pharmacokinetics单词基本解析:
n.药物(代谢)动力学n. 药物动力学, 药物与人体之间相互作用
pharmacokinetics变化用词:
pharmacokinetics英英释义:
Noun1. the study of the action of drugs in the body: method and rate of excretion; duration of effect; etc.
名词 pharmacokinetics:
the study of the action of drugs in the body: method and rate of excretion; duration of effect; etc.
pharmacokinetics中文词源:
pharmacokinetics用法和例句:
The pharmacokinetics of IDEBENONE have not been extensively studied.
有关艾地苯醌的药代动力学性质尚未作广泛研究.
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Objective To study the human pharmacokinetics and bioequivalence of erythromycin ethylsuccinate suspension.
目的研究琥乙红霉素干混悬剂的人体药代动力学和生物等效性.
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Objective To study the distribution and pharmacokinetics of Gd andGd - DTPA in mice.
目的研究钆喷酸葡胺脂质体在小鼠体内的分布与药代动力学.
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AIM : To study pharmacokinetics of lorazepam injection in healthy ese volunteers.
目的: 研究劳拉西泮注射液在中国健康人体内的药动学.
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Objective : To study the pharmacokinetics and bioavailability of danshensu in rat.
目的: 研究丹参素在大鼠体内药动学和口服生物利用度.
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Objective : To study the pharmacokinetics and bioavailability of cefalexin capsule.
目的: 研究头孢氨苄胶囊在人体内的药物动力学及其相对生物利用度.
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Professor Saltzman starts the lecture with an introduction to pharmacokinetics and pharmacodynamics.
教授索兹曼始于对药代动力学和药效学介绍讲座.
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AIM To study the pharmacokinetics and bioavailability of clinafloxacin in rats.
目的研究克林沙星在大鼠体内的药动学和生物利用度.
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Pharmacokinetics ( PK ) and pharmacodynamics ( PD ) are two important parts of pharmacology.
药代动力学(PK ) 和药效动力学 ( PD ) 是药理学重要组成部分.
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CONCLUSION: Pharmacokinetics of CFR and TMR are similar.
结论: CFR与TMR药物 动力学特点基本一致.
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AIM : To study the pharmacokinetics of brodimoprim ( BDP ).
目的: 测定国产溴莫普林 ( BDP ) 片在人体内的药物动力学.
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Objective : To determine pharmacokinetics parameters of Diammonium Glycyrrhizinic.
目的: 测定甘草酸二铵的体内药物动力学参数.
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The article describes its pharmacokinetics, the mechanism of action, and clinical trials as an anti - depressant.
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.
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OBJECTIVE: Pharmacokinetics and bioavailability of domestic and imported moclobemide tablets after single - dose oral administration.
目的: 研究国产吗氯贝胺片剂与进口同种产品的生物利用度及其药动学特征.
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Aim To determine scutellarin in dog plasma and study the pharmacokinetics of scutellarin in the dog.
目的 建立高效液相色谱法测定家犬血浆中灯盏花素主要有效成分灯盏乙素的浓度,研究灯盏花素在家犬体内的药代动力学.
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pharmacokinetics
Tilmicosin E.colli endotoxin, Blood Stagnation SyndromeModel, XueYuZhuFu decoction, Hemorheology, Pharmacokinetics.
01替米考星,大肠杆菌内毒素,血瘀证模型,血府逐瘀汤,血液流变学,药代动力学
Pharmacokinetics of CFR and TMR are similar.
CFR与TMR药物动力学特点基本一致.
SD rats are ideal animal in clinical Pharmacokinetics research for its little individual difference, low cost, blood re-collectable.
D大鼠是药代动力学的动物实验理想动物,它有个体差异小、成本低、适合药代动力学重复采血的优点。
HCV-796 was found to be generally well tolerated, with favorable pharmacokinetics and no dose-limiting toxicities.
HCV-796 被发现通常很好地被宽容,藉由有利的药物动力学和没有剂量限值毒性。
To supply datas for clinic using of microencapsulated catechin, studies on the toxicology,immune function , pharmacokinetics of microencapsulated catechin is a very meaningful work.
为了给儿茶素微胶囊的临床利用提供试验依据,因此开展了儿茶素微胶囊的毒理学,药物动力学及其对动物免疫功能的调节作用的研究,是一项很有意义的工作。
The main tasks for post-doctoral fellow include research in pharmacokinetics and clinical pharmacology, especially in drug metabolism, pharmacokinetics, and pharmacogenetics.
主要开展药物代谢(药物相互作用)以及遗传药理学与药物基因组学方面的研究工作。
This paper reviewed the in vitro antifungal activity,pharmacokinetics and drug interactions of micafungin.
介绍了米卡芬净的体外抗菌活性、药动学以及药物相互作用方面的研究进展。
However, Some of them also have adverse reaction, especially cardiotoxicity, which is related to antihistamines drugs interaction, pharmacokinetics and drug molecular structure.
但第2代抗组胺药仍有一些不良反应,尤以心脏的毒性作用,这与抗组胺药物相互作用、药动学、以及药物的分子结构有关。
Chunna Yu, Shuqing Chen, Su Zeng. Reporter Gene Assay to predict and Rank the Inducibility of CYP3A4 by TCMs. Asian Journal of Pharmacodynamics and Pharmacokinetics, 2006, 6 (3): 250.
俞春娜,陈枢青,曾苏,采用报告基因分析法预测中药对CYP3A4的诱导作用,第八次全国药物与化学异物代谢学术会议,大连,2006年10月。
Relative bioavailability and pharmacokinetics of clarithromycin in healthy volunteers. ......
克拉霉素;药动学;生物利用度;生物等效性
To determine pharmacokinetics parameters of baicalin and QRHJ by pharmacology effect method ......
关键词:黄芩苷;清热合剂;药物动力学;药理效应法
Areas of emphasis include pharmaceutics, pharmacokinetics, analytical chemistry, quality assurance, drug safety and manufacturing processes.
其中重点是药剂学,药效动力学,分析化学,质量保险,药物安全,制作过程。
Compound B1,B2 change pharmacokinetics of Venlafaxine, improve competence of penetrate BBB, possess brain-targeting effect, deserve for continued research, B5 excepted.
化合物B1,B2改变了文拉法辛的药代动力学性质,提高了其穿透血脑屏障能力,具有脑靶向效应,值得进一步研究; 而化合物B5缺乏该效应。
The upcoming study will examine a 21 days (b.i.d) regime and monitor pharmacokinetics and dose-response parameters.
即将进行的研究将审查21天(申办)制度和监测药代动力学和剂量反应参数。
The pharmacokinetics of the liposome after intravenous injection was studied.
同时考察包合物脂质体的体内药物动力学性质。
Bowmer C J,Yates MS,Emmerson J,etal.The effects of acute renal failure on the pharmacokinetics of indocyanine green in the rat.Biochem Pharmacol,1982,31(5):2531.
周瑾,涂晋文,邵朝弟.肾衰合剂防治大鼠急性肾衰竭的实验研究.湖北中医学院学报,2002,4(1):17.
What drug interactions may occur with warfarin? 2What drugs alter prothrombin time by interacting with warfarin levels (pharmacokinetics)? 3What drugs alter prothrombin time, but not by changing warfarin levels (pharmacodynamics)?
哪些药物可与华法林相互影响?2哪些药物可通过影响华法林水平改变凝血酶原时间(药代动力学角度)?3哪些药物不是通过影响华法林水平而改变凝血酶原时间(药效动力学角度)?
The bioequivalence and pharmacokinetics of domestic dextromethorphan hydrobromide extended release suspension was investigated in 18 healthy man volunteers, according to randomized crossover design.
在18名男性健康受试者中研究国产右美沙芬缓释混悬液的药物动力学特性及生物等效性。
Finally, the trophodynamics and pharmacokinetics of DDTs, HCB and PAHs were also investigated in this food web and the high trophic level animals.
在对二恶英类物质研究的同时,本研究调查了有机氯、六氯苯和多环芳烃类物质的食物网传递行为和高等生物体内的毒理动力学过程,得到了这些物质的食物网放大系数和代谢速率。
In this study, we first hypothesized that DEX potentiates CPA toxicity by inducing CYP3A4 and therefor changing its metabolic fate and pharmacokinetics.
在本研究中,先假设DEX通过诱导CYP3A4而改变CYP的两条代谢途径的相对比例,并使其药代动力学发生改变,从而增加CPA的毒性。
By using improved simplex method and residuals method,a calculation based on the parameters of compartment model of pharmacokinetics is presented.
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。
Multidrug resistance-associated protein(MRP) plays an important role in the pharmacokinetics of a drug in the body.However,the function of MRP can be affected by probenecid.
多药耐药相关蛋白(MRP)载体在药物的体内处置过程中发挥了重要的作用,丙磺舒对MRP有较好的抑制作用。
S studies on pharmacokinetics showed that the mean residence time of HEPC-SSL in blood is 23.3h, while that of EPC-SSL is 12.0h, and the area under the curve (AUC) of concentration of HEPC-SSL is larger than that of EPC-SSL.
大鼠体内药物动力学研究结果表明,HEPC长循环阿霉素脂质体在血中平均驻留时间(MRT)为23.3h,EPC长循环阿霉素脂质体在血中平均驻留时间(MRT)为12.0h。
Fueseau E,Sheiner LB.Simultaneous modeling of pharmacokinetics and pharmacodynamics with a nonparametric pharmacodynamic model.
姬汴生、张银娣.美托洛尔药动学、药效学结合模型的研究.河南医科大学学报,1995;
And gave the grey pharmacokinetics model according to blood concentration of compounded Captopril.
并根据抗高血压药复方卡托普利片的血药浓度给出了灰色药物动力模型。
To research pharmacokinetics model of glipizide tablets in health volunteer with grey theories.
应用灰色理论研究格列吡嗪片剂在健康志愿者体内的药物动力学模型。
Cardiopulmonary Bypass Has Minimal Effects on the Pharmacokinetics of Fentanyl in Adults Hudson RJ, et al.
心肺转流对成人芬太尼药效动力学影响轻微。
Achymthes bidentata Blume decoction can increase concentrations of clindamycin in cardia, hepar, lung and kidney; can influence pharmacokinetics parameters of clindamycin in rabbits.
怀牛膝水煎液对克林霉素在兔体内的药代动力学过程有影响,怀牛膝水煎液与克林霉素联用可以提高心、肝、肺、肾组织中克林霉素浓度。
Gender differences have aroused much attention in the area of pharmacokinetics.Gender differences in pharmacokinetics are the major factors causing interindividual differences in drug therapy.
性别对药代动力学的影响越来越受到重视,药代动力学的性别差异是药物作用个体差异的主要因素。
Shafer SL. Advances in propofol pharmacokinetics and pharmacodynamics. J Clin Anesth 1993,5:145.
戴体俊,叶妙,傅英.羟丁酸钠对氯胺酮药效学影响.中华麻醉学杂志1996,16:357.
The antifungal activity, pharmacokinetics and clinical evaluation of voriconazole,a new triazole antifungal drug with broad antifungal spectrum,are reviewed.
抗生素类,抗真菌;;药代动力学;;循证医学;;三唑类;;微生物敏感性试验;;文献检索课程;;图书馆服务;;信息存储和检索;;药物过敏
Abstract :The effect of traditional Chinese medicine and its preparation on pharmacokinetics of cyclosporin is reviewed in this paper.
摘 要 :本文综述了相关中药及中药制剂对环孢素药动学参数的影响。
AIM To study liver targeting and pharmacokinetics of tegafur magnetic long-circulating liposomes (TMLCL) which were given rats by hepatic artery.
摘要 目的 研究替加氟磁性长循环脂质体经肝动脉给药的药代动力学和组织靶向性。
Enantiomer accounts for quite large percentage in medicines, which has great difference in pharmacodynamics and pharmacokinetics.
摘要对映异构体在药物中占有很大比例,对映异构体药物在体内往往呈现很大药效学、药动学差异。
The purpose of this study was to investigate the effects of Ketoconazole to the pharmacokinetics of Pantoprazole in Wistar rats.
摘要目的研究酮康唑对泮托拉唑在大鼠体内药动学的影响,为临床合理用药提供参考。
Aim To investigate the tissue distribution and pharmacokinetics of hydroxycamptothecin (HCPT) after aerosol inhalation in rabbits.
摘要目的研究雾化吸人羟基喜树碱在兔体内的组织分布特点。
The recent progress of the Stable Isotopes(SI) research on pharmacokinetics is reviewed. With development of MS and GC-MS, it will be an important method for studying drugs.
摘要综述了稳定同位素在药物动力学研究中的最新发展,随着质谱和色-质联用等仪器的普及,它将成为药物研究中的一种重要手段。
Novel Starches: Single-dose Pharmacokinetics and Effects on Blood Coagulation.
新颖的淀粉:单次剂量的药代学和对血液凝固的作用。
Methods: (1) The pharmacokinetics, bioditribution and excretion of rhTNT-IL-2 were investigated with radiolabels combined with Trichloroacetic acid (TCA) precipitation or single photon emission computed tomography (SPECT).
方法:(1)采用同位素标记示踪法结合三氯醋酸(TCA)沉淀法和单光子发射计算机断层扫描(SPECT)技术研究~(125)I-rhTNT-IL-2的药代动力学。
Methods:Time and ways of medication were analyzed in terms of chronology,pharmacokinetics,pharmacodynamics and medicine application.
方法:从时间、药动学及药效学和给药系统等方面分析临床用药时间和方案。
Methods: Based on the theory of accumulated generating opposite-direction GOM (1,1) of the set-up model, the grey pharmacokinetics model of fleetness intravenous infusion was made.
方法:根据反向累加生成GOM(1,1)的建模原理,给出快速静脉推注药物动力学的灰色模型。
METHODS the pharmacokinetics of EPC and HEPC sterically stabilized liposomes (EPC-SSL, and HEPC-SSL) were studied by HPLC.
方法用高效液相色谱法研究EPC和HEPC长循环阿霉素脂质体在大鼠体内的药物动力学。
Methods The role of action, pharmacokinetics, adverse drug reaction,tolerance and development of fluoroquinolone were analyzed and concluded by reviewing domestic and abroad literature.
方法通过检索、查阅国内外文献,分析、归纳了新喹诺酮类药物在作用机制、抗菌活性、药代动力学、不良反应、耐药性及未来的研究方向。
Methods:HPLC was used to the data of determine FU, ADM and CDDP, and AAS method to deal with practical pharmacokinetics programs (3p87).
方法:以高效液相色谱法测定氟尿嘧啶、阿霉素,以原子吸收分光光度法测定顺铂,应用3P87实用药物动力学软件处理数据,以半衰期(T1/2)及生物利用度(AUC)为评价指标。
A stereoselective elimination of propafenone was observed in chinese subjects.Enantiomer/enantiomer interaction in pharmacokinetics and pharmacodynamics was also occurred.
普罗帕酮在人体内消除存在立体选择性,且两对映体产生了药效学上的相互作用。
The pharmacokinetics of IDEBENONE have not been extensively studied.
有关艾地苯醌的药代动力学性质尚未作广泛研究。
We studied PCD in NB4 and HL-60 cells and in vitro cellular pharmacokinetics of m-AMSA in synchronized and asynchronized cells.
本实验研究了NB4及HL-60细胞的程序化死亡及细胞药代动力学特征。
This review evaluates pregnancy-induced pharmacokinetics changes from aspects of absorption, distribution, metabolism and excretion.
本文从药物的吸收、分布、代谢和排泄4个方面概述了因妊娠而引起的药动学改变。
This abbreviated review outlines the physiologic changes associated with aging, and examines how these changes may affect the pharmacokinetics and pharmacodynamics of anticancer therapies.
本文列出了老年相关的生理变化并试图研究其相应的生理变化有可能会影响抗癌药物的药代学和药效学。
This review will summarize recent literature on the pharmacokinetics and pharmacodynamics of inhaled morphine as well as the utility in clinic.
本文对吗啡雾化吸入呼吸道给药的药物代谢动力学和药效学以及临床应用的研究进展进行综述。
The pharmacokinetics and bioavailability of acyclovir (ACV)were studied in 10 hepatitis B surface antigen carriers.
本文报道无环鸟苷在10名乙型肝炎表面抗原阳性患者体内的药代动力学及口服片剂的生物利用度。
The article describes its pharmacokinetics, the mechanism of action, and clinical trials as an anti-depressant.
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。
This paper reviews the progress of telithromycin in pharmacology, pharmacokinetics, clinical application and so on.
本文简要概述替利霉素药理学、药动学及其临床应用。
In this article, the mechanism, pharmacokinetics and advances in clinical application of ezetimibe are summarized.
本文综述了依折麦布的作用机制、药动学特性及其在临床应用中的最新进展。
The preclinical study, clinical pharmacokinetics, clinical evaluvation and adverse reactions of risedronate sodium as a new drug for treatment of metabolic bone disease are reviewed...
本文综述了利塞膦酸钠作为一种新型抗代谢性骨病药物的临床前研究概况、临床药代动力学、临床评价及不良反应。
Pharmacokinetics,toxicological functions,drug residue,withdrawal time and the application perspective are summarized in this article.
本文综述了喹烯酮的药代动力学、毒理作用、药物残留、休药期和应用前景等内容。
In this paper, it was reviewed that the most recent results on the study of the stereoselectivity in pharmacokinetics and its related factors.
本文综述了手性药物药代动力学立体选择性及其影响因素方面的最新研究进展。
This article summarizes the process mechanism, pharmacokinetics,pharmacodynamics,clinical studies and safety profile of clofarabine.
本文综述了氯法拉滨的作用机制、药动学、药效学、临床研究及不良反应。
The effect of traditional Chinese medicine and its preparation on pharmacokinetics of cyclosporin is reviewed in this paper.
本文综述了相关中药及中药制剂对环孢素药动学参数的影响。
By analyzing the clinical indications, adverse reactions and the character of pharmacokinetics of injection puerarin , this article explores the necessity of oral medication of Puerarin.
本文通过对葛根素注射液的临床适应症、不良反应、药动学特性,探讨葛根素口服给药的必要性;
In this study, we investigated the effects of HLJDT on the pharmacokinetics of two probe drugs MTX and CSP in rats.
本研究以大白鼠为模型,探讨黄连解毒汤对二探针药物MTX及CSP动力学之影响。
The aim of this study was to inestigate the effect of food composition on the pharmacokinetics of oral TU.
本研究旨在探索食物成分对口服TU药代动力学的影响。
A series of experiments were carried out for studies on pharmacokinetics and residues determination of furazolidonum .
本论文对呋喃唑酮的药效及其药代动力学与残留检测进行了系列研究。
This course, composed of biopharmaceutics and pharmacokinetics, is designed for the graduate and under graduate students in school of pharmaceutical science.
本课程面向药学专业高年级学生,由生物药剂学与药物动力学两部分构成。
To study the pharmacokinetics, tissue distribution and excretion of 125I-rhTPO in SD rats using radioisotopic tracing method in this paper.
本课题目的是建立125I标记重组人血小板生成素(125I-rhTPO)的分析方法,研究rhTPO在SD大鼠体内的药动学特性,观察在大鼠体内的组织分布和经尿、粪排泄的情况。
Pharmacokinetics of an Implanted Osmotic Pump Delivering Sufentanil for the Treatment of Chronic Pain Fisher DM, et al.
植入性苏芬太尼传输渗透泵治疗慢性疼痛的药效动力学。
Experimental study on pharmacokinetics of sustained release drug implant piece containing ofloxacine in vitreous.
氧氟沙星缓释植片在玻璃体腔药代动力学实验研究。
The mechanism of action,pharmacodynamics,pharmacokinetics,clinical applications and safety of clopidogrel,an ADP receptor antagonist,are reviewed in this paper.
氯吡格雷是一种新颖的抗血小板药物 ,通过阻断二磷酸腺苷 (ADP)受体而抑制血小板活性。 本文综述了氯吡格雷的作用机制、药效学和药代动力学特性及其临床应用和安全性
Grey theory can be used to study the single peak sequence in pharmacokinetics.
灰色理论可用于药物动力学中单峰序列的研究。
This paper introduced the pharmacodynamics,pharmacokinetics,the clinical efficacy and safety of mildronate.
现主要介绍其药效学、毒理学、药动学、临床评价等方面的研究进展。
This paper introduces mechanism of action,pharmacokinetics and determination of Memantine.
现综述其作用机制、体内过程与测定技术。
The pharmacological action,pharmacokinetics and clinical research of zoledronic acid are reviewe...
现综述唑来膦酸的药理作用、药动学和临床评价。
The pharmacological ac-tions,pharmacokinetics,clinical trial and tolerance of tenofovir DF are reviewed in this article.
现综述替诺福韦DF的药理作用、药动学、临床试验和耐受性。
Biological sample ana-lytical methods are the basis of pharmacokinetics research.
生物样品分析方法是进行药物体内动力学研究的基础。
Formulate the distribution of photosensitizer in vessels by pharmacokinetics.
用药代动力学描述光敏剂在血管中的变化规律;
OBJECTIVE To develop an HPLC-fluorescence metho d for determination trans tramadol and its active metabolite, O-demethyltrama dol (M1), in human serum, and study the pharmacokinetics.
目的 :建立人血清中反式曲马多 (transT)及其活性代谢物反式氧去甲基曲马多 (M 1)同时测定的HPLC荧光分析法并研究其人体药动学。
AIM: To compare the pharmacokinetics and bioavailability of 3 levodopa tablets (A, B, C).
目的 :比较 3种左旋多巴片剂 (A、B和 C片 )的生物利用度和药物动力学。
AIM: To study the pharmacokinetics of brodimoprim (BDP).
目的 :测定国产溴莫普林 (BDP)片在人体内的药物动力学。
Objective:To study on in vivo pharmacokinetics of carboplatin liposomes (CPL) after intralymphatic vessel perfusion (ILVP) with animal experiment.
目的 :研究卡铂脂质体 (CPL)经淋巴管内灌注 (ILVP)的体内药代动力学。
AIM: To study the pharmacokinetics of conjugate of urokinase with bispecific monoclonal antibody against urokinase and fibrin (UK BI9E 11 ) in mice.
目的 :研究尿激酶 -抗尿激酶抗纤维蛋白双特异单克隆抗体复合物 (U K- BI9E1 1 )在小鼠体内的药物动力学特征。