简介:因为他们联合了木头和无机的混合物的优点,混合木头材料吸引了可观的注意。这个工作调查了微结构形态学,热稳定性,紫外(紫外)用wood/ZnO混血儿材料做通过的composites的稳定性,和抗菌剂性质一灵巧在原处化学合成方法。X光检查衍射(XRD)和thermogravimetric分析(TGA)结果显示综合ZnO粒子有大约10.8nm的一种平均谷物尺寸。扫描电子显微镜学(SEM)观察证明与nanosheets自我装配的ZnOnanoflowers在木头房间腔被介绍并且与增加Zn2+集中增加了。ZnOnanoparticles也在木头房间墙中被产生,它被精力散的光谱学(版本)的结果证实。TGA测试也显示wood/ZnO混血儿材料的热稳定性在ZnO无机的粒子的形成以后被改进。最后,抗菌剂功效测试的结果和紫外抵抗测试表明ZnOnanoparticles对Escherichiacoli作为抗菌剂代理人显示出有希望的未来(E。coli)并且为木头保护的紫外抵抗代理人。
简介:我们为把坚持、有效的抗菌剂性质合并到广泛地使用的聚合物报导灵巧的策略,poly(甲基methacrylate)(PMMA),由异分子聚合有2-(tert-butylamino)的甲基methacrylate(MMA)在经由原子转移基聚合(ATRP)的一个壶的乙醇methacrylate(TA)。随后自己组装结果poly(甲基methacrylate)-block-poly[(2-tert-butylamino)ethylmethacrylate](PMMA20-b-PTA15)diblock共聚物负担得起明确的水可分散的泡,它能轻易地为有效抑制在医院里在墙上被喷洒并且细菌杀死。1H-NMR和胶化浸透层析(GPC)研究证实了良好共聚物的成功的合成。传播电子显微镜学(TEM),原子力量显微镜学(AFM)和散布的动态光(DLS)学习与狭窄的尺寸分发证明了泡的形成。DLS研究在各种各样的温度揭示了泡的优秀稳定性。抗菌剂测试对克积极、克否定的细菌显示出聚合物泡的有效抗菌剂活动。而且,这策略可以为在许多领域里为灵巧的抗菌剂应用准备大量聚合材料被扩大。
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简介:Magnesium(Mg)alloyshaveattractedconsiderableresearchattentionaspotentialbiocompatibleimplantmaterials.However,themajorbarrierstotheextendeduseofsuchmedicaldevicesarethepossibilityofhighcorrosionrateandimplantassociatedinfections.Tosolvethem,anovelpolyacrylicacid(PAA)/gentamicinsulfate(GS)-hydroxyapatite(HAp)coatingwassynthesizedbyaone-stephydrothermaldepositionmethod.CharacteristicsoffunctionalcoatingswereinvestigatedbySEM,FTIRandXRD.Corrosionpropertiesofsampleswereevaluatedbyelectrochemicalandhydrogenevolutiontests.AntibacterialactivitiesofthecoatingsagainstStaphylococcusaureus(S.aureus)weremeasuredbytheplate-countingmethod.Resultsshowedthattheas-preparedHApcoatingwithdenseandflawlessmorphologiescouldnotonlyenhancethecorrosionresistanceofMgalloys,butalsoimprovetheadhesionstrengthbetweentheHApcoatingandthesubstrate.Inaddition,theinductionoftheapatitecoatingduringimmersionconfirmedtheexcellentmineralizationabilityoftheHApcoating.Moreover,theobtainedHApcoatingpossessedantibacterialpropertiesandcouldprolongthereleaseofGS.Thus,thePAA/GS-HApcoatedMgalloycouldserveasabettercandidateforbiomedicalapplicationswithgoodanti-corrosionandantibacterialproperties.
简介:AninorganicnanomaterialscombinationofSm,Ag,andTiO2wassynthesizedusingsupercriticalfluiddrying(SCFD)combinedwithsol-geltechniques.Thestructure,photocatalysisandbacteriostaticactivityofthematerialswerecharacterizedbyX-raydiffraction(XRD),transmissionelectronmicroscopy(TEM),X-rayphotoelectronspectroscopy(XRPS),photocatalyticperformance,andantibacterialactivityexperiments.TheXRDresultsshowedthattheaverageparticlediameterofSm/Ag/TiO2was14.62nmandAgandSmionsweredispersedonthesurfaceofTiO2inahighlydispersed,amorphousform.TheTEMimageshowedthatthesizeoftheparticlewas12nmusingtheschererformula.TheXPSresultshowedthattheelementSmwasdopedandAgwasloadedinorganicnanomaterialssuccessfully.Sm/Ag/TiO2exhibitedoptimalphotocatalyticpropertiesat600oC,thephotocatalyticoptimalproportionofSm/Ag/TiO2was2:2:100.Whenthemolarratiowas2:2:100,thebacteriostaticcirclediameterwas16mmforStaphylococcusaureus,theminimumbacteriostaticconcentrationwas200μg/mLforwhitebeadscoccus,andtheminimumbactericidalconcentrationwas2×104μg/mLforwhitebeadscoccus.TheSEMresultsshowedthattheantibacterialmaterialattachedtothecandidaalbicanscellsurface,cellsappearedfolddeformation.ThereforetheinorganicnanomaterialsSm/Ag/TiO2hadhightemperatureresistance,goodphotocatalyticandantibacterialcharacteristicsinvisiblelight.
简介:NocathiacinI,aglycosylatedthiopeptideantibiotic,displaysexcellentantibacterialactivitiesagainstmultidrugresistantbacterialpathogens.Previously,anovelnocathiacinIformulationforintravenousadministrationhasbeensuccessfullydevelopedanditsaqueoussolubilityisgreatlyenhancedforclinicalapplication.ThepurposeofthepresentstudywastoincreasethefermentationtiterofnocathiacinIandreduceoreliminateanalogousimpuritiesbyscreeningthemediumingredientsusingresponsesurfacemethodology.Afterasysmaticoptimization,awater-solublemediumcontainingquality-controllablecomponentswasdevelopedandvalidated,resultinginanincreaseintheproductionofnocathiacinIfrom150to405.8mg·L-1at150-Lscale.Meanwhile,theanalogousimpuritiesexistedinreportedprocessesweregreatlyreducedoreliminated.Usingoptimizedmediumforfermentation,nocathiacinIwithpharmaceuticallyacceptablequalitywaseasilyobtainedwitharecoveryof67%.Inconclusion,theresultsfromthepresentstudyofferapracticalandefficientfermentationprocessfortheproductionofnocathiacinIasatherapeuticagent.
简介:Antibacterialpoly(D,L-lactide)(PDLLA)fibrousmembranesweredevelopedviaelectrospinning,followedbysurfacemodificationwhichinvolvedplasmapretreatment,UV-inducedgraftcopolymerizationof4-vinylpyridine(4VP)andquaternizationofthegraftedpyridinegroupswithhexylbromide.ThesuccessofmodificationwithquatemizedpyridiniumgroupsonthePDLLAfibrousmembraneswasascertainedbyX-rayphotoelectronspectroscopy(XPS).TheantibacterialactivitiesofthesemembraneswereassessedagainstGram-positiveStaphylococcusaureus(S.aureus)andGram-negativeEscherichiacoli(E.coli).ThePDLLAfibrousmembranesmodifiedwithquaternizedpyridiniumgroupsshowedantibacterialefficiencyagainstbothbacteriaashighas99.999%.Theresultsdemonstratedthattheantibacterialactivitywasbasedontheinteractionofthepositivechargeofpyridiniumgroupandnegativelychargedcellmembraneofbacteria,resultinginlossofmembranepermeabilityandcellleakage.
简介:Asystematicstudyonthesynthesisandantibacterialactivityofthequaternary"onium"saltsgraftedonaninsoluble"gel-type"stryene-7%divinylbenzenecopolymerbypolymer-analogousreactionsisshowed.Antibacterialactivityofquaternaryammoniumand/orphosphoniumsaltsgraftedonpolymer-supportshasbeenstudiedagainststaphylococcusaureusandEscherichiacoli.Awidevarietyof"onium"saltsboundtomacromolecularsupportswithdifferentquaternarygroupsanddifferentquaternarychainlengthsubstituentswereexamined.Theantibacterialactivityofmixed"onium"saltsincreasesasaconsequenceoftheassociationofammoniumandphosphoniumsaltsgraftedonthesamepolymericsupport.
简介:Thepurposeofthisstudywastoevaluatethelongtimeantibacterialpropertiesandshearbondstrengthofexperimentalnanosilver-containingcements(NSC).Nanosilverbaseinorganicantibacterialpowderwasaddedtothereinforcedglassionomercementatfivedifferentweightratiostoobtainaseriesofnanosilver-containingcements,thentheantibacterialpropertiesofthreeorthodonticcementproductsandfiveNSCsampleswereevaluatedbythedirectcontacttest(DCT)andtheagardiffusiontest(ADT).TheDCT,whichwasbasedonturbidnessdeterminationofbacterialgrowthin96-wellmicrotiterplates,wasperformedinbothfreshandagedfor1day,1week,2weeks,3weeks,4weeks,6weeks,and8weekstestedmaterials.TheshearbondstrengthesofthreeorthodonticcementproductsandfiveNSCsampleswereexaminedusingauniversaltestingmachine.TheADTresultsindicatedthattherewerenosignificantdifferencesbetweenNSCsandORTHOLCfreshspecimens.IntheDCTexperiment,allfreshsilvernanoparticles-containingtestedsamplespresentedpowerfulantibacterialproperties,buttheygraduallylosttheeffectiveantimicrobialagentswiththeextensionofagingtime.Finally,noneofthetestedmaterialsmaintaineditsantibacterialpropertyafteragingfor8weeks.Agraduallydecreasingtrendofbondstrengthpresentedwiththeincreasingincorporationofnanosilverbaseinorganicantibacterialpowderintotheglassionomercement,eventhoughallthetestedmaterialspecimensreachedtheidealbondstrengthrange.WemayconcludethatNSCscancontributetodecreasethedemineralizationratearoundbracketswithoutcompromisingbondstrength.
简介:TheantibacterialeffectofcarryingsilverB2O3-SiO2-Na2Oglassmaterialwasstudiedbymeansofantibacterialring,nephelometery,MICvalue,thinfilmattachmentandmicrocalorimetry,respectively.TheexperimentalresultsoffivekindsofantibacterialtestmethodsarealmostidenticalandcanverifythatcarryingsilverB2O3-SiO2-Na2Oglassmaterialexertsanexcellentantibacterialperformance.Antibacterialringandnephelometeryaresimple,quick,buttheprecisionisrestrictive.MICvalue,thinfilmattachmentmethodandmicrocalorimetrycanquantitativelycomparetheantibacterialeffectsoftheantibacterialglassmaterial.Comparedwiththetraditionalmicrobetestmethods,themicrocalorimetrycananalyzetheinhibitingeffectofthecell'sgrowthandmetabolismontheantibacterialglassmaterialbymonitoringthethermaleffectcontinuouslyandautomatically.
简介:Lactivicin,anovelinhibitorofbacterialcellwallsynthesis,wasisolatedfromtheculturefil-tratesofmicroorganismYK-258andYK-422.Itexhibitsbiologicalactivitiessimilartothoseoftheβ-lactamantibiotics,althoughitdoesnothaveaβ-lactamringinitsmolecule.Sincethediscoveryoflactivicin,hundredsofitsderivativeshavebeensynthesized.Most
简介:6/3-(4-Chlorophenyl)-s-triazolo[3,4-b][1,3,4]thiadiazoles(2a-e)and(5a-e)weresynthesizedrespectivelybyintermolecularcyclizationof5-aryl/4-chlorophenyl-4-amino-3-mercapto-1,2,4-triazoles(1a-e)and(4)with4-chlorobenzoicacid/arylacids,whichwerecondensedwithpiperazineunderphasetransfercatalystTBABtoyieldthecorrespondingfreebasesofmonopiperazinederivativesandfollowedtoformwater-solublesalts(3a-e)and(6a-e)withhydrochloricacidingoodyields.Theinvitrobiologicalresultsshowedthatpiperazinegroupconjugatedwiththeabovefusedheterocyclesplayedanimportantroleinantibacterialactivity.ThestructuresofnovelcompoundswereconfirmedbyIR,1HNMR,MSandelementalanalysis.
简介:Treatmentof4-amino-3-(1-aryl-5-methyl-1,2,3-triazol-4-yl)-5-mercapto-1,2,4-triazoles/2-amino-5-(1-aryl-5-methyl-1,2,3-triazole-4-yl)-1,3,4-thiadiazoleswithbenzaldehyde,acetoneandω-bromoacetophenonewastestedandcompared.ThetitlecompoundsSchiffbases,amides,imidazolo[2,1-b]-1,3,4-thiadiazolesand7H-s-triazolo[3,4-b]-1,3,4-thiadiazineshavebeenconfirmedbyelementalanalyses,^1HNMR,IRandMSspectra.AllthecompoundshavealsobeenscreenedfortheirantibacterialactivitiesagainstB.subtilis,S.aureusandE.coli.