生理盐水

Used for the wound has not to be stitched up, can Direct sprayed the low and small wound without enswathed after cleanout the wound by saline water.

对无需缝合的浅小创面可先用生理盐水或清水清洗，然后直接喷洒本品后不用包扎，每日2-3次。

The surface tension of silicone oil can be reduced to 12 to 14 ergs/cm2 by the absorption of lipoprotein.

实验测得气体与生理盐水交界面的表面张力约为60ergs/cm2，而硅油的表面张力实测为33 ergs/cm2，当注入眼内以后，随着硅油理化性质的改变，表面张力还会进一步下降。

Methods The immunofluorescency, Western blotting and RT-PCR were performed on mouse liver tissue obtained from 4 experimens pcDNA3.1(+-HBX and 1 normal control, 24 h after delivery the HBX gene eukaryon expression vector pcDNA3.1-HBX into mouse by the means of hydrodynamic injection.

实验动物分成模型组和对照组，模型组利用已构建的含有HBX基因的真核表达质粒pcDNA3.1-HBX，对照组以等量生理盐水代替，采用流体动力学法将质粒经尾静脉高压注入小鼠体内，24h后取小鼠肝组织，行免疫荧光、RT-PCR和Western blot法从不同水平检测HBX在小鼠肝组织内的表达情况。

Five weeks later, comedones on rabbit in group Zi had mostly extincted, which were near to that on normal rabbit, and there was a faint or negative SP expression; In group sulfur, comedones on rabbit had a lot change and SP was positive or faint positive. While in group 0.9% normal saline nothing had happened, SP was positive.

外用药3周后紫金霜组兔耳粉刺大部分消退，基本接近正常对照兔，SP呈弱阳性或阴性；硫磺粉刺组粉刺部分减少，SP呈阳性或弱阳性；生理盐水组无明显变化，SP呈阳性。

MethodsWe divided rats into five groups:A,B(group of Fuhuangshengjiyuchuang factis),C,D and E,and then treated them by different therapeutic methods.The changes of TGF-β1,Smad3 by immunohistochemistry at 18th day were observed.

方法采用改良付氏大鼠模型为研究对象，分为生理盐水组、复黄生肌愈创油膏组、补虚方组、祛瘀方组、康复新组，运用免疫组化法分别研究各组第18天创面瘢痕组织中转化生长因子β1（TGF-β1）、Smad3的变化。

Mg.kg-1.d-1 by gavage for 12 weeks, and the IR and NC groups were given an identical volume of physiological saline.

mg.kg-1.d-1）12周，IR组和NC组给予相同体积的生理盐水。

At the same time, Rats in normal and model groups were given a dose (O.lml ?kg"1) of normal saline, rats in other two groups were given Verapamil 0.4mg "kg"1 -. SSM 22.5mg ?kg"1 respectively by gastric gavages.

正常组及模型组于造模同时均予以生理盐水0.1ml·kg~(-1)灌胃，西药组及中药组则分别予以Vp0.4mg·kg~(-1)、SSM22.5g·kg~(-1)灌胃，并按此剂量每天灌胃1次，直至处死。

Methods BTXA labeled with125Iwas obtained. The radioactivitymeasurementwas taken tomeasure the solubility ofBTXA in gel and BTXA solution. The rightgastrocnemiusmuscles of12 SD ratswere injectedwithBTXA geland the leftgastrocnemiusmuscles injectedwith normal salinewere used as controls. HE staining and 1% gold chloride stainingwere used to study the tissue changes 6 months and 12 months afterBTXA gel injection and transmission electronmicroscopy was used to observe the ultrastructural changes.

将BTXA行示踪标记配制125I-BTXA水凝胶与125I-BTXA水溶液，进行样品放射性强度测定。12只SD大鼠用随机数字表法分为A、B两组，每组6只，大鼠右侧腓肠肌注射BTXA水凝胶，左侧腓肠肌注射等体积生理盐水作对照，于注射后6个月、12个月切取腓肠肌标本，常规病理HE染色、1%氯化金染色，透射电子显微镜观察组织结构变化。

Haemolysis test: With distilled water and stroke-physiological saline solution as positive and negative controls respectively, the rate of haemolysis of 100% and 50% eluent of PLGA/RIP were studied.

溶血实验：以蒸馏水和生理盐水分别为阳性、阴性对照，观察PLGA/RIP洗提液原液和0.5 g/L洗提液的溶血率。

Methods The purified general bacteria in broth culture for46hourswerepreserved in glycerol-physiological saline,the purified streptococcus and Neisseria scraped from the agar culture were preserved in fresh sheep-blood which was added suitable glycerol-physiological saline,the purified fungi were cultivated in half-solid culture;-20℃general bacteria and fungi,-80℃streptococcus and Neisseria.

将普通细菌的菌种纯化后接种于普通肉汤管，4～6h增菌后，加入适量甘油-生理盐水保存液，-20℃冰箱保存；链球菌属和奈瑟氏菌属的菌株纯化后，用接种环取菌置于新鲜脱纤维绵羊血中，加入适量保存液，-80℃低温冰箱保存；真菌菌种纯化后接种于带硅胶塞的半固体培养基，25℃培养24h后，-20℃冰箱保存。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。