A typical release behavior was observed for 30 days.
在30天内能观察到药物特有的释放行为。
The release behavior of the drug from liposome was studied by the third method for dissolution.
用溶出度第三法考察了脂质体的释放规律。
After filling capsules, compare the release behavior in vitro with that of the reference preparation.
填充胶囊后与参比制剂比较体外释放行为。
The effects of many factors including formulation and technique on the release behavior of tablets were investigated.
从处方因素和工艺因素等方面详细考察了各种因素对药物释放行为的影响。
At the same time, the influences of the drug-fed amount on PMT and release behavior in vitro of PMT were investigated.
同时，还研究了投药量对PMT的影响及PMT的体外药物释放行为。
Aim To prepare ondansetron hydrochloride osmotic pump tablets (OND-OPT) and investigate their in vitro drug release behavior.
目的制备盐酸昂丹司琼渗透泵型控释片剂(OND - OPT)并考察体外释药特性。
AIM To test gelatin microspheres of low molecular weight heparin (LMWH-GMS) release behavior; lung target behavior and stability.
目的考察低分子肝素肺靶向微球缓释性、稳定性和靶向性。
Aim To prepare Clarithromycin floating beads and investigate its buoyancy, entrapment efficiency and drug release behavior in vitro.
目的制备克拉霉素胃漂浮小丸，考察其漂浮性，包封率和体外释药行为。
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。
Objective to establish a UV method to determine the release degree of rotundine sustained-release tablets and to evaluate its in-vitro release behavior.
目的建立罗通定缓释片体外释放度测定方法，评价其体外释药行为。
OBJECTIVE To optimize the preparation method of the oridonin-loaded polylactic-acid nanoparticles, and investigate its properties and release behavior in vitro.
目的优化冬凌草甲素聚乳酸纳米粒的制备工艺，并对其理化性质和体外释药特性进行考察。
The aim of this study was to find the release behavior of active aluminum in red soil added with paper mill sludge compost(PSC) by simulating cultivating experiment.
通过室内模拟培养实验，研究赤红壤中添加富含铝盐的造纸污泥堆肥后，土壤中活性铝的释放特性。
Aim To prepare glucagon-like peptide1(GLP-1) loaded long-acting injectable microspheres and to evaluate their in vitro release behavior as well as its pharmacodynamics.
目的制备载胰高血糖素样肽-1（GLP-1）的长效注射微球，并对其体外释放特性及药效学进行考察。
Objective: To prepare compound metformin hydrochloride sustained-release capsules, and investigate the release behavior of metformin hydrochloride (MH) and glimepiride.
目的：研制复方盐酸二甲双胍缓释胶囊，并对盐酸二甲双胍(MH)和格列美脲进行释放度研究。
The cornea permeation test of formulation was studied by using rabbit corneas. Results:The formulation release behavior in vitro followed the first order kinetic equation.
结果 ：亲水凝胶材料含量越小 ，盐酸地匹福林从凝胶基质中释放越快 ，凝胶体外释药符合一级释放动力学方程 ，离体角膜渗透行为符合一级释放规律。
Conclusions Ibuprofen sustained release tablets with ideal release behavior could be prepared by selecting HPMC with different viscosity and adjusting the content of HPMC.
结论联合应用不同黏度和用量的HPMC，可制备具有理想释药行为的布洛芬骨架缓释片。
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。
Amphiphilic copolymer micelles play an important role in the field of drug delivery and their drug release behavior is strongly influenced by size and morphology of micelles.
两亲性共聚物胶束在药物控释方面有着重要应用，而胶束的尺寸形态与其药物传递行为密切相关。
Effects of formulation of drug layer, push layer and membrane on the release behavior of controlled release tablets were investigated and the optimal formulation was obtained.
考察含药层促渗聚合物、乳糖用量、助推层聚氧乙烯用量、助推层氯化钠用量及包衣液中含水量、醋酸纤维素浓度对释放度的影响，并对处方进行优化。
The factors which affect the lag time and drug release behavior were investigated, such as the thickness of the inner and outer layers, the amount of PVPP and other excipients, etc.
单因素考察发现，影响释药时滞和释药速率的主要因素为溶胀层中高效崩解剂比例、溶胀层增重及控释层增重。
CONCLUSION the adhesive property of the tablets and the release behavior of drug are relevant. Also, the formulation of buccal adhesive tablets is optimized by adjusting the composition.
结论口颊黏附片的生物黏附性与体外释药行为具有一定的相关性，通过调整处方可筛选出生物黏附性和体外释药均较理想的处方。
Objective: to develop the methods to determine the in vitro release of multi-target ingredients in Compound Danshen Sustained-release Tablets and to evaluate its release behavior in vitro.
目的：建立复方丹参缓释片多指标成分的体外释放度测定方法，评价其体外释药行为。
The factors which affect the lag time and drug release behavior were investigated, such as the type and thickness of the inner and outer layers, the type and amount of the plasticizer, etc.
本文考察了溶胀层种类和厚度、控释层包衣液类型和包衣层厚度、增塑剂种类和用量等因素对时滞及药物释放速率的影响。
The factors that influence the nutrients release behavior are as followings: membrane thickness, granule radius, diffusion coefficient, nutrients composition and nutrient dissolving property.
影响聚合物包膜肥料养分释放的因素主要有：膜厚、颗粒半径、扩散系数、养分组成及其溶解特性。
The effect of the size, surface area and porosity of particles, the property and content of drugs, as well as the properties of polymer on the drug release behavior of microcapsules are elucidated.
阐述了高分子包囊的粒径、表面积、孔度、药物性能和药含量，以及高分子包囊材料的性能对药物释放行为的影响。
Tip: To preserve the behavior of the previous release, the Check resources option was chosen as the default.
提示：要维持先前版本的行为，这个检查资源选项是默认选择的。
With the release of Ruby 1.9, this has changed: Ruby 1.9 has some changes that aren't compatible or at least change the behavior of some code.
但是有了Ruby 1.9发布以后，情况就有了变化：Ruby 1.9有了些不兼容性的变化，或是至少修改了一些代码的行为。
In this release, Xobni has also included additional user controls which will allow users to better customize Xobni's behavior.
在这次正式版本的发布中，Xobni也新增添了额外的用户控制，这一功能可以用户更好的自定义xobni的行为。
If they release it over another page element with the mouseup (fn) defined, what behavior should take place?
如果用户用所定义的mouseup (fn)在另一个页面元素之上释放鼠标，那么应该发生什么行为呢？
If they release it over another page element with the mouseup (fn) defined, what behavior should take place?
如果用户用所定义的mouseup (fn)在另一个页面元素之上释放鼠标，那么应该发生什么行为呢？
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