片语

oxidative drug metabolism药物氧化代谢

hepatic drug metabolism肝脏药物代谢

hepatic drug metabolism enzymes肝脏药物代谢酶

drug metabolism enzymes药物代谢酶

first pass drug metabolism首过药物代谢

phase drug metabolism相药物代谢

drug metabolism research药物代谢研究

drug metabolism enzyme药酶

英汉例句

• Predicting of drug metabolism in humans based on animal experiments is complicated by species differences in the catalytic properties of these enzymes.

  根据动物实验来预测人体的药物代谢时，代谢酶的种属差异性会使这项研究工作变得非常困难。

• CYP450 is regulated by genetic genes. Once the gene mutates, the CYP450 enzyme that coded and the drug metabolism then will change.

  CYP450的合成受着遗传基因的调控，一旦基因发生变异，它所调控合成的CYP450酶及酶所催化的药物代谢即发生变化。

• It was suggested that Bama miniature pigs and Guizhou miniature pigs were both feasible for experimental animal model for evaluating drug metabolism in some degree.

  提示巴马香猪、贵州小型香猪作为药物评价的实验动物具有一定可行性。

• The process of drug metabolism is such which may exert influence on the development of the effectiveness and the production of the toxicity of drugs.

  药物代谢过程是影响药物发挥作用及产生毒性的过程。

• OBJECTIVE: to study the selective inhibitory effect of diltiazem (DZ) on hepatic drug metabolism by using antipyrine (AP) as a model drug.

  目的：研究钙离子拮抗剂地尔硫(DZ)对模型药安替比林(AP)在人体内代谢的选择性抑制作用。

• Pharmacogenomics testing analyzes genes that are related to drug metabolism & activity, which can influence how a person responds to certain medications.

  药物基因组检测是对影响药物代谢和活性的基因进行检测和分析，这些基因会影响个体对药物的反应。

• Choosing the suitable drugs and dosages according to cytochrome P450 and drug metabolism would improve the pharmacotherapy efficacy and reduce the adverse drug reaction and toxic effect of drugs.

  根据细胞色素P 450和药物的生物转化来选择合适的药物及合适的剂量将有助于最大程度地提高药物治疗效应，同时减少药物不良反应和毒副作用。

• When renal function declined, drug excretion slow, and drug metabolism altered.

  肾功能减退时，不但药物排泄缓慢，而且药物代谢也会发生改变。

• CYP3A29 is the most important key enzyme for drug metabolism in pig's liver.

  CYP3A29是猪肝脏最重要的药物代谢关键酶。

• Results Varied genes related to drug metabolism have SNP phenomenon, which are closely associated with interindividual diversity in drug response.

  结果多种药物代谢相关基因存在SNP现象，且与药物效应个体多样性有着密切联系。

• CONCLUSION In situ liver perfusion is an appropriate organ model for drug metabolism and disposition research.

  结论大鼠原位肝灌流是良好的整体器官药物代谢模型，是体外实验有力的补充。