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。
Objective To study the preparation technique and in vitro drug release of adriamycin gelatin microspheres (ADM-GMS).
目的对阿霉素明胶微球（ADM-GMS）的制备工艺及体外释药特性进行研究。
OBJECTIVE To evaluate drug release properties in vitro of the hydrogel films made of cross-linked hyaluronic acid derivatives.
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 study the preparation process, assay and in vitro drug release of adriamycin polylactic acid microspheres.
目的：对阿霉素聚乳酸微球的制备工艺、含量测定及体外释药特性进行初步研究。
According to the literature, UV spectrophotometry was developed for the investigation of physicochemical properties, content and drug release in vitro.
建立了紫外分光光度法，用于盐酸氯米帕明基本理化性质、片剂释放度和含量的测定；
Objective:To study the release characters in vitro of Vinpocetine self- microemulsifying drug delivery system (VIN-SEDDS).
目的：研究长春西汀自乳化释药系统（VIN-SEDDS）的体外释药特性。
OBJECTIVE To study the preparation of aciclovir loaded albumin microspheres (ACV BSA MS) and evaluate its morphology, drug loading and release in vitro.
目的优化阿昔洛韦白蛋白微球的制备工艺，并对其形态学性质、载药量、体外释药进行考察。
Test of weight, size, drug concentration, mechanical function and antibacterial test and in vitro release study were done to evaluate the DDS.
对DDS药棒进行重量、大小、含药量、机械性能测试和抑菌实验、体外释放实验研究。
Microscopic morphology, diameter and drug-loaded amount of the micelles were examined by means of TEM, DLS and UV respectively, and their in vitro drug release rates were measured.
通过透射电镜观察、动态光散射测定、紫外吸光度测定等手段分析胶束的微观形态、粒径大小和载药量、测定了载药胶束的体外释药速率。
AIM To develop a novel pulsatile drug delivery system of which the lag time is cont rolled by an erodible plug (EP) and evaluate its release characteristics in vitro.
目的制备一种由溶蚀塞控制时滞的新型脉冲给药系统并对其体外释药行为进行评价。
A few of evaluation methods for drug release in vitro of sustained-controlled matrix tablets were introduced in this review.
本文简要介绍了几种缓控释骨架片药物体外释放行为的评价方法。
Objective To compare in vitro antitumor effects of controlled biodegradable drug release system and simplex anti-tumor drug in the patients with glioma.
目的比较可生物降解药物缓释体与单纯抗瘤药物体外抗胶质瘤细胞的作用。
The in vitro test of IBU loading and release illustrated the system had a great potential use for thermo-responsive controlled drug-release.
对最终体系进行的体外药物布洛芬（IBU）的装载和释放测试表明，该体系在温度响应控制药物释放方面有着较大的潜在应用前景。
OBJECTIVE:To investigate the characteristics of drug release and the factors affecting the in vitro dissolubility of diclofenac potassium double-layer tablets(DPD).
目的：考察双氯酚酸钾双层片的体外释放特征及其影响因素。
RESULTS Using the release rate of Rhein from film as an evaluation index, the in vitro drug releases were well.
结果以膜剂中大黄酸的释放度为评价指标，膜剂体外缓释效果良好。
The in vitro drug release profile of the HPCD complex and liposomes entrapping cinnarizine-HPCD complex were evaluated.
评价单纯包合物和包合物脂质体的体外释放行为；
The solubility of CH331 in outer aqueous phase played a significant role in encapsulation efficiency and in vitro drug release of microspheres.
CH331在外水相中的溶解度影响微球的包封率和体外释药行为。
The drug loading rate, encapsulation efficiency, particle distribution and in vitro release of Lac-NCTD from liposomes were investigated, respectively.
考察了药物与磷脂的复合率，磷脂复合物脂质体的包封率，粒径大小和分布，以及体外释药特性。
The pattern of drug release for 30 days in vitro fitted to zero order release plot, with an initial burst effect at the first day.
体外释放第一天呈突释效应，而后药物释放基本符合零级动力学过程。
The drug-loading rate of this chitosan-levofloxacin sustained-release microsphere is 43.88%. Its in vitro dissolubility is good.
该方法制备的左氧氟沙星-壳聚糖缓释微球载药量为43.88%，体外累积释放度的线形关系良好。
In vitro release study showed that polyanhydride erosion is the mechanism of drug controlled release.
体外释放研究表明，聚酸酐的溶蚀是控释的机理。
Methods Orthogonal design was used to optimize the formulation of the tablets, and in vitro drug release was investigated with an UV method.
方法采用正交试验设计法对片剂处方进行筛选与优化，确定最佳处方并制备马来酸罗格列酮胃漂浮缓释片剂；
CONCLUSION: the molecular mass of dextran has great influence on the drug release of conjugates in vitro. PLD2 and PLD50 have potentials in colon specific delivery of prednisolone.
结论：葡聚糖分子质量对强的松龙葡聚糖连接物的体外释药有明显影响，PLD 2,PLD5 0具有结肠定位释放潜力。
The entrapment efficiency, drug load content, in vitro release and stability of Bre-CS-NP were studied.
并进行了灯盏花素壳聚糖纳米粒包封率、载药量、体外释放度、稳定性等试验研究。
The drug loading, entrapment efficiency, diameter of nanoparticles and particle diameter distribution, shape and release curve of nanoparticles were investigated in vitro.
对纳米粒的载药量、大小及分布、形态及体外释放等进行了研究。
OBJECTIVE To prepare clindamycin hydrochloride microcapsule by means of intra liquid desiccation and to determine its in vitro drug release.
目的 采用液中干燥法制备盐酸克林霉素微囊，并考察其体外释药特性。
CONCLUSION the drug release percents and the tumor control rates of CCNU-TSL are improved significantly compared with lomustine solution in vitro.
结论洛莫司汀热敏脂质体在相变温度时，体外释药明显增加，体外抑瘤效果明显提高。
METHODS The microcapsule was prepared using ethyl cellulose as coating material. The influencing factors of in vitro drug release were investigated by paddle method.
方法以乙基纤维素为囊材制备微囊．用浆法研究其体外释药的影响因素。
Conclusions The glipizide film-controlled sustained-release pellets were successfully prepared and the in-vitro drug release conformed to the requirements of the sustained-release formulation.
结论成功制备了膜控型格列吡嗪缓释微丸，体外释放符合缓释制剂要求。
Conclusions The glipizide film-controlled sustained-release pellets were successfully prepared and the in-vitro drug release conformed to the requirements of the sustained-release formulation.
结论成功制备了膜控型格列吡嗪缓释微丸，体外释放符合缓释制剂要求。
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