对维拉唑酮的药理作用、药动学以及临床评价进行了回顾。
The pharmacology, pharmacokinetics and clinical evaluation of vilazodone were reviewed.
目的：研究药动学房室模型的辨识问题。
OBJECTIVE: To study the identification problems of pharmacokinetic compartment models.
用非房室模型参数估算法计算药动学参数。
The pharmacokinetic parameters were calculated according to non - compartment model.
目的对中药复方的药动学研究进展进行综述。
OBJECTIVE To review the development of pharmacokinetic research on compound prescriptions of TCM.
可以利用药物来改变某种毒剂的药动学性质。
Drugs may be utilized to alter the pharmacokinetic profile of a toxicant.
目的测定注射用甲磺酸帕珠沙星的药动学参数。
Purpose To study the pharmacokinetics characteristics of pazufloxacin in healthy volunteers.
结论：该药动学研究结果可为临床用药提供参考。
CONCLUSION: the study on pharmacokinetics can be used as a reference in the clinical medication.
目的考察中国癫痫患者卡马西平的群体药动学参数。
AIM To investigate the pharmacokinetic profile of carbamazepine (CBZ) in Chinese epilepsy patients.
目的介绍老年期药动学及药效学变化及合理使用药物。
OBJECTIVE To introduce the pharmacokinetics and pharmacodynamics of gerontic and rational administration of drug.
目的：测定布洛芬糖浆剂的药动学及相对生物利用度。
OBJECTIVE: To determine the pharmacokinetics and relative bioavailability of ibuprofen syrup.
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.
目的研究硝酸异山梨酯注射剂在中国志愿者中的药动学。
OBJECTIVE To study the pharmacokinetic profiles of isosorbide dinitrate injection in Chinese healthy volunteers.
目的用迭代二步法估算肌注妥布霉素的群体药动学参数。
OBJECTIVE to estimate the population pharmacokinetic parameters of tobramycin by iterative two stage method.
麻醉兔静脉注射间硝苯地平后，观察其药动学和药效学。
Pharmacokinetics and pharmacodynamics ofm-nifedipine were studied in anaesthetic rabbits after an intravenous injection.
目的：创建缓释植入剂局部给药治疗系统的药动学模型。
Objective:To establish the pharmacokinetic model for a target therapeutic system of sustained-release implants.
结论：本法可为羟乙基芦丁的药动学研究提供一检测方法。
Conclusion: The present study provides a reliable quantitative method for pharmacokinetic studies of troxerutin.
目的研究氯雷他定胶囊与片剂的人体药动学和生物等效性。
Aim To study the pharmacokinetics and relative bioavailability of domestic loratadine capsules and tablets in healthy volunteers.
结论本方法简便、准确、精密度好，可用于临床药动学研究。
Conclusion The method appeared to be simple, accurate and precise. It is suitable for clinical pharmacokinetic study.
探讨采用血液微透析技术研究青藤碱药动学的可行性和优越性。
To explore the feasibility and advantages of blood microdialysis technique for the pharmacokinetic study of sinomenine.
目的：研究盐酸雷尼替丁咀嚼片剂的人体药动学和生物等效性。
OBJECTIVE To study the pharmacokinetics and relative bioavailability of ranitidine hydrochloride chewable tablets in healthy volunteers.
本文概述了奈米非肽的药动学、药理作用机制以及临床试验情况。
The article describes its pharmacokinetics, the mechanism of action, and clinical trials as an anti-depressant.
目的：研究替硝唑结肠定位肠溶片在健康受试者中的药动学特征。
Objective:To study the pharmacokinetics of tinidazole colon-specific enteric-coated tablets in healthy volunteers.
目的研究硝酸异山梨酯(ISDN)注射剂在中国志愿者中的药动学。
OBJECTIVE To study the pharmacokinetic profiles of isosorbide dinitrate (ISDN) injection in Chinese healthy volunteers.
结论本方法适用于药动学研究，测定结果为临床合理用药提供了依据。
Concusion The method can be used in pharmacokinetics of cefathiamidine and provided evidence for clinical application.
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 method is accurate and rapid. It can be used to study pharmacokinetics of gatifloxacin mesylate and to monitor the plasma drug concentration.
目的：研究氢溴酸右美沙芬片在健康人体的药动学及相对生物利用度。
AIM: To study the pharmacokinetics and relative bioavailability of dextromethorphan hydrobromide tablet in healthy volunteers.
目的：测定国产与进口拉西地平片剂的血药浓度，进行药动学参数比较。
OBJECTIVE: To determine the blood concentration of domestic and foreign lacidipine tablets, and compare their pharmacokinetic parameters.
目的研究盐酸川芎嗪(TMPH)经大鼠鼻腔给药后的脑内药动学特性。
OBJECTIVE To investigate the brain pharmacokinetics of tetramethylpyrazine hydrochloride (TMPH) after intranasal administration in rats.
药物浓度对时间数据作房室模型和统计矩解析，并求出相应的药动学参数。
Analysis of the data was executed by compartmental model and statistical moment calculation from which pharmacokinetic parameters were obtained.
药物浓度对时间数据作房室模型和统计矩解析，并求出相应的药动学参数。
Analysis of the data was executed by compartmental model and statistical moment calculation from which pharmacokinetic parameters were obtained.
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