药物动力学参数在性别间没有明显差异。
The main pharmacokinetic parameters showed no difference in genders.
由非房室和房室模型评价药物动力学参数。
Pharmacokinetic parameters were assessed with noncompartment model and model-dependent method.
目的：建立快速推注的灰色药物动力学模型。
Objective: To establish the grey pharmacokinetics model of the fleetness intravenous infusion.
结果表明两者的各药物动力学参数均无明显差异。
The results showed that there was no significant difference in each pharmacokinetic parameters between them.
目的：研究莫西沙星在感染家兔模型中的药物动力学。
OBJECTIVE: To study the pharmacokinetics of moxifloxacin in a rabbit tissue cage model.
结论：灰色理论可用于建立静脉注射药物动力学模型。
Conclusion: the gray theories can be used for establishing the fleetness intravenous injection pharmacokinetics model.
结论该方法可用于野黄芩苷的临床前药物动力学研究。
Conclusions the method is proved to be accurate, simple, and suitable for the preclinical pharmacokinetics scutellarin in dogs.
目的：测定肺部感染患者静脉注射替硝唑的药物动力学。
OBJECTIVE: To determine pharmacokinetics of tinidazole in patients with lung infection.
联苯苄唑的药物动力学研究结果表明它是一个安全的药物。
The results of pharmacokinetics studies show that it is a safety drug.
研究了恩诺沙星长效注射液给猪肌注后的药物动力学特征。
The pharmacokinetic properties of enrofloxacin long acting injection were studied.
眼部药物动力学过程的考察是药物眼部作用研究的重要方面。
The ophthalmic pharmacokinetics investigation is an important research aspect of drug ophthalmic action.
结论：此方法灵敏、准确，适用于药物动力学和药效学研究。
Conclusion: the method is sensitive and accurate, fit for the research of pharmacokinetics and pharmacodynamics.
目的：为研究格列吡嗪的药物动力学及其制剂的开发提供方法。
AIM: To provide a method for study of glipizide pharmacokinetics and development of it's products.
结果：灰色物动力学模型比传统的药物动力学模型拟合精度高。
Results: The mimesis accuracy of Grey pharmacokinetics model was higher than that of traditional ones.
目的研究格列齐特片的健康人体药物动力学及相对生物利用度。
Objective To study the relative bioavailability of gliclazide in healthy volunteers.
目的研究国产和进口硝苯地平控释片的药物动力学和生物等效性。
ObjectiveTo investigate the pharmacokinetics and bioequivalence of domestic and imported nifedipine controlled release tablets.
托吡酯吸收迅速完全，呈线性药物动力学特征，生物利用度高。
TPM can be absorbed quickly and completely, it takes on linely drug dynamical characteristic, has high-level organism usefulness.
目的对苯妥英钠进行药物动力学研究，制定苯妥英钠个体化给药方案。
Objective Making researches into pharmacokinetics for phenytoin and laying down individuation drug delivery scheme for phenytoin sodium.
PCNONLIN程序进行药物动力学房室模型数据拟合和参数计算；
The modelling data were performed with a compartment pharmacokinetic modelling program (PCNONLIN).
采用药物动力学软件（PK- GRAPH）分析药物浓度-时间数据。
目的：了解加入新型增粘剂后氯霉素滴眼液在兔泪眼中的药物动力学差别。
OBJECTIVE: to assess the pharmacokinetic difference after new densifier adding into chloramphenicol eye drops in rabbits tear.
本文针对药物动力学的特点，利用控制模型，给出了对其稳定性分析的方法。
This paper established a control model and proposed the stabilization methods aimed at the characteristic of pharmacokinetics for bolus injection.
还需要对庆大霉素和氯霉素的毒性以及头孢曲松和环丙沙星的药物动力学做进一步的研究。
Further research into gentamicin and chloramphenicol toxicity and into the pharmacokinetics of ceftriaxone and ciprofloxacin is also required.
目的：研究甲硝唑磷酸酯钾PMP及甲硝唑MTZ在家兔血中的药物动力学参数。
Objective: To study the pharmacokinetics of potassium metronidazole phosphate (PMP) and metronidazole (MTZ) in rabbits.
目的评价氟尿嘧啶动物胃左动脉灌注和外周静脉化疗药物动力学的基础实验比较。
Objective To compare the pharmacokinetics on rabbit after left gastric regional arterial infusion chemotherapy with peripheral intravenous administration.
前言：目的：根据文献资料综述抗菌药物新剂型在细胞、组织的药物动力学特点。
Objective: Pharmacokinetic features of newer antibacterial dosage forms in infected cells and tissues were reviewed on the basis of literature.
本文进行了新西兰兔口服新基质复方丹参滴丸和原滴丸对照品的药物动力学研究。
Pharmacokinetics on the comparison between new and original pill were evaluated in rabbits by oral taken.
药物动力学表明，此药在更高剂量的情况下对处置表达CD56的肿瘤细胞更有效。
Pharmacokinetics showed that drug was able to tackle tumour cells expressing CD56 more effectively at the higher doses.
它被广泛应用于生物技术、药物动力学、物理、经济、种群动力学、流行病学等领域。
It is widely applied in various domains such as biological technology, medicine dynamics, physics, economy, population dynamics and epidemiology.
基于改进的单纯形算法和残数法，对药物动力学房室模型中的有关参数计算进行了研究。
By using improved simplex method and residuals method, a calculation based on the parameters of compartment model of pharmacokinetics is presented.
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