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.
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.
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.
本发明公开了该缓释制剂的体外释药特性及制备方法。
The invention also provides relative external releaser character and preparation.
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.
目的制备磷酸苯丙哌林缓释微丸,评价其体外释药特性。
Objective To prepare benproperine phosphate sustained-release pellets and study its release characteristics.
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 study the preparation technique and in vitro drug release of adriamycin gelatin microspheres (ADM-GMS).
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。
OBJECTIVE To study the preparation process, assay and in vitro drug release of adriamycin polylactic acid microspheres.
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.
目的制备盐酸昂丹司琼渗透泵型控释片剂(OND - OPT)并考察体外释药特性。
Aim To prepare ondansetron hydrochloride osmotic pump tablets (OND-OPT) and investigate their in vitro drug release behavior.
目的优化冬凌草甲素聚乳酸纳米粒的制备工艺,并对其理化性质和体外释药特性进行考察。
OBJECTIVE To optimize the preparation method of the oridonin-loaded polylactic-acid nanoparticles, and investigate its properties and release behavior in vitro.
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 drug loading rate, encapsulation efficiency, particle distribution and in vitro release of Lac-NCTD from liposomes were investigated, respectively.
目的建立卡铂热敏脂质体包封率和含量测定方法,并对其体外热敏释药特性进行考察。
OBJECTIVE To establish a method for determining carboplatin content and entrapment efficiency of thermo-sensitive liposomes and to study temperature-sensitive release property in vitro.
以盐酸维拉帕米为模型药物,制备了口服渗透泵片。通过考察渗透泵片体外释药各过程的速率,研究口服渗透泵制剂释药的基本过程及其特性。
The main processes of the drug delivery of oral osmotic pump system were studied to investigate its delivery characteristics, with verapamil hydrochloride as the model drug.
本发明公开了该缓释制剂的体外释 药特性及制备方法。
The invention discloses in vitro drug release characteristics and preparation method thereof.
本发明公开了该缓释制剂的体外释 药特性及制备方法。
The invention discloses in vitro drug release characteristics and preparation method thereof.
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