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1)  nucleus pulpous concentration
髓核药物浓度
2)  Drug concentration
药物浓度
1.
AIM To establish a simple and practical method for the estimation of the inter-patient variability of cytochrome P450(CYP3A)enzyme activity and to predict drug concentration and parmacokinetics of etoposide with the variability of CYP3A in chidren patients with leukemia.
方法采用HPLC测定药物浓度,一点法计算药物消除半衰期,尿样法测定体内CYP3A酶活性。
2.
Objective: To establish a HPLC method for the determination of the drug concentration in bile after the injection of lomefloxacine.
目的:建立用HPLC方法测定注射洛美沙星后不同时间的胆汁药物浓度。
3.
It was found that SM2 was absorbed quickly and distributed widely, the concentrations in the tissues of heart, liver, lung, kidney and small intestine were all higher,facially, the drug concentration in the tissue of small intestine was highest.
5h药物浓度高达27。
3)  plasma concentration
药物浓度
1.
Association between valproic acid plasma concentration and CYP2C19 gene ploymorphism;
丙戊酸药物浓度与 CYP2C19 基因多态性关系的研究
4)  drug gradient generator
药物浓度梯度
1.
The device consisted of an array of 6×6 cell culture chambers, a drug gradient generator and fluidic control valves.
本研究介绍了一种利用SU-8负性光刻胶模具和PDMS制作双层结构的微流控细胞阵列芯片的方法,该芯片通过C型的坝结构将进样细胞拦截在芯片的细胞培养的固定区域,键合双层PDMS构成阀控制层,阀网络的开关作用成功实现了芯片通道内微流体的操控,同时芯片设计了药物浓度梯度网络,产生6个不同浓度的药物刺激细胞。
5)  free drug monitoring
游离药物浓度
1.
In this review,we introduce the method used in the sample preparing and determination of free drug monitoring.
血浆中游离药物浓度与受体部位药物平衡,因而其与药效或药物不良反应密切相关。
6)  plasma concentration
血浆药物浓度
补充资料:髓核


髓核
nuelcus pulposus

为乳白色半透明胶状体,富于弹性,为椎间盘结构的一部分,位于两软骨板与纤维环之间。
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