. In this study, G2 PAMAM dendrimer conjugates modified with caproic acid was synthesized, the pulmonary absorption of insulin as models with or without G2-AC were evaluated. The results indicated that G2-AC6 exhibited a greatest AEE for insulin in various caproylation levels of G2-AC. G2-AC6 could significantly enhance the absorption of insulin, and the AEE of G2-AC6 was concentration-dependent. In toxicity tests, G2-AC6 displayed no measurable cytotoxicity to the pulmonary membranes over a concentration range from 0.1% (w/v) to 1.0% (w/v). Measurements of the TEER and permeability showed that G2-AC6 significantly reduced the TEER value of CF and increased its Papp value. The results suggested that G2-AC6 could cross epithelial cells by means of a combination of paracellular and transcellular pathways. These findings suggested G2-AC6 at lower concentrations (below 1.0%, w/v) might be promising absorption enhancers for increasing the pulmonary absorption of peptide and protein drugs.

5ß-Cholanic Acid/Glycol Chitosan Self-Assembled Nanoparticles (5ß-CHA/GC-NPs) for Enhancing the Absorption of FDs and Insulin by Rat Intestinal Membranes.

The absorption-enhancing effects of glycol chitosan modified by 5ß-cholanic acid nanoparticles (5ß-CHA/GC-NPs) on a drug with poor absorption in the intestine were studied by the method of in situ closed loop. We chose fluorescein isothiocyanate-labeled dextrans (FDs) and insulin as the model drugs. 5ß-CHA/GC-NPs loaded to different drugs were prepared by the dialysis method, and the physicochemical characteristics and in vitro release profiles of nanoparticles were also estimated. The results showed that 5ß-CHA/GC-NPs markedly increased the absorption of insulin and FDs in the jejunum, ileum, and colon. The ratios of absorption for all the drugs in the jejunum were higher than those in the ileum and colon. In addition, the enhancing effect of 5ß-CHA/GC-NPs for the absorption of FDs from the jejunum was decreased with increasing molecular weights. In the toxicity test, 5ß-CHA/GC-NPs did not significantly increase the release of protein and the activities of LDH, indicating that the nanoparticles did not cause any membrane damage to the intestine. These findings suggested that 5ß-CHA/GC-NPs were safe and useful carriers for enhancing the absorption of the drug with poor absorption by intestinal membranes.

Improved intestinal absorption of water-soluble drugs by acetylation of G2 PAMAM dendrimer nanocomplexes in rat.

In search of an effective and less toxic absorption enhancer, we synthesized primary amine acetylation of generation 2 polyamidoamine (G2 PAMAM) dendrimer (Ac-G2) by the reaction of G2 PAMAM dendrimer with acetic anhydride, and evaluated the effects of Ac-G2 on the intestinal absorption of poorly absorbable water-soluble drugs using an in situ closed-loop method in rats. The results indicated that Ac50-G2 had a greatest absorption enhancing effect for 5(6)-carboxyfluorescein (CF) in various acetylation levels of G2 PAMAM dendrimers. Ac50-G2 with various concentrations (0.1-1.0%, w/v) could significantly improve the intestinal absorption of alendronate, CF, and fluorescein isothiocyanate-labeled dextrans (FD4), although they did not enhance the absorption of macromolecular drug of FD10, and the absorption enhancement effect of Ac50-G2 was concentration-dependent. Furthermore, we examined the intestinal membrane damage with or without Ac50-G2. The results displayed Ac50-G2 at lower concentrations (0.1-0.5%, w/v) did not cause any observed toxic effect to the intestinal membranes. These findings suggested Ac50-G2 at lower concentrations (below 0.5%, w/v) might be promising as an effective and safe absorption enhancers to promote the intestinal absorption of poorly absorbable drugs.

Oxidase-like mimic of Ag@Ag3PO4 microcubes as a smart probe for ultrasensitive and selective Hg(2+) detection.

An oxidase-like mimic system based on facilely synthesized Ag@Ag3PO4 microcubes (Ag@Ag3PO4MCs) was designed and utilized to detect mercury ions with high selectivity and ultrasensitivity. Ag@Ag3PO4MCs with an average size of ca. 1.6 µm were synthesized by the reaction of [Ag(NH3)2](+) complex and Na2HPO4 and subsequent photoreduction under ultraviolet light. The as-prepared Ag@Ag3PO4MCs can effectively catalyze the oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) and o-phenylenediamine (OPD) in the presence of dissolved oxygen in slightly acidic solution, exhibiting oxidase-like activities rather than peroxidase-like activity. Interestingly, the introduction of Ag nanoparticles (AgNPs) on the surfaces of Ag3PO4MCs can dramatically enhance the oxidase-like activities due to a synergistic effect between AgNPs and Ag3PO4MCs, as evidenced by the faster oxidation speed of TMB and OPD than that of native Ag3PO4MCs in the presence of dissolved oxygen. The enzyme kinetics can be well-explained by the Michaelis-Menten equation. As "poisoning" inhibitor, Hg(2+) ions can inhibit the enzyme reaction catalyzed by Ag3PO4MCs or Ag@Ag3PO4MCs. On the basis of this effect, a colorimetric Hg(2+) sensor was developed by the enzyme inhibition reaction of Ag3PO4MCs or Ag@Ag3PO4MCs. The excellent specific interaction of Hg-Ag or Hg(2+)-Ag(+) provides high selectivity for Hg(2+) over interfering metal ions. Meanwhile, the sensitivity of this sensor to Hg(2+) is extremely excellent with a limit of detection as low as 0.253 nM for Ag@Ag3PO4MCs. Considering the advantages of low detection limit, low cost, facile preparation, and visualization, the colorimetric Ag@Ag3PO4MCs sensor shows high promise for the testing of Hg(2+) in water samples.

Study of the luminescence properties of a novel rare earth complex Tb(DPC)(2)2H2O.

Rare earth complex Tb(DPC)(2)2H(2)O was synthesized by introducing Pyridine-2,6-dicarboxylic acid(H(2)DPC) as the ligand and characterized by UV, fluorescent and infrared spectra as well as elemental analysis. The complex exhibited ligand-sensitized green emission, and it has the higher sensitized luminescent efficiency and longer lifetime. The effect and mechanism of the ligand (H(2)DPC) on the luminescence properties of terbium complex was discussed. In device ITO/PVK/Tb(DPC)(2)2H(2)O/Al, Tb(3+) may be excited by intramolecular energy transfer from ligand as observed by electroluminescence. The main emitting peak at 545 nm can be attributed to the transition of (5)D(4)-->(7)F(5) of Tb(3+) ion and this process results in the enhancement of green emission from electroluminescence device.

Enhanced luminescence of novel rare earth complexes Eu(3,5-DNBA)3Phen in nano-TiO2.

Eu(3+) (or Tb(3+)) of 3,5-dinitrobenzoic acid and 1,10-phenanthroline ternary rare earth complexes were synthesized and characterized by thermal analysis, infrared spectroscopy, elemental analysis and fluorescence spectroscopy. In this study an organic-inorganic combined device indium tin oxide/poly(N-vinylcar-bazole):RE(3,5-DNBA)(3)Phen:TiO(2)/Al was fabricated. The nano-TiO(2) has been used in the luminescence layer to change the electroluminescence property of RE(3,5-DNBA)(3) Phen (RE=Eu(3+)or Tb(3+)).

Enhanced luminescence of rare-earth complexes Tb(1-x)Eu(x)(m-NBA)3Phen in ZnS.

Rare-earth ternary complexes Tb(1-x)Eu(x)(m-NBA)(3)Phen (X=1, 0.25, 0.5, 0.75, 1.0) were synthesized and characterized by IR, DTA-TG, UV, fluorescent spectra and elemental analysis. It was found that luminescence of Eu(3+) complex was enhanced by doped with Tb(3+). It is proved by TG curve that the complexes are stable, ranging from ambient temperature to 360 degrees C in air. The organic-inorganic combined structural device was fabricated, and the electroluminescence intensity of the combined structural device was improved compared with the device of the purely organic components.

The study on the effect and mechanism of the second ligands on the luminescence properties of terbium complexes.

The binary complex of Tb(III) with N-phenylanthranilic acid (N-HPA) was synthesized, and the ternary complexes were synthesized by introducing 1,10-phenanthroline (Phen), 2,2'-dipyridyl (Bipy), trioctylphosphine oxide (TPPO) as the second ligand, respectively. These complexes were characterized by infrared spectra, UV spectra and fluorescence spectra. The effect and mechanism of different second ligands on the fluorescent intensity of the terbium N-phenylanthranilic acid complexes was discussed. It showed that all the complexes exhibited ligand-sensitized green emission. The luminescence intensity increased in the sequence of Tb(N-PA)(3)Phen