Synergistic Bonding of Poly(N-isopropylacrylamide)-Based Hybrid Microgels and Gold Nanoparticles Used for Temperature-Responsive Controllable Catalysis of p-Nitrophenol Reduction.

Stimuli-responsive hybrid nanoparticles used for controllable catalysis have been attracting increasing attention. This study aims to prepare hybrid microgels with excellent temperature-sensitive colorimetric and catalytic properties through combining the surface plasmon resonance properties of gold nanoparticles (AuNPs) with the temperature-sensitive properties of poly(N-isopropylacrylamide) (PNIPAM)-based microgels. Microgels with hydroxy groups (MG-OH) were prepared by soap-free emulsion polymerization, using N-isopropylacrylamide as the main monomer, hydroxyethyl methylacrylate as the functional monomer, N,N'-methylene bisacrylamide as the crosslinker, and 2,2'-azobis(2-methylpropionamidine) dihydrochloride as an initiator to ensure the microgels are positively charged. Furthermore, chemical modification on the surface of MG-OH was carried out by 3-mercaptopropyltriethoxysilane to obtain thiolated microgels (MG-SH). Two kinds of hybrid nanoparticles, AuNPs@MG-OH and AuNPs@MG-SH, were self-assembled, through electrostatic interaction between positive MG-OH and negative citrate-stabilized AuNPs as well as through synergistic bonding of electrostatic interaction and Au-S bonding between positive MG-SH and negative AuNPs. The morphology, stability, temperature-sensitive colorimetric properties, and catalytic properties of hybrid microgels were systematically investigated. Results showed that although both AuNPs@MG-OH and AuNPs@MG-SH exhibit good temperature-sensitive colorimetric properties and controllable catalytic properties for the reduction reaction of p-nitrophenol, AuNPs@MG-SH with synergistic bonding has better stability and higher catalytic performance than AuNPs@MG-OH. This work has good competitiveness against known PNIPAM-based materials and may provide an effective method for preparing smart catalysts by self-assembly with stimuli-responsive polymers, which has a great potential application for catalyzing a variety of reactions.

Bio-Based Waterborne Polyurethane Coatings with High Transparency, Antismudge and Anticorrosive Properties.

Green and environment-friendly preparation are of the utmost relevance to the development of transparent antismudge coatings. To prepare a waterborne polyurethane (WPU) coating with antismudge property, it is challenging to balance the stability of dispersion and the antismudge property of coating. Herein, we prepare a transparent bio-based WPU coating grafted with a minor proportion of poly(dimethylsiloxane) (WPU-g-PDMS) using renewable castor oil, monocarbinol-terminated PDMS, hexamethylene diisocyanate trimer, and 2,2-bis(hydroxymethyl)propionic acid as raw materials. Effects of the dosage of monocarbinol-terminated PDMS, the curing temperature, and the curing time on the antismudge performance were studied. Results showed that rigorous stirring (3000 rpm) is necessary to obtain a stable WPU-g-PDMS dispersion with a storage time longer than 6 months. A high curing temperature (>160 °C) and a period of curing time (>1 h) are indispensable to obtain the excellent antismudge property because they would facilitate the grafted low-surface-tension PDMS chains to migrate from the interior to the coating surface. The facts that simulated contaminated liquids such as water, HCl solution, NaOH solution, artificial blood, and tissue fluid could slide off easily and cleanly, and marker ink lined on the coating surface could shrink, indicated that the WPU-g-PDMS coating has good antismudge properties, which could be self-compensated shortly after deterioration. Due to the high cross-linking degree caused by multifunctional polyol and isocyanate, the WPU-g-PDMS coating has high hardness and good anticorrosive performance. The antismudge functionalization and waterborne technology of bio-based polyurethane coatings proposed in this work could be a promising contribution to the green and sustainable development of functional coatings. This kind of WPU-g-PDMS coating is expected to protect and decorate electronic screens, vehicles, and buildings, especially endoscopes.

Autofluorescence free detection of carcinoembryonic antigen in pleural effusion by persistent luminescence nanoparticle-based aptasensors.

Carcinoembryonic antigen (CEA) is an important biomarker in the diagnosis of cancer. The increase of CEA in malignant pleural effusion appears earlier and possesses higher clinical diagnostic value than that in the serum. Conventional fluorescent probes suffer from the interference of strong biotissue auto-fluorescence, which limits severely their applications in biology detection. Herein, a novel fluorescence aptasensor was designed with near-infrared persistent luminescence nanoparticles (PLNPs) for accurate detection of carcinoembryonic antigen in pleural effusion by FRET quenching and recovery mechanism. The strong background interference from the autofluorescence of pleural effusion samples can be effectively eliminated and extra increments of measured values originated from the background of different samples were ruled out, benefit from the long decay time of PLNPs and time-resolved fluorescence technology. The detection results show high accuracy of the measured values of carcinoembryonic antigen both in cancer and benign disease group with low detection limit up to 0.0851 pg mL-1. Furthermore, excellent selectivity from coexisting biomarker was achieved by the hybridization between the aptamer and the complementary DNA on PLNPs surface. Hence, the established near-infrared PLNPs-based aptasensors offer excellent performance with high selective, accuracy and signal-to-noise ratio for detection of carcinoembryonic antigen in pleural effusion.

Ultrahigh Flux and Strong Affinity Poly(N-vinylformamide)-Grafted Polypropylene Membranes for Continuous Removal of Organic Micropollutants from Water.

The rapid and effective removal of organic micropollutants (OMPs) from water remains a huge challenge for traditional water treatment techniques. Compared with powder adsorbents such as polymers and nanomaterials, the free-standing adsorptive membrane is possible for large-scale applications and shows promise in removing OMPs. Herein, inspired by aquatic plants, a novel free-standing adsorptive membrane (NPPM) with high water flux, strong adsorption affinity, and excellent reproducibility was prepared by one-step UV surface grafting. N-Vinylformamide (NVF) was employed to introduce multiple hydrophilic and hydrogen bonding sites on the surface of commercial polypropylene fiber membranes (PPM). The NPPM exhibits excellent water permeability and ultrahigh water flux (up to 40 000 L/(m2 h)) and could continuously remove a broad spectrum of OMPs from water. Its adsorption performance is 5-100 times higher than that of PPM and commercial membranes. Even in natural water sources such as tap water and river water, the NPPM shows unchanged adsorption performance and high OMPs removal efficiency (>95%). Notably, the NPPM has excellent regeneration performance and can be regenerated by hot water elution, which provides an environmentally friendly regeneration method without involving any organic solvent. Moreover, the synergy between hydrogen bonding and hydrophobic interaction is revealed, and the hydrophobic interaction provided by the hydrophobic substrate is proved to play a fundamental role in OMPs adsorption. The strong hydrogen bonds between the grafts and the OMPs are demonstrated by variable-temperature FTIR spectroscopy (vt-FTIR), 13C nuclear magnetic resonance spectroscopy (13C NMR), and simulation calculations. The strong hydrogen bonds could increase the enthalpy change and enhance the adsorption affinity, so the NPPM has a strong adsorption affinity, which is 100 times that of similar adsorption membranes. This study not only presents an adsorptive membrane with great commercial potential in the rapid remediation of a water source but also opens a pathway to develop an adsorptive membrane with high water flux and strong adsorption affinity.

Preparation and Self-Assembling of PLA-b-PNIPAM-b-PS Triblock Copolymer Thin Films.

Polylactide-b-poly(N-isopropylacrylamide)-b-polystyrene (PLA-b-PNIPAM-b-PS) triblock copolymers (tri-BCPs) with various chemical compositions (block ratio) were prepared from the combination of ring-opening polymerization and reversible addition-fragmentation chain transfer polymerization. Subsequently, the self-assembling behaviors of these tri-BCP films obtained from spin-coating were investigated by annealing them under different solvent atmosphere. We found that these films could self-assemble into various morphologies due to the microphase separation of incompatible copolymer blocks. Atomic force microscopy confirmed the perpendicular cylindrical morphology self-assembled from PLA4.5k-b-PNIPAM5.2k-b-PS22.4k tri-BCP film under mixed solvent atmosphere of toluene/acetone (7:3, v/v). Self-assembled PLA cylinders are evenly distributed among the PS matrix and perpendicular to the film surface, with PNIPAM component taking place at the PLA/PS interphase. Furthermore, by etching the degradable PLA component, porous PS film decorated with PNIPAM "brushes" hoisting channels were generated. This work provides a facile method and detailed protocol for fabricating stimuli-responsive porous films which are promising for thermoresponsive "smart" separation technologies.

Facile and Safe Synthesis of Novel Self-Pored Amine-Functionalized Polystyrene with Nanoscale Bicontinuous Morphology.

The chloromethyl-functionalized polystyrene is the most commonly used ammonium cation precursor for making anion exchange resins (AER) and membranes (AEM). However, the chloromethylation of polystyrene or styrene involves highly toxic and carcinogenic raw materials (e.g., chloromethyl ether) and the resultant ammonium cation structural motif is not stable enough in alkaline media. Herein, we present a novel self-pored amine-functionalized polystyrene, which may provide a safe, convenient, and green process to make polystyrene-based AER and AEM. It is realized by hydrolysis of the copolymer obtained via random copolymerization of N-vinylformamide (NVF) with styrene (St). The composition and structure of the NVF-St copolymer could be controlled by monomeric ratio, and the copolymers with high NVF content could form bicontinuous morphology at sub-100 nm levels. Such bicontinuous morphology allows the copolymers to be swollen in water and self-pored by freeze-drying, yielding a large specific surface area. Thus, the copolymer exhibits high adsorption capacity (226 mg/g for bisphenol A). Further, the amine-functionalized polystyrene has all-carbon backbone and hydrophilic/hydrophobic microphase separation morphology. It can be quaternized to produce ammonium cations and would be an excellent precursor for making AEM and AER with good alkaline stability and smooth ion transport channels. Therefore, the present strategy may open a new pathway to develop porous alkaline stable AER and AEM without using metal catalysts, organic pore-forming agents, and carcinogenic raw materials.

Hemp derived N-doped highly porous carbon containing Co nanoparticles as electrocatalyst for oxygen reduction reaction.

Biomass derived porous carbon was wildly used in non-precious metal carbon based electrocatalysts for ORR due to its low cost and sustainability. Here, we develop a facile route to prepare Co/N doped hemp derived highly porous carbon (Co/NHPC) as ORR electrocatalyst. The prepared Co/NHPC-90 possess 3D hierarchically porous nanostructure with high specific surface areas (1251 m2 g-1) and large pore volumes (0.99 cm3 g-1) due to the chemical activation of NaHCO3, which is benefit for the mass/electron transfer and exposure of active sites. In addition, melamine and cobalt nitrate were selected as nitrogen and metal source respectively to enrich the density of active sites. Thus, Co/NHPC-90 exhibits excellent ORR electrocatalytic performance with high half-wave potential (0.826 V), superior catalytic stability and tolerance to methanol.

PDMS-Infused Poly(High Internal Phase Emulsion) Templates for the Construction of Slippery Liquid-Infused Porous Surfaces with Self-cleaning and Self-repairing Properties.

Advanced liquid-repelling materials that resist both water-based and oil-based contaminants have significant applications in many fields. Herein, a novel protocol for the fabrication of a robust poly(high internal phase emulsion) (polyHIPE)-based slippery liquid-infused porous surface (SLIPS) system with combined self-repairing and self-cleaning properties is developed. Specifically, polystyrene-based polyHIPE (PS-HIPE) membranes with an interconnected porous structure were prepared from polymerization of the continuous oil phase in the water-in-oil HIPE templates. These polyHIPE membranes were used, for the first time, as porous substrates for loading low surface tension silicone oils as lubricating liquids for the fabrication of polyHIPE-based SLIPS membranes. These polyHIPE-based SLIPS membranes could easily repel both water- and oil-based contaminants (e.g., ink, milk, and coffee) with very low sliding angles (3.0 ? 1.3?) and could even repel solid contaminants (e.g., dust) upon washing with water. Meanwhile, such membranes exhibit excellent self-repairing properties so that physical scratching damage, such as cutting a trench, does not affect the liquid-repelling performance. The liquid-repelling ability could be recovered completely within 10 s. More significantly, such a SLIPS membrane shows excellent durability so that the water sliding angle of the SLIPS could be maintained at less than 5.0? for about 80 cycles owing to the regenerated poly(dimethylsiloxane) layer on the surface. This work represents a robust methodology to enrich the development of hydrophobic and oleophobic slippery surfaces, which is promising for many areas, such as biomedical, self-cleaning, antifouling, and self-repairing materials.

Glycerol aerobic oxidation to glyceric acid over Pt/hydrotalcite catalysts at room temperature.

Glycerol (GLY) aerobic oxidation in an aqueous solution is one of the most prospective pathways in biomass transformation, where the supported catalysts based on noble metals (mainly Au, Pd, Pt) are most commonly employed. Herein, Pt nanoparticles supported on rehydrated MgxAl1-hydrotalcite (denoted as re-MgxAl1-LDH-Pt) were prepared via impregnation-reduction method followed by an in situ rehydration process, which showed high activity and selectivity towards GLY oxidation to produce glyceric acid (GLYA) at room temperature. The metal-support interfacial structure and catalyst basicity were modulated by changing the Mg/Al molar ratio of the hydrotalcite precursor, and the optimal performance was achieved on re-Mg6Al1-LDH-Pt with a GLY conversion of 87.6% and a GLYA yield of 58.6%, which exceeded the traditional activated carbon and oxide supports. A combinative study on structural characterizations (XANES, CO-FTIR spectra, and benzoic acid titration) proves that a higher Mg/Al molar ratio promotes the formation of positively charged Ptδ+ species at metal-support interface, which accelerates bond cleavage of α-C-H and improves catalytic activity. Moreover, a higher Mg/Al molar ratio provides a stronger basicity of support that contributes to the oxidation of terminal-hydroxyl and thus enhances the selectivity of GLYA. This catalyst with tunable metal-support interaction shows prospective applications toward transformation of biomass-based polyols.

[Preparation and drug release of curcumin-loaded poly (α-isobutyl cyanoacrylate) microspheres].

Curcumin-loaded poly (α-isobutyl cyanoacrylate) microspheres (Cur-HP-ß-CD-PiBCA) were prepared by one-step emulsification with α-isobutyl cyanoacrylate as materials, poloxamer 188 as emulsifier, and curcumin complex with hydroxypropyl-ß-cyclodextrin (Cur-HP-ß-CD) as drug prepared by kneading method. Effects of emulsifier and drug concentration on microspheres size and distribution, drug loading and encapsulation efficiency were investigated in detail. And the curcumin release of drug-loaded microspheres was also studied. Results showed that as the emulsifier concentration increased from 0.01% to 0.07%, particle size of the drug-loaded microspheres decreased while particle size distribution, drug loading and entrapment efficiency increased. The optimized concentration of surfactant was 0.05%. With increasing the concentration of drug from 0.03% to 0.07%, drug loading of Cur-HP-ß-CD-PiBCA increased, but encapsulation efficiency decreased. Additionally, the results of drug release experiments revealed that the higher drug loading of Cur-HP-ß-CD-PiBCA was, the lower cumulative release percentage was. Drug-loading of cumulative inclusions in HP-ß-CD by PiBCA can improve its wettability, and increase the degree of dissolution and bioavailability.

Synthesis and Self-Assembly of Block Copolymers Containing Temperature Sensitive and Degradable Chain Segments.

In this work, polylactide-b-poly(N-isopropylacrylamide) were synthesized by the combination of controlled ring-opening polymerization and reversible addition fragmentation chain transfer polymerization. These block copolymers with molecular weight range from 7,900 to 12,000 g/mol and narrow polydispersity (≤1.19) can self-assemble into micelles (polylactide core, poly(N-isopropylacrylamide) shell) in water at certain temperature range, which have been evidenced by laser particle size analyzer proton nuclear magnetic resonance and transmission electron microscopy. Such micelles exhibit obvious thermo-responsive properties: (1) Poly(N-isopropylacrylamide) blocks collapse on the polylactide core as system temperature increase, leading to reduce of micelle size. (2) Micelles with short poly(N-isopropylacrylamide) blocks tend to aggregate together when temperature increased, which is resulted from the reduction of the system hydrophilicity and the decreased repulsive force between micelles.

Highly Porous Poly(high internal phase emulsion) Membranes with "Open-Cell" Structure and CO2-Switchable Wettability Used for Controlled Oil/Water Separation.

Polymer membranes with switchable wettability have promising applications in smart separation. Hereby, we report highly porous poly(styrene-co-N,N-(diethylamino)ethyl methacrylate) (i.e., poly(St-co-DEA)) membranes with "open-cell" structure and CO2-switchable wettability prepared from water-in-oil (W/O) high internal phase emulsion (HIPE) templates. The open-cell porous structure facilitates fluid penetration through the membranes. The combination of CO2-switchable functionality and porous microstructure enable the membrane with CO2-switchable wettability from hydrophobic or superoleophilic to hydrophilic or superoleophobic through CO2 treatment in an aqueous system. This type of membrane can be used for gravity-driven CO2-controlled oil/water separation, in which oil selectively penetrates through the membrane and separates from water. After being treated with CO2 switching wettability of the membrane, a reversed separation of water and oil can be achieved. Such a wettability switch is fully reversible, and the membrane could be regenerated through simple removal of CO2 and oil residual through drying. This facile and cost-effective approach represents the development of the first CO2-switchable polyHIPE system, which is promising for smart separation in a large volume.

Breathable Microgel Colloidosome: Gas-Switchable Microcapsules with O2 and CO2 Tunable Shell Permeability for Hierarchical Size-Selective Control Release.

Microcapsules enabling precise delivery and controlled release are highly desirable. However, it is still challenging to control the release profile by regulating the microcapsule shell permeability. In this work, gas-switchable microgel colloidosome (MGC) with oxygen (O2) and carbon dioxide (CO2) dual gas-tunable shell permeability has been developed and tested for control release of water-soluble cargo molecules, based on the size exclusion mechanism. The O2 and CO2 dual gas-switchable poly(2-(diethylamino)ethyl methacrylate-co-2,3,4,5,6-pentafluorostyrene), P(DEA-co-FS), microgels having surface modified with amino group (-NH2) were synthesized and used to stabilize oil-in-water (O/W) Pickering emulsions. The oil-soluble poly(propylene glycol) diglycidyl ether (PPGDGE) was added as an intermicrogel cross-linker. The cross-linking between adjacent microgel particles at the water-oil interface was achieved through the amine-epoxy reaction of PPGDGE with the amine groups at the particle surface. Fluorescent-labeled dextran model cargo molecules of 10 kDa (D1) and 2000 kDa (D2) were uploaded under CO2 treatment and locked inside the MGC with N2 treatment. The O2 and CO2 dual-gas switchable properties offered the MGC with tunable shell permeability, which allowed the hierarchical release of D1 and D2 based on size exclusive mechanism. This work provides a robust method for preparation of gas-switchable microcapsules with tunable permeability and size-exclusive hierarchical release profile, promising for multiple ingredient controllable release, separation, and reaction.

High internal phase emulsion with double emulsion morphology and their templated porous polymer systems.

This paper reports synthesis of the first high internal phase emulsion (HIPE) system with double emulsion (DE) morphology (HIPE-DE). HIPE is a highly concentrated but highly stable emulsion system, which has a dispersed/internal phase fraction over 74vol%. DE represents an emulsion system that hierarchically encapsulates two immiscible phases. The combination of HIPE and DE provides an efficient method for fabrication of complex structures. In this work, HIPE-DE having a water-in-oil-in-water (W/O/W) morphology has been prepared for the first time via a simple one-step emulsification method with poly(2-(diethylamino)ethyl methacrylate) (PDEA) microgel particles as Pickering stabilizer. An oil phase fraction up to 90vol% was achieved by optimizing the microgel concentration in aqueous phase. The mechanism of the DE formation has been elucidated. It was found that while PDEA microgels stabilized the oil droplets in water, small amount protonated DEA monomers acted as surfactant and formed water-containing micelles inside the oil droplets. It was demonstrated that the W/O/W HIPE-DE could be precisely converted into porous polymer structures. With styrene as the oil phase in W/O/W HIPE-DE, porous polystyrene particles were obtained upon polymerization. With dissolved acrylamide as the aqueous phase and toluene as the continuous phase, porous polyacrylamide matrixes were prepared. Elevating temperature required for polymerization did not change the W/O/W HIPE-DE morphologies. This simple approach provides a versatile platform for synthesis of a variety of porous polymer systems.

Oxygen and Carbon Dioxide Dual Gas-Switchable Thermoresponsive Homopolymers.

Herein, we report the first oxygen (O2) and carbon dioxide (CO2) dual gas-switchable thermoresponsive polymers based on a newly synthesized monomer N-(2-fluoroethyl amide)-N-(2-(diethylamino)ethyl) acrylamide, that is, AM(F1EA-DEAE), which bears both O2-switchable fluorinated ethyl amide (F1EA) and CO2-switchable N,N-diethylamino ethyl (DEAE) moieties on its side chain. PolyAM(F1EA-DEAE) samples prepared from reversible addition-fragmentation chain transfer (RAFT) polymerization exhibited good temperature-responsive properties. Their inherent low critical solution temperature (LCST) could be reversibly tuned to different levels by respectively purging O2 or CO2 into its aqueous solution. The O2-treatment shifted LCST to a higher temperature, while the CO2-treatment made the polymer fully water-soluble. The polymer could be readily recovered to its initial state by washing off the trigger gas with an inert gas such as nitrogen. This work provides an effective monomer design approach for the preparation of O2 and CO2 dual gas-responsive polymers.

Oxygen and carbon dioxide dual gas-responsive and switchable microgels prepared from emulsion copolymerization of fluoro- and amino-containing monomers.

We report herein the design and preparation of microgels that are responsive to both O2 and CO2 gases. The microgels were synthesized through soap-free emulsion copolymerization of O2-responsive monomer 2,3,4,5,6-pentafluorostyrene (FS) and CO2-responsive monomer 2-(diethylamino)ethyl methacrylate (DEA) with N,N'-methylenebis(acrylamide) (BisAM) as the cross-linker. The P(DEA-co-FS) microgels dispersed in aqueous solution could undergo volume phase transitions triggered by O2 and/or CO2 aeration. The particles were very responsive to CO2, while their responsivity to O2 was moderate. Microgels having different levels of the responsivity could be designed and prepared by varying the FS content in the copolymer. The phase transitions were also highly reversible, and the initial states of microgels could be easily recovered by "washing off" the trigger gases with N2. Multicycle O2, CO2, and N2 aerations were applied, and no loss in the dual gas responsivity and switchability was observed.

A chiroptical switch based on DNA/layered double hydroxide ultrathin films.

A highly oriented film was fabricated by layer-by-layer self-assembly of DNA and MgAl-layered double hydroxide nanosheets, and its application in chiroptical switch was demonstrated via intercalation and deintercalation of an achiral molecule into the DNA cavity. DNA molecules are prone to forming an ordered and dispersive state in the interlayer region of rigid layered double hydroxide (LDH) nanosheets as confirmed by scanning electron microscopy and atomic force microscopy. The induced chiroptical ultrathin film (UTF) is achieved via the intercalation of an achiral chromophore [5,10,15,20-tetrakis(4-N-methylpyridyl)porphine tetra(p-toluenesulfonate) (TMPyP)] into the spiral cavity of DNA stabilized in the LDH matrix [denoted as TMPyP-(DNA/LDH)20]. Fluorescence and circular dichroism spectroscopy are utilized to testify the intercalation of TMPyP into (DNA/LDH)20 UTF that involves two steps: the electrostatic binding of TMPyP onto the surface of (DNA/LDH)20 followed by intercalation into base pairs of DNA. In addition, the TMPyP-(DNA/LDH)20 UTF exhibits good reversibility and repeatability in induced optical chirality, based on the intercalation and deintercalation of TMPyP by alternate exposure to HCl and NH3/H2O vapor, which can be potentially used as a chiroptical switch in data storage.

A relationship between p27(kip1) and Skp2 after adult brain injury: implications for glial proliferation.

S-phase-associated kinase protein-2 (Skp2) is involved in ubiquitination and proteasome-mediated degradation of p27(kip1), which plays an important role in mammalian cell-cycle regulation and neurogenesis in the developing central nervous system. To investigate their expression and function in central nervous system injury and repair, we used a brain-penetrating injury model in adult rats. Western blot analysis showed a significant downregulation of p27(kip1) and a concomitant upregulation of Skp2 following brain injury, and their expression profiles were temporally correlative (r = -0.910, p = 0.037). Immunofluorescence double-labeling revealed that p27(kip1) was highly expressed in neurons (51%), astrocytes (72%), and microglia (76%) in the sham group, while its expression was decreased prominently in microglia (26%) and astrocytes (32%) at 3 days after injury. Meanwhile, Skp2 expression was very low in all cell types in the sham group; however, 3 days after injury, its expression was increased significantly in microglia (51%) and astrocytes (31%) (p < 0.001), and less significantly in neurons (8%) (p = 0.038), and the astrocytes and microglia had proliferated. We also examined the expression profiles of CDK2, threonine-187 phosphorylated p27(kip1), proliferating cell nuclear antigen (PCNA), and Ki67, and their changes correlated with the expression profiles of p27(kip1) and Skp2. Moreover, co-immunoprecipitation data suggested that the protein-protein interactions between p27(kip1) and Skp2 were enhanced after injury. Taken with results of previous reports, we hypothesize the Skp2 is related to the downregulation of p27(kip1) expression after brain injury, and such an event may be associated with glial proliferation, including that of astrocytes and microglia.

[Preparation and properties of poly (acrylic ester) hydrogel as basic materials for intraocular lens].

Poly (acrylic ester) hydrogel materials were widely used in intraocular lens and contact lens because of their excellent optical performance and biocompatibility. In this paper, the bulk copolymerization behavior of hydrophilic hydroxyethyl methacrylat with hydrophobic methyl metharylate was studied; and the optical performance, calcium deposits, equilibrium water content of polymers and its hydrogels obtained by different ratios of monomers were systematically investigated. The experimental results showed that the average light transmittance and the equilibrium water content of the obtained hydrogels increased with the increasing of the hydrophilic monomer content from 0 to 100%; however, the hardness decreased. The highest light transmittance reached 97% and the hardness of Shore A fell from 92 to 25, the equilibrium water content of hydrogel increased from 16% to 64%. The absorbent capacity of copolymers reduced with the adding of cross-linking monomer. When m(hydrophilic monomer): m(hydrophobic monomer) = 90 : 10, the combination property of the polymer and its hydrogel obtained is optimum.

Peripheral nerve injury induces down-regulation of Foxo3a and p27kip1 in rat dorsal root ganglia.

FOXO3a, as a forkhead transcription factor, can control cell cycle through transcriptionally down-regulating p27(kip1) level, which is a key regulator of the mammalian cell cycle and a good candidate to regulate multiple aspects of neurogenesis. To elucidate their expression and function in nervous system lesion and repair, we performed an acute sciatic nerve crush model and studied differential expressions of Foxo3a and p27(kip1) in lumbar dorsal root ganglia. Temporally, Foxo3a protein level was reduced 1 day after injury, and following Foxo3a down-regulation, p27(kip1) mRNA and protein levels were also decreased after injury. Spatially, decreased levels of Foxo3a and p27(kip1) were predominant in neurons and glial cells, which were regenerating axons and largely proliferated after injury, respectively. Together with previous reports, we hypothesized decreased levels of Foxo3a and p27(kip1) in lumbar dorsal root ganglia were implicated in axonal regeneration and the proliferation of glial cells after sciatic nerve injury.