Abstract: Objective: To develop the quality standard of ondansetron hydrochloride sustained release capsules.
文章摘要：目的：制定盐酸恩丹西酮缓释胶囊的质量标准。
The invention relates to compound tamsulosin and finasteride sustained release capsules and a preparation method thereof.
本发明涉及一种复方缓释胶囊及其制备方法。
Objective: To study the floating and sustained release performance of Xiaojin Cinnabar Floated sustained release Capsules.
目的：研究小金丹漂浮缓释胶囊的漂浮、缓释性能。
To establish a method using HPLC to determine the assay of Isosorbide 5 - mononitrate (ISMN) in its sustained release capsules.
建立了高效液相色谱法测定5—单硝酸异山梨酯缓释胶囊中5—单硝酸异山梨酯的含量方法。
It might, for example, be used to package together drugs in slow-release capsules of greater sophistication than is now possible.
举个例子，它可能被用来把多种药物包裹在胶囊中，然后在比现在更复杂的环境中缓慢释放。
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。
OBJECTIVE to prepare sustained-release capsules Loaded with silymarin solid dispersions and to evaluate its releasing features in vitro.
目的：制备水飞蓟素固体分散缓释胶囊并考察其体外释放度。
Methods Dextromethorphan Sustained-Release capsules of lasting antitussive were observed by acid citric induced cough model of guinea pig.
目的观察氢溴酸右美沙芬缓释胶囊的镇咳作用及镇咳作用时间。
CONCLUSION the method is an accurate for the drug release determination of Glipizide Sustained release Capsules, the analysis is out of interference of excipients.
结论方法结果准确，不受制剂中辅料的干扰，适用于格列吡嗪缓释胶囊的释放度测定。
OBJECTIVE: To optimize the conditions for the extraction and purification of the active components of Epimedium Herb and Drynaria in Gugu sustained-release capsules.
目的：优选固骨缓释胶囊中淫羊藿、骨碎补有效部位提取和分离纯化工艺的最佳条件。
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。
A laboratory method of preparing controlled release capsules floated in artificial gastric juice was developed by crosslinking the gelatin capsules with formaldehyde vapor.
以对乙酰氨基酚为模型药物，采用甲醛蒸汽交联明胶胶囊的方法制备了胃内滞留型控释胶囊。
Bioadhesive study showed that the bioadhesive ability of bioadhesive sustained release capsules to rats stomach and small intestine muscle strip mucosa was stronger than that of conventional ones.
生物粘附性研究表明缓释胶囊的内容物与大鼠离体胃、肠组织的粘附力明显大于普通胶囊。
Hydroxypropyl methylcellulose (HPMC) was used as the main sustained release excipient of Naoluotong sustained release Capsules, and the formula was optimized by the orthogonal experimental design.
以羟丙甲基纤维素作为主要的缓释辅料，采用正交设计方法优化处方研制成脑络康缓释胶囊。
The capsules can be made to release the pesticides at a predetermined time.
可使这些胶囊在预定时间释放出杀虫剂。
When the polymer cracks, the capsules break open and release the healing agent, which becomes polymer solid and seals the crack and restores the material's properties.
当材料断裂，荚囊就会打开并释放出修复介体，介体变成实体的复合物填补裂缝从而恢复材料的特性。
RESULTS Hydroxypropyl cellulose is extensively used in tablets, capsules, mucous membrane adhesion preparation, sustained or controlled release preparation, and film coating, etc.
结果羟丙基纤维素在片剂、胶囊剂、黏膜黏附制剂、缓控释制剂等多种制剂以及薄膜包衣方面均有良好应用。
The results indicate that the higher the concentration of chitosan in the capsules, the slower the release rate of capsules.
结果表明，随着胶囊中壳聚糖浓度的增大，肝素的释放速率变慢。
Method: To determine the dissolution of the rifampicin gastric capsules by UV spectrum method and the release of rifampicin micro pill capsules by HPLC respectively.
方法：用高效液相色谱法与紫外分光光度法分别同时测定利福平胃溶胶囊的溶出度与利福平微丸胶囊的释放度。
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 results showed that the amount of HPMC and Carbomer had remarkable effects on the in vitro release of capsules.
结果表明羟丙甲纤维素与卡波姆对阻滞胶囊体外释放度影响较大。
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。
Aim To prepare Maodongqing sustained release pellet capsules and study the dissolution rate.
目的制备膜控释毛冬青缓释微丸胶囊并研究其体外释药性能。
Results of high performance liquid chromatography (HPLC) and bacterial inhibition tests indicated that the capsules release high concentrations of active vancomycin for up to 144 hours.
高效液相色谱分析法和抑菌试验结果表明，此种颗粒可释放高浓度活性万古霉素多达144小时。
The invention also includes capsules, soft capsules, controlled-release capsule, osmotic pump capsules or other proper types of preparation which are prepared through the medicine combination.
本发明也包括利用该药物组合物制备的硬胶囊、软胶囊、缓控释胶囊、渗透泵型胶囊或其他合适的剂型。
The invention also includes capsules, soft capsules, controlled-release capsule, osmotic pump capsules or other proper types of preparation which are prepared through the medicine combination.
本发明也包括利用该药物组合物制备的硬胶囊、软胶囊、缓控释胶囊、渗透泵型胶囊或其他合适的剂型。
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