1) coating
[英]['kəʊtɪŋ] [美]['kotɪŋ]
药皮
1.
Study on the temperature rising of stainless steel electrode coating based on uniform design method;
基于均匀设计方法研究不锈钢焊条的药皮温升
2.
In order to analyze quantitatively the effect of coating ingredients on the usability of electrode,the slag detachability of stainless steel electrode was studied,using the computer software UST4.
为了定量地分析药皮辅料对焊条工艺性能的影响,利用中国数学会均匀设计分会推荐的UST4。
3.
Through the addition of rare earth oxidation La_2O_3 and CeO_2 into the electrode coating, the effect of rare earth oxidation on high temperature oxidation and sulphidation resistance is studied and the rational addition amount is suggested.
通过A402,A302,A202及Cr24Ni7不锈钢焊条熔敷金属的抗高温氧化腐蚀性能对比试验分析,设计了新的专用焊条合金系统Cr26Nil6,并在焊条药皮中分别添加微量稀土氧化物La2O3及CeO2,研究不同稀土氧化物添加量对焊条熔敷金属在空气中和含硫气氛中抗高温氧化及腐蚀性能的影响,从而确定了合理的稀土氧化物加入量。
2) double layers welding rod
药皮焊条
1.
Introduces the experimenting process that made by Russian scholars and de-phosphor effect with adding barium in weld,advantages of double layers welding rod that contain barium and the best content of barium.
介绍了俄罗斯学者在双层药皮焊条中添加钡元素脱磷的试验过程以及焊缝添加钡元素后的脱磷效果,含钡的双层药皮焊条的优越性和最佳的钡含量。
3) coating components
药皮辅料
1.
Effect of interactions among coating components on slag detachability of stainless steel electrode;
药皮辅料的交互作用对不锈钢焊条脱渣性的影响
4) transdermal drug delivery
经皮给药
1.
Characteristic analysis of electroporation apparatus for transdermal drug delivery;
经皮给药电穿孔仪的性能分析
2.
Advances on enhancement of permeability by transdermal drug delivery;
经皮给药系统促渗方法研究的新进展
3.
It is very important to disrupt the stratum corneum structure and to create pathways allowing transport of macromolecules, as the traditional transdermal drug delivery has been severely limited by the skin barrier.
传统经皮给药严重受限于皮肤的阻碍,如何破坏角质层打开一条允许大分子药物通过的通道是一个重要课题。
5) coated
[英]['kəutid] [美]['kotɪd]
药皮涂层
1.
Research and development of continuous coated electrode;
药皮涂层连续电焊条的研制
6) transdermal drug delivery
透皮给药
1.
The application and the safetyof the electroporation in transdermal drug delivery are also introduced.
电致孔可显著提高药物的经皮吸收,有望用于多肽和蛋白质类生物大分子药物的透皮给药。
2.
Objective In order to study the tissue distribution of Praziquantel(PZQ) and the pharmacokinetics after transdermal drug delivery.
目的研究透皮给药后吡喹酮在小鼠体内的组织分布及药代动力学。
补充资料：透皮给药系统
分子式：
CAS号：
性质：是一种经皮肤给药的制剂。组成：以硝酸甘油为例，背膜是不透药液的涂铝塑料，中间为药液储库，硝酸甘油吸附在乳糖，胶状二氧化硅上，药液储库的下侧复以控释膜，其表面有一层贴在皮肤上的黏合剂，粘贴皮肤不应引起过敏反应，粘贴层外面有一层铝膜覆盖，在使用时撕去。透皮剂型的优点：避免口服药物在消化道中遇酸酶破坏或食物吸附及消化道功能的影响；无首过代谢；无注射给药的不便；一次用药代替几次用药；药物储库释放持久使半衰期短的药物的药效明显延长；可任意终止给药。透皮剂型的缺点为对皮肤有刺激性或过敏反应；有耐受现象；制作工艺困难，价格昂贵。
CAS号：
性质：是一种经皮肤给药的制剂。组成：以硝酸甘油为例，背膜是不透药液的涂铝塑料，中间为药液储库，硝酸甘油吸附在乳糖，胶状二氧化硅上，药液储库的下侧复以控释膜，其表面有一层贴在皮肤上的黏合剂，粘贴皮肤不应引起过敏反应，粘贴层外面有一层铝膜覆盖，在使用时撕去。透皮剂型的优点：避免口服药物在消化道中遇酸酶破坏或食物吸附及消化道功能的影响；无首过代谢；无注射给药的不便；一次用药代替几次用药；药物储库释放持久使半衰期短的药物的药效明显延长；可任意终止给药。透皮剂型的缺点为对皮肤有刺激性或过敏反应；有耐受现象；制作工艺困难，价格昂贵。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条