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release carrier
相关语句
  释载体
    As new oral sustained release carrier, alginate gel has been highly recommended to controlled-release of many drugs.
    海藻酸盐微粒给药系统是近年来研究较多的一类新型口服药物缓控释载体,已成功应用于多种药物的控制释放。
短句来源
    RESULTS The plasticizer was used as the sustained release carrier and improved the characteristics of the commercial material.
    结果 加入的改性剂具有药物缓释载体和改善市售骨修复材料的特性。
短句来源
    Finally,the controlled release behavior of BH in polymer beads were studied and the release rate of BH kept almost constant after 24h. Release rate of BH was higher at pH 1.4 than that at pH 7.4.Conclusion: β-CDP beads may be an ideal controlled drug release carrier.
    BH在β-CDP微球中的释放速率存在明显的零级释放规律,且pH=1.4下的释放速率比pH=7.4下的快。 结论:β-环糊精聚合物微球是一理想的药物控释载体
短句来源
  缓释载体
    RESULTS The plasticizer was used as the sustained release carrier and improved the characteristics of the commercial material.
    结果 加入的改性剂具有药物缓释载体和改善市售骨修复材料的特性。
短句来源
  “release carrier”译为未确定词的双语例句
    The release properties could be expressed by the following equation: Q = 2.1811 t + 13.50 ( r =0.9527). These materials have good prospect as a controlled or sustained release carrier.
    阐明了载体中加入D ,L PLA材料 ,改善了以PHBV单一材料为载体的微球释药性能 ,体外释药方程为Q =2 .1811t +13.5 0 (r =0 .95 2 7)
短句来源
    Polysaccharides for therapeutical protein controlled release carrier
    多糖对口服蛋白药物的控释研究(英文)
    Conclusions Water-in-oil nanoemulsion is a potential controlled release carrier for water-soluble drugs.
    结论W/O型纳米乳可作为水溶性药物的缓控释制剂的载体。
短句来源
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  release carrier
Protein incorporation within Ti scaffold for bone ingrowth using Sol-gel SiO2 as a slow release carrier
      
The average pore size of PVA sponges used in this study was 30, 60, 110, 250, 350, and 700 μm and gelatin microspheres were employed as release carrier of bFGF.
      
Characteristics of clay as a slow-release carrier of Zn by direct implantation into tree trunks
      
EO105PO27EO105 copolymer is expected to be useful as a novel sustained-release carrier that maintains constant release rates for the volatility of perfume compounds over a wide temperature range.
      
Poly(ethylene oxide)/poly(propylene oxide)/poly(ethylene oxide) triblock copolymer as a sustained-release carrier for perfume co
      
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This article presents 149 cases of peridental diseases treated with carboxymethyl cellulose as peridental sustained release membrane for local application with good therapeutic effect. The results showed that this treatment had the advantages of smaller dose, high local concentration, satisfactory curative effect, no adverse reaetions, being not liable to produce drug-fast bacteria strains and ready reception from the patients. The paper also discusses the merits of taking the carboxymethylcellulose natrium...

This article presents 149 cases of peridental diseases treated with carboxymethyl cellulose as peridental sustained release membrane for local application with good therapeutic effect. The results showed that this treatment had the advantages of smaller dose, high local concentration, satisfactory curative effect, no adverse reaetions, being not liable to produce drug-fast bacteria strains and ready reception from the patients. The paper also discusses the merits of taking the carboxymethylcellulose natrium as peridental sustained release carrier: it can be dissolved in saliva, gingival sulcus fluid and blood; release slowly so that it may mantain a longer effective concentration in the local part, being beneficial to kill the bacteria.

以羧甲基纤维素钠作牙周缓释剂局部应用治疗牙周病149例。结果表明本药具有用药剂量小、局部浓度高、效果好、无副作用、不易形成耐药菌株、且病人易于接受等优点。还进一步讨论了以羧甲基纤维素钠作牙周缓释剂载体材料,能被唾液、龈沟液、血液等溶解而药物缓慢、持久释放,使局部维持有效药物浓度时间较长,有利于杀菌。

PHBV used as slowreleased carrier of progesterone was investigated in this paper. PHBV microspheres containing progesterone were prepared by an emulsion solvent evaporation method. It was found that release behaviour and content of progesterone in the microspheres depended on the concentration of PHBV in chloroform, the ratio of progesterone to PHBV and the temperature of preparation. The optimal conditions of PHBV contont in chloroform,the ratio of propesterone to PHBV and temperature for preparing...

PHBV used as slowreleased carrier of progesterone was investigated in this paper. PHBV microspheres containing progesterone were prepared by an emulsion solvent evaporation method. It was found that release behaviour and content of progesterone in the microspheres depended on the concentration of PHBV in chloroform, the ratio of progesterone to PHBV and the temperature of preparation. The optimal conditions of PHBV contont in chloroform,the ratio of propesterone to PHBV and temperature for preparing the microspheres were obteined respectively as 100 g/L 0.06:1 40℃.

对用PHBV作为药物缓释载体进行了研究,采用乳化溶剂挥发法制备得到药物缓释微球。研究表明,药物释放及药物包含量受PHBV在氯仿中的浓度、黄体酮与PHBV的比例以及制备温度的影响。用PHBV制备黄体酮缓释微球的最佳条件为PHBV在氯仿中的浓度为100g/L黄体酮的加入量为PHBV质量的6%,温度为40℃.

The sustained release microspheres have been prepared by the solvent evaporation methods, using poly(hydroxybutyrate co hydroxyvalerate)/polylactide blend as carrier and diazepam as modal drug. The mean diameter of microspheres is in a range of 18~25 μm. The change of surface morphology with the composition of carrier was observed by scanning electron microscope. In this paper, drug loading and incorporation efficiency vary with the composition of carrier for four kinds of microspheres, which was also discussed....

The sustained release microspheres have been prepared by the solvent evaporation methods, using poly(hydroxybutyrate co hydroxyvalerate)/polylactide blend as carrier and diazepam as modal drug. The mean diameter of microspheres is in a range of 18~25 μm. The change of surface morphology with the composition of carrier was observed by scanning electron microscope. In this paper, drug loading and incorporation efficiency vary with the composition of carrier for four kinds of microspheres, which was also discussed. The release properties could be expressed by the following equation: Q = 2.1811 t + 13.50 ( r =0.9527). These materials have good prospect as a controlled or sustained release carrier.

用溶剂蒸发法制备了以新型生物可降解材料聚羟基丁酸酯 羟基戊酸酯共聚物 (PHBV)与L ,DL 聚乳酸 (PLA)共混物为载体的 ,以地西泮为模药的缓释微球 ,微球的平均粒径为 18~ 2 5 μm。电镜观察表明 ,微球表面形态结构随载体成分改变而变化。文章还阐述了四种微球实际载药量与包封率随载体成分变化而改变的规律。阐明了载体中加入D ,L PLA材料 ,改善了以PHBV单一材料为载体的微球释药性能 ,体外释药方程为Q =2 .1811t +13.5 0 (r =0 .95 2 7)

 
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