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.
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。
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.
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.
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.
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