1.
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。
2.
Transport of Ecdysterone in Caco-2 Cell Monolayers;
蜕皮甾酮的体外转运模型以及药物转运动力学研究
3.
Sodium-coupled monocarboxylate transporters and their actions in drug delivery
Na~+偶联单羧酸转运蛋白及其在药物转运中的作用
4.
The polymorphisms of drug transporters on the effect of telmisartan pharmacokinetics
药物转运蛋白基因的遗传多态性对替米沙坦药动学的影响
5.
Development of Drug Transport Cell Models, Their Application and Preliminary Study on the Associated Mechanism;
药物转运细胞模型的建立、应用和相关机制的初步研究
6.
Establishment and evaluation of corneal epithelial cell culture models based on transport of drug
基于药物转运研究的角膜上皮细胞培养模型的建立及评价
7.
Drug-Metabolizing Enzymes and Transporters: Roles in the Human Prostate Cancer Chemotherapy
药物代谢酶及转运体与前列腺癌药物治疗
8.
The role of organic anion transporters in renal drug transport and durg-drug interaction
有机阴离子转运蛋白在药物肾脏转运中的作用
9.
Study of the Association between Single Nucleotide Polymorphisms of Drug Metabolism and Transport Related Genes and the Outcomes of Anti-tumor Drugs;
药物代谢转运相关基因多态性与抗肿瘤药物作用关联性研究
10.
Transport Model of Drug in Vitro and the Study of Transport Kinetics of Propranolol Enantiomers;
药物体外转运模型及普萘洛尔异构体转运动力学研究
11.
Current research progress in glutamate transporter subtype GLT-1 and its regulated drugs
谷氨酸转运体亚型谷氨酸转运体1与其调控药物的研究进展
12.
Liposome Electrokinetic Chromatography and Its Application in Profiling Drug Membrane Transport;
脂质体电动色谱及其用于评价药物膜转运
13.
Consideration of research on intestinal transportation and metabolism of herbal polysaccharide compounds
中药多糖类化合物肠内转运与代谢研究的思考
14.
Process of drug movement from the administration site to the systemic circulation.
吸收是指药物由用药部位进入体循环的转运过程。
15.
Preparation and Preclinical Pharmacological Study of ~(18)F-FECNT as a Dopamine Transporter Tracer
多巴胺转运蛋白示踪药物~（18）F-FECNT的制备与临床前药理研究
16.
Role of transporters in the drug excretion and its significance in new drug development
转运体在药物排泄中的作用及在新药研发中的意义
17.
Drug delivery via the transferrin receptor-mediated endocytosis pathway
转铁蛋白-转铁蛋白受体系统在药物运输中的应用(英文)
18.
Active transport appears to be limited to drugs structurally similar to endogenous substances.
主动转运似乎只限于其结构类似于机体内源性物质的那些药物。