动学

Drugs may be utilized to alter the pharmacokinetic profile of a toxicant.

可以利用药物来改变某种毒剂的药动学性质。

The intestinal everted sacs study will be conducted to assess the relationship between the hydrophobicity of linear peptides and their Pgp inhibitory effect. Subsequently, drug interaction in pharmacokinetics will be evaluated using in vivo study in rats.

以小肠翻肠实验来探讨Linear peptide的脂溶性与P醣蛋白抑制作用的关系，进一步以老鼠体内试验来评估药动学上的变化。

AIM: Study the pharmacokinetic characteristics of paclitaxel lyophilized nanoemulsions in rats.

目的：研究紫杉醇冻乾纳米乳在大鼠体内的药动学特徵。

The MTX was preluded in children with ALL by the single compartment model.

MTX在ALL患儿体内的经时过程呈一房室模型，各个体间药动学参数存在一定的差异。

The results summarized as follows:(1)The main pharmacokinetic parameters Tmax was about 2h, Cmax was 8.365, 7.519, 1.871, 6.485, 4.060μg/mL in blood, gill, kidney, liver, and muscle respectively, after oral administration at a dose of 30 mg/kg; while t1/2 were 8.180~23.249h. These showed that the NFLX absorption was rapid after oral administration of NFLX in Scophthalmus maximus, but the residence time in the fish was long.(2) T1/2 were 74.88~200.45h after oral administration at dose of 30 mg/kg for five consecutive days, which showed that the attenuation of NFLX in the fish body was slow and the residue concentration in the kidney was the highest.

另外，本文测定了大菱鲆成鱼体内NFLX的药物浓度，用MCP-KP药动学程序对所得的药物浓度-时间数据进行分析，结果表明：1单次混饲口灌(30 mg/kg体重日)NFLX，药物在大菱鲆体内的达峰时间为2h，血液、腮、肾脏、肝脏、肌肉达峰浓度分别为：8.365、7.519、1.871、6.485、4.060μg/mL，消除半衰期为8.180～23.249h，说明NFLX在大菱鲆体内吸收较迅速，但滞留时间较长。2连续五天混饲口灌(30 mg/kg体重日)NFLX，消除半衰期为74.88～200.45h，说明混饲口灌NFLX在大菱鲆体内消除缓慢，其中以肾脏中残留最显著。

A HPLC method for determination of lidocaine in rabbit plasma was established.

建立了HPLC法测定兔血浆中利多卡因的浓度，并研究家兔经不同途径给药后的药动学。

Objective To prepare the long-circulating paclitaxel-containing liposomes and evaluate its pharmacokinetics in rats.

目的制备紫杉醇长循环脂质体并观察其在大鼠体内的药动学。

OBJECTIVE To study the pharmacokinetics of zidovudine in young healthy volunteers. METHODS The separation was performed on Hypersil C18 (5 μm, 4.6 mm×200 mm) column.

目的：建立反相高效液相色谱法，研究齐多夫定在健康人体内的药动学。

This therapy is the reflection of wholism treatment by quantum medicine,information and biotechnique,biological agents,regulation of collaterals,compounds of drugs and physiotherapy.

这是现代量子医学，及信息与生物技术、制剂，经络功能调控，药物复方、证治药动学，和理疗效应等相互融合的&整体疗法&表现。

It was incorporated the number of the grades of CYP2D6 genotype and physiologic factors as covariances into modeling study.

之后将CYP2D6基因型分成四种等级以数字表示及生理因子当作共变数代入药动学模式中。

Breath, muscle contraction of the buttocks; arch body, as far as possible to hold his head, right leg straight towards the ceiling (peg-leg knee in order to avoid muscle tension).

呼气，收缩臀部肌肉；拱起身体，尽量抬起头来，右腿伸直朝向天花板（膝微屈，以避免肌肉紧张）。

The cost of moving grain food products was unchanged from May, but year over year are up 8%.

粮食产品的运输费用与5月份相比没有变化，但却比去年同期高8％。