结论药物释放主要取决于凝胶溶蚀。
Conclusion the drug release mainly depends on the gel erosion.
提高明胶浓度能进一步延缓药物释放度。
The rate of release can be slowed down by increasing the concentration of gelatin.
磁性药物微球的组成直接影响其药物释放速度。
The constitution of the microspheres affects the rate of the drug's release.
目的验证微型药物释放胶囊及遥控装置的可靠性。
Objective To verify the credibility of the miniature medicine release capsule and the remote control device.
它可以是特别有用的药物释放的应用，如在离子导入设备。
It can be particularly useful in drug delivery applications such as in iontophoresis devices.
结论辅料用量和性质对药物释放的影响随骨架类型不同而不同。
CONCLUSION The effects of contents and properties of excipients on drug release from matrices vary with matrix types.
结果凝胶溶蚀和药物释放随着振荡频率和释放面积的增加而加快。
Results the gel erosion and drug release were increased with the increase of surface area and shaking frequency.
结果表明：甲氨喋呤脂质体的药物释放速率符合一级动力学方程。
The results showed that the drug release from MTX liposomes was in conformity with the first-order dynamic equation.
比较凝胶小球在溶出前后的形态变化，进行药物释放机理的探讨。
Through analysing the changes of gel beads before and after dissolution testing, the release mechanism of drug was studied.
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。
At the same time, the influences of the drug-fed amount on PMT and release behavior in vitro of PMT were investigated.
分别考察了上述因素对于控释片体外释放度的影响以及药物释放机制。
The factors that control the drug release character of the tablets were investigated. The drug release mechanism of the formulation was also studied.
体外药物释放评价结果表明该药物载体具有良好的缓释效果和显影性。
The results of drug release in situ showed the materials have good sustained drug release effect.
药物释放结果表明，此凝胶对难溶药物乙酰水杨酸具有增溶缓释作用。
The experimental results showed that the hydrogel was a promising material for causing solubilization and developing a long-term controlled release system.
目的对交联透明质酸衍生物制备的载药水凝胶膜进行体外药物释放研究。
OBJECTIVE To evaluate drug release properties in vitro of the hydrogel films made of cross-linked hyaluronic acid derivatives.
科汉解释说，我们得到的药物释放率远远超过我们熟知的其他药物释放镜片。
"The rates of drug efflux that we got from these are vastly more than any other drug-eluting lens that we are familiar with," Kohane said.
方法采用相似因子法考察影响药物释放速率的因素，并考察了其释药机理。
Methods the influencing factors on the drug release were investigated by use of similarity factor method.
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。
The effects of many factors including formulation and technique on the release behavior of tablets were investigated.
概述了塑料微孔膜在分离、保鲜、助长、药物释放、人造器官等领域的应用。
The application of the membranes in separation, preservation, fosterage, medicament release and artificial organ etc is also reviewed.
在本次研究中对药物释放效率的考察表明每日给药一次足够用于对病毒的治疗。
The efficiency of drug release in this study has also confirmed that one single dose a day is most likely enough in treating the virus.
理想的纳米粒载体应有特异靶向性、药物释放可控性，无毒性以及可生物降解等。
The perfect nanoparticle vectors should be specific-targeting, controlled release, nontoxicity? biodegradation, and so on.
目的考察阳离子型壳寡糖硬脂酸嫁接物胶团的理化性质及载药胶团的体外药物释放。
Aim to prepare the micelles of stearic acid grafted chitosan oligosaccharide and investigate the drug release from micelles.
目的用人工神经网络模型定量的预测HPMC的量和其固有黏度对药物释放的影响。
Objective To use ANN to quantitatively predict the influence of the amount of HPMC and its internal viscosity on allopurinol release from HPMC sustained release tablets.
方法采用无膜溶出模型，考察释放面积、振荡频率对眼用凝胶溶蚀及药物释放的影响。
Methods The non-membrane model was introduced to observe the influence on the drug release and gel erosion for surface area and shaking frequency.
经口给药的DDS大多以延长药剂在胃内滞留时间和改善药物释放为其设计出发声点。
The formalation design for oral DDS or GIDS is essential to achieveprolonging stomach residence time and improving drug release.
对模型参数的最佳评价通过最小化模型模拟和实验测定间的药物释放动力学差别来获得。
Optimal estimates of the model parameters were obtained by minimizing the difference between model simulation and experimentally measured drug release kinetics.
聚合物间的这种特殊的互聚物复合形成现象可用于设计具有不同释药行为的药物释放系统。
This specific property of interpolymer complexation may be utilized to design drug delivery systems of various release behaviors.
下一步是要找到比注射更好的药物释放系统；胶体与火柴棒大小的植入剂都已在讨论范围内。
The next step is to find a more appealing delivery system than shots; both a gel and a matchstick-sized implant have been discussed.
甲氨喋呤脂质体在不同输液中药物释放速率常数不同。温度升高、药物释放速率常数增大。
MTX liposomes in different infusion solution gave different release rate constant when the temperature was going up the release rate constant was going up too.
医生也会根据一些信息对其遥控，这些信息包括药物释放时间、病人的年龄、体重、病史等。
A doctor would also program into a remote control information such as when the drug should be administered, and the patient's age, weight and medical history.
医生也会根据一些信息对其遥控，这些信息包括药物释放时间、病人的年龄、体重、病史等。
A doctor would also program into a remote control information such as when the drug should be administered, and the patient's age, weight and medical history.
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