凝胶染色扫描法快速定量冬虫夏草中蛋白质方法的初步研究

目的建立一种冬虫夏草蛋白质含量快速测定方法,弥补Bradford法不足,为研究过程中快速准确定量蛋白质奠定基础。方法本研究用牛血清蛋白(bovine serum albumin,BSA)作为已知浓度的定量标准,用它来计算其它带的量。根据Quantity One来降低图像噪音和背景强度,并确定泳道,定义带并建立光密度与已知浓度的定量标准蛋白线性关系,通过每个带的光密度定量计算凝胶上每个带的质量。结果本实验所建立的凝胶染色扫描法能够较为快速、简便、准确地测定冬虫夏草蛋白含量。结论凝胶染色扫描法用于蛋白质定量,准确度、精密度、重复性均符合要求,为测定方法的进一步完善奠定了基础。

超声处理对黑豆蛋白凝胶性能的影响

测定不同超声条件处理的黑豆蛋白凝胶的持水性、流变性、质构性及其显微结构,研究超声处理对黑豆蛋白凝胶性能的影响。结果表明:超声处理虽可明显改善黑豆蛋白凝胶的持水性,但质构特性,如硬度、弹性、内聚性、回弹性均较未处理的黑豆蛋白凝胶有所下降,且中功率处理后凝胶的质构特性明显优于低功率和高功率。流变学测试表明,温度扫描图谱中不同超声条件处理的黑豆蛋白凝胶G′平缓期表现出一定的差异,频率扫描图谱表现出超声处理后黑豆蛋白凝胶的G′、G″值均低于未处理样品,而未经处理样品和中功率超声处理的蛋白凝胶样品的tanδ值远大于其它样品值。超声条件处理后黑豆蛋白凝胶性能的改变与蛋白聚集和解聚以及聚集体的尺寸相关。

蜂毒素的SDS-PAGE质控方法研究

目的 建立以 SDS- PAGE进行蜂毒素质量控制的方法。方法 将通过凝胶色谱法从蜜蜂毒中分离纯化所得到的蜂毒素 ,以 SDS- PAGE法测定其相对分子质量 ,并通过凝胶成像扫描测定蜂毒素纯度。结果 蜂毒素样品电泳后在凝胶块上显示为均一条带 ,相对分子质量约为 2 80 0 ,含量为 (90 .5 9± 0 .85 ) % ,与 HPL C测定结果平行。结论 SDS- PAGE法作为蜂毒素的质控方法 ,结果准确、可靠。

Preparation and Characterization of TiO_2/Expanded Graphite

In order to obtain anatase TiO2/expanded graphite with high expansion volume, titania gel was introduced to expandable graphite surface by sol-gel process, and then the composite was expanded and calcined at high tempera- ture. The samples were analysed by using scanning electron microscope （SEM）, X-ray diffraction（XRD）, energy disperse spectroscopy （EDS）, and differential scanning calorimetry （DSC）. The optimal conditions for preparation are as follows： the molar ratio of tetrabutyl orthotitanate to triethanolamine is 1 ： 0.4, and the calcination and expansion temperature is in the range of 650--750 ~C. Under such conditions, the expansion volume of composites could reach 98 mE/g, and the mass loss ratio is less than 5%. The analysis shows that lower temperature and smaller particle size of graphite are helpful to the formation of anatase-type of TiO2, but larger particle size will lead to lower mass loss ratio, and higher temperature and larger particle size will lead to higher expansion volume.

Microstructure and electrical properties of La_2 O_3-doped ZnO-based varistor thin films by sol-gel process

Microstructure and electrical properties of La2 O3-doped ZnO-Bi2 O3 thin films prepared by sol–gel process have been investigated.X-ray diffraction shows that most diffraction peaks of ZnO are equal,and the crystals of ZnO grow well.Scanning electron microscopy and atomic force microscopy results indicate that the samples have a good structure and lower surface roughness.The nonlinear V–I characteristics of the films show that La2 O3 develops the electrical properties largely and the best doped content is 0.3% lanthanum ion,with the leakage current of 0.25 mA,the threshold field of 150 V/mm and the nonlinear coefficient of 4.0 in detail.

Hydration mechanism of low quality fly ash in cement-based materials

The hydration mechanism of low quality fly ash in cement-based materials was investigated. The hydration heat of the composite cementitious materials was determined by isothermal calorimetry, and the hydration products, quantity, pore structure and morphology were measured by X-ray diffraction(XRD), thermalgravity-differential thermal analysis(TG-DTA), mercury intrusion porosimetry(MIP) and scanning electron microscopy(SEM), respectively. The results indicate that grinding could not only improve the physical properties of the low quality fly ash on particle effect, but also improve hydration properties of the cementitious system from various aspects compared with raw low quality fly ash(RLFA). At the early stage of hydration, the low quanlity fly ash acts as almost inert material; but then at the later stage, high chemical activity, especially for ground low quality fly ash(GLFA), could be observed. It can accelerate the formation of hydration products containing more chemical bonded water, resulting in higher degree of cement hydration, thus denser microstructure and more reasonable pore size distribution, but the hydration heat in total is reduced. It can also delay the induction period, but the accelerating period is shortened and there is little influence on the second exothermic peak.

Electrochemical performance of LiFePO_4/(C+Fe_2P) composite cathode material synthesized by sol-gel method

A LiFePO4/（C＋Fe2P） composite cathode material was prepared by a sol-gel method using Fe（NO3）3.9H20, LiAc·H2O）, NHaH2PO4 and citric acid as raw materials, and the physical properties and electrochemical performance of the composite cathode material were investigated by X-ray diffractometry （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and electrochemical tests. The Fe2P content, morphology and electrochemical performance of LiFePOa/（C＋Fe2P） composite depend on the calcination temperature. The optimized LiFePO4/（C＋FeeP） composite is prepared at 650 ~C and the optimized composite exhibits sphere-like morphology with porous structure and Fe2P content of about 3.2% （mass fraction）. The discharge capacity of the optimized LiFePO4/（C＋FeRP） at 0.1C is 156 and 161 mA.h/g at 25 and 55 ℃, respectively, and the corresponding capacity retentions are 96% after 30 cycles; while the capacity at 1C is 142 and 149 mA.h/g at 25 and 55 ℃, respectively, and the capacity still remains 135 and 142 mA-h/g after 30 cycles at 25 and 55℃, respectively.

人心肌磷酸化肌球蛋白轻链的测定

采用等电聚焦、银染、凝胶光密度扫描技术相结合，分离人心室肌内磷酸化肌球蛋白轻链（ｐ－ＭＬＣ），实验周期短，结果可靠，重复性好，可为临床进行心肌收缩力改变的研究提供直接线索。湿重心肌低于１０ｍｇ时，ｐ－ＭＬＣ难以在等电聚焦板上显示。

Synthesis and Characterization of Sol-Gel Derived MgO/CNTs Nanocomposite

In this research, synthesis of magnesium oxide-multi walled carbon nanotube （MgO/MWCNTs） nanocomposite is reported using sol-gel method in which magnesium nitrate is added to aqueous solution. The structure of MWCNTs and MgO/MWCNTs composite has been characterized by analyzing the X-ray diffraction pattern （XRD）, Fourier Transform Infrared （FT-IR） spectra and Scanning Electron Microscopy （SEM） images. Experimental results indicate that the surface of purified MWCNTs sample is covered homogenously by a layered of MgO nanoparticles.

Investigation of Swelling and Dissolution Process of Natural Rubber in Aromatic Oil

Aromatic oil has been used to promote the properties of crumb rubber modified asphalt which is an ideal method to deal with the resource utilization of waste rubber tires and by-product of refinery. Furfural extract oil(FEO) was separated into the light fraction and the heavy fraction. Swelling and dissolution process of natural rubber sheet in these three oil samples was investigated to shed light on the interaction mechanism. Crumb rubber also interacted on FEO and asphalt respectively. Energy dispersive spectrometer(EDS), thermo-gravimetric analysis(TGA) and scanning electron microscope(SEM) were used to characterize the chemical and structural properties of processed rubber. The chemical composition of processed oils and asphalt was investigated by using the hydrocarbon group analysis(SARA) and gel permeation chromatography. The results revealed that the swelling rate and mass loss of rubber in oils were much higher than those in asphalt and rose with an increasing processing temperature. The heavy fraction of FEO had more diffusion and dissolving capability than the light fraction, whilst compatibility was observed between the heavy fraction and the light fraction. Selective absorption was not observed in the study and detachment of dissolved rubber was disseminated from the outside to the inside. The cross-linking degree of the residue rubber was unchanged with the processing time, and sulfur predominantly remained in the undissolved rubber. Dissolution of crumbed rubber in oils was attributed to devulcanization, while that in the asphalt was mainly attributed to depolymerization.

Synthesis and Gel Properties of Sorbitol Derivative Gelators

1,3:2,4-di-p-methylbenzylidene-D-sorbitol(MDBS)is known to be an efficient sorbitol derivative gelator.Two new sorbitol derivative gelators were designed and synthesized in contrast to MDBS in order to study the gel properties of gelators with different structures.Their gelation behavior to 30 solvents was investigated.It was found that the gelation behavior was related to the molecular structure of gelators.Compared with MDBS,the gelator with more hydroxyl in the molecular structure could gel water and that with more aromatic ring could gel aromatic solvent.The fibrous and three-dimensional network of the gels was obtained by scanning electron microscopy(SEM).Ultraviolet-visible(UV-Vis)spectroscopy revealed thatπ-πinteraction was one of the main driving forces for the formation of gels.Theπ-πstacking of gelation increases with the number of aromatic rings in the molecular structure of gelator.Fourier transform infrared(FT-IR)spectroscopy revealed that the hydrogen bonding was also the main driving force for the formation of gels.The layered structure of the gels was studied by X-ray diffraction(XRD).

Synthesis and Characterization of Novel Copolymers Based on 3(S)-Methyl-Morpholine-2,5-Dione

A series of novel copolymers were successfully synthesized by ring-opening polymerization （ROP） of 3 （S）-methyl-morpholine-2,5-dione （MMD） and 5-methyl-5-benzyloxycarbonyl-1,3-dioxan-2-one （MBC） using stan- nous octoate as catalyst. The copolymers were characterized by means of ~H-NMR and FT-IR spectroscopy. Gel permeation chromatography （GPC） test shows that the average-number relative molecular mass and average-weight rela- tive molecular mass slightly increase with the increase of MBC content in feed. The results of differential scanning calorimetry （DSC） demonstrate that the glass transition temperature of copolymers increases with the increase of MBC content in copolymers. The copolymers of MMD and MBC are amorphous copolymers, as indicated by DSC results, while the homopolymer of MMD is semicrystalline.

Non-isothermal crystallization kinetics of reactive microgel/nylon 6 blends

The non-isothermal crystallization kinetics of reactive microgel/nylon 6 blends was investigated by differential scanning calorimetry(DSC). The Mo equation was employed to analyze the non-isothermal crystallization data. The crystallization activation energies were also evaluated by the Kissinger method. The results show that the crystallization onset temperature(T onset) and crystallization peak temperature(T p) decrease with the increase of the content of reactive microgel, while ΔT(T onset–T p), the crystallization half-time(t1/2) and the crystallization enthalpy(ΔH c) increase. The required cooling rates of blends are higher than that of neat nylon6 in order to achieve the same relative crystallinity in a unit of time. The crystallization activation energies of the reactive microgel/nylon 6 blends are greater than those of the neat nylon 6. When the content of reactive microgel is 30%, the relative crystallinity(X t) reaches the maximum.

Radiation-Induced Synthesis of Polyvinylpyrrolidone （PVP） Nanogels

Nanogels-particles of polymer gels having the dimensions in the order of nanometers-are gaining attention for their wide application as biomaterials. Mainly, the nanogels are promising novel pharmaceutical carriers for small biologically active agents, bin macromolecules and can be chemically modified to incorporate various ligands for targeted drug delivery. This important factor has stimulated research on dissimilar science field such as nanotechnology and biotechnology, polymer and materials sciences, biochemistry, radiation chemistry and pharmaceutical sciences. A multitude of techniques have been described for the synthesis of this nanomaterial from polymers. However, the use of ionizing radiation （γ, e-） has demonstrated to be especially suitable for obtaining polymeric nanogels with a high degree of purity for biomedical applications, although the gamma radiation has not been widely utilized for these purposes. The aim of this paper is to develop the synthesis of PVP （polyvynilpyrrolidone） nanogels by gamma irradiation, for their evaluation as potential pharmaceutical carriers. Experiments were performed using argon saturated solution of PVP （0.1-1%）. Crosstinking reactions were carried out in a gamma irradiation chamber with a 60Co source （ISOGAMMA LLCo）, at room temperature. The PVP concentration influence was evaluated in PVP solutions （0.1% and 0.25%） at 15 kGy. The SEM （scanning electron microscopy）, ATR （attenuate total reflection spectroscopy）, DLS （dynamic light scattering）, and viscosimetry were used as characterization techniques.

Preparation and electrochemical performance of Li_2Mn_(0.5)Fe_(0.5)SiO_4 cathode material with sol-gel method for lithium ion batteries

Li2Fe0.5Mn0.5SiO4 material was synthesized by a citric acid-assisted sol-gel method. The influence of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+) on the electrochemical properties of Li2Fe0.5Mn0.5SiO4 was studied. The final sample was identified as Li2Fe0.5Mn0.5SiO4 with a Pmn21 monoclinic structure by X-ray diffraction analysis. The crystal phases components and crystal phase structure of the Li2Fe0.5Mn0.4SiO4 material were improved as the increase of the stoichiometric ratio value of n(citric acid) to n(Fe2+-Mn2+). Field-emission scanning electron microscopy verified that the Li2Fe0.5Mn0.5SiO4 particles are agglomerates of Li2Fe0.5Mn0.5SiO4 primary particles with a geometric mean diameter of 220 nm. The Li2Fe0.5Mn0.5SiO4 sample was used as an electrode material for rechargeable lithium ion batteries, and the electrochemical measurements were carried out at room temperature. The Li2Fe0.5Mn0.5SiO4 electrode delivered a first discharge capacity of 230.1 mAh/g at the current density of 10 mA/g in first cycle and about 162 mAh/g after 20 cycles at the current density of 20 mA/g.

Enhanced electrochemical property of FePO_4-coated LiNi_(0.5)Mn_(1.5)O_4 as cathode materials for Li-ion battery

Pristine LiNi0.5Mnl.5O4 and FePO4-coated one with Fd-3m space groups were prepared by a sol-gel method. The structure and performance were studied by X-ray diffraction （XRD） rietveld refinement, scanning electron microscopy （SEM）, high resolution transmission electron microscopy （HRTEM）, energy dispersive spectrometer （EDS） mapping, electrochemical impedance spectroscopy （EIS） and charge- discharge tests, respectively. The lattice parameters of all samples almost remain the same from the Rietveld refinement, revealing that the crystallographic structure has no obvious difference between pris- tine LiNi0.5Mn1.5O4 and FePO4-coated one. All materials show similar morphologies with uniform particle distribution with small particle size, and FePO4 coating does not affect the morphology of LiNi0.5Mnl05O 4 material. EDS mapping and HRTEM show that FePO4 may be successfully wrapped around the surfaces of LiNio.sMnl.s04 particles, and provides an effective coating layer between the electrolyte and the surface of LiNi0.5Mn1.5O4 particles. FePO4 （1 wt%）-coated LiNio.sMnl.504 cathode shows the highest discharge capac- ity at high rate （2 C） among all samples. After 80 cycles, the reversible discharge capacity of FePO4 （1 wt%） coated LiNi0.5Mn0.5O4 is 117 mAh g^-1, but the pristine one only has 50 mAh g^-1. FeP04 coating is an effec- tive and controllable way to stabilize the LiNi0.5Mn1.5O4/electrolyte interface, and avoids the direct con- tact between LiNi0.5Mn1.5O4 powders and electrolyte, then suppresses the side reactions and enhances the electrochemical performance of the LiNi0.5Mn1.5O4.

Fabrication of porous scaffolds with protein nanogels

A novel type of porous scaffold was fabricated from single protein nanogels. The nanogels with single protein as core and crosslinked polymer network as shell were prepared through a two-step procedure including surface acryloylation and in situ radical polymerization. The formation of single protein nanogels was verified by matrix assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometer, transmission electron microscopy (TEM) and dynamic light scattering (DLS) analyses. Subsequently, the porous scaffolds were fabricated through a solvent evaporating process of aqueous nanogel solutions. The porous scaffolds were characterized by Fourier transform infrared (FTIR), scanning electronic microscopy (SEM), atomic force microscopy (AFM), and fluorescence microscopy. Interestingly, the obtained porous nanogel scaffolds presented multi-level porous morphologies with macro and nano scale pores, providing better spaces and microenvironments than normal macro porous scaffolds. Cell proliferation assay of nanogels showed low cytotoxicity. Considering that both the protein species and polymer constitutes can be pre-designed and adjusted, these multi-level porous nanogel scaffolds are promising candidates for tissue culture applications.

Tunable supramolecular hydrogels from polypeptidePEG-polypeptide triblock copolymers

A series of ABA triblock copolymers of poly(?-(2-methoxy ethoxy)esteryl-glutamate)-block-poly(ethylene glycol)-blockpoly(?-(2-methoxy ethoxy)esteryl-glutamate) with poly(ethylene glycol) as middle hydrophilic B block and oligo(ethylene glycol)-functionalized polyglutamate(poly-L-EG2Glu) as terminal A blocks were prepared via ring-opening polymerization of EG2 Glu N-carboxyanhydride(NCA). The resulting P(EG2Glu)-b-PEG-b-P(EG2Glu) triblocks can spontaneously form hydrogels in water. The intermolecular hydrogen bonding interactions between polypeptides blocks were responsible for the formation of gel network structure. These hydrogels displayed shear-thinning and rapid recovery properties, which endowed them potential application as injectable drug delivery system. The mechanical strength of hydrogels can be modulated by copolymer composition, molecular weight and concentrations. Also, it was found that the hydrogels' strength decreased with temperature due to dehydration of polypeptide segments. Atomic force microscopy and scanning electron microscopy images revealed that these hydrogels were formed through micelle packing mechanism. Circular dichroism and Fourier transform infrared spectroscopy characterizations suggested the poly-L-EG2 Glu block adopted mixed conformation. A preliminary assessment of drug release in vitro demonstrated the hydrogels can offer a sustained release of doxorubicin(DOX) and the release rate could be controlled by varying chemical composition.

Ultrasound responsive organogels based on cholesterol-appended quinacridone derivatives with mechanochromic behaviors

A series of cholesterol-appended quinacridone (QA) derivatives 1a-1d have been synthesized,in which 1b and 1c could form stable organogels in a wide range of organic solvents upon ultrasound irradiation.Field emission scanning electronic microscope (FESEM) and transmission electron microscopy (TEM) of xerogels or precipitates indicated that 1b and 1c formed 1D fibrous nanostructure,while 1a assembled into 3D flower-like microstructures.The ultrasound-induced organogel process was characterized by kinetic UV-vis and photoluminescence spectroscopic methods suggesting the formation of ?-? aggregates in the gel state.Experimental results demonstrated that the ultrasound could promote molecules to contact frequently in the solution and induce semistable initial aggregates,which propagate to form nano/micro superstructures.The aggregation model was optimized by semiempirical AM1 calculation suggesting the hierarchical self-assembly process.In addition,the formed xerogel film exhibited mechanochromic property,and the phase transition process was accompanied by the fluorescence changes between yellowish green and orange.

States of Water in Hydrogels Containing with Glyceryl Methacrylate

Hydrogel materials were prepared by thermopolymerization with different content of glyceryl methacrylate and hydroxyethyl methacrylate. The different states of water in swelling hydrogels were described and studied by differential scanning calorimetry(DSC). It was found that the hydrophilicity of GMA was stronger than HEMA,the water content and bound water of GMA hydrogel are higher than HEMA hydrogel.With the increase of GMA content, the content of free water in hydrogel increased. When GMA content was lower than 50%, the increase of GMA content also increased the content of bound water; but when GMA content was higher than 50%, the increase of GMA content decreased the content of bound water, which was caused by the chain hydrogen bond formed on the GMA chain with hydroxyl group each other.