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1)  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。
2)  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。
3)  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。
4)  hot dispersion-ultrasonic technique
熔融超声分散法
1.
Method: To prepare solid lipid nanoparticles(SLN) loaded with Xionggui powder-supercritical carbon dioxide fluid extraction(XG-CO_2-SFE) using a hot dispersion-ultrasonic technique,establishing the best prescription of XG-CO_2-SFE-SLN through orthogonal design methods using entrapment efficiency of nanoparticles as index,and investig.
方法:采用熔融超声分散法制备芎归散超临界CO2萃取物固体脂质纳米粒混悬液,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;采用动态透析法考察其在不同介质中的释药特性。
5)  film-ultrasonic wave dissolving technique
薄膜-超声分散法
1.
Preparation of β-elemene solid lipid nanoparticles by film-ultrasonic wave dissolving techniques;
薄膜-超声分散法制备β-榄香烯固体脂质纳米粒
6)  film dispersion-ultrasonic
薄膜分散-超声法
1.
Methods The liposomes were prepared by film dispersion-ultrasonic and reverse phase evaporation technique.
方法薄膜分散-超声法、逆相蒸发法制备脂质体,HPLC测定硫酸多黏菌素E脂质体包封率,正交设计法优化脂质体处方。
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