查询词典 release from

Release agents, carbon black; tire release agents, mold release agents brakes, aluminum alloy release agent; friction material release agent; Alloy release agent; polyurethane elastomer release agent; cement product release agent; epoxy release agent; conveyor belt release agent; solar release agent; Rubber release agent; red pomade

脱模剂，碳黑；轮胎脱模剂、刹车片脱模剂、铝合金脱模剂；摩擦材料脱模剂；铝合金脱模剂；聚氨酯弹性体脱模剂；水泥制品脱模剂；环氧树脂脱模剂；输送带脱模剂；太阳能脱模剂；橡塑脱模剂；冲头油

Taijiquan Wushi to hire a sixth-generation direct-to-human transmission, Sakyamuni disciples are headed for the release; employ extended spring release Shaolin Masters (martial arts star's father, Chen release dragons with his disciples Hill) for the deputy head; employ fifth-generation Wushi Taijiquan immediate successor the state for two Sun Jianguo, deputy head of referees; employ Chinese calligraphy, martial arts tai chi Shenquan Warren Zhang - Zhang Ying-Min, deputy head for; recruit the best young boxer with Chen Shan (Little Dragons martial arts star's father, release) for the special guidance; hired martial arts star release dragons performances for invited representatives of friendship.

聘请武氏太极拳第六代直系传人、释迦弟子释为正为团长；聘请少林寺大师释延春（武打明星释小龙的父亲陈同山的弟子）为副团长；聘请武氏太极拳第五代直系传人、国家二级裁判孙建国为副团长；聘请中华太极武术书法奇人神泉张-张映敏为副团长；聘请十佳青年拳师陈同山为特技指导；聘请武打明星释小龙为特邀友情演出代表。

All enhancers did not significantly change the transcorneal lag time of ENX. The irritancy of poloxamer and Azone was observed.? The results of in vitro release studies showed that the ENX gel based 3% HPMC K4M and 3%HPMC F4M povided sustained release of the drug over an 8-h period in vitro.Diffusion area has significantly effect on drug release, and pH value of medium and rotation rate have effcet on drug release.However, the diffusion shield has no effect on drug release. The P_ value of the preparation based on 3% HPMC F4M was 1.34-fold of conventional eye drops of ENX.

体外溶出度试验结果表明，以3％的HPMC K4M和F4M为基质制备的ENX凝胶剂的体外释放行为符合眼用缓释制剂的要求；体外释放度影响因素试验结果表明，释放面积对释放度有显著性影响，pH值和转速略有影响，而扩散屏障没有影响；离体角膜透过实验结果表明，以F4M为基质制备的凝胶剂中ENX的表观渗透系数P_(app是对照组的1.34倍，说明F4M与眼角膜的相容性较好，是一种理想的眼用制剂增稠剂，可以在眼用制剂中广泛采用。

The IR analyses proved that the polymerization effects really occurred. The BET adsorption test indicated that the adsorption amount of MIPMs to LMD was as three times as that of non-imprinted microspheres. The controlled release test indicated that the release ratio of LMD on NIPMs was linearly increased with increasing time, which suggests that the release process is completely controlled by diffusion. Meanwhile, the release ratio of LMD on MIPMs was curvedly increased with increasing time, which indicates that the release process is controlled by both diffusion and the imprinting effect.

药物扩散实验表明， LMD在非印迹微球上的释药率几乎与时间呈直线关系，说明其释药过程完全受扩散控制；而LMD在MIPMs上的释药率则呈曲线上升趋势，说明其释药过程除了受扩散控制外，还受到药物模板分子与MIPMs之间的印迹效应的协同作用的控制，从而达到了缓释药物分子的目的。

No entire nitrendipine crystals were observed visually in SEM photos. The results of X-ray diffraction and differential scanning calorimetry analysis indicated that the crystalline form of nitrendipine was highly dispersed in microspheres, so as amorphous state. The drug release rate of microspheres could be controlled with adjusting the ratio of solid dispersion carriers and retarding agents formulated. The agitation speed and temperature of the preparation process have distinct effect on micromeritic properties of microspheres. The release profiles of the microspheres were mainly affected by the stirring rate of paddle, the concentration of SDS and pH of dissolution medium. Cooling speed and time, however, have no evident influence on the drug release rate of the microspheres. The dissolution data showed that the mechanism of drug release from microsphers was mainly diffusion-controlled. The incorporation efficiencies of 3 batches sample were exceed 96. 8％, which implied that the current method was suitable for design sustained-release dosage form for poorly water-soluble drug.

在扫描电子显微镜下观察，在微球内外未发现尼群地平的完整结晶，X-射线粉末衍射和差示扫描量热试验结果也显示，尼群地平已经被高度分散在微球中；微球的释药速度可通过调整处方中固体分散体载体和阻滞剂的比例控制；制备温度和搅拌速度对微球的质量影响较大；溶出仪的搅拌速度，释放介质的浓度和pH对微球的释放有较大的影响；制备过程中的冷却速度和冷却时间对微球的释放行为影响不很明显；方程拟合的结果表明缓释微球的释药行为符合扩散机制；测定三批微球样品的包封率均在96.8％以上，表明该法适合于制备难溶性药物的缓释微球。

The vitro release result which used theophylline as model drug showed, the release behavior can divide to sharp release 、 relaxedly release and equilibrium release periods.

以茶碱为模型药物，模拟体外释放的结果表明，共聚物胶束对茶碱的体外释药可分为突释、缓慢释放、平衡释放三个阶段。

The slow-release performance of these films and the factors influence the slow-release performance of films were also studied. The time that algaecide need to release out from film completely was between 20 min and 48 h, indicating all of the drug films had the slow-release property.

此外，本论文以异噻唑啉酮作为除藻剂，甲壳素、壳聚糖、聚乙烯醇等高分子材料作为载体，研究了异噻唑啉酮缓释药膜的制备、缓释性能以及各因素对其缓释性能的影响。

The results calculated by the Elovich rate equation showed that K release rates from 1 mol.L-1 HNO3 extraction ＞those from 2 mol.L-1 HNO3 extraction ＞those from H-resin extraction. Elovich equations combining with the data of H-resin and 2 mol.L-1 HNO3 successive extraction could well described the release characteristics of soil K. The correlation coefficients of the equations reached most significant levels (r＝0.956**—0.999**), and standard errors of specific K release capacities between the vaules calculated by the equations and those measured by both successive extractions were smaller(s=1.61 and 3.52). The specific release rates of soil K calculated by the Elovich rate equations were significantly correlated with the indices of soil K availability (the amounts of easily available K, nonexchangeable K, total available K in soils and K absorbed by ryegrass).

研究结果表明：1 mol.L-1 HNO3提取法的释K速率＞2 mol.L-1 HNO3提取法的释K速率＞氢饱和交换树脂提取法的释K速率；氢质交换树脂和2 mol.L-1 HNO3提取法结合Elovich模型较理想地描述了土壤K素的释放特性，拟合方程的相关系数均达极显著水平(r＝0.956**-0.999**)，土壤特征累积释K量的计算值与实测值的标准差较小(s=1.61和3.52)，且通过速率方程计算的土壤特征释K速率与K素有效性指标(速效K、缓效 K、有效K及黑麦草总吸K量)的相关性也较为密切。

The loading method and the quantity of linker had greater effect on in-vitro release curve. Release curve of incubation-absorption and entrapping method had two phases—quick release phase and slow release phase. And the first phase lasted about one hour and released 70% drug.

载药方法和交联剂用量对释药曲线有显著影响，吸附法和包埋法制备的载药DSMs的释药曲线明显分为快速释药阶段和缓慢释药阶段，第一阶段持续约1 h，释放药物的70%左右。

Oxalic acid loading substantially stimulated soil P release from A1 horizon, showing a linear relationship; but its effect on B horizon soil was relatively negligible, especially at low oxalic acid concentrations mmol L^(-1. Oxalate solutions 0.5~20.0 mmol L^(-1 oxalic acid adjusted to pH 5.16 with 10.0 mmol L^(-1) NaOH had a much higher (1.51~2.98 times) soil-P-release effect than oxalic acid solution the same in oxalate concentration. Therefore, the mechanism of oxalic acid/oxalate triggering release of soil phosphorus is assumed to be dominated by ligand-exchange or complexing reactions of oxalate anionC2O(superscript 2- subscript 4 but not simply acid-dissolving effect. The effect of oxalate anion on soil phosphorus release was found to be somewhat cumulative, i.e. the amount of P released was primarily controlled by the cumulative oxalate loading rate, relatively independent of the manner of oxalate addition (one-time or sequential).

结果表明，草酸能显著促进暗棕壤A层磷的释放，土壤磷溶出量随草酸溶液浓度升高而线性增加；但对B层土壤磷的释放效应相对较弱，草酸浓度低於5mmolL^(-1)时B层磷的释放不明显。pH5.16草酸钠溶液比相同浓度的草酸溶液具有更高的解磷效率，在设置二者浓度为0.5~20.0mmolL^(-1)时，前者的解磷量是后者的1.51~2.98倍，推断草酸盐溶液或凋落物淋洗液中草酸类物质促进暗棕壤磷释放的主要机理在於草酸阴离子C2O(上标 2-下标 4配位反应。

You have to walk your own alk in this life.

次生中你必须走自己的路。

To start with, the thesis analyses ***ism in terms of the generic masculine words, word order and semantic derogation of women in greater detail.

论文首先从阳性词泛指，词序，词义的贬降等方面对英语中的性别歧视现象进行了详细的分析。