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单词 pharmacokinetic
释义
  • pharmacokinetic

    • [?fɑ:m?ko?knet?k]

    释义

    • [医]药物代谢动力学
  • 实用场景例句

    • 全部

    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.

    辞典例句

    The fundamental pharmacokinetic principles are based upon the most elementary kinetic model.

    药动学的基本原理是以最基本的动力学模型为依据.

    辞典例句

    Drug protein binding changes involved in numerous factors in vivo may cause changes of pharmacokinetic parameters.

    体内各种因素引起的药物与血浆蛋白结合的改变,可能导致相应的药代动力学参数变化.

    互联网

    Induction and inhibition of cytochrome P 450 ( CYP 450 ) catalytic activity has been concluded to be pharmacokinetic drug - drug interaction.

    细胞色素P450酶 ( CYP450 ) 活性的诱导或抑制,是引起临床药物代谢性相互作用的主要作用机制.

    互联网

    Objective To evaluate the pharmacokinetic properties and bioequivalence of two different capsules of ampicillin probenecid capsules.

    目的比较两种氨苄西林丙磺舒胶囊的药代动力学参数及人体生物等效性.

    互联网

    Objective To measure the pharmacokinetic parameter and bioavailability of aciclovir in healthy human body.

    目的测定阿昔洛韦片在健康人体内的药代动力学参数及相对生物利用度.

    互联网

    And to investigate and compare with the pharmacokinetic parameters of t - Res and t - PD in rats.

    目的:建立大鼠血浆中t-Res 及t-PD 浓度的HPLC测定方法,研究比较t-Res及 t-PD在大鼠体内的药代动力学行为.

    互联网

    Aim To develop a pharmacokinetic model for the enterohepatic circulation of mycophenolic acid ( MPA ).

    目的建立麦考酚酸肠肝循环的药动学模型.

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    Conclusion The pharmacokinetic parameters of roxithromycin enterosoluble capsules revealed the character of the dosage form.

    结论罗红霉素系肠溶胶囊药代动力学参数符合该剂型的特征.

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    The statement of " aconite counteracts fritillaria " is preliminarily validated by our pharmacokinetic studies.

    从药动学角度初步验证了 “ 乌头反贝母 ” 理论的科学性.

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    Abstract: articlethe first to study on pharmacokinetic and eliminate of OTC in turbot after oral administration.

    摘要: 首次研究大菱鲆口服土霉素的药代动力学特征及残留消除规律.

    互联网

    It was showed that the metabolism of oleanolic acid in rabbit accorded with one - room pharmacokinetic model.

    结果表明,齐墩果酸在家兔体内的代谢符合一室药动学模型.

    互联网

    Patients an initial SQV formulation change or a CART change to SQV - RTV - ATV with intense pharmacokinetic sampling.

    受试者从开始就接受SQV配方设计改变或由CART转为SQV -RTV-ATV,同时加强药物代谢动力学采样.

    互联网

    Aim To investigate the pharmacokinetic characteristics of after multiple oral dose administration in healthy Chinese volunteers.

    目的研究中国健康男性志愿者多剂量口服吗氯贝胺缓释片的药代动力学特征.

    互联网

    Ritonavir - boosted double ? protease inhibitor ( PI ) ? only regimens are such an option but are prone to pharmacokinetic interactions.

    单独的利托那韦用量增加的双蛋白酶抑制剂 ( PI ) 疗法正是其中之一,但在药代动力学上两者易于产生相互作用.

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