- 更多网络例句与排泄药相关的网络例句 [注：此内容来源于网络，仅供参考]
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In the present study, the new sensitive and specific LC/MS/MS method was developed for the simultaneous determination of magnesium lithospermate B, rosmarinic acid and lithospermic acid and their major metabolites in biological samples. The pharmacokinetics of S. miltiorrhiza depside salts in dogs, rats, and humans conducted the developed LC/MS/MS method, and they would be useful for new drug development and design.
在此基础上，系统研究了创新中药丹参多酚酸盐多个成分在Beagle犬及大鼠体内的药物代谢动力学特征，包括多剂量、多种给药方式的影响，及吸收、分布、代谢、排泄特征；同时进行人体药物代谢动力学研究，为设计合理给药方案和临床安全有效用药提供了理论依据，对传统中药的现代化研究具有显著的示范作用。
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Results: For CRF rats which made by fed with feedingstuff contains 0.75% of adenine for 4 weeks, the weight of model control group rats were lighter than that of Yi Shen Granule groups rats. The water wastage of Yi Shen Granule groups rats were less than that of model control group rats. Compared urine volume, the ejectable quantity of Na, K, Cl and proteinuria in 12 hours , the data of Yi Shen Granule groups rats were less than that of model control rats. The specific gravity of Yi Shen Granule groups rats was higher than that of model control rats. The numerical value of RBC, HGB, HCT, MCV, MCH in model control group was lower than that in Yi Shen Granule groups. The content of BUN and Cre in serum of model control groups rats were higher than that of Yi Shen Granule groups. The results of excretion test of phenolsulfonphthalein showed that the RPF of Yi Shen Granule groups rats was larger than that of model control group rats.
结果： 益肾颗粒可以使0.75%腺嘌呤饲喂法致大鼠慢性肾衰模型动物体重增长加快；给药后观察，给药组动物饮水量较少，12小时尿量、12小时钠、氯、尿蛋白排泄总量均显著低于模型组动物，尿液比重值较大；模型组动物的RBC、HGB、HCT、MCV、MCH等指标的数值较给药组动物的数值小；给药组动物血清中BUN和Cre的含量较低；给药组动物酚红排泄率均高于模型组动物；给药30天，处死各组动物，尸解观察，模型对照组动物肾脏呈灰白色，各给药组动物肾脏表面均出现不同程度的红、白相兼的颗粒状纹理，各组动物肾脏均肿大，切面可见不同程度的腺嘌呤结晶沉积。
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AIM: To study the pharmacokinetics of astragaloside Ⅳ in rabbits and its excretion in rats.
目的 ：研究黄芪甲苷在家兔体内的药动学和在大鼠的排泄。
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Then,the accumulated excretion rate of luteolin and apigenin in the three courses were calculated.
与此同时，在胆汁中两者也有一定的累积排泄量，分别占给药剂量的2.05%和6.34%。
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It must be cautiously used for animals with renal dysfunction because of delay of sulfanilamide excretion.
肾功能障碍时，磺胺药排泄延缓，应慎用。
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Objective: A HPLC-ECD method was established to determine scutellarin in rat bile.
中文摘要：目的：建立大鼠胆汁中灯盏花乙素的高效液相-电化学色谱测定方法，研究灌胃给药灯盏花乙素苷元200 mg·kg-1后，代谢产物在胆汁中的排泄方式。
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In order to investigate the profile of absorption, excretion and retainment of As〓S〓, and to estimate the influence of Semen platycladi and other excipient in As〓S〓 absorption, we studied the pharmacokinetics in humans and mice respectively.
为了了解As〓S〓复方胶囊在人体内吸收、排泄、蓄积等规律，我们进行了临床药代动力学研究，同时，为了比较复方制剂及不同赋形剂对As〓S〓吸收的影响，进行了动物药代动力学实验。
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Because elderly patients with a lower basal metabolism, body reserve capacity is poor, and drug metabolism in liver and kidney functions closely related to the poor so that a reduced ability to excrete drugs, high blood concentration, and therefore need to take full advantage of the process of medication dosage, to ensure the safety of the treatment.
由于老年患者基础代谢较低，机体储备能力差，与药物代谢关系密切的肝肾功能不佳，从而使药物排泄能力下降，血药浓度偏高，因此在用药过程中需要充分把握药物的剂量，保证治疗的安全性。
- 更多网络解释与排泄药相关的网络解释 [注：此内容来源于网络，仅供参考]
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urinary alkalinization：尿鹼性化
uricosuria 尿酸尿(尿酸排泄) | uricosuric 排尿酸藥 排尿酸药 | urinary alkalinization 尿鹼性化
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anticancer drug：抗癌药
包括: 抗微生物药(antimiczobial drug)抗寄生虫药(antiparasitic drug)抗癌药(anticancer drug)(2) 化疗目的1. 化学治疗学(chemotherapy, 化疗)药物机体防治作用与不良反应药效学药动学吸收、分布、代谢、排泄病原微生物抗微生物药抗菌作用耐药性抗病能力致病作用不良反应体内过程机体(3) 评价指标 化疗指数 (chemotherapeu
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eccritic：排泄剂 排泄药 促排剂 促排泄的
eccrisiology 分泌学 | eccritic 排泄剂 排泄药 促排剂 促排泄的 | eccyclomastoma 局限性乳腺结缔织增生 局限性乳腺结缔织增生
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evacuant：排除的 排除药
euxinicdeposition 滞海沉积 | evacuant 排除的 排除药 | evacuate 排空 排泄干 抽空 搬空
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evacuant：排泄药
euxenite 黑稀金矿 | evacuant 排泄药 | evacuantexcretive 促进排泄的
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biological half life：生物半衰期
生物半衰期(Biological Half Life)简称血浆半衰期,系指药物自体内消除半量所需的时间,以符号T1/2表示. 一般情况下,代谢快、排泄快的药物,其生物半衰期短,而代谢慢、排泄慢者的生物半衰期较长. 临床上可根据各种药物的半衰期来确定适当的给药间隔时间(或每日的给药次数),
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Drug, hard：烈性药物
Drug, elimination药物的排泄 | Drug, hard烈性药物 | Drug, long-acting长效药
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lithium carbonate：碳酸锂
碳酸锂 碳酸锂(lithium carbonate)口服吸收快而完全,2~4小时血药浓度达峰值. 锂离子先分布于细胞外液,然后逐渐蓄积于细胞内. 锂虽吸收快,但通过血脑屏障进入脑组织和神经细胞需要一定时间. 因此,锂盐显效较慢. 主要自肾排泄,
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Anisic acid：茴香酸
其余的30%产物为茴香酸(anisic acid)和2-吡咯烷酮(2-pyrrolidone). 服药后24小时,77%-85%以代谢产物形式从尿中排出,4%从大便排泄. 原药形式排泄极少.
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Diazepam：地西泮
5.2.7 地西泮(diazepam) 有报道此药能迅速控制新生儿撤药综合征的症状,比较安全和疗程较短. 剂量为每次0.3~0.5 mg/kg,每8小时1次,肌注或口服[8]. 但存在以下缺点[1]:新生儿对本药的代谢和排泄能力较差,总排泄期长达1月以上;