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1)  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。
2)  free drug level
游离血药浓度
3)  free concentration
游离浓度
4)  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。
5)  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
6)  free drug
游离药物
1.
Centrifugation of minicolumn to remove free drugs from liposomes to determine the encapsulation efficiency by calculation the drug-to-phospholipid ratio;
方法以氟吡洛芬、酮洛芬、拓扑替康为模型药物脂质体,通过葡聚糖凝胶(Sephadex G-50)微柱离心去除游离药物,以HPLC法测定药物含量,以定磷法测定磷脂含量,通过药脂比测定药物包封率。
补充资料:游离基浓度
分子式:
CAS号:

性质:又称游离基浓度。单位体积中所含自由基的量。一般常以M·或R·来表示自由基,以[M·]或[R·]来表示自由基的浓度,其单位为mol/L。

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