The drug release model and the envelop rates of the testing group remained stable within the storage date.
试验组在贮存期内的释药模式及包封率均维持稳定。
Furthermore, our model incorporates mechanisms by which the processes underlying drug release from a polymer matrix can be quantitatively analyzed.
另外，我们的模型整合机制使药物从聚合物基质中释放的过程可以被定量分析。
Methods The non-membrane model was introduced to observe the influence on the drug release and gel erosion for surface area and shaking frequency.
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。
A mathematical model describing the drug release from porous polymer was established by using the species continuity equation.
以组分的连续性方程为基础，建立了药物从多孔骨架聚合物系统中释放的数学模型。
Vitamin B12 was selected as a model drug and the in vitro release properties was studied.
以维生素b12为模型药物，研究药物的释放性质。
The drug release experiment of compression spring model with pure magnetic mechanism trigger was successful.
用纯磁力机构的压缩弹簧释放方式成功模拟了药物释放试验。
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。
OBJECTIVE To develop a novel rapidly release oral solid dosage form orally disintegrating tablet using acetaminophen as the model drug.
目的以对乙酰氨基酚(扑热息痛)为模型药物制备新型口服速释剂型口腔崩解片。
Optimal estimates of the model parameters were obtained by minimizing the difference between model simulation and experimentally measured drug release kinetics.
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。
Aim: to explore the effects of granulomatous inflammation model in rats established by the application of drug sustained release and Bacillus Calmette-Guerin (BCG).
目的：观察应用药物缓释剂和卡介苗构建大鼠局限性炎性肉芽肿模型的效果。
Taking Ib as a model drug, the drug release behaviors of the capsules were studied.
以布洛芬为模型药物，初步研究了微囊载体的缓释行为。
Objective To prepare pulsed-release capsule(PRC) using famotidine(FM) as a model drug and to explore the way of preparing pulsed-release pellets(PRP).
目的制备以法莫替丁为模型药物的脉冲控释胶囊；探索制备脉冲微丸的方法。
OBJECTIVE To predict drug release from the extended formulations by grey maths model.
目的运用灰色数学理论预测长效缓释蛋白微球的体外释药过程。
The mechanism of release results from the matrix rode and drug diffusion of matrix by describing the drug release curve using Ringer-Peppas model.
释药机制探讨表明：经膜控和骨架杂化控制释药的模型用一级动力学方程解释较好。
The effects of different drug loadings on the drug release rate were simulated and compared with other data to validate this model.
模拟不同载药量对药物释放速率的影响并与其它数据进行比较，以此来验证此模型。
Objective To prepare indomethacin immediate release capsules by means of hot-melt extrusion (HME) using indomethacin as the model drug.
目的以热熔挤出技术制备吲哚美辛速释胶囊。
Using insulin as the model drug, the encapsulation capability and sustained release of the nanoparticles were studied.
以胰岛素为模型药物，研究纳米粒的包封和释药性能。
Using insulin as the model drug, the encapsulation capability and sustained release of the nanoparticles were studied.
以胰岛素为模型药物，研究纳米粒的包封和释药性能。
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