为了使输出结果更具可操作性，建立了标准工艺块和标准动素库。
Some standard process modules and standard therblig base had been created to improve the maneuverability of the outputs.
如果你需要喝许多水，那么就喝佳得乐，Propel，动乐或其他类似的除了含水外还含有维生素和电解质的饮料。
And if you need to drink large amounts of fluid, use Gatorade, Propel, Powerade, or other similar drinks that have vitamins and electrolytes besides just water.
在某些情况中，细菌本身的酶产生了使抗生素丧失活性的能力，抗生素失去活性之后，细菌再择机而动。
In some cases, enzymes native to the bacteria develop the ability to inactivate antibiotics before they have a chance to work.
有的理论认为快速眼动帮助调剂人体体温和神经传递素的水平。
Some theories suggest that REM helps regulate body temperature and neurotransmitter levels.
目的：了解肾上腺素对丁哌卡因肌间沟臂丛神经阻滞的药效学及药动学影响。
Objective: To investigate the effects of adrenaline on pharmacodynamics and pharmacokinetics of bupivacaine for interscalene plexus block.
结论天麻素注射液的人体药动学符合药动学二室模型。
Conclutions The pharmacokinetics of gastrodin injection in volunteers was accorded with two compartment model.
目的：研究多西环素肠溶微粒胶囊和多西环素片的人体生物等效性与药动学。
AIM: To study the bioequivalence and pharmacokinetics of doxycycline enteric-coated microsomes capsules and doxycycline tablets.
其次，有在生成的基础上总结了重动句的生成原因：内部义素和外部因素。
Then, on the pretext of this supposition, the thesis summarizes the cause of generation of Verb-copying sentence: internal cause and external cause.
对臼-内酰胺类抗生素的新的药动学参数，“超过MIC的时间”进行评价。
Objective To evaluate the new pharmacokinetic parameter, the duration of time that serum concentrations exceed the MIC(T > MIC)for beta - lactams.
目的采用尿药法进行去甲斑蝥素人体药动学研究。
OBJECTIVE To study pharmacokinetics of norcantharidin in human by urinary excretion method.
以自制芹菜素混悬液为对照组，考察了大鼠口服芹菜素固体脂质纳米粒的药动学过程。
The pharmacokinetic processes of oral AP-SLN of the rats were also studied, while apigenin suspension was used as control group.
目的本研究对所制得的芹菜素固体脂质纳米粒的制剂学性质和药动学进行研究。
OBJECTIVE To investigate the pharmacy characters and pharmacokinetic processes of the prepared apigenin loaded solid lipid nanoparticles (AP-SLN).
结论尿药法估算去甲斑蝥素人体药动学参数取样方便，样本处理简单。
CONCLUSION it's suitable to estimate the pharmacokinetic parameters by urinary excretion method, with the merits of convenient sample collection and simply specimen disposal.
结论尿药法估算去甲斑蝥素人体药动学参数取样方便，样本处理简单。
CONCLUSION it's suitable to estimate the pharmacokinetic parameters by urinary excretion method, with the merits of convenient sample collection and simply specimen disposal.
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