A simple, quick and accurate HPLC method was adopted to assay the drug concentration in plasma.
并介绍了一种简单、快速、准确的高效液相方法检测硝苯地平的血药浓度。
The method is accurate and rapid. It can be used to study pharmacokinetics of gatifloxacin mesylate and to monitor the plasma drug concentration.
本方法准确快速，适用于加替沙星的药动学研究及临床血药浓度监测。
The drug concentration in liver, kidney and plasma was determined by HPLC.
采用HPLC法测定大鼠肝、肾和血浆中的药物浓度。
After equilibrium is attained, drug concentrations in tissues and in extracellular fluids are reflected by the plasma concentration.
达到分布平衡后，便可通过血浆浓度反映组织和细胞外液的药物浓度。
Drug concentration in rats plasma was detected by high performance lipid chromatography (HPLC) after curcumin liposomes administered to rats.
姜黄素脂质体大鼠口服给药后，以高效液相色谱(hplc)法测定大鼠血浆中的药物浓度。
To set up the local plasma drug concentration-space-time equation of the local embedding administration.
按实例建立局部植入给药的局部药物浓度时空方程。
Only recently have the peroral or dermal use been evaluated. Drugs encapsulated into SLN showed a reduced peak plasma concentration and prolonged therapeutic drug level following oral administration.
近年来，SLN的口服和经皮给药逐渐受到重视，研究发现，口服经过SLN包裹后的药物能降低其血药浓度峰值，并延长药物作用时间。
Bioavailability determinations based on the peak plasma concentration can be misleading, because drug elimination begins as soon as the drug enters the bloodstream.
单靠峰时血浆浓度来确定生物利用度会导致误解，因为药物一进入血流就会开始药物消除。
Plasma protein binding influences distribution and the apparent relationship between pharmacologic activity and total plasma drug concentration.
血浆蛋白的结合作用会影响药物的分布，并影响药理活性和总血浆药物浓度间的表观关系。
When the weak acid is given orally, the concentration gradient for un-ionized drug between stomach and plasma tends to be large, favoring diffusion through the gastric mucosa.
当这种弱酸性药物经口服给药时，胃与血浆之间的非解离型药物浓度梯度很大，从而有利于透过胃粘膜扩散。
When it was applied in sample analysis, bupivacaine was successfully separated and determined from the rat plasma after drug injection, and its concentration monitoring in plasma was carried out.
在样品分析中，成功分离测定了注射药物的大鼠血浆中的布比卡因，实现了布比卡因血药浓度的快速监测。
Methods: the factors that made the determined plasma drug concentration changed on the course of TDM were analyzed.
方法：针对分析前、分析中、分析后的主要环节可能产生血药浓度变化的因素进行分析。
Objective: To set up the local plasma drug concentration-space-time equation of the local embedding administration.
目的：按实例建立局部植入给药的局部药物浓度时空方程。
AIM To set up the local plasma drug concentration space time equation of the local embedding.
目的建立局部植入给药的药物浓度时空方程。
Objective: To set up the local plasma drug concentration space time equation of the local embedding.
目的：建立局部植入给药的药物浓度时空方程。
In patients with hypertension, the plasma drug concentration and blood pressure versus time curves mirrored each other, indicating a close relationship between concentration and effect.
在高血压患者中，药物血浆浓度与血压-时间曲线相互对应，这表明药物浓度与降压疗效之间密切相关。
In patients with hypertension, the plasma drug concentration and blood pressure versus time curves mirrored each other, indicating a close relationship between concentration and effect.
在高血压患者中，药物血浆浓度与血压-时间曲线相互对应，这表明药物浓度与降压疗效之间密切相关。
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