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- OBJECTIVE To study the preparation process,asssy and in vitro drug release of temozolomide polylactic-co-glycolic acid microspheres. 目的:对替莫唑胺聚乳酸-羟基醋酸微球的制备工艺、含量测定及体外释药特性进行初步研究。
- OBJECTIVE To 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。
- Objective To prepare docetaxel nanostructured lipid carriers (Docetaxel-NLC) and investigate their pharmaceutical properties and their in vitro drug release behavior. 目的 制备多西他赛纳米脂质载体,并考察其剂型性质及体外释药行为。
- Keywords Irinotecan hydrochloride;Liposome;In vitro drug release; 盐酸伊立替康;脂质体;体外释药;
- In vitro drug release of composite matrix transdermal delivery system 复合基质型经皮给药控释系统体外释放的传质规律
- IN VITRO DRUG RELEASE BEHAVIOR OF CARRIER MADE OF POROUS GLASS CERAMICS 多孔微晶玻璃作为缓释药物载体的体外实验研究
- Preparation and in Vitro Drug Release Behavior Study of Porous Phosphate Glass Ceramic 多孔微晶玻璃作为药物载体材料的制备及其体外释药研究
- Study on the preparation and in vitro drug release of gentamycin hemostasia collagen sponge 庆大霉素止血胶原海绵的制备及体外释放度
- In vitro drug release of enteric-coated sustained-release budesonide pellet and its residue drug amount in various intestine segments of rats 布地奈德肠溶缓释微丸的体外释药特性及其在大鼠各肠段的药物残余量
- Influence of PEG chain length on in vitro drug release and in vivo pharmacokinetics of hydroxycamptothecin(HCPT) loaded PEG-PHDCA niosomes 不同聚乙二醇相对分子质量对包载羟基喜树碱的PEG-PHDCA纳米囊泡 体外释放和体内药动学行为的影响
- Keywords Huperzine A;microspheres;poly(d;l-lactic acid)(PLA);l-lactic-co-glycollic acid)(PLGA);in vitro drug release; 石杉碱甲;微球;聚乳酸;聚乳酸聚乙醇酸共聚物;体外释放;
- Keywords Amsacrine;Solid lipid nanoparticles;Emulsification solvent evaporation method;Compritol 888 ATO;Lyophilization;In vitro drug release;Pharmacokinetics;Tissue distribution; 安吖啶;固体脂质纳米粒;乳化-溶剂挥发法;山嵛酸甘油酯;冷冻干燥;体外释放;药动学;组织分布;
- In vitro Drug release 体外释药
- Objective To prepare colchicine sustained-release pellets and investigate the drug release mechanism in vitro. 目的 制备秋水仙碱缓释微丸,并对其体外释药规律进行考察。
- Objective: To prepare nefopam hydrochloride sustained-release tablets and investigate the drug release in vitro. 目的:研制盐酸奈福泮缓释片,并考察其体外释放度。
- Objective To prepare paracetamol sustained-release pellets and investigate the drug release mechanism in vitro. 目的制备扑热息痛缓释微丸,并对其体外释药情况进行研究。
- OBJECTIVE To prepare thymopentin microspheres and investigate the drug release in vitro. 目的制备胸腺五肽微球并对其体外释放进行考察。
- Conclusion The nifedipine-PEG solid dispersion could accelerate the in vitro drug dissolution. 结论 硝苯地平PEG固体分散体能加快药物的体外溶出速率。
- OBJECTIVE To study the drug release mechanism of helicid(HD) bioadhesive sustained-release tablet and to determine the adhesive force in vitro. 目的研究生物黏附性神衰果素缓释片的体外释放度及释药规律,并测定其体外黏附力。
- We consider that in vitro drug sensitivity test could guide clinical vse of drug to get satisfactory efficacy. 体外药敏实验结果能指导临床用药,而且疗效较满意。