给药

It can be used to make artificial dialysers,artificial skins,oral ulcer membranes,and periodontal tissue GTR membranes and drug membranes.

为对医药领域开发和研制壳聚糖膜提供一些借鉴，综述了壳聚糖膜可以应用于医药领域的优良性能：易降解性、生物相容性、促创伤愈合性、抗菌性和药物缓释性；以及壳聚糖膜剂的一些医药用途，有人工肾膜、人工皮肤、口腔溃疡膜、牙周 GTR膜、不同给药途径药膜等。

The effect and adverse drug reaction of Diazepam were statistically analyzed.

统计分析地西泮不同给药方式的治疗效果和不良反应。

For example, find all mention of medications, dosages, routes of administration, etc.

例如，找出所有提到的药物、剂量、给药途径，等。

F951 distributes extensively into tissues,but the relative affinity varies enormously, being higher for kidney, liver, spleen and bone marrow and lower for heart, lung, brain, intestine, skin, fat and reproductive gland. At about 2 hours postdose, the concentrations of F951 reached the maximums and began to reduce slowly.

结果显示，F951在小鼠体内的分布不均匀，在肾、肝、脾、骨髓中分布浓度明显高于其它器官，在给药后8小时内单位重量组织中的F951含量教高，以后开始缓慢下降；F951在小鼠的心、肺、脑、肠、皮肤、脂肪、生殖腺中也有低水平的分布。

An animal model of DM was established byinjecting a little dosage ofSTZ in high fat-fed rats. When the model was establishedsuccessfully, corresponding medicine were supplied for 12 weeks and then the ratsweight、biochemical criterions, blood glucose, GSP and the content of NO, ET, hs-CRP,AR, IL-6, TNF-a in rats serum were mensurated.

给药12周后，观察冬连胶囊对大鼠生长状态、体重、生化指标、血糖、糖化血清蛋白、血浆一氧化氮、内皮素、血清高敏C—反应蛋白、醛糖还原酶、白细胞介素—6(IL-6)、肿瘤坏死因子的影响，及大鼠视网膜微血管形态学、病理改变。

RESULTS:The concentration-time curves of two preparations fitt ed to a one-compartment model.The peak plasma levelsof ambroxol test drug and reference drug were(385.5±98.3)and(378.9±90.3)μg .

结果：经3p97计算程序拟合，两者在体内的过程皆符合血管外给药一室模型，采用梯形法计算的两者AUC0-t均值分别为(2421.2±761.3)μg 。

METHODS:Freund′s complete adjuvant was injected into the footpads and tails of rats,to induce experimental arthritis.Aceclofenac was orally administered from 19th day when the secondary response was clear,its therapeutic effects on the footpad swelling and weights of thymus,spleen and adreal were observed.

大鼠足跖及尾部注射弗化完全佐剂，形成实验性关节炎，19d后明显出现继发性反应，此时分组给药，观察醋氯芬酸对关节炎大鼠左、右后足跖肿胀及胸腺、脾脏和肾上腺重量的影响。

Results: fops had inhibitory effect on o 2 production in vitro, having a 50% of inhibitory concentration (ic50) of 3.866×10-6 g/ml, and a weak inhibitory effect on h2o2 production with a ic50 of l.668×10-3 g/ml but showed a potent inhibitory effect on the various free radicals produced by "respiratory burst" of human leukocyte. fops (20, 40, 80 mg/kg) increased the sod activity in myocardial tissue, liver and kidney of mice and decreased the mda content of myocardial tissue, liver, kidney and spleen of mice.

结果：在体外阿里红多糖可有效的清除o 2，其ic50为3.866×10-6；对h2o2的清除作用很弱，但能抑制人血嗜中性粒细胞&呼吸爆发&产生的多种自由基，ic50为1.668×10-3；阿里多红糖（20、40、80 mg/kg）可明显增加小鼠心脏和肝脏中sod的活性，其中剂量为40、80 mg/kg的阿里红多糖可明显增加肝脏中sod的活性，同时各给药组均可明显减少小鼠心脏、肝脏、肾脏和脾中mda的含量，与对照组相比较差异有统计学意义（p.05）。

We discuss the benefits and challenges of oral chemotherapy from the perspectives of patients, healthcare providers and healthcare funders.

本文主要从患者、护理和保健者的角度讨论口服给药化疗的益处和难处。

Objective To modify the method of gavage administration in guinea pigs.

目的 改良豚鼠灌胃给药的方法。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。