Facile fabrication of chitin/ZnO composite hydrogels for infected wound healing.

When ordinary wounds are infected, the skin's self-healing capacity declines; thus appropriate dressings with both antibacterial ability and healing ability for bacteria-associated wounds are indispensable. In this work, multifunctional chitin/ZnO composite hydrogels have been designed as an infected full-thickness skin wound-healing material. The hydrogels are fabricated by a facile one-pot strategy through the sequential addition of commercial ZnO powders into aqueous alkaline chitin solutions, crosslinking and regeneration. The regenerated nanoscale ZnO particles aggregate into microscale particles and are embedded in the chitin matrix with tight interactions, including hydrogen bonding and coordination interactions. The decoration of ZnO endows the chitin/ZnO composite hydrogels with excellent antibacterial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus), with acceptable biocompatibility. More importantly, the chitin/ZnO composite hydrogels show an outstanding accelerated infectious full-thickness wound-healing performance with more fibroblast proliferation, more collagen deposition, and more neogenesis of the epithelium and granulation tissue. Therefore, it is expected that the chitin/ZnO composite hydrogels can serve as competitive skin wound dressings for the prevention and control of infections.

Magnetic chitosan microspheres: An efficient and recyclable adsorbent for the removal of iodide from simulated nuclear wastewater.

The efficient and recyclable magnetic chitosan microspheres (MCMs) were successfully synthesized to remove iodide from nuclear wastewater and characterized through XRD, FTIR, SEM, EDS, VSM, TGA and XPS. The characterization results indicated that the MCMs exhibited smooth spherical morphology and good magnetic properties. The removal potential of MCMs was investigated for iodide (I-) anions at different conditions. From pH 3 to pH 9, MCMs performed the high I- removal efficiency (>90%). The maximum I- removal capacity of MCMs was up to 0.8087 mmol g-1 at 298 K, well-fitting with the pseudo-second-order and Sips models. Furthermore, the I- removal efficiency of MCMs still maintained more than 91% after five adsorption-desorption cycles, performing good regeneration and reusability. This study is expected to prompt the MCMs to become an efficient and recyclable biosorbent for iodide removal from nuclear wastewater.

Preparation of Quaternary Ammonium Salt-Modified Chitosan Microspheres and Their Application in Dyeing Wastewater Treatment.

An efficient adsorbent (a quaternary ammonium salt-modified chitosan microsphere, CTA-CSM) was synthesized via an emulsion cross-linking reaction between 3-chloro-2-hydroxypropyl trimethyl ammonium chloride (CTA) and chitosan (CS). The adsorption efficiency of the CTA-CSM as an adsorbent was studied using methyl orange dye to evaluate its suitability for wastewater purification. The characterization results showed that the CTA groups were successfully grafted onto the CS microspheres, and the as-prepared CTA-CSM samples exhibited a smooth surface and good dispersibility. The modification of CTA on CTA-CSM significantly improved its ability to remove methyl orange dye. The adsorption process of methyl orange by CTA-CSM was well described by the Langmuir isotherm model and followed the pseudo-second-order kinetic model. Under the optimal conditions, the maximum removal rate (98.9%) and adsorption capacity (131.9 mg/g) of CTA-CSM was higher than those of other previous reports; its removal rate for methyl orange was still up to 87.4% after five recycles. Hence, CTA-CSM is a very promising material for practical dyeing wastewater purification.

Synthesis and characterization of magnetic chitosan microspheres for drug delivery.

A novel magnetic microsphere was prepared by simple microemulsion polymerization for protein drug delivery systems. The Fe3O4 magnetic nanoparticles were successfully encapsulated in chitosan microspheres, which endowed the chitosan microspheres with good magnetism. The drug loading performance results indicated that the prepared magnetic chitosan microspheres exhibited a superior drug loading capacity, and the drug loading amount reached 947.01 mg g-1. Furthermore, the magnetic chitosan microspheres also showed a higher drug release rate (87.8%) and evident sustained-release performance in vitro. The magnetic microsphere carrier will be widely used in the biomedical field as a promising drug carrier.

Preparation and Characterization of Sulfonated Magnetic SiO2 Microspheres as the Solid Acid Catalysts for Esterification.

The sulfonated magnetic SiO2 microsphere solid acid catalysts were prepared by the impregnation and grafting methods with iron oxide magnetic nanoparticles (Fe3O4 MNPs) as the magnetic cores. The catalytic properties of the magnetic SiO2 solid acid catalyst were studied in detail. The characterization results showed that the SiO2 was successfully coated on the Fe3O4 MNPs. Compared with the grafting method, impregnated solid acid exhibits higher catalytic performance, which reached an esterification rate of up to 99.00% when the reaction temperature was 105 °C, the molar ratio of n-butanol/adipic acid was 3:1, and the ratio of the catalyst (the mass of magnetic solid acid) to liquids (the total volume of n-butanol and adipic acid) was 2.95%. The magnetic solid acid exhibited great separation ability and reusability. After six times of recycle, the conversion of the grafted magnetic solid acid still attained 85.61% compared with that of the impregnated magnetic solid acid, which reduced to 81.35%, holding great potential for green chemical processes.

Thermo-responsive magnetic liposomes for hyperthermia-triggered local drug delivery.

We prepared and characterised thermo-responsive magnetic liposomes, which were designed to combine features of magnetic targeting and thermo-responsive control release for hyperthermia-triggered local drug delivery. The particle size and zeta-potential of the thermo-responsive magnetic ammonium bicarbonate (MagABC) liposomes were about 210 nm and -14 mV, respectively. The MagABC liposomes showed encapsulation efficiencies of about 15% and 82% for magnetic nanoparticles (mean crystallite size 12 nm) and doxorubicin (DOX), respectively. The morphology of the MagABC liposomes was visualised using transmission electron microscope (TEM). The MagABC liposomes showed desired thermo-responsive release. The MagABC liposomes, when physically targeted to tumour cells in culture by a permanent magnetic field yielded a substantial increase in intracellular accumulation of DOX as compared to non-magnetic ammonium bicarbonate (ABC) liposomes. This resulted in a parallel increase in cytotoxicity for DOX loaded MagABC liposomes over DOX loaded ABC liposomes in tumour cells.

Crystallization of AlPO4-5 aluminophosphate molecular sieve prepared in fluoride medium: a multinuclear solid-state NMR study.

In the present work, multinuclear solid-state NMR techniques, combined with powder X-ray diffraction (PXRD) and infrared (IR) spectroscopy, are employed to monitor the crystallization of AlPO4-5 aluminophosphate prepared in the presence of HF under hydrothermal condition. The crystallization process is characterized by the evolution of intermediate gels, in which the long-rang ordering arrangement is probed by PXRD, revealing the threshold of the crystallization around 120 min. The appearance of 31P signals at ca. -22 and -29 ppm due to the structural P-O-Al unit and 19F signal at -120 ppm due to the structural F-Alpen-O-P unit in the NMR spectra of the series gels indicates that the crystalline framework is starting to form. The onset of the crystallization is also evidenced by the presence of the pentacoordinated Al in the structural F-Alpen-O-P unit which is considered to be associated with the ordered framework. More information about the local ordering of the gels is obtained from two-dimensional 27Al --> 31P heteronuclear correlation (HETCOR) and 31P/27Al double-resonance experiments. In combination with 1H --> 31P cross-polarization/magic-angle spinning (CP/MAS) experiments, two microdomains can be identified in the 120 min heated gel. A possible evolution mechanism of the gels consisting of three successive stages is proposed for the crystallization process.

Covalent functionalization of multiwalled carbon nanotubes with a low molecular weight chitosan.

Covalent functionalization of shortened multiwalled carbon nanotubes (MWNTs) with a natural low molecular weight chitosan (LMCS) was accomplished by a nucleophilic substitution reaction. Amino and primary hydroxyl groups of the LMCS contributed mainly to the formation of MWNT-LMCS conjugates. The LMCS content in the MWNT-LMCS is approximately 58 wt %, and approximately four molecular chains of the LMCS are attached to 1000 carbon atoms of the nanotube sidewalls. Most interestingly, the amorphous packing structure of the LMCS changed dramatically when it attached to the MWNTs. The MWNTs might induce the crystalline character of the LMCS. As a novel derivative of MWNTs, the MWNT-LMCS is soluble in dimethylformamide, dimethyl acetamide, dimethylsulfoxide, and acetic acid aqueous solution. The confirmation of the chitosan-based covalent functionalization route might lead to further studies aiming for potential applications in catalysis and environmental protection.

Acidity of mesoporous MoO(x)/ZrO2 and WO(x)/ZrO2 materials: a combined solid-state NMR and theoretical calculation study.

The acidity of mesoporous MoO(x)/ZrO2 and WO(x)/ZrO2 materials was studied in detail by multinuclear solid-state NMR techniques as well as DFT quantum chemical calculations. The 1H MAS NMR experiments clearly revealed the presence of two different types of strong Brønsted acid sites on both MoO(x)/ZrO2 and WO(x)/ZrO2 mesoporous materials, which were able to prontonate adsorbed pyrine-d5 (resulting in 1H NMR signals at chemical shifts in the range 16-19 ppm) as well as adsorbed trimethylphosphine (giving rise to 31P NMR signal at ca. 0 ppm). The 13C NMR of adsorbed 2-(13)C-acetone indicated that the average Brønsted acid strength of the two mesoporous materials was stronger than that of zeolite HZSM-5 but still weaker than that of 100% H2SO4, which was in good agreement with theoretical predictions. The quantum chemical calculations revealed the detailed structures of the two distinct types of Brønsted acid sites formed on the mesoporous MoO(x)/ZrO2 and WO(x)/ZrO2. The existence of both monomer and oligomer Mo (or W) species containing a Mo-OH-Zr (or W-OH-Zr) bridging OH group was confirmed with the former having an acid strength close to zeolite HZSM-5, with the latter having an acid strength similar to sulfated zirconia. On the basis of our NMR experimental and theoretical calculation results, a possible mechanism was proposed for the formation of acid sites on these mesoporous materials.

High-resolution magic-angle spinning (13)C spectroscopy of brain tissue at natural abundance.

High-resolution magic-angle spinning (MAS) (1)H and (13)C magnetic resonance spectroscopy (MRS) has recently been applied to study the metabolism in intact biological tissue samples. Because of the low natural abundance and the low gyromagnetic ratio of the (13)C nuclei, signal enhancement techniques such as cross-polarization (CP) and distortionless enhancement by polarization transfer (DEPT) are often employed in MAS (13)C MRS to improve the detection sensitivity. In this study, several sensitivity enhancement techniques commonly used in liquid- and solid-state NMR, including CP, DEPT and nuclear Overhauser enhancement (NOE), were combined with MAS to acquire high-resolution (13)C spectra on intact rat brain tissue at natural abundance, and were compared for their performances. The results showed that different signal enhancement techniques are sensitive to different classes of molecules/metabolites, depending on their molecular weights and mobility. DEPT was found to enhance the signals of low-molecular weight metabolites exclusively, while the signals of lipids, which often are associated with membranes and have relatively lower mobility, were highly sensitive to CP enhancement.