给药

Effect of A_3 on dimethylbenzene-induced mice ear edema Method:After peroral A_3 3 days, the mice ear edema models induced by dimethylbenzene were prepared. The mice ear edema was tested at 1 h.

A_3对二甲苯所致小鼠耳廓肿胀的影响方法：连续灌胃给药3天(1次/天)后，采用二甲苯制备小鼠耳廓肿胀的炎症模型，观察二甲苯致炎后1 h药物对小鼠耳肿胀的影响。

As one of aliphatic polyether-ester, poly (p-dioxanone) shows not only excellent biodegradability, biocompatibility and bio-absorbability, but also good flexility, tensile strength and knot strength. The PPDO has already been used in some biomedical materials such as suture, bone repair device and may have potential application in peroral or parenteral drug delivery systems.

聚对二氧环己酮是脂肪族聚醚酯的一种，不仅具有优良的生物降解性、生物相容性和生物可吸收性，而且具有出色的柔韧性、抗拉强度和结节强度，可应用于生物医用材料，例如手术缝合线、骨科修复材料等，并在口腔和非肠道给药系统中具有潜在的应用前景。

Effect of A_3 on carrageenin-induced rats paw edema Method:After peroral A_3 4 days, the rats paw edema models induced by CGN were prepared. The rat paw edema was tested at

A_3对角叉菜胶所致大鼠足肿胀的影响方法：连续灌胃给药4天(1次/天)后，采用角叉菜胶制备大鼠足趾肿胀的炎症模型，观察角叉菜胶致炎后1，2，4，6 h药物对大鼠足趾肿胀的影响。

Results Phagocytize ac-tivity and the production ability of IL-1and NO in the mice treated with marine algal polysaccharide were increased obvi-ously than that in non-medication group.

结果 海藻多糖处理组小鼠腹腔巨噬细胞吞噬功能、产生IL-1和NO能力较未给药照射组明显增强（P均。05）。

The composition may optionally be formulated with a pharmaceutically acceptable carrier for systemic or topical administration.

组合物可以可选地与用于全身或局部给药的可药用载体配制在一起。

Many patients experience anxiety in the immediate preoperative period, and pharmacologic management is quite acceptable.

大多病人在术前刻都存在焦虑状态，因此术前给药是被广泛接受的。

Drug absorption is determined by physicochemical properties of drugs, their formulations, and routes of administration.

药物的吸收是由药物的理化性质、药剂的配方及给药途径所决定的。

Objective:To observe the effect of Yunkang Capsule on mice cerebral pial microcirculation. Methods: The

组、阳性对照组和正常对照组，分别灌胃给药10 天后，开颅窗观察小鼠软脑膜微循环；然后在软脑膜局部滴加去甲肾上腺素复制

The pial arteriolar dilator response to hypercapniawas significantly attenuated in the clonidine group (14%±4%, 4%± 4%, 6%± 6%, and 5%± 7% for beforeand 30, 60, and 90 min, respectively).

可乐定组软膜小动脉对高碳酸血症的扩张反应明显减轻（给药前及后30， 60， and 90 min 时分别为14%±4%，4%±4%，6%±6%和5%±7%）。

Results compared with the control group, the rats in the lactacystin group began gradually to have some behavioral symptoms, for example, the spontaneous motors decreased progressively, tardive dyskinesia, piloerection, tremor, contralateral rotations induced by apomorphine increased gradually.

结果 实验组给药后，随着时间推移大鼠开始出现渐进性自发性活动减少、动作缓慢、对外界刺激不自主竖毛、震颤；阿扑吗啡诱导的向健侧旋转运动逐渐增多。

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。