1) emulsification dispersion-ultrasonication
乳化分散-超声法
1.
Methods IB-SLNs were prepared by an emulsification dispersion-ultrasonication method.
方法采用乳化分散-超声法制备布洛芬固体脂质纳米粒,以包封率为评价指标,进行正交实验筛选最优处方,并对最优处方的外观、粒径、zeta电位和体外释放度进行考察;以兔关节肿胀度和兔体内抗卵清蛋白抗体的效价为指标对药效学进行评价。
2) microemulsion ultrasonication method
微乳超声分散法
1.
Method:Prepared nanostructured lipid carriers (NLC) loaded with supercritical carbon dioxide fluid extraction of Xionggni powder (XG-CO_2-SFE) with a microemulsion ultrasonication method,established the best prescription of XG-CO_2-SFE-NLC by orthogonal design methods with entrapment efficiency of nanoparticles as index,and investigated their physicochemical characterizations.
方法:采用微乳超声分散法制备芎归散超临界CO_2萃取物纳米结构脂质载体混悬液,以总苯酞的含量作为工艺研究中包封率的评价指标,以包封率为考察指标,采用正交试验筛选最佳处方,并考察其物理化学性质。
3) Ultrasonic emulsification-solvent diffusion method
超声乳化溶剂扩散法
4) supersound method
超声乳化法
1.
Vc liposomes were prepared by the supersound method with glyceryl dilaurate as synthetic materials.
以自制月桂酸甘油酯为原料,选择超声乳化法制备了抗坏血酸类脂质体。
5) ultrasonic technique
超声分散法
1.
Objective To prepare solid lipid nanoparticles containing praziquantel(PZQ-SLN) by ultrasonic technique,and investigate the main factors in the process of preparing PZQ-SLN.
目的采用超声分散法制备吡喹酮固体脂质纳米粒,并考察制备过程中的主要影响因素。
2.
Aim To prepare solid lipid nanoparticles (SLN) loaded with all-trans retinoic acid using an ultrasonic technique with Compritol 888 ATO as matrix material, and investigate properties of nanoparticles in vitro and in vivo.
目的 以山嵛酸甘油酯(Compritol888ATO)为脂质材料,采用超声分散法制备维甲酸固体脂质纳米粒,并考察其体内外性质。
6) film-dispersion and hydration-sonication method
薄膜分散-水化超声法
1.
METHODS PEG-PHDCA niosomes were prepared by film-dispersion and hydration-sonication method and lyophilized.
方法采用薄膜分散-水化超声法制备了羟基喜树碱的PEG-PHDCA纳米囊泡,在研究该纳米囊泡的形态、粒径、载药量、包封率、冷冻干燥工艺后对其体外释药特征及体内药动学参数进行测定。
补充资料：微乳
分子式：
CAS号：
性质：见微乳液。
CAS号：
性质：见微乳液。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条