给药
- 与 给药 相关的网络例句 [注:此内容来源于网络,仅供参考]
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Methods: 26 patients with tubercular meningitis were treated with traditional methods combined with intrathecal injection, and to investigate the clinical effect and biochemical indexes and cerebrospinal fluid of protein, glucose and chlorides.
在收治的26例结核性脑膜炎患者常规抗结核治疗基础上合并使用鞘内给药;观察患者临床症状与体征变化,脑脊液的蛋白、糖、氯化物变化。
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The mice were orally given correspondence drug for 7 days in every group, and after the seventh day of giving drug the mice were experimentized. Hot board method and vinegar twist body method were used to observe the analgesia effect, and experiments of dimethylbenzene inducing tumefaction of ears and osmosis of abdomen capillary vessel were done to obseve anti-inflammatory effect.
各组小鼠分别连续灌胃7 d,分别在末次给药后做热板法实验和醋酸扭体法实验两种疼痛模型观察镇痛作用;二甲苯致小鼠耳肿胀实验和小鼠腹腔毛细血管通透性的实验,研究抗炎作用;并且与阳性对照组及空白模型组作对比观察。
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After administerded for 30 days, all rats were killed and anatomized. The nephric exterior of model control group rats was offwhite, instead, that of Yi Shen Granule groups rats showed red grain in offwhite exterior. There were tumefaction of tissue and sediment of adenine in all kidney.
病理组织学观察发现,与空白组比较,造模动物肾小管均有扩张,给药后其扩张程度有显著性差异,采用半定量的方法对肾小管扩张程度进行分级比较,结果显示大剂量组动物肾小管扩张程度较轻。
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After 40 days, the blood fat and the function of vascular endothelial cell were determined. The pathomorphology of aortic tunica intima was observed.
给药组灌服补肾活血中药,连续用药40 d后,测定血脂及血管内皮细胞功能,观察主动脉内膜的病理形态学变化。
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Methods We treated those casea with combined operation which had oral medicine for a long tine or had been treated with medicine in nasal cavity, at the same time, their nasal ventilation were bad because they had a deflection of nasal septum or/and turbinal intumescentia, nasal polyps.
对于已经长期口服药物或鼻腔局部给药治疗效果差,并有鼻中隔偏曲或伴有鼻甲肥大、息肉形成而影响鼻通气的患者给予联合手术治疗。
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Results Ningxin compound extract had obvious anxiolytic effects on rats, with effective inhibition of the rise of blood pressure in combination with exogenous tyramine.
结果 宁心416 mg/kg、208 mg/kg、104 mg/kg灌胃给药均有明显的抗焦虑作用;宁心在实验剂量下(288 mg/kg)能抑制外源酪胺引起的升压作用。
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Accord- ing to the observation that the compounds were stable in low pH aqueous solution and their sta- bility decreased when pH increased, and they rapidly decomposed to form α-methylenecyclopen- tanones derivative when pH reached 6 to 7, we postulated that the compounds were unabsorbable in stomack (where pH1-3) and unstable in small intestine (where pH5-8). The decomposed product was indeed inactive.
对Ⅰ类化合物在稀溶液中的稳定性研究表明,低pH时化合物较稳定,随着pH值的升高稳定性逐渐降低,pH6~7时,化合物迅速分解成α-亚甲基环戊酮类化合物,由此而推测Ⅰ类化合物经口给药无效的原因为:它们在强酸性的胃中(pH1-3)呈离子状态,因而不易吸收,经胃的排空运动进入肠道后,随着pH逐渐升高(pH5-8)化合物迅速分解,而分解产物α-亚甲基环戊酮类化合物证明是无效的。
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Here we show that the simple systemic delivery of a unconjugated, PBS-formulated locked-nucleic-acid-modified oligonucleotide (LNA-antimiR) effectively antagonizes the liver-expressed miR-122 in non-human primates.
结果显示采用非结合的PBS配制的锁核酸改良寡核酸(LNA-antimiR)单一全身给药可以有效地干扰非人类的灵长类动物体内肝脏表达的miR-122。
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UH2/Ura basic value of body liquid can reflect circadian variation and individual difference of DPD activity in vivo, and has significant correlation with fluoropyrimidine pharmacokinetics, curative effect and toxicity.
这种时辰变化规律的研究结果对于时辰给药方案的设计和调整很有意义。
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The rabbits were feeded by estradiol valerate everyday as follows. Group A: E〓V 1. 8mg/d, group B: E〓V 3. 6mg/d, group C: E〓V 7. 2mg/d, group D: E〓V 3. 6mg/d+MPA 3. 6mg/d, group E was the untreated control group, group F was the untreated sham control group.
之后给予口服雌激素或联合应用孕激素共16周,给药方案如下:A组〓V 1.8mg/天,B组〓V 3.6mg/天,C组〓V 7.2mg/天,D组〓V 3.6mg/天+MPA 3.6mg/天,E组和F组均不用药。
- 推荐网络例句
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They weren't aggressive, but I yelled and threw a rock in their direction to get them off the trail and away from me, just in case.
他们没有侵略性,但我大喊,并在他们的方向扔石头让他们过的线索,远离我,以防万一。
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In slot 2 in your bag put wrapping paper, quantity does not matter in this case.
在你的书包里槽2把包装纸、数量无关紧要。
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Store this product in a sealed, lightproof, dry and cool place.
密封,遮光,置阴凉干燥处。