烧瓶振荡法是动态测试抗菌性的方法，与浸渍法相对，原为非溶出性纺织品而设计。
Flask shaking method is commonly used for dynamic test antimicrobial activity. In contrast to leaching antimicrobial test, this method is especially designed for non-permeable textile products.
通常以硅酸钠水溶液作为单体硅源，氢氧化钠溶液作为碱激发剂以提高原料的溶出性。
Generally, sodium silicate solutions are used for monomer sources added with caustic soda solutions for activation of leaching out of fillers.
如果所研究的溶出度平均值显示随时间的下降趋势，该趋势预示了在有效期内保持高于所注册Q值的难度，这种事实可能预示符合性警戒。
If the study's dissolution average shows a decreasing trend with time that indicates difficulty remaining above the registered Q-value through expiration, this fact could indicate a compliance alert.
方法试验采用稀盐酸做为溶出介质，依法确证辅料的干扰程度及含量测定方法的可行性。
METHODS Used diluted hydrochloric acid as dissolvent, to ensure the disturbance degree of accessories and proof the feasibility of testing method.
分析了高压溶出系统脉冲缓冲器设置安全连锁的必要性，介绍了压力连锁及料位连锁的实现。
This paper analyzes on the importance of pulse buffer's safe interlock control, and introduces the realization of the pressure interlock and level interlock.
本文就石灰活性对氧化铝溶出率的影响和提高石灰活性的方法进行研究，提出了提高活性的必要性和方法。
The paper studies the influence of lime activation on the digesting efficiency of alumina and the method of advancing the lime activation, proposing the necessity and the method upgrading activation.
简述了溶出磨系统集中监控系统软、硬件的构成及各子系统的功能，溶出磨系统集中监控的必要性。
This essay introduce the necessity of using mill concentrate supervise and control and the mill concentrate supervise and control system soft - and hardware structure.
有必要进行制剂溶出度的实时监测，确保药品的内在质量，保证用药的安全性及有效性。
It suggests that we should take the real-time dissolution test to ensure the intrinsic quality of medicines and drug safety and efficacy.
结果：各厂家溶出参数之间有极显著性差异（P＜0．01）。
RESULTS: There is significant differentiation in dissolution parameter of each pharmaceutical factory(P < 0 . 01 ) .
结果显示，桑沟湾沉积物中POC、TN和TP的再溶出速率存在明显的区域差异和季节性变化。
It was indicated the release rates of POC, TN and TP from sediment manifested obvious region diversity and seasonal variation.
目的：探讨中药制剂蝙蝠葛酚性碱片的溶出度，为临床用药提供参考。
Objective: To investigate the dissolution of phenolic alkaloids of menispermum dauricum tablet(PAMDT), and supply some information for clinical medication.
分析了分散片的处方和工艺特点，及其在药物溶出度和生物利用度方面的优越性。
The formulation, technological characteristics, the superiority in drug dissolution and bioavailability of dispersible tablets are summarized.
结果不同批号样品间的溶出度有显著性差异。
Results The dissolution parameters of Huanglianshangqing Tablets of different batch number showed significant difference.
目的通过对甘羟铝片溶出度进行方法学研究，提高甘羟铝片的质量可控性，确保药品的临床疗效。
OBJECTIVE Through dissolution behavior study of Dihydroxyaluminium Aminoacetate to enhance its quality controllability, and guarantee clinical curative effect.
分光光度法和数粒法测定不同释放天数的树脂包衣尿素溶出氮相关性均较好。
There are good correlated coefficient between the test by granular counted and the test by spectrophotometer.
抗菌瓷砖具有良好的抗菌耐久性，瓷砖表面仅存在银离子溶出抗菌作用。
It was shown that the antibacterial tile was antibacterial durable and the silver ion eluted from the surface of the tile was the only reason for its antibacterial activity.
试验结果表明，适当的微波处理不但可以提高大豆异黄酮的溶出率，同时可提高提取操作的选择性，是一种有效的处理方法。
The result showed that the adaptive microwave treatment not only enhanced the extracting rate, but also increased the selectivity of extracting operation. So it's a very efficient processing method.
方法：转篮法，以对乙酰氨基酚为溶出指标，用紫外分光光度法检测，提取参数，并对参数进行相关性分析。
METHODS: By using circle basket test with paracetamol as the dissolution index, detected by UV, to abstract parameters and make correlation analysis.
方法参照美国药典中溶出度仪的系统适用性校正方法。
Methods the way of apparatus suitability test is described in the United States pharmacopoeia.
质量一致性评价体外溶出曲线对比。
Dissolution curve comparison in-vitro for quality consistency evaluation;
方法采用分光光度法测定罗红霉素胶囊的体外溶出度，并对溶出参数进行相关性分析。
Methods The dissolution of roxithromycin capsules was analyzed with spectrophotometry. The dissolutive parameters of different products were compared.
目的考察维生素E淀粉软胶丸的溶出度，对其生物利用等效性进行评估。
Objective To investigate the dissolution rate of Vitamin E starch soft capsule.
通过对滴丸的质量标准如含量测定、溶出度的研究表明滴丸具有可控性、稳定性。
The ligustilide pill's quality was estimated synthetically by the study of quality standard, which proved that XiongBing-pill is stable and controllable.
方法将羧甲基淀粉钠、微晶纤微素按一定比例混合，作为片剂基本处方，以分散片的外观、崩解时限、体外溶出度及混悬性为指标进行处方筛选。
METHOD s Mixing the CMSNa and MCC in certain proportion as the basic formulation of the tablets, the appearance, disintegration, dissolution and the suspensibility were investigated.
采用离体黏附模型及二喹啉甲酸（BCA）法测定黏附微丸的黏附性及溶出度。
The BCA method and in vitro adhesive analogue were adopted to determine release behavior of the adhesive pellets and their adhesiveness.
采用离体黏附模型及二喹啉甲酸（BCA）法测定黏附微丸的黏附性及溶出度。
The BCA method and in vitro adhesive analogue were adopted to determine release behavior of the adhesive pellets and their adhesiveness.
应用推荐