1) thin-film dispersion method
薄膜-振荡分散法
2) Film dispersion method
薄膜分散法
1.
Basing on the synthesis of pH-sensitive amphiphilic block copolymer poly(2-ethyl-2-oxazoline)-poly(D,L-lactide)(PEOz-PDLLA),this paper presents the preparation of docetaxel-loaded pH-sensitive block copolymer micelles using film dispersion method.
本文在合成pH敏感两亲性嵌段共聚物聚(2-乙基-2-噁唑啉)-聚乳酸(PEOz-PDLLA)的基础上,采用薄膜分散法制备多西他赛pH敏感嵌段共聚物胶束,利用芘荧光探针技术测定胶束的临界胶束浓度(CMC);通过高效液相色谱测定胶束的载药量及包封率;分别利用透射电镜、动态光散射法和zeta电位分析仪对胶束的形态、粒径和表面电位进行了表征;采用透析法考察了载药聚合物胶束的体外释放行为。
2.
Basing on the synthesis of pH-sensitive amphiphilic block copolymer Poly(2-ethyl-2-oxazoline)-Poly(D,L-lactide)(PEOz-PDLLA),this paper prepared docetaxel-loaded pH-sensitive block copolymer micelles using film dispersion method.
本文在合成pH敏感两亲性嵌段共聚物聚(2-乙基-2-噁唑啉)-聚乳酸(PEOz-PDLLA)的基础上,采用薄膜分散法制备了多西他赛pH敏感嵌段共聚物胶束,利用芘荧光探针技术测定胶束的临界胶束浓度(CMC);通过高效液相色谱测定胶束的载药量及包封率;分别利用透射电镜、动态光散射法和Zeta电位分析仪对胶束的形态、粒径和表面电位进行了表征;采用透析法考察了载药聚合物胶束的体外释放行为。
3) 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
4) 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。
5) Membrane-sonic method
薄膜超声分散法
1.
METHODS The sterically stabilized nanoliposomes were prepared with membrane-sonic method, the effect of some factors on the encapsulation efficiency, including lecithins, the weight ratio of bee venom to SPC, the weight ratio of SPC to chol,the pH of water phase, the electricity of lipids and the iron strength of water phase, was investigated.
方法采用薄膜超声分散法制备蜂毒多肽长循环脂质体,以包封率为指标,分别考察药脂比、胆固醇用量、磷脂种类、不同相对分子质量PEG-胆固醇、不同pH值、离子强度等对脂质体的影响,在此基础上采用正交设计[L9(4])]对处方进行优化。
6) film ultrasonic wave dissolving technique
薄膜超声分散法
1.
Methods:The ligustrazine solid lipid nanoparticles were prepared by film ultrasonic wave dissolving techniques,And the optimum formula was selected through orthogonal design test according to the entrapment efficiency.
方法:采用薄膜超声分散法制备,并以包封率为指标采用正交设计法优化川芎嗪固体脂质纳米粒的制备工艺。
2.
Methods:The ligustrazine solid lipid nanoparticles were prepared by film ultrasonic wave dissolving techniques,And the optimum formula was selected through orthogonal design test according to the entrapment efficiency oading.
方法:采用薄膜超声分散法制备,并以包封率为指标采用正交设计法优化川芎嗪口服固体脂质纳米粒的制备工艺。
3.
[Methods] The ligustrazine solid lipid nanoparticles were prepared by film ultrasonic wave dissolving techniques.
[方法]采用薄膜超声分散法制备,并以包封率为指标采用正交设计法优化川芎嗪固体脂质纳米粒的制备工艺。
补充资料：振荡培养法
分子式：
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CAS号：
性质：见摇瓶培养法。
分子量：
CAS号：
性质：见摇瓶培养法。
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