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ID:32363902
大小:5.22 MB
页数:46页
时间:2019-02-03
《低分子硫酸软骨素制备及对软骨修复作用地研究》由会员上传分享,免费在线阅读,更多相关内容在学术论文-天天文库。
1、与模型组相比,给予ChS的组别,其血清中的钙磷含量也相对较少(P2、通过对上述因子的影响,从而产生积极的作用。硕士研究生裴彤(药物化学)指导教师高华教授关键词:硫酸软骨素;低分子量;降解;软骨修复;炎性因子ResearchoftheMethodforPreparingLowMolecularWeightChondroitinSulfateandEffectofitonCartilageRepairObjectiveAbstractToinvestigatethemethodforpreparinglowmolecularweightchondroitinsulfate,andtoexploretheeff3、ectofitonCartilageRepair.Methods1、Weighacertainamountofchondroitinsulfate,itsmolecularweightisapproximately50000.DegradingwithHCl,H202andChSaseEACatacertaintemperatureandconditions.Aftercompletionofthereaction,utilizing95%ethanoltoprecipitateanddehydrate.Theproducts’molec4、ularweightweredeterminedbyhighperformanceliquidchromatography.2、EstablishkneearticularcartilagedefectmodelsonNewZealandrabbits.36NewZealandrabbitswererandomlydividedinto6groups(6ineachgroups):controlgroup[distilledwater0.49/(kg’d)],modelgroup[distilledwater0.49/(kg’d)],lo5、w—doseoflowmolecularweightChSgroup[10wmolecularweightChS0.29/(kg‘d)],high—doseoflowmolecularweightChSgroup[10wmolecularweightChS0.49/(kg’d)],low—doseofhighmolecularweightChSgroup[highmolecularweightChS0.29/(kg’d)]andhigh-doseofhighmolecularweightChSgroup[highmolecularweig6、htChS0.49/(kg。d)].Respectivelygavage.Recordingtheweight,survivaltimeandlivingfettleoftherabbitsineachgroup.Observethesituationofcartilagedefectandhistologicalsections.Theexpressionofcytokines,suchasIL一1p,TNF一0【andTGF—pinsynovialfluidwasdetectedbyELISA,determiningcontentof7、calciumandphosphorusinserumofrabbitbyautomaticbiochemicalanalyzerkit.Resuits1、Determinedbyhighperformanceliquidchromatography,themolecularweightofchondroitinsulfateis55426beforedegrading.Themolecularweightofchondroitinsulfateis3936afterdegradingwithHCl.Thecolorofthesoluti8、onchangedfromwhitetored-brownintheprocessofdegradation.Theproducts’viscosityislargeanditsyieldis
2、通过对上述因子的影响,从而产生积极的作用。硕士研究生裴彤(药物化学)指导教师高华教授关键词:硫酸软骨素;低分子量;降解;软骨修复;炎性因子ResearchoftheMethodforPreparingLowMolecularWeightChondroitinSulfateandEffectofitonCartilageRepairObjectiveAbstractToinvestigatethemethodforpreparinglowmolecularweightchondroitinsulfate,andtoexploretheeff
3、ectofitonCartilageRepair.Methods1、Weighacertainamountofchondroitinsulfate,itsmolecularweightisapproximately50000.DegradingwithHCl,H202andChSaseEACatacertaintemperatureandconditions.Aftercompletionofthereaction,utilizing95%ethanoltoprecipitateanddehydrate.Theproducts’molec
4、ularweightweredeterminedbyhighperformanceliquidchromatography.2、EstablishkneearticularcartilagedefectmodelsonNewZealandrabbits.36NewZealandrabbitswererandomlydividedinto6groups(6ineachgroups):controlgroup[distilledwater0.49/(kg’d)],modelgroup[distilledwater0.49/(kg’d)],lo
5、w—doseoflowmolecularweightChSgroup[10wmolecularweightChS0.29/(kg‘d)],high—doseoflowmolecularweightChSgroup[10wmolecularweightChS0.49/(kg’d)],low—doseofhighmolecularweightChSgroup[highmolecularweightChS0.29/(kg’d)]andhigh-doseofhighmolecularweightChSgroup[highmolecularweig
6、htChS0.49/(kg。d)].Respectivelygavage.Recordingtheweight,survivaltimeandlivingfettleoftherabbitsineachgroup.Observethesituationofcartilagedefectandhistologicalsections.Theexpressionofcytokines,suchasIL一1p,TNF一0【andTGF—pinsynovialfluidwasdetectedbyELISA,determiningcontentof
7、calciumandphosphorusinserumofrabbitbyautomaticbiochemicalanalyzerkit.Resuits1、Determinedbyhighperformanceliquidchromatography,themolecularweightofchondroitinsulfateis55426beforedegrading.Themolecularweightofchondroitinsulfateis3936afterdegradingwithHCl.Thecolorofthesoluti
8、onchangedfromwhitetored-brownintheprocessofdegradation.Theproducts’viscosityislargeanditsyieldis
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