Pinocytosis probably plays a minor role in drug transport, except for protein drugs.
除蛋白质类药物外，胞饮在药物转运过程作用不大。
Numerical results have shown that hyperthermia significantly improved drug transport in tumor.
数值计算结果显示热作用能有效促进肿瘤内脂质体药物的传输。
The drug loaded nanoparticle is a new technology produced by nanotechnology combined with modern medicine. Its a new carrier of drug transport.
载药纳米微粒是纳米技术与现代医药学结合的产物，是一种新型的药物输送载体。
Study on these transporters could attribute to elucidate the action of the drug at the BCSFB, regulate the drug transport behavior and guide the research & d…
对这些转运蛋白的研究使人们能深入地解析药物在血脑脊液屏障上的动态，更有效地调控药物转运行为，指导脑靶向与非脑靶向药物的研发设计。
The mechanisms responsible for drug transport across the BBB, the drug delivery systems (DDS) to the brain and the administration methods were all described in this paper.
从药物穿透血脑屏障的途径、药物传输系统及给药方法三个方面进行阐述。
We focused on several key pathways, including nucleotide excision repair, drug transport and metabolism. Both expression and germline DNA variation were evaluated in these key pathways.
由于核苷酸切除修复、药物转运和药物代谢通路在铂金药物功能中的重要性，这篇综述重点总结了这些通路中的基因表达和非癌细胞DNA变异与铂金疗效的关系。
Reactants in radiopharmaceutical kits, or inactive ingredients that physically or chemically combine with active ingredients to facilitate drug transport are considered inactive ingredients.
放射性药物组成中的反应物，或为了便于药物运输将非活性成分与活性成分以物理或者化学而结合都被认为是非活性成分。
US planes gave the Hmong the opportunity to do something they hadn’t previously—transport and sell large quantities of the drug, including to US soldiers.
美国的飞机为苗族人提供了机会让他们做从来没做过的事——运输并贩卖大量毒品，包括卖给美国士兵。
The model characterizes many dynamic transport and complexation processes that include radial diffusion, excipient complexation and crystalline drug dissolution.
模型利用径向扩散，辅料络合作用和晶体药物的溶出度来表征多个动力学运输和络合过程。
Pharmaceutical Drug Room different characteristics to the needs of the market, research and development for pharmaceutical production, storage, transport, Sales and use of the preparation method.
药物制剂室根据药物的不同特性，结合市场的需要，研究开发适合药品生产，保存，运输，销售和使用的制剂方法。
CONCLUSION Bergenin was absorbed badly at all segments of intestine in rats. The absorption of the drug conforms to the passive transport mechanism.
结论岩白菜素在大鼠肠道内吸收较少，吸收机制可能为被动扩散。
Due to overlapping specificities of the transport proteins, drug interactions at the level of tubular secretion is an event that may occur in clinical situation.
由于转运蛋白的特异性之间存在重叠，药物在肾小管分泌过程中产生的药物的相互作用将是今后临床上值得注意的问题。
By disrupting the stratum corneum structure and create pathways allowing transport of macromolecules, microneedles array can improve the transdermal drug delivery and increase the efficiency.
传统的被动式经皮给药严重受限于皮肤角质层的阻碍，利用微针阵列破坏角质层可改善皮肤对药物的渗透性，大大提高经皮给药效率。
By disrupting the stratum corneum structure and create pathways allowing transport of macromolecules, microneedles array can improve the transdermal drug delivery and increase the efficiency.
传统的被动式经皮给药严重受限于皮肤角质层的阻碍，利用微针阵列破坏角质层可改善皮肤对药物的渗透性，大大提高经皮给药效率。
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