体外释药速率符合一级动力学模型。
The in vitro release characteristics investigated fitted to first order pharmacokinetic model.
目的：研究香荷药条的体外释药特性。
OBJECTIVE To study the drug-releasing characteristics in vitro of Xianghe medicinal strip.
研制了二羟丙茶碱双层片并考察其体外释药特征。
The objective was to prepare the diprophylline double-layer tablet and study the factors affecting its dissolubility in vitro.
并考察脂质体的体外释药特性和体外抗肿瘤活性。
The release characteristics and anti-tumor activities of CCNU-TSL in vitro were investigated.
目的：研制萘普生肠溶微丸，评价其体外释药特性。
OBJECTIVE To develop naproxen enteric-coated pellets and evaluate its release characteristics in vitro.
以其为载体制备纳曲酮微球，比较了体外释药速率。
Invitro release of naltrexone microspheres prepared with the various PLGA were compared.
目的研究新藤黄酸骨架片体外释药速率的影响因素。
Objective To study the influential factors of the release rate of neogambogic acid from sustained release matrix tablets.
目的：制备氟比洛芬包衣小丸，评价其体外释药特性。
Objective: To prepare flurbiprofen coated pellets and evaluate its release characteristics in vitro.
结果：制备的黄杨宁渗透泵控释片体外释药速度较平稳。
Results:Preparation of Huangyangning osmotic pump controlled release tablets in vitro release rate of more stable.
目的制备氧化苦参碱缓释片剂，并评价其体外释药特性。
OBJECTIVE To prepare oxymatrine sustained-release tablets and evaluate the drag release property.
目的探讨羧甲基壳聚糖包药微球体的制备及体外释药特性。
Objective to prepare carboxymethyl chitosan microspheres of fluorouracil (FU-CMCS-MS), and measure the releasing of FU-CMCS-MS in vitro.
目的制备酒石酸托特罗定渗透泵片，考察其体外释药特性。
OBJECTIVE to prepare the tolterodine osmotic pump tablet and study its release profiles in vitro.
目的探讨羧甲基壳聚糖包药微球体的制备及体外释药特性。
Objective to study the release characteristics of fluorouracil-loaded carboxymethyl chitosan microspheres (Fu-CMCS-MS) in vitro.
结论：氟尿嘧啶微球体外释药以药物扩散和材料降解为主。
Conclusion: The fluorouracil release from microspheres with polylactic acid as carriers was controlled by drug diffusion and polymeric erosion.
结果：该处方、制备工艺简单，体外释药符合缓释片的规律。
RESULTS Prescription and process are simple and the in vitro drug released complied with relevant requirement.
目的制备阿昔洛韦缓释微丸，并对其体外释药情况进行研究。
Objective To prepare aciclovir sustained-release pellets and investigate the drug release mechanism in vitro.
目的：制备小剂量阿司匹林胃漂浮胶囊并研究其体外释药特征。
OBJECTIVE: to prepare aspirin gastric floating capsule and to study its in vitro drug-release characteristics.
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。
OBJECTIVE To predict drug release from the extended formulations by grey maths model.
目的研究磷酸川芎嗪丙烯酸树脂水分散体包衣缓释小丸的体外释药。
OBJECTIVE To study the dissolution profile of phosphate tetramethylpyrazine sustained release pellets coated with Eudragit pseudolatex.
目的制备盐酸氨溴索药物树脂复合物并对其体外释药动力学进行考察。
The drug release kinetics were also investigated in different releasing mediums(deionic water, 0.
目的制备度米芬渗透泵片，以控制体外释药维持零级释放达80%以上。
Objective To prepare Domiphen osmotic tablets of zero release above 80% in vitro.
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。
OBJECTIVE To prepare clindamycin hydrochloride microcapsule by means of intra liquid desiccation and to determine its in vitro drug release.
目的：考察影响双氯芬酸钠乙基纤维素水性分散体包衣片体外释药的因素。
OBJECTIVE:To study the factor of influencing drug release from diclofenac sodium(DS)tablet coated with ethylcellulose aqueous dispersion.
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。
METHODS The microcapsule was prepared using ethyl cellulose as coating material. The influencing factors of in vitro drug release were investigated by paddle method.
目的探讨对以羧甲基壳聚糖为载体的氟尿嘧啶微球体外释药特性的影响因素。
Objective to study the release characteristics of fluorouracil-loaded carboxymethyl chitosan microspheres (Fu-CMCS-MS) in vitro.
目的：比较退障凝胶与退障眼膏的体外释药特性，为研制退障凝胶提供依据。
Objective: to prepare Tuizhang gel to cure cataract, the characteristics of Tuizhang gel on the drug-releasing in vitro were evaluated by compared with Tuizhang oculentum.
目的探讨对以羧甲基壳聚糖为载体的氟尿嘧啶微球体外释药特性的影响因素。
Objective to prepare carboxymethyl chitosan microspheres of fluorouracil (FU-CMCS-MS), and measure the releasing of FU-CMCS-MS in vitro.
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 release characters in vitro of Vinpocetine self- microemulsifying drug delivery system (VIN-SEDDS).
以聚乳酸为载体材料制备阿奇霉素微球（AZMMS）并考察其体外释药特性。
To prepare microsphere containing Azithromycin(AZM) with polylactic acid, and investigate the characteristics of AZM microsphere (AZMMS)in vitro release.
目的制备酮咯酸氨丁三醇的海藻酸钠-壳聚糖微囊，对其体外释药特性进行考察。
OBJECTIVE To prepare ketorolac tromethamine(KT)alginate-chitosan microcapsules, and to investigated the behavior of KT microcapsules in vitro.
应用推荐