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   诱导交联 的翻译结果: 查询用时:0.251秒
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诱导交联
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  “诱导交联”译为未确定词的双语例句
     Conclusion At low concentrations formaldehyde could not induce DPC; but at high concentrations, it could induce DPC significantly.
     结论 在低浓度时 ,甲醛诱导 DNA-蛋白质交联现象不明显或不诱导该现象 ,在高浓度时可显著诱导交联现象。
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     Objective The main goal of this paper was to prepare vMIP-loaded chitosan nanoparticles and to investigate the physico-chemical characteristics, drug efficacy, and pharmacokinetics.
     目的探讨利用离子诱导交联法制备vMIP-壳聚糖纳米粒的理化性质及体外释药的研究。
  相似匹配句对
     in troducing stimulus;
     诱导刺激;
短句来源
     Crosslinking of Polypropylene
     聚丙烯的交联
短句来源
     Nickel chloride induced DNA-protein crosslinks in rats in vivo
     氯化镍在体内诱导大鼠DNA-蛋白质交联
短句来源
     An In Vivo Study DNA-protein Crosslinks Induced by Nickel Chloride
     氯化镍诱导DNA-蛋白质交联物的体内研究
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     Trial-preparation of Crosslinked Polyvinylpyrrolidone
     交联聚乙烯吡咯烷酮的试制
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  induced crosslinking
Some specific features of the radiation-induced emulsion copolymerization of butyl acrylate and acrylonitrile and radiation-induced crosslinking of the resulting copolymer in the latex form were studied.
      
Radiation-Induced Crosslinking of Thymine with Cysteamine: Cysteamine Attachment to the Methyl Group of Thymine
      
The results were used to explain that PPF-based networks undergo a biphasic degradation behavior due to the competing hydrolytic degradation and thermal induced crosslinking.
      
One type of binding was identified as L1-induced crosslinking of cysteine residues 93 and 112 of the β-globin chain.
      
Gamma-ray induced crosslinking of polynorbornene and its copolymer containing a stabilizing group
      
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Objective To explore the action of formaldehyde inducing DNA protein crosslinks(DPC) and to test the detection method. Methods This study took human blood lymphocyte as experimental material, chose 0、0 005、0 025、0 125、0 625 mmol/L five formaldehyde concentrations, and used KCl SDS method to detect DPC. Results At low concentrations(0 005, 0 025 mmol/L) formaldehyde cold not induce DPC(P>0 05); but at high concentrations(0 125, 0 625 mmol/L), it could induce DPC significantly(P<0 01), and there...

Objective To explore the action of formaldehyde inducing DNA protein crosslinks(DPC) and to test the detection method. Methods This study took human blood lymphocyte as experimental material, chose 0、0 005、0 025、0 125、0 625 mmol/L five formaldehyde concentrations, and used KCl SDS method to detect DPC. Results At low concentrations(0 005, 0 025 mmol/L) formaldehyde cold not induce DPC(P>0 05); but at high concentrations(0 125, 0 625 mmol/L), it could induce DPC significantly(P<0 01), and there was good dose dependent relation. Conclusion At low concentrations formaldehyde could not induce DPC; but at high concentrations, it could induce DPC significantly. KCl SDS method was effective.

目的 探讨甲醛致 DNA-蛋白质的交联作用以及交联的检测方法。方法 以人血淋巴细胞为材料 ,设定 0、0 .0 0 5、0 .0 2 5、0 .1 2 5、0 .6 2 5 mmol/ L 五个甲醛浓度梯度 ,采用 KCl- SDS沉淀法来检测染毒后细胞中 DNA-蛋白质交联的含量。结果 甲醛浓度在 0、0 .0 0 5、0 .0 2 5 mm ol/ L 时 ,交联现象不明显或不能诱导DPC(P>0 .0 5 ) ;在 0 .1 2 5、0 .6 2 5 mm ol/ L 时交联程度显著增加 (P<0 .0 1 ) ,并有较好的剂量 -效应关系。结论 在低浓度时 ,甲醛诱导 DNA-蛋白质交联现象不明显或不诱导该现象 ,在高浓度时可显著诱导交联现象。KCl- SDS沉淀法检测 DNA-蛋白质交联的含量是有效的

>=Objective The main goal of this paper was to prepare vMIP-loaded chitosan nanoparticles and to investigate the physico-chemical characteristics, drug efficacy, and pharmacokinetics. Methods The surface morphology and particle size distributions of the NPs were examined by transmission electron microscopy and laser diffraction, respectively. The entrapment efficiency was determined by the method of Bradford after separating the NPs from the suspension under size exclusion chromatography. The loading pattern...

>=Objective The main goal of this paper was to prepare vMIP-loaded chitosan nanoparticles and to investigate the physico-chemical characteristics, drug efficacy, and pharmacokinetics. Methods The surface morphology and particle size distributions of the NPs were examined by transmission electron microscopy and laser diffraction, respectively. The entrapment efficiency was determined by the method of Bradford after separating the NPs from the suspension under size exclusion chromatography. The loading pattern of different sizes of NPs was assayed by dialysis. Using Hplc to evaluation the concentration of the drug in vivo. Results The NPs prepared in our experiment regular and well-distributed with a mean diameter of 181.8nm, the zeta potential is 28.53?.81mV and an average encapsulation efficiency up to 75.75%, The release behavior in vitro showed an initial burst released, following by a slower raze stage. Conclusion The results showed that vMIP-CS-NPs were suitable to oral administration. This research provides a base for our lab's drug to go to the oral market.

目的探讨利用离子诱导交联法制备vMIP-壳聚糖纳米粒的理化性质及体外释药的研究。方法: 采用透射电镜和激光粒度散射分析仪对纳米粒的形态、粒径和zeta电位进行了测定,分子筛层析法和紫外分光光度法测定纳米粒的包封率,利用透析法测定了vMIP的体外释药特性。结果vMIP-壳聚糖纳米粒呈圆形,粒子较均一,平均粒径为181.8nm,zeta电位为28.53±3.81 mV。采用硫酸葡聚糖掩盖vMIP的电荷,优化包封率为(75.75%);vMIP-壳聚糖纳米粒体外透析发生凝胶化,释放缓慢,初期有个突释过程。结论vMIP-壳聚糖纳米粒有做口服给药的前景。

 
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