简介:该研究旨在筛选盐酸青藤碱与JAK/STAT信号通路的药物靶点,并对其抑菌活性与抗氧化活性进行评估.实验采用Autoduck软件筛选出药物在JAK/STAT信号通路上的药物靶标,然后用滤纸片法检测盐酸青藤碱对苏芸金杆菌和金葡萄球菌的抑菌活性,同时用DPPH法和ABTS法检测盐酸青藤碱不同溶剂提取物的抗氧化活性.结果显示:盐酸青藤碱在JAK/STAT信号通路上的药物靶点为STAT1.抑菌实验中,药物浓度为5-60mg/mL的浓度范围时,两种菌中均形成8-10mm大小不等的抑菌圈形成.且其对金葡萄球菌的抑菌效果优于苏芸金杆菌.抗氧化实验中:酸青藤碱不同溶剂提取物对[DPPH.]自由基力为:在0.1-0.4mg/mL浓度范围内,乙醇(95%)〉丙酮〉稀碱,在0.4-1.0mg/mL的浓度范围内,稀碱〉丙酮〉乙醇(95%);不同溶剂对[ABTS.]自由基的清除力为:丙酮〉乙醇(95%).盐酸青藤碱有很好的抗氧化活性,但弱于VC.本实验可以为盐酸青藤碱作为新型药物开发提供实验依据,更深入探讨其潜在的药用价值提供一定的理论参考.
简介:Ni2P/ZrO2-SBA-15catalystswithdifferentzirconiumn-propoxide/SBA-15massratiosweresynthesizedtoevaluatetheirdibenzothiophenehydrodesulfurizationcatalyticactivity.EffectofZrO2introductionwasinvestigated.SupportsandcatalystswerecharacterizedbyBET,XRD,29SiNMR,XPSandFTIR.TheresultsindicatedthatzirconiumwasincorporatedintoSBA-15intheformsof[(–O–)2Si(–O–Zr)2]and/or[(–O–)3Si–O–Zr],andthattheSBA-15frameworkstructurewasmaintainedafterincorporationofZrO2.Withzirconiumcontentincreasing,ZrO2wastransformedfromamorphousphasetotetragonalphase.ZirconiumincorporationintoSBA-15supportscouldfacilitatetoformmoredispersedNi2Pactivephase.TheremightbesomeinteractionoccurringbetweenthePandZrspecies.InadditiontoNi2P,anotherkindofactivephase,ZrP,wasformed,whichmightexhibitabetterHDSactivitythanNi2P.Itwasobservedthatatatemperatureof280°C,pressureof3.0MPa,WHSVof6.5h?1andH2tooilratioof450,theNi2P/Zr-SBA(1.5)catalyst,where1.5representszirconiumn-propoxide/SBA-15massratio,showedthehighestDBTconversion,whichwas86.6%,almost35%higherthanthatoftheNi2P/Zr-SBA(0)catalyst.
简介:实验选择四溴二苯醚(BDE-47)与高氯酸盐(PER)作为研究对象,系统研究了二者联合暴露对成年斑马鱼肝脏抗氧化系统的影响。实验设置(BDE-478.5+PER335)mg/L,(BDE-470.85+PER33.5)mg/L,(BDE-470.085+PER3.35)mg/L三种联合暴露组及二者各自单一的暴露组。暴露14天后,分别测定雌雄斑马鱼肝脏内超氧化物歧化酶(SOD)活性、过氧化氢酶(CAT)活性、谷胱甘肽过氧化物酶(Gpx)活性以及脂质过氧化物(MDA)水平。结果显示,与两种物质单一暴露相比,联合暴露致使肝脏内SOD,CAT的活性增加,MDA水平增加,而GSH活性降低,实验说明,PER诱导加剧了BDE-47对成年斑马鱼肝脏抗氧化酶的影响,进一步产生了氧化应激。
简介:以硝酸镍为金属离子源、对苯二甲酸为配体,N,N-二甲基甲酰胺为溶剂。采用溶剂热法合成了金属-有机骨架Ni-MOF,采用X射线粉末衍射、N2吸附/脱附、扫描电镜、红外光谱和热重分析等方法对样品进行表征,考察了反应时间对样品结构及吸附性能的影响,测试了样品的c0,的吸附性能。结果表明,150℃反应4h后得到Ni-MOF球形晶体,延长反应时间对Ni-MOF的结构及性能没有明显影响。样品的BET面积为1200~1221m2/g,平均孔径为1.95nm,在常压27℃时,对CO2的吸附量为17.9%,经10次吸附/脱附循环实验后,吸附量稳定在16.5%~17.9%,是一个良好的吸附材料。
简介:BrookiteTiO2,thelatestTiO2photocatalyst,promisestobeaninterestingcandidateforphotocatalyticapplicationsbecauseofitsuniquephysicalandchemicalproperties.Inthisstudy,pure-phasebrookiteTiO2withaquasi-sphericalnanostructurewassuccessfullysynthesizedviaasolvothermalmethodusingtetrabutyltitanate(Ti(OC4H9)4,TBOT)astheTisourceinthepresenceofoxalicacid.NaOHwasusedtoregulatethepHofsolution.Thestructureandmorphologyofthesampleswerethenanalyzedusingmultiplemethods,suchasX-raydiffraction(XRD),Ramanspectroscopy,scanningelectronmicroscopy(SEM),transmissionelectronmicroscopy(TEM),Brunauer–Emmett–Teller(BET)measurementsandultraviolet–visiblediffusespectroscopy(UV–Vis).Photocatalyticactivitiesoftheas-synthesizedbrookiteTiO2wereevaluatedbydegradingaqueousmethylenebluesolutionunderUVlightirradiation.Theeffectofthermaltreatmenttemperatureonphotocatalyticactivityofthesampleswasalsoinvestigated.TheproducedbrookiteTiO2nanopowderscalcinedat500°Cfor2hshowedthehighestphotocatalyticactivity,andthecorrespondingdegradationrateofmethyleneblue(10mg/L)reached96.7%after90minofillumination.Inaddition,theformationmechanismofpure-phasebrookiteTiO2wasinvestigated.Itwasfoundthattheformationofpure-phasebrookiteTiO2inthisstudywasascribedtothecombinedactionofoxalicacidandsodiumhydroxide.
简介:以纳米TiO2作为光催化剂的非均相半导体光催化法被视为最具应用前景的有机污染物处理技术,在被大于或等于禁带能的光子激发后,TiO2可产生价带空穴和导带电子,其中价带空穴能够直接氧化吸附的化学物质或者通过和表面键合的OH-离子和或吸附的H2O分子反应产生强氧化性的羟基自由基,从而无选择性降解多种污染物。紫外LED技术相比于传统紫外汞灯,具有能耗低、寿命长、构造简单、波长不唯一、无二次污染等优势,无毒无汞的紫外LED已成为未来紫外光发射器研制的重点发展方向。本文综述了水中PPCPs处理技术研究现状和紫外LED协同纳米TiO2光催化技术处理水中PPCPs的可行性,为探寻一种高效稳定的PPCPs处理技术,开发绿色节能的PPCPs降解方法提供了参考意义。
简介:Alow-costandeasilypreparedmanganesecarbonate(MnCO3)hasbeensynthesizedforcatalyticconversionof5-hydroxymethylfurfural(5-HMF)to2,5-diformylfuran(DFF).ThepropertiesandmorphologyofthemanganesecarbonateweremeasuredbySEM,XRD,TGA,BETandXPS.Inthismethod,noharshreactionconditionswererequired,anditwasasimpleandgreenprocessfortheoxidationof5-HMFintoDFF.ToachieveanoptimumDFFyield,differentreactionconditions,includingreactiontemperature,reactiontime,catalystamount,andsolventswereinvestigated.ResultsfromtheexperimentsindicatedthatthehighestDFFyieldof86.9%wasobtainedat120°Cunderatmosphericoxygenpressureafter6h.Finally,MnCO3couldbeusedatleastfivetimeswithconsiderablestability.
简介:采用高效液相色谱法测定针叶樱桃提取物中VB1和VB2的含量,优化样品制备方法及HPLC色谱条件,并将该方法用于针叶樱桃提取物中VB1和VB2的含量测定。方法:采用HPLC法,色谱柱DiamonsilC18柱(250mm×4.6mm,5μm),柱温为40℃,进样体积20μL,流速1.0mL/min,检测波长280nm,流动相组成为乙腈和5mol/L庚烷磺酸钠溶液,采用梯度洗脱模式。方法学考察表明,VB1和VB2分别在0.089μg/mL-0.89μg/mL和0.086μg/mL-0.86μg/mL范围内线性关系良好,方法的精密度和重复性均符合要求,平均回收率为99.5%~101.1%。该方法操作简单,能够用于针叶樱桃提取物中VB1和VB2的含量测定。